Contents

1 Oil and Gas Resources and Reserves 7
1.1 Terminology and Definitions . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
1.2 Methods for Resources/Reserve Estimation . . . . . . . . . . . . . . . . . . . 9
1.2.1 Analogy-Based Approach . . . . . . . . . . . . . . . . . . . . . . . . 9
1.2.2 Volumetric Estimates . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
1.2.3 Performance Analysis . . . . . . . . . . . . . . . . . . . . . . . . . . 11
I Fundamentals 15
2 Basic Concepts of Petroleum Geology 17
2.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
2.2 The Basic Concepts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
2.2.1 Clastic Sedimentary Rocks . . . . . . . . . . . . . . . . . . . . . . . . 18
2.2.2 Nonclastic Sedimentary Rocks . . . . . . . . . . . . . . . . . . . . . . 19
2.3 The Origin and Habitat of Petroleum . . . . . . . . . . . . . . . . . . . . . . . 20
2.3.1 Source Rock and Generation of Petroleum . . . . . . . . . . . . . . . . 20
2.3.2 Petroleum Migration and Accumulation . . . . . . . . . . . . . . . . . 23
2.3.3 Classification of Petroleum Reservoir-Forming Traps . . . . . . . . . . 24
2.4 Types of Hydrocarbon Traps on the Norwegian Continental Shelf . . . . . . . . 28
3 Basic Concepts and Definitions
in Reservoir Engineering 31
3.1 Continuum Mechanics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
3.2 Porosity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
3.3 Saturation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
3.3.1 Residual Saturation . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
3.3.2 Laboratory Determination of Residual Oil and Water Saturation . . . . 34
3.4 Reservoir Pressure and Distribution of Fluid Phases. . . . . . . . . . . . . . . . 38
3.5 Pressure Distribution in Reservoirs . . . . . . . . . . . . . . . . . . . . . . . . 40
3.6 Exercises . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44
4 Porosity 45
4.1 General Aspects . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
4.2 Models of Porous Media . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
4.2.1 Idealised Porous Medium Represented by Parallel Cylindrical Pores . . 46
i
4.2.2 Idealised Porous MediumRepresented by Regular Cubic-Packed Spheres
47
4.2.3 Idealised Porous MediumRepresented by Regular Orthorhombic-Packed
spheres . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47
4.2.4 Idealised Porous MediumRepresented by Regular Rhombohedral-Packed
spheres . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48
4.2.5 Idealised Porous Medium Represented by Irregular-Packed Spheres
with Different Radii . . . . . . . . . . . . . . . . . . . . . . . . . . . 48
4.3 Porosity Distribution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50
4.4 Measurement of Porosity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50
4.4.1 Full-Diameter Core Analysis . . . . . . . . . . . . . . . . . . . . . . . 50
4.4.2 Grain-Volume Measurements Based on Boyle’s Law . . . . . . . . . . 51
4.4.3 Bulk-Volume Measurements . . . . . . . . . . . . . . . . . . . . . . . 53
4.4.4 Pore-Volume Measurement . . . . . . . . . . . . . . . . . . . . . . . . 54
4.4.5 Fluid-Summation Method . . . . . . . . . . . . . . . . . . . . . . . . 55
4.5 Uncertainty in Porosity Estimation . . . . . . . . . . . . . . . . . . . . . . . . 57
4.6 Porosity Estimation from Well Logs . . . . . . . . . . . . . . . . . . . . . . . 58
4.7 Exercises . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60
5 Permeability 63
5.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63
5.2 Darcy’s Law . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63
5.3 Conditions for Liquid Permeability Measurements. . . . . . . . . . . . . . . . 68
5.4 Units of Permeability . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 69
5.5 Gas Permeability Measurements . . . . . . . . . . . . . . . . . . . . . . . . . 71
5.5.1 Turbulent Gas Flow in a Core Sample . . . . . . . . . . . . . . . . . . 74
5.6 Factors Affecting Permeability Values . . . . . . . . . . . . . . . . . . . . . . 76
5.6.1 The Klinkenberg Effect . . . . . . . . . . . . . . . . . . . . . . . . . . 76
5.7 Exercises . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 79
6 Wettability and Capillary Pressure 83
6.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 83
6.2 Surface and Interfacial Tension . . . . . . . . . . . . . . . . . . . . . . . . . . 83
6.3 Rock Wettability . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 84
6.4 Contact Angle and Interfacial Tension . . . . . . . . . . . . . . . . . . . . . . 86
6.5 Capillary Pressure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 88
6.5.1 Capillary Pressure Across Curved Surfaces . . . . . . . . . . . . . . . 88
6.5.2 Interfacial Tension . . . . . . . . . . . . . . . . . . . . . . . . . . . . 90
6.5.3 Capillary Pressure in a Cylindrical Tube . . . . . . . . . . . . . . . . . 90
6.6 Capillary Pressure and Fluid Saturation . . . . . . . . . . . . . . . . . . . . . 93
6.7 Pore Size Distribution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 95
6.8 Saturation Distribution in Reservoirs . . . . . . . . . . . . . . . . . . . . . . . 98
6.9 Laboratory Measurements of Capillary Pressure . . . . . . . . . . . . . . . . . 101
6.10 Drainage and Imbibition Processes. . . . . . . . . . . . . . . . . . . . . . . . 103
6.10.1 Hysterisis in Contact Angle . . . . . . . . . . . . . . . . . . . . . . . 105
6.10.2 Capillary Hysterisis . . . . . . . . . . . . . . . . . . . . . . . . . . . . 105
ii
6.11 Exercises . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 107
7 Relative Permeability 111
7.1 Definitions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 111
7.2 Rock Wettability and Relative Permeabilities . . . . . . . . . . . . . . . . . . 113
7.3 Drainage/Imbibition Relative Permeability Curves . . . . . . . . . . . . . . . . 114
7.4 Residual Phase Saturations . . . . . . . . . . . . . . . . . . . . . . . . . . . . 115
7.5 Laboratory Determination of Relative Permeability Data . . . . . . . . . . . . 116
7.6 Exercises . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 118
8 Compressibility of Reservoir Rock and Fluids 121
8.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 121
8.2 Compressibility of Solids, Liquids and Gases . . . . . . . . . . . . . . . . . . 121
8.2.1 Rock Stresses and Compressibility . . . . . . . . . . . . . . . . . . . . 122
8.2.2 Compressibility of Liquids . . . . . . . . . . . . . . . . . . . . . . . . 125
8.2.3 Compressibility of Gases . . . . . . . . . . . . . . . . . . . . . . . . . 126
8.3 Deformation of Porous Rock . . . . . . . . . . . . . . . . . . . . . . . . . . . 128
8.3.1 Compressibility Measurements. . . . . . . . . . . . . . . . . . . . . . 129
8.3.2 Betti’s Reciprocal Theorem of Elasticity. . . . . . . . . . . . . . . . . 130
8.4 Compressibility for Reservoir Rock Saturated with Fluids . . . . . . . . . . . . 131
8.5 Exercises . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 134
9 Properties of Reservoir Fluids 135
9.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 135
9.2 Definitions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 136
9.3 Representation of hydrocarbons . . . . . . . . . . . . . . . . . . . . . . . . . 137
9.3.1 Ternary diagrams . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 140
9.4 Natural gas and gas condensate fields . . . . . . . . . . . . . . . . . . . . . . 142
9.5 Oil fields . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 143
9.6 Relation between reservoir and surface volumes . . . . . . . . . . . . . . . . . 144
9.7 Determination of the basic PVT parameters . . . . . . . . . . . . . . . . . . . 148
9.8 Exercises . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 150
II Reservoir Parameter Estimation Methods 153
10 Material Balance Equation 155
10.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 155
10.2 Dry gas expansion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 156
10.3 A general oil reservoir . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 157
10.3.1 A1: Expansion of oil . . . . . . . . . . . . . . . . . . . . . . . . . . . 158
10.3.2 A2: Expansion of originally dissolved gas . . . . . . . . . . . . . . . . 159
10.3.3 B: Expansion of gas cap gas . . . . . . . . . . . . . . . . . . . . . . . 159
10.3.4 C: Reduction in HCPV due to expansion of connate water and reduc-
tion of pore volume . . . . . . . . . . . . . . . . . . . . . . . . . . . . 160
10.3.5 Production terms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 161
10.4 The material balance equation . . . . . . . . . . . . . . . . . . . . . . . . . . 161
iii
10.5 Linearized material balance equation . . . . . . . . . . . . . . . . . . . . . . . 161
10.6 Dissolved gas expansion drive . . . . . . . . . . . . . . . . . . . . . . . . . . 162
10.7 Gas cap expansion drive . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 165
10.8 Water influx . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 167
10.9 Exercises . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 170
11 Well Test Analysis 173
11.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 173
11.1.1 Systems of Uunits Used in Well Test Analysis . . . . . . . . . . . . . . 174
11.2 Wellbore Storage Period . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 175
11.3 Semi Logarithmic Period . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 177
11.3.1 Diffusivity Equation . . . . . . . . . . . . . . . . . . . . . . . . . . . 177
11.3.2 Solution of the Diffusitivity Equation . . . . . . . . . . . . . . . . . . 178
11.3.3 Gas Reservoir . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 180
11.3.4 The Solution of the Diffusitivity Equation in Dimensionless Form . . . 181
11.3.5 Wellbore Pressure for Semi Logarithmic Data . . . . . . . . . . . . . . 181
11.4 Semi Steady State Period . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 184
11.4.1 Average Reservoir Pressure . . . . . . . . . . . . . . . . . . . . . . . 185
11.4.2 Well Skin Factor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 186
11.4.3 Wellbore Pressure at Semi Steady State . . . . . . . . . . . . . . . . . 187
11.5 Wellbore Pressure Solutions . . . . . . . . . . . . . . . . . . . . . . . . . . . 188
11.5.1 Transition Time Between Semi Logarithmic Period and Semi Steady
State Period . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 189
11.5.2 Recognition of Semi Logarithmic Data . . . . . . . . . . . . . . . . . 189
11.6 Exercises . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 190
12 Methods of Well Testing 193
12.1 Pressure Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 193
12.2 Pressure Drawdown Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 194
12.2.1 Pressure Drawdown Test Under Semi Logarithmic Conditions . . . . . 195
12.2.2 Pressure Drawdown Test Under Semi Steady State Conditions . . . . . 196
12.3 Pressure Build-Up Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 197
12.4 Pressure Test Analysis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 199
12.4.1 Miller - Dyes - Hutchinson (MDH) Analysis . . . . . . . . . . . . . . 199
12.4.2 Matthews - Brons - Hazebroek (MBH) Analysis (Horner plot) . . . . . 201
12.5 Exercises . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 205
iv
Preface
The topics covered in this book represent a review of modern approaches and practical methods
for analysing various problems related to reservoir engineering.
This textbook, part I Fundamentals and part II Reservoir Parameter Estimation Meth-
ods, constitutes the main content of the book. The subjects presented, are based on the course
of lectures in Reservoir Engineering 1 held by the authors at the Rogaland University Centre
in the period from 1989 to 1995. Part III Fluid Flow in Porous Media and part IV Enhanced
Oil Recovery are a collection of subjects extending the fundamental knowledge into areas of
more advanced theoretical description. The last part VProjects Exercises presents quite a few
exercises of the type students are asked to solve at their examination test.
The book contains a short introduction to important definitions for oil and gas reservoirs
(Chapter 1). The two main parts of the book is related to petro-physics (Chapter 2 to 10), and
related to two important methods in Reservoir Engineering, namely Material Balance (Chapter
11) and Well Testing (Chapter 12, 13 and 14). Modelling of fluid flow in porous media is pre-
sented through different examples using various mathematical techniques (Chapter 15 to 20).
Classification and description of several methods used in enhanced oil recovery are associated
with examples for oil and gas fields in the North Sea (Chapter 21 to 27)
The Preface contains a list of some of the most commonly used parameters and systems of
units used in petroleum engineering.
In Chapter 1 some basic definitions of gas and oil reserves are given and the methods of
their evaluation.
Chapter 2 is a brief introduction to the basics of petroleum geology, with some illustra-
tive examples relevant to the Norwegian Continental Shelf. This chapter contains some basic
concepts and definitions related to the origin, habitat and trapping of petroleum
In Chapter 3 some basic concepts and definitions used in Reservoir Engineering are pre-
sented. Some laboratory techniques are explained and examples of equipment are shown. A
short description of reservoir pressure distribution is also presented.
Chapter 4 introduces porosity and some examples of experimental techniques used to
estimate porosity. Some examples describing the method of error propagation are also given.
Permeability is introduced in Chapter 5. A short deduction of Darcy’s law is given and
some examples of its use is described. Measurements of gas permeability is exemplified and
together with laminar and turbulent gas flow, some additional factors affecting permeability are
discussed.
In Chapter 6, viscosity is introduced and some basic equations, describing laminar fluid
flow are derived. Examples of different viscosity measuring techniques are discusses and some
flow characteristics are mentioned.
1
2
Wettability and capillary pressure are discussed in Chapter 7. In this chapter we intro-
duce the term surface energy to replace interfacial tension and an important relation between
surface energies are derived. Examples of the effect of capillary forces are given and different
experimental techniques are discussed.
Relative permeability is introduced briefly inChapter 8. There has been no attempt made,
to give a broad and consistent description of relative permeability in this book. The chapter is
meant as an introduction to basic concepts of relative permeability and possibly an inspiration
for further reading.
In Chapter 9, some basic aspects of compressibility related to reservoir rock and fluids are
introduced. Examples are related to the behaviour of porous reservoir rocks and core samples
under laboratory conditions.
Chapter 10 lists some basic definitions and properties related to reservoir fluids. Volume-
factors and other important relations are explained and examples of their use are given.
The Material Balance Equation is deduced inChapter 11. The equation is applied in sev-
eral examples, describing different types of reservoirs, such as gas-reservoir and oil- reservoirs
with and without a gas cap.
Well test analysis is introduced in Chapter 12. A somewhat simplified derivation of the
pressure solution for three important production periods are presented, i.e., the wellbore storage
period, the semi-logaritmic period and the semi-steady state period. Dimension-less parameters
are used and the set of pressure solutions are presented.
Chapter 13 introduces some basic methods of well testing, like drawdown test, build-up
test and combinations of the two, are presented. Examples of two "classical" well test analysis
is also included.
Modern well test analysis, like transient testing techniques, is presented inChapter 14.
Use of type curves and matching techniques are shortly presented.
Part III Fluid Flow in Porous Media gives an introduction to mathematical modelling
of oil displacement by water-flooding. This part presents a broad classification of models
describing fluid flow in porous media. Basic principles behind equations of Buckley- Leverett
theory and their application are presented, as well as various analytical solution techniques.
Some few exercises are included at the end of this part.
Enhanced Oil Recovery is presented in part IV. A basic mathematical description of EOR
methods are given and various methods are classified. Examples of polymer flooding is pre-
sented as well as EOR related to surfactants and different solvents. Various techniques using
WAG, foams and Microbial methods are also briefly described.
Most chapters in part I and II contain several exercises, illustrating the concepts and meth-
ods presented, while all exercises in part III and IV are added at the end.
This book does not contain complicated mathematical equations or calculus. The math-
ematical prerequisite required are minimal, though necessary. The student should know the
elements of matrix and linear algebra, probability theory and statistics, and also be acquainted
with single and partial-differential equations and methods of their solution. In part III and IV,
however some slightly more advanced mathematical formalism is used.
A reference list is given at the end of the book. The book does not cover all the relevant
literature, nor is the reference list intended to be a complete bibliography. Only some necessary
references and key publications are included in the reference list.
3
J.-R. Ursin & A. B. Zolotukhin
Stavanger, 1997
4
Units and conversion factors
The basic knowledge of units and conversion factors is absolutely necessary in reservoir engi-
neering, although the choice of industrial units depend on company, country or simply tradition.
Since the choice of units has been largely a question of preference, the knowledge of conversion
factors is practical necessary.
English and American units are most commonly used in the petroleum industry, but there is
a tendency to turn to SI-units or practical SI-units, especially in the practice of the Norwegian
and the other European oil companies.
In this book we will use both SI-units and industrial units in explaining the theory as well
as in examples and in exercises. Since both set of units are widely used in the oil industry, it is
important to be confident with both systems, -simply due to practical reasons.
A selection of some of the most frequently used parameters are listed in the table below.
The Metric unit is seen as a practical SI-unit, often used in displaying data or calculations.
Metric unit = Conversion factor Industry unit,
i.e. metric unit is found by multiplying a given industry unit by an appropriate conversion
factor.
5
Parameter (SI unit) Industry unit Conversion factor Metric unit
Area, m
2
sq mile 2.589988 km
2
acre 4046.856 m
2
sq ft 0.09290304 m
2
sq in. 6.4516 cm
2
Compressibility, Pa
−1
psi
−1
0.1450377 kPa
−1
Density, kg/m
3
g/cm
3
1000.0 kg/m
3
lbm/ft
3
16.01846 kg/m
3
o
API 141.5/(131.5 +
o
API) (γ
sg
)

Flow rate, m
3
/s bbl/d 0.1589873 m
3
/d
ft
3
/d 0.02831685 m
3
/d
Force, N lbf 4.448222 N
pdl 138.2550 mN
dyne 0.01 mN
Length, m mile 1.609344 km
ft 30.48 cm
in. 2.54 cm
Pressure, Pa atm 101.325 kPa
bar 100.0 kPa
lbf/in.
2
(psi) 6.894757 kPa
mm Hg (0
o
C) 1.333224 kPa
dyne/cm
2
0.1 Pa
Mass, kg ton 1000 kg
lbm 0.4535924 kg
Temperature, K
o
C + 273.15 K
o
F (
o
F-32)/1.8
o
C
R 5/9 K
Surface tension, N/m dyne/cm 1.0 mN/m
Viscosity, Pas cp (poise) 0.001 Pas
Volume, m
3
acre-ft 1233.489 m
3
cu ft 0.02831685 m
3
bbl 0.1589873 m
3
U.S. gal 3.785412 dm
3
liter 1.0 dm
3

Spesific gravity of oil.
6
Chapter 1
Oil and Gas Resources and Reserves
1.1 Terminology and Definitions
In the period from 1936 to 1964, the American Petroleum Institute (API) set some guiding stan-
dards for the definition of proved reserves. They were presented in a joint publication of API
and the American Gas Association (AGA), "Proved reserves of crude oil, natural gas liquids
and natural gas", in 1946. In 1964, the Society of Petroleum Engineers (SPE) recommended
reserve definitions following the revised API definitions. In 1979, the U.S. Security and Ex-
change Commission (SEC) issued a newer set of definitions, whereby also the SPE definitions
were updated in 1981. In 1983, the World Petroleum Congress issued a set of petroleum reserve
definitions, which included categories ranging fromproved to speculative reserves [2].
Fig. 1.1 shows a conceptual scheme of the oil and gas resources and reserves, where the
following definitions are used [2]:
Reserves are estimated volumes of crude oil, condensate, natural gas, natural
gas liquids, and associated substances anticipated to be commercially recoverable
from known accumulations from a given date forward, under existing economic
conditions, by established operating practices, and under current government regu-
lations. Reserve estimates are based on geologic and/or engineering data available
at the time of estimate.
The relative degree of an estimated uncertainty is reflected by the categorisation of reserves
as either "proved" or "unproved"
Proved Reserves can be estimated with reasonable certainty to be recoverable
under current economic conditions. Current economic conditions include prices
and costs prevailing at the time of the estimate.
Reserves are considered proved is commercial producibility of the reservoir is
supported by actual engineering tests.
Unproved Reserves are based on geological and/or engineering data similar to
those used in the estimates of proved reserves, but when technical, contractual,
economic or regulatory uncertainties preclude such reserves being classified as
proved. They may be estimated assuming future economic conditions different
from those prevailing at the time of the estimate.
7
8 Chapter 1. Oil and Gas Resources and Reserves
Undiscoveed
Nonrecoverable
Resources
Recoverable
Resources
Reserves
Cumulative
Production
Proved
Reserves
Unproved
Reserves
Probable
Reserves
Possible
Reserves
Discovered
Total Oil and Gas Resource
Figure 1.1: Conceptual scheme for oil and gas resources and re-
serves.
Unproved reserves may further be classifiedprobable and possible, see Fig. 1.1.
Probable Reserves are less certain than proved reserves and can be estimated with
a degree of certainty sufficient to indicate they are more likely to be recovered than
not.
Possible Reserves are less certain than proved reserves and can be estimated with
a low degree of certainty, insufficient to indicate whether they are more likely to
be recovered than not.
The estimation of reserves will depend upon the actual mode of petroleum recovery, which
may involve either a natural-drive mechanism improved by water or gas injection, or some
special technique of enhanced oil recovery (EOR).
In general, "possible" reserves may include:
• Reserves suggested by structural and/or stratigraphic extrapolation beyond areas classi-
fied as probable, based on geological and/or geophysical interpretation.
• Reserves in rock formations that appear to be hydrocarbon-bearing based on logs or
cores, but may not be productive at a commercial level.
• Incremental reserves based on infill drilling are subject to technical uncertainty.
1.2 Methods for Resources/Reserve Estimation 9
• Reserves attributable to an improved or enhanced recovery method when a pilot project
is planned (but not in operation) and the rock, fluid and reservoir characteristics are such
that a reasonable doubt exists whether the estimated reserves will be commercial.
• Reserves in a rock formation that has proved to be productive in other areas of the field,
but appears to be separated from those areas by faults and the geological interpretation,
indicates a relatively low structurally position.
1.2 Methods for Resources/Reserve Estimation
1.2.1 Analogy-Based Approach
Another producing reservoir with comparable characteristics can be used as a possible analogue
for the reservoir under consideration, either by a direct well-to-well comparison or on a unit-
recovery basis. This can be done by determining an average oil or gas recovery per well in
the analogue reservoir (e.g., 100,000 bbl/well) and applying a similar or adjusted recovery
factor to the wells in the reservoir considered. The unit-recovery approach refers to a recovery
calculated in barrels per acre-foot or Mcf per acre-foot.
In an analogue approach, one has to consider similarities of well spacing, reservoir rock
lithofacies, rock and fluid properties, reservoir depth, pressure, temperature, pay thickness and
drive mechanism. All possible differences between the analogue reservoir and the reservoir in
question need to be considered to make a realistic adjustment of the recovery estimates.
The use of an analogue may be the only method available to estimate the reserves in a situ-
ation where there are no solid data on well performance or reservoir characteristics. However,
an analogue-based approach is also the least accurate and little reliable method of petroleum
reserve estimation, simply because perfect analogues can seldom be found.
1.2.2 Volumetric Estimates
The methods of reserve estimation based on reservoir data are volumetric and can be divided
into deterministic and probabilistic (stocastic) estimates. The main difficulty in a volumetric
estimate of resources/reserves is in the transfer of data obtained at a small scale (core analysis,
lithofacies data, well logs, etc.) into a much larger scale ( i.e. data "upscaling" for interwell
space).
Deterministic Methods
The principle of a deterministic approach to resources/reserve estimates is to "upscale" the
information derived from the wells and supported by seismic survey, into the interwell space
by using an interpolation technique.
The main parameters used for a volumetric estimate in this approach are:
• The reservoir "gross" isopach map, which means the bulk thickness of the reservoir rocks
(formation).
• The reservoir "net" isopach map, which means the cumulative thickness of the permeable
rock units only. The Net-to-Gross ratio (N/G) is an important parameter indicating the
productive portion of the reservoir.
10 Chapter 1. Oil and Gas Resources and Reserves
• The reservoir rock porosity (as a volume-based weighed average):
φ =

i
φ
i
A
i
h
i

i
A
i
h
i
,
where φ is the local porosity, A
i
is a subarea and h
i
is a subthickness (of permeable rock).
• The permeability and net-thickness product (kh
N
) is important for the estimation of well
production capacity:
(kh
N
) = h
N

i
k
i
h
i

i
h
i
=
N
G

i
k
i
h
i
,
where k
i
is the local permeability (other symbols as above).
• Volume-based average saturation of water, gas and oil. For example water saturation:
S
w
=

i
S
wi
φ
i
A
i
h
i

i
φ
i
A
i
h
i
.
Plotting these parameters as contoured maps (isopachs, isoporosity, isopermeability, etc.)
provides the crucial information on their variation and distribution in the reservoir and makes
it possible to evaluate the reservoir pore volume and its fractions saturated with oil and gas
(hydrocarbon volume). The numerical value of hydrocarbon resources/reserve estimate their
represents an outcome of "integrated" map analysis.
Stochastic Methods
An alternative approach is a probabilistic estimation of resources/reserves, which takes more
account of the estimate uncertainty. Stochastic reservoir description is usually based on the pro-
cedure of random-number generator. This numerical technique assumes that the main reservoir
properties (porosity, permeability, N/G, ect.) all have random, possibly normal, frequency dis-
tributions, with the range of values included by core and well-log data. The maximum and
minimum values are specified for each of the reservoir parameters and the random number
generator then "drowns data", so to speak, and then simulates their actual density distribution
in the whole reservoir.
In practice, it is necessary to repeat the stochastic simulation for different "seeds" (initial
boundary values) in order to asses and quantify the actual variation of a given parameter. Each
numerical realisation bears an uncertainty for the reservoir characterisation, where the prob-
abilistic rather than deterministic, is an estimate of resources/reserves. Different realisations
lead to different volumetric estimates, with different probabilities attached. The cumulative
frequency distributions of these estimates, that is used to asses their likelihood will be a very
unclear formulation. See Fig. 1.2.
In common usage [8] we have:
– An estimate with 90 % or higher probability is the level regarded as aproven value.
– An estimate with 50 % or higher probability is the level regarded as aproven + probable
value.
1.2 Methods for Resources/Reserve Estimation 11
F
r
e
q
u
e
n
c
y

o
f

c
u
m
u
l
a
t
i
v
e
p
r
o
b
a
b
i
l
i
t
y
Value Min Max
0.0
1.0
Probability, that a given
value of resources will
be at least as great
as shown
F
r
e
q
u
e
n
c
y
Min Max Value
Figure 1.2: Example of stochastic volumetric estimate based on a se-
ries of random-number simulations.
– An estimate with 10 % or higher probability is the level regarded as aproven +probable
+ possible value.
As more information on the reservoir becomes available, the cumulative frequency graph
may change its shape and the uncertainty of our resource/reserve estimates may decrease, see
Fig. 1.3.
More generally, the problem of certainty can be considered in terms of "fuzzy" [61], prob-
abilistic and deterministic estimates based on the data available at a particular time, as seen
in Fig. 1.4. A comparison of these estimates may be more revealing that each of them is in
isolation.
At the very early stages of field appraisal, the data are usually too limited for using statis-
tical analysis and, hence, a fuzzy estimate of the resources/reserves may be best or only option
[22, 28, 56]. The lack or scarsity of data in such cases is compensated by a subjective assess-
ment of the reservoir characteristics (i.e. the shape of the distribution and the maximum and
minimum values of a given reservoir parameter), Based on the knowledge from other reservoirs
or simply a theoretical guess. A rectangular distribution means no preference and a triangular
distribution means that strong preference distributions are used.
When more data have been collected and statistical analysis becomes possible, aprobabilis-
tic estimate can be made. The range in the possible values of the reservoir parameters would
then be narrower, compared to a fuzzy assessment. When the data available are abadundant, a
deterministic estimate can be made based on a well- specified value of a particular parameter
for a particular part (zone, subunit or layer) of the reservoir.
1.2.3 Performance Analysis
The methods of performance analysis presently used include:
• Analysis based on Material Balance Equation (MBE) [33, 34].
• Reservoir Simulation Models (RSM) [10, 45].
12 Chapter 1. Oil and Gas Resources and Reserves
F
r
e
q
u
e
n
c
y
o
f
c
u
m
u
l
a
t
i
v
e
p
r
o
b
a
b
i
l
i
t
y
Value Min Max
0.0
1.0
F
r
e
q
u
e
n
c
y
o
f
c
u
m
u
l
a
t
i
v
e
p
r
o
b
a
b
i
l
i
t
y
Value Min Max
0.0
1.0
F
r
e
q
u
e
n
c
y
o
f
c
u
m
u
l
a
t
i
v
e
p
r
o
b
a
b
i
l
i
t
y
Value Min Max
0.0
1.0
F
r
e
q
u
e
n
c
y
o
f
c
u
m
u
l
a
t
i
v
e
p
r
o
b
a
b
i
l
i
t
y
Value Min Max
0.0
1.0
F
r
e
q
u
e
n
c
y
o
f
c
u
m
u
l
a
t
i
v
e
p
r
o
b
a
b
i
l
i
t
y
Value Min Max
0.0
1.0
F
r
e
q
u
e
n
c
y
o
f
c
u
m
u
l
a
t
i
v
e
p
r
o
b
a
b
i
l
i
t
y
Value Min Max
0.0
1.0
Pre-drilling Discovery Appraisal
Delineation/
early production
Mature
production
Late time
depletion
Figure 1.3: Changes in the uncertainty resources estimate with in-
creasing data acquisition (after Archer and Wall, 1992).
• Decline Curve Analysis (DCA) [53].
The aim of all of these methods is to obtain the best reservoir performance prediction on
the basis of available data.
The MBE method is based on the data obtained from previous reservoir performance and
PVT analysis, but involves some assumptions for the reservoir driving mechanism in order
to minimise the range of possible predictions from the dataset. The method is thus adjusted
differently to reservoirs containing oil, gas or oil with a gas cap (primary or secondary).
The RSM method involves a numerical simulation technique, with the matching of the
production and the reservoir’s previous performance (history). The discrepancy between the
simulation results (prediction) and the available data is minimised by adjusting the reservoir
parameters and taking into account the most likely reservoir drive mechanism (history match).
The DCA method is to predict future performance of the reservoir by matching the ob-
served trend of the production decline with one or several standard mathematical methods of
the production rate-time (hyperbolic, harmonic, exponential, ect.). If successful, such a perfor-
mance analysis allows to estimate both the reserves and the future performance of the reservoir.
The following "decline curves" from production wells are commonly used in the DCA:
– Production rate vs. time.
– Production rate vs. cumulative oil production.
– Water cut vs. cumulative oil production.
1.2 Methods for Resources/Reserve Estimation 13
F
r
e
q
u
e
n
c
y

o
f

c
u
m
u
l
a
t
i
v
e
p
r
o
b
a
b
i
l
i
t
y
Value
0.0
1.0
M.L.V V.P.V
V.O.V
Fuzzy
Probabilistic
Deterministic
Figure 1.4: The concept of uncertainty in resources/reserves estima-
tion illustrated by fuzzy, probabilistic and deterministic
approach (data set).
– Gas-oil ratio vs. cumulative production.
– Percentage oil production vs. cumulative oil production.
– The (p/z) ratio vs. cumulative gas production.
Some of these decline curves are shown in Fig. 1.5.
14 Chapter 1. Oil and Gas Resources and Reserves
0
0 0
Cumulative oil producction Cumulative oil producction
Cumulative oil producction
Economic
limit
Economic
limit
Economic
limit
Economic
limit
G
q
0
Np
Np
Np Gp
q
Time
O
i
l
p
r
o
d
u
c
t
i
o
n
,

%
100
(
p
z
)
Figure 1.5: Different ways of data representation for a decline curve
analysis.
Part I
Fundamentals
15
Chapter 2
Basic Concepts of Petroleum Geology
2.1 Introduction
Reservoir Engineering is a part of Petroleum Science that provides the technical basis for the
recovery of petroleum fluids from subsurface sedimentary-rock reservoirs.
The Fig. 2.1 below indicates the place and role of Reservoir Engineering in the broad field
of Petroleum Science.
Geology and
Geophysics
Reservoir
Engineering
Production
Engineering
Facilities
Engineering
Reservoir correlation
Reservoir characterization
Geochemical studies
Workover reserve analysis, well completion design, production
facility design, production log interpretation, prediction of
production schedules
Design proposals for
separation, treating, metering
and pipeline facilities
Final facility design and
operation
Reserve estimates for well
proposal evaluation
Reserve estimates, material balance calculations, fluid flow
equations, reservoir simulation, pressure transient analysis,
well test design and evaluation
Reservoir screening for
improved recovery projects
Improved recovery project
design and maintenance
Figure 2.1: Reservoir engineering and petroleum science.
This chapter pertains to the basic concepts of Petroleum Geology and covers the following
17
18 Chapter 2. Basic Concepts of Petroleum Geology
main topics:
• The source rock of hydrocarbons.
• The generation, maturation, migration and accumulation of hydrocarbons.
2.2 The Basic Concepts
Petroleum is a mineral substance composed of hydrocarbons and produced from the natural
accumulations of organic matter of a faunal and/or floral provenance. Petroleum is a gaseous,
liquid or semisolid substance, present in the pore space of porous rocks, referred to as reservoir
rocks, which are mainly of sedimentary origin.
2.2.1 Clastic Sedimentary Rocks
Sedimentary rocks results from the deposition of sedimentary particles, known as clastic mate-
rial or detritus (from the Latin "worn down"), consisting of mineral grains and rock fragments.
Sedimentary particles are derived from weathered and fragmented older rocks, igneous, meta-
morphic or sedimentary, usually with some chemical changes. Sediment comprising loose
mineral detritus or debris is referred to as clastic sediment (from the Greek word "klastos",
meaning broken). Some clastic sediments consist of the accumulations of skeletal parts or
shells of dead organisms, commonly fragmented, and are referred to as bioclastic rocks (see
next section). The particles of clastic sediment may range widely in size, and the predominant
grain-size fraction is the primary basis for classifying clastic sediments and clastic sedimentary
rocks. As shown in Table 2.1 clastic sediments can be divided into 4 main classes: gravel, sand,
silt, and clay [49], where mud is a mixture of clay and silt, possibly including also some very
fine sand. The narrower the grain-size range of a given sediment, the better its "sorting". Both
the grain size and sorting have direct implications for the sediment permeability to fluids.
Table 2.1: Definition of grain-size and the terminology for sediments
and sedimentary rocks.
Sediment Grain-size limits Unconsolidated Consolidated
grain-size fraction in mm sediment rock
Boulder More than 256 Boulder gravel Boulder conglomerate

Cobble 64 to 256 Cobble gravel Cobble conglomerate

Pebble 4 to 64 Pebble gravel Pebble conglomerate

Granule 2 to 4 Granule grawel Granule coglomerate

Sand 1/16 to 2 Sand Sandstone
Silt 1/256 to 1/16 Silt Siltstone
Clay Less than 1/256 Clay Claystone (clayshale, if fissile)
Clay & slit mixture Mud Mudstone (mudshale, if fissile)

The term "gravelstone" is preferred by some authors on semantic basis [51].
2.2 The Basic Concepts 19
2.2.2 Nonclastic Sedimentary Rocks
Chemical Deposits
Some sedimentary rocks contain little or no clastic particles. Such a sediment, formed by the
precipitation of minerals from solution in water, is achemical sediment. It forms by means of
either biochemical or purely chemical (inorganic) reactions [51]. The primary porosity of such
rocks is practically zero, and their possible porosity is totally dependent on the development of
secondary porosity, chiefly in the form of microfractures.
Biogenic Deposits
Sedimentary rocks commonly contain fossils, the remains of plants and animals that died and
were buried and preserved in the sediment as it accumulated. A sediment composed mainly
or entirely of fossil remains is called a biogenic sediment. If the fossil debris has not been
homogenised by chemical processes, the deposit can be regarded as a bioclastic sediment [51].
Main nonclastic rocks are: limestone, dolomite, salt, gypsum, chert, and coal. Chalk is a
special type of biogenic limestone, composed of the sheletal parts of pleagic coccolithophorid
algea, called coccoliths. The main types of sedimentary rocks and their chemical compositions
are shown in list below, containing main sedimentary rock types and their chemical composi-
tion of categories [37].
Sandstone a siliciclastic rock formed of sand, commonly quartzose or arhosic, cemented with
silica, calcium carbonate, iron oxide or clay.
Chemical composition: SiO
2
. Density: ∼ 2.65 g/cm
3
.
Shale a fissile rock, commonly with a laminated structure, formed by consolidation of clay or
mud ( mainly siliciclastic)
Argillite (mud rock) – any compact sedimentary rock composed mainly of siliciclastic mud.
Chemical composition: SiO
2
.
Dolomite a carbonate rock, consisting largely of the mineral dolomite (calcium magnesium
carbonate)
Chemical composition: CaMg(CO
3
)
2
. Density: ∼ 2.87 g/cm
3
.
Limestone a carbonate rock consisting wholly or mainly of the mineral calcite.
Chemical composition: CaCO
3
. Density: ∼ 2.71 g/cm
3
.
Calcarenite a sandstone composed of carbonate grains, typically a clastic variety of limestone.
Chemical composition: CaCO
3
. Density: ∼ 2.70 g/cm
3
.
Marl a friable rock consisting of calcium carbonate and siliciclastic mud/clay.
Chemical composition: SiO
2
+CaCO
3
. Density: ∼ 2.68 g/cm
3
.
Salt (rock salt) – a chemical rock composed of the mineral halite.
Chemical composition: NaCl.
20 Chapter 2. Basic Concepts of Petroleum Geology
Gypsum a chemical, evaporitic rock composed of the mineral gypsum
Chemical composition: CaSO
4
2H
2
O.
Anhydrite a chemical, evaporitic rock composed of the mineral anhydrite.
Chemical composition: CaSO
4
.
Some of the typical reservoir rocks are shown in Fig. 2.2
2.3 The Origin and Habitat of Petroleum
2.3.1 Source Rock and Generation of Petroleum
Local large concentrations of organic matter in sedimentary rocks, in the form of coal, oil or
natural gas are called the fossil fuels.
A rock rich in primary organic matter is called a source rock, because it is capable of
releasing large amounts of hydrocarbons in natural burial conditions. Usually this is ashale
or mudrock which itself is a very common rock type, consisting about 80% of the world’s
sedimentary rock volume. Organic carbon-rich shale and mudrock are characteristically black
or dark greyish in colour, which indicates a non-oxidised primary organic matter.
Many hypotheses concerning the origin of petroleum have been advanced over the last
years. Currently, the most favoured one is that oil and gas are formed from marine phytoplank-
ton (microscopic floating plants) and to a lesser degree from algae and foraminifera [51]. In the
ocean, phytoplankton and bacteria are the principal of organic matter buried in sediment. Most
of organic matter is trapped in clay mud that is slowly converted into shale under burial. Dur-
ing this conversion, the organic compounds are transformed (mainly by the geothermal heat)
into petroleum, defined as gaseous, liquid or semisolid natural substances that consist mainly
of hydrocarbons.
In terrestrial sedimentary basins, it is plants such as trees, bushes, and grasses that con-
tribute to most of the buried organic matter in mud rocks and shales. These large plants are rich
in resins, waxes, and lignins, which tend to remain solid and form coal, rather than petroleum.
Many organic carbon-rich marine and lake shales never reach the burial temperature level
at which the original organic molecules are converted into hydrocarbons forming oil and nat-
ural gas. Instead, the alteration process is limited to certain wax-like substances with large
molecules. This material, which remains solid, is called kerogen, and is the organic substance
of so-called oil shales. Kerogen can be converted into oil and gas by further burial by mining
the shale and subjecting it to heat it in a retort.
Petroleum is generated when the kerogen is subjected to a sufficient high temperature in
the process of the sediment burial. The alteration of kerogen to petroleum is similar to other
thermal-cracking reactions, which usually require temperatures greater than 60
o
C. At lower
temperatures, during the early diagenesis, a natural biogenic methane called marsh gas, is
generated through the action of microorganisms that live near the ground surface.
A temperature range between about 60
o
C and 175
o
C is most favourable for the generation
of hydrocarbons, and is commonly called theoil window. See Fig 2.3.
At temperatures much above 175
o
C, the generation of liquid petroleum ceases and the for-
mation of gas becomes dominant. When the formation rock temperature exceeds 225
o
C, most
of the kerogen will have lost its petroleum-generating capacity [49],as illustrated by Fig. 2.3 .
2.3 The Origin and Habitat of Petroleum 21
Figure 2.2: Typical reservoir rocks.
The long and complex chain of chemical reactions involved in the conversion of raw or-
ganic matter into crude petroleum is called maturation. Additional chemical changes may
occur in the oil and gas even after these have been generated or accumulated. This explains,
for example, why the petroleum taken from different oil fields has different properties, de-
spite a common source rock. Likewise, primary differences in the source composition may be
reflected in the chemistry of the petroleum.
22 Chapter 2. Basic Concepts of Petroleum Geology
Generation Intensity
Biogenic Methane
Heavy
Light
Oil
Wet Gas
Dry Gas
T
e
m
p
e
r
a
t
u
r
e
,
°
C
100
175
225
315
60
Dry
Gas
Zone
Wet
Gas
Zone
Oil
Zone
Immature
Zone
Figure 2.3: Generation of petroleum vs. burial temperature.
Two types of evidence support the hypothesis that petroleum is a product of the decompo-
sition of natural organic matter [51],
• oil has the optical properties of hydrocarbons that are known only to derive from organic
matter and
• oil contains nitrogen and certain other compounds that are known to originate from living
organic matter only.
Oil source rocks are chiefly marine shales and mudrocks. Sampling of mud on the conti-
nental shelves and along the bases of continental slopes has shown that the shallowly buried
mud contains up to 8% organic matter. Similar or even higher total organic-carbon (TOC)
content characterizes many ancient marine shales. Geologists conclude therefore that oil is
originated primarily from the organic matter deposited in marine sediments.
The fact is that most of the world’s largest hydrocarbon fields are found in marine sedimen-
tary rock successions representing ancient continental shelves. However, some lake sediments
may be just as oil-prone as marine source rocks. Many oil fields in various parts of the world
are in ancient lacustrine deposits (formed at the bottom or along the shore of lakes, as geo-
logical strata). Fig. 2.4 shows the distribution of the world’s sedimentary basin and petroleum
accumulations (from [51]).
2.3 The Origin and Habitat of Petroleum 23
- Areas where major
amounts of oil and gas
have been found
- Areas of ocean deeper than
2000m underlain by thick
accumulations of sedimentary rock
Legend:
Figure 2.4: World’s main sedimentary basins and petroleum accu-
mulations.
2.3.2 Petroleum Migration and Accumulation
The accumulation of petroleum occur in only those areas, where geological conditions have
provided the unique combination of both hydrocarbon prone source rocks and hydrocarbon
traps.
Hydrocarbons are less dense than water. Once released from the source rock, they thus
tend to migrate upwards in the direction of the minimum pressure, until they either escape at
the ground surface, or an impervious barrier, called atrap.
In a trap, the oil and gas accumulate by displacing pore water from the porous rock. The top
may be imperfectly sealed, which means that gas and possibly also some oil may "leak" to yet
higher lying traps or up to the ground surface. The part of the trap that contains hydrocarbons
is called a petroleum reservoir.
Water generally underlines the hydrocarbons in a trap. The water bearing part of the trap
is called an aquifer, and is hydrolically connected with the reservoir. This means that any
pressure change in the aquifer will also affect the reservoir, and the depletion of the reservoir
will make the aquifer expand into this space.
Both oil and gas are generated together, in varying proportions, from a source rock which
results in a primary gas cap above the oil in the reservoir. Likewise, a secondary gas cap may
develop when the reservoir pressure has decreased and the lightest hydrocarbon begin to bubble
out from the oil. Some "leaky" or limited-capacity traps may segregate oil and gas that have
been generated together, such that these accumulate in separate reservoirs.
24 Chapter 2. Basic Concepts of Petroleum Geology
In summary, several factors are required for the formation of a petroleum reservoir [49]:
1. There must be a source rock, preferably rich in primary organic matter (carbon- rich
marine or lacustrine shale). This source rock must be deeply buried to reach efficient
temperatures to cause the organic matter to mature and turn into petroleum.
2. There has to be a migration pathway that enables the shale-released petroleum to migrate
in a preferential direction.
3. There must be a reservoir rock that is sufficiently porous and permeable to accumulate
the petroleum in large quantities.
4. There must be a trap that is sealed sufficiently to withhold the petroleum. Otherwise,
the majority of petroleum will bypass the porous rock and be dispersed or escape to the
ground surface.
5. An impermeable seal or caprock, is critical in preventing the petroleum from leaking out
from the reservoir or escaping to the surface.
If any of these key factors is missing or inadequate, a petroleum reservoir field cannot be
formed. A large isolated reservoir or group of closely adjacent reservoirs is referred to as an
oil field.
2.3.3 Classification of Petroleum Reservoir-Forming Traps
In this section, a general classification of petroleum reservoir-forming traps is discussed (after
[1]). In broad terms, one may distinguish between structual traps (related to tectonic struc-
tures) and sratigraphic traps (related to the sealing effect of unconformities and rock-type, or
lithofacies, changes).
Domes and Anticlines
Domes and anticlines are structures formed by the tectonic uplift and/or folding of sedimentary
rocks. When viewed from above, a dome is circular in shape as in Fig. 2.5, whereas an anticline
is an elongate fold as in Fig. 2.6.
Salt Domes
This type of geological structure is caused by the upward intrusion of a diapiric body of salt,
volcanic rock, or serpentine. In pushing up or piercing through the overlaying sedimentary
rocks, the diapir may cause the formation of numerous traps on its flanks, in which petroleum
may accumulate, as seen in Fig. 2.7. Some salt domes may be highly elongated, rather than
cylindrical, and are called salt walls (e.g. southern North Sea region). Salt itself is a perfect
sealing rock.
2.3 The Origin and Habitat of Petroleum 25
Im
b
p
r
e
m
e
a
le
Bed
Porous Strata
G
A
S
O
IL
W
A
T
E
R
Figure 2.5: Oil and gas accumulation in a dome structure.
I
m
le
p
r
m
a
e
b
e
B
e
d
Porous Strata
G
A
S
O
IL
W
A
T
E
R I
e
m
e
m
e
p
r
a
b
l
S
trata
Figure 2.6: Oil and gas accumulation in an anticline structure.
Fault Structures
Many petroleum traps are related to faults, which commonly displace permeable rocks against
the impervious one. The fault plane, where lined with a shear-produced gouge or heavily
cemented by the percolating groundwater fragments of rock, acts on impermeable barrier that
further increases the trapping effect on the migration of oil and gas. See Fig. 2.8.
Structures Unconformity
This type of structure is a sealing unconformity, with the permeable rocks tilted, erosionally
truncated and covered by younger impermeable deposits. A reservoir may be formed where
the petroleum is trapped in the updip part of the bluntly truncated and sealed, porous rock unit,
as seen in Fig. 2.9.
26 Chapter 2. Basic Concepts of Petroleum Geology
Gas
Oil
Oil
Oil
Water
Water
Salt Mass
Figure 2.7: Hydrocarbon accumulation associated with a salt dome.
Gas
Oil
Water
Fault
Figure 2.8: Hydrocarbon accumulation related to a fault.
Lenticular Traps
Oil and gas may accumulate in traps formed by the bodies of porous lithofacies (rock types)
embedded in impermeable lithofacies, or by the pinch-outs of porous lithofacies within imper-
meable ones, as seen in Fig. 2.10.
Examples of such lenticular traps include: fluvial sandstone bodies embedded in floodbasin
mudrocks, deltaic or mouth-bar sandstone wedges pinching out within offshore mudrocks, and
turbiditic sandstone lobes embedded in deep marine mudrocks. Similar traps occur in various
limestones, where their porous lithofacies (e.g. oolithic limestone or other calcarenites) are
embedded in impermeable massive lithofacies; or where porous bioclastic reefal limestones
pinch out in marls or in mudrocks.
The approximate percentages of the world’s petroleum reservoirs associated with those
2.3 The Origin and Habitat of Petroleum 27
Gas
Oil
Water
Impermeable
Beds
Figure 2.9: Oil and gas trapped below an unconformity.
Oil
Water
Tight-increasing
Shale Content
Figure 2.10: Petroleum trap formed by lithofacies change (Sand-
stone pinch-out).
major trap types are given in Fig. 2.11.
On of the present-day Earth’s surface, over half of the continental areas and adjacent ma-
rine shelves have sediment covers either absent or too thin to make prospects for petroleum
accumulation. Even in an area where the buried organic matter can mature, not all of it re-
sults in petroleum accumulations. The following statistical data may serve as a fairly realistic
illustration [49]:
• Only 1% by vol. of a source rock is organic matter,
• < 30% by vol. of organic matter matured to petroleum,
• > 70% by vol. of organic matter remains as residue and
• 99% by vol. of petroleum is dispersed or lost at the ground surface in the process of
migration, and only 1% by vol. is trapped.
These data lead to the following estimate: only 0.003 vol.% of the world’s source rocks
actually turn into petroleum that can be trapped and thus generate our petroleum resources.
28 Chapter 2. Basic Concepts of Petroleum Geology
Structural
Traps
Stratigraphic
Traps
Combination
Traps
F
a
u
l
t
s
S
a
l
t

D
i
a
p
i
r
s
U
n
c
o
n
f
o
r
m
i
t
y
R
e
e
f
O
t
h
e
r
S
t
r
a
t
i
g
r
a
p
h
i
c
C
o
m
b
i
n
a
t
i
o
n
0.75
0.50
0.25
0
A
n
t
i
c
l
i
n
e
s
Figure 2.11: Percentages of world’s petroleum accumulations asso-
ciated with the major traps types.
2.4 Types of Hydrocarbon Traps on the Norwegian Continental
Shelf
Structural traps, particularly fault and dome structures, are the most common type of trap in the
Norwegian Continental Shelf [4]. Stratigraphic traps are far less common for this region, al-
though there are several reservoirs associated with unconformities or porous lithofacies pinch-
outs (e.g. fluvial sandstone in the Snorre filed and turbiditic sandstone in the Frigg and Balder
fields).
Table 2.2 summarises the regional information about some of the hydrocarbon fields be-
longing to the most common types of traps in the Norwegian continental shelf [4].
2.4 Types of Hydrocarbon Traps on the Norwegian Continental Shelf 29
Table 2.2: Types of petroleum trap in the main fields of the Norwe-
gian Continental Shelf [4].
Field Type of Trap Reservoir Rock Rock Age
AGAT Stratigraphic Sandstone Cretaceous
BALDER Stratigraphic Sandstone Tertiary
DRAUGEN Stratigraphic Sandstone Jurassic
EKOFISK Dome Chalk Cretaceous
ELDFISK Dome Chalk Cretaceous
EMBLA Structural Sandstone Carboniferous
FRIGG Stratigraphic Sandstone Tertiary
GULLFAKS Structural Sandstone Jurassic
HEIDRUN Structural Sandstone Jurassic
MIDGARD Structural Sandstone Jurassic
OSEBERG Structural Sandstone Jurassic
SNORRE Structural Sandstone Jurassic
SN
˙
IHVIT Structural Sandstone Jurassic
STATFJORD Structural Sandstone Jurassic
TROLL Structural Sandstone Jurassic
VALHALL Dome Chalk Cretaceous
30 Chapter 2. Basic Concepts of Petroleum Geology
Chapter 3
Basic Concepts and Definitions
in Reservoir Engineering
3.1 Continuum Mechanics
The present understanding of the subsurface processes relevant to reservoir engineering is
based on the physical concepts of continuum mechanics [12]. According to these concepts,
a porous rock formation saturated with fluids forms a continuum, which means that all the
components involved (rock, water, oil and/or gas) are present in every element, or volumetric
part, of the reservoir space, even if the elementary volume considered is very small and ap-
proaches zero. This conceptual approach allows us to develop a useful theory for the flow of
liquid and gas through a porous medium, called thefiltration theory. All of the most important
numerical simulation programs (ECLIPSE, MORE, FRANLAB, FRAGOR, UTCHEM, etc.)
are based on this theory.
The flow of fluids that occurs in the partial volume of a porous rock, even if very small, can
only be described qualitatively, because of the great complexity of the phenomenon. However
there are some regularities in the behaviour of the "rock-fluids" systems that can be described
by continuum mechanics. For the purpose of the filtration theory, the laws of continuum me-
chanics are considered to be effective only if the elementary volume is sufficiently large to
render the number of pores and rock grains very large or "innumerable". This condition makes
the average parameters of the porous medium sufficiently representative for a description of
the fluid flow processes occurring in the rock. If the elementary volumes are too small and
comparable to the rock’s pore or grain size, the filtration theory cannot be successfully applied.
The need for this concept assumption can be explained as follows. Let us consider the flow
of liquids and gas in a natural reservoir, with the scale of the flow phenomenon varying from
very small to large, as seen in Fig. 3.1. In Fig. 3.1, many physical phenomena (capillary effects,
fluid adhesion effects associated, etc.) occur at a scale comparable to the rock’s grain size or
the dimension of a fractured rock’s fragment (10
−4
−10
0
m).
At a large scale, with the elementary volumes considered on the order of 10
2
−10
4
m,
the effect of the micro-scale phenomena "average" and can more readily be parameterizied.
Likewise, the concepts of continuum mechanics can be applied if the reservoir heterogeneity
is considered at a macro-scale level (lithofaces variation, bedding, ect.), whereas all micro-
heterogeneities on a scale comparable to the grain size are being considered as constants in
31
32
Chapter 3. Basic Concepts and Definitions
in Reservoir Engineering
A B C D
Fracture
A
B
Well
~ 10 m
-3
~ 10 m
0
~ 10 m
2
~ 10 m
4
C
Figure 3.1: Structure of a fractured-rock reservoir at different scales
of observation.
the equations of flow (parametrized connate-water saturation, residual-oil saturation, etc.) or
described by some empirical relationships (functions). The fundamental definitions in the fil-
tration theory include the distribution betweenporosity (i.e. the rock’s fluid storage capacity)
and permeability (i.e. the rock’s fluid flow capacity), as well as the consideration offluid satu-
ration (i.e. the pore volume percent occupied by water, oil and gas, respectively).
3.2 Porosity
The porosity constitute the part of the total porous rock volume which is not occupied by rock
grains or fine mud rock, acting as cement between grain particles. Absolute and effective
porosity are distinguished by their access capabilities to reservoir fluids. Absolute porosity is
defined as the ratio of the total void volumeV
p
a
, whether the voids are interconnected or not,
to the bulk volume V
b
of a rock sample,
φ
a
def
=
V
p
a
V
b
. (3.1)
Effective porosity implies the ratio of the total volume of interconnected voidsV
p
to the
bulk volume of rock,
φ
def
=
V
p
V
b
. (3.2)
Effective porosity depends on several factors like rock type, heterogeneity of grain sizes
and their packing, cementation, weathering, leaching, type of clay, its content and hydration,
etc. It should be noted that porosity is a static parameter, unlike permeability which makes
sense only if liquid or gas is moving in porous medium.
3.3 Saturation
Let us consider a representative elementary volume of the reservoir, with the pores filled with
oil, gas and water. In volumetric terms, this can be written as follows:
3.3 Saturation 33
V
p
=V
o
+V
g
+V
w
, (3.3)
which leads to the definition of saturation, S, as a fraction of the pore volume occupied by a
particular fluid:
S
i
def
=
V
i
V
p
, i = 1, ..., n
where n denotes the total number of fluid phases present in the porous medium.
Consequently,
n

i=1
S
i
= 1.
If two fluids coexist (say, oil and water), they are distributed unevenly in the pore space
due to the wettability preferences. See Fig. 3.2. Simply, the adhesive forces of one fluid against
the pore walls (rock-grain surface) are always stronger than those of the other fluid. In the vast
majority of petroleum reservoirs, both siliclastic and carbonate, the pore water is the wetting
phase and oil is a non-wetting phase.
Rock
Water
Oil
Figure 3.2: Distribution of water and oil phases in a water-wet
porous medium.
Importantly, the fluid saturation (S
o
, S
g
and S
w
) in a reservoir varies in space, most notably
from the water-oil contact to the reservoir top (see figures in previous chapter), and also in
time during the production. In short, different parts of the reservoir may have quite different
fluid saturations, and also the saturation in any elementary volume of the reservoir changes
progressively during the production.
3.3.1 Residual Saturation
Not all the oil can be removed from the reservoir during production. Depending on the produc-
tion method, or the actual "drive mechanism" of the petroleum displacement, the oil- recovery
factor may be as low as 5-10% and is rarely higher than 70%. Part of the oil will remain as
residue, this is called the residual oil. One has to distinguish between the residual oil and pos-
sibly gas saturation reached in a reservoir after the production stage, and the residual saturation
34
Chapter 3. Basic Concepts and Definitions
in Reservoir Engineering
of fluid phases in a reservoir-rock sample after a well coring operation. A fresh, "peel-sealed"
core sample is taken to the laboratory, where the reservoir saturation and the oil-recovery factor
are estimated. The laboratory process is illustrated in Fig. 3.3, where water is displacing the
initial oil in the core sample.
Water
Oil
Water
Sample holder
Core sample
Figure 3.3: Evaluation of residual oil saturation S
or
by a laboratory
displacement from a core sample.
If the pore volume V
p
of the core sample in known, then
S
or
=
V
oi
−V
o
V
p
, (3.4)
where V
oi
is the initial volume of trapped oil in the core sample, andV
o
is the displaced or
produced oil.
3.3.2 Laboratory Determination of Residual Oil and Water Saturation
The cores recovered from wells contain residual fluids (depleted due to the drilling-fluid inva-
sion, the changes in pressure and temperature, etc.) that are assumed to reflect:
• The fluid saturation at the reservoir conditions.
• The possible alterations due to the drilling-fluid invasion into the core.
• The efficiency of possible oil displacement from the reservoir rock represented by the
core.
The modern techniques of core-samples collection prevent dramatic alterations of the rock
fluid characteristics, (foam-based drilling fluid, rubber sleeves containing the core samples and
maintaining their reservoir pressure, deep freezing of retrieved cores, etc.)
Two laboratory techniques are commonly used for determining the residual oil and water
saturation,
• a high temperature retort distillation method and
• the Dean-Stark method.
3.3 Saturation 35
The Retort Distillation Method
The core sample is weighed and its bulk volume measured or calculated. The sample is then
placed in a cylindrical metal holder with a screw cup at the top and a hollow stem projecting
from the bottom. The top is sealed and the sample holder is placed in a retort oven. A ther-
mostat controller raises the temperature of the core to a selected level, at which point the water
within the core is vaporised and recovered. The temperature is then increased to∼ 650
o
C
(1200
o
F) to vaporise and then distil oil from the sample. The vaporised fluids are first collected
in the sample holder and then released vertically downwards through the hollow stem (down-
draft retort). They are subsequently condensed and measured in a calibrated receiving tube.
See Fig. 3.4.
Temperatur
controller
Oil
Water
Insulated
oven
Heating
elements
Sample cup
Condensing
tube
Water
bath
Receiving
tube
Termocouple
Water
inlet
Screen
Figure 3.4: The high temperature retort distillation method.
N.B.! Samples are usually destroyed in this test due to the high temperature and for this
reason small-diameter samples or "plugs" (small cores from the well core), are normally used.
The calculation of the oil and water saturation is straightforward. The following parameter
values are derived from the laboratory test:
36
Chapter 3. Basic Concepts and Definitions
in Reservoir Engineering
• V
b
, ρ
r
– the sample bulk volume and rock density, determined prior to the experiment.
• V
o
;V
w
– the recovered oil and water volumes, registered during the test..
• V
p
– the pore volume, which is calculated.
The water and residual oil saturation are calculated as follows:
S
w
=
V
w
V
p
, and S
o
=
V
o
V
p
, (3.5)
where the saturation are fractional parts of the pore volume. Frequently, saturation are also
given in %.
The Dean-Stark Apparatus for Measuring Initial Fluids
When the core to be analysed is weighed, the measurement includes the weight of rock grains,
and the pore fluid. The sample is then placed in the tare apparatus (to be sure that no sand grains
are lost from the core sample during its analysis, which might otherwise lead to an erroneously
high oil saturation!) and this unit is suspended above a flask containing a solvent, such as
toluene, as shown in Fig. 3.5.
There are several requirements for choosing a proper solvent,
• it must have a boiling temperature higher than that of water,
• it must be immiscible with water and
• it must also be lighter than water.
Toluene satisfies all of those requirements.
When heat is applied to the solvent, it vaporises. The hot solvent vapour rises, surrounds
the sample and moves up to the condensing tube, where it is cooled and condensed. The
condensate collects into the calibrated tube until the fluid there reaches the spill point, where
upon the solvent condensate drips back onto the sample containing the reservoir fluids. The
solvent mixes with the oil in the sample and both are returned to the solvent flask below. See
Fig. 3.5. The process continues until the sample’s temperature has risen above the boiling point
of water. At that point, the water vaporises, rises in the condensing tube, condenses therein
and falls back into the calibrated tube. Because it is heavier than the solvent, it collects at
the bottom of the tube, where its volume can be directly measured. When successive readings
indicate no additional water recovery, the water volume is recorded for further calculations.
After all the oil and water have been recovered from the sample, it is dried and weighed again.
The difference between the original and final weights equals to the weight of the oil and water
originally present in the sample. Because the water collected in the calibrated tube is distilled,
with a density of 1.0 g/cm
3
and a known volume, the weight of oil in the sample can be
calculated. This information is subsequently combined with the estimated porosity of the clean,
dry sample, the volumes of the oil and water can be converted into percent pore-space fraction
(saturation).
3.3 Saturation 37
Condensing
tube
Flask
Solvent
Tare
Sample
Water
Solvent
Offset
calibrated
tube
Figure 3.5: The Dean-Stark apparatus.
N.B. The samples in the process are not destroyed and can be further used in other mea-
surements, i.e., pore volume pycnometry or perhaps capillary measurements, ect..
The calculation of the oil and water saturation is straightforward. The following parameters
are derived from the laboratory test:
• W
i
– the initial weight of the core sample, determined prior to the tests.
• W
d
– the weight of the dry, clean core sample, determined directly after the tests.
• φ, V
b
– the rock’s porosity and the core sample’s bulk volume, determined after the tests.
• V
w
– the reservoir volume of water, registered during the test.
• V
o
– the recovered volume of oil, which is calculated.
Water and oil (residual) saturation is calculated according to Eqs. (3.5), where both the
retort distillation method and the Dean-Stark method are capable of yielding fluid saturation
values within ±5% of the true values.
38
Chapter 3. Basic Concepts and Definitions
in Reservoir Engineering
3.4 Reservoir Pressure and Distribution of Fluid Phases.
The migration and accumulation of petroleum in a reservoir leads to the replacement of the
original pore water by gas and oil , even though the rock pores remain "water-wet" (i.e, their
walls are covered with a thin filmof water). The density difference makes the gas accumulate at
the top of the reservoir, and the oil directly below. Water underlies the petroleum, as an aquifer,
but is continuously distributed throughout the reservoir as the wetting fluid. See Fig. 3.6.
GOC
OWC
FWL
crest
0.0 1.0
S
W
D
e
p
t
h
Gas cap
Gas
Oil zone
Oil
Water zone
Water
Water zone
c
Figure 3.6: The distribution of fluid phases in a reservoir.(S
w
is the
water saturation.)
The following fluid interfaces in the reservoir are important:
• The Gas-Oil Contact (GOC) – a surface separating the gas cap from the underlying oil
zone (also referred to as the oil "leg" or oil "column"). Below the GOC, gas can be
present only as a dissolved phase in oil.
• The Oil-Water Contact (OWC) – a surface separating the oil zone from the underlying
water zone. Below the OWC, oil is generally absent.
• The Free-Water Level (FWL) – an imaginary surface at which the pressure in the oil
zone equals to that in the water zone, i.e. p
o
= p
w
. In other words, FWL is the oil-water
contact in the absence of the capillary forces associated with a porous medium, i.e. in a
well.
However, the term "oil-water contact" does not have a single, unique meaning in reservoir
engineering considerations. The continuos distribution of water saturation in the reservoir zone
(see S
w
in Fig. 3.6) affects strongly the relative mobility of the oil phase, which in turn makes
it necessary to distinguish the following saturation interfaces:
• The Free-Oil Level (FOL) – the level above which the oil saturation is sufficiently high
to allow full oil mobility (100% oil productivity) and the water saturation is low enough
to make water immobile. In most reservoirs, this is the level whereS
o
exceeds ca. 70%,
which means S
w
< 30%.
• The Economic OWC – the level above which enough oil will be mobile, rendering the
whole overlying part of the reservoir economical viable. In most reservoirs, this is the
3.4 Reservoir Pressure and Distribution of Fluid Phases. 39
level where S
o
exceeds ca. 50%, although the actual threshold value may vary, depending
upon reservoir conditions.
• The Productive OWC – The level above which oil become mobility. This may meanS
w
as high as 80-85% and S
o
of merely 15-20%.
• The Edge-Water Level – which is the OWC as defined earlier (level of S
w
= 100%),
located below the productive oil-water contact. In strict terms, this is not always the
"100% water level", as our common terminology refers to it, because the oil saturation
may still be in the order of some percent. This is the base of the reservoir, or the oil- col-
umn level below which the capillary forces render oil completely arrested, or "imbibed",
by the rock pores (such that only thermal distribution can possibly remove the oil from
the "dead-end" pores). Therefore, some engineers prefer to refer to this surface as the
capillary oil displacement level or threshold pressure level.
Needless to add, the distribution of these surfaces is of crucial importance when it comes
to physical (fluid dynamics) and economical (oil recovery) considerations. The interfaces are
usually determined on the basis of analysis and well (drill-stem) tests. The FWL would then
appear to be the only rock-independent OWC, representing the absolute base of the oil column,
as shown in Fig. 3.6.
The total pressure at any reservoir depth, due to the weight of the overlying fluid saturated
rock column, is called the overburden pressure, p
ov
.
The total pressure at any depth is the sum of the overlaying fluid-column pressure (p
f
) and
the overlaying grain- or matrix-column pressure (p
m
), as sketched in Fig. 3.7, and thus,
p
ov
= p
f
+ p
m
.
Pressure
D
e
p
t
h
FP GP
Overburden
pressure
(OP)
underpressure
overpressure
normal hydrostatic
pressure
Figure 3.7: Overburden pressure as the combined grain- and fluid
column pressure.
40
Chapter 3. Basic Concepts and Definitions
in Reservoir Engineering
Because the overburden pressure p
ov
is constant at any particular depth D, then the differ-
ential overburden pressure is zero, i.e. [21]:
dp
f
=−dp
m
.
This means that any reduction of the fluid pressure, as it occurs during production, will
lead to a corresponding increase in the grain pressure. Rock compressibility is therefore an
important parameter to be considered when petroleum (preferably oil) production is estimated.
3.5 Pressure Distribution in Reservoirs
The hydrostatic water pressure at any depthD, can be calculated as follows:
p
w
(D) =

D
D
0
(
dp
dz
)
w
dz + p
w
(D
0
), (3.6)
where (dp/dz)
w
denotes the pressure gradient of the water phase at depthz, and D
0
is an arbi-
trary depth with a known pressure (for instance, the pressure at the sea bottom or the pressure
at the sea surface). The hydrostatic pressure is therefore identical to the water pressure, at any
reservoir depth, as long as there is a continous phase contact in the water, all the way up to the
sea surface.
If the hydrostatic pressure gradient considered to be constant we can write,
p
w
(D) = (
dp
dD
)
w
(D−D
0
) + p
w
(D
0
), (3.7)
and if D
0
is taken at the sea level, the equation becomes,
p
w
(D) = (
dp
dD
)
w
D+14.7 (in psia), or
p
w
(D) = (
dp
dD
)
w
D+1.0 (in bar) (3.8)
Typical "normal" pressure gradients for the water, oil and gas phases are:
(dp/dD)
w
= 0.45 psi/ft = 10.2kPa/m,
(dp/dD)
o
= 0.35 psi/ft = 7.9 kPa/m,
(dp/dD)
g
= 0.08 psi/ft = 1.8 kPa/m
Abnormally high or low reservoir pressure can appear when the reservoir is "sealed" off
from the surrounding aquifer, as a result of geological processes. The reservoir pressure can
then be corrected, relative the hydrostatic pressure, by using a constant (C) in the above pressure
equations. The constant C accounts for the fact that the reservoir pressure is not in hydrostatic
equilibrium, where the pressure in the reservoir is somewhat higher or lower than otherwise
expected.
The water pressure for a general reservoir is then as follows,
p
w
(D) = (
dp
dD
)
w
D+14.7+C, (in psia,) (3.9)
3.5 Pressure Distribution in Reservoirs 41
where C is positive when over-pressure is observed and negative for a under-pressured reser-
voir.
In order to evaluate the pressure distribution in a reservoir, let us consider the reservoir
which cross-section, as shown in Fig. 3.8 (see also [21]).
Gas
Oil
Water
GOC
OWC
FWL D
e
p
t
h
,
f
t
5000
5250
5500
5510
Figure 3.8: Cross-section of a reservoir.
Assuming normal pressure condition, we can evaluate the fluid-phase pressures at the dif-
ferent reservoir "key" levels.
• Water phase:
(p
w
)
FWL
= 0.45 5510+14.7 = 2494.2 psia
(p
w
)
OWC
= 0.45 5500+14.7 = 2489.7 psia
(p
w
)
GOC
= 0.45 5250+14.7 = 2377.2 psia
(p
w
)
top
= 0.45 5000+14.7 = 2264.7psia
• Oil phase:
(p
o
)
FWL
= = 0.35 5510+C
o
= 2494.2psia
which gives: C
o
= 565.7psia
(p
o
)
OWC
= 0.35 5500+565.7 = 2490.7psia
(p
o
)
GOC
= 0.35 5250+565.7 = 2403.2psia
(p
o
)
top
= 0.35 5000+565.7 = 2315.7psia
• Gas phase:
(p
g
)
GOC
= 0.08 5250+C
g
= 2403.2psia
which gives: C
g
= 1983.2psia
(p
g
)
top
= 0.08 5000+1983.2 = 2383.2 psia
The different phase pressures (water, oil and gas) are derived from a common reference
which normally is the FWL pressure, (p
w
)
FWL
. At this level there is no pressure difference
42
Chapter 3. Basic Concepts and Definitions
in Reservoir Engineering
between water and oil and the two pressures are identical, i.e., (p
w
)
FWL
= (p
o
)
FWL
. Ideally
there is no oil present in the zone between the FWL and the OWC, since the oil pressure is too
low to allow the oil phase to enter the pore space (the largest pore throats). Accordingly, the
OWC becomes the level in the reservoir where the water saturation becomes less than one and
consequently the water saturation is ideally considered to be 100% in this zone.
Similar to the FWL, the definition of the GOC, is the level in the reservoir where the pres-
sures in the oil and gas phases are identical. Often this pressure is referred to as thereservoir
pressure.
Different phase pressures are observed at the same elevation in the reservoir, as seen in
Fig 3.9. The pressure difference between two coexisting phases is calledcapillary pressure and
denoted (P
c
)
i j
, where the subscripts i and j refer to oil-water, gas-oil or gas-water.
Pressure, psia
Treshold
capillary
pressure
D
e
p
t
h
,

f
t
5000
5000
5250
5250
5500
5500
5510
5510
Gas
Oil
Water
GOC
OWC
FWL
2250
W O G
2375 2500
Figure 3.9: Pressure distribution in a reservoir (hypothetical exam-
ple).
The capillary pressure at the top of the reservoir, shown in Figs. 3.8 and 3.9, can be evalu-
ated as follows,
(P
c
)
top
ow
= (p
o
)
top
−(p
w
)
topt
= 2315.7−2264.7 = 51.0 psi(a) = 3.5 bar
(P
c
)
top
go
= (p
g
)
top
−(p
o
)
top
= 2383.2−2315.7 = 67.5 psi(a) = 4.6 bar
(P
c
)
top
gw
= (p
g
)
top
−(p
w
)
top
= 2383.2−2264.7 = 118.5 psi(a) = 8.1 bar
The capillary calculations and the Fig. 3.9, show that the phase pressures are different at
the same elevation in the reservoir, and that the capillary pressure is additive, i.e. [7]:
(P
c
)
gw
= (P
c
)
ow
+(P
c
)
go
, (3.10)
At static (initial reservoir) conditions, the distribution of phases within a reservoir is gov-
erned by counteracting gravity and capillary forces. While gravity forces tend to separate
3.5 Pressure Distribution in Reservoirs 43
reservoir fluids accordingly to their densities, the capillary forces, acting within and between
immiscible fluids and their confining solid substance, resist separation. The balance of these
two forces result in an equilibrium distribution of phases within the reservoir prior to its devel-
opment, as shown in Fig. 3.6
Example: Water pressure in a vertical cylindrical tube
The water pressure at a depth D is found using Eq. 3.6, where p
w
(D
0
) is the atmo-
spheric pressure, p
atm.
.
The water pressure at any depth is,
p =
F
A
⇒ dp = d

F
A

,
where F/A is force due to water weight per cross-section area. We may there-
fore write the pressure change as,
dp = d

mg
A

= d

ρ
w
gV
w
A

= d

ρ
w
gAD
A


w
gdD
In the equation above, ρ
w
is the water density, g is the gravitational constant
and D is the water depth.
Substituting the last results into Eq.3.6 we obtain the following general formula
for water pressure at depth D,
p
w
(D) =

D
0
ρ
w
gdD+ p
atm.
.
NB! The pressure variation in a reservoir is determined by the fluid densities
alone (when the gravitational coefficient is considered constant).
.
44
Chapter 3. Basic Concepts and Definitions
in Reservoir Engineering
3.6 Exercises
1. Determine the porosity and lithology of a core sample, given the following data:
Weight of dried core sample: 259.2 g
Weight of 100% water-saturated core sample: 297g
(the density of water is 1.0 g/cm
3
)
Weight of core sample in water: 161.4 g
Define the terms absolute and effective porosity and decide which term to use when
characterising the core sample.
2. A laboratory cylindrical cup contains 500cm
3
water and weighs 800 g. Carbonate sand
(limestone, CaCO
3
) is poured into the cup until the level of sand and water coincide.
Calculate the bulk volume and porosity of this saturated porous medium knowing that
the total weight of cup and its content (water and limestone) is 2734 g. How do you
define the porosity ?
3. A glass cylinder has been filled with dolomite grains up to the 2500cm
3
mark. The mass
of dolomite is 4714 g. Calculate and characterise the sand’s porosity.
4. Estimate numerically the change in carbonate-rock porosity caused by a complete dolomi-
tization of calcite, accounting to the chemical reaction,
2CaCO
3
+Mg
2+
=CaMg(CO
3
)
2
+Ca
2+
,
will yield a carbonate rock’s porosity of 13% .
5. Calculate the porosity of a sandstone core sample given the data from core analysis:
Bulk volume of dried sample: 8.1 cm
3
,
Weight of dried sample: 17.3 g,
Sand grain density: 2.67 g/cm
3
.
6. Calculate the density of formation water when the pressure gradient is measured,dp/dz
= 10.2 kPa/m.
7. Areservoir water pressure of 213bar is measured at a sub-sea depth of 2000m. Evaluate
the pressure situation in the reservoir and determind whether there is an over- /underbur-
den pressure, when the water pressure gradient is 10.2kPa/m.
8. Formation water salinity will influence hydrostatic pressure estimation. Given that un-
certainty in salinity may lead to an uncertainty in water density of ∆ρ = 1.11 - 1.31
g/cm
3
, determine the pressure change inside a reservoir where the depth from thetop
down to the FWL is 150 m.
(answ. 1. 28%, effective, 2.65 g/cm
3
, sandstone, 2. 41%, absolute, 3. 34%, absolute, 4.
4%, 6. 20%, 7. 1.4 g/cm
3
, 8. 8.1 bar, 9. 3 bar)
Chapter 4
Porosity
4.1 General Aspects
According to the definition, already presented, the porosity is the fluid-storage capacity of a
porous medium, which means the part of the rock’s total volume that is not occupied by solid
particles. It should also be noted that porosity is astatic parameter, defined locally as an average
over the representative elementary volume of porous rock media considered.
Genetically, the following types of porosity can be distinguished :
• Intergranular porosity.
• Fracture porosity.
• Micro-porosity.
• Vugular porosity.
• Intragranular porosity.
Rock media having both fracture and intergranular pores are called double-porous or fracture-
porous media.
Fromthe point of viewof pores susceptibility to mechanical changes one should distinguish
between consolidated and unconsolidated porous media. A consolidated medium means a rock
whose grains have been sufficiently compacted and are held together by cementing material.
An important characteristic of consolidated porous media is the ability to restore elastically, to
a great extent, to their shape (volume) after the removal of the overburden pressure.
Porosity is a statistical property dependent on the rock volume taken into consideration.
If the volume selected is too small, the calculated porosity can deviate greatly from the "true"
statistical average value [35]. Only a volume selected large enough (a representative volume)
will result in a representative and correct statistical average (see Fig. 4.1).
4.2 Models of Porous Media
The geometric character of rock’s permeable pore space is in reality quite complicated, and
may vary greatly from one rock type to another. In practice, it is impossible to counter the
45
46 Chapter 4. Porosity
Domain of
microscopic
effects
Domain of
porous
medium
Homogeneous
medium
Inhomogeneous
medium
Grain
Bulk
volume
0
1.0
0.0
V
b
Figure 4.1: Definition of a representative elementary volume for
porosity measurements [35].
pore-system geometry in a detailed and faithful way. Therefore, several idealised models have
been developed to approximate porous rock media and their varied characteristics.
4.2.1 Idealised Porous Medium Represented by Parallel Cylindrical Pores
V
b
V
p
Figure 4.2: Idealised porous medium represented by a system of par-
allel cylindrical pores (pipes).
Estimation of porosity accounting to this model, see Fig. 4.2, is as follows:
φ =
V
p
V
b
=
πr
2
n m
2rn 2rm
=
π
4
= 0.785, or 78.5%,
where r is the pipe radius and m n is the number of cylinders contained in the bulk volume.
It is rather obvious that rocks do not have pores like this and that this model gives a unre-
alistically high porosity value. This model may though, be used in some situations where fluid
flow under simplified conditions is modelled.
4.2 Models of Porous Media 47
4.2.2 Idealised Porous Medium Represented by Regular Cubic-Packed Spheres
2
r
Figure 4.3: Idealised porous medium represented by a regular sys-
tem of cubic-packed spheres.
The estimation of porosity according to this model, see Fig. 4.3, is as follows:
V
b
= (2r)
3
and V
m
=
1
8
(
4
3
πr
3
) 8 =
4
3
πr
3
,
and
φ =
V
b
−V
m
V
b
=
8r
3

4
3
πr
3
8r
3
= 1−
π
6
= 0.476 or 47.6%
where V
m
is the "matrix" volume or the volume of bulk space occupied by the rock.
4.2.3 Idealised Porous Medium Represented by Regular Orthorhombic-Packed
spheres
2
r
60
o
Figure 4.4: Idealised porous medium represented by a regular sys-
tem of orthorhombic-packed spheres.
The estimation of porosity according to this model, see Fig. 4.4, is as follows:
V
b
= 2r 2r h = 4r
2
2r sin(60
o
) = 4

3r
3
and V
m
=
4
3
πr
3
,
where h is the height of the orthorhombic-packed spheres. The matrix volume is unchanged
and thus,
48 Chapter 4. Porosity
φ = 1−
V
m
V
b
= 1−
4πr
3
12

3r
3
= 1−
π
3

3
= 0.395 or 39.5%
4.2.4 Idealised Porous Medium Represented by Regular Rhombohedral-Packed
spheres
2
r
45
o
Figure 4.5: Idealised porous medium represented by regular system
of rhombohedral-packed spheres.
The estimation of porosity according to this model, see Fig. 4.5 and it follows from Fig. 4.5
that,
h =

4r
2
−2r
2
=

2r,
where h is the height in the tetrahedron and
V
b
= 2r 2r

2r = 4

2r
3
and V
m
=
4
3
πr
3
,
which gives
φ = 1−
4πr
3
12

2r
3
= 1−
π
3

2
= 1−0.74 = 0.26 or 26.0%
4.2.5 Idealised Porous Medium Represented by Irregular-Packed Spheres with
Different Radii
Real reservoir rock exhibits a complex structure and a substantial variation in grain sizes and
their packing, which results in variation of porosity and other important reservoir properties,
often associated with the hetrogeniety of porous medium.
Fig. 4.6 shows an example of an idealised porous medium represented by four populations
of spheres (I - IV) sorted by different radii and the histogram showing the hypothetical grain
-size distribution.
By drawing a graph with radii of the spheres plotted on the horizontal axis and heights
equal to the corresponding frequencies of their appearance plotted on the vertical axis, one can
obtain a histogram of distribution of particles (spheres) in sizes.
4.2 Models of Porous Media 49
F
r
e
q
u
e
n
c
y
r
I
I
II
II
III
III
IV
IV
Figure 4.6: Idealised porous medium represented by an irregular sys-
tem of spheres with different radii.
The different models, described above, may serve as a "mental image" or idealised con-
cretization of a rather complex porous structure of porous rocks. The advantage of idealised
models, in general and in particular in the case of porous media, is the opportunity they offer for
simple quantification and representation of characteristic parameters. Since rock porosity has
so many representations, it is important to maintain a representative image, though idealized,
of the rock porosity, for further analysis and improved undersanding.
Example: Porous medium of irregular system of spheres
A porous medium is blended with three types of sediment fractions: fine pebble
gravel with porosity (φ
pebble
= 0.30), sand (φ
sand
= 0.38) and fine sand (φ
f .sand
=
0.33).
The three sediments are mixed in such proportions that the sand fills the pore
volume of the fine pebbles and that the fine sand fills the pore volume of the sand.
The volume of fine pebble gravel is equal to the bulk volume, i.e.,V
b
= V
pebble
.
Since the sand fills the pore volume of the pebble and the fine sand the pore volume
of the sand, the following table is listed:
Volume of sand: V
sand
= φ
pebble
V
pebble
.
Volume of fine sand: V
f .sand
= φ
sand
V
sand
.
Pore volume of fine sand: V
p
= φ
f .sand
V
f .sand
.
The total porosity is then defined,
φ =
V
p
V
b
=
φ
f .sand
φ
sand
φ
pebble
V
pebble
V
pebble
,
= 0.3 0.38 0.33 = 0.037.
The porosity of the porous medium is ∼ 4%.
.
50 Chapter 4. Porosity
4.3 Porosity Distribution
The multiple sampling of porosity measurements for reservoir rocks at different depths and in
different wells gives a data set that can then be plotted as a histogram, to reveal the porosity’s
frequency distribution. See Fig. 4.7. The distribution may appear to be unimodal (left) or
polymodal (right). Such histograms may be constructed separately for the individual zones,
or units, distinguished within the reservoir, and thus give a good basis for statistical estimates
(mean porosity values, standard deviations, etc.).
F
r
e
q
u
e
n
c
y
Porosity
Min Max
F
r
e
q
u
e
n
c
y
Porosity
Min Max
Figure 4.7: Unimodal and polymodal porosity distributions.
Numerical simulation of fluid flow in porous media, related to laboratory tests on core sam-
ples as well as full field production estimation, require a realistic picture of the rock porosity
and its variation throughout the reservoir. This picture is not easily obtainable since porosity
is measured locally (in the well) and porosity extrapolations introduce large uncertainty in the
estimated average values.
The grouping of porosity data according to the reservoir zones, depth profile or graphical
co-ordination, may reveal spatial trends in the porosity variation , see Fig. 4.8. The recognition
of such trends is very important for the development of a bulk picture of the reservoir as a
porous medium and representation of the reservoir porosity in mathematical simulation models
(reservoir characterisation, lateral correlation, numerical modelling, etc.)
Mechanical diagenesis (compaction) and chemical diagenesis (cementation) have a pro-
found effect on a sedimentary rock’s porosity. This burial effect is illustrated by the two typical
examples of sand and clay deposits in Fig. 4.9.
4.4 Measurement of Porosity
4.4.1 Full-Diameter Core Analysis
A full-diameter core analysis is used to measure the porosity of rocks that are distinctly hetero-
geneous, such as some carbonates, and fissured, vugular rocks, for which a standard core-plug
analyse is unsuitable. The same core-plug is a non-representative elementary volume for this
type of rock. The porosity measurement in such rocks requires samples that are as large as can
be obtained (portions of full-diameter drilling cores). In heterogeneous rocks, the local poros-
ity may be highly variable, as it may include micro-porosity, intergranular porosity, vugues,
4.4 Measurement of Porosity 51
+
+
+
+
+
+
+
+
+
+
+
+
+
+
Porosity
D
e
p
t
h
Figure 4.8: Examples of trends of porosity distribution in the depth
profiles of two reservoir sandstone.
sand
clay
0.5
0.4
0.3
0.2
0.1
0.0
0 300 600 900 1200 1500 1800
P
o
r
o
s
i
t
y
Depth, m
Figure 4.9: Sediment compaction burial and porosity change.
fractures, or various combinations of these. A full-diameter core sample usually has a diameter
of 5 inches (12.5 cm) and the length of 10 inches (25 cm).
The full-diameter core technique does not differentiate between the actual types of porosity
involved, but yields a singe porosity value that represents their effective combination. Several
laboratory techniques used for porosity measurements, and the procedure is generally similar
for full-diameter cores and core "plugs".
4.4.2 Grain-Volume Measurements Based on Boyle’s Law
This gas transfer technique involves the injection and decompression of gas into the pores of a
fluid-free (vacuum), dry core sample, see Fig. 4.10. Either the pore volume or the grain volume
can be determined, depending upon the instrumentation and procedures used.
52 Chapter 4. Porosity
Sample
Chamber
Valve Valve
Reference
volume
Pressure
gauge
Pressure
regulator
To gas
pressure
source
Figure 4.10: Porosity measurements based on the Boyle’s law.
To perform the laboratory measurement, Helium gas is often used due to its following
properties,
• the very small size of helium molecules makes the gas rapidly penetrate small pores,
• helium is an inert gas that and will not be absorbed on the rock surfaces and thus yield
erroneous results.
Other gases, such as N
2
and CO
2
, might be good alternatives to Helium. The advantage of
CO
2
is it’s hydrophilic ability, which increase the effect of dehydrating the core sample. N
2
is
also used, simply due to its availability.
The Calculation of the Grain Volume
Using the ideal gas law,
pV = nRT
where the temperature, T= const, one obtains p
1
V
1
= p
2
V
2
, and in the case of vacuum inside
the sample chamber (Fig. 4.10,
p
1
V
re f
= p
2
(V
re f
+V
s
−V
g
),
where V
re f
, V
s
and V
g
are the reference volume, the volume of the sample chamber and the
grain volume, respectively. See Fig. 4.10.
Assuming adiabatic conditions, one obtains,
V
g
=
p
2
V
re f
+ p
2
V
s
−p
1
V
re f
p
2
, (4.1)
where p
1
denotes initial pressure in the reference cell, and p
2
the final pressure in the system.
Successive measurements will increase the accuracy, due to effects of dehydration of the porous
core sample.
4.4 Measurement of Porosity 53
4.4.3 Bulk-Volume Measurements
This technique utilizes the Archimedes’ principle of mass displacement:
1. The core sample is first saturated with a wetting fluid and then weighed.
2. The the sample is then submerged in the same fluid and its submerged weight is mea-
sured.
The bulk volume is the difference between the two weights divided by the density of the
fluid.
Fluids that are normally used are,
• water which can easily be evaporated afterwards,
• mercury which normally not enters the pore space in a core sample due to its non-wetting
capability and its large interfacial energy against air.
The laboratory measurements, using this technique, are very accurate, where uncertainties
in the order of ± 0.2%, is normally obtained.
Example: Uncertainty analysis in measuring the bulk volume using Archimedes’
principle.
The bulk volume of a porous core sample can be measured in two steps, first by
weighing the sample in a cup of water; m
1
(assuming 100% water saturation) and
then weighing the sample in air as it is removed from the cup; m
2
.
The bulk volume is then written,
V
b
=
m
2
−m
1
ρ
w
.
Differentiating the equation above gives us,
dV
b
=
∂V
b
∂m
2
dm
2
+
∂V
b
∂m
1
dm
1
+
∂V
b
∂ρ
w

w
,
dV
b
=
m
2
−m
1
ρ
w
¸
dm
2
m
2
−m
1

dm
1
m
2
−m
1


w
ρ
w

.
If the density measurement as well as the two mass-measurements above, is
considered to be independent measurements, the relative uncertainty in the bulk
volume is written,

∆V
b
V
b

2
= 2

∆m
(m
2
−m
1
)

2
+

∆ρ
w
ρ
w

2
,
where the uncertainty introduced in the process of weighing the two masses is
considered to be identical, i.e., ∆m = ∆m
1
= ∆m
2
.
54 Chapter 4. Porosity
The uncertainty equation above may also be written,

∆V
b
V
b

2
= 2

∆m
ρ
w
V
b

2
+

∆ρ
w
ρ
w

2
.
If the relative uncertainty in determined the water density is estimated to 0.1%
and the weighing accuracy is equal to 0.1 g, we find a relative uncertainty in the
bulk volume of approximately 0.5%. The bulk volume of the core sample is ap-
proximately 30 cm
3
and water density is assumed equal to 1g/cm
3
.
(Note that the uncertainty related to the assumption of 100% water saturation
prior to the first mass measurement, in some experimental tests could be larger
than the effective uncertainty related to the measuring technique.)
.
4.4.4 Pore-Volume Measurement
Pore volume measurements can be done by using the Boyle’s law, where the sample is placed
in a rubber sleeve holder that has no voids space around the periphery of the core and on the
ends. Such a holder is called the Hassler holder, or a hydrostatic load cell, see Fig. 4.11.
Hydrostatic
pressure
To flow
meter
Rubber tubing
Core sample
Flow into
core
Figure 4.11: Hydrostatic load cell (Hassler holder) used for a direct
measurement of pore volume.
Helium or one of its substitutes is injected into the core plug through the end stem. The
calculation of the pore volumeV
p
is as follows:
p
0
V
p
+ p
1
V
re f
= nRT (4.2)
p
2
(V
p
+V
re f
) = nRT (4.3)
and
V
p
=
(p
1
−p
2
)
(p
2
−p
0
)
V
re f
where (p
1
> p
2
> p
0
)
It is important to notice that the Hassler core holder has to be coupled to a volume of known
reference V
re f
, as seen in Fig. 4.10, when the pore volumeV
p
, is measured.
4.4 Measurement of Porosity 55
4.4.5 Fluid-Summation Method
This technique is to measure the volume of gas, oil and water present in the pore space of a
fresh or preserved (peel-sealed) core of known bulk volume. If the core has been exposed to
the open air for some time, some of the oil and water can evaporate and the saturation will be
measured inaccurately.
The volumes of the extracted oil, gas and water are added to obtain the pore volume and
hence the core porosity.
The core sample is divided into two parts. One part (ca. 100 g) is crushed and placed in a
fluid-extraction retort (see figure in previous chapter), where the metal-holder unit has a cap to
prevent the evaporation of gases at the top.
The vaporised water and oil originally contained in the pores, move down and are subse-
quently condensed and collected in a calibrated glassware, where their volumes are measured.
The second part of the rock sample (ca. 30 g) with a roughly cylindrical shape, is weighed
and then placed in a pump chamber filled with mercury (a pycnometer) in which its bulk vol-
ume is determined, measuring the volume of the displaced mercury. Then the pressure of the
mercury, p
Hg
, is raised to 70 bar (1000 psi). At this pressure, the mercury enters the sample and
compresses the gas, filling the pore space originally occupied with the gas. With an appropriate
calculation, the volume of the mercury "imbibed" in the rock gives the gas volumeV
g
.
The bulk volume and weight of the fresh sample allow the computation of the effective bulk
density of the rock. This in turn is used to convert the weight of the first part of the sample,
which was 100 g (to be retorted), into an equivalent bulk volume.
The oil, water and gas volumes are each calculated as fractions of the bulk volume of the
rock sample and the three values are added to yield the porosity value .
The laboratory procedure provides the following information:
• First subsample gives the rock’s weight W
s1
and the volumes of oil V
o1
and water V
w1
are
recorded.
• Second subsample gives the volume of gasV
g2
and the rock’s bulk volumeV
b2
.
From the second subsample, the fraction of the bulk volume occupied by gas (i.e., the
fraction of the gas-bulk volume) can be calculated,
f
g
=
V
g
2
V
b
2
= φS
g
where the subscript 2 is omitted for f
g
, S
g
, and φ, because these values are representative for
both parts of the sample.
Denoting the apparent bulk density of the fluid-saturated rock sample asρ
app
, we can write,
W
s
1
=V
b
1
ρ
app
and W
s
2
=V
b
2
ρ
app
→V
b
1
=V
b
2
W
s
1
W
s
2
The formation oil- and water-volume factor are calculated as follow,
f
o
=
V
o
1
V
b
1
= φS
o
,
f
w
=
V
w
1
V
b
1
= φS
w
,
56 Chapter 4. Porosity
and the sum of the fluid-volume factor then gives the porosity value:
f
o
+ f
w
+ f
g
= φ(S
o
+S
w
+S
g
) = φ
Example: Use of pycnometer in matrix volume calculation.
The pycnometer is a lab-tool occasionally used for measuring bulk- and pore vol-
umes of core samples. A pycnometer is in principle a contained volume, a cell,
where a defined amount of mercury can be injected or withdrawn. The sketch
below illustrates the working principle of the pycnometer.
V
0
Hg
Figure 4.12: Sketch of the pycnometer.
In order to define the matrix volume, V
m
of a core sample, the following mea-
suring steps are carried out:
1. The pycnometer cell is fully saturated with mercury.
2. The pycnometer piston is withdrawn and a gas (air) volume of V
0
is mea-
sured.
3. The core sample is placed in the cell, and the cell volume is sealed. The
equilibrium condition inside the cell is written; p
0
(V
0
−V
m
), where p
0
is the
atmospheric pressure and V
m
is the matrix of the sample (the rock’s grain
volume).
4. Mercury is injected into the cell and a new gas volume,V
1
and gas pressure,
p
1
is measured. NB: The mercury does not enter the pore system of the core
sample, due to its high interfacial tension. (Mercury, as laboratory fluid, has
become less popular due to its toxic characteristics and is quite often replaced
by other fluids.)
5. New equilibrium is reached and we write; p
1
(V
1
−V
m
).
Finally, the matrix volume is found as follows:
V
m
=
p
1
V
1
−p
0
V
0
p
1
−p
0
.
.
4.5 Uncertainty in Porosity Estimation 57
4.5 Uncertainty in Porosity Estimation
Experimental data is always contaminated with measuring uncertainty. For characteristic pa-
rameter estimation, like determination of the porosity, we will expect the uncertainty in the
measured parameters to introduce an error in the estimate of the porosity found.
Porosity will normally be a function of V
p
, V
m
and/or V
b
. Since the three parameters are
dependent, i.e.
V
b
=V
p
+V
m
, (4.4)
only two of them should appear in the uncertainty analysis.
If we define porosity as,
φ =
V
p
V
b
,
we may differentiate the equation and we obtain,

φ
=
dV
p
V
p

dV
b
V
b
.
The pore- and bulk volumes are independent measurements, i.e., the resultsV
p
and V
b
are
independent parameters and so are their uncertainties, ∆V
p
and ∆V
m
.
The relative error or uncertainty in the porosity is then given by
∆φ
φ
=

∆V
p
V
p

2
+

∆V
b
V
b

2
. (4.5)
In laboratory experiments we wish to reduce uncertainties to a minimum. Eq. (4.5) tells
us that it is not sufficient to reduce the uncertainty in only one of the measured parameters,
leaving the other unchanged, since the total relative uncertainty is mainly influenced by the
largest relative uncertainty.
Example: Error propagation
From laboratory measurements one has estimated the relative uncertainty related
to the pore volume to be, ´V
p
/V
p
= 5.0% and the relative uncertainty related to
the matrix is, ´V
m
/V
m
= 7%.
The porosity is defined,
φ =
V
p
V
b
=
V
p
V
p
+V
m
.
We could start to differentiate the porosity with respect toV
p
and V
m
, given the
equation above, but instead we intend to differentiate Eq. (4.4) and then substitute
the results into Eq. (4.5).
Differentiation of Eq. (4.4) gives,

´V
b
V
b

2
=

´V
p
V
p
+V
m

2
+

´V
m
V
p
+V
m

2
,
58 Chapter 4. Porosity
and substitution in Eq. (4.5) gives,
´φ
φ
=

´V
p
V
p

2
+

´V
p
V
p
+V
m

2
+

´V
m
V
p
+V
m

2
,
or written differently,
´φ
φ
=

(1+φ
2
)
´V
p
V
p

2
+

(1−φ)
2
´V
m
V
m

2
.
If the porosity is, φ = 0.2 (or 20%), then the relative uncertainty in the porosity
is ∼ 7.57% and the porosity with uncertainty is written,
φ ±´φ = (20 ±1.5)%.
Note that if the equation φ =V
p
/(V
p
+V
m
) is differentiated directly, the result
would be slightly different because the differentiation was used only once, com-
pared to the process above where a two step differentiation is performed. Every
extra operation in the error propagation increases the final uncertainty.
.
4.6 Porosity Estimation from Well Logs
Porosity of reservoir rock can be estimated not only by using methods, as has been described
above, but also from geophysical well logs, often called wireline logs. This method of porosity
evaluation is not very accurate, but has the advantage of providing continous porosity data.
Once these logs are obtained and converted into a porosity log, they can be calibrated using
core-sample porisity data and serve as additional reliable source of porosity distribution evalu-
ation.
Porosity can be estimated from:
• Formation resistivity factor (F).
• Microresistivity log (from which F can be derived).
• Neutron - gamma log.
• Density (gamma - gamma) log.
• Acoustic (sonic) log.
The Formation resistivity factor is defined as the ratio of the resistivity of the porous sample
saturated with an ionic solution R
o
of the bulk resistivity of the same solutionR
w
, i.e. [23]
F =
R
o
R
w
. (4.6)
The Formation resistivity factor measures the influence of pore structure on the resistance
of the core sample. There are several relationships which can be used for the porosity evaluation
using F-values [23],
4.6 Porosity Estimation from Well Logs 59
• F = φ
−m
, where m is the cementation constant (Archie, 1942).
• F = (3−φ)/2φ (Maxwell, 1881).
• F = X/φ, where X is the electric tortuosity of the sample (Wyllie, 1957).
For more information regarding porosity evaluation using geophysical well logs, see refer-
ence [7, 23, 37].
60 Chapter 4. Porosity
4.7 Exercises
1. Calculate the bulk volume of a preserved (paraffin-coated) core sample immersed in
water, given the following data:
weight of dry sample in air: 20 g,
weight of dry sample coated with paraffin: 20.9 g (density of paraffin is : 0.9 g/cc),
weight of coated sample immersed in water: 10 g (density of water is: 1g/cc)
Determine the rock’s porosity, assuming a sand-grain density of 2.67 g/cc.
2. Calculate the bulk volume of a dry core sample immersed in mercury pycnometer, given
the following data:
weight of dry sample in air: 20 g,
weight of mercury-filled pycnometer at 20
o
C: 350 g,
weight of mercury-filled pycnometer with the sample at 20
o
C; 235.9 g.
density of mercury: 13.546 g/cc.
3. Determine the sandstone’s grain density and porosity, given the following data:
weight of crushed dry sample in air: 16 g,
weight of crushed sample plus absorbed water: 16.1 g,
weight of water-filled pycnometer: 65 g,
weight of water-filled pycnometer with the sample: 75 g.
4. Determine the sandstone’s grain volume and porosity using Boyl’s law, given the follow-
ing data:
volume of chamber containing the core sample: 15 cc,
volume of chamber containing air: 7 cc,
bulk volume of core sample: 10 cc
5. Calculate the effective porosity of a sandstone sample using the following data:
weight of dry sample in air: 20 g,
weight of saturated sample in air: 22.5 g,
density of water is : 1.0 g/cc),
weight of saturated sample in water: 12.6 g.
6. A core sample is saturated with an oil (ρ
o
= 35
o
API), gas and water. The initial weight
of the sample is 224.14 g. After the gas is displaced by water (ρ
w
=1g/cm
3
), the weight
is increased to 225.90 g. The sample is the placed in aSoxhlet distillation apparatus, and
4.4 cm
3
water is extracted. After drying the core sample, the weight is now 209.75 g.
The sample bulk volume, 95 cm
3
is measured in a mercury pycnometer.
Find the porosity, water saturation, oil saturation, gas saturation and lithology of the core
sample. (Notice that the oil density is ρ[g/cm
3
] = 141.4/(131.5 +ρ[
o
API]), when the
water density at that particular temperature and pressure is 1g/cm
3
)
7. Another core sample is brought to the laboratory for compositional analysis, where 80
g of the sample is placed in a mercury pycnometer and the volume of gas found is 0.53
cm
3
. A piece of the same sample, weighing 120 g is placed in a retorte, where the water
and oil volume is measured to 2.8 cm
3
and 4.4 m
3
, respectively. A third piece of the
4.7 Exercises 61
sample, weighing 90 g is placed in a pycnometer and the bulk volume is measured to
be 37.4 cm
3
. Assume oil and water densities as in the exercise above and find the same
characteristic parameters.
8. Calculate the porosity of the sample described below:
mass of dry sample: 104.2 g,
mass of water saturated sample: 120.2 g,
density of water 1.001 g/cm
3
,
mas of saturated sample immersed in water: 64.7g.
Is this effective porosity or the total porosity of the sample? What is the most probable
lithology of the matrix material? Explain .
9. A core, 2.54 cm long and 2.54 cm in diameter has a porosity of 22%. It is saturated with
oil and water, where the oil content is 1.5cm
3
.
a) What is the pore volume of the core?
b) What are the oil and water saturations of the core?
10. If a formation is 2.5 m thick, what is the volume of oil-in-place (in m
3
and in bbl) of a
40.47 hectare large area, if the core described in the excercise above is representative of
the reservoir?
Answer to questions:
1. 24.3%, 2. 9.95 cm
3
, 3. 2.67 g/cm
3
, 1.6%, 4. 20%, 5. 25%, 6. 19%, 14.5%, 75.8%, 9.6%,
2.73 g/cm
3
, 7. 16%, 35.1%, 55.1%,10%, 2.69 g/cm
3
, 8. 29%, 2.64 g/cm
3
, 9. 2.831 cm
3
, 53%,
47%, 10. 738235.6 bbl
62 Chapter 4. Porosity
Chapter 5
Permeability
5.1 Introduction
Permeability in a reservoir rock is associated with it’s capacity to transport fluids through a
system of interconnected pores, i.e. communication of interstices. In general terms, the per-
meability is a tensor, since the resistance towards fluid flow will vary, depending on the flow
direction. In practical terms, however, permeability is often considered to be ascalar, even
though this is only correct for isotropic porous media.
If there were no interconnected pores, the rock would be impermeable, i.e., it is natural
to assume that there exists certain correlations between permeability and effective porosity.
All factors affecting porosity will affect permeability and since rock permeability is difficult
to measure in the reservoir, porosity correlated permeabilities are often used in extrapolating
reservoir permeability between wells.
Absolute permeability could be determined in the laboratory by using inert gas (nitrogen
is frequently used) that fills the porous rock sample completely and limits the possibility of
chemical interaction with the rock material to a minimum. Since the gas molecules will pen-
etrate even the smallest pore-throats, all pore channels are included in the averaging process
when permeability is measured.
When several phases or mixtures of fluids are passing through a rock locally and simulta-
neously, each fluid phase will counteract the free flow of the other phase’s and a reduced phase
permeability (relative to absolute) is measured, i.e. effective permeability.
5.2 Darcy’s Law
The first important experiments of fluid flow through porous media, were reported by Dupuit in
1854, using water-filters. His results showed that the pressure drop across the filter is propor-
tional to the water filtration velocity. In 1856 Henry Darcy proved that flow of water through
sand filters, obeys the following relationship:
q = K A
h
∆l
, (5.1)
63
64 Chapter 5. Permeability
where h is a difference in manometer levels, i.e. hydrostatic height difference,
A is cross-sectional area of the filter,
∆l is thickness of the filter in the flow direction and
K is a proportionality coefficient.
In Darcy’s experimental results, as in Eq. (5.1), viscosityµ, was not included because only
water filters were investigated and hence, the effects of fluid density and viscosity had no real
experimental significance.
Experiments repeated after Darcy, have proved that if the manometric level, h, is kept
constant, the same flow rate (or flow velocity) is measured, irrespective of the orientation of
the sand filter (see Fig. 5.1).
Datum
plane
θ = 90
o
0 < < 90
o o
θ θ = 90
o
θ
I II III
Figure 5.1: Orientation of the sand filter with respect to the direction
of gravitation.
The pressure difference across the sand filter in Fig. 5.1, for the 3 cases are given,
I : ∆p
I
= ρg(h−∆l),
II : ∆p
II
= ρg(h−∆l sinθ),
III : ∆p
III
= ρgh,
where ∆l is the thickness or length of the sand filter in the flow direction.
Since the water velocity is proportional to the manometric level (observation made by
Darcy), the flow velocity is proportional to,
v ∝ (∆p+ρg∆z),
where ∆z is the elevation in the gravitational field. (∆z accounts for the inclined flow direction
relative to horizontal flow.)
If the sand filter is made longer, a reduced flow velocity is expected and similarly if the
water is replaced by a fluid of higher viscosity, a reduced flow velocity is expected.
5.2 Darcy’s Law 65
v ∝
1
µ
∆p+ρg∆z
∆l
.
The proportionality, above, can be replaced by equality, by introducing a proportionality
coefficient k,
v =
k
µ
∆p+ρg∆z
∆l
, (5.2)
where k is the permeability.
The pressure at any point along the flow path is related to a reference height or datum plane
z
0
, where ∆z = z −z
0
and e.g. z
0
= 0 at a level where the reference pressure is 1 atm. A
pressure difference ∆(p+ρgz) = (p+ρgz)
2
−(p+ρgz)
1
will create a fluid flow between the
two points, unless the pressure p is equal to the static pressure −ρgh. In these cases no flow
is expected and static equilibrium is established, as observed in any reservoir where the fluid
pressure increases with depth.
Fluid flow in a porous rock is therefore given by the pressure potential difference ∆(p +
ρgz), i.e. the sum of pressure difference and elevation in the gravity field. In a historical
context, the pressure potential has been associated with the energy potential (energy pr. mass)
and the following definition has been used,
Φ
def
=
p
ρ
+gz.
Substituting the pressure potential difference ∆Φ in Eq. (5.2), one can rewrite the equality
equation based on Darcy’s deduction,
q = A
k
µ
ρ
∆Φ
∆l
where k is the permeability of the porous medium (filter, core sample/plug, etc.), µ is the
viscosity of the fluid and l is the length of the porous medium in the direction of flow andΦ is
the pressure potential. The flow rate q = dV/dt, is volume pr. time.
The Darcy’s law in differential form is,
q = A
k
µ
ρ

dl
= lim
∆l→0

A
k
µ
ρ
∆Φ
∆l

. (5.3)
For linear and horizontal flow (parallel to the x-axis) of incompressible fluid, the elevation
is constant, i.e. dz/dx = 0, and Dracy’s law is written,
q =−A
k
µ
dp
dx
, (5.4)
where the minus sign "-", in front of the pressure gradient term, compensates for a negative
pressure gradient in the direction of flow (since fluids move from high to low potential). Ve-
locity and flow rate are pr. definition positive parameters (see the example below).
At this point it is important to notice that the permeability, k, is introduced in Eqs. (5.4)
and (5.3), as a proportionality constant and not as a physical parameter. The permeability
does pr. definition, not carry any characteristic information about the porous medium. When
66 Chapter 5. Permeability
permeability is related to the transport capability of the porous medium, as often is the case
in practical situations, the fact that this information about the porous medium is missing in
Eq. (5.4), is often overlooked. The proportionality constant k, called permeability, describes
not only the porous medium transport capability, as such, but represents all information about
the porous medium etc., which is otherwise not described by any of the other parameters in
Eq. (5.4).
Example: Linear horizontal core flow
The minus sign "-" in the horizontal flow equation Eq. 5.4 is justified by consider-
ing linear core flow.
Let’s assume a constant liquid flow rate q, through a core sample, as shown
in Fig. 5.2. The pressures p
1
, p
2
and the positions x
1
, x
2
are labelled according to
standard numbering and orientation.
x
x
2
p
1
p
2
x
1
q q
Figure 5.2: Horizontal flow in a core sample.
Assuming a homogeneous porous medium and integration from position 1 to
2, the pressure term is written as follows,
dp
dx
=
p
2
−p
1
x
2
−x
1
=−
p
1
−p
2
x
2
−x
1
,
where p
1
> p
2
in positive flow direction. Since x
2
obviously is larger than x
1
,
the value of dp/dx is pr. definition negative, i.e. the minus sign "-" is needed to
balance the equation.
.
The fluid velocity related to the cross-section areaA is called the superficial (i.e. filtration)
or bulk velocity, and the linear flow velocity is written,
u =
q
A
=−
k
µ
dp
dx
. (5.5)
The real velocity of fluid flow in the pores is called theinterstitial (true) velocity, v
pore
and
is necessarily higher than the bulk velocity, since the flow cross-section area is, on average,φ
times smaller than the bulk cross-section A. The directions of pore flow are inclined relative
to the general flow direction and a characteristic inclination angle α is assigned to describe
this effect. This effect will increase the pore velocity even more, as illustrated in Fig. 5.3. If,
in addition, the porous medium contains a residual saturation of a non-flowing phase, e.g. a
connate water saturation S
wc
, the pore flow velocity is affected through the reduction of the
5.2 Darcy’s Law 67
flow cross-section area. The sum of these effects will cause the pore flow velocity to become
considerably higher than the bulk velocity,
v
pore
=
q
A
1
φ
1
1−S
wc
1
cos
2
α
. (5.6)
α
α
z
x
y
v
q
v
pore
Figure 5.3: Pore flow velocity in a porous medium.
Experimental tests from different porous rocks have shown that an average inclination an-
gle, α ·36
o
and that this angle may vary between 12
o
to 45
o
. If a typical porosity of 25% and
a connate water saturation of 10% are assumed, then the pore velocity will be about 7 times
higher than the bulk velocity.
Example: Linear inclined core flow
When the direction of flow is inclined, with an angle θ to the horizontal flow
direction, the gravitational force has to be considered, since the fluids are moving
up or down in the gravitational field.
In order to keep a constant flow rate q, through a porous medium of length ∆l,
a pressure difference ∆p is applied. See Fig. 5.4.
l
l
2
p
1
p
2
l
1
q
q
x
θ
r
g
Figure 5.4: Core flow at a dip angle θ to the horizontal axis
Flow at an angle to the horizontal direction is described by Eq. (5.3), where the
minus sign is describing linear flow,
q =−A
k
µ
d(p+ρgz)
dl
.
68 Chapter 5. Permeability
z is the elevation in the gravitational field and from Fig.5.4 it’s evident that
z = l sinθ, where l is the direction of flow. The flow equation becomes,
q =−A
k
µ
dp
dl
−A
k
µ
ρgsinθ.
Integration from position 1 to 2, gives

q+A
k
µ
ρgsinθ

∆l = A
k
µ
∆p.
The pressure difference is given,
∆p =
µ∆l
Ak
q+ρg∆l sinθ,
where horizontal linear flow is ∆p
θ=0
= q(µ∆l)/(Ak).
In order to maintain a constant flow rate through the core sample, the pressure
difference needs to be adjusted relative to the inclination angle (dip angle). In a
up-dip situation, as in Fig. 5.4, the pressure difference has to be larger relative to
the horizontal case, since the fluid is pushed upwards in the gravitational fields,
i.e.,
0 ≤θ < 90
o
⇒ ∆p ≥∆p
0
−90
o
< θ < 0 ⇒ ∆p <∆p
0
.
5.3 Conditions for Liquid Permeability Measurements.
Permeability in core samples is measured in the laboratory using Darcy’s law for horizontal
flow, Eq. (5.4). In these tests, some important conditions have to be satisfied before permeabil-
ity could be estimated from the measured data. These conditions are the following:
• Horizontal flow.
• Incompressible fluid.
• 100% fluid saturation in the porous medium.
• Stationary flow current, i.e. constant cross-section in flow direction.
• Laminar flow current (satisfied in most liquid flow cases).
• No chemical exchange or - reactions between fluid and porous medium.
5.4 Units of Permeability 69
q
∆p
slope;
a = Ak/ l µ∆
Figure 5.5: Experimental determination of liquid permeability.
Having satisfied all the above conditions, permeability is found by integrating the linear
flow equation where the permeability is experimentally determined using the formula,
q =
Ak
µ∆l
∆p, (5.7)
where the flow rate q and the pressure difference ∆p are the measured data. Permeability is
found by plotting the measured data as shown in Fig. 5.5.
The linear best fit through all experimental data-points will give a slope, from which the
permeability can be calculated using Eq. (5.7) [54].
The importance of linear representation of the measured data is the advantage of visual
inspection, which may reveal non-linear effects in the data, e.g. at high or low flow rates, or
uncertainty in laboratory measurements, e.g. large spread in data around the linear fit.
5.4 Units of Permeability
Dimensional analysis applied to the Darcy’s law, shows that permeability has the dimension of
surface area, L
2
. It is not convenient to measure permeability of porous media in cm
2
or in m
2
.
By convention the unit for the permeability is called theDarcy. The following definition of the
Darcy has been accepted:
The permeability is 1 Darcy if a fluid with viscosity of 1cp is flowing at a rate of 1
cm
3
/s through a porous medium with a cross-section of 1cm
2
, creating a pressure
difference of 1 atm/cm.
Applying Darcy-units to Eq. (5.4), we get the following equality:
1
cm
3
s
=−1cm
2
1D
1cp


1atm
1cm

,
where the Darcy-units are preferably used in connection with laboratory tests.
There are two systems of units which are widely used in petroleum field engineering;
• Field units.
• SI units (international system of units).
70 Chapter 5. Permeability
The value 1 Darcy is defined in SI-units by substitution:
q = 10
−6
m
3
s
,
µ = 1cp = 10
−3
kg
m s
,
dp
dl
= 1
atm
cm
= 1.01 10
5
Pa
cm
= 1.01 10
7
kg
m
2
s
2
and
A = 10
−4
m
2
k =

A dp/dl
= 0.987 10
−12
m
2
= 0.987µm
2
.
Here: µm
2
= (µm)
2
.
It follows from these evaluations that,
1 D = 0.987 µm
2
.
Instead of the unit 1 Darcy, the 1/1000 fraction is used, which then is called millidarcy
(mD).
It is important to remember that permeability is a tensor, which means that permeability
might have different values in different directions. Vertical permeability (i.e. normal to the
bedding of formations) is usually much lower in comparison than the horizontal permeability
(measured along the bedding of formations). In its turn, the horizontal permeability can be
different in different directions. These permeability features should be taken into account while
measuring permeability.
Example: Core sample liquid permeability.
A cylindrical core sample is properly cleaned and all remains of hydrocarbons are
removed from the pore space. The core is saturated with water and then flushed
horizontally. The core length is 15cm, it’s diameter is 5 cm and the water viscosity
is 1.0 cp.
The permeability might be determined by plotting the data in a "rate/pressure"
diagram, as shown in Fig. 5.5, or more directly, by calculating the permeability
value for each data-pair, using the formula,
k =
µ∆l
A
q
∆p
,
where A = π(d/2)
2
and d is the core sample diameter.
The pressure drop ∆p, is measured for three different flow-rates and perme-
ability is calculated using the above formula,
q
w
[cm
3
/s] 1.0 3.0 10.0
∆p [atm] 7.2 24.5 76.0
k [D] 0.106 0.093 0.101
5.5 Gas Permeability Measurements 71
The average or representative permeability is k = 0.1 D or 100 mD.
Laboratory measurements, always contain uncertainty related to the technol-
ogy used to obtain the lab-data. This uncertainty could be examined by plotting
the data-pairs in an appropriate way, e.g. as shown in Fig. 5.5. The advantage
of data-plotting, compared to straight forward calculations, as in this example, is
the opportunity to verify that the data used in the averaging process are "good" or
representative .
.
5.5 Gas Permeability Measurements
Due to certain interactions between the liquids and the porous rock, absolute permeability is
routinely measured in the laboratory by flowing gas (usually inert gas) through the core sample.
Because gas is a highly compressible substance, i.e. the gas rate is pressure dependent, the
Darcy’s law may not be utilised directly. Considering mass flow of gasqρ, one can write,
qρ =−A

µ
dp
dx
,
where ρ is the density of the gas at certain pressure.
It follows from the perfect gas law (pV = nRT) that,
ρ(p) =
ρ(p
0
)
p
0
p, or simply ρ =
ρ
0
p
0
p,
which when substituted into the previous equation equation yields,
qρ =−A

0
p
µp
0
dp
dx
. (5.8)
Here the subscript "0" refers to a certain pressure value, for instance, the pressure at normal
or standard conditions.
Taking into account the invariant quantity,
qρ = q
0
ρ
0
,
one finally obtains,
q
0
=−A
kp
µp
0
dp
dx
, (5.9)
or integrated from p
1
to p
2
,
q
0
= A
k
2µp
0
p
2
1
−p
2
2
∆l
. (5.10)
Another useful form in which Eq. (5.10) can be written is,
q
0
= A
k
µ
p
p
o
∆p
∆l
, (5.11)
72 Chapter 5. Permeability
where p = (p
1
+ p
2
)/2 is a mean (average) pressure in the core during the measurements.
Combining the invariant mass flow; qρ =qρ and the results generated from the perfect gas
law; ρ p = ρp with Eq. (5.11), one obtains,
q =−A
k
µ
∆p
∆l
, (5.12)
where q is the mean or average flow rate. Eq. (5.12) has exactly the same form as Darcy’s
law for horizontal liquid flow, except for the fact that the flow rate is the mean flow rate. In a
homogeneous porous rock, the mean flow rate is equal to the gas rate at the centre of the core
sample.
The Hassler core holder is commonly used for permeability measurements. It provides
measurements of permeability in both vertical and horizontal directions.
For permeability measurements in the vertical direction gas is injected through the core
plug in the axial direction (see Fig. 5.6, left). The core plug is placed in an impermeable rubber
sleeve protecting the gas flow at the outer-face of the core plug.
High air
pressure
Core sample
Rubber tubing
Low air
pressure
To flow
meter
High air
pressure
Rubber
disk
Low air
pressure
To flow
meter
Metal plug
Screen
Screen
Flow
directions
Figure 5.6: Full diameter vertical and horizontal permeability mea-
surement apparatus (from IHRDC, 1991).
Horizontal permeability measurements require a sealing of the top surfaces of the core with
non-permeable rubber disks (see Fig. 5.6, right). The area of cylindrical surface at the inflow
and outflow openings is covered with a screen and the sample is then placed into the core
holder. Under high air pressure the rubber tubing is collapsed around the core. Low pressure
air is introduced into the center of the holder and passes through the rubber boot and intersects
with the screen, and then flows vertically through the screen. The air then flows through the full
diameter sample along its full height and emerges on the opposite side, where the screen again
allows free flow of the air to exit. The screen are selected to cover designated outer segments
of the full diameter sample. In most cases the circumference of the core is divided into four
equal quadrants. In this test the flow length is actually a function of the core diameter, and the
cross-sectional area of flow is a function of the length and diameter of the core sample.
It is common to furnish two horizontal permeability measurements on all full diameter
samples. The second measurement is made at the right angles to the first.
5.5 Gas Permeability Measurements 73
Example: Core sample gas permeability.
A gas permeability test has been carried out on a core sample, 1in in diameter and
length. The core has been cleaned and dried and mounted in a Hassler core holder,
of the type seen in Fig. 5.6.
The gas is injected and the pressure, p
1
measured, at one end of the core sam-
ple, while the gas rate, q
2
is measured at the other end, at atmospheric pressure,
i.e., p
2
= 1atm.
The gas permeability could be estimated using Eq. (5.10), written as follows,
q
2
= A
k
2µp
2
p
2
1
−p
2
2
∆l
.
Given the pressure p
1
and the gas rate q
2
, the mean pressure in the core sample,
p and the pressure drop across the core, ∆p, are calculated from the equation
above. The gas permeability k is found as a function of the mean core pressure.
The following data is given:
p
1
[mmHg] q
2
[cm
3
/min] p [atm.] ∆p [atm.] k [mD]
861 6.4 1.066 0.133 6.8
1276 35.6 1.33 0.667 6.3
2280 132.8 2.00 2.00 5.0
0 0.2 0.4 0.6 0.8 1
Reciprocal pressure: 1/p
m
[1/atm.]
2
3
4
5
6
7
P
e
r
m
e
a
b
i
l
i
t
y
:

k

[
m
D
]

Figure 5.7: Gas permeability plotted as the reciprocal of mean pres-
sure.
Note that the gas permeability is pressure dependent. As the mean pressure in
the core sample increases it is expected that the gas permeability will approach the
absolute (liquid) permeability, since at such high pressure the gas itself, will start
to behave as a liquid.(This asymptotic limit is not reached unless the pressure, e.g.
in air, is more than 1000 bar.)
74 Chapter 5. Permeability
The absolute gas permeability of the core sample is therefore found as the
asymptotic value of permeability, when p →∞or more conveniently, when 1/p →
0, as seen in Fig.5.7. The data, taken from the table is plotted and the absolute per-
meability is found k
liquid
= 3.0mD.
.
5.5.1 Turbulent Gas Flow in a Core Sample
When gas permeability in core samples are measured, turbulent flow may be experienced in
parts of the pore system, preferably in the larger pores and pore channels.
In order to adjust for the occurance of turbulence, the horizontal flow equation can be
expanded by adding a term particularly describing the turbulent flow situation. For this purpose
the Fanning Eq. (5.13), is used describing turbulent flow in a circular tube [7],
v
2
=
R
ρF
∆p
∆x
, (5.13)
where R is the tube radius, ρ is the gas density and F is the Fanning friction factor characteris-
ing the tube (i.e. roughness, wetting, etc.).
According to the Fanning equation one may assume that pressure drop across a pore chan-
nel is proportional to the square of the average gas velocity in the pore.
The horizontal flow equation, including a turbulent term can be written as,
∆p
∆x
=
µ
k
v +βv
2
,
where v is the average or mean flow velocity and β is the turbulent constant .
Considering the average gas flow velocity, v = q/A and rearranging the above equation
somewhat, one gets,
∆p
∆x
A
µ
1
q
=
1
k
+
β

q.
In an experimental situation one normally do not know the average core rateq. Instead the
gas rate is measured at the exhaust end, q
0
. Recall from above the relation,
q =
p
0
p
q
0
.
Substituting for average gas rate in the horizontal flow equation one gets an equation par-
ticularly adapted for experimental application,
A
∆xµp
0
∆pp
q
0
=
1
k
+
β p
0

q
0
p
. (5.14)
Eq. (5.14) is a linear equation where 1/k is the constant term.
In order to use Eq. (5.14), special care has to be taken to how data is plotted. Since
p = (p
1
+p
2
)/2 and ∆p = (p
1
−p
2
), are both functions of p
1
, one of them has to be kept fixed
when producing linear plots.
Assuming there are three sets of data; set a, b and c. For each set there are three measure-
ments; 1, 2 and 3, all together nine measurements.
5.5 Gas Permeability Measurements 75
p
a
∆p
a,1
q
0,a,1
p
a
∆p
a,2
q
0,a,2
p
a
∆p
a,3
q
0,a,3
p
b
∆p
b,1
q
0,b,1
p
b
∆p
b,2
q
0,b,2
p
b
∆p
b,3
q
0,b,3
p
c
∆p
c,1
q
0,c,1
p
c
∆p
c,2
q
0,c,2
p
c
∆p
c,3
q
0,c,3
For each data set; a, b and c, a straight line is plotted through the measured data points and
the constant 1/k is evaluated, as shown in the Fig. 5.8.
q /p
0 m
p
ma
p
mb
p
mc
1/k
a
1/k
b
1/k
c
A
p
p
x
p
q


ν
m
0










0
Figure 5.8: Plotting linear data where the average pressure p = p
m
is
kept constant.
The three permeability values found form Fig. 5.8; k
a
, k
b
and k
c
are now plotted, in accor-
dance with the linear Eq. (5.14), as shown in the Fig. 5.9.
k
a
k
c
k
b
1/p
m
k
,

D
k
L
Figure 5.9: Absolute permeability as function of inverse average
pressure, p = p
m
When turbulence is considered, gas permeability is found using a step like plotting process,
where data having the same average core pressure are plotted together in the first step. Sec-
ondly, permeabilities are plotted as functions of the inverse average pressure, from where the
absolute (liquid) permeability is found.
76 Chapter 5. Permeability
5.6 Factors Affecting Permeability Values
General considerations show that permeability is a characteristic parameter describing flow
behaviour in porous media. Since the permeability is introduced as a proportional coefficient
in Darcy’s law, it is evident that other characteristics than the porous medium have important
influence on the numeric value of the permeability. In the case of overburden pressure, exper-
iments have shown that the permeability is even more dependent on the overburden pressure
than the porosity.
Permeability measurements are also (sometimes strongly) affected by the fluid, e.g. used
in laboratory tests, due to some interaction between the fluid and the porous medium. To avoid
this effect, gases (helium, nitrogen, carbon-dioxide and air) are often used for permeability
measurements. The use of gases introduce other problems, such as turbulent flow behaviour,
increased uncertainty in gas rate measurements and at low pressure, theKlinkenberg effect.
It follows from Eq. (5.11), that the rock permeability to gas is not the same as for liquids,
since gas permeability is pressure dependent, i.e. k = k(p),
k =
q
o
µ
A
p
o
p
∆l
∆p
, (5.15)
where the latter statement means that different average core pressures p, provide different val-
ues of the rock permeability to gas.
These facts should be considered when permeability from laboratory measurements is re-
lated to reservoir permeability.
5.6.1 The Klinkenberg Effect
It has been observed that at low average pressures, measurements of gas permeability give
erroneously high results, as compared to the non-reactive liquid permeability measurements
(absolute permeability). This effect is known as the gas slippage effect or as the Klinkenberg
effect, investigated by Klinkenberg in 1941. Klinkenberg found that the gas permeability of a
core sample varied with both the type of gas used in the measurements and the average pressure
p, in the core.
One of the conditions for the validity of Darcy’s law, as presented in Eqs. (5.7) or (5.11), is
the requirement of laminar flow, i.e. that the fluid behaves "classically" with respect to inter-
molecular interactions in the gas. At low gas pressure, in combination with small (diameter)
pore channels, this condition is broken.
At low p, gas molecules are often so far apart, that they slip through the pore channels
almost without interactions (no friction loss) and hence, yield a increased flow velocity or flow
rate. At higher pressures, the gas molecules are closer together and interact more strongly
as molecules in a liquid. Compared to laminar flow, at a constant pressure difference, the
Klinkenberg dominated flow will yield a higher gas rate than laminar flow,
q
Klinkenberg
> q
laminar
.
Experiments show that when gas permeability is plotted versus the reciprocal average pres-
sure p, a straight line can be fitted through the data points. Extrapolation of this line to infinite
mean pressure, i.e. when 1/p →0, gives the absolute (liquid) permeability. The permeability
5.6 Factors Affecting Permeability Values 77
1.2 1.6 2.0
2.0
4.0
6.0
8.0
0.0
0.0 0.4 0.8
Reciprocal Mean Pressure, 1/bar
G
a
s
P
e
r
m
e
a
b
i
l
i
t
y
,
m
D
He
N
2
CO
2
Liquid or absolute
permeability, k
L
Figure 5.10: Klinkenberg permeability determination.
value at 1/p →0 is comparable to the permeability obtained if the core were saturated with a
non-reactive liquid (see Fig. 5.10.
In early core analysis the Klinkenberg permeability was estimated by using a steady-state
technique for permeability measurements, at different mean pressures p, or by using the fol-
lowing correlation’s;
k
m
= k
L

1+
b
p

, (5.16)
where k
m
and k
L
are the measured- and the absolute (liquid) permeability, respectively. The
parameter b depends on the type of gas used and reflects, to some extent, properties of the rock
(Fig. 5.10).
Corrections to measured gas permeability due to the Klinkenberg effect are normally mod-
erate to small corrections, as seen for the table below.
Non-corrected Klinkenberg corrected
permeability, [mD] permeability, [mD]
1.0 0.7
10.0 7.8
100.0 88.0
1000.0 950.0
In most laboratory measurements of gas permeability, it is safe to neglect the Klinkenberg
effect if the gas pressure is higher than 10 bar. In reservoirs, the pressure will be much higher
and consequently the significance of the Klinkenberg effect of no importance.
Example: Onset of the Klinkenberg effect
The onset of the Klinkenberg effect is considered in a system comprised of a bun-
dle of identical capillary tubes. For such a system, using Poiseuille’s law for tube
flow, it is shown that the permeability can be written,
78 Chapter 5. Permeability
k =
π
4
r
2
8
, (5.17)
where r is the individual tube radius.
Irrespective of the fact that a bundle of cylindrical tubes is far from being a
realistic model of a porous medium, one can estimate the permeability at which
the Klinkenberg effect starts to become a significant effect.
As an example helium gas might be chosen in the flow experiment. Helium
has a mean free path, λ
He
=0.18 10
−6
m at atmospheric pressure and temperature
of 20
o
C [59]. At higher pressures, lower mean free paths are observed, i.e. λ <
λ
He
.
Since the Klinkenberg effect is said to become important when themean free
path of the gas and the size (diameter) of the pore channels are comparable, there
is a maximum permeability limit, below which the Klinkenberg effect becomes
active.
Substituting the helium mean free path for the diameter of the tube radius in
Eq. (5.17); r = λ
He
/2, it follows,
k
He
=
π
4

He
/2)
2
8
, (5.18)
Using helium gas, the Klinkenberg effect would be active at standard condi-
tions in a "porous" medium, as above, for permeabilities less thank
He
= 0.8 mD. In
an experiment where N
2
or CO
2
is used, the expected mean free paths are shorter
and consequently the permeability limits are lower than in theHe case.
For many gases, the mean free paths of their molecules at standard conditions
(room temperature and atmospheric pressure) are in the range: 0.01 to 0.1 µm,
whereas the mean free paths of CO
2
and N
2
are respectively 0.04 µm and 0.06
µm.
.
5.7 Exercises 79
5.7 Exercises
1. Prove that the numeric constant for convertingdyn/cm
2
to atm, is equal to 1.013310
6
,.
2. Darcy’s law is given,
q = A
k
µ
∆p
∆L
,
where; k:[Darcy], µ:[cp], A:[cm
2
], q:[cm
3
/s], L:[cm] and p:[atm].
Convert this equation to "Oil Field Units" where; k:[mD], µ;[cp], A:[ f t
2
], q:[bbl/d],
L:[ft] and p:[psi].
3. The cylindrical pore model consists of cylindrical tubes stacked on top of each other.
Assuming a tube radius equal to r and that the fluid flow velocity through the tubes, is
given by Poiseuilles equation,
v =
r
2

∆p
∆l
.
a) Calculate the porosity of the cylindrical pore model φ,
b) Show that the permeability is written as k = φr
2
/8.
c) Consider the average permeability of a serial coupling of two tubes with tube radius
R and r, where R r. Find an expression for the average permeability and evaluate
the consequences of relative increase/decrease in the pore radius, as shown in the
figure below.
∆l
∆l
r R
4. A reservoir has cylindrical geometry where the following parameters are defined;
p
e
[atm] Pressure at the outer boundary
p
w
[atm] Pressure in the well
r
w
[cm] Well radius
r
e
[cm] Radius at the outer boundary
h [cm] Reservoir height
Use Darcy’s law to derive a general equation for a cylindrical reservoir in the cases of
horizontal flow, when we have,
a) incompressible fluid and
b) ideal gas.
80 Chapter 5. Permeability
5. Use the laws of Darcy and Poiseuilles to estimate the lowest measurable permeability of
a sandstone core sample, without detecting the Klinkenberg effect. The measurements
are done under laboratory conditions, usingN
2
.
6. Calculate the air permeability, in two ways, for a cylindrical core sample where the
following data is given. Verify that the two approaches used above give the same answer.
(Use the equation for gas rate at the effluent endq
o
and the equation for the average gas
rate q.)
Length 3.0 in, p
1
55 psig,
Diameter 1.5 in, p
2
20 psig,
q
b
75 cm
3
/s, Atm. pressure 13 psia,
p
b
14.65 psia, µ 0.0185 cP.
q
b
and p
b
is the flow rate and back pressure, respectively.
(NB: p
psia
= p
psig
+ p
atm.pressure
)
7. An oil well is producing from a cylindrical reservoir with a drainage area of 20 acres.
Calculate the well pressure, given the following data:
r
w
= 6 in, µ = 5 cP,
k = 75 mD, h = 10 ft,
p
e
= 5000 psia, q = 175 BOPD,
BOPD is short for "Barrel of Oil Produced per Day".
Calculate the pressure in the reservoir at a distance 5 ft from the well. What is the
pressure drop from the well to this position, in percentage of the total pressure difference
in the reservoir?
8. Show that the average permeability
¯
k for n horizontal layers, stacked on top of each other
(in parallel), is given by the formula [8] (see Figure below),
¯
k =

n
j=1
k
j
h
j

n
j=1
h
j
,
where k
j
and h
j
are the permeability and thickness of the layers.
k
1
k
2
k
3
h
1
h
2
h
3
q
q
9. Linear flow in horizontal layers.
Calculate the total flow rate in f t
3
/d at the pressure p
b
for gas flow through parallel
layers, where the following data is given:
5.7 Exercises 81
width 200 ft, length 400 ft, p
atm.
15.0 psia,
h
1
2 ft, k
1
200 mD, p
in
500 psig,
h
2
6 ft, k
2
150 mD, p
out
400 psig,
h
3
4 ft, k
3
400 mD, p
b
14.65 psia.
Gas viscosity µ
g
= 0.0185cp. (Notice: p
psia
= p
psig
+ p
atm.
)
10. Show that the average permeability of rectangular porous media coupled in series is
given by the formula [8] (see Figure below),
¯
k =

n
j=1
L
j

n
j=1
L
j
/k
j
,
where L
j
is the length of the media in the direction of flow.
k
1
k
2
k
3
L
1
L
2 L
3
L
q q
11. Linear and horizontal flow through linear beds in series.
Calculate the total oil rate bbl/d through all media, when the following data is given:
width 100 ft, height 50 ft, µ
o
10 cP,
L
1
100 ft, k
1
100 mD, p
in
100 psig,
L
2
200 ft, k
2
50 mD, p
out
50 psig,
L
3
200 ft, k
3
200 mD, p
atm.
15.0 psia,
12. Show that the average permeability for n radial layers in a cylindrical reservoir is given
by the formula [8] (see Figure below),
¯
k =
ln(r
e
/r
w
)

n
j=1
ln(r
j
/r
j−1
)/k
j
,
where r
e
and r
w
is the radius to the outer boundary of the reservoir and the well radius,
respectively. k
j
is permeability to the layer with outer radius r
j
.
Are the formulas above valid both for gas- and liquid flow?
13. Radial and horizontal flow through cylindrical layers.
An oil well has a intermediate zone with reduced reservoir permeability k
1
. Calculate
the pressure at the outer boundary p
e
when the oil rate is 100 bbl/d and the following
data is given:
r
w
6 in, k
1
50 mD, p
w
2000 psia,
r
1
10 ft, k
2
200 mD, µ
o
5 cp,
k
3
330 ft, h 20 ft.
82 Chapter 5. Permeability
What is the pressure at outside the damaged zone (r
1
) ?
14. Absolute permeability of a core sample is being measured by water flooding. The core
sample is mounted in a transparent cylindrical tube, as shown in the figure below, and
the air-water surface is monitored as function of time.
The tube is placed in a vertical position and the water is assumed to flow through the
whole core sample, evenly distributed over the surface.
Calculate the absolute permeability of the sample when the air–water surface uses 400
seconds to move 18 cm.
Water
Core
sample
q
82 cm
100 cm
2 cm
Additional data;
Density of water 1 g/cm
3
Water viscosity 1 cp
Gravitational constant 980 cm/s
2
Thickness of core sample 2 cm
Answers to questions:
3. π/4, 5. 0.1 mD, 6. 0.1 D, 7. 262 atm, 288 atm,
9. 1.57 10
6
f t
3
/d, 11. 4710 bbl/d, 13. 2272 psi, 14. 1 D.
Chapter 6
Wettability and Capillary Pressure
6.1 Introduction
The exploitation of hydrocarbons is a complex process of controlling interactions in systems
involving crude oil, water, gas and rock formations. In such complicated systems, it is impor-
tant to recognise the effect of the surface properties of oil/rock, water/rock and, in combination,
the interface oil/water. A central property, when giving an overall picture of the interfacial con-
ditions, is the surface or interfacial tension (or more correctly the surface or interfacial energy).
This property is very sensitive to chemical changes at the interface.
In this chapter, the interaction between wettability and surface tension is revealed. Due
to the great significance of the surface/interfacial tension, several experimental methods have
been developed in order to measure this physical property. Some of the most commonly used
techniques are reviewed.
6.2 Surface and Interfacial Tension
An interface is known as the boundary region between two adjacent bulk phases. The equilib-
rium bulk phases can be:
• Liquid-vapor (LV).
• Liquid-liquid (LL).
• Liquid-solid (LS).
• Solid-vapor (SV).
(Gases are basically miscible and thus, no interfacial tension is observed between gases.)
Any surface that is in the state of lateral tension, leads to the concept ofsurface tension.
For curved interfaces, the definition is similar but slightly more complex. The surface tension,
denoted by σ, can be related to the work or energy required to establish the surface area.
If two fluids, say water and oil is forming an interface, as seen in Fig. 6.1, the molecules at-
tached to the oil-water interface do necessarily have less kinetic energy than the bulk molecules,
on average. The molecules on or close to the interface may not move with the same degree of
freedom and speed, due to the constraint put on them by the interface. Since the total energy of
83
84 Chapter 6. Wettability and Capillary Pressure
the molecules is mainly a function of temperature, the potential energy of molecules attached
to the interface is greater than the potential energy of the bulk molecules.
water
oil
Figure 6.1: Molecular motion in bulk and close to the oil-water in-
terface.
Generally speaking, a molecule at a surface is in a state of higher potential energy than a
bulk molecule, due to anisotropy and intermolecular interactions. This means that energy is
required to move a molecule from the interior to the surface of a phase, i.e., to increase the
surface area of the system. Since a proportionality exist between surface area and potential
energy of the system of molecules and since equilibrium is reached at minimum potential
energy (actually minimum Gibbs energy), the surface area of a system is always minimised.
Keeping the temperature, pressure and amount of material in the system constant, the fol-
lowing expression for surface tension may be written,
σ =

∂G
∂A

T,p,n
i
. (6.1)
Here G is the Gibbs free energy and A is the surface area. The unit of surface tension is
therefore, the unit of energy pr. area, i.e., J/m
2
or more commonly N/m. Note, that what is
called surface or interface tension is in fact surface or interface energy and quite often it is more
advantageous to use the energy perspective than it is to deal with tension and forces.
The surface tension between a pure liquid and its vapour phase is usually in the range of 10
to 80 mN/m. The stronger the intermolecular attractions in the liquid, the greater is the work
needed to bring bulk molecules to the surface, i.e., the larger is the interfacial tensionσ. In
Table 6.1 some typical values for surface - and interfacial tensions are listed.
6.3 Rock Wettability
Laboratory experiments have proved that rock wettability affects oil displacement. The term
wettability can be defined as "the tendency of one fluid to spread or to adhere to a solid surface
in the presence of other immiscible fluids" [29].
The evaluation of reservoir wettability can be made through measurements of interfacial
tensions, i.e., tensions acting at the fluid-fluid and rock-fluid interfaces, and thecontact angle.
Note that wettability itself is a microscopic characteristic, that has to be measured by using
micro-scale laboratory investigation techniques.
6.3 Rock Wettability 85
Table 6.1: Surface tension, σ
LV
and interfacial tension to water, σ
LW
for some liquids at temperature, T = 293
o
K. Note: Sur-
face tension σ
LV
, is here defined as the interfacial tension
between a liquid and its vapor.
Liquid σ
LV
(mN/m) σ
LW
(mN/m)
Water 72.8 –
n-octane 21.7 51.7
n-dodecane 25.4 52.9
n-hexadecane 27.5 53.8
dichoromethane 28.9 27.7
benzene 28.9 35.0
mercury 476.0 375.0
The angle θ is influenced by the tendency of one of the fluids, i.e. water, of the immiscible
pair, to spread on the pore wall surface in preference to the other (oil). The qualitative recog-
nition of preferred spread is called a wettability preference, and the fluid which spreads more
is said to be the wetting phase fluid. Contact angles are measured, by convention, through the
fluid whose wettability is studied or through the fluid which is wetting the solid surface. A ta-
ble of typical fluid pairs of interest in reservoir engineering is shown in the Table 6.2, together
with contact angles and interfacial tensions [8].
Table 6.2: Fluid pair wettability under reservoir and laboratory con-
ditions.
System Conditions
Wetting Non-wetting T = temperature θ σ
phase phase P = pressure (dynes/cm)
Brine Oil Reservoir, T, P 30 30
Brine Oil Laboratory, T, P 30 48
Brine Gas Laboratory, T, P 0 72
Brine Gas Reservoir, T, P 0 (50)
Oil Gas Reservoir, T, P 0 4
Gas Mercury Laboratory, T, P 140 480
The degree of wettability exhibited, depends both on the chemical compositions of the
fluid pair, particularly the asphaltine content of the oil, and on the nature of the pore wall.
Pure quartz sandstone or calcite surfaces are likely to be wetted preferentially by water. The
presence of certain authigenic clays, particularly chamosite, may promote oil wet character.
The differences in contact angle somehow indicate different wettability preferences which
86 Chapter 6. Wettability and Capillary Pressure
can be illustrated by the following rule of thumb presented in Table 6.3 and in Fig. 6.2 [19].
Table 6.3: Wettability preference expressed by contact angle.
Contact angle values Wettability preference
0 – 30 Strongly water wet
30 – 90 Preferentially water wet
90 Neutral wettability
90 – 150 Preferentially oil wet
150 – 180 Strongly oil wet
s s s
o
o
o
w
w
w
θ = 0 θ = 90 θ ~ 180
Figure 6.2: Example of wetting preference.
6.4 Contact Angle and Interfacial Tension
With two immisible fluids (oil and water) present in the reservoir, there are three interfacial
tension parameters to be assessed; σ
os
, σ
ws
and σ
wo
. The three interfacial tension are not
independent parameters, and in order to reveal the relationship between them a "gedanken"
experiment is carried out on a droplet of water, surrounded by oil, placed in a contact with a
water-wet reservoir rock, as seen in Fig. 6.3.
R
θ
θ
r
h
Water
Oil
Rock
Figure 6.3: Geometry of the water droplet in oil, placed in a contact
with a water-wet reservoir rock.
The following definitions will be used:
• surface tension between the oil and solid; σ
os
,
6.4 Contact Angle and Interfacial Tension 87
• surface tension between the water and solid; σ
ws
,
• interfacial tension between the oil and water phases; σ
ow
,
• contact angle at the oil-water-solid interface measured through the water;θ,
• surface area of the water droplet; A
d
,
• area of the reservoir rock occupied by the water droplet; A
s
.
The water droplet is assumed to be in equilibrium with the surrounding medium. A small
deformation of the surface area, will deform the droplet slightly and force the droplet to expand
on the solid surface. The deformation is described by the equilibrium equation, expressing the
change in energy due to the change in area.
σ
ws
dA
s
+(−σ
os
dA
s
) +σ
ow
dA
d
= 0 (6.2)
Elaborating on Eq. (6.2), the following relationships are valid (see also Fig. 6.3),
A
s
= πr
2
⇒ dA
s
= 2πrdr
A
w
=π(r
2
+h
2
) ⇒ dA
w
= 2π(rdr +hdh)
V
w
=
πh
6
(3r
2
+h
2
)
Incompressible liquids give,
dV
w
=
∂V
w
∂r
dr +
∂V
w
∂h
dh = 0,
which leads to
dh =−
2rh
h
2
+r
2
dr.
Using these results, Eq. (6.2) is rewritten,
σ
ws
−σ
os

ow

1−
2h
2
h
2
+r
2

= 0, (6.3)
and taking into account that (see Fig. 6.3),
Rsinθ = r
Rcosθ = R−h
and
(1−
2h
2
h
2
+r
2
) = cos θ,
a final result is obtained,
σ
os
−σ
ws
= σ
ow
cos θ, (6.4)
which is known as the Young-Dupre equation [15].
88 Chapter 6. Wettability and Capillary Pressure
6.5 Capillary Pressure
Capillary pressure may be defined as the pressure difference across a curved interface between
two immiscible fluids. By convention, the P
c
term is positive for unconfined immiscible fluid
pairs, where P
c
is defined as the pressure difference between the non- wetting and the wetting
phase.
P
w
P
o
Water
Oil
*
*
Figure 6.4: Pressure difference across a curved (spherical) interface.
Using an example with an oil drop floating in water where the density of oil and water are
assumed similar, as seen in Fig. 6.4, the capillary pressure is written,
P
c
= p
o
−p
w
.
If the droplet is small, one may assume the interfacial tension to be far more important
than the gravitational force acting on the droplet and thus, since the surface area is minimised,
the droplet takes the form of a perfect sphere. A small perturbation, i.e. a small reduction of
the sphere volume, is described by an equation taking into account the energy change due to
the volume and the surface change. The equilibrium condition is ecpressed as the change in
potential and surface energy,
p
w
dV +σ
ow
dA = p
o
dV.
Substituting definition of the capillary pressure p
c
, in the latter equation, one we succes-
sively obtain,
P
c
= σ
ow
dA
dV
= σ
ow
dA
dr

dV
dr

−1
= σ
ow
8πr
4πr
2
= σ
ow
2
r
.
Capillary pressure can be of significant magnitude, since this is the energy needed to form
a droplet that can pass through a porous channel . Taking typical values of a pore radius and
an interfacial tension of oil and water, the capillary pressure can be obtained by the following
evaluation:
r ∼1µm and σ
ow
= 0.025
N
m
⇒P
c
·10
4
N
m
2
= 0.5 bar
6.5.1 Capillary Pressure Across Curved Surfaces
For two immiscible liquids as part of a real physical system, a spherical interface is an odd
observation. Normally, a curved surface is characterised by two radii of curvature;R
1
and R
2
,
as seen in Fig 6.5.
6.5 Capillary Pressure 89
Figure 6.5: Curved surface and radii of curvature.
With a pressure difference across the interface in the two phases, the interface will show
a net curvature with the larger pressure on the concave side. The relationship between the
pressure difference ∆p = P
c
and the curvature is given by Laplace equation,
P
c
= σ

1
R
1
+
1
R
2

, (6.5)
where R
1
and R
2
are the principal radii of curvature and σ is the interfacial tension. For a
spherical droplet R
1
= R
2
= r and ∆p = 2σ/r. Across a planar interface/surface R
1
= R
2
=∞
and ∆p = 0.
Example: Surface tension and surface energy
The process of displacing water through a porous medium is comparable to the
formation of droplets of sizes equal to the capillary pore throats.
What is then the energy needed to transform 1 cm
3
of pure water to droplets
with an average radius of 1 µm, when the surface tension of water to vapor is 0.073
mN/m?
The energy in question, is the energy needed to increase the initial water sur-
face A, of the initial volume V to N number of droplets with area, A
d
and volume
,V
d
.
The area increase is,
∆A = N A
d
−A =
V
V
d
A
d
−A =
3
r
V −A,
where the droplet area and volume are respectively; 4πr
2
and (4/3)πr
3
.
Since the increased area ∆A is directly proportional to the increase in potential
energy ∆E
p
, which can be expressed by Eq. (6.1),
∆E
p
= σ
air,w
∆A =σ
air,w

3
r
V −A

.
If the initial water area is considered to be small (or negligible) to the area of
the droplets, a potential energy equal to about 0.22J is found.
90 Chapter 6. Wettability and Capillary Pressure
.
6.5.2 Interfacial Tension
Assuming pairs of immicsible unconfined fluids the following phenomena, as illustrated in
Fig. 6.6 can be observed, depending on the sign of interfacial tension:
σ > 0
σ < 0
σ ~ 0
Figure 6.6: Formation of interface as function of the sign of the in-
terfacial tension in pairs of immicsible unconfined fluids.
• When the surface tension is positive, σ > 0, confined molecules, have a preference for
keeping their own company. The surface against the second type of molecules is min-
imised and in the case of small droplets, spherical interfaces are formed.
• In the cases when σ ≈ 0, liquids are classified as "truely" miscible. In these cases no
preference with respect to mixing of the two fluids is observed. (However, diffusion will
lead to mixing of the two fluids.)
• When the surface tension is negative, σ < 0, molecules of one type will prefer (have
affinity for) the company of the second type of molecules. We may observe a chemical
reaction where the final state is stable in time. An example of such a process is the
hydrophilic ability of pure ethanol to mix with air more or less instantaneously.
6.5.3 Capillary Pressure in a Cylindrical Tube
When a non-wetting fluid is displacing a wetting fluid, as is the case when oil is displacing
water in a water-wet porous rock, a curved interface is formed in the capillary tube. To reveal
the relation between the capillary pressure, the interfacial tension and the radius in a cylindrical
tube, two immiscible fluids (oil + water) are confined in a cylindrical capillary of radiusr
c
, as
shown in Fig. 6.7.
Using the Eq. (6.5) for the pressure difference between the two sides of the interface,
6.5 Capillary Pressure 91
θ
c
θ
c
r
c
R Water
Oil
Figure 6.7: Idealised model of a pore channel filled with two immis-
cible fluids forming a curved interface between them.
p
o
−p
w
= σ
ow

1
R
1
+
1
R
2

,
where R
1
and R
2
are main radii of the curvature, expressing the radius of the interfacial surface
R by means of the contact angle θ
c
and the capillary radius r
c
in the cylindrical tube. When
R
1
= R
2
= R and
R =
r
c
cosθ
c
,
the capillary pressure is written,
P
c
= p
o
−p
w
= σ
ow

1
R
1
+
1
R
2

=

ow
cos θ
c
r
c
, (6.6)
where Eq. (6.6) is the capillary pressure in a cylindrical tube of radiusr.
Example: Oil - water displacement in a capillary tube
Displacement processes in porous media are very often a competition between
viscous- and capillary forces. In this example, the process by which oil displaces
water in a cylindrical tube is considered in analogy with the production of oil from
a water-wet reservoir where oil is forced through capillary pores which initially
contained water.
Consider a dynamical situation, as sketch in Fig. 6.8 where the oil front has
reached a position x in to the cylinder (pore). The pressure drop along the cylin-
drical tube is partly the viscous pressure drop ∆p
o
+ ∆p
w
, in the oil- and water
zone and partly the capillary pressure drop, P
c
across the oil-water interface:
∆p
V
= ∆p
o
+∆p
w
=
q
Ak

o
x +µ
w
(L−x)] ,
P
c
=

ow
cosθ
r
.
92 Chapter 6. Wettability and Capillary Pressure
Water Oil
0
x
L
∆p
o
∆p
c
∆p
w
Figure 6.8: Cross-section view of a cylindrical "pore channel".
The flow rate is q = Av, where A and v is respectively the cross-section area
and the pore velocity. The permeability of the tube is known as,k = r
2
/8, and r is
the tube radius.
The strength between the two forces is considered by simply comparing their
pressure drops,
∆p
V
P
c
= 4
¸

o
σ
ow
cosθ
x
r
+

w
σ
ow
cosθ
L−x
r

.
In the equation above, the relation vµ/(σ cosθ) is the only term contain-
ing dynamical parameters. In analogy with the definition of Reynolds number, a
dimension-less number could be defined,
N
c
=

σ cosθ
.
The Capillary number N
c
, describes the competition between the viscous- and
the capillary force.
In a situation where the two forces are assumed to be equally important, i.e.
∆p
v
/P
c
∼1, a set of "typical values" could be chosen and the average pore velocity
is found,
∆p
V
/P
c
= 1
θ = 60
o
L/r = 5
µ
o
≈µ
w
= 1mPa s
σ
ow
= 50mN/m

v
pore
≈1.3m/s.
Reservoir flow is commonly considered to be of the order of 1 foot pr. day,
which is equal to 3.5 µm/s. From this comparison , it is obvious (even when the
appropriate bulk velocity u = v
pore
/(φ(1−S
r
)cos
2
α) is taken into account) that
under reservoir flow conditions, capillary forces are totally predominant and that
viscous forces play a minor role when microscopic flowpattern is considered. This
means that the capillary forces alone decide which pore channels are going to be
swept and which are not, in the reservoir.
The Capillary number for reservoir flow becomes N
c
= 1.5 10
−5
(using the
numbers above), while the Capillary number at the "breaking point" when the
viscous force becomes equally important to the capillary force is 8 10
−3
.
6.6 Capillary Pressure and Fluid Saturation 93
The capillary number for field water-floods ranges from 10
−6
to 10
−4
. Labo-
ratory studies have shown that the value of the Capillary number is directly related
to the ultimate recovery of oil, where an increase in the Capillary number im-
plies an increase in the oil recovery. The Capillary number is generally varied by
increasing the flow rate (pore velocity) and/or lowering the interfacial tension.
.
6.6 Capillary Pressure and Fluid Saturation
Results from drainage and imbibiation laboratory experiments have shown that the capillary
pressure P
c
= p
o
−p
w
is dependent on the following parameters (see Fig. 6.9):
• surface tensions; σ
os
, σ
ws
and σ
ow
,
• contact angle measured through the water phase; θ
c
,
• rock porosity; φ,
• rock permeability; k,
• fluid saturations; S
w
and S
w
σ
ow σ
ow
θ
c
θ
c
σ
ws
σ
ws
σ
os
σ
os
Oil
Oil
Water
Water
Oil-wet Water-wet
Figure 6.9: Wettability of oil-water-solid system.
The task is to define (if possible) a correlation between capillary pressureP
c
and the param-
eters, mentioned above, being responsible for the numeric variation of the capillary pressure in
the experiments.
Relying upon the data obtained, the following dependency can be expressed,
P
c
= f (φ, k, σ
os
, σ
ws
, σ
ow
, θ
c
, S
o
, S
w
) (6.7)
Since some of the parameters are dependent on others,
S
o
= 1−S
w
,
σ
os
−σ
ws
= σ
ow
cosθ
c
,
the list of independent parameters is shortened and Eq. (6.7) is written;
P
c
= f (φ, k, σ
ow
cosθ
c
, S
w
) (6.8)
A dimensional analysis of Eq. (6.8) can be carried out using the following notation for
dimensions,
94 Chapter 6. Wettability and Capillary Pressure
M – mass, L – length, and T – time,
which gives the following dimensions for all the parameters in Eq. (6.8):
[P
c
] = M L
−1
T
−2
, [k] = L
2
, [σ
ow
cosθ
c
] = M T
−2
,
[φ] = 1, [S
w
] = 1
(6.9)
Comparing all the parameters of the right-hand side of Eq. (6.8), it appears that both di-
mension parameters k and σ
ow
have independent dimensions. This means that dimension of
the capillary pressure can be defined through dimensions of those parameters, i.e.,
[P
c
] = [k]
α

ow
cosθ
c
]
β
.
Using notation (6.9), the last relation is written in the form,
M L
−1
T
−2
= L

M
β
T
−2β
,
which is followed by,
M : 1 = β,
L : −1 = 2α, ⇒ α =−1/2 and β = 1.
T : −2 = −2β,
Thus, a dimension-less parameter F can be composed,
F =
P
c
σ
ow
cosθ
c


k,
and by making use of this result, Eq. (6.8) can be rewritten in dimension-less form,
F = F(φ, S
w
),
or using the initial notation,
P
c
=
σ
ow
cosθ
c

k
F(φ, S
w
).
It can be shown that parameters φ and S
w
and their functions, can only appear in correla-
tions where they form a product,
P
c
=
σ
ow
cosθ
c

k
F
1
(φ) F
2
(S
w
) (6.10)
Thus by using the dimension analysis (the π-theorem) [11], the number of independent
variable parameters is reduced and an almost exact formof the correlation between the capillary
pressure P
c
, fluids and rock parameters is obtained.
The following correlation is widely used for reservoir simulation tasks [13, 15],
P
c
=
σ
ow
cosθ
c

(k/φ)
J(S
w
), (6.11)
where J(S
w
) is known as the J-function (after Leverett).
6.7 Pore Size Distribution 95
6.7 Pore Size Distribution
It is obvious that the capillary pressure is strongly affected by the distribution of pore chan-
nel sizes, represented by the 1/r relationship. The capillary pressure does also represent the
response of interfacial tensions and rock wettability. Generally, is the capillary pressure char-
acteristic of the reservoir heterogeneity.
To reveal the relation between the capillary pressure and the microscopic heterogeneity of
the reservoir, the following example is considered: An idealised model of the porous medium
consisting of cylindrical capillaries with different radii r
i
, where all pore channels have the
same type of wettability and, as a consequence, a fixed contact angleθ
c
. It is also assumed, that
a certain invariant distribution-function χ(r) defines a fraction of pore channels with capillary
radii belonging to the interval (r, r +dr) as,
χ(r) =
n(r, r +dr)
N
,
where N is the total number of pore channels.
Let V
i
be the pore volume of a single capillary with radiusr
i
and V be the total pore volume
of the porous medium considered, i.e.,
V =
N

i=1
V
i
.
Now let us consider a process of imbibition for a strongly water-wet rock initially saturated
with oil, as shown in Fig. 6.10.
Water Oil
Rock
Figure 6.10: Illustration of imbibition process in an idealised model
of porous medium.
Assume that at the starting point, the pressure in the oil phase p
o
, is high enough to protect
the water invading the pore channels. Then gradually decreasing the outlet pressure (pressure
in the oil phase), the water will invade the pores. It is quite obvious that the water enters only
those capillary channels with capillary pressureP
c
, exceeding the difference between the outlet
and inlet pressure ∆p
o
(t). Hence, at a certain time only those channels will be filled with water,
which satisfy the condition,
P
c
≥∆p
o
(t),
96 Chapter 6. Wettability and Capillary Pressure
or, substituting Eq. (6.6) into the last inequality,
r
c


ow
cos θ
c
∆p
o
(t)
.
Then the volume of water which has invaded the porous medium can be defined as,
V
c
= N

r
c
0
χ(r)πr
2
ldr,
where l is the length of a single pore channel.
Defining the total pore volume as,
V = N


0
χ(r)πr
2
ldr,
the relations between the water saturation S
w
, and the capillary pressure P
c
, is
S
w
=
V
c
V
=

r
c
0
χ(r)r
2
dr


0
χ(r)r
2
dr
, and
P
c
=

ow
cos θ
c
r
c
, (6.12)
which explicitly indicates that microscopic reservoir heterogeneity strongly affects the capillary
pressure.
Since the pore size distribution varies between the different layers in a reservoir, it is ex-
pected that the capillary pressure curve shape will also vary from layer to layer. This phe-
nomenon is frequently observed in laboratory tests, by using a mercury injection technique, on
core samples taken from different elevations in the same well.
Example: Pore size distribution and capillary pressure curve
In this example, it will be shown how data from a mercury drainage experiment
could be used to produce a capillary pressure curve and how these data could be
used further, to define the pore size distribution for the core sample tested.
First, the core sample is properly cleaned, dried and placed in vacuum for some
time, before it is sealed in a mercury pycnometer. A series ofN+1, representative
pressure measurements p
i
, is recorded inside the pycnometer and the injection
volume V
i
is read as the pore sample is invaded by more and more mercury. The
experimental data is as follows:
p
Hg
p
0
p
1
p
2
p
3
p
N
V
Hg
V
0
V
1
V
2
V
3
V
N
The capillary pressure P
c
, is here the pressure difference between the mercury
pressure p
Hg
, and the gas pressure in the core sample p
g
,
P
c
= p
Hg
−p
g
=
2σ cosθ
r
.
6.7 Pore Size Distribution 97
The gas is the wetting phase since mercury definitely does not wet any core
sample. The wetting saturation is therefore written,
S
g
= 1−S
Hg
=
V
N
−V
i
V
N
−V
0
.
Based on the data in the table above, the following parameters are calculated,
S
g
1 S
1
S
2
S
3
0
r r
0
r
1
r
2
r
3
r
N
P
c
P
c,0
P
c,1
P
c,2
P
c,3
P
c,N
The pore size distribution D(r) is representing the relative increase in pore
volume as function of the pore throat radius,
D(r)
de f
= −
1
∆V
dV
dr
,
where ∆V =V
N
−V
0
and dV =V
i
−V
i−1
, taken from the above tabulated data. The
minus sign "-" is added due to convenience.
The pore size distribution is then rewritten,
D(r) =−
1
∆V
1
dr
∂V
∂S
∂S
∂P
c
dP
c
.
Remembering the definition of the wetting phase saturation
S
g
= (V
N
−V)/(V
N
−V
0
), one may write,
∂S
∂V
=−
1
∆V

∂V
∂S
=−∆V,
and by substituting in the pore size distribution equation, one gets,
D(r) =
1
dr
dP
c
(∂P
c
/∂S)
.
Using the definition of the capillary pressure P
c
= 2σ cosθ/r, gives
dP
c
=
∂P
c
∂r
dr =−
P
c
r
dr.
Substituting this last expression into the pore size distribution, one gets,
D(r) =−
P
c
r
1
(∂P
c
/∂S)
.
Fig. 6.11 shows the two curves for the capillary pressure and the pore size
distribution, respectively. When P
c
(S
g
) is known, then D(r) can be calculated,
using the following steps.
1. For a certain gas saturation S
g
, the corresponding capillary pressureP
c
(S
g
) is
calculated.
98 Chapter 6. Wettability and Capillary Pressure
Pore radius, r
P
o
r
e
r
a
d
i
u
s
d
i
s
t
r
i
b
u
t
i
o
n
,
D
(
r
)
C
a
p
i
l
l
a
r
y
P
r
e
s
s
u
r
e
,
P
c
Water saturation, S
w
Incremental
Mercury
Injection
D(r)
P
c
r
dS
w
dP
c
=
Figure 6.11: Capillary pressure curve and corresponding pore size
distribution [8].
2. The pore radius related to this pressure is r = 2σ cosθ/P
c
.
3. The tangent to the curve P
c
(S
g
) through the co-ordinate (S
g
, P
c
(S
g
)) gives the
slope defined by ∂P
c
/∂S.
In Fig. 6.11 the pore size distribution is drawn in accordance with the enumer-
ated list.
.
6.8 Saturation Distribution in Reservoirs
The equilibrium fluid saturation distribution in a petroleum reservoir, prior to production is
governed by the pore space characteristics. This is as a result of the non-wetting phase, nor-
mally hydrocarbons, entering pore space initially occupied by the wetting fluid, normally water,
during migration of hydrocarbons from a source rock region into a reservoir trap. A pressure
differential is required for the non-wetting phase to displace wetting phase and this is equivalent
to a minimum threshold capillary pressure and is dependent on pore size.
The physical significance of threshold pressure in an oil reservoir may be appreciated by
the analogy with a capillary rise of water in different vertical glass tubes suspended in an open
tray of water, as seen in Fig. 6.12. Since P
c
∝ 1/r it is observed that entry of the non-wetting
phase should be most difficult in the smallest tube (highest threshold pressure). For a water-air
system, the following relation exist,
P
c
= gρ
w
h, ⇒ P
c(3)
> P
c(2)
> P
c(1)
where r
3
< r
2
< r
1
.
The threshold capillary pressure, found in reservoir is proportional to the height above the
free water level (FWL), where a 100% water saturation is found.
The FWL is a property of the reservoir system, while an oil-water contact observed in a
particular well will depend on the threshold pressure of the rock type present in the vicinity of
the well.
6.8 Saturation Distribution in Reservoirs 99
h
1
h
3
h
2
Figure 6.12: Capillary water elevation in cylindrical tubes as func-
tion of tube radii.
The relation between height above the free water level and the capillary pressure is derived
from consideration of the gravity-capillary pressure force equilibrium. Using a free water level
as the datum plane and defining its position in the reservoir as the place where the oil phase
pressure p
o
equals the water phase pressure p
w
, one obtains,
P
c(FWL)
= p
o
−p
w
= 0.
At some height h, above FWL, the pressures are,
p
o
= p
FWL
−ρ
o
gh
p
w
= p
FWL
−ρ
w
gh
Therefore, the capillary pressure at a depth equivalent toh above the FWL is,
P
c
= p
o
−p
w
= (p
FWL
−ρ
o
gh) −(p
FWL
−ρ
w
gh) = gh(ρ
w
−ρ
o
)
Since P
c
= P
c
(S
w
, r) there exist a dependence,
h = h(S
w
, r),
which indicated that saturation at height h, will depend on both the water saturation and the
pore radius (see example: "Equilibrium in a capillary channel"),
h
S
w
=

ow
cosθ
c
rg(ρ
w
−ρ
o
)
.
Similarly, the threshold height h
t
is equivalent to the height of an observed water-oil contact
above FWL. In a particular rock type, this height is given,
h
t
=
P
ct
g(ρ
w
−ρ
o
)
.
In real reservoir systems it is expected that a number of rock type units or layers will
be encountered. Each unit can have its own capillary pressure characteristic and the static
saturation distribution in the reservoir will be a superposition of all units, as seen in Fig. 6.13.
100 Chapter 6. Wettability and Capillary Pressure
FWL
OWC
OWC
OWC
OWC
Well
k
1
k > k > k > k
1 4 3 2
k
2
k
3
k
4
Figure 6.13: Observed water-oil contacts and their relationship with
free water level (FWL) in a layered reservoir with a
common aquifer [8].
Example: Equilibrium in a capillary tube
In this example, the relation between elevation of water above FWL in reservoirs
is coupled to the pore dimension (pore radius).
Equilibrium in a vertical water wet capillary tube, as shown in Fig. 6.14, is
related to the saturation of water in a reservoir, where oil is the non-wetting fluid.
For a small perturbation ∆h, a small part of the tube surface will experience
a change in fluid coverage, when oil is replacing water as being the contact fluid.
The change in surface energy, caused by oil displacing water in a small fraction of
the capillary tube (see close up in Fig. 6.14), is given by the difference in surface
tension (or surface energy),
∆E
s
= 2πr(σ
os
−σ
ws
)∆h.
Water
w
Oil
o
∆h
h
r
Figure 6.14: Perturbation around equilibrium in a water-wet capil-
lary tube.
6.9 Laboratory Measurements of Capillary Pressure 101
The corresponding potential energy change, due to change in elevation is writ-
ten,
∆E
p
= πr
2
∆h(ρ
w
−ρ
o
)gh.
If small perturbations close to equilibrium are considered, the surface- and
the potential energy changes is expected to be equal, i.e. ∆E
s
= ∆E
p
. Using the
Young- Dupre equation, the following relation is given,
σ
ow
cosθ =
g
2

w
−ρ
o
)rh.
In a oil reservoir where the fluids are well defined , i.e. where the densities
and the oil- water interfacial tension are known parameters, the pore radiusr and
the height above FWLh are reciprocal variables. This means that the saturation of
initial water present in the reservoir above a certain height h is localised in those
pores having a radii less than r.
From the above consideration, the capillary pressure has a "dual" characteris-
tic,
P
c
= g(ρ
w
−ρ
o
)h =

ow
cosθ
r
,
where the capillary pressure is the pressure difference between oil- and water
phase at a certain elevation h in the reservoir, and at the same time, the pressure
difference across a curved surface in inside a pore channel of radiusr. This dual
characteristic of the capillary pressure gives the condition for the coexistence of
oil and water in porous rock.
.
6.9 Laboratory Measurements of Capillary Pressure
Laboratory measurements of capillary pressure are based on the fact thatP
c
∝σ cos θ/r, where
r characterizes the porous medium with respect to the pore throats and the pore size distribu-
tion . This implies that for any given porous medium and any pairs of fluids, the following
relationship is valid,
P
c1
(σ cos θ
c
)
1
=
P
c2
(σ cosθ
c
)
2
.
Practical use is made of this relationship in conducting laboratory tests with fluids other
than reservoir condition fluids. For example, air and brine with a (σ cos θ
c
)
lab
value of 72
dynes/cm may be used to measure capillary pressure for air- brine in the laboratory. The
relationship for the reservoir oil-brine pair capillary pressure is obtained using the appropriate
value of (σ cos θ
c
)
res
=26 dynes/cm, where,
P
c,res
= P
c,lab
(σ cosθ
c
)
res
(σ cosθ
c
)
lab
.
102 Chapter 6. Wettability and Capillary Pressure
The migration of hydrocarbons into an initially water filled reservoir rock and subsequent
equilibrium vertical saturation distribution is modelled in the laboratory by a non-wetting phase
displacing a wetting phase (drainage capillary pressure test). Air and brine are frequently used
as the pseudo reservoir fluids, and the displacement is affected by increasing air pressure in
a series of discrete steps in water saturated core plugs sitting on a semi-permeable porous
diaphragm. As a result of an increase in pressure (equivalent to P
c
since P
c
= p
air
− p
brine
)
the water saturation decreases and its value is established by weighting the core plugs. The
apparatus layout is shown in Fig. 6.15.
Core plug
Capillary
contact
powder
Neoprene
diaphragm
Screen
Porous
plate
Air
pressure
Figure 6.15: Gas-liquid drainage capillary pressure measurement.
Portion of liquid in saturated core is displaced at a par-
ticular pressure level by either gas or liquid. Liquid sat-
uration measured after equilibrium saturation has been
reached. Repetition for several successive pressure lev-
els [8].
In laboratory tests the final irreducible wetting phase saturation value is often beyond the
breakdown pressure of the porous plate and is sometimes obtained by centrifuge spinning at
a rotational force equivalent to about 150 psi (10.34 bar), and measuring the quantity of any
produced wetting phase.
The pore size distribution in a given rock type is usually determined by a mercury injection
test. Although this test is destructive, in the sense that the sample cannot be used again, it has
the advantage that high pressures can be attained, where mercury, the non-wetting phase with
respect to air, can be forced into very small pores.
Example: Height of water - oil transition zone.
A laboratory air-brine capillary pressure of 1.25 bar has been measured in a reser-
voir core sample at residual water saturation. The air-brine interfacial tension is
0.070 N/m and the brine-oil interfacial tension for the reservoir fluids is 0.022
N/m.
The height of the water-oil transition zone is the height from FWL and up to
the point in the reservoir where connate water saturation is reached,
6.10 Drainage and Imbibition Processes. 103
h
res
=
P
c,res
g(ρ
brine
−ρ
oil
)
,
where P
c,res
is the capillary pressure in the reservoir at this water saturation. ρ
brine
and ρ
oil
is respectively 1074 kg/m
3
and 752 kg/m
3
.
In the case of identical wetting preferences for the core sample and the reser-
voir, one may assume proportionality between capillary pressure and the interfa-
cial tension in the two situations,
P
c,res
= P
c,lab
σ
res
σ
lab
.
Combining these two equation, the height of the transition zone is found,
h
res
=
σ
res
σ
lab
P
c,lab
g(ρ
brine
−ρ
oil
)
,
which gives, h
res
= 12.5 m.
.
6.10 Drainage and Imbibition Processes.
When two or more fluids flow through a porous medium simultaneously, the phase pressures
p
i
, generally speaking, are not identical. The difference between the phase pressures of two
coexisting phases is defined as the capillary pressure. The capillary pressure is inversely pro-
portional to a generalised interfacial curvature, which is usually dominated by the smallest
local curvature (radius) of the interface, as illustrated in Fig. 6.16.
r
R
oil
water
rock
Figure 6.16: Local curvature of the interface of two coexisting liq-
uids.
An idealised permeable medium is considered by the arrangements of decreasing pore sizes
(a single pore bounded by the decreasing sizes sphere assemblage) and initially saturated with
a wetting phase (w) into which a non-wetting phase (nw) is alternatively injected and then
104 Chapter 6. Wettability and Capillary Pressure
withdrawn. The forcing of a non-wetting phase into a pore (non-wetting saturation increasing)
is a drainage process. The reverse (wetting saturation increasing) is animbibition process. We
imagine the pores have an exit for the wetting fluid somewhere on the right.
Beginning at zero non-wetting saturation, injection up to the saturation shown incondition
1 in Fig. 6.17, is first considered. At static conditions, the pressure difference between the exit
and entrance of the assemblage is the capillary pressure at that saturation. When the wetting
fluid is introduced into the pore from the right, the non-wetting fluid disconnects leaving a
trapped or non-flowing glob in the largest pore (condition 2).
The capillary pressure curve from condition 1 to condition 2 is an imbibition curve that is
different from the drainage curve because it terminates (P
c
= 0) at a different saturation. At the
static condition 2, the entrance - exit pressure difference is zero since both pressures are being
measured in the same wetting phase.
1
3 4
5
6
Oil
Water
Rock
5
1
2 4 6
3
C
a
p
i
l
l
a
r
y
p
r
e
s
s
u
r
e
Non-wetting phase saturation
2
Figure 6.17: The distribution of a non-wetting phase at various satu-
rations.
Going from condition 2 to condition 3 is a second drainage process, that results in even
higher non-wetting saturation, a higher capillary pressure, and a higher trapped non-wetting
phase saturation after imbibition (condition). At the highest capillary pressure (condition 5), all
pores of the subtracted volume contain the non- wetting phase, and a post - imbibition trapped
saturation is maximum. The capillary pressure curve going from the largest non-wetting phase
saturation to the largest trapped non-wetting phase saturation is the imbibition curve (condition
6). Note, that the termination of any imbibition curve is at zero capillary pressure.
This representation, being quite simple, explains many features of actual capillary pres-
sure curves. Imbibition curves are generally different from drainage curves, but the difference
shrinks at high non-wetting phase saturations where more of the originally disconnected globs
6.10 Drainage and Imbibition Processes. 105
are connected. This phenomenon is called trapping hysteresis or drag hysteresis and is caused
by differences in advancing and receding contact angles.
6.10.1 Hysterisis in Contact Angle
When oil is moving to cover a rock surface which previously has been wetted by water, it
has been experimental proven that the contact angle is smaller than in the case when water is
replacing oil, over the same surface.
This effect is called the hysterisis in contact angle and has to do with the inherent memory
of a physical system, which relates prehistoric events to present experience. In practical terms
this means that the back and forth movement is energy dependent, typical for non-reversible
systems.
The hysterisis is detected by measuring the advancingθ
a
, and residing θ
r
contact angles of
an oil drop suspended between two horizontal plates (made of polished rock material; quartz
or calcite) submerged in water, as shown in Fig. 6.18. One plate is fixed and the other can
move smoothly to either side. The oil drop is left to age between the plates for some time, until
the two contact angles are equal. When the mobile plate is moved, the two contact angles are
measured. The test is repeated after some time, when the two angles have stabilised.
s
oil
water
θ
r
θ
a
Figure 6.18: Measurement of hysterics in contact angle.
The hysterics observed, where the receding angle is smaller than the advancing angle, is
an expression of the fact that energy is lost in cyclic systems. In relation to multiphase flow in
porous media, the hysterics has two important effects:
• One is to stabilise the capillary surfaces (interfaces) between the fluids in the pore system,
such as to preserve the fluid distribution in the reservoir, unless a finite capillary pressure
difference is imposed.
• The second effect is related to the dissipation of energy towards the capillary walls, when
the interface is advancing through the pore. The effect of this dissipation of energy is
experienced as a resistance towards flow and is often materialised through "rip off" of
small droplets, which then becomes practically immobile.
6.10.2 Capillary Hysterisis
It is seen that capillary pressure depends both on wetting phase saturation and the direction of
its variation. A typical curve of the capillary pressure in case of two-phase flow, is shown in
the Fig. 6.19.
106 Chapter 6. Wettability and Capillary Pressure
P
cb
P
(
S
)
c
w
S
nc
S
w
S
wc
1.0 0.0
1
2
3
Figure 6.19: Typical type of capillary pressure curve for a two-phase
flow problem: 1 drainage, 2 imbibition and 3 secondary
drainage.
Two ways in which one phase can be substituted by the other in a porous medium are usu-
ally considered. The first is the process of displacement where the wetting phase is displaced
by the non-wetting one, and the second is the process of imbibition, where the non-wetting
phase is displaced by the wetting one. The value P
cb
is defined as threshold capillary pressure
which should be exceeded to provide displacement. If displacement is preceded by imbibition
the capillary pressure curve is as the curve 3 in the Fig. 6.19, which is different from the curve
1. The presence of two different curves of imbibition and displacement is called capillary hys-
teresis. The presence of the negative capillary pressure near the saturation pointS
w
= S
nc
was
first discovered by Welge (1949). The hysteresis effect i demonstrated by the two curves 2 and
3 in Fig. 6.19.
6.11 Exercises 107
6.11 Exercises
1. Calculate the energy needed to transform 1 cm
3
of water into droplets with an average
radius of 1 µm. In analogy with displacement processes in porous media, assume an
interfacial tension σ
o,w
= 0.025 N/m.
2. Show that the general expression for capillary pressure
P
c
= σ

1
R
1
+
1
R
2

,
could be written
P
c
=
2σ cos θ
r
,
for a cylindrical tube. Define the parameters; r, R
1,2
, θ and σ.
3. A capillary glass-cylinder is positioned vertically in a cup of water. Calculate the height
of water inside the cylinder when the inner diameter is 0.1 cm. The surface tension
between water and air is 72 dyn/cm, and the water is assumed to wet the glass 100 %.
4. In order to displace water by air form a porous plate, a pressure of 25 psig is needed.
Find the diameter, given in µm, of the largest pore channel disconnecting the porous
plate, when the surface tension σ
air,w
is 72 dyn/cm.
5. A horizontal cylinder, filled with oil, is 0.1m long and has a inner diameter of 0.01 mm.
The oil has a viscosity similar to water, 1 mPa s. What is the pressure drop along the
cylinder, when the average flow velocity is found to be 0.01mm/s ?
An equal amount of water and oil is pumped through the cylinder and the water and oil
is assumed to move through the tube as droplets, with an average length of 0.03mm pr.
droplet. The advancing contact angle is 40
o
and the receding angle is 20
o
. Calculate the
pressure drop through the tube, assuming the same flowvelocity as above. The interfacial
tension between water and oil is 25 mN/m.
6. A core sample is placed in a core holder in a centrifuge. The radial distance to the
core sample is given by the two position vectors r
1
and r
2
. The length of the sample is
therefore; r
2
−r
1
. At a rotation frequency ω, air will displace some of the water in the
sample. The radial distance r
d
, corresponds to the threshold pressureP
d
at that particular
rotation frequency. See the figure below.
a) Show that the pressure difference for one phase is given by:
P
2
−P
1
=
1
2
ρω
2
(r
2
2
−r
2
1
), when P
2
= P(r
2
), P
1
= P(r
1
)
b) Show that
P
c
(r) =
1
2
∆ρω
2
(r
2
2
−r
2
)
108 Chapter 6. Wettability and Capillary Pressure
ω
r
S
w
r
1
r
2
r
d
1.0
0.0
when its known that
P
c1
= P
c
(r
1
) =
1
2
∆ρω
2
(r
2
2
−r
2
1
)
and when
P
d
=
1
2
∆ρω
2
(r
2
2
−r
2
d
)
It is assumed that P
c2
= P
c
(r
2
) = 0.
c) The water saturation can be written,
S
w1
= S
w
(r
1
) =
d(
¯
S
w
P
c1
)
dP
c1
when r
1
∼r
2
, assuming the length of core sample to be short compared to the radius
of rotation. (This is an approximation, only partly true.)
Use the equations above to derive the a formula giving the capillary pressure as
function of the water saturation (P
c
–curve), when the capillary pressure is given in
kPa.
The following data is given for a core sample, saturated with sea-water and rotated
in air.
r
1
= 4.46 cm
r
2
= 9.38 cm
∆ρ = 1.09 g/cm
3
V
p
= 8.23 cm
3
RPM

415 765 850 915 1005 1110 1305
∆V[cm
3
] 0.00 0.00 0.10 0.15 0.30 0.50 1.10
RPM 1550 1835 2200 2655 3135 3920 4850
∆V[cm
3
] 2.20 2.90 3.61 4.21 4.72 5.24 5.75
RPM

: Rotation pr. Minute and ∆V: produced volume.
6.11 Exercises 109
7. In the laboratory, a capillary pressure difference of 5 psi has been measured between
water and air in a core sample. Calculate the corresponding height above the OWC in
the reservoir from where the core originates, when the following information is given
(assume capillary pressure at the OWC to be zero).
Laboratory Reservoir
σ = 75dyn/cm σ = 25dyn/cm
∆ρ
w/air
= 1.0g/cm
3
∆ρ
o/w
= 0.2g/cm
3
8. In a laboratory experiment, capillary data from two water saturated core samples was
obtained by using air as the displacing fluid.
1000 mD core sample 200 mD core sample
P
c
[psi] S
w
P
c
[psi] S
w
1.0 1.00 3.0 1.00
1.5 0.80 3.6 0.90
1.8 0.40 4.0 0.60
2.2 0.20 4.5 0.30
3.0 0.13 5.5 0.20
4.0 0.12 7.0 0.18
5.0 0.12 10.0 0.18
Calculate the distribution of vertical water saturation in the stratified reservoir given by
the figure below, i.e. determine S
w
as function hight in the reservoir.
12 ft
4 ft
6 ft
3 ft
4 ft
5 ft
FWL
Additional data:
Laboratory: σ
w/air
= 50dyn/cm
Reservoir: σ
o/w
= 23dyn/cm
ρ
o
= 0.81g/cm
3
ρ
w
= 1.01g/cm
3
9. Use the air - water capillary pressure curve for laboratory conditions, below, to calculate
the saturations; S
o
, S
g
and S
w
at the reservoir level (hight) 120 f t above the oil-water
contact (assume P
c
= 0 at this level). The distance between the contacts (OWC and
GOC) is 70 f t.
Additional data:
110 Chapter 6. Wettability and Capillary Pressure
Laboratory: σ
w/air
= 72dyn/cm
Reservoir: σ
o/g
= 50dyn/cm
σ
w/o
= 25dyn/cm
ρ
o
= 53lb/ f t
3
ρ
w
= 68lb/ f t
3
ρ
g
= 7lb/ f t
3
20 30 40 50 60 70 80 90 100
Water saturation [%]
0
10
20
30
40
50
60
70
80
90
C
a
p
i
l
l
a
r
y

p
r
e
s
s
u
r
e

[
p
s
i
]

10. An oil water capillary pressure experiment on a core sample gives the following results:
P
c,o/w
[psi] 0 4.4 5.3 5.6 10.5 15.7 35.0
S
w
[%] 100 100 90.1 82.4 43.7 32.2 29.8
Given that the sample was taken from a point 100 ft above the oil-water contact, what
is the expected water saturation at that elevation? If the hydrocarbon bearing thickness
from the crest (top) of the structure to the oil-water contact in 175 ft, what is the average
water saturation over this interval? (ρ
w
= 64lbs/ f t
3
and ρ
o
= 45lbs/ f t
3
)
11. If we assume an interfacial tension; σ cosθ = 25 dyn/cm and a permeability and porosity
respectively 100 mD and 18 %, in the exercise above, we may construct the capillary
curve for a laboratory experiment using mercury as non-wetting phase. In the laboratory
experiments one assume the lithology to be unchanged, but the permeability and porosity
to be respectively 25 mD and 13 %. Find laboratory capillary curve when the interfacial
tension to mercury is 370 dyne/cm.
Answers to questions:
1. ∆E = 0.075J, 3. h = 3cm, 4. d = 0.5µm, 5. ∆p = 3.2mbar, ∆p = 29bar, 7. h = 5.8m, 9.
S
o
= 0.2, S
g
= 0.62 , S
w
= 0.36, 11. S
w
= 0.41.
Chapter 7
Relative Permeability
7.1 Definitions
Relative permeability is a concept used to relate the absolute permeability (100% saturation
with a single fluid) of a porous system, to the effective permeability of a particular fluid in the
system, when that fluid occupies only a fraction of the total pore volume.
When measuring a flow-rate of a fluid versus the pressure difference in a core sample, we
can obtain (single phase flow),
q =
k
e
A
µ
´p
´x
,
and
k
e
=
q
A
µ´x
´p
.
Here k
e
is called effective permeability. For 100% saturation, the effective permeability is
identical to the absolute permeability; i.e. k
e
= k.
In multiphase flow a generalisation of Darcy law has been accepted [12],
q
j
= k
je
A
µ
j
´p
j
´x
,
where j denotes a fluid phase j, and k
je
is called the effective (phase) permeability.
According to the last equation we can obtain,
k
je
=
q
j
A
µ
j
´x
´p
j
.
In a vast number of laboratory experiments it has been observed that a sum of effective
permeability’s is less than the total or absolute permeability, i.e.,
n

j=1
k
je
< k.
Moreover, effective (phase) permeability was noticed to be a function of quite a number of
parameters, such as: fluid saturation, rock property, absolute permeability, fluid property, and
reservoir conditions (pressure, temperature),
k
je
= f (k, p, T, S
1
, S
2
, . . . , S
n
, . . .) j ∈ [1, n].
111
112 Chapter 7. Relative Permeability
In two phase systems the latter relationship is expressed as functions of a single (by con-
vention, wetting) saturation.
The effective permeability can be decomposed into the absolute permeability and the rela-
tive permeability, as shown below,
k
e j
= k
r j
k.
The relative permeability is a strong function of the saturation of phaseS
j
. Being a rock-
fluid property, the functionality between k
r j
and S
j
is also a function of rock properties (e.g.
pore size distribution) and wettability. It is not, in general, a strong correlation between relative
permeability and fluid properties, though when certain properties (e.g. interfacial tension)
change drastically, relative permeability can be affected [40].
It is important to note that the phase permeability is a tensorial function (as the absolute
permeability) and that the relative permeability is not.
Though there have been attempts to calculate relative permeability on theoretical grounds,
by far the most common source of them, has been experimental measurements. This implicates
that it is important to keep definitions of mobility, phase permeability and relative permeability
separate and clear.
Functions k
j
(S
j
) depend both on the structure of the porous medium and on the saturation
distribution of the phases. However in mathematical modelling of two-phase and multi-phase
flowit is conventional to assume that relative permeabilities are the functions of saturation only.
This assumption considerably simplifies the task of laboratory experiments carried out in order
to determine relative permeabilities.
In the presence of two coexisting phases, the typical curves of relative permeability are as
shown in Fig. 7.1.
S
wc
S
w
S
nc
k
c k
w
1.0
1.0
0.0
0.0
Figure 7.1: Typical type of relative permeability characteristics for a
two-phase flow, where S
w
is the wetting phase and S
n
is
the non-wetting phase.
One important feature in the behaviour of the rel.perm.-curves should be emphasised. If
saturation of one of the phases becomes less than some definite value: S
w
< S
wc
or S
n
< S
nc
,
then the corresponding relative permeability for that phase becomes zero and the phase be-
comes immobile. This means that continuity of the phase is broken or disturbed and the phase
7.2 Rock Wettability and Relative Permeabilities 113
remains in a passive or loose state. The values S
jc
, j = w, where n
1
are defined as residual
saturation of the i-th phase. Let us note that those values depend on thermodynamic condition
of the reservoir (reservoir pressure, temperature, number of phases, type of rock, etc.).
7.2 Rock Wettability and Relative Permeabilities
It should be noted that evaluations of phase- and relative permeabilities can be done through
measurements of capillary pressure, which shows the evidence of strong correlation between
them. Because of certain links between them, we would expect micro-heterogeneity and rock
wettability to have a certain influence on relative (phase) permeability. Typical water-oil rela-
tive permeabilities are presented for strongly water-wet and oil-wet formations in Fig. 7.2 (left)
and 7.2 (right), respectively.
0.0 0.2 0.4 0.6 0.8 1.0
1.0
0.8
0.6
0.4
0.2
0.0
Oil
Water
S
w
k
r
0.0 0.2 0.4 0.6 0.8 1.0
1.0
0.8
0.6
0.4
0.2
0.0
Oil
Water
S
w
k
r
Figure 7.2: Characteristics of typical relative permeability for a two-
phase flow, where S
w
is the wetting phase and S
n
is the
non-wetting phase (left: a water-wet formation and right:
an oil-wet formations).
The difference in the flow properties that indicates different wettability preferences can be
illustrated by the following rule of thumb [29]:
1
Here w and n denote wetting and non-wetting phase, respectively.
114 Chapter 7. Relative Permeability
Water-wet Oil-wet
Connate water satura-
tion
Usually greater than
20 to 25 percent PV
Generally less than 15
percent PV, frequently
less than 10 percent
Saturation at which
oil and water per-
meabilities are equal
(crossover saturation)
Greater than 50 per-
cent water saturation
Less than 50 percent
water saturation
Relative permeabili-
ties to water at maxi-
mum water saturation;
i.e. flood-out
Generally less than 30
percent
Greater than 50 per-
cent and approaching
100 percent
Let us note that the endpoint values of the relative permeabilities are usually (if not always)
less than 1 and which are measures of wettability. The non-wetting phase occurs in isolated
globules, several pore diameters in length, that occupy the center of the pores. Trapped wetting
phase, on the other hand, occupies the cavities between rock the grains and coats the rock
surfaces. Thus we would expect the trapped non-wetting phase to be a bigger obstacle to the
wetting phase, then the trapped wetting phase is to the non-wetting phase. The wetting phase
endpoint relative permeability will, therefore, be smaller than the non-wetting phase endpoint.
The ratio of wetting to non-wetting endpoints proves to be a good qualitative measure of the
wettability of the medium. For extreme cases of preferential wetting, the endpoint relative
permeability to the wetting phase can be 0.05 or less. Others view the crossover saturation
(k
r2
= k
r1
), of the relative permeabilities is a more appropriate indicator of wettability, perhaps
because it is less sensitive to the value of the residual saturations (see the rule of thumb, above).
7.3 Drainage/Imbibition Relative Permeability Curves
In a gas-oil systems, the direction of displacement is particularly important, as the process can
represent a drainage process, such as gas drive (gas displacing oil immiscibily) or an imbibition
process, such as:
1. Movement of an oil zone into receding depleting gas cap.
2. Movement of an aquifer into receding depleting gas cap.
In gas-oil systems the third phase, water, which is always present in the reservoir, is consid-
ered to stay at irreducible saturation and play no part in the displacement processes. It is there-
fore argued that experiments in the laboratory can be conducted with or without irreducible
water present and that effective permeabilities could be correlated to total liquid saturation
(S
L
), rather than gas saturation. The relation is based on a definition of liquid saturation,
S
L
= S
o
+S
w
= 1−S
g
.
7.4 Residual Phase Saturations 115
1.0
1.0
0.0
S
gc
S
g
S
gmax
k
ro
k
rg
k
=

k
/

k
r
o
1.0
1.0
0.0
S
gr
S
g
S
gmax
k
ro
k
rg
k
=

k
/

k
r
o
Figure 7.3: Gas-oil relative permeabilities [8].
In a system where gas saturation increases from zero, as in a liquid drainage process, it
is observed that gas does not flow until some critical gas saturation (S
gc
) has been attained.
This is attributed to the physical process of the gas phase becoming continuous through the
system, as a condition for gas flow. In liquid imbibition processes (gas saturation decreasing
from a maximum initial value) the gas permeability goes to zero when the residual or trapped
gas saturation (S
gr
) is reached. See Fig. 7.3.
7.4 Residual Phase Saturations
As we know from the previous discussion, increasing pressure gradients force the non-wetting
phase into the pore channels, causing the wetting phase to retreat into the concave contacts
between the rock grains and other cavities in the pore body. At very high pressure differences,
the wetting phase approaches mono-layer coverage and a low saturation.
The residual non-wetting phase is trapped in the large pores in globules several pore di-
ameters in length. Repeated experimental evidence has shown that under most conditions, the
S
nwr
could be as large as S
wr
.
According to experimental observations there is a strict evidence of a relationship between
residual non-wetting or wetting phase saturations and the so-called local capillary number. This
relationship is called the capillary de-saturation curve (CDC). Typically, these curves are plots
of percent residual (non-flowing) saturation for the non-wetting (S
nwr
) or wetting (S
wr
) phases
on the y axis versus a capillary number on a logarithmic x axis. The capillary number N
c
is a
dimension-less ratio of viscous forces to local capillary forces, and can be variously defined.
One of the examples is shown below (after Dombrovsky and Brownell):
N
c
=
k [ ∇

Φ[
σ
ow
cosθ
c
116 Chapter 7. Relative Permeability
where

Φ is the potential of flow.
10 10 10 10 10 10
-7 -6 -5 -4 -3 -2
Wetting phase
Normal range
waterfloods
Nonwetting
critical N
c
30
20
10
0
Nonwetting
phase
Wetting
critical N
c
Capillary number N
c
R
e
s
i
d
u
a
l

n
o
n
-
w
e
t
t
i
n
g

o
r
w
e
t
t
i
n
g

s
a
t
u
r
a
t
i
o
n
,

%
Figure 7.4: Schematic capillary de-saturation curve [40].
It is important to mention that chemical additives reduce capillary forces at the interface
of the oil/water system, resulting in increased capillary number N
c
and reduced residual oil
saturation, being either wetting or non-wetting phase. The reduction of interfacial tension at
the interface allows the trapped oil to become mobile and be displaced by the water.
7.5 Laboratory Determination of Relative Permeability Data
Laboratory determination of effective permeability is generally conducted as a special core
analysis test on representative and carefully preserved core plug samples. A reservoir condition
test is conducted at reservoir pore pressure conditions and reservoir temperatures with real
or simulated reservoir fluids. Such reservoir condition tests may model displacement under
unsteady state, or steady state conditions. Different equipment arrangements for those test are
shown in Figs. 7.5 and 7.6.
Unsteady state rel.perm. test simulate the flooding of a reservoir with an immiscible fluid
(gas or water). The determination of rel. perm. is based on observation of the fractional flow
of displacing phase fluid from the outlet end of the core plug and its relationship with satu-
ration. The displacement theory of Buckley and Leverett is combined with that of Weldge in
a technique described by Johnson, Bossler and Naumann [38]. The detection of the break-
through time of the displacing phase at the outlet core face is critical in the representation of
relative permeability, and severe errors can occur with heterogeneous samples. Flow rates are
determined according to the method of Rappoport and Leas in order to minimize the effect
of capillary pressure forces in retaining wetting phase fluid at the outlet end face discontinu-
ity. The unsteady state or dynamic displacement test is most frequently applied in reservoir
analysis of strong wetting preference, and with homogeneous samples.
For reservoirs with more core-scale heterogeneity and with mixed wettability, the steady
state laboratory test is preferred. The steady state process provides simultaneous flow of dis-
placing and displaced fluids through the core sample at a number of equilibrium ratios. At each
7.5 Laboratory Determination of Relative Permeability Data 117
Hg
res.
Ruska
pump
Hg
Brine Oil
Chart
recorder
Oil
colector
Sample
3 way
valve
Brine
colector
Hg
Hg
B
r
i
n
e
Oil
Chart
recorder
0 - 50 psig
Transducer
Oil
colector
Sample
3 way
valve
Brine
colector
Soltrol
O
i
l

S
o
l
t
r
o
l
300
cc
300
cc
1000
cc
Figure 7.5: Unsteady state relative permeability measurement at
constant rate (above) and at constant pressure (below).
ratio from 100% displaced phase to 100% displacing phase an equilibrium condition must be
reached at which the inflow ratio of fluids equals to the outflow ratio, and at which the pressure
difference between inlet and outlet is constant. At such a condition the Darcy law equation is
applied to each phase to calculate effective permeability at the given steady state saturation.
Capillary pressure tends to be ignored and a major difficulty is the determination of saturation
at each stage. Between five and ten stages are usually needed to establish rel.perm. curves.
118 Chapter 7. Relative Permeability
Hg
res.
Hg
Oil
res.
Brine
Oil
Oil
Chart
recorder
Sample
Constant displacement
Ruska pumps
Pressure
transducer
Figure 7.6: Steady state relative permeability measurement [8].
7.6 Exercises
1. Use Darcy’s law for radial flow and show that the fractional flow for water, f
w
, can be
written:
f
w
=
q
w
q
w
+q
o
=
1
1+k
ro
µ
w
/k
rw
µ
o
Assume the capillary forces to be negligible anddP
o
/dr = dP
w
/dr.
The following laboratory data is given:
S
w
k
ro
k
rw
P
lab
c
[psi]
1.00 0.00 1.00 1.0
0.90 0.04 0.78 3.4 ρ
o
= 0.85g/cm
3
0.80 0.14 0.58 3.9 ρ
w
= 1.00g/cm
3
0.70 0.29 0.39 4.5 σ
res.
= 22dyn/cm
0.60 0.49 0.23 5.7 σ
lab
= 75dyn/cm
0.50 0.73 0.09 8.4 µ
o
= 15.0cp
0.40 1.00 0.00 18.0 µ
w
= 1.0cp
0.30 1.00 0.00 ∞
Use critical oil saturation, S
oc
= 0.05 and the data above to construct a graph showing
the water fraction as function of height above the WOC.
What is the water fraction at 15 m above the WOC ?
7.6 Exercises 119
2. The laboratory data below is recorded at stationary conditions, measuring the relative
permeability for a oil-water injection experiment.
q
o
[cm
3
/time] q
w
[cm
3
/time] ∆P [psi] V
w
[cm
3
]
90 0 49.25 2.17
75 5 91.29 2.87
60 9 109.52 3.63
45 20 123.30 4.65
30 34 137.05 5.93
15 85 164.30 7.95
0 122 147.00 9.86
V
w
is the volume of water in the core sample, determined by weighing. q
o
and q
w
is the
oil- and water rate through the sample, respectively. ∆P is the pressure drop.
Additional data is given:
Absolute permeability 16.7 mD length of core sample 9 cm
Diameter of core sample 3.2 cm Oil viscosity 2.0 cp
Water viscosity 1.1 cp Porosity 0.20
1 atm. equals 14.65 psi
Draw the rel.perm. curves for k
ro
and k
rw
using the data above.
Answers to questions:
1. 25%
120 Chapter 7. Relative Permeability
Chapter 8
Compressibility of Reservoir Rock and
Fluids
8.1 Introduction
Compressibility is a universal phenomenon, of significant importance where all substances are
compressible, some more compressible than others. Compressibility is therefore an important
"drive mechanism" in underground petroleum production.
Oil and gas are naturally existing hydrocarbon (HC) mixtures, quite complex in chemical
composition which exist at elevated temperatures and pressures in the reservoir. When pro-
duced to the surface, the temperature and pressure of the mixture are reduced, where the state
of the HC mixture at the surface depends upon the composition of the HC fluid found in the
reservoir. The fluid remaining in the reservoir at any stage of depletion undergoes physical
changes as the pressure is reduced due to removal of quantities of oil, gas and initial water
from the reservoir.
It is necessary to study the physical properties of these naturally existing HC and in partic-
ular, their variation with pressure and temperature, in order to fully understand and control the
production process. This information is important in estimating the performance of the fluids
in the reservoir.
Compressibility, as physical phenomenon, plays a key role in general underground petroleum
production. Nearly all production of oil, gas and formation water is related to volume expan-
sion when the reservoir pressure decreases due to removeal of reservoir fluids.
8.2 Compressibility of Solids, Liquids and Gases
For a mixture of HC it is quite obvious that pressure and temperature are essential parameters.
The state of equilibrium is defined by these two parameters and consequently also the phase
behaviour of the fluid, i.e. the fractional volume of oil and gas.
In the case of formation rock and the saturation of fluids contained therein, pore volume
and fluid changes due to the pressure decline is the dominating phenomenon, responsabile for
reservoir fluid production, since the reservoir temperature changes slightly or remain constant
in most cases. Volumes of reservoir fluid brought to the surface will experience change in both
121
122 Chapter 8. Compressibility of Reservoir Rock and Fluids
pressure and temperature, i.e. the final state of oil and gas is characterised by volume changes
due to both drop in pressure and in temperature.
The general behaviour of materials can be described by the compressibility and expansion
terms;
c = −
1
V

∂V
∂ p

T
, (8.1)
β =
1
V

∂V
∂T

p
, (8.2)
where c is the isothermal compressibility, c ≥0 and β is the isobaric thermal expansion, β ≥0.
In practice, it is normal to use an average compressibility factor of the different HC com-
ponents. In relation to reservoir production, it is common practise to distinguish between the
following definitions of compressibility:
• Rock matrix compressibility; c
r
.
• Rock bulk compressibility; c
b
.
• Liquid compressibility (oil or initial water); c
o
and c
w
.
• Gas compressibility; c
g
.
8.2.1 Rock Stresses and Compressibility
When rocks are subjected to external load or force, internal stresses are developed and if the
stresses are sufficiently strong, deformation such as volume and shape changes of the rock will
be the result. The stresses on any plane surface through a rock sample under in situ. conditions
are composed of a normal stress vector (perpendicular to the plane) and two shear stresses,
parallel to the plane surface. The general stress condition may be characterised by a stress
tensor, with nine components as shown in Fig. 8.1. The stress tensor is often written in matrix
form;

¸
σ
x
τ
xy
τ
xz
τ
yx
σ
y
τ
yz
τ
zx
τ
zy
σ
z
¸

Due to the general conditions of equilibrium, the stress tensor will be symmetric around
the diagonal, which means that τ
xy
= τ
yx
and so on. There are thus only six independent stress
components in the stress tensor:
3 normal stresses: σ
x
, σ
y
and σ
z
and
3 tangential (shear stresses): τ
xy
, τ
yz
, τ
zx
.
Underground gas and oil reservoirs experience stresses due to the overload of rock material
and water and the lateral confinement stresses exerted on the reservoir from the surrounding
rock masses, see Fig. 8.2. It is possible to show that there exist one set of ortogonal axis with
8.2 Compressibility of Solids, Liquids and Gases 123
σ
z
σ
y
σ
x
τ
zy
τ
zy
τ
zx
τ
zx
τ
xy
τ
xy
z
x
y
Figure 8.1: Stress conditions of formation rock media.
σ
z
σ
y
σ
x
Figure 8.2: Principal stresses on reservoir rock..
respect to which all shear stresses are zero and the normal stresses have their extreme values.
These stresses are called the principal stresses
For most reservoirs, the principal normal stresses are orientated as shown in Fig. 8.2, where
the major principle stress σ
z
is acting parallel to the force of gravity, while the two lateral
stresses σ
x
and σ
y
are acting in the horizontal plane, e.g. σ
z
> σ
x
, σ
y
.
The average normal stress is generally defined by,
σ =
1
3

x

y

z
). (8.3)
The collective action of the principal stresses will cause the rock material to deform. The
relative longitudinal deformation is given by theprincipal strain,
ε
i
=
∆l
i
l
i
=
l
i
−l
/
i
l
i
, where i = x, y, z, (8.4)
where l
i
is the initial length of the rock in the i’th direction, l
/
is the length after deformation.
The sum of principal strains will give the relative volume change∆ε = (ε
x

y

z
), where
ε
V
=∆V/V. (In case of non-zero shear stresses, a displacement or rotation of the rock may be
experienced.)
The stress - strain relationship is dependent on several parameters of which the following
are the most important; the composition and lithology of the rocks, the degree of cementation
of the rock material, the type of cementing material, the compressibility of the rock matrix, the
porosity of the rock material and the pressure and temperature in the reservoir.
124 Chapter 8. Compressibility of Reservoir Rock and Fluids
In the following, the rock will be assumed to be isotropic, which means equal properties
in all directions. For simplicity, it is also assumed that the stresses are refered to the principal
stress directions.
Within the elastic limit of volume deformation of any rock material, Hooke’s law states
that there exist a proportionality between stress, σ and strain, ε, where σ
1
, σ
2
and σ
3
are the
principar stress directions.
σ
1
= Eε
1
, (8.5)
where E is the Young’s modulus of elasticity and the subscript indicate change in stress and
strain in the same direction and where the stresses normal to this direction are constant.
If a cylindrical rock sample is subjected to a compressive stress, σ
1
, parallel to its long
axis, it will shorten, ε
1
and the diameter will increase. The ratio of transverse strain to the axial
strain is expressed by the Poisson ratio ν. If the transverse strain is defined by ε
2
and ε
3
, then
the transverse deformation is given,
ν =
ε
2
ε
1
=
ε
3
ε
1
, (8.6)
where ε
1
is the principal strain direction.
The significance of Poisson’s ratio, coupling axial and transverse strain, indicates that de-
formation along one principal axis is caused by a combination of all three principal stresses.
This observation is presented in Hooke’s law in three dimensions:

x
= σ
x
−ν(σ
y

z
), (8.7)

y
= σ
y
−ν(σ
x

z
), (8.8)

z
= σ
z
−ν(σ
x

y
). (8.9)
In writing Hooke’s law this way, the strains are reddered to the condition of zero stresses.
It is often convenient to write Hooke’s law in changes of stresses, ∆σ
x
etc. In that case srain
are refered to the initial conditions.
The total deformation due to all three principal stresses acting on the rock material is given
by ∆V = (ε
x

y

z
)V. Using Hooke’s law, Eqs. (8.7) to (8.9), the relative volume change is
given,
∆V
V
=
3σ(1−2ν)
E
(8.10)
Relative volume deformation of the rock is also described by the compressibility Eq. (8.1)
on differential from,
∆V
V
= c
r
∆σ. (8.11)
In introducing c
r
, one assumes that the rock is completely solid with no pores or cracks
within it.
Combining equation Eq. (8.10) and Eq. (8.11) proves that the compressibility and the elas-
ticity are "two sides of the same case",
8.2 Compressibility of Solids, Liquids and Gases 125
c
r
=
3(1−2ν)
E
, (8.12)
where also the elastic constants E and ν, refer to the solid rock material.
In Eq.(8.12) the important relation between the compressibility and the elastic properties
of the rock material is established. Under the assumption that the deformation of the rock is
within the range of the elasticity (see Fig. 8.3), compressibility is constant, i.e.
dV
V
=−c
r
dσ, (8.13)
according to Eq.(8.1) the deformed volumeV is equal to,
V =V
0
e
−c
r
(σ−σ
0
)
·V
0
[1−c
r
(σ −σ
0
)]. (8.14)
The approximation is valid when c
r
∆σ is small, i.e. c
r
(σ −σ
0
) <1.
V
p p
0
V
0
0
Within the range
of elasticity
Figure 8.3: Deformation of rock bulk volume under conditions of
elastic behaviour (constant compressibility factor).
The dimension of compressibility c
r
is reciprocal pressure, as follows from Eq.(8.1) or
(8.14), i.e.
[c
r
] = [σ]
−1
For normal reservoir rock like quarts, the compressibility is;c
quarts
∼2.5 10
−6
bar
−1
.
8.2.2 Compressibility of Liquids
Deformation of liquids can be explained, following the same chain of arguments as seen for
solid (rock) material. Within the elastic limit of the liquid, one can expect the compressibility
to be constant and in accordance to Eq.(8.1) and in analogy with Eq.(8.14),
V
l
=V
l
0
e
−c
l
(p−p
0
)
·V
l
0
[1−c
l
(p−p
0
)], (8.15)
126 Chapter 8. Compressibility of Reservoir Rock and Fluids
where the last approximation is valid whenc
l
(p−p
o
) <1.
Various liquids may behave quite differently depending on the composition of that liquid.
Water is not particularly compressible and has a compressibility factorc
w
∼ 4.6 10
−5
bar
−1
.
Oil, on the other hand, may have a varying compressibility factor, depending on the compo-
sition of oil, i.e. the mixture of light and heavy HC and the amount of gas contained in the
oil.
Black oils may have a compressibility ∼25 10
−5
bar
−1
, while light oils can have substan-
tially higher compressibility, depending on the content of the solution gas.
8.2.3 Compressibility of Gases
Experience tells us that gases are very compressible. Gas compressibility can be defined
equally to solids and liquids, using the definition in Eq.(8.1), in an attempt to consistently
describe the nature of compressibility as a universal characteristic, also valid for gases.
In the case of a perfect gas,
pV = nRT, (8.16)
where
p: absolute pressure of the gas phase,
V: volume which it occupies,
T: absolute temperature of gas,
n: number of moles of gas equal to its mass divided
by its gaseous molecular weight and
R: the gas constant.
Combining Eqs.(8.1) and (8.16) one obtain,
c
g
=−
1
V
∂V
∂ p
=
1
p
. (8.17)
Form this deduction it must be conclude that compressibility of gases is notconstant, but
varies as the reciprocal pressure (under the assumption of constant temperature).
Example: Compressibility of real gas
The real gas law is,
pV = znRT,
where z is the deviation factor, expressing the non-ideal deviation from perfect gas
behaviour.
Since compressibility describes the volume deformation, we may assume the
volume to be a function of pressure, temperature and a non-ideal factor, i.e. V =
V(p, T, z).
Differentiation of the volum function,
dV =
∂V
∂ p
dp+
∂V
∂T
dT +
∂V
∂z
dz,
= −
V
p
dp+
V
T
dT +
V
z
dz.
8.2 Compressibility of Solids, Liquids and Gases 127
At reservoir condition, T is constant and consequently,

1
V
dV
dp
=
1
p

1
z
dz
dp
.
Compressibility for real gases in the reservoir is then given by,
c
g
=
1
p

1
z
dz
dp
.
The deviaton factor z, is a non-trivial function of pressure and temperature.
The z-factor is usually expressed as a function of the so-called pseudo reduced
pressure p
pr
and pseudo reduced temperature T
pr
, as seen in Fig. 8.4, i.e.
z = z(p
pr
, T
pr
),
where pseudo reduced pressure and temperature are defined as,
p
pr
=
p
p
pc
, T
pr
=
T
T
pc
,
where p
pc
and T
pc
are pseudo critical pressure and pseudo critical temperature,
respectively.
Z
p
pr
1.0
0
T
pr
n
T
pr
T
pr
1
Figure 8.4: z-factor as a function of pseudo reduced pressurep
pr
and
temperature T
pr
.
Critical pressure and temperature for a mixture of m numbers of HC compo-
nents are defined,
p
pc
=
m

i
n
i
p
ci
, T
pc
=
m

i
n
i
T
ci
,
where p
ci
and T
ci
are critical pressure and temperature of the different HC compo-
nents and n
i
is the volume fraction or the mole fraction of each component given
by Avogadro’s law.
.
128 Chapter 8. Compressibility of Reservoir Rock and Fluids
8.3 Deformation of Porous Rock
The elastic deformation or compressibility of porous rock is complicated by the fact that it is
subjected to an external confining stressσ, and in addition to an internal pore pressure p, acting
on the surface of the pore walls. The total external stress acting on the porous rock is partly
counterbalanced by the pore presssure and the forces acting through the rock matrix. This is
depicted in Fig. 8.5, where the total stress will be the pressure acting on the outer surface, while
the pore pressure and the forces acting through the rock matrix are the counteracting pressures
[62].
p
p
σ
σ
σ
Figure 8.5: Stresses working on a porous rock.
Experience in rock and soil mechanics has shown that the deformation of porous and pre-
meable materials depend on the effective stress which is the difference between the applied
total stress and the pore pressure. Effective stress was originally introduced by Terzaghi and is
defined as,
σ
/
= σ −p, (8.18)
later the defineition of effective stress has been generalized to,
σ
/
= σ −αp,
where the constant α, often called the Biot constant is a number equal or less than one,α ≤1.
For most reservoir rocks α will become close to one and may be neglected. It should be
noted however that the consept of effective stress does not follow from strictly theoretical
considerations, but must be regarded as a close approximation. For porous rocks, the stresses
in Hooke’s law should be replaced by effective stresses.
When a reservoir is produced the reservoir pressure will in most cases be reduced. The
overburden load will however remain more or less constant and thus the vertical effective
stress will increase, causing compaction of the reservoir rock. The horizontal stresses may
also change with pore pressure and the development of complete stress conditions may be
difficult to determine.
For reservoir engineering, it is first of all the volumetric behaviour that is important. The
volumetric changes are given by the average applied stress and one will therefore for simplicity
in the following assume a hydrostatic applied stress field on the porous rock.
8.3 Deformation of Porous Rock 129
Variation of the effective stress on the rock due to withdrawal of reservoir fluid (oil, gas or
initial water) will cause deformation in the bulk volumeV
b
, as well as deformation in the pore
volume V
p
. Generally, both the external stress σ and the pore pressure p may provoke changes
in the bulk or/and pore volume. The bulk and pore volume are therefore defined as function of
both external stress and pore pressure, i.e.
V
b
= V
b
(σ, p),
V
p
= V
p
(σ, p). (8.19)
Differentiation of Eqs. (8.19) gives the relative volume change,
dV
b
V
b
=
1
V
b

∂V
b
∂σ

dσ +
1
V
b

∂V
b
∂ p

dp,
dV
p
V
p
=
1
V
p

∂V
p
∂σ

dσ +
1
V
p

∂V
p
∂ p

dp. (8.20)
Using Eq. (8.1) the definition of isothermal compressibility, a set of four compressibilities
may be defined and Eq. (8.20) is written,
dV
b
V
b
= −c

dσ +c
bp
dp,
dV
p
V
p
= −c

dσ +c
pp
dp, (8.21)
where the "minus" sign demonstrates the fact that when σ increases, both the bulk and pore
volume will decrease, while when p increases, then the bulk and pore volume will increase.
The four compressibilites defined in Eqs. (8.21) are all not independent and through elastic
theory it is possible to resolve the relation between them. The purpose of this process is to
express the pore compressibility as function of the compressibilities of bulk volume and rock
material, c
p
= c
p
(c
b
, c
r
).
8.3.1 Compressibility Measurements.
If a porous rock sample is brought to the laboratory and the external stressσ, on the sample
is increase while the pore pressure is kept constant dp = 0, as seen in Fig. 8.6, left, Eqs. (8.21)
gives,
dV
b
V
b
=−c

dσ, (8.22)
Since c

depends on the elastic moduli of the matrix rock material and the geometry of
the pore space, it must in general be considered to be an independent parameter, characterised
as the bulk compressibility, i.e. c

= c
b
.
If, on the other hand, the rock sample is exposed to an external stress equal to the internal
pressure, such that dσ = dp, see Fig. 8.6, right, then Eqs. (8.21) is written,
130 Chapter 8. Compressibility of Reservoir Rock and Fluids
σ σ = p
dp = 0
Figure 8.6: Stresses working on a porous rock.
dV
b
V
b
= (−c
b
+c
bp
)dσ,
dV
p
V
p
= (−c

+c
pp
)dσ, (8.23)
where dσ = dp and where c

= c
b
.
When the pore pressure increases/decreases equally to the confining stress, then the effect
of the pores with respect to the deformation of the porous rock, is only related to the rock matrix
material itself. Seen from the outside the material would behave as a completly solid rock.
Under these condition, the compressibility of the rock sample is equal to the compressibility
of the rock material c
r
. From Eqs. (8.23), the following relation between compressibilities are
deduced;
−c
b
+c
bp
= −c
r
,
−c

+c
pp
= −c
r
, (8.24)
where the minus sign for c
r
reflects the fact that the rock will compress under these conditions.
8.3.2 Betti’s Reciprocal Theorem of Elasticity.
If both the external stress and the pore pressure are changing, then the bulk and pore volume
are deformed accordingly,
dV
b
= dV
b
(σ) +dV
b
(p),
dV
p
= dV
p
(σ) +dV
p
(p), (8.25)
where dV(σ) is the volume change relative to the external stress and dV(p) is the volume
change relative to the pore pressure.
Betti’s theorem states that the hypothetical work given by the volume expansion of the bulk
volume due to the pore pressure dV
b
(p) times the change in the external stress dσ, is equal to
the work given by the volume expansion of the pore volume due to the external stressdV
p
(σ)
times the change in the pore pressure dp, i.e.
8.4 Compressibility for Reservoir Rock Saturated with Fluids 131
dV
b
(p) dσ = dV
p
(σ) dp. (8.26)
Using Eqs. (8.21) in Eq. (8.26), one gets,
−V
b
c
bp
dp dσ =−V
p
c

dσ dp, (8.27)
where c
bp
= c
b
. The minus sign for the first term reflects that the force and displacement are in
opposite directions. Since porosity is definedφ =V
p
/V
b
, the bulk compressibility is given,
c
bp
= φc

(8.28)
Combining Eqs. (8.24 and Eq. (8.28) on gets,
c
p
=
c
b
−(1+φ)c
r
φ
, (8.29)
where c
pp
= c
p
is the pore volume compressibility. This formula, developed by Geertsma [31],
relates the pore compressibility to the bulk and rock compressibilities which are the parameters
normally measured, like in experiments sketched in Fig. 8.6.
8.4 Compressibility for Reservoir Rock Saturated with Fluids
Compressibility of homogenous matter like the rock material c
r
and the contained saturations
of fluids, e.g. oil, water and/or gas, are all defined by Eq. (8.1). A discrete version of this
definition, where the pressure drop ∆p is sufficiently small, gives
c =
1
V
∆V
∆p
⇒ ∆V = cV∆p. (8.30)
The compressibility of the fluids c
f
contained in the pore volume is defined by the com-
pressibility of the different phases; c
w
, c
o
and c
g
. Since the pore volume is expanded by the
fluid phase volumes: V
f
= V
w
+V
o
+V
g
, a change in the pore pressure will cause the fluid
volume to change. The fluid compressibility is written,
∆V
f
= ∆V
w
+∆V
o
+∆V
g
,
c
f
= c
w
V
w
V
p
+c
o
V
o
V
p
+c
g
V
g
V
p
,
= c
w
S
w
+c
o
S
o
+c
g
S
g
, (8.31)
where S is the fluid phase saturation (S
w
+S
o
+S
g
= 1).
Of interest in relation to the production of oil and gas, is the total compressibility of the
rock - fluid system. This compressibility accounts for the expansion of fluid, given by the fluid
compressibility c
f
and the reduction of the pore volume when the pore pressure is reduced,
given by c
p
in Eq. (8.29),
132 Chapter 8. Compressibility of Reservoir Rock and Fluids
c
t
= c
p
+c
f
,
=
c
b
−(1+φ)c
r
φ
+c
w
S
w
+c
o
S
o
+c
g
S
g
,
=
1
φ
[c
b
−(1+φ)c
r
+φ(c
w
S
w
+c
o
S
o
+c
g
S
g
)]. (8.32)
The effective HC compressibility is a useful term, related to the pore space occupied by the
hydrocarbons,
c
HC
= c
o
S
o
+c
g
S
g
.
An equally important term is the effective compressibility responsible for the expansion
of initial water and reduction of the pore volume, when pressure is released as a result of HC
production. This term, a non-HC compressibility is defined,
c
non−HC
=
c
b
−(1+φ)c
r
+φc
w
S
w
φ
.
Example: Porosity variation in the reservoir
When the reservoir pore pressure is reduced, due to oil or gas production, the
equilibrium of stresses in the reservoir is changed. This change in the effective
stress on the rock material will cause the porosityφ =V
p
/V
b
to change.
By differentiation the porosity one gets,

φ
=
dV
p
V
p

dV
b
V
b
. (8.33)
Substituting Eqs. (8.21) in Eq. (8.33) and remembering that c
pp
is the pore
compressibility c
p
and c

is the bulk compressibility c
b
,

φ
= (c
p
dp−c

dσ) −(c
bp
dp−c
b
dσ). (8.34)
Combining Eqs. (8.24) and Eq. (8.29) with Eq. (8.34) gives,
dφ =−c
b
(1−φ) −c
r
d(σ −p), (8.35)
where the porosity change dφ is proportional to the change in the effective stress.
It should be noted that in this case, the dependence on the effective stress is an
exact theoretical result.
Under reservoir conditions, the confinement stress is constant, i.e. dσ = 0 and
thus the change in porosity is,
∆φ = c
r

c
b
c
r
(1−φ) −1

∆p, (8.36)
where the pressure drop ∆p, due to fluid production from the reservoir is small
enough to keep the material within the elastic limit.
8.4 Compressibility for Reservoir Rock Saturated with Fluids 133
In a non-porous rock, i.e. when φ →0, the bulk compressibility will be equal
to the rock matrix compressibility, c
b
= c
r
, which then define the lower bound,
where by c
b
/c
r
≥ 1. In typical sandstone porous rocks, the ratio c
b
/c
r
is often
found to be between 4 to 100. For sandstone reservoirs with a typical porosity
larger than 5-10 %, the terms in the bracket in Eq. (8.36) will always be positive.
When the pore pressure is reduced, p
1
> p
2
(Fig. 8.7), a porosity deforma-
tion is observed, φ
1
> φ
2
, i.e. the porosity is reduced in the reservoir when the
pressure is reduced, which is an important drive mechanism for undersaturated oil
reservoirs.
p
1
p
2
V :
p
φ
1
φ
2
Figure 8.7: Constant confinement pressure and reduced pore pres-
sure leads to a reduction in the pore volume.
.
Example: Porosity variation in formation core samples
Reservoir porosity is seen to decrease with the pore pressure, under the assumption
of constant confinement stress. What about the porosity change in rock samples
which are brought to the surface for further experimental investigations? This
question is quite important since laboratory measurements on core material from
wells, is one of the very few direct sources of information available regarding
reservoir characteristics.
Eq. (8.35) gives the porosity change relative to the change in the pressure dif-
ference (σ − p). At initial conditions in the reservoir, the pressure difference is
normally such that the confinement pressure is larger than the pore pressure, i.e.
(σ −p)
R
> 0. In the laboratory or at normal atmospheric condition, the confine-
ment pressure and the pore pressure will be close to equal, i.e. (σ −p)
L
= 0.
For a porous rock sample, where the bulk and rock matrix compressibilities
are such that (c
b
(1 −φ) −c
r
) > o, which is the case for practically all porous
rock materials, the porosity will increase when the rock sample is brought to the
surface, i.e. φ
R
< φ
L
.
.
134 Chapter 8. Compressibility of Reservoir Rock and Fluids
p
R
p
L
φ
R
φ
L
Figure 8.8: Variation of bulk volume during surfacing of core mate-
rial.
8.5 Exercises
1. The reservoir pressure is 1923 psi, connate water saturation is 0.24 and gas saturation is
0.31.
Find the total compressibility and the effective hydrocarbon compressibility when the
following fluid and formation compressibility are known; c
o
= 10 10
−6
psi
−1
, c
w
= 3
10
−6
psi
−1
, c
g
= 1/p psi
−1
and c
r
= c
b
= 5 10
−6
psi
−1
.
2. A reservoir with an initial pressure of 6500 psia has an average porosity of 19 %. Bulk
compressibility is 3.810
−6
psi
−1
, and estimated abandonment pressure is 500 psia.
Find the formation porosity when the field is abandoned?
3. A gas reservoir has a gas deviation factor (at 150
o
F),
p [psia] 0 500 1000 2000 3000 4000 5000
z 1.00 0.92 0.86 0.80 0.82 0.89 1.00
Plot z versus p and graphically determine the slope at 1000 psia, 2200 psia and 4000
psia. Then, find the gas compressibility at these pressures.
Answers to questions:
1. 171.4 10
−6
psi
−1
, 224.6 10
−6
psi
−1
, 2. 18.6 %,
3. 1.11 10
−3
psi
−1
, 0.45 10
−3
psi
−1
, 0.14 10
−3
psi
−1
Chapter 9
Properties of Reservoir Fluids
9.1 Introduction
Production of oil and gas can be compared to a process where volumes of the reservoir fluids
are transformed to the stock tank volumes of oil and gas, see Fig. 9.1. During this process both
pressure and temperature are significantly changed. The reservoir production rates of oil and
gas will in the event of continuously decreasing pressure and temperature transform, where the
phase ratio of oil and gas is changed as well as the gas-oil ratio and the composition of both
phases.
Q = V / t
gn gn
∆ ∆
Q = V / t
g g
∆ ∆
Q = V / t
on on
∆ ∆
Q = V/ t
o o
∆ ∆
Reservoir
Sea
Figure 9.1: Volume transformation of oil and gas.
Primary reservoir production takes place without any temperature change, while the reser-
voir pressure drops substantially near the well. The composition of oil and/or gas will therefore
changed slightly during production. In an oil reservoir we may experience the shrinkage of oil
due to the solution gas liberation near the well and in a rich gas reservoir we expect condensa-
135
136 Chapter 9. Properties of Reservoir Fluids
tion of liquid hydrocarbons (oil) when the pressure is reduced.
When the reservoir fluid is produced and brought to the surface, pressure is further reduced
through different stages of separation. In these processes, temperature is also reduced and
consequently the composition of oil and gas undergoes significant change.
In this chapter focus is put on some characteristic aspects of hydrocarbon mixtures and the
separation of oil and gas as function of pressure and temperature. We will look at how oil and
gas behave in the reservoir and their expansion to stock tank condition.
9.2 Definitions
The process by which the different hydrocarbon (HC) components form phases through various
chemical reactions is governed by a natural (entropy driven) development towards equilibrium
or the lowest energy level. This could be expressed more precisely referring to the Gibbs phase
rule.
The Gibbs phase rule shows a relationship among the number of componentsN
C
,
number of phases N
P
, number of chemical reactions N
R
, and degrees of freedom
N
F
, where;
N
F
= N
C
−N
P
+2−N
R
.
The number 2 accounts for the intensive properties p, T, and N
C
−N
R
defines the
number of independent components.
For a pure component (like H
2
O), then N
C
−N
R
= 1 and
N
F
= 3−N
P
.
For pure components the phase rule says that no more than three phases can form at any tem-
perature and pressure, i.e.
When N
P
= 1 N
F
= 2 Both intensive properties can be changed
arbitrarily
When N
P
= 2 N
F
= 1 Only one intensive property can be
independent – there are three lines
on a (p, T)-plot reflecting this occurrence
(sublimation line, melting point line, and
vapour pressure line)
When N
P
= 3 N
F
= 0 No degrees of freedom – a single triple
point in the phase diagram
We know that water may appear in different phases like ice, liquid and vapour, all depend-
ing on temperature and pressure. The co-existence of different phases, is shown in Fig. 9.2.
The different regions are separated by phase boundaries. The phase boundary between water
and vapour ends in a critical point where the two phases cease to co-exist. Beyond this point,
for temperatures T > T
C
and pressures p > p
C
, there is no distinct difference between water
and vapour, hence we call this state the fluid state. (For pure water, i.e. H
2
O, the critical
temperature is 374.1
o
C and the critical pressure is 218.3 atm.)
9.3 Representation of hydrocarbons 137
p
c
T
c
Critical
point
Ice
Water
Vapour
1 atm.
100 °C
Figure 9.2: PT-diagram for H
2
O.
9.3 Representation of hydrocarbons
Naturally occurring HC are complex in composition and contain a great many members of
paraffins (alkanes), naphthenes (cyclo-alkanes) and aromatic series and often some non-hydrocarbon
impurities.
Some of the components in the paraffin series are listed below:
Methane CH
4
C
1
Heptane C
7
H
16
Ethane C
2
H
6
C
2
Octane C
8
H
18
Propane C
3
H
8
C
3
Nonane C
9
H
20
Butane C
4
H
10
C
4
Decane C
10
H
22
Pentane C
5
H
12
C
5
Hexane C
6
H
14
C
6
Some typical non-hydrocarbon impurities are represented by,
Nitrogen N
2
Carbon Dioxide CO
2
Hydrogen Sulphide H
2
S
For mixtures of HC components, C
7
H
16
and higher, it is quite common to writeC
+
7
, mean-
ing all component in the series. The C
+
7
characteristic is then the average for all components
higher then C
6
.
In gases, typically light components likeC
1
, C
2
and C
3
dominate the composition. For light
oils, C
4
, C
5
and C
6
are the important components and for heavier oils the presence of various
decanes and asfaltenes are quit common. However, intermediate components likeC
4
−C
5
can be in both gaseous and liquid state depending on prevailing pressure and temperature.
Components C
+
7
are heavy and in most interesting cases of petroleum engineering, can not be
evaporized.
For pure components of oil, say, Ethane (C
2
H
6
) and Heptane (C
7
H
16
), and their mix-
ture (50% of C
2
H
6
and 50% of C
7
H
16
) the phase PT-diagram is shown in Fig. 9.3. The PT-
characteristics of the pure components are somewhat similar to theH
2
O case, shown in Fig. 9.2.
When two or more HC components are mixed, the phase boundaries form a closed boundary
138 Chapter 9. Properties of Reservoir Fluids
area in the PT-diagram, where the two phases of oil and gas co-exists. This area is called the
two-phase region and has a characteristic shape for that particular composition.
p
T
Liquid
Gas
p
T
Liquid
Gas
p
T
Liquid
Gas
Liquid +
Gas
a) 100% Ethane b) 100% Heptane c) 50% Ethane 50% Heptane
C
C
C
Figure 9.3: PT-diargam for Ethane, Heptane and their mixture.
The equilibrium state is defined as function of p and T and consequently also the volume
ratio of oil and gas is PT-dependent. Volume is therefore a dependent function of p and T,
as shown by the law of real gases. These relations between pressure, volume and temperature
are often referred to as PVT-relations. For a mixture of hydrocarbons, a PVT-diagram can be
drawn, as shown in Fig. 9.4.
G
a
s
G
a
s
L
iq
u
id
L
i
q
u
i
d
T
e
m
p
e
r
a
t
u
r
e
V
a
p
o
r
-
P
r
e
s
s
u
r
e
C
u
r
v
e
C
r
i
t
i
c
a
l
p
o
i
n
t
P
r
e
s
s
u
r
e
P
r
e
s
s
u
r
e
B
u
b
b
l
e
p
o
i
n
t
c
u
r
v
e
D
e
w
p
o
i
n
t
c
u
r
v
e
V
o
l
u
m
e
Figure 9.4: PVT diagram for a mixed component system.
The existence of a super critical fluid region to the right of the critical point where phases
can not be distinguished, is seen in the PT-diagram in Fig. 9.4 (lower right).
The PV-diagram (upper left) shows how the oil volume is increasing when pressure is
9.3 Representation of hydrocarbons 139
decreasing. For a given temperature, we observe a monotonously volume increase or swelling
of the oil phase down to a certain pressure level. At this pressure the volume continues to
increase by separation into co-existing oil - and gas phases. Continued volume increase means
gradually increased gas-oil ratio at constant pressure. The two-phase region is left when the
pressure starts to decrease again and further volume increase is due to gas expansion only.
Another way of representing the PVT discontinuity, represented by the two-phase region,
is to present the intensive property of specific - or molar volume, see Fig. 9.5.
Gas
Gas
Liquid
Liquid
Temperature
P
r
e
s
s
u
r
e
T
1
T
1
T
2
T
2
T
3
T
3
T
4
T
4
Specific volume
Two-phase
region
Critical
point
Figure 9.5: Pressure-specific volume diagram for mixed component
system.
Specific volume is volume occupied by a unit of mass of a substance, i.e. [V
s
] = m
3
/kg
(ft
3
/lb). Molar volume is equal to volume occupied by one mole of a substance, i.e. [V
m
] =
m
3
/kg-mole or cm
3
/g-mole (ft
3
/lb-mole).
For temperatures higher than T
3
, in Fig. 9.5, there is no phase change when pressure is
decreased. For lower temperatures, however, a phase transformation will pass through a two-
phase region confined by a bubble point locus and a dew point locus where the oil and gas are
in equilibrium.
The PT-diagram for a more complex mixtures is presented in Fig. 9.6. It is important to
notice that the shape of an envelope A-CP-CT-B depends on the composition of HC mixture,
with the following definitions:
CP: Cricondenbar – a pressure point, above which a liquid can not be vaporised.
CT: Cricondentherm – a temperature point, above which a gas can not be condensed.
C: Critical Point – a pressure and temperature point, at which two phases become identical.
All the quality lines merge at this point, lines which defines the fractional oil-gas ratio.
A reservoir with initial conditions as indicated by position1 in Fig. 9.6 is what we would
call a gas reservoir. When this reservoir is produced at constant temperature, from1 to 2, no
phase boundary is crossed, i.e. only gas is produced. If, on the other hand, the production
follows the dotted line from 1 to x, then oil will gradually drop out of the gas both in the
reservoir and on the way to location x. The composition of the gas will have changed, where
the heavier components are condensed.
140 Chapter 9. Properties of Reservoir Fluids
A reservoir located at point 3 in Fig. 9.6, should be called a gas condensate reservoir. When
this reservoir is produced at constant temperature, from 1 to 5, condensation of gas in the
reservoir starts as soon as the two-phase region is entered, at point 4. When the pressure
continues to decrease, and the dew point line is approached, vaporisation of residual oil can
happen and the gas composition may become richer until the dew point line is crossed. Form
that point onwards, no change in the composition will occur.
As we have mentioned before, the two-phase region is characterising the reservoir fluid,
such that an oil reservoir would have a different shaped two-phase region than seen in Fig. 9.6.
Having said this, we can imagine that an oil reservoir is located somewhere in the upper left
corner in Fig. 9.6. When this reservoir is produced at constant temperature, no gas will exist in
the reservoir until the bubbel point line is crossed. At this time, solution gas will slowly build
up to a continuous phase and flow towards the well with a considerably higher mobility than
the oil itself.
p
T
Liquid
Gas
CP
A
B
C
CT
80%
60%
40%
20%
1
2
3
4
x
5
Figure 9.6: PT- diagram for a complex HC mixture.
9.3.1 Ternary diagrams
Binary diagrams are often used for representing an overall behaviour of hydrocarbons and
for detailed analysis of phase behaviour when the number of components or groups of pure
components, do not exceed three . Natural hydrocarbons are complex mixtures of different
components and are usually represented by pseudo-components (normally 2 or 3). In order to
predict phase behaviour for such compositions ternary diagrams are often used, see Figs. 9.7
and 9.8.
One of the advantages of ternary diagrams is that they enable us to represent both the
phase compositions and the overall composition of mixture. Let us assume that the overall
composition is represented by point M. Then the overall compositions C
i
can be expressed
through the phase compositions C
i j
,
C
i
=C
i1
S
1
+C
i2
S
2
, i = 1, 2, 3
9.3 Representation of hydrocarbons 141
Plait point
Binodal
curve
Tie line
2-phase region
C
2
C
1
C
3
1-phase
region
Figure 9.7: Two-phase ternary diagram.
Plait
point
Tie line
C
2
C
1
C
3
2-phase
region
3-phase region
1-phase
region
a
b
c
d
e
f
- invariant point
Figure 9.8: Three-phase ternary diagram.
Note that the fraction of each component is 1 at their apex and 0 at the opposite edge. Any unit
can be used (mole-, weight- or volume fraction).
Using the fact that S
1
+S
2
= 1, we can obtain the following expression for the relative
amounts of phases S
i j
in the overall composition,
S
1
=
C
i
−C
i2
C
i1
−C
i2
, S
2
=
C
i
−C
i1
C
i2
−C
i1
,
which is called "the lever rule".
It follows from the Gibbs phase rule that in case of 3 (pseudo) components and 2 phases,
where (p and T are expected to be known), the system has only one degree of freedom. This
means that if one of the parameters is specified all the other can be easily evaluated.
Fig. 9.8 shows the case when the composition has a 3-phase region which is indicated by the
embedded smaller triangle. All sides of this triangle are surrounded by 2- phase regions. There
is no degrees of freedom in the three phase region. It means that the compositions of the three
phases are given by the apexes of the 3 phase triangle (invariant points). Any total composition
M within this triangle gives three phases with the same overall composition. Moving inside the
triangle we can only change the fraction of phases and not the overall composition. The lever
rule enables us to calculate the relative amounts of these phases,
142 Chapter 9. Properties of Reservoir Fluids
S
1
=
a
a+b
, S
2
=
c
c +d
, S
3
=
e
e + f
.
In Figs. 9.7 and 9.8 both triangles have a common baseline, which is usually the case for
surfactant+oil+brine systems.
9.4 Natural gas and gas condensate fields
In a dry gas field, the reservoir temperature is always larger than the critical temperature of the
same gas, i.e. the following initial condition is important,
T
r
> T
CT
.
If initial conditions in the reservoir coincide with point 1 in Fig. 9.6 and gas recovery is
performed in such a way that the pressure will decline from1 to 2, than the dew point line will
never be crossed and only dry gas will exist in the reservoir at any pressure.
When producing the gas to the surface, however, both p and T will decrease and the final
state will be at some point x within the two-phase envelope, the position of the point being
dependent on surface separation.
Let us imagine initial pressure and temperature at point 3 in Fig. 9.6. During isothermal
depletion liquid will start to condense in the reservoir when the pressure has fallen below the
dew point at 4.
The maximum liquid saturation deposited in the reservoir is when the pressure is between
points 4 and 5 in the two-phase region. The condensation is generally rather small and fre-
quently below the critical saturation which must be exceeded before the liquid becomes mobile.
The process of condensation is called retrograde liquid condensation, where the retrograde liq-
uid condensate is not recovered and, since the heavier components tend to condense first, this
represents a loss of a valuable part of the hydrocarbon mixture.
Continued pressure depletion below the point of maximum condensation would lead to re-
vaporisation of the liquid condensate. However, this does not occur because once the pressure
falls below point 4 the overall composition and hence, the molecular weight of the HC remain-
ing in the reservoir increases and is left behind in the reservoir as retrograde condensate while
the light components are mobile and will be produce.
The composite phase envelope for the reservoir fluids tends to move downwards and to the
right, thus inhibiting re-vaporisation. Sometimes it is economically advantageous to produce
a gas condensate field by the process of gas re-cycling. Starting at point 3 in Fig. 9.9 and
separating the liquid condensate from the dry gas at the surface and re-injecting the latter into
the reservoir in such a way that the dry gas displaces the wet gas towards the producing wells.
However, in practical field developments this is not easily accomplished.
The reservoir pressure is kept almost at the initial level but the composition of the reservoir
gas is gradually changed in such a way, that the phase envelope moves to the left and upwards.
After breakthrough of the dry gas occurs, the injection is terminated and the remaining dry gas
produced. The objective of the gas re-cycling process is to keep reservoir conditions above/or
to the right from the dew point curve, as seen in Fig. 9.9.
9.5 Oil fields 143
p
T
Initial
composition
Intermediate
composition
Final
composition
3
Figure 9.9: Development of the gas field by the gas re-cycling pro-
cess.
9.5 Oil fields
Since the oil contains more of the heavier HC components, a phase diagram for oil will be
more elongated in horizontal direction, as compared with gas fields and as shown in Fig. 9.10.
Initial
composition
Intermediate
composition
Final
composition
p
T
A
B
X
Unfavourable conditions
of production
Figure 9.10: Development of the oil field.
If initial conditions in the reservoir coincide with pointA in Fig. 9.10, there will be only one
phase present, namely liquid oil containing dissolved gas. Reducing the pressure isothermally
will eventually bring the oil to the bubble point B. Further reduction in pressure will lead to
solution gas production and the presence of two phases in the reservoir;
• liquid oil, containing an amount of dissolved gas which commensurate with the pressure
and
• liberated gas, originally dissolved in the oil.
144 Chapter 9. Properties of Reservoir Fluids
Keeping production at point X below the bubble point, in Fig. 9.10, the overall reservoir
HC composition will change due to the fact that the gas, being more mobile, will flow with a
much greater velocity than the oil towards the well.
The composition will change to such an extent, that the liquid phase is finally becoming
less and less mobile. The relative content of heavier components in oil will increase, and the
shape of the phase diagram will change towards more and more unfavourable conditions for oil
production. It is therefore preferable to maintain oil production close to, or above the bubble
point by using water flooding, gas injection or other enhanced oil recovery methods.
The phase diagram for an oil reservoir with a gas cap must necessarily have a phase enve-
lope which is characterised by both the gas and oil contained in the reservoir. The two-phase
area of the reservoir fluid is overlapping the appropriate oil and gas reservoir, as shown in Fig.
9.11.
p
T
A
Reservoir
gas
Reservoir
oil
Reservoir
fluid
Initial
reservoir
conditions
Figure 9.11: Phase diagram for the oil reservoir with a gas cap.
9.6 Relation between reservoir and surface volumes
The amount of oil and gas produced form the reservoir, measured in standard volume quantities
(at normal pressure and temperature) are converted to reservoir volumes by the use of volume
factors; B
o
, B
g
, R
s
and R. These factors are defined in accordance to Fig. 9.12.
Volumes defined at reservoir conditions (or at the surface) are transformed to surface vol-
umes (or reservoir volumes) by use of volume factors. The volume factors are defined by lab-
oratory experiments performed on samples taken from the reservoir oil or gas. The definition
of these factors are [21]:
R
s
: The solution gas-oil ratio, which is the number of standard cubic meters (feet) of gas
which will dissolve in one stock tank cubic meter (barrel) of oil when both are measured
at surface conditions.
R
s
=
V
ogn
V
on
¸
Sm
3
Sm
3

.
9.6 Relation between reservoir and surface volumes 145
V
p
V
g
V
ogn
V
on
V
gn
V
o
V
on
V
ggn
Reservoir: , p T Surface: , p T
n n
Figure 9.12: Stock tank production through expansion of reservoir
oil and -gas from an oil reservoir.
B
o
: The oil formation volume factor is defined as the volume of oil in cubic meters (or bar-
rels) occupied in the reservoir at the prevailing p and T divided by the volume of oil in
stock tank cubic meter (barrel),
B
o
=
V
o
V
on
¸
Rm
3
Sm
3

.
B
g
: The gas formation volume factor is defined as the volume of gas in cubic meters (or
barrels) in the reservoir divided by the volume of the same gas at standard cubic meter
(foot),
B
g
=
V
g
V
ggn
¸
Rm
3
Sm
3

.
R: The gas-oil ratio (GOR), is the volume of gas in standard cubic meters (feet) produced
divided by volume of stock tank cubic meter (barrel) of oil at surface conditions,
R =
V
gn
V
on
¸
Sm
3
Sm
3

.
The following useful relationships between the volume factors can be deduced, simply
using Fig. 9.12:
V
gn
= RV
on
(9.1)
V
g
= B
g
(R−R
s
)V
on
(9.2)
V
o
+V
g
= [B
o
+(R−R
s
)B
g
]V
on
(9.3)
146 Chapter 9. Properties of Reservoir Fluids
V
g
= B
g
(1−
R
s
R
)V
gn
(9.4)
The volume factors B
o
, R
s
, B
g
and R are all pressure dependent functions, as seen from
Fig. 9.13.
p
p
p
p
B
o
B
g
p
b
p
b
p
b
p
b
R
s
R
Figure 9.13: Dependency of PVT volum parameters on pressure.
In order to explain the characteristic behaviour of the different volume factors it is natural
to follow a decreasing pressure development, i.e. from right to left in Fig. 9.13.
The oil volume factor B
o
is seen to increase linearly when pressure is decreasing towards
the bubble point pressure p
b
. This increase in B
o
is directly linked to the oil compressibility,
i.e. when pressure is released, then volume is increased. For pressure lower then the bubble
point, solution gas is gradually leaving the oil phase which leads to a shrinking volume of oil.
Finally all gas will evaporate and the oil is said to bedead and B
o
≈1. This process continues
until standard condition is reached.
The solution gas-oil ratio R
s
is constant for pressures higher than the bubble point pressure,
since no gas is produced in the reservoir. A unit sample of oil at different pressures (p > p
b
)
will therefore contain the same amount of gas and oil at standard condition. For pressures
lower than the bubble point pressure, we will find a decreasing amount of gas in the reservoir
oil sample because some gas has already evaporated and been produced as gas.
In the case of the volum factor for gas, gas in equilibrium with oil can only exist up to its
bubble point pressure. For pressure higher than p
b
, all free gas will be dissolve in the oil. For
decreasing pressure lower than the bubble point pressure, the volume of gas will expand as the
reciprocal pressure.
9.6 Relation between reservoir and surface volumes 147
The gas-oil ratio R, shown in Fig. 9.13, is given as a function of decreasing reservoir pres-
sure. When the pressure is above the bubble point pressure, no change is observed in the gas-oil
ratio at surface condition. Shortly after the reservoir pressure has dropped below the bubble
point pressure, the process of solution gas vaporisation will take place, first near the wellbore.
For a short while, the gas is not mobile due to gas saturation below critical gas saturation. The
presence of discontinuous gas will block some of the path ways for the oil and consequently oil
with less gas are being produced. The minimum gas-oil ratio is reached as the gas saturation
becomes continuous and starts to flow. When pressure is further decreased, more gas than oil
is produced than initially, since gas liberated in the reservoir is more mobile and therefore is
produced faster than the oil it originally evaporated from.
Example: Importance of the GOR
The GOR is an important parameter, not only because it gives the gas-oil ratio as
function of pressure and time, but also because it carries important information
about the mobility ratio of gas and oil in the reservoir.
With reference to Figs. 9.1 and 9.12 we may define the gas-oil ratio for a satu-
rated oil reservoir, i.e. with a reservoir pressure lower than bubble point pressure,
R =
V
gn
V
on
=
Q
gn
Q
on
,
where Q
on
= Q
o
/B
o
and where Q
o
is the oil rate in the reservoir. Using the rela-
tions Eqs.(9.1) - (9.4) we find,
Q
gn
= RQ
on
,
Q
on
= Q
g
/[B
g
(R−R
s
)],
where Q
g
is the gas rate in the reservoir.
Using the GOR, defined above, and the two relations giving the gas- and oil
rate, we may write the following expression for the GOR factor,
R =
Q
g
B
g
B
o
Q
o
+R
s
.
For reservoir flow, we assume Darcy’s law to be valid, both for oil- and gas
flow, i.e.
Q
i
=
k
i
µ
i
A
dp
i
dr
, i = o, g.
where Q
i
are the reservoir flow rates.
For reservoir flowin the vicinity of the well, we may safely neglect all capillary
effects, and the reservoir gas-oil flow ratio is written,
Q
g
Q
o
=
k
g
µ
g
µ
o
k
o
.
Substituting this ratio in the GOR equation, we may express the GOR in terms
of reservoir parameters,
148 Chapter 9. Properties of Reservoir Fluids
R =
k
g
µ
g
µ
o
k
o
B
o
B
g
+R
s
, (9.5)
where the mobility of oil- and gas is defined, λ
i
= k
i

i
, and i = o, g.
Eq.(9.5) gives the relation between gas - and oil mobility in the reservoir and
the observed gas-oil ration, where the volume factors B
o
, B
g
and R
s
are known
from laboratory measurements. The GOR as presented in Eq.(9.5) gives a ideal-
ized approximation of reservoir dependence and should therefore be interpretated
with care.
Example: Initial reservoir fluids
The definition of initial in place volumes are somewhat different for oil- and gas
reservoirs.
For a general reservoir we may define the following parameters,
V
R
Reservoir bulk volume.
φ Porosity.
B
o
, B
g
Formation factor.
R
s
Solution gas-oil ratio.
The hydrocarbon pore volume, HCPV = V
R
φ, is important in defining the
reserves in an oil reservoir,
Oil reserves: OIIP = HCPV/B
o
,
Gas reserves: GIIP = OIIP R
s
.
The reserves coming from a gas reservoir is defined,
Gas reserves: GIIP = HCPV/B
g
,
Oil reserves: OIIP = GIIP/R
s
.
9.7 Determination of the basic PVT parameters
Conventional analysis of basic PVT parameters follow well established procedures by which
the different volume factors are measured:
• Flash expansion of the fluid sample is used to determine the bubble point pressurep
b
.
• Differential expansion of the fluid sample is used to determine the basic parametersB
o
,
R
s
and B
g
.
• Flash expansion of fluid samples through various separator combinations is used to en-
able the modification of laboratory derived PVT data to match field separator conditions.
The process differential - and flash expansion, shown in Fig. 9.14, illustrates the difference
between flash and differential expansion of the fluid sample.
9.7 Determination of the basic PVT parameters 149
Initial
composition
Final
composition
p
T
p
T
Flash expansion Differential expansion
1
1
1 1
2 2
2 2
3
3
3 3
p > p
i b
p < p
b
p
b
p
b
p
b new
Hg
Gas
Gas
Oil
Oil
Oil
Oil
Oil Oil
Figure 9.14: Flash and differential expansion of fluid samples.
Note that the flash expansion experiment does not change the overall hydrocarbon compo-
sition in the cell while in the differential liberation experiment, at each stage, depletion gas is
liberated physically and removed from the cell. Therefore, there is a continous compositional
change in the PVT-cell. The remaining hydrocarbones are becoming progressively richer in
heavier components and the average molecular weight is increasing. Consequently flash ex-
pansion leaves smaller oil volumes then differential expansion.
Reservoir production is most likely reproduced by a non-isothermal differential expansion,
where multi-stage separation at the surface is commonly used because differential liberation
will normally yield a larger final volume of equilibrium oil than the corresponding flash expan-
sion.
150 Chapter 9. Properties of Reservoir Fluids
9.8 Exercises
1. Calculate the density expressed in SI-units,
– for a crude oil API gravity of 57.2 and
– for a natural gas API gravity of 70.7,
when water density is 1000 kg/m
3
at standard condition (1 atm. and 20
0
C).
2. A gas consists of 50% – 50% mixture by weight of two hydrocarbons. The pressure
is increased isothermally until two phases appear. The liquid phase consists of 40%
by weight of the more volatile component and the vapour phase 65% by weight of this
component. What are the weight functions of the liquid and the vapour phase?
3. The following data are obtained in a PVT analysis at 90
0
C.
Pressure [bar] 276 207 172 138 103
Celle (system) volume [cm
3
] 404 408 410 430 450
a) Estimate the bubble point pressure.
The system is re-compressed, expanded to 138 bar and the free gas is removed at constant
pressure and then measured by further expansion to standard condition. The contained
liquid volume is 388 cm
3
and the measured gas volume (at 1 atm. and 15.6
0
C) is 5.275
litres.
The pressure is reduced to normal condition, as above, and residual liquid volume is
found to be 295 cm
3
and the liberated gas volume is 21 litres.
Estimate the following PVT parameters,
b) c
o
, liquid compressibility at 207 bar,
c) B
o
factor at 207 bar,
d) B
o
and R
s
at 172 bar and 138 bar and
e) B
g
and z at 138 bar.
4. Calculate the gas-oil capillary pressure for the following reservoir:
Gas saturation [%] Elevation [ft]
75 -5420
50 -5424
25 -5426
0 -5428
Additional data:
Oil API gravity; 45.1
Gas specific gravity; 0.65
Oil formation volume factor; 1.18 RB/STB
Gas formation volume factor; 0.0025 RB/SCF
Solution gas-oil ratio; 480 SCF/STB
9.8 Exercises 151
Answers to questions:
1. 749.5 kg/m
3
, 699.8 kg/m
3
, 2. 2/3, 3. a) 172 bar, b) 14.1 10
−5
bar
−1
,
c) 1.383 Rm
3
/Sm
3
, d)1.3898 Rm
3
/Sm
3
, 1.315 Rm
3
/Sm
3
,
89.07 Sm
3
/Sm
3
, 71.2 Sm
3
/Sm
3
, e) 0.0079 Rm
3
/Sm
3
, 0.887 4. ρ
o
= 735.5 kg/Rm
3
, ρ
g
= 55.7
kg/Rm
3
.
152 Chapter 9. Properties of Reservoir Fluids
Part II
Reservoir Parameter Estimation
Methods
153
Chapter 10
Material Balance Equation
10.1 Introduction
The basic principle behind the Material Balance Equation is very fundamental:
The mass of hydrocarbons (HC) initially in place is equal to sum of the mass
produced and the mass still remaining in the reservoir,
M
i
=∆M+M.
In material balance calculations we implicitly consider the reservoir as being a tank of
constant volume. The pressure in this tank is defined by the volumetric average pressure,
p =
1
V
i

V
i
pdV,
where V
i
is the initial hydrocarbone volume, i.e. the hydrocarbon pore volume (HCPV).
If we assume the fluid density in the reservoir to be constant during the depletion process,
i.e. ρ ∼constant, we may write the mass conservation law in terms of volume conservation,
V
i
−V =∆V when p
i
→p. (10.1)
Eq.(10.1) is often referred to as the golden principle, where
Expansion = Production.
Even though material balance techniques use crude approximations of the reservoir, with
limited reference to local information, their application and use have proven to be of great
importance in various situations. Being simple in principle, methods based on the material
balance equation are commonly used in the following cases:
• Extrapolation of production curves for oil, water and gas (production decline curve anal-
ysis).
• Identification of the drive mechanism.
• History matching.
In this chapter we will develop the Material Balance Equation for a general oil and gas
reservoir and illustrate the use of the equation by various examples.
155
156 Chapter 10. Material Balance Equation
10.2 Dry gas expansion
Let us consider a dry gas reservoir where the production is modelled using material balance
calculations. The HCPVis constant in absence of water influx. The production of gas at surface
conditions is G
p
.
The material balance equation given by Eq.(10.1) is slightly redefined where the volumeof
gas in the reservoir initially in place is obviously equal to the volumeof gas in the reservoir at
a given pressure p,
G B
gi
= (G−G
p
)B
g
, (10.2)
where the following definitions are used,
G: resources of gas initially in place, [Sm
3
],
G
p
: cumulative volume of gas produced, [Sm
3
],
B
gi
: initial gas formation volume factor, [Sm
3
/Rm
3
] and
B
g
: gas formation volume factor at current reservoir pressure, [Sm
3
/Rm
3
].
The relation presented in Eq.(10.2) is illustrated in Fig. 10.1, where the purpose is to visu-
alise the transformation of gas volume under reservoir condition to surface conditions. When
a surface volume of G
p
has been produced, the volume of gas left in the reservoir isG−G
p
,
in standard units. At a reservoir pressure p, the volume occupied by the gas in the reservoir, is
equal to (G−G
p
)B
gp
, i.e Eq.(10.2).
G B
gi G [Sm ]
3
p p
n
(G-G )B
p g
G-G
p
G
p
Figure 10.1: Volume transformation using volume formation factors.
It follows from Eq.(10.2) that,
B
gi
B
g
= 1−
G
p
G
. (10.3)
Using the equation of state for a real gas pV = znRT, and assuming isothermal conditions
of production one can obtain the relations,
B
gi
=
V
i
V
n
=

p
zT

n

zT
p

i
and
10.3 A general oil reservoir 157
B
g
=
V
p
V
n
=

p
zT

n

zT
p

p
,
where the indices i and p refer to the initial and current pressures respectively .
Eq.(10.3) can now be written,

p
z

=

p
z

i

1−
G
p
G

. (10.4)
Using Eq.(10.4), p/z vs. cumulative gas production exhibits a straight line trend, allowing
us to estimate the resources of gas, as shown in Fig. 10.2. Two important characteristics are
displayed by plotting the data as shown in the figure. When the data follows a linear trend, this
serves as a proof for the assumption of no or negligible water influx during gas production and
that the main driving force behind the production is gas expansion. Secondly, when a straight
line is fitted through the data, the intersection point with the x-axis gives us an estimate for
initial gas in place, G.
G
G
p
0
p
z
( )
i
Figure 10.2: Gas reservoir exhibiting a straight line trend in p/z vs.
cumulative gas production.
10.3 A general oil reservoir
In a general oil reservoir, hydrocarbons will be represented as oil and/or gas. Dependent on
the composition of the fluid, reservoir temperature and initial pressure, there may exist a gas
cap above the oil zone, as schematically indicated in Fig. 10.3. The gas in the gas cap is in
equilibrium with the oil in the oil zone and the volume part of the reservoir occupied by gas
relative to oil is constant.
The following nomenclature is used in the derivation of the material balance equation:
HCPV: Part of pore volume occupied by hydrocarbons.
N: Resources of oil (initial oil in place) inSm
3
.
m: Ratio between the resources of gas in the gas cap and resources of oil in the oil zone
measured at reservoir conditions.
158 Chapter 10. Material Balance Equation
Gas cap
Oil zone
Oil zone
mNB
oi
(Rm )
3
NB
oi
(Rm )
3
Gas cap
C
B
A
Initial reservoir
conditions
Current reservoir
conditions
A, B, C - produced volumes
Figure 10.3: Oil reservoir with a gas cap: Illustration of material bal-
ance.
mNB
oi
: Resources of gas (initial gas in place) inRm
3
.
N
p
: Volume of oil produced in Sm
3
.
Production from the oil reservoir (with a gas cap, see Fig. 10.3) is explained as expansion
of the oil zone, volume - A, expansion of the gas cap, volume - B and as expansion of initial
water present plus reduction of pore volume due to expansion of reservoir formation matrix and
possible reduction of bulk volume, volume - C. In dealing with the development of the material
balance equation, it is therefore convenient to break up the expansion term into its components.
Note that we are here considering underground withdrawal of hydrocarbon fluids, measured in
Rm
3
.
A1: Expansion of oil.
A2: Expansion of originally dissolved gas.
B: Expansion of gas cap gas.
C: Reduction in HCPV due to expansion of connate water and reduction of pore volume.
Reservoir expansion is equal to production, hence: ∆V
prod
= A1 + A2 + B + C.
10.3.1 A1: Expansion of oil
The oil (liquid phase) expansion at reservoir condition can be defined as,
V
o
(p) −V
o
(p
i
) =∆V
o
(p).
Here V
o
(p
i
) is the oil volume at initial conditions andV
o
(p) is the volume of the oil initial in
place at pressure p, see Fig. 10.4. ∆V
o
is the volume oil produced at reservoir pressure p.
10.3 A general oil reservoir 159
p p
i
∆V
o
V
o
Figure 10.4: Expansion of oil at reservoir pressure.
Oil expansion is written,
∆V
o
= N B
o
−N B
oi
= N(B
o
−B
oi
), (10.5)
where ∆V
o
is measured in Rm
3
. N is the initial oil in place [Sm
3
] and is defined; N =V
p
(1−
S
w
)/B
oi
, where S
w
is the average water saturation andV
p
the pore volume.
10.3.2 A2: Expansion of originally dissolved gas
At initial conditions oil and gas in the gas cap are in mutual equilibrium . Reducing the pressure
below the bubble point pressure, p
b
will cause the liberation of solution gas.
The total amount of solution gas in the oil is NR
si
, measured in surface volumes. The
amount of gas still dissolved in the oil at current reservoir pressure and temperature isNR
s
,
also in surface volumes. Therefore, the gas volume liberated during the pressure drop, fromp
i
to p, is,
NR
si
−NR
s
= N(R
si
−R
s
).
This gas volume is measured at surface condition, but since we want to express all expanded
volumes at reservoir condition, we have to multiply the surface volume by the volume factor
for gas at reservoir pressure, i.e. B
g
,
∆V
og
= N(R
si
−R
s
)B
g
. (10.6)
10.3.3 B: Expansion of gas cap gas
The expansion of gas cap gas follows the same principle as observed for the expansion/production
of dry gas given by Eq.(10.2),
GB
gi
= (G−G
p
)B
g
.
The total volume of the gas cap as part of the oil volume in the reservoir, measured at
reservoir condition,
GB
gi
= mNB
oi
.
The gas production at current reservoir pressure is then,
160 Chapter 10. Material Balance Equation
G
p
B
g
=
mNB
oi
B
gi
(B
g
−B
gi
).
The expansion of the gas cap (in reservoir volumes) is therefore written,
∆V
gg
= mNB
oi

B
g
B
gi
−1

. (10.7)
10.3.4 C: Reduction in HCPV due to expansion of connate water and reduction
of pore volume
Reduction in HCPV due to expansion of connate water and reduction of pore volume is in
practice equal to the increased production by the same volume. Expansion of connate water
and reduction of pore volume are controlled by the compressibility of water and pore volumes,
i.e. c
w
and c
p
.
The HCPV compressibility as the compressibility for connate water and formation matrix
are defined in accordance with the general law of thermal compressibility,
c =
1
V
∆V
∆p
⇒ ∆V = cV∆p,
where the absolute volume change in the HC pore space due to expansion of connate water and
reduction of pore volume is,
∆V
HCPV
=∆V
w
+∆V
p
.
∆V
w
and ∆V
p
are the volume changes due to expansion of connate water and that due to
reduction in pore volume, respectively.
Using the definition of compressibility, we get,
∆V
HCPV
= c
w
V
w
∆p+c
p
V
p
∆p.
From previous considerations, we found that: V
w
= S
w
V
p
and V
p
=V
HCPV
/(1−S
w
) and we
get,
∆V
HCPV
=V
HCPV

c
w
S
w
+c
p
1−S
w

∆p,
where the pore volume compressibility is; c
p
= (c
b
−(1+φ)c
r
)/φ and V
HCPV
=V
o
+V
g
=
NB
oi
+mNB
oi
= (1+m)NB
oi
.
The volume expansion due to initial water and reduction in the pore volume, gives the
expansion of the HCPV or volume -C,
∆V
HCPV
= (1+m)NB
oi

c
w
S
w
+c
p
1−S
w

∆p. (10.8)
10.4 The material balance equation 161
10.3.5 Production terms
The production of oil and gas at surface conditions is, N
p
+G
p
. The expansion volumes,
A1, A2, B and C, are measured at reservoir conditions. In order to compare the two types of
volumes, we have to transform the production volumes to reservoir volumes, i.e. N
p
B
o
+G
p
B
g
.
Using the relation between gas and oil produced at standard condition, Eqs.(9.1) to (9.4),
G
p
= (R−R
s
)N
p
,
where R is the gas-oil ratio (GOR) and R
s
is the solution gas-oil ratio.
We can now write the overall production term as,
∆V
prod
= N
p
[B
o
+(R−R
s
)B
g
]. (10.9)
10.4 The material balance equation
Combining Eqs.(10.5) to (10.9) we can write the material balance equation for a general oil
reservoir,
N
p
[B
o
+(R−R
s
)B
g
] = NB
oi
¸
(B
o
−B
oi
) +(R
si
−R
s
)B
g
B
oi
+
m(
B
g
B
gi
−1) +(1+m)(
c
w
S
w
+c
p
1−S
w
)∆p

+(W
e
−W
p
)B
w
. (10.10)
(W
e
−W
p
)B
w
on the right-hand side of Eq.(10.10) accounts for water influx into the reservoir
and production of water, respectively.
It is important to notice under which circumstances the material balance equation is devel-
oped. The equation gives a static representation of the reservoir and does not include any terms
describing the energy loss in the reservoir due to fluid flow behaviour. The following features
of the MBE should be noted:
• MBE generally exhibits a lack of time dependence although the water influx has a time
dependence.
• Although the pressure only appears explicitly in the water and pore volume compress-
ibility terms, it is implicit in all the other terms of Eq.(10.10) since the PVT parameters
B
o
, R
s
and B
g
are functions of pressure. The water influx is also pressure dependent.
• Eq.(10.10) is evaluated, in the way it was derived, by comparing the current volumes at
pressure p to the original volumes at p
i
. Note that the material balance equation is not
evaluated in a step-wise or differential fashion.
10.5 Linearized material balance equation
The linearized material balance equation is particular interesting in connection with reservoir
parameter estimation. Results published in 1963-64 by Havlena and Odeh opened a wide range
162 Chapter 10. Material Balance Equation
of applications of the MBE to reservoir engineering [33, 34]. The linear form of equation
(10.10) is,
F = N(E
o
+mE
g
+E
c
) +W
e
B
w
, (10.11)
where the following definitions are used:
The underground withdrawal:
F = N
p
[B
o
+(R−R
s
)B
g
] +W
p
B
w
Expansion of oil and its originally dissolved gas:
E
o
= (B
o
−B
oi
) +(R
si
−R
s
)B
g
Expansion of the gas cap gas:
E
g
= B
oi

B
g
B
gi
−1

Expansion of the connate water and reduction of pore volume:
E
c
= (1+m)

c
w
S
w
+c
p
1−S
w

B
oi
∆p
Eq.(10.11) is especially important for revealing the drive mechanism of the reservoir and
for estimation of initial oil and gas.
10.6 Dissolved gas expansion drive
Fluid samples taken from an oil reservoir, indicate a reservoir pressure larger than the bubble
point pressure, i.e. p > p
b
. From this information alone, important deductions are made:
1. The reservoir fluid exists in only one phase, as undersaturated oil.
2. Production is driven by expansion of undersaturated oil.
3. No gas cap can exist.
4. All produced gas comes from the oil, i.e. R
si
= R
s
= R.
5. Production of oil is controlled by compressibility of oil, -water and -formation.
With these restrictions in mind, a simplified material balance equation is written,
N
p
B
o
= NB
oi
¸
B
o
−B
oi
B
oi
+
c
w
S
w
+c
p
1−S
w
∆p

.
We have seen earlier that the slow decline of the volume factorB
o
, for increasing pressures
higher than the bubble point pressure, is described by the law of compressibility,
10.6 Dissolved gas expansion drive 163
c
o
=
1
V
o
∆V
o
∆p
,
where we may use the definitions; ∆p = p
i
−p, V
o
=V
on
B
oi
and ∆V
o
=V
on
(B
o
−B
oi
). Note the
notation: N =V
on
, in accordance with Fig. 9.12.
Oil compressibility is therefore written,
c
o
=
1
V
on
B
oi
V
on
(B
o
−B
oi
)
∆p
=
B
o
−B
oi
B
oi
1
∆p
, (10.12)
and the simplified material balance equation above is therefore,
N
p
B
o
= NB
oi
¸
c
o
S
o
+c
w
S
w
+c
p
1−S
w
∆p

.
By introducing a total compressibility; c
t
= c
o
S
o
+c
w
S
w
+c
p
, we may write the equation
above,
N
p
B
o
= N B
oi
c
t
1−S
w
∆p, (10.13)
and by introducing the reservoir pore volume using the expression,V
p
S
o
=N B
oi
, we may find
a simple relation between produced oil, N
p
and observed pressure drop, ∆p given by,
N
p
=
V
p
c
t
B
o
∆p.
The linear relationship between oil production N
p
and pressure drop ∆p can be used to
estimate unknown reservoir parameters such as pore volume V
p
or total compressibility c
t
.
Fig. 10.5 shows a linear representation of the data, used to determineV
p
and c
t
.
N
p
∆p
Figure 10.5: Reservoir parameter estimation for dissolved gas ex-
pansion data.
164 Chapter 10. Material Balance Equation
c
w
= 3 10
−6
psi
−1
p
i
= 4000 psi B
oi
= 1.2417 RB/STB
c
p
= 8.6 10
−6
psi
−1
p
b
= 3330 psi B
ob
= 1.2511 RB/STB
S
w
= 0.2
Example: Oil recovery factor at bubble point pressure
An undersaturated oil reservoir has been produced down to its bubble point pres-
sure. What is the oil recovery at this time when the following parameters are
given?
From Eq.(10.13) we may write,
N
p
N
=
B
oi
B
ob
c
t
∆p
1−S
w
,
where c
t
= c
o
S
o
+c
w
S
w
+c
p
. Using Eq.(10.12) we have the total compressibility,
c
t
=
B
ob
−B
oi
B
oi
∆p
(1−S
w
) +c
w
S
w
+c
p
.
Inserting for the numbers from the table above, we find the total compressibil-
ity; c
t
= 18.24 10
−6
psi
−1
, and the relative production becomes,

N
p
N

3330psi
= 0.01516,
which gives an oil recovery at the bubble point pressure equal to 1.5%.
.
After some time with continuous production, the reservoir pressure will finally decrease
below bubble point pressure. When this happens, gas is produced in the reservoir and the
expansion of this gas will become increasingly important for the process of oil production. The
material balance equation Eq.(10.10) can now be expressed as,
N
p
[B
o
+(R−R
s
)B
g
] = N
¸
(B
o
−B
oi
) +(R
si
−R
s
)B
g
+
c
w
S
w
+c
p
1−S
w
∆p

.
When we consider the significance of the different expansion factors, we may assume the
gas expansion to be gradually more important than the expansion due to compressibility of
initial water and the formation. Consequently, we may neglect the compressibility term and
write the simplified material balance equation as,
N
p
[B
o
+(R−R
s
)B
g
] ≈N[(B
o
−B
oi
) +(R
si
−R
s
)B
g
]. (10.14)
The use of this approximate equation is justified through a comparison of the different
volumes A and C in Fig. 10.3. For reservoir pressures p < p
b
, we will find that A C in all
practical cases.
10.7 Gas cap expansion drive 165
R
si
(4000psi) = 510 SCF/STB B
g
(900psi) = 0.00339 RB/SCF
R
s
(900psi) = 122 SCF/STB B
o
(900psi) = 1.0940 RB/STB
Example: Oil recovery below the bubble point pressure
Using the same example as above, we can now calculate the oil recovery down to
a pressure p = 900psi,where the volume factors are given:
The solution gas produced in the reservoir will change the compressibility in
the reservoir drastically. The formula for gas compressibility can be given by
c
g
= 1/V(∆V/∆p), indicating a gas compressibility of c
g
·300 10
−6
psi
−1
. This
is about 15 times larger than the total compressibility at pressures above the bubble
point pressure.
From this simple consideration we may assume all compressibility terms in the
material balance equation, Eq.(10.10), to be negligible compared to the solution
gas compressibility. We may therefore use the approximation Eq.(10.14),
N
p
N
=
(B
o
−B
oi
) +(R
si
−R
s
)B
g
B
o
+(R−R
s
)B
g
,
where R is the gas-oil ratio (GOR).
Using the numbers from the tables above, we find the oil recovery equal to,

N
p
N

900psi
=
344.4
R+200.7
. (10.15)
In order to numerically define the oil recovery, information about the GOR is
necessary. On the other hand it is quite obvious that oil recovery is maximised
when R is kept as small as possible, i.e. gas should remain in the reservoir if oil
production is to be optimized.
.
From the example above we may state an improtant production strategy for oil reservoirs,
namely that:
All production should come from the oil zone.
Since the gas is considered as the driving force in the reservoir production, it should, if
possible be produced after the oil is produced. If the gas is produced first, we will not only
loose some of the driving force, but the oil will also be smeared out due to the withdrawal of
the gas zone. This oil, due to capillary effects, is most probably lost.
10.7 Gas cap expansion drive
The presence of a gas cap at initial conditions indicates a saturated oil in equilibrium with
the gas. As learned from the example above, production of gas should be minimised since
gas acts as the driving force behind oil production. The wells should therefore be drilled and
166 Chapter 10. Material Balance Equation
completed with the purposed of optimising oil production, keeping as much gas in the reservoir
as possible.
When a gas cap is discovered in connection with an oil reservoir, we can safely neglect
all terms in the material balance equation, Eq.(10.10), containing expansion of connate water
or formation matrix. In the case of gas cap expansion drive we therefore get the somewhat
simplified material balance equation,
N
p
[B
o
+(R−R
s
)B
g
] =
NB
oi
¸
(B
o
−B
oi
) +(R
si
−R
s
)B
g
B
oi
+m(
B
g
B
gi
−1)

+(W
e
−W
p
)B
w
,
where the linearized material balance equation is,
F = N(E
o
+mE
g
) +W
e
B
w
.
If we could assume no water influx during oil production, i.e. W
e
= 0, the linearized mate-
rial balance equation could then be written,
F
E
o
= N +mN
E
g
E
o
, (10.16)
which clearly indicates the advantage with linearization, wheremN is the slope and N is the
constant term (N is the intersection point with the y-axis). The assumption of negligible water
influx is rather plausible for reservoirs with a gas cap since the expansion of initial water and
formation matrix is small compared to the expansion of gas cap gas, unless the aquifer size is
large compared to the oil reservoir.
Example: Linearization of material balance equation
The pressure decline in a saturated oil reservoir with a gas cap is driven by ex-
pansion of liberated solution gas E
o
, and gas cap expansion E
g
, as presented in
Eq.(10.16).
In order to estimate initial oil in place N, and the size of the gas cap mN, we
need to know the production data, like produced oil volume at surface condition
N
p
, in addition to the gas-oil ratio R. Further information is also acquired with
respect to the different volume factors B
o
, B
g
and R
s
.
The linearized terms used in Eq.(10.16) are defined as below,
F = N
p
[B
o
+(R−R
s
)B
g
],
E
o
= (B
o
−B
oi
) +(R
si
−R
s
)B
g
,
E
g
= B
oi
(
B
g
B
gi
−1),
where we assume no water production or water influx.
For an oil reservoir with a gas cap, we have the following data,
The data in the table above is plotted in Fig. 10.6 which shows a linearization fit
taking into account all data points. From the figure we find the initial oil volume
10.8 Water influx 167
p [psia] F/E
o
10
6
[STB] E
g
/E
o
3150 398.8 4.94
3000 371.8 4.51
2850 368.5 4.29
2700 355.7 4.25
2550 340.6 3.99
2400 340.7 3.93
0 1 2 3 4 5
E
g
/E
o
0
50
100
150
200
250
300
350
400
450
F/E
o
[STB]
Measurements
Linear fit
Figure 10.6: Extrapolation of lineraized gas cap expansion data.
Note that the units on the y- axis (F/E
o
) is given in
10
6
STB.
to be N = 109.5 10
6
STB and the slope or gas cap size mN = 58.7 10
6
STB,
indicating a fractional gas cap size of m = 0.54.
.
10.8 Water influx
Water influx is more the rule, than the exception for normal oil and gas production, i.e. we
expect some influx of water to be present in all situations where reservoir production takes
place over some period of time.
Generally we may expect the influx of water to be both time and pressure dependent and
we write,
W
e
= f (p, t),
where f is some function which will depend on the reservoir and the extent and volume of the
aquifer itself.
168 Chapter 10. Material Balance Equation
This picture could be clarified by considering a reservoir model, as shown in Fig. 10.7,
where the periphery pressure (pressure near the boundary) in the aquifer zone is equal top
e
.
The pressure difference induced, will then cause water to flow into the reservoir volume. This
flow will obey Darcy’s law,
q
w
=C(p
e
−p),
where C is a constant depending on the various reservoir parameters.
r
e
p
p
e
q
w
q
w
q
w
q
w
q
w
Figure 10.7: Water influx from external aquifer.
The cumulative water influx can be found by integrating over the time this process takes
place,
W
e
=

t
0
q
w
dt ·

i
q
i
∆t
i
=C

i
∆p
i
∆t
i
.
In the equation above we move from a continuous case to a discrete case by summing over
all pressure drops ∆p for all time periods ∆t.
The use of this equation is important when real data is supposed to be fitted in accordance
with a material balance model. The constant C is adjusted in such a way as to secure the match
between the model and the real data.
Example: Pressure maintenance through water injection
In an attempt to maintain the reservoir pressure we may inject water into the reser-
voir. Injection water rate will be proportional to the oil production rate and the
following simplified material balance equation is applied,
N
p
[B
o
+(R−R
s
)B
g
] =W
p
B
w
.
Key data for a typical oil reservoir is,
N
p
= 10000 STB B
o
= 1.2002 RB/STB R = 3000 SCF/STB
B
g
= 0.00107 RB/SCF R
s
= 401 SCF/STB
10.8 Water influx 169
If pressure is maintained, we can conclude from the data above that the relation
between produced oil and injected water has to be,
W
p
= 4.0N
p
,
measured in [STB].
.
170 Chapter 10. Material Balance Equation
10.9 Exercises
1. The following PVT-data is used in material balance calculations.
p [psia] B
o
R
s
B
g
4000 1.2417 510 –
3500 1.2480 510 –
3330 1.2511 510 0.00087
3000 1.2222 450 0.00096
2700 1.2022 401 0.00107
2400 1.1822 352 0.00119
2100 1.1633 304 0.00137
1800 1.1450 257 0.00161
1500 1.1115 214 0.00196
1200 1.0940 167 0.00249
900 1.0940 122 0.00339
600 1.0763 78 0.00519
300 1.0583 35 0.01066
a) Find the recovery N
p
/N, when the pressure decreases from p
i
= 4000 psia to the
bubble point, p = p
b
.
Compressibility is given; c
w
= 3.0 10
−6
psi
−1
, c
p
= 8.6 10
−6
psi
−1
and connate
water saturation is S
wc
= 0.2.
b) Calculate the recovery N
p
/N for declining pressure, from p
i
= 4000 psia to p =
600 psia.
What is the gas saturation at 600psia, when R = 1000 SCF/STB ?
c) The oil rate is 10000 STB/d at pressure p = 2700 psia and the gas-oil ratio is R =
3000SCF/STB.
What is the injection water rate necessary to maintain the production at p=2700
psia ? Use B
w
= 1.0RB/STB.
2. For an oil reservoir with gas cap, the water injection rate is not known. The material
balance equation with no water production is,
N =
N
p
[B
t
+B
g
(R−R
si
)] −W
i
B
w
(B
t
−B
oi
) +(B
g
−B
gi
)mB
oi
/B
gi
,
where B
t
= B
o
+(R
si
−R
s
)B
g
and W
i
is the water volume injected given in STB.
a) Calculate the initial oil in place and the size of the gas cap when the following PVT-
and production data is given.
The boiling point pressure is 1850 psia.
10.9 Exercises 171
p [psia] 1850 1600 1300 1000
R
s
[SCF/STB] 690 621 535 494
B
o
[RB/STB] 1.363 1.333 1.300 1.258
B
g
[RB/SCF] 0.00124 0.00150 0.00190 0.00250
B
t
[RB/STB] 1.363 1.437 1.594 1.748
ρ
o
[psi/ft] 0.3014 0.3049 0.3090 0.3132
N
p
[STB] – 3.1 10
8
5.5 10
8
5.9 10
8
R [SCF/STB] – 1100 1350 1800
W
i
[STB] – 1.594 10
8
2.614 10
8
3.12 10
8
Water saturation is 0.24, porosity is 0.17 and the water volume factor is approxi-
mately 1.0 RB/STB.
b) Geological information indicates that the reservoir could be approximated to a right
circular cone. Calculate the height of the cone when the pressure at the bottom
level of the oil zone (cone) is 1919 psia ( –the water-oil contact). [Volume of a
right circular cone is πr
2
h/3].
3. Define an expression giving the gas-oil ratio, GOR [SCF/STB] in a reservoir with super-
critical gas saturation.
Find the GOR using the following data;
µ
o
=0.8 cp B
o
=1.363 RB/STB
µ
g
=0.018 cp B
g
=0.001162 RB/SCF
k
o
=1000 mD R
s
= 500 SCF/STB
k
g
=96 mD
4. The data in the table below is taken form an oil reservoir.
p N
p
R B
o
R
s
B
g
[psia] [10
6
STB] [SCF/STB] [RB/STB] [SCF/STB] [RB/SCF]
3330 – – 1.2511 510 0.00087
3150 1.024 1050 1.2353 477 0.00092
3000 1.947 1060 1.2222 450 0.00096
2850 2.928 1160 1.2122 425 0.00101
2700 – – 1.2022 401 0.00107
a) First, assume there is no gas cap present and the production mechanism is dissolved
gas drive. Estimate the initial oil volume in the reservoir.
b) Estimate oil production at p = 2700 psia, by a method of comparing R, calculated
from the material balance equation and secondly calculated from the GOR– equa-
tion (as done in Exercise 1),
R = R
s
+
k
g
k
o
B
o
µ
o
B
g
µ
g
.
A relation k
g
/k
o
exists experimentaly and the gas saturation dependency has been
established:
172 Chapter 10. Material Balance Equation
log(k
g
/k
o
) = 34.5 S
g
−2.54,
where S
wc
=0.30, µ
o
=1.0 cp and µ
g
=0.1 cp.
c) Data from an other well indicates the existence of a small gas cap. Calculate the
initial oil volume, in view of this new information.
Answer to questions:
1. a) 1.52%, b) 46%, 0.43, c) 39830 STB/d 2. a) 2.22 10
9
STB, 0.49, b) 738 ft, 3. 5505
SCF/STB,
4. a) 122.8 10
6
STB, b) by iteration c) 108.6 10
6
STB
Chapter 11
Well Test Analysis
11.1 Introduction
In order to optimise a development strategy for an oil or gas field, we have to consider a reser-
voir model capable of realistically predicting the dynamic behaviour of the field in terms of
production rate and fluid recovery. Such a model is constructed using geological, geophysical
and well data. The necessary parameters are obtained from direct measurements (cores, cut-
tings, formation fluid samples, etc.) and from interpreted data (surface seismic, well logs, well
tests, PVT analysis, etc.). While seismic data and well logs provide a static description of the
reservoir, only well testing data provide information on dynamic reservoir response. The well
test data is therefore a key element in the reservoir model construction, see Fig.11.1.
Geophysics
Interpretation
Reservoir
Engineering
Electric Log PVT, Core Well Test
Geophysical
Model
Log
Model
Well Test
Model
Reservoir Model
Measurement
Figure 11.1: Stages of reservoir modelling.
Interpretation of these data leads to individual "models" (what the geophysicist, the petro-
physicist and well analyst think the reservoir looks like). A brief understanding of the fun-
damental aspects of well testing is necessary in order to incorporate dynamic well test data
into the reservoir model and it is the function of the reservoir engineer to incorporate these
173
174 Chapter 11. Well Test Analysis
individual models into a cohesive reservoir model [50].
In the initial phase of well tests, pressure measurements are dominated by wellbore storage
effects. During this time, fluid contained in the wellbore and its direct connected volumes are
produced. Then, as the production of the reservoir fluid starts, the fluid near the well expands
and moves towards the area of lower pressure. This movement will be retarded by friction
against the pore walls and the fluid’s own inertia and viscosity. However, as the fluid moves
it will, in turn, create a pressure imbalance and this will induce neighbouring fluid to move
towards the well. This process continues until the drop in pressure, created by the start-up
of production, is dissipated throughout the reservoir. The tail portion of the well test data for
the test of sufficient duration, is affected by the interference from other wells or by boundary
effects such as those that occur when the pressure disturbance reaches the edge of a reservoir.
From this time and onwards, the average pressure in the reservoir will decrease in a way similar
to emptying a confined volume, like a tank of gas.
In this chapter we will develop simple models that can explain the measured well test data.
The models give a rather simplified and idealistic view of the reservoir, characterised by:
• isotropic and homogenous reservoir volume,
• constant porosity, - absolute permeability, - viscosity and - reservoir height (reservoir
thickness),
• test production with relative small pressure gradients, i.e. c∇p ∇p is small (compress-
ibility times pressure gradient squared) ,
• horizontal radial flow paths (no cross flow) and
• constant flow rate.
Even though these items place tight restrictions on the reservoir itself, some important
information can be extracted from the models, explaining reservoir behaviour on basis of the
well test data.
The wellbore pressure data is subdivided into three different production periods, each de-
scribing characteristic well and reservoir pressure response profile:
1. Wellbore storage period. Production from the wellbore and nearby cavities.
2. Semi logarithmic period. Production from an infinite acting reservoir where no bound-
ary effects are observed.
3. Semi steady state period. Production from a confined reservoir (closed volume) where
the interference from the boundary dominates pressure decline.
11.1.1 Systems of Uunits Used in Well Test Analysis
The following systems of units are traditionally used in well test analysis: SI-Units and Field
Units, as presented in Table 11.1.
Some conversion factors mostly used in well test analysis are listed below:
11.2 Wellbore Storage Period 175
Table 11.1: System of units used in well test analysis
Parameter Nomenclature SI-units Field units
Flow rate q Sm
3
/d STB/d
Volume factor B Rm
3
/Sm
3
RB/STB
Thickness h m ft
Permeability k µm
2
mD
Viscosity µ mPas cp
Pressure p kPa psia
Radial distance r m ft
Compressibility c (kPa)
−1
psi
−1
Time t hrs hrs
1 STB/d = 0.159 Sm
3
/d
1 ft = 0.3048 m
1 mD = 0.98710
−3
µm
2
1 cp = 1 mPas
1 psi = 6.895 kPa
11.2 Wellbore Storage Period
Let us consider the initiation of well production at a constant rate at timet
0
=0. First, the fluids
contained in the wellbore itself and its continuous cavities will be produced. This production is
characterised by the expansion of oil and gas in the well, defined by the fluid compressibility,
c
f
and the well storage volume, V
w
.
The definition of the wellbore fluid compressibility is c
f
= ∆V
w
/(V
w
∆p) and the well
flowrate is qB = ∆V
w
/∆t, where the pressure drop in the well is, ∆p. (B is the wellbore fluid
volume factor, measured in reservoir volume pr. standard volume.)
∆p =
qB
c
f
V
w
t, (11.1)
where ∆p = p
i
−p
w
(t) is the difference between initial and wellbore pressure.
The compressibility is often redefined, where the wellbore storage, c
ws
= c
f
V
w
is used to
characterise particular wells.
Example: Wellbore storage effect
A well has a certain volume capacity for fluids. A real well, with an average well
radius of r
w
= 0.1m, at a well depth of H = 2000m has a volume V
w
, accessible to
fluids close to 17 m
3
.
176 Chapter 11. Well Test Analysis
t, hrs
10 10 10 10
-3 -2 -1 0
Slope = 1
l
o
g
(
-
)
p
p
i
w
f
Figure 11.2: Logarithmic analysis of the pressure drawdown data at
early times of well testing, i.e. in the wellbore storage
period
If well production is measured in standard cubic meter pr. day [Sm
3
/d] and
time in hours [hr], the well pressure is then given by,
p
i
−p
w
=
qB
24c
ws
t,
and the logarithmic pressure difference can be given by,
log(p
i
−p
w
(t)) = log(t) +log

qB
24c
ws

,
where p
w
is the wellbore pressure.
The latter equation, in a logarithmic scale, exhibits the linear relation between
time and pressure drop. This straight line behaviour seen in Fig. 11.2, has a slope
equal to unity.
The technique of using log-log plots is commonly used in well test analysis for
model recognition, but also as here, for estimation of the wellbore storage constant
c
ws
:
c
ws
=
qB
24(p
i
−p
w
(1hr))
, (11.2)
with p
w
(1 hr) picked from the unit slope line.
.
When the well is opened (shut-in) to flow, it is opened at the surface. Due to the wellbore
storage, where the well itself contains a certain volume of compressible fluid, there is a delay
in a flow-rate response at the sand-face (bottom of the well), as seen in Fig. 11.3. This effect
must be incorporated into the interpretation model of the pressure test data.
11.3 Semi Logarithmic Period 177
q
t
t ∆
Sandface
flow rate
Surface flow rate
∆t
q
t
Sandface
flow rate
t
p
Surface flow rate
∆t
Figure 11.3: The wellbore storage effect on flow-rate during the
drawdown (left) and build- up tests (right).
11.3 Semi Logarithmic Period
In this section we will focus our attention on what happens in the reservoir when the fluid is
drawn towards the well due to the pressure drop in the wellbore. We shall develop a theory for
fluid flow in a cylindrical and somewhat idealistic reservoir (see introductory remarks). The
production profile in this period is characterised by a semi logarithmic pressure dependence,
hence the title of this section.
11.3.1 Diffusivity Equation
Transport of oil in porous media is generally described by the law of continuity and Darcy’s
law. If we consider a volume element, as shown in Fig.11.4, we may define the flow of oil in
the x-direction by the equations,
d(ρv
x
)
dx
= −
∂(φρ)
∂t
,
v
x
= −
k
µ
dp
dx
.
where ρ is density, φ is porosity, µ is viscosity, k is permeability and v
x
is flow velocity in
x-direction.
Using an independent co-ordinate system, we may write the same equations as,
∇ (ρv) = −
∂(φρ)
dt
,
v = −
k
µ
∇p,
Substituting these two equations gives us,

ρ
k
µ
∇p

=
∂(φρ)
∂t
. (11.3)
178 Chapter 11. Well Test Analysis
v
x
v
x+ x ∆
x x
x+ x ∆
p
x
p
x+ x ∆
Figure 11.4: Flow of oil in the x-direction through a volume element.
In accordance with an idealistic view of the reservoir, as mentioned above, we will consider
both permeability and viscosity to be constant, while oil density and reservoir porosity may
vary with pressure, i.e. ρ = ρ(p) and φ = φ(p). From these relations we can define the liquid
compressibility as well as the matrix compressibility as,
c
l
=
1
ρ
∂ρ
∂ p
and c
m
=
1
φ
∂φ
∂ p
.
Eq.(11.3) is further developed using the newly defined compressibilities, c
l
and c
m
, and we
write,
c
l
∇p∇p+∇
2
p =
1
η
∂ p
∂t
, (11.4)
where η = k/(φcµ) and c = c
l
+c
m
, where c is the total compressibility.
Further simplification of Eq.(11.4) rests on the assumption that c
l
∇p∇p <[∇
2
p[, which
is the case in almost all real cases. With this last simplification in mind, we can write the
Diffusitivity equation (independent of co-ordinate systems),

2
p =
1
η
∂ p
∂t
. (11.5)
The diffusitivity equation in cylindrical co-ordinates gives,
1
r

∂r

r
∂ p
∂r

+

2
∂z
2
=
1
η
∂ p
∂t
. (11.6)
With no crossflow in the reservoir, the linearized diffusitivity equation is written,
1
r

∂r

r
∂ p
∂r

=
1
η
∂ p
∂t
. (11.7)
11.3.2 Solution of the Diffusitivity Equation
The solution of the diffusivity equation can be simplified by usingthe linear source approxi-
mation implicating a zero wellbore radius. In case of a constant flow rate the following Initial-
and Boundary condition are defined. Initial conditions are described by the pressure start-up
conditions in the reservoir, while the boundary condition is deduced from Darcy’s law.
11.3 Semi Logarithmic Period 179
Initial condition:
i) p(r, 0) = p
i
, ∀r,
ii) lim
r→∞
= p
i
, ∀t.
Boundary condition:

r
∂ p
∂r

r=r
w
=
qBµ
2πhk
, ∀t > 0,
Line-source solution: lim
r→∞

r
∂ p
∂r

=
qBµ
2πhk
, ∀t. > 0
In solving the linear diffusitivity Eq.(11.7) we may use the well known Boltzmann trans-
formation,
y =
r
2
4t
,
which gives the following partial derivatives:
∂r = (r/2y)∂y and ∂t =−(t/y)∂y.
When the Boltzmann transformation is applied to Eq.(11.7), the variable of time is made
implicit and the diffusivity equation is reduced to only one variable,

∂y

y
∂ p
∂y

=
y
η
∂ p
∂y
. (11.8)
We may solve Eq.(11.8), by direct integration and we get,
y
∂ p
∂y
= K
3
e
−r
2
/(4ηt)
,
where K
3
is a constant that could be defined, using the boundary condition for the line-source
solution, i.e. K
3
= (qBµ)/(4πhk).
Second integration of Eq.(11.8), gives the following expression,
p
i
−p(r, t) =
qBµ
4πhk


r
2
/(4ηt)
e
−s
s
ds. (11.9)
The integral in Eq.(11.9) is known as the Exponential integral and is originally defined as,
Ei(ξ) ≡

ξ
−∞
e
s
s
ds,
−Ei(−ξ) =


ξ
e
−s
s
ds.
The general solution of the linear diffusitivity equation, Eq.(11.7), can then be presented
as,
p
i
−p(r, t) =
qBµ
4πhk
¸
−Ei


r
2
4ηt

, (11.10)
where η = k/(φµc).
Values of the function −Ei(−ξ) is tabulated in Table 11.2.
180 Chapter 11. Well Test Analysis
Table 11.2: Table of the function Ei(ξ) for 0.01 ≤ξ ≤ 10.
ξ [−Ei(−ξ)] ξ [−Ei(−ξ)] ξ [−Ei(−ξ)] ξ [−Ei(−ξ)]
0.01 4.0379 0.12 1.6595 0.35 0.7942 0.90 0.2602
0.02 3.3547 0.14 1.5241 0.40 0.7024 1.00 0.2194
0.03 2.9591 0.16 1.4092 0.45 0.6253 1.50 0.1000
0.04 2.6813 0.18 1.3098 0.50 0.5598 2.00 0.0489
0.05 2.4679 0.20 1.2227 0.55 0.5034 2.50 0.0249
0.06 2.2953 0.22 1.1454 0.60 0.4544 3.00 0.0130
0.07 2.1508 0.24 1.0762 0.65 0.4115 4.00 0.0038
0.08 2.0269 0.26 1.0139 0.70 0.3738 5.00 0.0011
0.09 1.9187 0.28 0.9573 0.75 0.3403 7.00 0.0001
0.10 1.8229 0.30 0.9057 0.80 0.3106 10.00 0.0000
11.3.3 Gas Reservoir
The general form of the basic (material balance) equation, given by Eq. (11.7), is valid for both
liquid and gas flow. In the case of more compressible fluids, like gases, some modifications are
necessary in order to use the diffusivity equation.
Attempting to obtain a linear type of the diffusivity equation for a highly compressible gas
flow, Al-Hussainy, Ramey and Crawford (1966), replaced the dependent variable p by the real
gas pseudo pressure m(p) in the following manner,
m(p) = 2

p
p
b
p
µz
dp, (11.11)
where p
b
is an arbitrary (datum) pressure.
Using the equation of state for a real gas,
ρ =
Mp
zRT
,
and a pseudo pressure function m(p) from Eq.(11.11) they derived a simplified linear equation
for a real gas flow:
1
r

∂r
(r
∂m(p)
∂r
) =
1
η
∂m(p)
∂t
, (11.12)
which is precisely the same as Eq.(11.7) where the term p is replaced by a pseudo pressure
function m(p).
It follows from Eq.(11.12) that the behaviour of m(p) vs. time in gas well testing should
have identical trends as pressure vs. time in oil well testing. This fact is commonly used in a
gas well test analysis.
11.3 Semi Logarithmic Period 181
11.3.4 The Solution of the Diffusitivity Equation in Dimensionless Form
In connection with model recognition and practical application of the well test data it is quite
often advantageous to plot the measured data in such a way as to initially compare it with
a standard and well known function. It is therefore convenient to introduce dimensionless
variables, such as,
r
D
=
r
r
w
,
t
D
=
kt
φµcr
2
w
,
p
D
=
2πhk
qBµ
[p
i
−p(r, t)].
Depending on the units preferred; standard- or field units, the above normalisation can be
written,
SI- units:
r
D
=
r
r
w
, t
D
=
0.0036kt
φµcr
2
w
and p
D
=
πhk
1.842qBµ
[p
i
−p(r, t)],
Field units:
r
D
=
r
r
w
, t
D
=
0.000264kt
φµcr
2
w
and p
D
=
πhk
141.2qBµ
[p
i
−p(r, t)],
Using dimensionless variables for the solution of the linear diffusivity equation, as pre-
sented in Eq.(11.10), we get,
p
D
(r
D
, t
D
) =−
1
2
Ei


r
2
D
4t
D

, (11.13)
where the factor 1/2 in front of the exponential function is of purely historical reasons, related
to the presentation of semi logarithmic data.
11.3.5 Wellbore Pressure for Semi Logarithmic Data
The wellbore pressure (r
D
= 1) is given by,
p
wD
(t
D
) =−
1
2
Ei

−1
4t
D

.
From mathematical tables we have the following approximation,
−Ei(−ξ) =


ξ
e
−s
s
ds ≈(−lnξ −γ) +ξ −
ξ
2
2 2!
+
ξ
3
3 3!
− ,
where γ ·0.5772157 is Euler’s constant.
The interesting question now is related to the validity of the approximation: −Ei(−ξ) ≈
−lnξ −γ, i.e.
p
wD
(t
D
) =−
1
2
Ei


1
4t
D

≈−
1
2

ln
1
4t
D

. (11.14)
182 Chapter 11. Well Test Analysis
We may write the dimensionless wellbore pressure as,
p
wD
(t
D
) ≈ −
1
2
(ln1−ln4−lnt
D
+γ),

1
2
(lnt
D
+0.80907),
where the next term in the series expansion of Eq. (11.14), is 1/(4t
D
), is thought to be insignif-
icant.
In order to check the accuracy of this approximation we may look at the relative importance
of the next term not included in the approximation Eq.(11.14), i.e.
Error =
1/(4t
D
)
lnt
D
+0.80907
. (11.15)
If we assume the dimensionless time; t
D
≥25, then we would expect the Error always to
be less then 0.25 %.
In order to illustrate the implication of the restrictiont
D
≥25, we can consider the constraint
on time (in hours), for a "typical" oil reservoir with the following parameters (in field units),
k = 100 mD φ = 25 % µ = 1.0 cP
c = 5 10
−6
psi
−1
r
w
= 1 ft
Using the definition of the dimensionless time in field units from above, we find that the
real time that passes before the approximation, Eq.(11.14) is valid, is not more than 0.0012 hrs,
or 4.3 seconds. We therefore conclude that the error done in applying the approximation in
Eq.(11.14), is insignificant for all practical purposes.
In cases where the pressure drop observed in one well is induced by an other well a certain
lateral distance apart from the observation well, we have to consider the restriction imposed
above very carefully. In these cases the approximation may usually not hold.
Generally we may therefore use the following approximation,
p
wD
(r
D
, t
D
) =
1
2

ln
t
D
r
2
D
+0.80907

, (11.16)
with the restriction of t
D
/r
2
D
≥25.
Example: Semi logarithmic analysis of pressure drawdown data
The wellbore pressure is given by the approximation (in dimensionless form),
p
wD
(t
D
) =
1
2
(lnt
D
+0.80907)
Using the definition of dimensionless variables, given above, we may write,
p
i
−p
w
(t) =
qBµ
2πhk
1
2

ln
kt
φµcr
2
w
+0.80907

.
Rewriting this equation using log term instead of ln and standard units,
11.3 Semi Logarithmic Period 183
p
i
−p
w
(t) =
2.1208qBµ
hk

logt +log
k
φµcr
2
w
−2.0923

,
and in field units,
p
i
−p
w
(t) =
162.6qBµ
hk

logt +log
k
φµcr
2
w
−3.2275

.
When the well test data is presented in a semi logarithmic plot as shown in
Figure 11.5, we may use one of the two equations above in order to extract vital
information about the reservoir. In the figure, some early data originates from
the wellbore storage period and some late data originates from the period when
boundary effects starts to mask the pressure data. These data does not comply with
the straight line and should therefore be disregarded when the semi logarithmic
data is matched.
p
,

k
P
a
t, hrs
10 10 10 10 10 10
-3 -2 -1 0 1 2
Wellbore storage
effect
Outer boundary
effect
Slope m
Figure 11.5: Pressure drawdown data.
The straight line through the semi logarithmic data points in Figure 11.5, is
defined by the equation,
p(t) ∼−mlogt,
where m is the slope of the straight line. This line is compared with the model
above, and from this comparison we get the following equality (using SI - units),
m = 2.1208
qBµ
hk
.
The reservoir permeability, k could be estimated when information about reser-
voir height, oil viscosity, oil volume factor and oil rate are known.
.
184 Chapter 11. Well Test Analysis
11.4 Semi Steady State Period
After a period of reservoir production from an infinite reservoir, there comes a period of pro-
duction where the influence from neighbouring wells or reservoir boundaries, such as lateral
extension, faults or sands thinning out, are going to play an increasingly important role. This
period is called the semi steady state period and a steadily decreasing reservoir pressure is
observed (decreased average pressure in a confined reservoir volume). Simultaneously, the
pressure profile in the reservoir is maintained unchanged.
It should be emphasised that this is an idealised model of how we think the reservoir re-
sponds to boundaries effects, and as such, prudent interpretation of steady state data is highly
recommendable.
In Figure 11.6, several pressure profiles are plotted. At constant well production, the draw-
down pressure profile is assumed to be constant, i.e. ∂ p(r)/∂t = constant, in the reservoir.
p
e
p
r
w
r
e
Figure 11.6: Steady state pressure profiles.
Since the pressure profile is assumed to be constant, we expect the diffusitivity equation to
be time independent, i.e. a constant K
1
balances the diffusitivity equation,
1
r

∂r

r
∂ p
∂r

= K
1
.
Integration of the time independent diffusivity equation gives,
r
∂ p
∂r
=
1
2
K
1
r
2
+K
2
, (11.17)
where K
2
is also a constant.
The boundary conditions in the semi steady state are partly defined as for the case of the
logarithmic period, but in addition we have assumed that the pressure profile does not signifi-
cantly vary after the reservoir boundary limit is reached. At this limit, the reservoir pressure is
steadily decreasing while the pressure profile is conserved.
11.4 Semi Steady State Period 185
Boundary condition in the well:

r
∂ p
∂r

r=r
w
=
qBµ
2πhk
.
Boundary condition at infinite reservoir radius:

r
∂ p
∂r

r=r
e
= 0.
Using the boundary conditions to define the constantsK
1
and K
2
, and integrating Eq.(11.17)
from the well (r = r
w
), gives,
p(r) = p(r
w
) +
qBµ
2πhk

ln
r
r
w

1
2
r
2
r
2
e

, (11.18)
where r
e
is the radial distance to the boundary of the confined reservoir, i.e. r
e
r
w
and so
r
w
/r
e
→0.
11.4.1 Average Reservoir Pressure
The average reservoir pressure is not an observable quantity. The average pressure is a weighted
function of the pressure in the whole reservoir and could be defined as,
p =

r
e
r
w
pdV

r
e
r
w
dV
.
Substituting for p given by Eq.(11.18) and integrating, we find the average reservoir pres-
sure,
p = p(r
w
) +
qBµ
2πhk

ln
r
e
r
w

3
4

, (11.19)
Eq.(11.19) gives the average pressure in a cylindrical reservoir with an outer radius equal
to r
e
and where the well is located in the centre. In real cases, however, the reservoir shape is
seldom cylindrical and more so, the well position is most frequently off centred. In these real
cases we may not use Eq.(11.19) directly. Instead a slight modified version given by Eq.(11.20)
is used, where A is the top area of the reservoir andC
A
is a parameter characterising the shape
and relative position of the well.
The average pressure for a general reservoir is then written,
p = p(r
w
) +
qBµ
2πhk

1
2
ln
4A
e
γ
C
A
r
2
w

, (11.20)
where γ is Euler’s constant.
In the case of a cylindrical reservoir, with a centred well location, i.e. A = π(r
2
e
−r
2
w
), we
find the shape-factor C
A
·4πe
(3/2−γ)
= 31.6206 (Dietz,1965).
186 Chapter 11. Well Test Analysis
11.4.2 Well Skin Factor
When a well is drilled it is always necessary to have a positive differential pressure acting from
the wellbore to the formation to prevent inflowof the reservoir fluids (blow-out). Consequently,
some of the drilling fluid penetrates the formation and particles suspended in the mud can
partially penetrate the pore spaces, reducing permeability, and creating a so-calleddamaged
zone next to the wellbore.
Assuming modification of the permeability in the damaged zone (r
w
< r < r
s
) is k
s
, and
within the rest of the reservoir (r
s
< r < r
e
) is k, as shown in Fig. 11.7.
p
e
p
s
p
wf
r
e
r
s
r
w
Figure 11.7: Skin effect caused by formation damage.
For the steady state inflow we can write the following equations for a cylindrical reservoir
with a centred well, as stated for formation beds in series,
p
s
−p
w

qBµ
2πk
s
h
ln
r
s
r
w
,
p
e
−p
s

qBµ
2πkh
ln
r
e
r
s
.
Note the approximation made due to the fact that r
e
r
w
and r
e
r
s
.
The total pressure drop from the wellbore through the reservoir is given by,
p
e
−p
w
= p
e
−p
s
+ p
s
−p
w
=
qBµ
2πkh
¸
ln
r
e
r
w
+(
k
k
s
−1)ln
r
s
r
w

, (11.21)
where the last term is called the mechanical skin factor S,
S = (
k
k
s
−1)ln
r
s
r
w
. (11.22)
Hence,
p
e
−p
w
=
qBµ
2πkh
(ln
r
e
r
w
+S), (11.23)
11.4 Semi Steady State Period 187
where the skin is a number characterising the cylindrical volume next to the wellbore.
As seen from Eq.(11.23), the skin may be associated with a characteristic pressure drop
∆p
skin
caused by the reduction in permeability in the skin zone,
∆p
skin
=
qBµ
2πkh
S. (11.24)
From this equation it is evident that when the skin S is positive, an increased pressure drop
towards the well is observed, while when S is negative the pressure drop is less than expected.
Skin is associated with the condition of reservoir permeability in the closed volume next to
the well. If the permeability in the skin zone is reduced, due to drilling or well treatments, then
the well will experience an increased pressure drop in this region while the skin is positive. If
the well, on the other hand, has a permeability higher than expected, then the skin is negative,
i.e.
• Skin factor is positive, S > 0 when k
s
< k and
• Skin factor is negative, S < 0 when k
s
> k.
11.4.3 Wellbore Pressure at Semi Steady State
The reservoir pressure development in a closed reservoir could be compared to the production
from a pressurised closed tank of oil. Production is maintained through volume expansion
where the combined compressibility of oil and reservoir rock ,c, is the important parameter.
The total compressibility of oil and reservoir rock is defined by, c = −dV/(Vdp), which
can be rewritten as,
dp
dt
=−
qB
cV
,
where qB is the oil flow in the reservoir andV = φAh is the reservoir pore volume.
At constant reservoir flow rate, we may integrate from initial pressure, p
i
to the average
pressure p and we get the following simple relation between reservoir pressure and time,
p
i
−p(t) =
qB
cV
t. (11.25)
Combining Eq.(11.19) which describes the semi steady state analysis, with Eq.(11.25), we
get,
p
i
−p(r
w
) =
qBµ
2πhk

1
2
ln
4A
e
γ
C
A
r
2
w
+S

+
qB
cV
t (11.26)
Note that we in Eq.(11.26) have introduced the skinS as an extra term in the equation, account-
ing for a partly damaged zone around the well.
Dimensionless variables are introduced, following the same definitions as for the case of
semi steady state, with the exception of the dimensionless timet
DA
, which is defined,
t
DA
=
kt
φAcµ
. (11.27)
In t
DA
dimensionless time is referenced to the reservoir drainage areaA.
188 Chapter 11. Well Test Analysis
Hence, Eq.(11.26) can be rewritten using dimensionless variables and we get,
p
wD
=

2πt
DA
+
1
2
ln
4A
e
γ
C
A
r
2
w
+S

. (11.28)
11.5 Wellbore Pressure Solutions
To this time we have developed the pressure function for the three periods of reservoir produc-
tion, referring to the wellbore storage period, the semi logarithmic period and the semi steady
state period, as if they were independent sequences reservoir production. In reality, well test
data, originating from the different periods are not easily distinguishable and quite a lot of
effort is spent identifying which data belongs to which period of production.
Summing up what we already know, we may write the following three pressure equations,
Well storage period:
p
i
−p
w
=
qB
c
ws
t.
Semi logarithmic period:
p
i
−p
w
=
qBµ
2πhk
1
2

ln
kt
φµcr
2
w
+0.80907+2S

.
Semi steady state period:
p
i
−p
w
=
qBµ
2πhk

2πk
φAcµ
t +
1
2
ln
4A
e
γ
C
A
r
2
w
+S

.
Using the following set of dimensionless variables,
SI- units:
r
D
=
r
r
w
, t
DA
=
0.0036kt
φAcµ
, p
D
=
hk
1.842qBµ
(p
i
−p(r, t)),
Field units:
r
D
=
r
r
w
, t
DA
=
0.000264kt
φAcµ
, p
D
=
hk
141.2qBµ
(p
i
−p(r, t),
we get the three wellbore pressure equations in dimensionless form,
Well storage period:
p
WS
wD
=
A
c
D
t
DA
, where c
D
=
c
st
2πhφc
.
Semi logarithmic period:
p
SL
wD
=
1
2

ln
4A
r
2
w
e
γ
t
DA
+2S

.
Semi steady state period:
p
SS
wD
=

2πt
DA
+
1
2
ln
4A
e
γ
C
A
r
2
w
+S

.
11.5 Wellbore Pressure Solutions 189
11.5.1 Transition Time Between Semi Logarithmic Period and Semi Steady State
Period
The difficulties in recognising the semi logarithmic data is primarily related to identification
of the time when the wellbore pressure, changes from being semi logarithmic to being semi
steady state dominated.
p
wD
p
wD
SL
p
wD
SS
t
DA
semi
logaritmic state
semi
steady state
Figure 11.8: Transition between semi logarithmic period and semi
steady state period.
Since the wellbore pressure development in the two periods are principally different, as
seen in the Fig.11.8, we may define the transient time when one period is followed by the
other, by the minimum pressure difference min¦p
SS
wD
−p
SL
wD
¦, such that
d(p
SS
wD
(t
DA
) −p
SL
wD
(t
DA
))
dt
DA
= 0.
Carrying out the derivation we find the transition time, t
DA
= 1/(4π), which can be transferred
to real time by using the definition of dimenisonless time.
11.5.2 Recognition of Semi Logarithmic Data
Appropriate plotting of the well test data is an important tool in the process of differentiating
the different reservoir production periods.
In a linear-linear plot as shown in Fig. 11.9, we can identify the semi logarithmic data,
following a non linear time development. For real data, such identification could be rather
difficult to perform and therefore of less practical importance.
The purpose of plotting data is partly to be able to identify the different production periods,
but equally important, to facilitate quantitative data analysis. This analysis is mainly performed
by plotting the interesting data linearly, i.e. data plotted as a straight line. This technique is
shown in Fig. 11.10 where we have plotted the semi logarithmic data as shown in Fig. 11.9, in
a linear-log plot. The semi logarithmic data is plotted as a straight line and from the slope of
this line, we can get important reservoir information.
190 Chapter 11. Well Test Analysis
p
wD
p
wD
SL
p
wD
SS
p
wD
WS
t
DA
1/4π
Figure 11.9: Linear-linear plot of well test data..
p
wD
p
wD
SL
p
wD
SS
p
wD
WS
log(t )
DA
1/4π
Figure 11.10: Linear-log plot of well test data.
11.6 Exercises
1. Claculate the dimensionless time t
D
for the following cases,
a) with data:
φ = 0.15 r = 10cm
µ = 0.3cp t = 10s
c = 15 10
−5
atm
−1
k = 0.1D
b) with data: φ, µ and c as above and
r = 10cm t = 1000s k = 0.01D
2. Find the exponential intergrals and pressure drops for the following cases,
a) with data:
φ = 0.12 r = 10cm
µ = 0.7cp t = 1s
c = 10 10
−5
atm
−1
k = 0.05D
h = 2400cm q = 10000cm
3
/s
11.6 Exercises 191
b) with data: φ, µ, c and h as above and
r = 30000cm t = 24h
3. In a reservoir at initial pressure, a well with a flow rate of 400 STB/D is shut-in. The
reservoir is characterised by the following parameters:
k= 50 mD φ = 0.3 c= 10 10
−6
psi
−1
h= 30 ft µ = 3.0 cp B
o
= 1.25 RB/STB
r
w
= 0.5 ft
a) At what time, after the shut-in, will the approximationEi(−x) =−ln(xe
γ
) be valid
? (Eulers constant γ=0.5772.
b) What is the pressure draw-down in the well after 3 hours of production?
c) For how long must the well produce, at constant flow rate, until a pressure drop of
1 psi is observed in a neighbouring well 2000 f t away?
4. Use the diffusivity equation,
3

i=1
d
dx
i

ρ
dp
dx
i

=
φµ
k

dt
,
and the expression for the compressibility at constant temperature,
c =
1
ρ

dp
,
to derive the diffusivity equation for one phase liquid flow. (Assume the liquid com-
pressibility to be small and constant for the pressures in mind.) Show that:
3

i=1
d
2
p
dx
2
i
=
φµc
k
dp
dt
.
5. For a reservoir at initial pressure with 3 wells (W1, W2 and W3) where W1 is an obser-
vation well, the following data is given:
P
i
= 4483 psia B
o
= 1.15 RB/STB h=30 ft
k
o
= 7.5 mD S
o
= 0.80 c
o
= 8.0 10
−6
psi
−1
µ
o
= 1.15 cp S
w
= 0.20 c
w
= 3.0 10
−6
psi
−1
c
f
= 4.0 10
−6
psi
−1
r
w
= 0.276 ft
Use the total compressibility c
t
= S
o
c
o
+S
w
c
w
+c
f
in the calculations.
A pressure drop of 4439 psi is observed in well W1 after 1600 hours of production at a
constant flow rate of 190 STB/D from well W2 and after 1550 hours of production of 80
STB/D from W3. Well W2 is located 2000 f t north of W1 and W3 is 1900 f t west of
W1.
Estimate the average reservoir porosity between the wells.
192 Chapter 11. Well Test Analysis
Answers to questions:
1. a) 1481, b) 14815, 2. a) 4.895, b) 0.62, 3. a) 15.4 s, b) 51.3 bar, c) 227 hr, 5. 0.175
Chapter 12
Methods of Well Testing
12.1 Pressure Tests
Well testing has become a widely used tool for reservoir characterisation and parameter identi-
fication. The development of well testing has accelerated from rudimentary productivity tests
into a powerful technique which is strengthening the understanding of complex reservoir char-
acteristics. Analysis of pressure trends enables us to evaluate several important reservoir pa-
rameters and to appraise the drainage zone.
Pressure tests are classified in accordance with their operation.
• Pressure drawdown test (Fig. 12.1,upper left): The well is opened to flow at a constant
rate causing pressure drawdown.
• Pressure build-up test (Fig. 12.1,upper right): Production of constant flow rate well is
shut-in, causing pressure build-up.
• Falloff test (Fig. 12.1,lower left): Injecting at constant rate and injection well shut-in,
causing pressure falloff.
• Multiple rate (Fig. 12.1,lower right): Well tested at different flow rates, each lasting until
the flowing pressure stabilises. This is followed by a shut-in period, which again lasts
until the pressure stabilises.
Drawdown and build-up tests are the two most common types of well tests and the selection
of which one to use depends on the practical field requirements.
A drawdown test simply involves flow rate measurements and pressure decline in a flowing
well. In a conventional drawdown test, the well is first shut-in until wellbore pressures stabilise,
and then opened and produced at a steady rate while the pressure decrease within the well bore
is monitored.
Unfortunately, flowrates are still measured at the surface in most well tests. Such flowrates
do not reflect the true downhole conditions as they are considerably affected by wellbore stor-
age, fluid segregation and gas liberation. This poses a problem as well testing theory requires
downhole flow rates.
Build-up tests are basically the opposite of drawdown tests. Instead of measuring pressures
in a flowing well, as in drawdown testing, the well is shut-in and the increase or build-up in
193
194 Chapter 12. Methods of Well Testing
q
t
t
0
0
p
q
t
t
0
0
p
q
t
t
0
0
p
q
t
t
0
0
p
Figure 12.1: Methods of well testing.
pressure is monitored. Nevertheless, as with drawdown tests, build-up tests are still affected
by wellbore storage effects during the initial stages or "early time"-part of the test. Therefore
pressure readings taken from the beginning of the test has to be ignored and all analysis is done
on the later part of the pressure response, even though it has been realised that this discarded
early time data contains a considerable amount of information.
In practice, it is not so easy to carry out a "pure" drawdown or build-up test as the produc-
tion schedule prior to the test, is usually complex. For example, a Drill-Stem Test (DST) is per-
formed by carrying out a series of build-up and drawdown tests in relatively quick succession.
The observed pressure build-up/drawdown response, within a given time, incorporates all the
pressure transient effects caused by every previous step-change in production rate. However,
multiple rate tests are not as simple as it might appear, while it relies on additional reservoir in-
formation as well as complex interpretation of pressure data using analysis based on theoretical
models.
12.2 Pressure Drawdown Test
Drawdown test analysis are done by direct application of the wellbore pressure solutions, pre-
sented in the previous chapter.
12.2 Pressure Drawdown Test 195
A plot of pressure versus the log of time (p, log(t)), will show the radial flow solution as a
straight line, see Fig. 12.2. This fact provides us with an easy and seemingly precise graphical
procedure for interpretation of the pressure data. The slope and intercept of the portion of the
curve forming a straight line is used for permeability and skin factor calculations.
The early portion of the data is unfortunately, distorted by wellbore storage and skin effects
as indicated in Fig. 12.2. Well tests have therefore to be made long enough to overcome both
effects and to produce a straight line in a semi logaritmic plot.
But even this approach presents drawbacks. Sometimes more than one "apparent" straight
line appears and analysis finds it difficult to decide which one to use. An alternative straight
line could be the signature of a fault located near the well.
The latter portion of the pressure transient is affected by the interference from other wells
or by boundary effects such as those that occur when the pressure response reaches the edge of
the reservoir.
12.2.1 Pressure Drawdown Test Under Semi Logarithmic Conditions
From the previous chapter in section "Wellbore pressure solutions", we may formulate the semi
logarithmic pressure solutions inSI-units and Field-units as:
SI-units:
p
w
= p
i
−2.1208
qBµ
kh
(logt +log
k
φµcr
2
w
−2.0923+
S
1.151
). (12.1)
Field-units:
p
w
= p
i
−162.6
qBµ
kh
(logt +log
k
φµcr
2
w
−3.2275+
S
1.151
). (12.2)
p
,

k
P
a
t, hrs
10 10 10 10 10 10
-3 -2 -1 0 1 2
Wellbore storage
effect
Outer boundary
effect
Slope m
Figure 12.2: Semi-logarithmic plot of pressure drawdown test data.
196 Chapter 12. Methods of Well Testing
In Fig. 12.2 we recognise the semi logarithmic data, as the data points being plotted on
a straight line, where m is the slope of the straight line. If we define the slope as a positive
number,
m =
(p
i
−p
w
(t
1
)) −(p
i
−p
w
(t
2
))
log(t
1
) −log(t
2
)
> 0,
we may use Eqs. (12.1) or (12.2), to define the reservoir permeability, k. The known m-value
yields a permeability value.
SI-units: Field-units:
k =
2.1208qBµ
mh
[µm
2
], k =
162.6qBµ
mh
[mD].
The skin factor S is conventionally identified from the same plot, see Fig. 12.2. The linear
pressure at time t = 1 hr is used in Eqs. (12.1) or (12.2) and the skin is directly calculated.
(Note that p
w
(1hr) in the equations below, is a data point on the straight line which needs not
necessarily correspond to an observed pressure.)
SI-units:
S = 1.151
¸
p
i
−p
w
(1hr)
m
−log
k
φµcr
2
w
+2.0923

.
Field-units:
S = 1.151
¸
p
i
−p
w
(1hr)
m
−log
k
φµcr
2
w
+3.2275

.
12.2.2 Pressure Drawdown Test Under Semi Steady State Conditions
When the pressure transient is affected by the interference from boundary effects or other
wells, the pressure curve deviates downwards from the straight line behaviour. Sometimes
such disturbances overlap with other kinds of "early time" effects like large scale reservoir
inhomogeneity, neighbouring sealing faults or other pressure disturbing zones. These effects
can completely mask the all-important pressure response such that proper pressure analysis
becomes impossible.
Under semi steady state test conditions we are investigating a sealed-off reservoir, where
the well is producing from its own drained area. At these late times in the development of
the well test procedure we may likely observe complicated pressure data which is masked
by several effects. Semi steady state tests are therefore normally not preferred when typical
reservoir parameters like permeability, productivity and skin are estimated. The analysis of
semi steady state data is more rigorous than might possible be interpreted by the wellbore
pressure equation.
The semi steady state equation is written,
p
w
(t) = p
i

qBµ
2πkh

2πkt
φcµA
+
1
2
ln
4A
e
γ
C
A
r
2
w
+S

, (12.3)
12.3 Pressure Build-Up Test 197
where the pressure is a linear function of time.
Semi steady state data is plotted as a straight line in a line-line plot, as seen in Fig. 12.3.
The asymptotic pressure value p
0
= p
w
(t = 0), in the figure, enables us to define the Dietz
shape factor C
A
. In Field Units, Eq. (12.3) can re-written,
p
0
= p
i

162.6qBµ
kh

log
4A
e
γ
r
2
w
−logC
A
+
S
1.151

. (12.4)
t, hrs
0
p
w
f
,
p
s
i
p
o
Figure 12.3: Semi steady state analysis of pressure drawdown data.
12.3 Pressure Build-Up Test
In analysing drawdown data, we could directly apply the "Wellbore pressure solutions" from
the previous chapter, since pressure is decreasing with time, at constant wellbore rate. In the
case of pressure build-up, when the well is closed, the "Wellbore pressure solutions" may not be
used directly. Fortunately, the same equations can be applied since the process, the bottomhole
pressure drawdown is, in principle, similar too the process of pressure build-up.
Normally, the build-up pressure data is considered to be more reliable than the pressure
drawdown data, since the influence fromdynamical effects near the well is of lesser importance.
If a well is shut-in at a certain time t, the no-flow conditions, as shown in Fig. 12.4, can be
described by a superposition technique.
As a theoretical assumption we may consider the wellbore rate to be both positive,
+q and negative, −q, as indicated in Fig. 12.4. The no-flow condition is obtained
when the positive and negative well rate are summed, i.e. (+q) +(−q) = 0. Con-
sequently, the no-flow condition can be described by adding the pressure solutions
for the positive flow rate and the pressure solution for the negative flow rate, using
the "Wellbore pressure solutions" (drawdown pressure analysis).
The technique of superposition is depicted in Fig. 12.5. At timet when the well is shut-in,
the wellbore pressure is influenced by the continuos production at positive rate+q causing
the pressure to decrease. The influence by the negative rate −q is to increase the wellbore
pressure. For times greater than t, we will observe a combined pressure development caused
198 Chapter 12. Methods of Well Testing
q
q = 0
+q
-q
time
∆t t
0
Figure 12.4: Pressure build-up test. Representation of a non-flowing
well performance by a superposition technique.
by a decreasing pressure due to the positive well rate (−q) and a increasing pressure due to the
negative well rate (−q).
p
i
p ( t)
w

p (t+ t)
w

0
0
t t+∆t
∆t ∆t
∆t
∆t
t
A
A"
B
B"
Figure 12.5: Pressure formation by superposition in build-up tests.
Using wellbore pressure, we define,
p
w
(∆t): Pressure in the well after shut-in.
p
w
(t +∆t): Pressure in the well given by continuos production at
positive well rate.
p
i
−p
w
(∆t): Pressure in the well given by start-up of continuos
production at negative well rate (increasing pressure contribution).
12.4 Pressure Test Analysis 199
The superposition principle gives,
p
w
(∆t) = p
w
(t +∆t) + p
i
−p
w
(∆t),
where p
w
on the left side of the equallity is the well shut-in pressure, whilep
w
on the right side
is the well flow pressure. Using dimensionless pressures, the well shut-in pressure is given,
p
i
−p
w
(∆t) =
qBµ
2πhk
[p
wD
(t
D
+∆t
D
) −p
wD
(∆t
D
)].
If skin is included and the wellbore pressure at shut-in is p
w
(∆t
D
= 0) = p
ws
, we have
p
i
−p
ws
=
qBµ
2πhk
[p
wD
(t
D
) +S].
From the above equations, we may derive the following expressions for the wellbore pres-
sure.
p
w
(∆t) = p
i

qBµ
2πhk
[p
wD
(t
D
+∆t
D
) −p
wD
(∆t
D
)], (12.5)
p
w
(∆t) = p
ws
+
qBµ
2πhk
[p
wD
(t
D
) −p
wD
(t
D
+∆t
D
) + p
wD
(∆t
D
) +S], (12.6)
p
w
(∆t) = p−
qBµ
2πhk
[p
wD
(t
D
+∆t
D
) −p
wD
(∆t
D
) −2πt
DA
]. (12.7)
Pressure build-up data is analysed using the three equations above, where Eq. (12.6) is
applied to estimate the reservoir permeability and skin, while Eq. (12.7) is used to determine
the average pressure p. Eq. (12.7) is derived on the basis of average pressure development,
where
p
i
−p =
qB
c
t
V
t =
qBµ
2πhk
2πt
DA
, t
DA
=
k
φAcµ
t.
It is important to notice that the dimensionless pressures p
D
in Eqs. (12.5) to (12.7) could
represent the equations describing both semi logarithmic period as well as semi steady state
period, i.e. depending on the analysis to be performed, we may chose which set of equations
we think will fit the data best.
12.4 Pressure Test Analysis
Based on Eqs. (12.5) to (12.7), we may perform different analysis, where certain assumptions
are made about the nature of pressure test data. In the following, two examples are give on how
pressure build-up data might be analysed.
12.4.1 Miller - Dyes - Hutchinson (MDH) Analysis
In this analysis [43] we will assume that the semi logarithmic period is long enough to recognise
a straight line behaviour in a semi logarithmic plot, i.e. we need to be able to differentiate
between the three different periods, described in the previous chapter.
200 Chapter 12. Methods of Well Testing
p
i
p(t+ t)~ p(t) ∆
t t+∆t
Figure 12.6: Pressure approximation in MDH-analysis.
Shortly after the well is shut-in, at timet, we start to monitor the wellbore pressure p
w
(∆t).
For some period of time we may assumet ∆t and during this period the dimensional pressure
approximation p
wD
(t
D
+∆t
D
) · p
wD
(t
D
) is valid, as depicted in Fig. 12.6.
Combining Eq. (12.6) and the above assumption, gives the wellbore pressure
p
w
(∆t) = p
ws
+
qBµ
2πhk
[p
wD
(∆t
D
) +S]. (12.8)
If the pressure development is assumed to have reached the semi logarithmic state, after
shut-in of the well, we may write: p
wD
(∆t) = p
SL
wD
(∆t
D
), with reference to the definitions of
semi logarithmic solutions in the previous chapter.
Using the definitions of dimensionless time and pressure for semi logarithmic data, we get
the following pressure expression,
p
w
(∆t) = p
ws
+m
¸
log∆t +log
k
φµcr
2
w
−2.0923+
S
1.151

,
where m is the slope of the linearized semi logarithmic data (see Fig. 12.7) and the number
2.0923 is a conversion factor to SI-units.
SI-units or Field units depends on preference and the following definitions.
SI-units: m =
2.1208qBµ
hk
and −2.0923
Field units: m =
162.6qBµ
hk
and −3.2275
From Eq. (12.8), we find the skin factor by direct substitution, see also Fig. 12.7,
S = 1.151
¸
p
w
(∆t = 1hr) −p
ws
m
−log
k
φµcr
2
w
+2.0923

.
The average reservoir pressure p, could be evaluated on the basis of Eq. (12.7), using the
same approximation as above, namely; p
wD
(t
D
+∆t
D
) · p
wD
(t
D
).
p
w
(∆t) = p−
m
1.151
[p
wD
(t
D
) −p
wD
(∆t
D
) −2πt
DA
].
12.4 Pressure Test Analysis 201
p
w
p
w
( =1hr) ∆t
0.1 1 10 100
∆t
∆t =
φ µ c A
k C 0.0036
A
p
Figure 12.7: MDH analysis of semi logarithmic pressure data.
We shall now assume that the reservoir had reached its semi steady state period before or
shortly after the well was shut-in. The interpretation of the different dimensionless pressures
are accordingly,
p
wD
(t
D
) = p
SS
wD
(t
D
) and p
wD
(∆t
D
) = p
SL
wD
(∆t
D
),
and the wellbore pressure is the written,
p
w
(∆t) = p−
m
1.151
[p
SS
wD
(t
D
) −p
SL
wD
(∆t
D
) −2πt
DA
],
= p−
m
1.151
¸
2πt
DA
+
1
2
ln
4A
e
γ
C
A
r
2
w

1
2
ln
4∆t
D
e
γ
−2πt
DA

,
= p−
m
1.151
¸
1
2
ln
A
C
A
r
2
w
∆t
D

.
Using SI-units we get,
p
w
(∆t) = p−
m
1.151
¸
1
2
ln
φµcA
0.0036kC
A
∆t

.
If the reservoir has reached its semi steady state period before (or shortly after) the well
was shut-in, the average reservoir pressure p is found by following the semi logarithmic line to
the time ∆t = φµcA/(0.0036kC
A
), as shown in Fig. 12.7, where the average pressure is,
p = p
w

∆t =
φµcA
0.0036kC
A

.
12.4.2 Matthews - Brons - Hazebroek (MBH) Analysis (Horner plot)
Following the same approach as in the above section, we have assumed the pressure difference
p
wD
(t
D
+∆t
D
) −p
wD
(t
D
) to be small but finite, i.e.,
202 Chapter 12. Methods of Well Testing
p
wD
(t
D
+∆t
D
) −p
wD
(t
D
) =
1
2
ln
t +∆t
t
. (12.9)
In practical terms, compared to MDH - analysis, this means that the well could be closed
somewhat earlier in the MBH - analysis [36]. The pressure difference is depicted in Fig. 12.8,
which points out that the time of shut-in t
D
, may come earlier and further up on the pressure
decline curve. In Fig. 12.8 we have p
w
(t) ≥ p
w
(t +∆t), while for dimension less pressures
p
wD
(t
D
+∆t
D
) ≥ p
wD
(t
D
), since p
wD
∝ (p
i
−p
w
).
p
i
p(t+ t) ∆
p(t)
t t+∆t
Figure 12.8: Wellbore pressure difference at the shut-in time, in
MBH - analysis.
Combining the approximation given by Eq. (12.9) and the wellbore pressure solution Eq. (12.6),
we get
p
w
(∆t) = p
ws
+
m
1.151
¸

1
2
ln
t +∆t
t
+ p
wD
(∆t
D
) +S

, (12.10)
where p
wD
(∆t
D
) = p
SL
wD
(∆t
D
), is considered to be in the semi logarithmic period.
Using SI-units this gives,
p
w
(∆t) = p
ws
+m
¸
−log
t +∆t
t
+log∆t +log
k
φµcr
2
w
−2.0923+
S
1.151

,
= p
ws
+m
¸
log
∆t
t +∆t
+logt +log
k
φµcr
2
w
−2.0923+
S
1.151

. (12.11)
Permeability and skin are estimated by plotting the build-up pressures p
w
(∆t) against the
time function ∆t/(t +∆t) on a semi logarithmic plot, as indicated by Eq. (12.11). The slope of
the linear data is m and hence k or kh are found by substitution. The skin is calculated at the
time ∆t = 1, where t +1 ·t is assumed, i.e.,
S = 1.151
¸
p
w
(∆t = 1hr) −p
ws
m
−log
k
φµcr
2
w
+2.0923

.
The pressure p
w
(∆t = 1) is read directly from the plot, as shown in Fig. 12.9.
12.4 Pressure Test Analysis 203
p
w
p
w
( =1) ∆t
1
10
-2
10
-3
10
-4
10
-1
p


t
t+ t


t
t+ t
1
C t
A DA
=
p
i
Figure 12.9: Horner plot. Wellbore pressure data plotted for MBH -
analysis.
The pressure approximation Eq. (12.9) may be applied in a similar way as done above, for
defining the average reservoir pressure p. Substituting Eq. (12.9) in Eq. (12.7), we get
p
w
(∆t) = p−
m
1.151
¸
1
2
ln
t +∆t
t
+−p
wD
(∆t
D
) −2πt
DA

,
= p−
m
1.151
¸
1
2
ln
t +∆t
t
+ p
wD
(t
D
) −
1
2
(ln∆t
D
+0.80907) −2πt
DA

,
= p−
m
1.151
¸
1
2
ln
t +∆t
∆t
+ p
wD
(t
D
) −
1
2
(lnt
D
+0.80907) −2πt
DA

,
= p−
m
1.151
¸
1
2
ln
t +∆t
∆t
+ p
wD
(t
D
) −p
SL
wD
(t
D
) −2πt
DA

. (12.12)
If we then assume that the well is in its semi steady state at the time of shut-in, i.e.
p
wD
(t
D
) = p
SS
wD
(t
D
), the we get
p
w
(∆t) = p−
m
1.151
¸
1
2
ln
t +∆t
∆t

1
2
ln
4t
D
e
γ
+2πt
DA
+
1
2
ln
4A
e
γ
C
A
r
2
w
−2πt
DA

,
= p−m
¸
log

t +∆t
∆t
A
C
A
r
2
w
1
t
D

. (12.13)
Since t
D
in Eq. (12.13) is a well defined time (time of shut-in), we may estimate the average
reservoir pressure as the pressure on the straight line (see Fig. 12.9) at the time,
∆t
t +∆t
=
A
C
A
r
2
w
t
D
=
1
C
A
t
DA
.
If we now assume that the well is in its semi logarithmic state at the time of shut-in, i.e.
p
wD
(t
D
) = p
SL
wD
(t
D
), we then get by substitution into Eq. (12.12),
204 Chapter 12. Methods of Well Testing
p
w
(∆t) = p
m
1.151
¸
1
2
ln
t +∆t
∆t
−2πt
DA

At the time ∆t/(t +∆t) = 1, we get
p
w

∆t
t +∆t
= 1

= p+
m
1.151
[2πt
DA
],
= p
qBµ
2πhk
¸

kt
φAcµ

,
= p+
qBt
Vc
, where V = φAh (12.14)
Under semi steady state conditions we have seen that,
p
i
−p =
qBt
Vc
,
and consequently we may write,
p
w

∆t
t +∆t
= 1

= p+(p
i
−p) = p
i
.
The initial reservoir pressure is defined in Fig. 12.9 on the straight line at time∆t/(t +∆t) =
1.
12.5 Exercises 205
12.5 Exercises
1. A well is tested by exploiting it at a constant rate of 1500 STB/d for a period of 100
hours. It is suspected, from seismic and geological evidence, that the well is draining
an isolated reservoir block which has approximately a 2:1 rectangular geometrical shape
and the extended drawdown test is intended to confirm this. The reservoir data and the
flowing bottom hole pressures recorded during the test are detailed below.
h = 20 f t c = 15 10
−6
psi
−1
r
w
= 0.33 f t µ
o
= 1cp
φ = 0.18 B
o
= 1.20RB/STB
Time p
w
Time p
w
Time p
w
(hours) (psi) (hours) (psi) (hours) (psi)
0 3500 (p
i
) 7.5 2848 50 2597
1 2917 10 2830 60 2545
2 2900 15 2794 70 2495
3 2888 20 2762 80 2443
4 2879 30 2703 90 2392
5 2869 40 2650 100 2341
a) Calculate the effective permeability and skin factor of the well.
b) Make an estimate of the area being drained by the well and the Dietz shape factor.
(after L.P.Dake)
2. A discovery well is produced for a period of approximately 100 hours proir to closure
for an initial pressure buildup survey. The production data and estimated reservoir and
fluid properties are listed below.
q = 123STB/d φ = 0.2
N
p
= 500STB µ = 1cp
h = 20 f t B
oi
= 1.22RB/STB
r
w
= 0.3 f t c = 20 10
−6
psi
−1
(c
o
S
o
+c
w
S
w
+c
f
)
A = 300acers
Time p
w
Time p
w
Time p
w
(hours) (psi) (hours) (psi) (hours) (psi)
0.0 4506 1.5 4750 4.0 4766
0.5 4675 2.0 4757 6.0 4770
0.66 4705 2.5 4761 8.0 4773
1.0 4733 3.0 4763 10.0 4775
a) What is the initial reservoir pressure?
b) If the well is completed across the entire formation thickness, calculated the effec-
tive permeability.
206 Chapter 12. Methods of Well Testing
c) Calculate the value of the mechanical skin factor.
d) What is the additional pressure drop in the wellbore due to the skin?
e) If it is initially assumed that the well is draining from the centre of a circle, is it
valid to equate p
i
to the asymptotic value log(t +∆t)/(∆t) = 0?
(after L.P.Dake)
3. A reservoir has 3 wells; W1, W2 and W3. Well W1 has been producing at a constant
flow rate of 120 STB/D for 70 hours and is then converted to an observation well. Well
W2, located 2500 f t straight north of well W1, is producing at a flow rate of 190 STB/D.
Well W3, located 1900 f t west of W1, is producing at a rate of 80 STB/D. At the time
when well W1 was shut-down, well W2 had produced for 100 hours and well W3 for 50
hours.
Pressure data from well W1 is given in the table:
∆t [hours] 0 5 10 20 30 40 50 100 150
P
ws
[psia] 4213 4380 4413 4433 4443 4450 4455 4466 4472
∆t 200 250 300 400 500 800 1200 1500 –
P
ws
4473 4474 4478 4480 4470 4461 4448 4439 –
Additional reservoir data:
µ
o
= 0.8 cp B
o
= 1.15 RB/STB c
f
= 4.0 10
−6
psi
−1
S
o
= 0.80 S
w
= 0.20 c
o
= 8.0 10
−6
psi
−1
h = 30 ft r
w
= 0.276 ft c
w
= 3.0 10
−6
psi
−1
Assume that the pressure development in well W1 can be expressed by the formula
below:
P
ws
= P
i
−162.6
Q
1
µB
kh
log

t
1
+∆t
∆t

−70.6
Q
1
µB
kh
¸
Q
2
Q
1
Ei(x
1
) +
Q
3
Q
1
Ei(x
2
)

where
x
1
=
φµc
t
d
2
12
0.00105kt
2
x
2
=
φµc
t
d
2
13
0.00105kt
3
and where d
12
and d
13
is the distance between W1 and W2 and W1 and W3, respectively.
t
1
is the time of production for well W1.
a) Calculate the average reservoir compressibilityc
t
.
b) Estimate the initial pressure P
i
, assuming the interference between well W2 and
W3 is negligible for early pressure data.
c) Calculate the average reservoir oil permeability ,k
o
.
d) Calculate the mechanical skin, S.
e) Use the pressure observation form∆t = 1500 hours to find the average reservoir
porosity between the wells.
12.5 Exercises 207
4. An oil well has been producing 1484 STB at a flow rate of 124 STB/D, when it was shut
down. The pressure build-up data is given in the table below:
∆t [hours] 4 8 12 16 20 24
P
ws
[psia] 2857 3027 3144 3252 3283 3298
∆t 28 32 36 40 44 48
P
ws
3308 3315 3323 3331 3338 3342
Additional reservoir data:
µ = 3.2 cp B
o
= 1.21 RB/STB
h = 8.4 ft c
t
= 12 10
−6
psia
−1
φ = 0.02
a) Find the reservoir pressure at the outer boundary, P
e
.
b) Calculate the average reservoir oil permeability, k
o
.
Answers to questions:
1. a) 240 mD, b) 4.5, 2. a) 4800 psi, b) 50 mD, c) 6.0, d) 128 psi, 3. a) 11 10
−6
psi
−1
, b) 4485
psi, c) 7.6 mD, d) -3.5, e) 0.135, 4. a) 3475 psi, b)58 mD.
208 Chapter 12. Methods of Well Testing
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4.3 4.4

4.5 4.6 4.7 5

Idealised Porous Medium Represented by Regular Cubic-Packed Spheres 47 4.2.3 Idealised Porous Medium Represented by Regular Orthorhombic-Packed spheres . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.2.4 Idealised Porous Medium Represented by Regular Rhombohedral-Packed spheres . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.2.5 Idealised Porous Medium Represented by Irregular-Packed Spheres with Different Radii . . . . . . . . . . . . . . . . . . . . . . . . . . . Porosity Distribution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Measurement of Porosity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.4.1 Full-Diameter Core Analysis . . . . . . . . . . . . . . . . . . . . . . . 4.4.2 Grain-Volume Measurements Based on Boyle’s Law . . . . . . . . . . 4.4.3 Bulk-Volume Measurements . . . . . . . . . . . . . . . . . . . . . . . 4.4.4 Pore-Volume Measurement . . . . . . . . . . . . . . . . . . . . . . . . 4.4.5 Fluid-Summation Method . . . . . . . . . . . . . . . . . . . . . . . . Uncertainty in Porosity Estimation . . . . . . . . . . . . . . . . . . . . . . . . Porosity Estimation from Well Logs . . . . . . . . . . . . . . . . . . . . . . . Exercises . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4.2.2

47 48 48 50 50 50 51 53 54 55 57 58 60 63 63 63 68 69 71 74 76 76 79

Permeability 5.1 Introduction . . . . . . . . . . . . . . . . . . . . . 5.2 Darcy’s Law . . . . . . . . . . . . . . . . . . . . . 5.3 Conditions for Liquid Permeability Measurements. 5.4 Units of Permeability . . . . . . . . . . . . . . . . 5.5 Gas Permeability Measurements . . . . . . . . . . 5.5.1 Turbulent Gas Flow in a Core Sample . . . 5.6 Factors Affecting Permeability Values . . . . . . . 5.6.1 The Klinkenberg Effect . . . . . . . . . . . 5.7 Exercises . . . . . . . . . . . . . . . . . . . . . . Wettability and Capillary Pressure 6.1 Introduction . . . . . . . . . . . . . . . . . . . . . 6.2 Surface and Interfacial Tension . . . . . . . . . . . 6.3 Rock Wettability . . . . . . . . . . . . . . . . . . 6.4 Contact Angle and Interfacial Tension . . . . . . . 6.5 Capillary Pressure . . . . . . . . . . . . . . . . . . 6.5.1 Capillary Pressure Across Curved Surfaces 6.5.2 Interfacial Tension . . . . . . . . . . . . . 6.5.3 Capillary Pressure in a Cylindrical Tube . . 6.6 Capillary Pressure and Fluid Saturation . . . . . . 6.7 Pore Size Distribution . . . . . . . . . . . . . . . . 6.8 Saturation Distribution in Reservoirs . . . . . . . . 6.9 Laboratory Measurements of Capillary Pressure . . 6.10 Drainage and Imbibition Processes. . . . . . . . . 6.10.1 Hysterisis in Contact Angle . . . . . . . . 6.10.2 Capillary Hysterisis . . . . . . . . . . . . . ii

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83 83 83 84 86 88 88 90 90 93 95 98 101 103 105 105

6.11 Exercises . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 107 7 Relative Permeability 7.1 Definitions . . . . . . . . . . . . . . . . . . . . . . . . . 7.2 Rock Wettability and Relative Permeabilities . . . . . . 7.3 Drainage/Imbibition Relative Permeability Curves . . . . 7.4 Residual Phase Saturations . . . . . . . . . . . . . . . . 7.5 Laboratory Determination of Relative Permeability Data 7.6 Exercises . . . . . . . . . . . . . . . . . . . . . . . . . 111 . 111 . 113 . 114 . 115 . 116 . 118 121 . 121 . 121 . 122 . 125 . 126 . 128 . 129 . 130 . 131 . 134 135 . 135 . 136 . 137 . 140 . 142 . 143 . 144 . 148 . 150

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8

Compressibility of Reservoir Rock and Fluids 8.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . 8.2 Compressibility of Solids, Liquids and Gases . . . . . . . 8.2.1 Rock Stresses and Compressibility . . . . . . . . . 8.2.2 Compressibility of Liquids . . . . . . . . . . . . . 8.2.3 Compressibility of Gases . . . . . . . . . . . . . . 8.3 Deformation of Porous Rock . . . . . . . . . . . . . . . . 8.3.1 Compressibility Measurements. . . . . . . . . . . 8.3.2 Betti’s Reciprocal Theorem of Elasticity. . . . . . 8.4 Compressibility for Reservoir Rock Saturated with Fluids . 8.5 Exercises . . . . . . . . . . . . . . . . . . . . . . . . . . Properties of Reservoir Fluids 9.1 Introduction . . . . . . . . . . . . . . . . . . . 9.2 Definitions . . . . . . . . . . . . . . . . . . . . 9.3 Representation of hydrocarbons . . . . . . . . 9.3.1 Ternary diagrams . . . . . . . . . . . . 9.4 Natural gas and gas condensate fields . . . . . 9.5 Oil fields . . . . . . . . . . . . . . . . . . . . . 9.6 Relation between reservoir and surface volumes 9.7 Determination of the basic PVT parameters . . 9.8 Exercises . . . . . . . . . . . . . . . . . . . .

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II Reservoir Parameter Estimation Methods
10 Material Balance Equation 10.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10.2 Dry gas expansion . . . . . . . . . . . . . . . . . . . . . . . . . . 10.3 A general oil reservoir . . . . . . . . . . . . . . . . . . . . . . . 10.3.1 A1: Expansion of oil . . . . . . . . . . . . . . . . . . . . 10.3.2 A2: Expansion of originally dissolved gas . . . . . . . . . 10.3.3 B: Expansion of gas cap gas . . . . . . . . . . . . . . . . 10.3.4 C: Reduction in HCPV due to expansion of connate water tion of pore volume . . . . . . . . . . . . . . . . . . . . . 10.3.5 Production terms . . . . . . . . . . . . . . . . . . . . . . 10.4 The material balance equation . . . . . . . . . . . . . . . . . . . iii

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10.5 10.6 10.7 10.8 10.9

Linearized material balance equation Dissolved gas expansion drive . . . Gas cap expansion drive . . . . . . Water influx . . . . . . . . . . . . . Exercises . . . . . . . . . . . . . .

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11 Well Test Analysis 173 11.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 173 11.1.1 Systems of Uunits Used in Well Test Analysis . . . . . . . . . . . . . . 174 11.2 Wellbore Storage Period . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 175 11.3 Semi Logarithmic Period . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 177 11.3.1 Diffusivity Equation . . . . . . . . . . . . . . . . . . . . . . . . . . . 177 11.3.2 Solution of the Diffusitivity Equation . . . . . . . . . . . . . . . . . . 178 11.3.3 Gas Reservoir . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 180 11.3.4 The Solution of the Diffusitivity Equation in Dimensionless Form . . . 181 11.3.5 Wellbore Pressure for Semi Logarithmic Data . . . . . . . . . . . . . . 181 11.4 Semi Steady State Period . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 184 11.4.1 Average Reservoir Pressure . . . . . . . . . . . . . . . . . . . . . . . 185 11.4.2 Well Skin Factor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 186 11.4.3 Wellbore Pressure at Semi Steady State . . . . . . . . . . . . . . . . . 187 11.5 Wellbore Pressure Solutions . . . . . . . . . . . . . . . . . . . . . . . . . . . 188 11.5.1 Transition Time Between Semi Logarithmic Period and Semi Steady State Period . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 189 11.5.2 Recognition of Semi Logarithmic Data . . . . . . . . . . . . . . . . . 189 11.6 Exercises . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 190 12 Methods of Well Testing 12.1 Pressure Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12.2 Pressure Drawdown Test . . . . . . . . . . . . . . . . . . . . . . . . 12.2.1 Pressure Drawdown Test Under Semi Logarithmic Conditions 12.2.2 Pressure Drawdown Test Under Semi Steady State Conditions 12.3 Pressure Build-Up Test . . . . . . . . . . . . . . . . . . . . . . . . . 12.4 Pressure Test Analysis . . . . . . . . . . . . . . . . . . . . . . . . . 12.4.1 Miller - Dyes - Hutchinson (MDH) Analysis . . . . . . . . . 12.4.2 Matthews - Brons - Hazebroek (MBH) Analysis (Horner plot) 12.5 Exercises . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 193 . 193 . 194 . 195 . 196 . 197 . 199 . 199 . 201 . 205

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iv

and related to two important methods in Reservoir Engineering. Chapter 4 introduces porosity and some examples of experimental techniques used to estimate porosity. namely Material Balance (Chapter 11) and Well Testing (Chapter 12. The two main parts of the book is related to petro-physics (Chapter 2 to 10). Permeability is introduced in Chapter 5. A short deduction of Darcy’s law is given and some examples of its use is described. The last part VProjects Exercises presents quite a few exercises of the type students are asked to solve at their examination test. Some laboratory techniques are explained and examples of equipment are shown.Preface The topics covered in this book represent a review of modern approaches and practical methods for analysing various problems related to reservoir engineering. This textbook. habitat and trapping of petroleum In Chapter 3 some basic concepts and definitions used in Reservoir Engineering are presented. This chapter contains some basic concepts and definitions related to the origin. Measurements of gas permeability is exemplified and together with laminar and turbulent gas flow. The subjects presented. 13 and 14). part I Fundamentals and part II Reservoir Parameter Estimation Methods. viscosity is introduced and some basic equations. The book contains a short introduction to important definitions for oil and gas reservoirs (Chapter 1). constitutes the main content of the book. Chapter 2 is a brief introduction to the basics of petroleum geology. with some illustrative examples relevant to the Norwegian Continental Shelf. Part III Fluid Flow in Porous Media and part IV Enhanced Oil Recovery are a collection of subjects extending the fundamental knowledge into areas of more advanced theoretical description. Classification and description of several methods used in enhanced oil recovery are associated with examples for oil and gas fields in the North Sea (Chapter 21 to 27) The Preface contains a list of some of the most commonly used parameters and systems of units used in petroleum engineering. are based on the course of lectures in Reservoir Engineering 1 held by the authors at the Rogaland University Centre in the period from 1989 to 1995. Modelling of fluid flow in porous media is presented through different examples using various mathematical techniques (Chapter 15 to 20). Some examples describing the method of error propagation are also given. describing laminar fluid flow are derived. 1 . A short description of reservoir pressure distribution is also presented. In Chapter 6. Examples of different viscosity measuring techniques are discusses and some flow characteristics are mentioned. In Chapter 1 some basic definitions of gas and oil reserves are given and the methods of their evaluation. some additional factors affecting permeability are discussed.

Most chapters in part I and II contain several exercises. such as gas-reservoir and oil. The equation is applied in several examples. The book does not cover all the relevant literature. Examples of two "classical" well test analysis is also included. to give a broad and consistent description of relative permeability in this book. while all exercises in part III and IV are added at the end. In part III and IV. some basic aspects of compressibility related to reservoir rock and fluids are introduced. A somewhat simplified derivation of the pressure solution for three important production periods are presented. though necessary. like drawdown test.. This book does not contain complicated mathematical equations or calculus. A basic mathematical description of EOR methods are given and various methods are classified. A reference list is given at the end of the book. Use of type curves and matching techniques are shortly presented. Volumefactors and other important relations are explained and examples of their use are given.reservoirs with and without a gas cap. Examples of polymer flooding is presented as well as EOR related to surfactants and different solvents. build-up test and combinations of the two. In this chapter we introduce the term surface energy to replace interfacial tension and an important relation between surface energies are derived. Various techniques using WAG. Part III Fluid Flow in Porous Media gives an introduction to mathematical modelling of oil displacement by water-flooding. Some few exercises are included at the end of this part. illustrating the concepts and methods presented. the wellbore storage period. like transient testing techniques. Chapter 10 lists some basic definitions and properties related to reservoir fluids. The Material Balance Equation is deduced in Chapter 11. as well as various analytical solution techniques. Examples are related to the behaviour of porous reservoir rocks and core samples under laboratory conditions.e. The student should know the elements of matrix and linear algebra. Basic principles behind equations of Buckley. The mathematical prerequisite required are minimal. In Chapter 9. foams and Microbial methods are also briefly described. however some slightly more advanced mathematical formalism is used.Leverett theory and their application are presented. There has been no attempt made. Well test analysis is introduced in Chapter 12. probability theory and statistics. i. Only some necessary references and key publications are included in the reference list. . Modern well test analysis. Enhanced Oil Recovery is presented in part IV. are presented. is presented in Chapter 14. The chapter is meant as an introduction to basic concepts of relative permeability and possibly an inspiration for further reading. Chapter 13 introduces some basic methods of well testing. Relative permeability is introduced briefly in Chapter 8. describing different types of reservoirs. Dimension-less parameters are used and the set of pressure solutions are presented.2 Wettability and capillary pressure are discussed in Chapter 7. Examples of the effect of capillary forces are given and different experimental techniques are discussed. and also be acquainted with single and partial-differential equations and methods of their solution. the semi-logaritmic period and the semi-steady state period. nor is the reference list intended to be a complete bibliography. This part presents a broad classification of models describing fluid flow in porous media.

-R. 1997 . Ursin & A. B. Zolotukhin Stavanger.3 J.

but there is a tendency to turn to SI-units or practical SI-units. In this book we will use both SI-units and industrial units in explaining the theory as well as in examples and in exercises. country or simply tradition.4 Units and conversion factors The basic knowledge of units and conversion factors is absolutely necessary in reservoir engineering. metric unit is found by multiplying a given industry unit by an appropriate conversion factor. although the choice of industrial units depend on company. it is important to be confident with both systems. Since the choice of units has been largely a question of preference. -simply due to practical reasons. The Metric unit is seen as a practical SI-unit. Metric unit = Conversion factor × Industry unit. . Since both set of units are widely used in the oil industry.e. often used in displaying data or calculations. A selection of some of the most frequently used parameters are listed in the table below. the knowledge of conversion factors is practical necessary. especially in the practice of the Norwegian and the other European oil companies. i. English and American units are most commonly used in the petroleum industry.

Pa−1 Density.1 1000 0.856 0.0 0.01 1. m2 Industry unit sq mile acre sq ft sq in.8 5/9 1.0 6.1450377 1000.02831685 0.448222 138.01846 141. psi−1 g/cm3 lbm/ft3 o API bbl/d ft3 /d lbf pdl dyne mile ft in.589988 4046. kg Temperature. K R Surface tension.489 0. m Pressure.4535924 + 273.48 2.5 Parameter (SI unit) Area.2550 0. N/m Viscosity. .5/(131.54 101. m3 /s Force.1589873 0.0 16.S. kg/m3 Flow rate.785412 1.4516 0.894757 1.09290304 6.2 (psi) mm Hg (0o C) dyne/cm2 ton lbm oC oF Conversion factor 2. Pa·s Volume. m3 dyne/cm cp (poise) acre-ft cu ft bbl U.5 + o API) 0.333224 0.15 (o F-32)/1.609344 30.1589873 3.02831685 4.0 Metric unit km2 m2 m2 cm2 kPa−1 kg/m3 kg/m3 (γsg )∗ m3 /d m3 /d N mN mN km cm cm kPa kPa kPa kPa Pa kg kg K oC Compressibility. gal liter K mN/m Pa·s m3 m3 m3 dm3 dm3 ∗ Spesific gravity of oil.001 1233. N Length.325 100. atm bar lbf/in. Pa Mass.

6 .

Current economic conditions include prices and costs prevailing at the time of the estimate.S.1 Terminology and Definitions In the period from 1936 to 1964. in 1946. In 1964. Unproved Reserves are based on geological and/or engineering data similar to those used in the estimates of proved reserves. and associated substances anticipated to be commercially recoverable from known accumulations from a given date forward. Fig. condensate. "Proved reserves of crude oil. which included categories ranging from proved to speculative reserves [2]. but when technical. Reserve estimates are based on geologic and/or engineering data available at the time of estimate. In 1979.Chapter 1 Oil and Gas Resources and Reserves 1. The relative degree of an estimated uncertainty is reflected by the categorisation of reserves as either "proved" or "unproved" Proved Reserves can be estimated with reasonable certainty to be recoverable under current economic conditions. the U. 1. and under current government regulations. by established operating practices. natural gas. where the following definitions are used [2]: Reserves are estimated volumes of crude oil.1 shows a conceptual scheme of the oil and gas resources and reserves. the Society of Petroleum Engineers (SPE) recommended reserve definitions following the revised API definitions. whereby also the SPE definitions were updated in 1981. They may be estimated assuming future economic conditions different from those prevailing at the time of the estimate. Security and Exchange Commission (SEC) issued a newer set of definitions. the American Petroleum Institute (API) set some guiding standards for the definition of proved reserves. economic or regulatory uncertainties preclude such reserves being classified as proved. under existing economic conditions. natural gas liquids. natural gas liquids and natural gas". contractual. the World Petroleum Congress issued a set of petroleum reserve definitions. They were presented in a joint publication of API and the American Gas Association (AGA). 7 . Reserves are considered proved is commercial producibility of the reservoir is supported by actual engineering tests. In 1983.

8 Chapter 1. Oil and Gas Resources and Reserves Total Oil and Gas Resource Discovered Undiscoveed Nonrecoverable Resources Recoverable Resources Reserves Cumulative Production Unproved Reserves Possible Reserves Proved Reserves Probable Reserves Figure 1. • Reserves in rock formations that appear to be hydrocarbon-bearing based on logs or cores. • Incremental reserves based on infill drilling are subject to technical uncertainty. see Fig. Possible Reserves are less certain than proved reserves and can be estimated with a low degree of certainty. based on geological and/or geophysical interpretation. or some special technique of enhanced oil recovery (EOR). Unproved reserves may further be classifiedprobable and possible. Probable Reserves are less certain than proved reserves and can be estimated with a degree of certainty sufficient to indicate they are more likely to be recovered than not. "possible" reserves may include: • Reserves suggested by structural and/or stratigraphic extrapolation beyond areas classified as probable.1. which may involve either a natural-drive mechanism improved by water or gas injection. but may not be productive at a commercial level. In general. The estimation of reserves will depend upon the actual mode of petroleum recovery. 1. insufficient to indicate whether they are more likely to be recovered than not.1: Conceptual scheme for oil and gas resources and reserves. .

one has to consider similarities of well spacing. The use of an analogue may be the only method available to estimate the reserves in a situation where there are no solid data on well performance or reservoir characteristics. temperature. into the interwell space by using an interpolation technique. However. 1.2. pay thickness and drive mechanism. which means the bulk thickness of the reservoir rocks (formation).2 Methods for Resources/Reserve Estimation 1. indicates a relatively low structurally position. 100. data "upscaling" for interwell space). lithofacies data. reservoir depth.) into a much larger scale ( i. simply because perfect analogues can seldom be found. • The reservoir "net" isopach map.g. The Net-to-Gross ratio (N/G) is an important parameter indicating the productive portion of the reservoir. All possible differences between the analogue reservoir and the reservoir in question need to be considered to make a realistic adjustment of the recovery estimates.000 bbl/well) and applying a similar or adjusted recovery factor to the wells in the reservoir considered. reservoir rock lithofacies.1. but appears to be separated from those areas by faults and the geological interpretation. In an analogue approach. rock and fluid properties. . which means the cumulative thickness of the permeable rock units only. an analogue-based approach is also the least accurate and little reliable method of petroleum reserve estimation. 1. pressure. well logs. The main parameters used for a volumetric estimate in this approach are: • The reservoir "gross" isopach map.e.2 Methods for Resources/Reserve Estimation 9 • Reserves attributable to an improved or enhanced recovery method when a pilot project is planned (but not in operation) and the rock. The unit-recovery approach refers to a recovery calculated in barrels per acre-foot or Mcf per acre-foot. etc. • Reserves in a rock formation that has proved to be productive in other areas of the field..2. The main difficulty in a volumetric estimate of resources/reserves is in the transfer of data obtained at a small scale (core analysis.1 Analogy-Based Approach Another producing reservoir with comparable characteristics can be used as a possible analogue for the reservoir under consideration. fluid and reservoir characteristics are such that a reasonable doubt exists whether the estimated reserves will be commercial. This can be done by determining an average oil or gas recovery per well in the analogue reservoir (e.2 Volumetric Estimates The methods of reserve estimation based on reservoir data are volumetric and can be divided into deterministic and probabilistic (stocastic) estimates. either by a direct well-to-well comparison or on a unitrecovery basis. Deterministic Methods The principle of a deterministic approach to resources/reserve estimates is to "upscale" the information derived from the wells and supported by seismic survey.

G i ∑i hi where ki is the local permeability (other symbols as above). so to speak. is an estimate of resources/reserves. ∑i Ai hi where φ is the local porosity. See Fig. • Volume-based average saturation of water. Ai is a subarea and hi is a subthickness (of permeable rock). and then simulates their actual density distribution in the whole reservoir.) all have random. ∑i φi Ai hi Plotting these parameters as contoured maps (isopachs. This numerical technique assumes that the main reservoir properties (porosity. isoporosity.2. 1. with different probabilities attached. possibly normal. Stochastic reservoir description is usually based on the procedure of random-number generator. isopermeability. • The permeability and net-thickness product (khN ) is important for the estimation of well production capacity: ∑ ki hi N (khN ) = hN i = ∑ ki hi . etc. . In practice. The cumulative frequency distributions of these estimates. it is necessary to repeat the stochastic simulation for different "seeds" (initial boundary values) in order to asses and quantify the actual variation of a given parameter. In common usage [8] we have: – An estimate with 90 % or higher probability is the level regarded as aproven value. where the probabilistic rather than deterministic. gas and oil. – An estimate with 50 % or higher probability is the level regarded as aproven + probable value. which takes more account of the estimate uncertainty. Oil and Gas Resources and Reserves • The reservoir rock porosity (as a volume-based weighed average): φ= ∑i φi Ai hi . with the range of values included by core and well-log data. N/G. that is used to asses their likelihood will be a very unclear formulation. Each numerical realisation bears an uncertainty for the reservoir characterisation. permeability. The maximum and minimum values are specified for each of the reservoir parameters and the random number generator then "drowns data". Different realisations lead to different volumetric estimates. Stochastic Methods An alternative approach is a probabilistic estimation of resources/reserves. ect.10 Chapter 1.) provides the crucial information on their variation and distribution in the reservoir and makes it possible to evaluate the reservoir pore volume and its fractions saturated with oil and gas (hydrocarbon volume). For example water saturation: Sw = ∑i Swi φi Ai hi . The numerical value of hydrocarbon resources/reserve estimate their represents an outcome of "integrated" map analysis. frequency distributions.

The lack or scarsity of data in such cases is compensated by a subjective assessment of the reservoir characteristics (i.3 Performance Analysis The methods of performance analysis presently used include: • Analysis based on Material Balance Equation (MBE) [33. the problem of certainty can be considered in terms of "fuzzy" [61]. 1. probabilistic and deterministic estimates based on the data available at a particular time.1. as seen in Fig. 34]. When the data available are abadundant. At the very early stages of field appraisal. hence. . Based on the knowledge from other reservoirs or simply a theoretical guess. As more information on the reservoir becomes available.2.e. A comparison of these estimates may be more revealing that each of them is in isolation. aprobabilistic estimate can be made. When more data have been collected and statistical analysis becomes possible. 45].4. the cumulative frequency graph may change its shape and the uncertainty of our resource/reserve estimates may decrease. see Fig.2 Methods for Resources/Reserve Estimation 11 1. The range in the possible values of the reservoir parameters would then be narrower.0 Min Value Max Min Value Max Figure 1. 1. A rectangular distribution means no preference and a triangular distribution means that strong preference distributions are used. 1. a fuzzy estimate of the resources/reserves may be best or only option [22. – An estimate with 10 % or higher probability is the level regarded as aproven +probable + possible value.3.0 Frequency of cumulative probability Frequency Probability. compared to a fuzzy assessment. the data are usually too limited for using statistical analysis and. More generally. that a given value of resources will be at least as great as shown 0. 28. subunit or layer) of the reservoir.specified value of a particular parameter for a particular part (zone.2: Example of stochastic volumetric estimate based on a series of random-number simulations. • Reservoir Simulation Models (RSM) [10. 56]. the shape of the distribution and the maximum and minimum values of a given reservoir parameter). a deterministic estimate can be made based on a well.

0 Late time depletion Min Value Max 0. cumulative oil production.0 Min Value Max 0. The MBE method is based on the data obtained from previous reservoir performance and PVT analysis. Oil and Gas Resources and Reserves Frequency of cumulative probability Frequency of cumulative probability 0.0 Delineation/ early production 1.0 Frequency of cumulative probability 1.0 Min Value Max Frequency of cumulative probability Frequency of cumulative probability 0. . The RSM method involves a numerical simulation technique. time.3: Changes in the uncertainty resources estimate with increasing data acquisition (after Archer and Wall.0 Min Value Max Figure 1. harmonic. but involves some assumptions for the reservoir driving mechanism in order to minimise the range of possible predictions from the dataset.12 Chapter 1. The following "decline curves" from production wells are commonly used in the DCA: – Production rate vs.0 Appraisal Max 0. The method is thus adjusted differently to reservoirs containing oil.0 Discovery 1. If successful.0 Pre-drilling 1. The discrepancy between the simulation results (prediction) and the available data is minimised by adjusting the reservoir parameters and taking into account the most likely reservoir drive mechanism (history match ). 1992). – Water cut vs. exponential. such a performance analysis allows to estimate both the reserves and the future performance of the reservoir.). The aim of all of these methods is to obtain the best reservoir performance prediction on the basis of available data. The DCA method is to predict future performance of the reservoir by matching the observed trend of the production decline with one or several standard mathematical methods of the production rate-time (hyperbolic. – Production rate vs. gas or oil with a gas cap (primary or secondary).0 Min Value Frequency of cumulative probability 1. • Decline Curve Analysis (DCA) [53].0 Min Value Max 0. with the matching of the production and the reservoir’s previous performance (history). ect.0 Mature production 1. cumulative oil production.

V Value Figure 1. probabilistic and deterministic approach (data set). 1. cumulative gas production.V V.4: The concept of uncertainty in resources/reserves estimation illustrated by fuzzy. – Percentage oil production vs. cumulative oil production. Some of these decline curves are shown in Fig.O. – The (p/z) ratio vs.0 V.0 Deterministic Frequency of cumulative probability Probabilistic Fuzzy 0.V M. cumulative production. – Gas-oil ratio vs.1.P. .L.2 Methods for Resources/Reserve Estimation 13 1.5.

5: Different ways of data representation for a decline curve analysis. Oil and Gas Resources and Reserves q q Np Np 0 Economic limit Cumulative oil producction 0 Economic limit Time 100 p (z ) Oil production.14 Chapter 1. . % Np Gp 0 Economic limit Cumulative oil producction 0 Economic limit G Cumulative oil producction Figure 1.

Part I Fundamentals 15 .

Chapter 2

Basic Concepts of Petroleum Geology
2.1 Introduction
Reservoir Engineering is a part of Petroleum Science that provides the technical basis for the recovery of petroleum fluids from subsurface sedimentary-rock reservoirs. The Fig. 2.1 below indicates the place and role of Reservoir Engineering in the broad field of Petroleum Science.
Reservoir characterization

Geology and Geophysics

Reserve estimates for well proposal evaluation

Reservoir correlation

Geochemical studies Reserve estimates, material balance calculations, fluid flow equations, reservoir simulation, pressure transient analysis, well test design and evaluation
Reservoir screening for improved recovery projects Improved recovery project design and maintenance

Reservoir Engineering

Production Engineering

Workover reserve analysis, well completion design, production facility design, production log interpretation, prediction of production schedules

Facilities Engineering

Design proposals for separation, treating, metering and pipeline facilities

Final facility design and operation

Figure 2.1: Reservoir engineering and petroleum science. This chapter pertains to the basic concepts of Petroleum Geology and covers the following 17

18

Chapter 2. Basic Concepts of Petroleum Geology

main topics: • The source rock of hydrocarbons. • The generation, maturation, migration and accumulation of hydrocarbons.

2.2 The Basic Concepts
Petroleum is a mineral substance composed of hydrocarbons and produced from the natural accumulations of organic matter of a faunal and/or floral provenance. Petroleum is a gaseous, liquid or semisolid substance, present in the pore space of porous rocks, referred to as reservoir rocks, which are mainly of sedimentary origin.

2.2.1 Clastic Sedimentary Rocks
Sedimentary rocks results from the deposition of sedimentary particles, known as clastic material or detritus (from the Latin "worn down"), consisting of mineral grains and rock fragments. Sedimentary particles are derived from weathered and fragmented older rocks, igneous, metamorphic or sedimentary, usually with some chemical changes. Sediment comprising loose mineral detritus or debris is referred to as clastic sediment (from the Greek word "klastos", meaning broken). Some clastic sediments consist of the accumulations of skeletal parts or shells of dead organisms, commonly fragmented, and are referred to as bioclastic rocks (see next section). The particles of clastic sediment may range widely in size, and the predominant grain-size fraction is the primary basis for classifying clastic sediments and clastic sedimentary rocks. As shown in Table 2.1 clastic sediments can be divided into 4 main classes: gravel, sand, silt, and clay [49], where mud is a mixture of clay and silt, possibly including also some very fine sand. The narrower the grain-size range of a given sediment, the better its "sorting". Both the grain size and sorting have direct implications for the sediment permeability to fluids. Table 2.1: Definition of grain-size and the terminology for sediments and sedimentary rocks.
Sediment grain-size fraction Boulder Cobble Pebble Granule Sand Silt Clay Clay & slit mixture

Grain-size limits in mm More than 256 64 to 256 4 to 64 2 to 4 1/16 to 2 1/256 to 1/16 Less than 1/256

Unconsolidated sediment Boulder gravel Cobble gravel Pebble gravel Granule grawel Sand Silt Clay Mud

Consolidated rock Boulder conglomerate ∗ Cobble conglomerate ∗ Pebble conglomerate ∗ Granule coglomerate ∗ Sandstone Siltstone Claystone (clayshale, if fissile) Mudstone (mudshale, if fissile)

The term "gravelstone" is preferred by some authors on semantic basis [51].

2.2 The Basic Concepts

19

2.2.2 Nonclastic Sedimentary Rocks
Chemical Deposits Some sedimentary rocks contain little or no clastic particles. Such a sediment, formed by the precipitation of minerals from solution in water, is a chemical sediment. It forms by means of either biochemical or purely chemical (inorganic) reactions [51]. The primary porosity of such rocks is practically zero, and their possible porosity is totally dependent on the development of secondary porosity, chiefly in the form of microfractures. Biogenic Deposits Sedimentary rocks commonly contain fossils, the remains of plants and animals that died and were buried and preserved in the sediment as it accumulated. A sediment composed mainly or entirely of fossil remains is called a biogenic sediment. If the fossil debris has not been homogenised by chemical processes, the deposit can be regarded as a bioclastic sediment [51]. Main nonclastic rocks are: limestone, dolomite, salt, gypsum, chert, and coal. Chalk is a special type of biogenic limestone, composed of the sheletal parts of pleagic coccolithophorid algea, called coccoliths. The main types of sedimentary rocks and their chemical compositions are shown in list below, containing main sedimentary rock types and their chemical composition of categories [37]. Sandstone a siliciclastic rock formed of sand, commonly quartzose or arhosic, cemented with silica, calcium carbonate, iron oxide or clay. Chemical composition: SiO2 . Density: ∼ 2.65 g/cm3 . Shale a fissile rock, commonly with a laminated structure, formed by consolidation of clay or mud ( mainly siliciclastic) Argillite (mud rock) – any compact sedimentary rock composed mainly of siliciclastic mud. Chemical composition: SiO2 . Dolomite a carbonate rock, consisting largely of the mineral dolomite (calcium magnesium carbonate) Chemical composition: CaMg(CO3 )2 . Density: ∼ 2.87 g/cm3 . Limestone a carbonate rock consisting wholly or mainly of the mineral calcite. Chemical composition: CaCO3 . Density: ∼ 2.71 g/cm3 . Calcarenite a sandstone composed of carbonate grains, typically a clastic variety of limestone. Chemical composition: CaCO3 . Density: ∼ 2.70 g/cm3 . Marl a friable rock consisting of calcium carbonate and siliciclastic mud/clay. Chemical composition: SiO2 +CaCO3 . Density: ∼ 2.68 g/cm3 . Salt (rock salt) – a chemical rock composed of the mineral halite. Chemical composition: NaCl.

This material. consisting about 80% of the world’s sedimentary rock volume. and grasses that contribute to most of the buried organic matter in mud rocks and shales. which remains solid. See Fig 2. . the most favoured one is that oil and gas are formed from marine phytoplankton (microscopic floating plants) and to a lesser degree from algae and foraminifera [51].3 . 2. a natural biogenic methane called marsh gas. Chemical composition: CaSO4 . which usually require temperatures greater than 60 C. Instead. bushes.3.3. evaporitic rock composed of the mineral anhydrite. Some of the typical reservoir rocks are shown in Fig. in the form of coal.2 2. during the early diagenesis.3 The Origin and Habitat of Petroleum 2. rather than petroleum. At temperatures much above 175oC. A temperature range between about 60oC and 175oC is most favourable for the generation of hydrocarbons. most of the kerogen will have lost its petroleum-generating capacity [49]. liquid or semisolid natural substances that consist mainly of hydrocarbons. the alteration process is limited to certain wax-like substances with large molecules. In terrestrial sedimentary basins. Kerogen can be converted into oil and gas by further burial by mining the shale and subjecting it to heat it in a retort. because it is capable of releasing large amounts of hydrocarbons in natural burial conditions. evaporitic rock composed of the mineral gypsum Chemical composition: CaSO4 2H2 O. Currently. waxes. The alteration of kerogen to petroleum is similar to other o thermal-cracking reactions. is called kerogen. Many hypotheses concerning the origin of petroleum have been advanced over the last years. When the formation rock temperature exceeds 225 C. Usually this is ashale or mudrock which itself is a very common rock type. Organic carbon-rich shale and mudrock are characteristically black or dark greyish in colour. it is plants such as trees.as illustrated by Fig. is generated through the action of microorganisms that live near the ground surface. the generation of liquid petroleum ceases and the foro mation of gas becomes dominant. In the ocean. the organic compounds are transformed (mainly by the geothermal heat) into petroleum. These large plants are rich in resins. and is commonly called the oil window. oil or natural gas are called the fossil fuels. which indicates a non-oxidised primary organic matter. A rock rich in primary organic matter is called a source rock. and lignins. and is the organic substance of so-called oil shales. defined as gaseous. Many organic carbon-rich marine and lake shales never reach the burial temperature level at which the original organic molecules are converted into hydrocarbons forming oil and natural gas. phytoplankton and bacteria are the principal of organic matter buried in sediment. which tend to remain solid and form coal.1 Source Rock and Generation of Petroleum Local large concentrations of organic matter in sedimentary rocks. At lower temperatures. Petroleum is generated when the kerogen is subjected to a sufficient high temperature in the process of the sediment burial. During this conversion. 2. Anhydrite a chemical.20 Chapter 2. Basic Concepts of Petroleum Geology Gypsum a chemical. Most of organic matter is trapped in clay mud that is slowly converted into shale under burial.

despite a common source rock. primary differences in the source composition may be reflected in the chemistry of the petroleum.2. Additional chemical changes may occur in the oil and gas even after these have been generated or accumulated.3 The Origin and Habitat of Petroleum 21 Figure 2.2: Typical reservoir rocks. for example. The long and complex chain of chemical reactions involved in the conversion of raw organic matter into crude petroleum is called maturation. . This explains. Likewise. why the petroleum taken from different oil fields has different properties.

The fact is that most of the world’s largest hydrocarbon fields are found in marine sedimentary rock successions representing ancient continental shelves. 2. .22 Chapter 2. • oil has the optical properties of hydrocarbons that are known only to derive from organic matter and • oil contains nitrogen and certain other compounds that are known to originate from living organic matter only. burial temperature.3: Generation of petroleum vs. °C Wet Gas Zone Dry Gas 225 Dry Gas Zone 315 Figure 2. Sampling of mud on the continental shelves and along the bases of continental slopes has shown that the shallowly buried mud contains up to 8% organic matter.4 shows the distribution of the world’s sedimentary basin and petroleum accumulations (from [51]). as geological strata). Many oil fields in various parts of the world are in ancient lacustrine deposits (formed at the bottom or along the shore of lakes. Similar or even higher total organic-carbon (TOC) content characterizes many ancient marine shales. Basic Concepts of Petroleum Geology Generation Intensity Immature Zone 60 Heavy Oil Zone 100 Light Biogenic Methane Oil Wet Gas 175 Temperature. However. Geologists conclude therefore that oil is originated primarily from the organic matter deposited in marine sediments. Two types of evidence support the hypothesis that petroleum is a product of the decomposition of natural organic matter [51]. Fig. some lake sediments may be just as oil-prone as marine source rocks. Oil source rocks are chiefly marine shales and mudrocks.

. and the depletion of the reservoir will make the aquifer expand into this space. Likewise.2. Once released from the source rock. Some "leaky" or limited-capacity traps may segregate oil and gas that have been generated together.3. Hydrocarbons are less dense than water.4: World’s main sedimentary basins and petroleum accumulations.Areas where major amounts of oil and gas have been found . or an impervious barrier. The water bearing part of the trap is called an aquifer.Areas of ocean deeper than 2000m underlain by thick accumulations of sedimentary rock Figure 2.3 The Origin and Habitat of Petroleum 23 Legend: . from a source rock which results in a primary gas cap above the oil in the reservoir. Both oil and gas are generated together. This means that any pressure change in the aquifer will also affect the reservoir. until they either escape at the ground surface. and is hydrolically connected with the reservoir. a secondary gas cap may develop when the reservoir pressure has decreased and the lightest hydrocarbon begin to bubble out from the oil. which means that gas and possibly also some oil may "leak" to yet higher lying traps or up to the ground surface. they thus tend to migrate upwards in the direction of the minimum pressure. in varying proportions. 2. Water generally underlines the hydrocarbons in a trap. called atrap. The part of the trap that contains hydrocarbons is called a petroleum reservoir. In a trap. such that these accumulate in separate reservoirs. The top may be imperfectly sealed.2 Petroleum Migration and Accumulation The accumulation of petroleum occur in only those areas. where geological conditions have provided the unique combination of both hydrocarbon prone source rocks and hydrocarbon traps. the oil and gas accumulate by displacing pore water from the porous rock.

24

Chapter 2. Basic Concepts of Petroleum Geology

In summary, several factors are required for the formation of a petroleum reservoir [49]: 1. There must be a source rock, preferably rich in primary organic matter (carbon- rich marine or lacustrine shale). This source rock must be deeply buried to reach efficient temperatures to cause the organic matter to mature and turn into petroleum. 2. There has to be a migration pathway that enables the shale-released petroleum to migrate in a preferential direction. 3. There must be a reservoir rock that is sufficiently porous and permeable to accumulate the petroleum in large quantities. 4. There must be a trap that is sealed sufficiently to withhold the petroleum. Otherwise, the majority of petroleum will bypass the porous rock and be dispersed or escape to the ground surface. 5. An impermeable seal or caprock, is critical in preventing the petroleum from leaking out from the reservoir or escaping to the surface. If any of these key factors is missing or inadequate, a petroleum reservoir field cannot be formed. A large isolated reservoir or group of closely adjacent reservoirs is referred to as an oil field.

2.3.3 Classification of Petroleum Reservoir-Forming Traps
In this section, a general classification of petroleum reservoir-forming traps is discussed (after [1]). In broad terms, one may distinguish between structual traps (related to tectonic structures) and sratigraphic traps (related to the sealing effect of unconformities and rock-type, or lithofacies, changes). Domes and Anticlines Domes and anticlines are structures formed by the tectonic uplift and/or folding of sedimentary rocks. When viewed from above, a dome is circular in shape as in Fig. 2.5, whereas an anticline is an elongate fold as in Fig. 2.6. Salt Domes This type of geological structure is caused by the upward intrusion of a diapiric body of salt, volcanic rock, or serpentine. In pushing up or piercing through the overlaying sedimentary rocks, the diapir may cause the formation of numerous traps on its flanks, in which petroleum may accumulate, as seen in Fig. 2.7. Some salt domes may be highly elongated, rather than cylindrical, and are called salt walls (e.g. southern North Sea region). Salt itself is a perfect sealing rock.

2.3 The Origin and Habitat of Petroleum

25

d ble Be mea GAS r Impe

OIL
TE WA R

Porous Strata

Figure 2.5: Oil and gas accumulation in a dome structure.

Im

le eab perm

Be d
GAS
OIL

e Imp

ab rme

rata l e St

TE WA

R

Porous Strata

Figure 2.6: Oil and gas accumulation in an anticline structure.

Fault Structures Many petroleum traps are related to faults, which commonly displace permeable rocks against the impervious one. The fault plane, where lined with a shear-produced gouge or heavily cemented by the percolating groundwater fragments of rock, acts on impermeable barrier that further increases the trapping effect on the migration of oil and gas. See Fig. 2.8.

Structures Unconformity This type of structure is a sealing unconformity, with the permeable rocks tilted, erosionally truncated and covered by younger impermeable deposits. A reservoir may be formed where the petroleum is trapped in the updip part of the bluntly truncated and sealed, porous rock unit, as seen in Fig. 2.9.

26

Chapter 2. Basic Concepts of Petroleum Geology

Gas Oil

Water

Oil Oil Salt Mass Water

Figure 2.7: Hydrocarbon accumulation associated with a salt dome.
Fault

Gas Oil Water

Figure 2.8: Hydrocarbon accumulation related to a fault. Lenticular Traps Oil and gas may accumulate in traps formed by the bodies of porous lithofacies (rock types) embedded in impermeable lithofacies, or by the pinch-outs of porous lithofacies within impermeable ones, as seen in Fig. 2.10. Examples of such lenticular traps include: fluvial sandstone bodies embedded in floodbasin mudrocks, deltaic or mouth-bar sandstone wedges pinching out within offshore mudrocks, and turbiditic sandstone lobes embedded in deep marine mudrocks. Similar traps occur in various limestones, where their porous lithofacies (e.g. oolithic limestone or other calcarenites) are embedded in impermeable massive lithofacies; or where porous bioclastic reefal limestones pinch out in marls or in mudrocks. The approximate percentages of the world’s petroleum reservoirs associated with those

2.3 The Origin and Habitat of Petroleum

27

Gas Oil Water

Impermeable Beds

Figure 2.9: Oil and gas trapped below an unconformity.
Tight-increasing Shale Content

Oil

Water

Figure 2.10: Petroleum trap formed by lithofacies change (Sandstone pinch-out). major trap types are given in Fig. 2.11. On of the present-day Earth’s surface, over half of the continental areas and adjacent marine shelves have sediment covers either absent or too thin to make prospects for petroleum accumulation. Even in an area where the buried organic matter can mature, not all of it results in petroleum accumulations. The following statistical data may serve as a fairly realistic illustration [49]: • Only 1% by vol. of a source rock is organic matter, • < 30% by vol. of organic matter matured to petroleum, • > 70% by vol. of organic matter remains as residue and • 99% by vol. of petroleum is dispersed or lost at the ground surface in the process of migration, and only 1% by vol. is trapped. These data lead to the following estimate: only 0.003 vol.% of the world’s source rocks actually turn into petroleum that can be trapped and thus generate our petroleum resources.

2.75 0. fluvial sandstone in the Snorre filed and turbiditic sandstone in the Frigg and Balder fields).4 Types of Hydrocarbon Traps on the Norwegian Continental Shelf Structural traps.g.50 Unconformity Other Stratigraphic 0 Structural Traps Stratigraphic Combination Traps Traps Figure 2. Reef 0. although there are several reservoirs associated with unconformities or porous lithofacies pinchouts (e. Table 2. particularly fault and dome structures.25 Salt Diapirs Combination Anticlines Faults . Basic Concepts of Petroleum Geology 0.11: Percentages of world’s petroleum accumulations associated with the major traps types. are the most common type of trap in the Norwegian Continental Shelf [4]. Stratigraphic traps are far less common for this region.28 Chapter 2.2 summarises the regional information about some of the hydrocarbon fields belonging to the most common types of traps in the Norwegian continental shelf [4].

4 Types of Hydrocarbon Traps on the Norwegian Continental Shelf 29 Table 2. Field AGAT BALDER DRAUGEN EKOFISK ELDFISK EMBLA FRIGG GULLFAKS HEIDRUN MIDGARD OSEBERG SNORRE ˙ SNIHVIT STATFJORD TROLL VALHALL Type of Trap Stratigraphic Stratigraphic Stratigraphic Dome Dome Structural Stratigraphic Structural Structural Structural Structural Structural Structural Structural Structural Dome Reservoir Rock Sandstone Sandstone Sandstone Chalk Chalk Sandstone Sandstone Sandstone Sandstone Sandstone Sandstone Sandstone Sandstone Sandstone Sandstone Chalk Rock Age Cretaceous Tertiary Jurassic Cretaceous Cretaceous Carboniferous Tertiary Jurassic Jurassic Jurassic Jurassic Jurassic Jurassic Jurassic Jurassic Cretaceous .2.2: Types of petroleum trap in the main fields of the Norwegian Continental Shelf [4].

Basic Concepts of Petroleum Geology .30 Chapter 2.

The need for this concept assumption can be explained as follows. many physical phenomena (capillary effects. UTCHEM. All of the most important numerical simulation programs (ECLIPSE. the laws of continuum mechanics are considered to be effective only if the elementary volume is sufficiently large to render the number of pores and rock grains very large or "innumerable". the effect of the micro-scale phenomena "average" and can more readily be parameterizied. water.) are based on this theory. This condition makes the average parameters of the porous medium sufficiently representative for a description of the fluid flow processes occurring in the rock. with the elementary volumes considered on the order of 10 − 104 m. 2 At a large scale. FRANLAB.). Likewise. as seen in Fig. with the scale of the flow phenomenon varying from very small to large. can only be described qualitatively. of the reservoir space. Let us consider the flow of liquids and gas in a natural reservoir. which means that all the components involved (rock. This conceptual approach allows us to develop a useful theory for the flow of liquid and gas through a porous medium. In Fig. the concepts of continuum mechanics can be applied if the reservoir heterogeneity is considered at a macro-scale level (lithofaces variation. FRAGOR. oil and/or gas) are present in every element. 3. bedding. whereas all microheterogeneities on a scale comparable to the grain size are being considered as constants in 31 . or volumetric part. even if very small. fluid adhesion effects associated.) occur at a scale comparable to the rock’s grain size or the dimension of a fractured rock’s fragment (10−4 − 100 m). For the purpose of the filtration theory. According to these concepts. However there are some regularities in the behaviour of the "rock-fluids" systems that can be described by continuum mechanics. etc. a porous rock formation saturated with fluids forms a continuum.1. even if the elementary volume considered is very small and approaches zero. because of the great complexity of the phenomenon. ect. MORE. If the elementary volumes are too small and comparable to the rock’s pore or grain size.1.1 Continuum Mechanics The present understanding of the subsurface processes relevant to reservoir engineering is based on the physical concepts of continuum mechanics [12].Chapter 3 Basic Concepts and Definitions in Reservoir Engineering 3. The flow of fluids that occurs in the partial volume of a porous rock. etc. the filtration theory cannot be successfully applied. 3. called the filtration theory.

Vb (3. its content and hydration. 3. with the pores filled with oil.e. type of clay. etc. respectively). the rock’s fluid flow capacity). φ= def Vp .1) Effective porosity implies the ratio of the total volume of interconnected voidsVp to the bulk volume of rock. gas and water. weathering. Basic Concepts and Definitions in Reservoir Engineering A Fracture B C D B A C Well ~ 10 m -3 ~ 10 m 0 ~ 10 m 2 ~ 10 m 4 Figure 3. the pore volume percent occupied by water. unlike permeability which makes sense only if liquid or gas is moving in porous medium. In volumetric terms. as well as the consideration offluid saturation (i. to the bulk volume Vb of a rock sample. φa = def Vpa . Absolute and effective porosity are distinguished by their access capabilities to reservoir fluids. acting as cement between grain particles. the rock’s fluid storage capacity) and permeability (i. The fundamental definitions in the filtration theory include the distribution between porosity (i. Vb (3.e. It should be noted that porosity is a static parameter. etc. cementation.1: Structure of a fractured-rock reservoir at different scales of observation.32 Chapter 3. heterogeneity of grain sizes and their packing.2 Porosity The porosity constitute the part of the total porous rock volume which is not occupied by rock grains or fine mud rock.) or described by some empirical relationships (functions). Absolute porosity is defined as the ratio of the total void volume Vpa . whether the voids are interconnected or not.e. 3. the equations of flow (parametrized connate-water saturation. oil and gas. leaching.3 Saturation Let us consider a representative elementary volume of the reservoir. residual-oil saturation.2) Effective porosity depends on several factors like rock type. this can be written as follows: .

Part of the oil will remain as residue.2: Distribution of water and oil phases in a water-wet porous medium. 3. Sg and Sw ) in a reservoir varies in space.recovery factor may be as low as 5-10% and is rarely higher than 70%. oil and water). this is called the residual oil. the pore water is the wetting phase and oil is a non-wetting phase. Water Oil Rock Figure 3.3 Saturation 33 Vp = Vo +Vg +Vw . Simply. the adhesive forces of one fluid against the pore walls (rock-grain surface) are always stronger than those of the other fluid. as a fraction of the pore volume occupied by a particular fluid: Si = def Vi . In the vast majority of petroleum reservoirs.3.1 Residual Saturation Not all the oil can be removed from the reservoir during production. most notably from the water-oil contact to the reservoir top (see figures in previous chapter). and also in time during the production. both siliclastic and carbonate. (3. One has to distinguish between the residual oil and possibly gas saturation reached in a reservoir after the production stage.3) which leads to the definition of saturation. 3. different parts of the reservoir may have quite different fluid saturations. i = 1. they are distributed unevenly in the pore space due to the wettability preferences. and the residual saturation . and also the saturation in any elementary volume of the reservoir changes progressively during the production. Consequently. n Vp where n denotes the total number of fluid phases present in the porous medium.3. Depending on the production method.. the fluid saturation (So .. S.. i=1 ∑ Si = 1. Importantly. the oil. n If two fluids coexist (say. . See Fig. In short.2. or the actual "drive mechanism" of the petroleum displacement.

• a high temperature retort distillation method and • the Dean-Stark method. where the reservoir saturation and the oil-recovery factor are estimated. deep freezing of retrieved cores. A fresh. 3.34 Chapter 3. • The efficiency of possible oil displacement from the reservoir rock represented by the core.) that are assumed to reflect: • The fluid saturation at the reservoir conditions. If the pore volume Vp of the core sample in known. . 3. etc. "peel-sealed" core sample is taken to the laboratory. Water Core sample Oil Sample holder Water Figure 3. The laboratory process is illustrated in Fig. Vp (3. the changes in pressure and temperature. Basic Concepts and Definitions in Reservoir Engineering of fluid phases in a reservoir-rock sample after a well coring operation.) Two laboratory techniques are commonly used for determining the residual oil and water saturation.4) where Voi is the initial volume of trapped oil in the core sample. The modern techniques of core-samples collection prevent dramatic alterations of the rock fluid characteristics. • The possible alterations due to the drilling-fluid invasion into the core.3.3: Evaluation of residual oil saturation Sor by a laboratory displacement from a core sample.3. etc. (foam-based drilling fluid. then Sor = Voi −Vo . where water is displacing the initial oil in the core sample.2 Laboratory Determination of Residual Oil and Water Saturation The cores recovered from wells contain residual fluids (depleted due to the drilling-fluid invasion. and Vo is the displaced or produced oil. rubber sleeves containing the core samples and maintaining their reservoir pressure.

4: The high temperature retort distillation method. The vaporised fluids are first collected in the sample holder and then released vertically downwards through the hollow stem ( ownd draft retort). The sample is then placed in a cylindrical metal holder with a screw cup at the top and a hollow stem projecting from the bottom. The temperature is then increased to ∼ 650o C (1200o F) to vaporise and then distil oil from the sample.B. 3. See Fig. are normally used. at which point the water within the core is vaporised and recovered.3. They are subsequently condensed and measured in a calibrated receiving tube. The top is sealed and the sample holder is placed in a retort oven. N.! Samples are usually destroyed in this test due to the high temperature and for this reason small-diameter samples or "plugs" (small cores from the well core). The following parameter values are derived from the laboratory test: .4. A thermostat controller raises the temperature of the core to a selected level.3 Saturation 35 The Retort Distillation Method The core sample is weighed and its bulk volume measured or calculated. The calculation of the oil and water saturation is straightforward. Termocouple Insulated oven Heating elements Sample cup Screen Condensing tube Water bath Water inlet Receiving tube Oil Water Temperatur controller Figure 3.

where its volume can be directly measured. • it must have a boiling temperature higher than that of water. Frequently. After all the oil and water have been recovered from the sample. The solvent mixes with the oil in the sample and both are returned to the solvent flask below. Toluene satisfies all of those requirements. • Vp – the pore volume.Vw – the recovered oil and water volumes. which is calculated. Vp Vp (3. saturation are also given in %. The Dean-Stark Apparatus for Measuring Initial Fluids When the core to be analysed is weighed. the weight of oil in the sample can be calculated. which might otherwise lead to an erroneously high oil saturation!) and this unit is suspended above a flask containing a solvent. the measurement includes the weight of rock grains. registered during the test. Because the water collected in the calibrated tube is distilled.5. Basic Concepts and Definitions in Reservoir Engineering • Vb . There are several requirements for choosing a proper solvent. condenses therein and falls back into the calibrated tube. • it must be immiscible with water and • it must also be lighter than water. 3. . with a density of 1. 3. where upon the solvent condensate drips back onto the sample containing the reservoir fluids. This information is subsequently combined with the estimated porosity of the clean. determined prior to the experiment.5. The hot solvent vapour rises. ρr – the sample bulk volume and rock density. it vaporises. The sample is then placed in the tare apparatus (to be sure that no sand grains are lost from the core sample during its analysis. • Vo . See Fig. The water and residual oil saturation are calculated as follows: Sw = Vw Vo . surrounds the sample and moves up to the condensing tube. the volumes of the oil and water can be converted into percent pore-space fraction (saturation). where it is cooled and condensed. rises in the condensing tube. the water volume is recorded for further calculations.0 g/cm3 and a known volume. as shown in Fig. the water vaporises. it is dried and weighed again.. dry sample. it collects at the bottom of the tube.5) where the saturation are fractional parts of the pore volume. and the pore fluid. At that point.36 Chapter 3. The difference between the original and final weights equals to the weight of the oil and water originally present in the sample. and So = . When successive readings indicate no additional water recovery. Because it is heavier than the solvent. The process continues until the sample’s temperature has risen above the boiling point of water. such as toluene. When heat is applied to the solvent. The condensate collects into the calibrated tube until the fluid there reaches the spill point.

Vb – the rock’s porosity and the core sample’s bulk volume. (3.3 Saturation 37 Condensing tube Offset calibrated tube Solvent Water Sample Tare Flask Solvent Figure 3.5). which is calculated. • Vw – the reservoir volume of water. • φ . N. determined directly after the tests.e. registered during the test. i. . The calculation of the oil and water saturation is straightforward.3.B. ect. Water and oil (residual) saturation is calculated according to Eqs. The following parameters are derived from the laboratory test: • Wi – the initial weight of the core sample. where both the retort distillation method and the Dean-Stark method are capable of yielding fluid saturation values within ±5% of the true values. • Wd – the weight of the dry. determined prior to the tests. pore volume pycnometry or perhaps capillary measurements. determined after the tests. clean core sample.5: The Dean-Stark apparatus. . • Vo – the recovered volume of oil. The samples in the process are not destroyed and can be further used in other measurements..

which in turn makes it necessary to distinguish the following saturation interfaces: • The Free-Oil Level (FOL) – the level above which the oil saturation is sufficiently high to allow full oil mobility (100% oil productivity) and the water saturation is low enough to make water immobile. In other words. Below the OWC.38 Chapter 3. unique meaning in reservoir engineering considerations. 3. • The Economic OWC – the level above which enough oil will be mobile. In most reservoirs. even though the rock pores remain "water-wet" (i. rendering the whole overlying part of the reservoir economical viable.e. FWL is the oil-water contact in the absence of the capillary forces associated with a porous medium. this is the .4 Reservoir Pressure and Distribution of Fluid Phases. in a well. Basic Concepts and Definitions in Reservoir Engineering 3. Water underlies the petroleum. 3.6: The distribution of fluid phases in a reservoir. • The Free-Water Level (FWL) – an imaginary surface at which the pressure in the oil zone equals to that in the water zone. but is continuously distributed throughout the reservoir as the wetting fluid. Below the GOC.6) affects strongly the relative mobility of the oil phase. i. • The Oil-Water Contact (OWC) – a surface separating the oil zone from the underlying water zone. However. as an aquifer. 70%.(Sw is the water saturation.0 SW 1. their walls are covered with a thin film of water). which means Sw < 30%. i.0 Figure 3. and the oil directly below. gas can be present only as a dissolved phase in oil. this is the level where So exceeds ca. oil is generally absent. The density difference makes the gas accumulate at the top of the reservoir.e. the term "oil-water contact" does not have a single.e. In most reservoirs. The continuos distribution of water saturation in the reservoir zone (see Sw in Fig. Gas Gas cap crest GOC Oil zone Depth Oil Water OWC c FWL Water zone Water zone 0.) The following fluid interfaces in the reservoir are important: • The Gas-Oil Contact (GOC) – a surface separating the gas cap from the underlying oil zone (also referred to as the oil "leg" or oil "column"). The migration and accumulation of petroleum in a reservoir leads to the replacement of the original pore water by gas and oil . See Fig. po = pw .6.

the distribution of these surfaces is of crucial importance when it comes to physical (fluid dynamics) and economical (oil recovery) considerations. 3. Pressure Overburden pressure (OP) FP GP overpressure Depth underpressure normal hydrostatic pressure Figure 3. located below the productive oil-water contact. as our common terminology refers to it.3. This may mean Sw as high as 80-85% and So of merely 15-20%. Needless to add. pov . The FWL would then appear to be the only rock-independent OWC. 50%. and thus. The total pressure at any depth is the sum of the overlaying fluid-column pressure (p f ) and the overlaying grain. due to the weight of the overlying fluid saturated rock column.column level below which the capillary forces render oil completely arrested. • The Edge-Water Level – which is the OWC as defined earlier (level of Sw = 100%). • The Productive OWC – The level above which oil become mobility. 39 level where So exceeds ca. The interfaces are usually determined on the basis of analysis and well (drill-stem) tests. some engineers prefer to refer to this surface as the capillary oil displacement level or threshold pressure level. This is the base of the reservoir.7. this is not always the "100% water level". as shown in Fig. or the oil. pov = p f + pm .or matrix-column pressure (pm ). because the oil saturation may still be in the order of some percent.7: Overburden pressure as the combined grain. 3. In strict terms. or "imbibed". The total pressure at any reservoir depth. as sketched in Fig. Therefore. representing the absolute base of the oil column. although the actual threshold value may vary.6. . is called the overburden pressure.4 Reservoir Pressure and Distribution of Fluid Phases. depending upon reservoir conditions. by the rock pores (such that only thermal distribution can possibly remove the oil from the "dead-end" pores).and fluid column pressure.

at any reservoir depth. (in psia.8) Typical "normal" pressure gradients for the water. and D0 is an arbitrary depth with a known pressure (for instance. i. [21]: d p f = −d pm . then the differential overburden pressure is zero. The hydrostatic pressure is therefore identical to the water pressure.35 psi/ft = 7. If the hydrostatic pressure gradient considered to be constant we can write. as a result of geological processes. the equation becomes.7 +C. oil and gas phases are: (d p/dD)w = 0. 3. (d p/dD)o = 0. where the pressure in the reservoir is somewhat higher or lower than otherwise expected. as it occurs during production.e. Rock compressibility is therefore an important parameter to be considered when petroleum (preferably oil) production is estimated. pw (D) = ( dp )w D + 14. relative the hydrostatic pressure.7) pw (D) = ( (3.40 Chapter 3. dz (3.5 Pressure Distribution in Reservoirs The hydrostatic water pressure at any depth D.2kPa/m.9) . will lead to a corresponding increase in the grain pressure.08 psi/ft = 1.45 psi/ft = 10. as long as there is a continous phase contact in the water. can be calculated as follows: D pw (D) = ( D0 dp )w dz + pw (D0 ). pw (D) = ( dp )w D + 14. This means that any reduction of the fluid pressure. The constant C accounts for the fact that the reservoir pressure is not in hydrostatic equilibrium. The water pressure for a general reservoir is then as follows. The reservoir pressure can then be corrected. (d p/dD)g = 0.0 (in bar) dD (3. Basic Concepts and Definitions in Reservoir Engineering Because the overburden pressure pov is constant at any particular depth D. the pressure at the sea bottom or the pressure at the sea surface). dD and if D0 is taken at the sea level. by using a constant ( ) in the above pressure C equations. all the way up to the sea surface.6) where (d p/dz)w denotes the pressure gradient of the water phase at depthz.9 kPa/m. or dD dp pw (D) = ( )w D + 1.8 kPa/m Abnormally high or low reservoir pressure can appear when the reservoir is "sealed" off from the surrounding aquifer. dp )w (D − D0 ) + pw (D0 ).) dD (3.7 (in psia).

2psia (po )top = 0.45 · 5510 + 14.2 = 2383.7 = 2377.7psia • Oil phase: (po )FW L = = 0.7psia • Gas phase: (pg )GOC = 0. we can evaluate the fluid-phase pressures at the different reservoir "key" levels.45 · 5250 + 14.35 · 5000 + 565.2psia (pg )top = 0.8: Cross-section of a reservoir. let us consider the reservoir which cross-section. as shown in Fig.7 psia (pw )GOC = 0.08 · 5000 + 1983.7psia (po )OWC = 0. Assuming normal pressure condition.7 = 2264.2 psia (pw )top = 0.7 = 2489.2psia which gives: Cg = 1983.5 Pressure Distribution in Reservoirs 41 where C is positive when over-pressure is observed and negative for a under-pressured reservoir.2 psia The different phase pressures (water. At this level there is no pressure difference .35 · 5500 + 565. 5000 Gas 5250 GOC Oil Depth.3.45 · 5000 + 14. ft 5500 OWC Water FWL 5510 Figure 3.2 psia (pw )OWC = 0.2psia which gives: Co = 565.35 · 5250 + 565. (pw )FW L .7 = 2494.8 (see also [21]).7 = 2315.08 · 5250 +Cg = 2403. In order to evaluate the pressure distribution in a reservoir. oil and gas) are derived from a common reference which normally is the FWL pressure.7 = 2403.7psia (po )GOC = 0.7 = 2490.45 · 5500 + 14. • Water phase: (pw )FW L = 0.35 · 5510 +Co = 2494. 3.

3. can be evaluated as follows. Basic Concepts and Definitions in Reservoir Engineering between water and oil and the two pressures are identical. (Pc )top = (po )top − (pw )topt = 2315. Similar to the FWL. the OWC becomes the level in the reservoir where the water saturation becomes less than one and consequently the water saturation is ideally considered to be 100% in this zone. 3.7 = 67.9: Pressure distribution in a reservoir (hypothetical example).9. Different phase pressures are observed at the same elevation in the reservoir.5 bar ow (Pc )top = (pg )top − (po )top = 2383.42 Chapter 3. (pw )FW L = (po )FW L .2 − 2264. as seen in Fig 3.7 = 118. ft 2375 O G 2500 5000 W GOC 5250 5500 Water 5510 OWC FWL 5500 5510 Treshold capillary pressure Figure 3. Often this pressure is referred to as thereservoir pressure. psia 2250 5000 Gas 5250 Oil Depth. show that the phase pressures are different at the same elevation in the reservoir. (3.e. While gravity forces tend to separate . Accordingly. The pressure difference between two coexisting phases is calledcapillary pressure and denoted (Pc )i j .5 psi(a) = 4.9. i.7 = 51. The capillary pressure at the top of the reservoir.9. and that the capillary pressure is additive. is the level in the reservoir where the pressures in the oil and gas phases are identical..e. the definition of the GOC. Ideally there is no oil present in the zone between the FWL and the OWC. shown in Figs. the distribution of phases within a reservoir is governed by counteracting gravity and capillary forces. [7]: (Pc )gw = (Pc )ow + (Pc)go .10) At static (initial reservoir) conditions. gas-oil or gas-water.6 bar go (Pc )top = (pg )top − (pw )top = 2383.1 bar gw The capillary calculations and the Fig.2 − 2315.5 psi(a) = 8. since the oil pressure is too low to allow the oil phase to enter the pore space (the largest pore throats). Pressure. i.0 psi(a) = 3.7 − 2264. where the subscripts i and j refer to oil-water.8 and 3.

6. The water pressure at any depth is.5 Pressure Distribution in Reservoirs 43 reservoir fluids accordingly to their densities. A where F/A is force due to water weight per cross-section area. as shown in Fig. . 3. ρw is the water density.3. p= F A ⇒ dp = d F . the capillary forces. Substituting the last results into Eq. patm. dp = d mg =d A ρw gVw A =d ρw gAD A = ρw g dD In the equation above.6 we obtain the following general formula for water pressure at depth D. acting within and between immiscible fluids and their confining solid substance. . 3. .3. resist separation. We may therefore write the pressure change as.6 Example: Water pressure in a vertical cylindrical tube The water pressure at a depth D is found using Eq. where pw (D0 ) is the atmospheric pressure. g is the gravitational constant and D is the water depth. The balance of these two forces result in an equilibrium distribution of phases within the reservoir prior to its development. NB! The pressure variation in a reservoir is determined by the fluid densities alone (when the gravitational coefficient is considered constant). . D pw (D) = 0 ρw g dD + patm.

absolute.1 bar. Calculate the density of formation water when the pressure gradient is measured. determine the pressure change inside a reservoir where the depth from the top down to the FWL is 150 m.6 Exercises 1. Formation water salinity will influence hydrostatic pressure estimation. 4. Sand grain density: 2.3 g.4 g/cm3 .67 g/cm3 .31 g/cm3 . 3 bar) . A reservoir water pressure of 213 bar is measured at a sub-sea depth of 2000 m.44 Chapter 3. absolute. A glass cylinder has been filled with dolomite grains up to the 2500cm3 mark. 9.d p/dz = 10. 4. given the following data: Weight of dried core sample: 259. 5. A laboratory cylindrical cup contains 500 cm3 water and weighs 800 g. will yield a carbonate rock’s porosity of 13% . 8.2 kPa/m. Given that uncertainty in salinity may lead to an uncertainty in water density of ∆ρ = 1. Weight of dried sample: 17. 6. 34%. 1.4 g Define the terms absolute and effective porosity and decide which term to use when characterising the core sample. effective. Calculate the porosity of a sandstone core sample given the data from core analysis: Bulk volume of dried sample: 8. Calculate and characterise the sand’s porosity./underburden pressure. Calculate the bulk volume and porosity of this saturated porous medium knowing that the total weight of cup and its content (water and limestone) is 2734 g. 8.2 kPa/m. 3.1 cm3 . Basic Concepts and Definitions in Reservoir Engineering 3. 7. 8. Determine the porosity and lithology of a core sample.1.11 . Estimate numerically the change in carbonate-rock porosity caused by a complete dolomitization of calcite. 6. 1. 2. 2. The mass of dolomite is 4714 g. CaCO3 ) is poured into the cup until the level of sand and water coincide. 41%. 4%. 7. accounting to the chemical reaction. 28%. sandstone.2 g Weight of 100% water-saturated core sample: 297 g (the density of water is 1.0 g/cm3 ) Weight of core sample in water: 161. (answ. 2.65 g/cm3 . 20%. How do you define the porosity ? 3. 2CaCO3 + Mg2+ = CaMg(CO3 )2 +Ca2+ . when the water pressure gradient is 10. Carbonate sand (limestone. Evaluate the pressure situation in the reservoir and determind whether there is an over.

Genetically. Only a volume selected large enough (a representative volume) will result in a representative and correct statistical average (see Fig. to a great extent. An important characteristic of consolidated porous media is the ability to restore elastically. A consolidated medium means a rock whose grains have been sufficiently compacted and are held together by cementing material. Porosity is a statistical property dependent on the rock volume taken into consideration. to their shape (volume) after the removal of the overburden pressure. defined locally as an average over the representative elementary volume of porous rock media considered. • Vugular porosity. the calculated porosity can deviate greatly from the "true" statistical average value [35]. In practice. • Fracture porosity. If the volume selected is too small. already presented. • Micro-porosity. the porosity is the fluid-storage capacity of a porous medium. the following types of porosity can be distinguished : • Intergranular porosity. and may vary greatly from one rock type to another.1 General Aspects According to the definition. 4. 4. It should also be noted that porosity is astatic parameter. it is impossible to counter the 45 .Chapter 4 Porosity 4. Rock media having both fracture and intergranular pores are called double-porous or fractureporous media. From the point of view of pores susceptibility to mechanical changes one should distinguish between consolidated and unconsolidated porous media.2 Models of Porous Media The geometric character of rock’s permeable pore space is in reality quite complicated. which means the part of the rock’s total volume that is not occupied by solid particles.1). • Intragranular porosity.

be used in some situations where fluid flow under simplified conditions is modelled. Vb 2rn · 2rm 4 where r is the pipe radius and m · n is the number of cylinders contained in the bulk volume.1: Definition of a representative elementary volume for porosity measurements [35]. see Fig.5%. is as follows: φ= Vp π r 2 · n · m π = = = 0.2. Porosity Domain of microscopic effects 1.46 Chapter 4.2: Idealised porous medium represented by a system of parallel cylindrical pores (pipes). 4. .1 Idealised Porous Medium Represented by Parallel Cylindrical Pores Vb Vp Figure 4. or 78. This model may though.2. 4. several idealised models have been developed to approximate porous rock media and their varied characteristics.0 0 Vb Grain Figure 4. pore-system geometry in a detailed and faithful way. Estimation of porosity accounting to this model. It is rather obvious that rocks do not have pores like this and that this model gives a unrealistically high porosity value.0 Domain of porous medium Inhomogeneous medium Bulk volume Homogeneous medium 0. Therefore.785.

4. The matrix volume is unchanged and thus. see Fig. is as follows: √ 4 Vb = 2r · 2r · h = 4r2 · 2r sin(60o ) = 4 3 r3 and Vm = π r3 . 4.6% Vb 8r3 6 where Vm is the "matrix" volume or the volume of bulk space occupied by the rock. see Fig. is as follows: 1 4 4 Vb = (2r)3 and Vm = ( π r3 ) · 8 = π r3 .2.4.3. .2 Idealised Porous Medium Represented by Regular Cubic-Packed Spheres 2r Figure 4.2. The estimation of porosity according to this model. 4.3: Idealised porous medium represented by a regular system of cubic-packed spheres.476 or 47.3 Idealised Porous Medium Represented by Regular Orthorhombic-Packed spheres 60o 2r Figure 4. The estimation of porosity according to this model. 8 3 3 and π Vb −Vm 8r3 − 4 π r3 3 φ= = = 1 − = 0.4: Idealised porous medium represented by a regular system of orthorhombic-packed spheres. 3 where h is the height of the orthorhombic-packed spheres. 4.2 Models of Porous Media 47 4.

5 and it follows from Fig. . h= 4r2 − 2r2 = √ 2 r.5: Idealised porous medium represented by regular system of rhombohedral-packed spheres.2.IV) sorted by different radii and the histogram showing the hypothetical grain -size distribution.48 Chapter 4. 4.5 that.26 or 26. which results in variation of porosity and other important reservoir properties.2. By drawing a graph with radii of the spheres plotted on the horizontal axis and heights equal to the corresponding frequencies of their appearance plotted on the vertical axis. Porosity φ = 1− π Vm 4π r3 = 1− √ = 1 − √ = 0. 4. one can obtain a histogram of distribution of particles (spheres) in sizes.5% 3 Vb 12 3 r 3 3 4.5 Idealised Porous Medium Represented by Irregular-Packed Spheres with Different Radii Real reservoir rock exhibits a complex structure and a substantial variation in grain sizes and their packing. 3 which gives φ = 1− π 4π r3 √ = 1 − √ = 1 − 0. where h is the height in the tetrahedron and √ √ 4 Vb = 2r · 2r · 2 r = 4 2 r3 and Vm = π r3 . often associated with the hetrogeniety of porous medium.0% 12 2r3 3 2 4.74 = 0.6 shows an example of an idealised porous medium represented by four populations of spheres (I . The estimation of porosity according to this model. 4.4 Idealised Porous Medium Represented by Regular Rhombohedral-Packed spheres 45 o 2r Figure 4.395 or 39. see Fig. Fig.

Pore volume of fine sand: Vp = φ f . in general and in particular in the case of porous media. The total porosity is then defined. i.33). the following table is listed: Volume of sand: Volume of fine sand: Vsand = φ pebbleVpebble . The volume of fine pebble gravel is equal to the bulk volume. The three sediments are mixed in such proportions that the sand fills the pore volume of the fine pebbles and that the fine sand fills the pore volume of the sand.sand .e.30).2 Models of Porous Media 49 I III IV Frequency II IV III II I r Figure 4. Example: Porous medium of irregular system of spheres A porous medium is blended with three types of sediment fractions: fine pebble gravel with porosity (φ pebble = 0.33 = 0. for further analysis and improved undersanding. Vp Vb φ= = φ f . Since the sand fills the pore volume of the pebble and the fine sand the pore volume of the sand. though idealized. Vpebble = 0.4. of the rock porosity. Since rock porosity has so many representations. sand (φsand = 0.sand V f .6: Idealised porous medium represented by an irregular system of spheres with different radii. it is important to maintain a representative image. The advantage of idealised models.sand = 0. may serve as a "mental image" or idealised concretization of a rather complex porous structure of porous rocks.sand φsand φ pebbleVpebble . V f . The different models.38 · 0. described above.. The porosity of the porous medium is ∼ 4%. .3 · 0.sand = φsand Vsand . is the opportunity they offer for simple quantification and representation of characteristic parameters.Vb = Vpebble . .38) and fine sand (φ f .037.

and thus give a good basis for statistical estimates (mean porosity values. see Fig. 4. The recognition of such trends is very important for the development of a bulk picture of the reservoir as a porous medium and representation of the reservoir porosity in mathematical simulation models (reservoir characterisation. 4.). The porosity measurement in such rocks requires samples that are as large as can be obtained (portions of full-diameter drilling cores). for which a standard core-plug analyse is unsuitable. In heterogeneous rocks. standard deviations. require a realistic picture of the rock porosity and its variation throughout the reservoir. This picture is not easily obtainable since porosity is measured locally (in the well) and porosity extrapolations introduce large uncertainty in the estimated average values. the local porosity may be highly variable. Porosity 4.7: Unimodal and polymodal porosity distributions.8. See Fig. Numerical simulation of fluid flow in porous media.4 Measurement of Porosity 4. . distinguished within the reservoir. etc. The distribution may appear to be unimodal (left) or polymodal (right).4. 4. Such histograms may be constructed separately for the individual zones. etc.) Mechanical diagenesis (compaction) and chemical diagenesis (cementation) have a profound effect on a sedimentary rock’s porosity. 4. numerical modelling.3 Porosity Distribution The multiple sampling of porosity measurements for reservoir rocks at different depths and in different wells gives a data set that can then be plotted as a histogram. depth profile or graphical co-ordination. vugues. may reveal spatial trends in the porosity variation .1 Full-Diameter Core Analysis A full-diameter core analysis is used to measure the porosity of rocks that are distinctly heterogeneous. intergranular porosity.50 Chapter 4. The same core-plug is a non-representative elementary volume for this type of rock. The grouping of porosity data according to the reservoir zones. such as some carbonates. vugular rocks. and fissured. or units. lateral correlation. to reveal the porosity’s frequency distribution. related to laboratory tests on core samples as well as full field production estimation. as it may include micro-porosity.7.9. Frequency Frequency Min Porosity Max Min Porosity Max Figure 4. This burial effect is illustrated by the two typical examples of sand and clay deposits in Fig.

Either the pore volume or the grain volume can be determined. A full-diameter core sample usually has a diameter of 5 inches (12. m Figure 4.5 0. .2 0.4 Measurement of Porosity 51 Porosity + + + + + + + + + Depth + + + + + Figure 4.10. but yields a singe porosity value that represents their effective combination.5 cm) and the length of 10 inches (25 cm).3 0.1 0. fractures. Several laboratory techniques used for porosity measurements. or various combinations of these.9: Sediment compaction burial and porosity change. 4.2 Grain-Volume Measurements Based on Boyle’s Law This gas transfer technique involves the injection and decompression of gas into the pores of a fluid-free (vacuum). depending upon the instrumentation and procedures used.4 Porosity sand 0.8: Examples of trends of porosity distribution in the depth profiles of two reservoir sandstone. 0. dry core sample. 4.4. see Fig. and the procedure is generally similar for full-diameter cores and core "plugs".0 0 300 600 900 clay 1200 1500 1800 Depth.4. The full-diameter core technique does not differentiate between the actual types of porosity involved.

4. p1Vre f = p2 (Vre f +Vs −Vg ). where Vre f . 4. p2 (4. respectively. one obtains p1V1 = p2V2 .10: Porosity measurements based on the Boyle’s law.10. Porosity Sample Chamber Reference volume Pressure gauge Valve To gas pressure source Pressure regulator Valve Figure 4. N2 is also used. The advantage of CO2 is it’s hydrophilic ability. might be good alternatives to Helium. one obtains. pV = nRT where the temperature. due to effects of dehydration of the porous core sample. Other gases.52 Chapter 4. • helium is an inert gas that and will not be absorbed on the rock surfaces and thus yield erroneous results. and p2 the final pressure in the system. and in the case of vacuum inside the sample chamber (Fig. the volume of the sample chamber and the grain volume. Vg = p2Vre f + p2Vs − p1Vre f . Helium gas is often used due to its following properties. The Calculation of the Grain Volume Using the ideal gas law.1) where p1 denotes initial pressure in the reference cell. . simply due to its availability. Assuming adiabatic conditions. which increase the effect of dehydrating the core sample.10. T = const. See Fig. Successive measurements will increase the accuracy. To perform the laboratory measurement. Vs and Vg are the reference volume. such as N2 and CO2 . • the very small size of helium molecules makes the gas rapidly penetrate small pores.

the relative uncertainty in the bulk volume is written.4. 2. i. Fluids that are normally used are. using this technique. The core sample is first saturated with a wetting fluid and then weighed. Example: Uncertainty analysis in measuring the bulk volume using Archimedes’ principle.4. • water which can easily be evaporated afterwards. ρw Differentiating the equation above gives us. first by weighing the sample in a cup of water.4 Measurement of Porosity 53 4. is normally obtained.e.2%.. • mercury which normally not enters the pore space in a core sample due to its non-wetting capability and its large interfacial energy against air. m1 (assuming 100% water saturation) and then weighing the sample in air as it is removed from the cup. . The the sample is then submerged in the same fluid and its submerged weight is measured. where the uncertainty introduced in the process of weighing the two masses is considered to be identical. where uncertainties in the order of ± 0. − − ρw m2 − m1 m2 − m1 ρw If the density measurement as well as the two mass-measurements above. are very accurate. The laboratory measurements. The bulk volume is the difference between the two weights divided by the density of the fluid. Vb = m2 − m1 . is considered to be independent measurements.3 Bulk-Volume Measurements This technique utilizes the Archimedes’ principle of mass displacement: 1. The bulk volume is then written. ∆m = ∆m1 = ∆m2 . ∂ m2 ∂ m1 ∂ ρw dVb = dm2 m2 − m1 dm1 d ρw .m2 . dVb = ∂ Vb ∂ Vb ∂ Vb dm2 + dm1 + d ρw . The bulk volume of a porous core sample can be measured in two steps. ∆Vb Vb 2 =2 ∆m (m2 − m1 ) 2 + ∆ ρw ρw 2 .

The calculation of the pore volume Vp is as follows: p0Vp + p1Vre f and Vp = (p1 − p2 ) Vre f where (p1 > p2 > p0 ) (p2 − p0 ) = nRT (4. we find a relative uncertainty in the bulk volume of approximately 0. If the relative uncertainty in determined the water density is estimated to 0. where the sample is placed in a rubber sleeve holder that has no voids space around the periphery of the core and on the ends. Hydrostatic pressure Core sample Flow into core To flow meter Rubber tubing Figure 4. The bulk volume of the core sample is approximately 30 cm3 and water density is assumed equal to 1 g/cm3 .) .54 Chapter 4.2) (4.5%.1% and the weighing accuracy is equal to 0. is measured. as seen in Fig. or a hydrostatic load cell.11.3) p2 (Vp +Vre f ) = nRT It is important to notice that the Hassler core holder has to be coupled to a volume of known reference Vre f .4 Pore-Volume Measurement Pore volume measurements can be done by using the Boyle’s law. 4. Helium or one of its substitutes is injected into the core plug through the end stem. when the pore volume Vp . see Fig.11: Hydrostatic load cell (Hassler holder) used for a direct measurement of pore volume. 4. ∆Vb Vb 2 ∆m =2 ρwVb 2 ∆ ρw + ρw 2 . 4.10. Such a holder is called the Hassler holder. (Note that the uncertainty related to the assumption of 100% water saturation prior to the first mass measurement. . in some experimental tests could be larger than the effective uncertainty related to the measuring technique.1 g.4. Porosity The uncertainty equation above may also be written.

Vo1 Vb1 Vw fw = 1 Vb1 fo = = φ So . gas and water are added to obtain the pore volume and hence the core porosity. The volumes of the extracted oil. This in turn is used to convert the weight of the first part of the sample.4. = φ Sw . is weighed and then placed in a pump chamber filled with mercury (a pycnometer) in which its bulk volume is determined. and φ .4 Measurement of Porosity 55 4. is raised to 70 bar (1000 psi). pHg . the fraction of the gas-bulk volume) can be calculated. where their volumes are measured. With an appropriate calculation. 100 g) is crushed and placed in a fluid-extraction retort (see figure in previous chapter). where the metal-holder unit has a cap to prevent the evaporation of gases at the top.4. At this pressure. . 30 g) with a roughly cylindrical shape. Sg . Then the pressure of the mercury. The vaporised water and oil originally contained in the pores. Ws1 = Vb1 · ρapp and Ws2 = Vb2 · ρapp → Vb1 = Vb2 Ws1 Ws2 The formation oil. filling the pore space originally occupied with the gas. the fraction of the bulk volume occupied by gas (i.and water-volume factor are calculated as follow. Denoting the apparent bulk density of the fluid-saturated rock sample asρapp . water and gas volumes are each calculated as fractions of the bulk volume of the rock sample and the three values are added to yield the porosity value . into an equivalent bulk volume. The core sample is divided into two parts. The bulk volume and weight of the fresh sample allow the computation of the effective bulk density of the rock. move down and are subsequently condensed and collected in a calibrated glassware.. One part (ca.5 Fluid-Summation Method This technique is to measure the volume of gas. because these values are representative for both parts of the sample. the volume of the mercury "imbibed" in the rock gives the gas volumeVg . oil and water present in the pore space of a fresh or preserved (peel-sealed) core of known bulk volume. the mercury enters the sample and compresses the gas. The laboratory procedure provides the following information: • First subsample gives the rock’s weightWs1 and the volumes of oil Vo1 and water Vw1 are recorded. some of the oil and water can evaporate and the saturation will be measured inaccurately. • Second subsample gives the volume of gasVg2 and the rock’s bulk volume Vb2 . measuring the volume of the displaced mercury. From the second subsample. we can write. The second part of the rock sample (ca. which was 100 g (to be retorted).e. If the core has been exposed to the open air for some time. The oil. fg = Vg2 = φ Sg Vb2 where the subscript 2 is omitted for fg .

and pore volumes of core samples. 4.) 5. New equilibrium is reached and we write. The pycnometer is a lab-tool occasionally used for measuring bulk. The pycnometer piston is withdrawn and a gas (air) volume of V0 is measured. and the cell volume is sealed. p1 (V1 −Vm ). as laboratory fluid. p1 − p0 .56 Chapter 4. . NB: The mercury does not enter the pore system of the core sample. where a defined amount of mercury can be injected or withdrawn. The pycnometer cell is fully saturated with mercury. Mercury is injected into the cell and a new gas volume. where p0 is the atmospheric pressure and Vm is the matrix of the sample (the rock’s grain volume). the following measuring steps are carried out: 1. 2. a cell. Hg V0 Figure 4. Finally. The equilibrium condition inside the cell is written. p0 (V0 −Vm ). Vm of a core sample. In order to define the matrix volume.V1 and gas pressure. (Mercury. p1 is measured. has become less popular due to its toxic characteristics and is quite often replaced by other fluids. Porosity and the sum of the fluid-volume factor then gives the porosity value: fo + fw + fg = φ (So + Sw + Sg ) = φ Example: Use of pycnometer in matrix volume calculation. The sketch below illustrates the working principle of the pycnometer. The core sample is placed in the cell. the matrix volume is found as follows: Vm = p1V1 − p0V0 . 3. due to its high interfacial tension.12: Sketch of the pycnometer. A pycnometer is in principle a contained volume.

The porosity is defined.5) In laboratory experiments we wish to reduce uncertainties to a minimum.5) tells us that it is not sufficient to reduce the uncertainty in only one of the measured parameters. Example: Error propagation From laboratory measurements one has estimated the relative uncertainty related to the pore volume to be. leaving the other unchanged. If we define porosity as.4) φ= Vp . (4. Vb Vb 2 = Vp Vp +Vm 2 + Vm Vp +Vm 2 . since the total relative uncertainty is mainly influenced by the largest relative uncertainty. Vm /Vm = 7%. Vb Vp +Vm We could start to differentiate the porosity with respect toVp and Vm . the resultsVp and Vb are independent parameters and so are their uncertainties.. dVp dVb dφ = − . only two of them should appear in the uncertainty analysis. (4. .4) and then substitute the results into Eq. φ= Vp Vp = . Vb we may differentiate the equation and we obtain. (4. (4. For characteristic parameter estimation. Since the three parameters are dependent.e.0% and the relative uncertainty related to the matrix is. ∆Vp and ∆Vm . Eq. φ Vp Vb The pore.and bulk volumes are independent measurements. Vp /Vp = 5. i.5 Uncertainty in Porosity Estimation 57 4.4.4) gives.5 Uncertainty in Porosity Estimation Experimental data is always contaminated with measuring uncertainty. Vb = Vp +Vm . (4. we will expect the uncertainty in the measured parameters to introduce an error in the estimate of the porosity found.e. i. given the equation above. Differentiation of Eq. like determination of the porosity. but instead we intend to differentiate Eq. (4.5). The relative error or uncertainty in the porosity is then given by ∆φ = φ ∆Vp Vp 2 + ∆Vb Vb 2 . Porosity will normally be a function of Vp . Vm and/or Vb .

Once these logs are obtained and converted into a porosity log. • Neutron . then the relative uncertainty in the porosity is ∼ 7. • Microresistivity log (from which F can be derived). (4. The Formation resistivity factor is defined as the ratio of the resistivity of the porous sample saturated with an ionic solution Ro of the bulk resistivity of the same solution Rw . Note that if the equation φ = Vp /(Vp +Vm ) is differentiated directly.2 (or 20%). but has the advantage of providing continous porosity data. often called wireline logs.57% and the porosity with uncertainty is written. Every extra operation in the error propagation increases the final uncertainty.6 Porosity Estimation from Well Logs Porosity of reservoir rock can be estimated not only by using methods. [23] Ro . φ = φ (1 + φ 2 ) Vp Vp 2 + (1 − φ )2 Vm Vm 2 . compared to the process above where a two step differentiation is performed. φ± φ = (20 ± 1. Porosity can be estimated from: • Formation resistivity factor (F). 4.gamma log. Porosity and substitution in Eq. There are several relationships which can be used for the porosity evaluation using F-values [23]. If the porosity is. F= .6) Rw The Formation resistivity factor measures the influence of pore structure on the resistance of the core sample. Vp Vp 2 + Vp Vp +Vm 2 + Vm Vp +Vm 2 . the result would be slightly different because the differentiation was used only once.5) gives. φ = 0.e. • Density (gamma .5)%. but also from geophysical well logs. φ = φ or written differently. they can be calibrated using core-sample porisity data and serve as additional reliable source of porosity distribution evaluation.gamma) log. This method of porosity evaluation is not very accurate. (4.58 Chapter 4. . • Acoustic (sonic) log. i. as has been described above.

6 Porosity Estimation from Well Logs 59 • F = φ −m . For more information regarding porosity evaluation using geophysical well logs. 23. 37]. see reference [7. • F = X /φ . where X is the electric tortuosity of the sample (Wyllie. • F = (3 − φ )/2φ (Maxwell. .4. 1942). 1881). 1957). where m is the cementation constant (Archie.

weight of mercury-filled pycnometer at 20 oC: 350 g. Calculate the bulk volume of a preserved (paraffin-coated) core sample immersed in water. weight of crushed sample plus absorbed water: 16. Determine the sandstone’s grain density and porosity. Determine the sandstone’s grain volume and porosity using Boyl’s law.5 + ρ [o API]). given the following data: weight of crushed dry sample in air: 16 g. when the water density at that particular temperature and pressure is 1g/cm3 ) 7. oil saturation.90 g.9 g (density of paraffin is : 0. given the following data: volume of chamber containing the core sample: 15 cc. 235. weight of mercury-filled pycnometer with the sample at 20 o C. 95 cm3 is measured in a mercury pycnometer. weight of water-filled pycnometer: 65 g. gas and water. After the gas is displaced by water (ρw = 1 g/cm3 ). the weight is now 209.9 g/cc). water saturation.4 m3 . (Notice that the oil density is ρ [g/cm3 ] = 141. weight of saturated sample in water: 12. given the following data: weight of dry sample in air: 20 g. Another core sample is brought to the laboratory for compositional analysis. gas saturation and lithology of the core sample. weight of dry sample coated with paraffin: 20. density of water is : 1.4/(131.14 g. volume of chamber containing air: 7 cc. The sample is the placed in aSoxhlet distillation apparatus. The sample bulk volume. 3. given the following data: weight of dry sample in air: 20 g. The initial weight of the sample is 224. 6. After drying the core sample. where 80 g of the sample is placed in a mercury pycnometer and the volume of gas found is 0.6 g. respectively. A piece of the same sample.8 cm3 and 4. weight of saturated sample in air: 22.53 cm3 . assuming a sand-grain density of 2. where the water and oil volume is measured to 2. bulk volume of core sample: 10 cc 5. and 4. Calculate the effective porosity of a sandstone sample using the following data: weight of dry sample in air: 20 g. weighing 120 g is placed in a retorte. Calculate the bulk volume of a dry core sample immersed in mercury pycnometer. weight of water-filled pycnometer with the sample: 75 g.0 g/cc).1 g.5 g.75 g.4 cm3 water is extracted. A core sample is saturated with an oil (ρo = 35o API).67 g/cc. the weight is increased to 225.546 g/cc. density of mercury: 13. 2. weight of coated sample immersed in water: 10 g (density of water is: 1g/cc) Determine the rock’s porosity. Porosity 4.60 Chapter 4. 4.9 g. Find the porosity.7 Exercises 1. A third piece of the .

75.95 cm3 .1%.2 g.6%. 9. 47%.73 g/cm3 . a) What is the pore volume of the core? b) What are the oil and water saturations of the core? 10. 29%.4 cm3 . 2.7 Exercises 61 sample. if the core described in the excercise above is representative of the reservoir? Answer to questions: 1. 2. 55. 2.67 g/cm3 . A core.64 g/cm3 . 1.47 hectare large area. mas of saturated sample immersed in water: 64. Is this effective porosity or the total porosity of the sample? What is the most probable lithology of the matrix material? Explain .1%. 9. 2.7 g. 24. 25%. 4. It is saturated with oil and water.831 cm3 . mass of water saturated sample: 120. 738235. 8. 20%.6%.6 bbl .5 m thick. 10. 9.2 g. 5. 53%. 7.5%.5 cm3 .001 g/cm3 . 2.54 cm in diameter has a porosity of 22%. density of water 1. 2. Assume oil and water densities as in the exercise above and find the same characteristic parameters. 6. 19%. 14. weighing 90 g is placed in a pycnometer and the bulk volume is measured to be 37. what is the volume of oil-in-place (in m3 and in bbl) of a 40. 9. 3.8%. 35. Calculate the porosity of the sample described below: mass of dry sample: 104.54 cm long and 2. If a formation is 2. 16%.4.69 g/cm3 . 8. where the oil content is 1. 2.10%.3%.

62 Chapter 4. Porosity .

since the resistance towards fluid flow will vary. obeys the following relationship: h . In general terms. His results showed that the pressure drop across the filter is proportional to the water filtration velocity. communication of interstices. When several phases or mixtures of fluids are passing through a rock locally and simultaneously. In 1856 Henry Darcy proved that flow of water through sand filters. permeability is often considered to be a scalar. using water-filters.e. If there were no interconnected pores.2 Darcy’s Law The first important experiments of fluid flow through porous media. however. the rock would be impermeable. each fluid phase will counteract the free flow of the other phase’s and a reduced phase permeability (relative to absolute) is measured.1) . In practical terms. were reported by Dupuit in 1854.Chapter 5 Permeability 5. i. effective permeability. 5. All factors affecting porosity will affect permeability and since rock permeability is difficult to measure in the reservoir.. all pore channels are included in the averaging process when permeability is measured.e.1 Introduction Permeability in a reservoir rock is associated with it’s capacity to transport fluids through a system of interconnected pores. Since the gas molecules will penetrate even the smallest pore-throats. the permeability is a tensor. Absolute permeability could be determined in the laboratory by using inert gas (nitrogen is frequently used) that fills the porous rock sample completely and limits the possibility of chemical interaction with the rock material to a minimum. depending on the flow direction. porosity correlated permeabilities are often used in extrapolating reservoir permeability between wells. it is natural to assume that there exists certain correlations between permeability and effective porosity. i. ∆l q = K ·A 63 (5.e. even though this is only correct for isotropic porous media. i.

is kept constant. the flow velocity is proportional to. (∆z accounts for the inclined flow direction relative to horizontal flow.1). a reduced flow velocity is expected.64 Chapter 5. i. a reduced flow velocity is expected and similarly if the water is replaced by a fluid of higher viscosity. hydrostatic height difference. have proved that if the manometric level. for the 3 cases are given. Since the water velocity is proportional to the manometric level (observation made by Darcy). was not included because only water filters were investigated and hence. is thickness of the filter in the flow direction and is a proportionality coefficient. viscosity µ . irrespective of the orientation of the sand filter (see Fig. The pressure difference across the sand filter in Fig. where ∆z is the elevation in the gravitational field. the effects of fluid density and viscosity had no real experimental significance. 5. (5. II : ∆pII = ρ g(h − ∆l · sin θ ). as in Eq.e. I : ∆pI = ρ g(h − ∆l). III : ∆pIII = ρ gh. v ∝ (∆p + ρ g∆z). h.1: Orientation of the sand filter with respect to the direction of gravitation.) If the sand filter is made longer. where ∆l is the thickness or length of the sand filter in the flow direction. is cross-sectional area of the filter. 5.1). In Darcy’s experimental results. . Permeability where h A ∆l K is a difference in manometer levels.1. the same flow rate (or flow velocity) is measured. Experiments repeated after Darcy. θ Datum plane I o θ = 90 II o o 0 < θ < 90 III o θ = 90 Figure 5.

in front of the pressure gradient term. (5. the pressure potential has been associated with the energy potential (energy pr.g. µ ∆l The proportionality. In a historical context.4) and (5. (5.2) where k is the permeability.e. The flow rate q = dV /dt. time. µ ∆l (5. is introduced in Eqs. etc.e. as observed in any reservoir where the fluid pressure increases with depth. i.5. the sum of pressure difference and elevation in the gravity field. q = −A k dp . ∆l→0 µ dl µ ∆l (5. When .2 Darcy’s Law 65 v∝ 1 ∆p + ρ g∆z . The pressure at any point along the flow path is related to a reference height or datum plane z0 .). definition.3) For linear and horizontal flow (parallel to the x-axis) of incompressible fluid.2). The permeability does pr. Velocity and flow rate are pr. definition positive parameters (see the example below). z0 = 0 at a level where the reference pressure is 1 atm. can be replaced by equality. Φ= def p + gz. as a proportionality constant and not as a physical parameter. i. where ∆z = z − z0 and e.3). In these cases no flow is expected and static equilibrium is established. ρ Substituting the pressure potential difference ∆Φ in Eq. A pressure difference ∆(p + ρ gz) = (p + ρ gz)2 − (p + ρ gz)1 will create a fluid flow between the two points. mass) and the following definition has been used. k dΦ k ∆Φ q=A ρ = lim A ρ . dz/dx = 0. k ∆Φ q=A ρ µ ∆l where k is the permeability of the porous medium (filter. The Darcy’s law in differential form is. µ is the viscosity of the fluid and l is the length of the porous medium in the direction of flow andΦ is the pressure potential. core sample/plug. the elevation is constant. compensates for a negative pressure gradient in the direction of flow (since fluids move from high to low potential). one can rewrite the equality equation based on Darcy’s deduction. unless the pressure p is equal to the static pressure −ρ gh. not carry any characteristic information about the porous medium. At this point it is important to notice that the permeability. and Dracy’s law is written. v= k ∆p + ρ g∆z .4) where the minus sign "-". k. by introducing a proportionality coefficient k. Fluid flow in a porous rock is therefore given by the pressure potential difference ∆(p + ρ gz). µ dx (5. above. is volume pr.

i. If. describes not only the porous medium transport capability. as such. since the flow cross-section area is. as shown in Fig.66 Chapter 5.φ times smaller than the bulk cross-section A. = dx x2 − x1 x2 − x1 where p1 > p2 in positive flow direction.4 is justified by considering linear core flow. This effect will increase the pore velocity even more. e. A µ dx (5. the pore flow velocity is affected through the reduction of the .2. and the linear flow velocity is written. through a core sample.2: Horizontal flow in a core sample. p2 and the positions x1 . Let’s assume a constant liquid flow rate q. as often is the case in practical situations. (5.e. which is otherwise not described by any of the other parameters in Eq. dp p1 − p2 p2 − p1 =− . the value of d p/dx is pr. on average. Example: Linear horizontal core flow The minus sign "-" in the horizontal flow equation Eq.3. x2 are labelled according to standard numbering and orientation. the porous medium contains a residual saturation of a non-flowing phase. The pressures p1 . Permeability permeability is related to the transport capability of the porous medium. Assuming a homogeneous porous medium and integration from position 1 to 2. the fact that this information about the porous medium is missing in Eq. definition negative. called permeability. u= q k dp =− .4). 5. but represents all information about the porous medium etc. in addition.4). 5.5) The real velocity of fluid flow in the pores is called the interstitial (true) velocity. The directions of pore flow are inclined relative to the general flow direction and a characteristic inclination angle α is assigned to describe this effect.g. The proportionality constant k. a connate water saturation Swc . p1 q x1 x2 x p2 q Figure 5.e. filtration) or bulk velocity. Since x2 obviously is larger than x1 . The fluid velocity related to the cross-section area A is called the superficial (i. the pressure term is written as follows. as illustrated in Fig.. the minus sign "-" is needed to balance the equation. . 5. is often overlooked. (5. v pore and is necessarily higher than the bulk velocity.

In order to keep a constant flow rate q.2 Darcy’s Law 67 flow cross-section area. 5. (5. See Fig. then the pore velocity will be about 7 times higher than the bulk velocity. the gravitational force has to be considered.4: Core flow at a dip angle θ to the horizontal axis Flow at an angle to the horizontal direction is described by Eq. since the fluids are moving up or down in the gravitational field.3). A φ 1 − Swc cos2 α (5. through a porous medium of length ∆l. Experimental tests from different porous rocks have shown that an average inclination angle. a pressure difference ∆p is applied. v pore = 1 q1 1 . The sum of these effects will cause the pore flow velocity to become considerably higher than the bulk velocity.5.6) z vpore α α x vq y Figure 5. with an angle θ to the horizontal flow direction. α 36o and that this angle may vary between 12o to 45o . Example: Linear inclined core flow When the direction of flow is inclined. q = −A k d(p + ρ gz) . where the minus sign is describing linear flow. If a typical porosity of 25% and a connate water saturation of 10% are assumed.4. p2 p1 l2 q l1 r q l g θ x Figure 5.3: Pore flow velocity in a porous medium. µ dl .

68 Chapter 5. In these tests. where l is the direction of flow. Permeability z is the elevation in the gravitational field and from Fig.e. Ak where horizontal linear flow is ∆pθ =0 = q(µ ∆l)/(Ak). µ µ The pressure difference is given.5.3 Conditions for Liquid Permeability Measurements. 5. (5..4). 5. since the fluid is pushed upwards in the gravitational fields. µ dl µ Integration from position 1 to 2. • 100% fluid saturation in the porous medium. • No chemical exchange or .e. constant cross-section in flow direction. • Stationary flow current.reactions between fluid and porous medium. the pressure difference needs to be adjusted relative to the inclination angle (dip angle). q = −A k dp k − A ρ g sin θ . In order to maintain a constant flow rate through the core sample. Eq. . • Incompressible fluid. some important conditions have to be satisfied before permeability could be estimated from the measured data. Permeability in core samples is measured in the laboratory using Darcy’s law for horizontal flow. gives k k q + A ρ g sin θ ∆l = A ∆p. i. 0 ≤ θ < 90o ⇒ ∆p ≥ ∆p0 −90o < θ < 0 ⇒ ∆p < ∆p0 . • Laminar flow current (satisfied in most liquid flow cases). The flow equation becomes. ∆p = µ ∆l q + ρ g∆l sin θ . In a up-dip situation. the pressure difference has to be larger relative to the horizontal case.4 it’s evident that z = l sin θ .4. i. These conditions are the following: • Horizontal flow. as in Fig.

from which the permeability can be calculated using Eq. . The linear best fit through all experimental data-points will give a slope. By convention the unit for the permeability is called theDarcy. which may reveal non-linear effects in the data. There are two systems of units which are widely used in petroleum field engineering. e. L2 . large spread in data around the linear fit. permeability is found by integrating the linear flow equation where the permeability is experimentally determined using the formula.5. e. a = Ak / µ∆ l ∆p Figure 5.5.5: Experimental determination of liquid permeability.4 Units of Permeability 69 q slope. The following definition of the Darcy has been accepted: The permeability is 1 Darcy if a fluid with viscosity of 1cp is flowing at a rate of 1 cm3 /s through a porous medium with a cross-section of 1cm2 . µ ∆l (5. s 1cp 1cm where the Darcy-units are preferably used in connection with laboratory tests. It is not convenient to measure permeability of porous media in cm2 or in m2 .g. q= Ak ∆p. creating a pressure difference of 1 atm/cm. • Field units. Permeability is found by plotting the measured data as shown in Fig. (5.g. shows that permeability has the dimension of surface area. 5. at high or low flow rates. 5. Having satisfied all the above conditions. we get the following equality: 1 cm3 1D 1atm = −1cm2 − . • SI units (international system of units).4 Units of Permeability Dimensional analysis applied to the Darcy’s law. (5. The importance of linear representation of the measured data is the advantage of visual inspection. or uncertainty in laboratory measurements. Applying Darcy-units to Eq.7) where the flow rate q and the pressure difference ∆p are the measured data.7) [54].4).

s kg . The core is saturated with water and then flushed horizontally. ms q = 10−6 µ = 1 cp = 10−3 dp Pa kg atm = 1 = 1.987 µ m2 . 5.987 · 10−12 m2 = 0. normal to the bedding of formations) is usually much lower in comparison than the horizontal permeability (measured along the bedding of formations).0 0. Permeability The value 1 Darcy is defined in SI-units by substitution: m3 .01 · 105 = 1. or more directly.e. is measured for three different flow-rates and permeability is calculated using the above formula.2 0. Example: Core sample liquid permeability.987µ m2 . 1 D = 0. In its turn.101 .5 0.106 3. which means that permeability might have different values in different directions. A ∆p where A = π (d/2)2 and d is the core sample diameter. These permeability features should be taken into account while measuring permeability.0 7. it’s diameter is 5 cm and the water viscosity is 1.0 76.0 cp. The permeability might be determined by plotting the data in a "rate/pressure" diagram. which then is called millidarcy (mD). The core length is 15 cm. A · d p/dl Here: µ m2 = (µ m)2 . the 1/1000 fraction is used. Vertical permeability (i. A cylindrical core sample is properly cleaned and all remains of hydrocarbons are removed from the pore space. qw [cm3 /s] ∆p [atm] k [D] 1.093 10. k= µ ∆l q .70 Chapter 5.5. The pressure drop ∆p.01 · 107 2 2 and dl cm cm m s −4 2 A = 10 m qµ k = = 0.0 24. It is important to remember that permeability is a tensor. It follows from these evaluations that. using the formula. the horizontal permeability can be different in different directions. by calculating the permeability value for each data-pair. as shown in Fig. Instead of the unit 1 Darcy.

one finally obtains.g. . Because gas is a highly compressible substance. (5. Laboratory measurements.5 Gas Permeability Measurements 71 The average or representative permeability is k = 0. This uncertainty could be examined by plotting the data-pairs in an appropriate way.1 D or 100 mD. the pressure at normal or standard conditions. Taking into account the invariant quantity. p0 p0 which when substituted into the previous equation equation yields. for instance. q0 = A (5. the Darcy’s law may not be utilised directly. as shown in Fig.11) . e. qρ = −A kρ d p . one can write. qρ = −A k ρ0 p d p . µ dx where ρ is the density of the gas at certain pressure. q0 = −A or integrated from p1 to p2 .10) Another useful form in which Eq. µ p0 dx (5. q0 = A kp d p .5 Gas Permeability Measurements Due to certain interactions between the liquids and the porous rock.e. 5. The advantage of data-plotting. i. 2µ p0 ∆l k p ∆p . µ po ∆l (5.10) can be written is. compared to straight forward calculations. 5. qρ = q0 ρ0 . always contain uncertainty related to the technology used to obtain the lab-data. the gas rate is pressure dependent. absolute permeability is routinely measured in the laboratory by flowing gas (usually inert gas) through the core sample. ρ (p) = ρ (p0 ) ρ0 p. µ p0 dx (5.5.9) k p2 − p2 1 2 . Considering mass flow of gasqρ . as in this example. It follows from the perfect gas law (pV = nRT ) that.8) Here the subscript "0" refers to a certain pressure value. or simply ρ = p.5. is the opportunity to verify that the data used in the averaging process are "good" or representative .

For permeability measurements in the vertical direction gas is injected through the core plug in the axial direction (see Fig. Low pressure air is introduced into the center of the holder and passes through the rubber boot and intersects with the screen. 1991). The core plug is placed in an impermeable rubber sleeve protecting the gas flow at the outer-face of the core plug. 5. ρ p = ρ p with Eq. The screen are selected to cover designated outer segments of the full diameter sample. Combining the invariant mass flow. qρ = qρ and the results generated from the perfect gas law. left). Metal plug Screen Core sample Low air pressure High air pressure Screen To flow Low air meter pressure Rubber disk To flow meter Flow directions High air pressure Rubber tubing Figure 5. and the cross-sectional area of flow is a function of the length and diameter of the core sample.6.11). 5. It is common to furnish two horizontal permeability measurements on all full diameter samples. (5.6.72 Chapter 5. µ ∆l q = −A (5. right). and then flows vertically through the screen. where the screen again allows free flow of the air to exit. . except for the fact that the flow rate is the mean flow rate. The area of cylindrical surface at the inflow and outflow openings is covered with a screen and the sample is then placed into the core holder.12) where q is the mean or average flow rate. one obtains. Under high air pressure the rubber tubing is collapsed around the core. the mean flow rate is equal to the gas rate at the centre of the core sample. Eq. Horizontal permeability measurements require a sealing of the top surfaces of the core with non-permeable rubber disks (see Fig. In a homogeneous porous rock. The air then flows through the full diameter sample along its full height and emerges on the opposite side.6: Full diameter vertical and horizontal permeability measurement apparatus (from IHRDC. Permeability where p = (p1 + p2 )/2 is a mean (average) pressure in the core during the measurements. (5.12) has exactly the same form as Darcy’s law for horizontal liquid flow. The Hassler core holder is commonly used for permeability measurements. In this test the flow length is actually a function of the core diameter. The second measurement is made at the right angles to the first. In most cases the circumference of the core is divided into four equal quadrants. It provides measurements of permeability in both vertical and horizontal directions. k ∆p .

As the mean pressure in the core sample increases it is expected that the gas permeability will approach the absolute (liquid) permeability.e.4 0.066 1.00 ∆p [atm. The gas permeability k is found as a function of the mean core pressure. while the gas rate.2 0.7: Gas permeability plotted as the reciprocal of mean pressure. the mean pressure in the core sample.] 0. ∆p. at atmospheric pressure. q2 is measured at the other end. is more than 1000 bar. will start to behave as a liquid. Note that the gas permeability is pressure dependent.133 0.3 5. are calculated from the equation above.g.00 k [mD] 6. p2 = 1atm.] 1.8 6.6. 2µ p2 ∆l Given the pressure p1 and the gas rate q2 .667 2. of the type seen in Fig. The core has been cleaned and dried and mounted in a Hassler core holder. written as follows.10).33 2. p and the pressure drop across the core. The gas permeability could be estimated using Eq..8 p [atm. at one end of the core sample.5.5 Gas Permeability Measurements 73 Example: Core sample gas permeability. The gas is injected and the pressure. The following data is given: p1 [mmHg] 861 1276 2280 q2 [cm3 /min] 6. (5. 1in in diameter and length.4 35. q2 = A k p2 − p2 1 2 .6 0.) .(This asymptotic limit is not reached unless the pressure. i. p1 measured.8 1 Reciprocal pressure: 1/p m [1/atm. in air.6 132. A gas permeability test has been carried out on a core sample.] Figure 5. 5. since at such high pressure the gas itself.0 7 6 Permeability: k [mD] 5 4 3 2 0 0. e.

13) ρ F ∆x where R is the tube radius. roughness.14) ∆xµ p0 q0 k Aµ p Eq. one gets.5.14). the horizontal flow equation can be expanded by adding a term particularly describing the turbulent flow situation.0 mD. R ∆p . when 1/p → 0. ρ is the gas density and F is the Fanning friction factor characterising the tube (i.14) is a linear equation where 1/k is the constant term. 2 and 3.74 Chapter 5. (5. (5. Since p = (p1 + p2 )/2 and ∆p = (p1 − p2 ). For this purpose the Fanning Eq. are both functions of p1 . = + ∆x µ q k Aµ In an experimental situation one normally do not know the average core rateq. (5.5.e. q0 . 1.7. is used describing turbulent flow in a circular tube [7]. preferably in the larger pores and pore channels. p Substituting for average gas rate in the horizontal flow equation one gets an equation particularly adapted for experimental application. wetting. taken from the table is plotted and the absolute permeability is found kliquid = 3. turbulent flow may be experienced in parts of the pore system. special care has to be taken to how data is plotted. v = q/A and rearranging the above equation somewhat. p0 q = q0 . According to the Fanning equation one may assume that pressure drop across a pore channel is proportional to the square of the average gas velocity in the pore. v2 = The horizontal flow equation. Assuming there are three sets of data. A ∆pp 1 β p0 q0 = + .). In order to use Eq. Recall from above the relation. Considering the average gas flow velocity. In order to adjust for the occurance of turbulence. (5. ∆p A 1 1 β q. all together nine measurements. 5. Permeability The absolute gas permeability of the core sample is therefore found as the asymptotic value of permeability. (5. Instead the gas rate is measured at the exhaust end. when p → ∞ or more conveniently. For each set there are three measurements. set a. etc. including a turbulent term can be written as. b and c. ∆p µ = v + β v2 . ∆x k where v is the average or mean flow velocity and β is the turbulent constant . .1 Turbulent Gas Flow in a Core Sample When gas permeability in core samples are measured. one of them has to be kept fixed when producing linear plots.13). as seen in Fig. . The data.

5 Gas Permeability Measurements 75 pa pa pa pb pb pb pc pc pc ∆pa.1 q0. A ∆ppm ∆xνp0 q0 pmc pmb pma 1/kc 1/kb 1/ka q0 /pm Figure 5.a. 5. where data having the same average core pressure are plotted together in the first step.2 q0.1 ∆pc.b. kb and kc are now plotted.3 For each data set. a.8. permeabilities are plotted as functions of the inverse average pressure.8: Plotting linear data where the average pressure p = pm is kept constant.9: Absolute permeability as function of inverse average pressure.3 q0.3 ∆pc. gas permeability is found using a step like plotting process.9.3 q0.14).3 ∆pb.c.1 ∆pa.1 ∆pb. as shown in the Fig. . Secondly.D ka kc kb kL 1/pm Figure 5.b.3 q0. (5. p = pm When turbulence is considered.2 ∆pc. in accordance with the linear Eq. ka .1 q0.2 q0. The three permeability values found form Fig. k. 5.2 ∆pb.b.2 ∆pa. 5.1 q0.5.c.2 q0.8. b and c.a.a. a straight line is plotted through the measured data points and the constant 1/k is evaluated. as shown in the Fig. from where the absolute (liquid) permeability is found.c.

in combination with small (diameter) pore channels.e. (5.11). due to some interaction between the fluid and the porous medium. Since the permeability is introduced as a proportional coefficient in Darcy’s law. at a constant pressure difference.1 The Klinkenberg Effect It has been observed that at low average pressures. as presented in Eqs. yield a increased flow velocity or flow rate. k= qo µ po ∆l . this condition is broken. measurements of gas permeability give erroneously high results. The permeability . Klinkenberg found that the gas permeability of a core sample varied with both the type of gas used in the measurements and the average pressure p. Extrapolation of this line to infinite mean pressure. Permeability measurements are also (sometimes strongly) affected by the fluid. (5. i. used in laboratory tests.g.76 Chapter 5. At higher pressures. These facts should be considered when permeability from laboratory measurements is related to reservoir permeability.6.11). is the requirement of laminar flow. carbon-dioxide and air) are often used for permeability measurements. gives the absolute (liquid) permeability. that the fluid behaves "classically" with respect to intermolecular interactions in the gas. gas molecules are often so far apart. i. the gas molecules are closer together and interact more strongly as molecules in a liquid. A p ∆p (5. in the core. nitrogen. This effect is known as the gas slippage effect or as the Klinkenberg effect. since gas permeability is pressure dependent. qKlinkenberg > qlaminar .e. To avoid this effect. i. such as turbulent flow behaviour. experiments have shown that the permeability is even more dependent on the overburden pressure than the porosity. gases (helium. At low p. theKlinkenberg effect. that they slip through the pore channels almost without interactions (no friction loss) and hence. when 1/p → 0. Permeability 5. investigated by Klinkenberg in 1941. the Klinkenberg dominated flow will yield a higher gas rate than laminar flow. increased uncertainty in gas rate measurements and at low pressure.15) where the latter statement means that different average core pressures p. Compared to laminar flow. 5. it is evident that other characteristics than the porous medium have important influence on the numeric value of the permeability. as compared to the non-reactive liquid permeability measurements (absolute permeability). Experiments show that when gas permeability is plotted versus the reciprocal average pressure p. a straight line can be fitted through the data points.6 Factors Affecting Permeability Values General considerations show that permeability is a characteristic parameter describing flow behaviour in porous media. e. provide different values of the rock permeability to gas. that the rock permeability to gas is not the same as for liquids. It follows from Eq. At low gas pressure. k = k(p).e. In the case of overburden pressure. The use of gases introduce other problems.7) or (5. One of the conditions for the validity of Darcy’s law.

5.0 950. .0 Figure 5. or by using the following correlation’s. In early core analysis the Klinkenberg permeability was estimated by using a steady-state technique for permeability measurements. value at 1/p → 0 is comparable to the permeability obtained if the core were saturated with a non-reactive liquid (see Fig. mD 6. at different mean pressures p. using Poiseuille’s law for tube flow.and the absolute (liquid) permeability.0 10. 5. 5.0 0.10).0 100. as seen for the table below.16) where km and kL are the measured.10. [mD] 0. For such a system.8 88.6 Factors Affecting Permeability Values 77 8.4 1. p (5. properties of the rock (Fig.0 2.2 Reciprocal Mean Pressure. kL 0. Corrections to measured gas permeability due to the Klinkenberg effect are normally moderate to small corrections. km = kL 1 + b . 1/bar 2.0 Gas Permeability. Non-corrected permeability.7 7. The parameter b depends on the type of gas used and reflects. [mD] 1.0 Klinkenberg corrected permeability. it is shown that the permeability can be written. respectively. Example: Onset of the Klinkenberg effect The onset of the Klinkenberg effect is considered in a system comprised of a bundle of identical capillary tubes.8 0.0 4.0 0.0 He N2 CO2 Liquid or absolute permeability.0 1000. to some extent. the pressure will be much higher and consequently the significance of the Klinkenberg effect of no importance.10: Klinkenberg permeability determination.0 In most laboratory measurements of gas permeability.6 1. In reservoirs. it is safe to neglect the Klinkenberg effect if the gas pressure is higher than 10 bar.

(5. the mean free paths of their molecules at standard conditions (room temperature and atmospheric pressure) are in the range: 0. Irrespective of the fact that a bundle of cylindrical tubes is far from being a realistic model of a porous medium. At higher pressures. for permeabilities less thankHe = 0. r = λHe /2. there is a maximum permeability limit.17).18 · 10−6 m at atmospheric pressure and temperature of 20o C [59]. Helium has a mean free path.8 mD. the expected mean free paths are shorter and consequently the permeability limits are lower than in theHe case.06 µ m. as above. the Klinkenberg effect would be active at standard conditions in a "porous" medium. As an example helium gas might be chosen in the flow experiment.17) where r is the individual tube radius. 4 8 (5. λ < λHe . i. For many gases. kHe = .e. (5. lower mean free paths are observed. Substituting the helium mean free path for the diameter of the tube radius in Eq. π (λHe /2)2 . In an experiment where N2 or CO2 is used. one can estimate the permeability at which the Klinkenberg effect starts to become a significant effect. below which the Klinkenberg effect becomes active. λHe = 0.1 µ m. Permeability k= π r2 . whereas the mean free paths of CO2 and N2 are respectively 0. . it follows.04 µ m and 0.78 Chapter 5. Since the Klinkenberg effect is said to become important when the mean free path of the gas and the size (diameter) of the pore channels are comparable.18) 4 8 Using helium gas.01 to 0.

q:[cm3 /s]. as shown in the figure below. µ ∆L where. µ :[cp].[cp]. is equal to 1. A:[ f t 2 ]. Assuming a tube radius equal to r and that the fluid flow velocity through the tubes. k:[mD]. k:[Darcy]. q=A k ∆p . r R ∆l ∆l 4. q:[bbl/d].. 2. . pe [atm] pw [atm] rw [cm] re [cm] h [cm] Pressure at the outer boundary Pressure in the well Well radius Radius at the outer boundary Reservoir height Use Darcy’s law to derive a general equation for a cylindrical reservoir in the cases of horizontal flow. Convert this equation to "Oil Field Units" where.7 Exercises 79 5. where R r. Prove that the numeric constant for converting dyn/cm2 to atm. r2 ∆p v= . Darcy’s law is given. The cylindrical pore model consists of cylindrical tubes stacked on top of each other.0133×106 . a) incompressible fluid and b) ideal gas.7 Exercises 1. c) Consider the average permeability of a serial coupling of two tubes with tube radius R and r. 3. Find an expression for the average permeability and evaluate the consequences of relative increase/decrease in the pore radius. 8µ ∆l a) Calculate the porosity of the cylindrical pore model φ . L:[cm] and p:[atm]. when we have. L:[ft] and p:[psi]. b) Show that the permeability is written as k = φ r2 /8. A:[cm2 ]. µ . A reservoir has cylindrical geometry where the following parameters are defined.5. is given by Poiseuilles equation.

Show that the average permeability k for n horizontal layers. given the following data: rw k pe = = = 6 in. 20 psig. is given by the formula [8] (see Figure below). 175 BOPD. Calculate the well pressure. in two ways. qb and pb is the flow rate and back pressure.pressure ) 7. 10 ft. stacked on top of each other (in parallel). 5000 psia. for a cylindrical core sample where the following data is given. Linear flow in horizontal layers. 13 psia.) Length Diameter qb pb 3. without detecting the Klinkenberg effect. 75 cm3 /s.0185 cP. q k1 k2 k3 h1 h2 h3 q 9. using N2 . (Use the equation for gas rate at the effluent end qo and the equation for the average gas rate q. Permeability 5. p1 p2 Atm.5 in. Use the laws of Darcy and Poiseuilles to estimate the lowest measurable permeability of a sandstone core sample. in percentage of the total pressure difference in the reservoir? ¯ 8. Calculate the pressure in the reservoir at a distance 5 ft from the well.0 in. The measurements are done under laboratory conditions. 1. n kh ¯ ∑ j=1 j j . respectively. 14. 75 mD. where the following data is given: . 0. BOPD is short for "Barrel of Oil Produced per Day". Calculate the total flow rate in f t 3 /d at the pressure pb for gas flow through parallel layers. k= n ∑ j=1 h j where k j and h j are the permeability and thickness of the layers. µ h q = = = 5 cP. Calculate the air permeability. (NB: p psia = p psig + patm. An oil well is producing from a cylindrical reservoir with a drainage area of 20 acres. What is the pressure drop from the well to this position.80 Chapter 5. 6. Verify that the two approaches used above give the same answer.65 psia. pressure µ 55 psig.

10 ft. 12. 500 psig. 20 ft. 5 cp. 200 mD. 150 mD. 200 ft. Linear and horizontal flow through linear beds in series.0185cp. 100 ft. length k1 k2 k3 400 ft. 400 psig. Are the formulas above valid both for gas. 15. k n ∑ j=1 L j /k j where L j is the length of the media in the direction of flow. q k1 k2 k3 q L1 L2 L3 L 11. patm.0 psia. An oil well has a intermediate zone with reduced reservoir permeability k1 . respectively. n L ¯ = ∑ j=1 j . 330 ft. Gas viscosity µg = 0. height k1 k2 k3 50 ft. (Notice: p psia = p psig + patm. Calculate the pressure at the outer boundary pe when the oil rate is 100 bbl/d and the following data is given: rw r1 k3 6 in.5. 200 ft. 400 mD. µo pin pout patm. ) 10. 100 psig.65 psia. pin pout pb 15. 4 ft. Radial and horizontal flow through cylindrical layers.and liquid flow? 13. pw µo h 2000 psia. . 2 ft. Calculate the total oil rate bbl/d through all media. 14. Show that the average permeability of rectangular porous media coupled in series is given by the formula [8] (see Figure below). k j is permeability to the layer with outer radius r j . 10 cP.7 Exercises 81 width h1 h2 h3 200 ft. n ln(r j /r j−1 )/k j ∑ j=1 where re and rw is the radius to the outer boundary of the reservoir and the well radius. k1 k2 50 mD. 50 psig. 50 mD.0 psia. 100 mD. 200 mD. 200 mD. ¯ k= ln(re /rw ) . 6 ft. when the following data is given: width L1 L2 L3 100 ft. Show that the average permeability for n radial layers in a cylindrical reservoir is given by the formula [8] (see Figure below).

evenly distributed over the surface. 2272 psi. 6. Calculate the absolute permeability of the sample when the air–water surface uses 400 seconds to move 18 cm. 7. 13. 11. 1 D.1 mD. π /4. Water 100 cm Core sample 82 cm 2 cm q Additional data. 0.82 Chapter 5. and the air-water surface is monitored as function of time. 4710 bbl/d. 14.1 D. Density of water Water viscosity Gravitational constant Thickness of core sample Answers to questions: 3. Permeability What is the pressure at outside the damaged zone (r1 ) ? 14. 1 g/cm3 1 cp 980 cm/s2 2 cm . The tube is placed in a vertical position and the water is assumed to flow through the whole core sample. 0.57 · 106 f t 3 /d. The core sample is mounted in a transparent cylindrical tube. 288 atm. 262 atm. Absolute permeability of a core sample is being measured by water flooding. 9. as shown in the figure below. 1. 5.

on average. In such complicated systems.2 Surface and Interfacial Tension An interface is known as the boundary region between two adjacent bulk phases. water/rock and. the interface oil/water.1 Introduction The exploitation of hydrocarbons is a complex process of controlling interactions in systems involving crude oil. as seen in Fig.) Any surface that is in the state of lateral tension. in combination. 6. The equilibrium bulk phases can be: • Liquid-vapor (LV). Due to the great significance of the surface/interfacial tension. If two fluids. can be related to the work or energy required to establish the surface area. (Gases are basically miscible and thus. • Liquid-solid (LS). water. several experimental methods have been developed in order to measure this physical property. the molecules attached to the oil-water interface do necessarily have less kinetic energy than the bulk molecules. The surface tension. Some of the most commonly used techniques are reviewed. due to the constraint put on them by the interface. A central property. The molecules on or close to the interface may not move with the same degree of freedom and speed. gas and rock formations. • Solid-vapor (SV). • Liquid-liquid (LL).Chapter 6 Wettability and Capillary Pressure 6.1. no interfacial tension is observed between gases. the interaction between wettability and surface tension is revealed. when giving an overall picture of the interfacial conditions. is the surface or interfacial tension (or more correctly the surface or interfacial energy). For curved interfaces. Since the total energy of 83 . This property is very sensitive to chemical changes at the interface. leads to the concept ofsurface tension. the definition is similar but slightly more complex. denoted by σ . it is important to recognise the effect of the surface properties of oil/rock. In this chapter. say water and oil is forming an interface. 6.

e. Wettability and Capillary Pressure the molecules is mainly a function of temperature.1) Here G is the Gibbs free energy and A is the surface area. the greater is the work needed to bring bulk molecules to the surface. a molecule at a surface is in a state of higher potential energy than a bulk molecule. The evaluation of reservoir wettability can be made through measurements of interfacial tensions.e. In Table 6. σ= ∂G ∂A .ni (6. that what is called surface or interface tension is in fact surface or interface energy and quite often it is more advantageous to use the energy perspective than it is to deal with tension and forces. the surface area of a system is always minimised. Since a proportionality exist between surface area and potential energy of the system of molecules and since equilibrium is reached at minimum potential energy (actually minimum Gibbs energy). J/m2 or more commonly N/m.3 Rock Wettability Laboratory experiments have proved that rock wettability affects oil displacement. i. The unit of surface tension is therefore. area. tensions acting at the fluid-fluid and rock-fluid interfaces. the following expression for surface tension may be written.. i.84 Chapter 6. the potential energy of molecules attached to the interface is greater than the potential energy of the bulk molecules. due to anisotropy and intermolecular interactions. Note that wettability itself is a microscopic characteristic. to increase the surface area of the system. the unit of energy pr. The stronger the intermolecular attractions in the liquid.1: Molecular motion in bulk and close to the oil-water interface.p.. pressure and amount of material in the system constant. The surface tension between a pure liquid and its vapour phase is usually in the range of 10 to 80 mN/m.and interfacial tensions are listed. oil water Figure 6.1 some typical values for surface .e.. and thecontact angle. the larger is the interfacial tension σ . This means that energy is required to move a molecule from the interior to the surface of a phase.. i. Note. Generally speaking. T. The term wettability can be defined as "the tendency of one fluid to spread or to adhere to a solid surface in the presence of other immiscible fluids" [29]. i.e. Keeping the temperature. 6. . that has to be measured by using micro-scale laboratory investigation techniques.

P θ σ (dynes/cm) 30 48 72 (50) 4 480 30 30 0 0 0 140 The degree of wettability exhibited.1: Surface tension. The differences in contact angle somehow indicate different wettability preferences which .5 28. particularly chamosite. through the fluid whose wettability is studied or through the fluid which is wetting the solid surface.0 σLW (mN/m) – 51. and on the nature of the pore wall. P Laboratory. by convention. T.2: Fluid pair wettability under reservoir and laboratory conditions.2. of the immiscible pair. may promote oil wet character.9 28. depends both on the chemical compositions of the fluid pair. T.e. σLW for some liquids at temperature.7 52. Note: Surface tension σLV . T. is here defined as the interfacial tension between a liquid and its vapor. T. Pure quartz sandstone or calcite surfaces are likely to be wetted preferentially by water.7 35. A table of typical fluid pairs of interest in reservoir engineering is shown in the Table 6. and the fluid which spreads more is said to be the wetting phase fluid. Contact angles are measured. water.0 The angle θ is influenced by the tendency of one of the fluids. P Reservoir. to spread on the pore wall surface in preference to the other (oil).9 476. particularly the asphaltine content of the oil. Liquid Water n-octane n-dodecane n-hexadecane dichoromethane benzene mercury σLV (mN/m) 72. System Wetting Non-wetting phase phase Brine Brine Brine Brine Oil Gas Oil Oil Gas Gas Gas Mercury Conditions T = temperature P = pressure Reservoir.0 375.7 25. i. T = 293o K.9 53. P Laboratory. The qualitative recognition of preferred spread is called a wettability preference.3 Rock Wettability 85 Table 6. T. T. The presence of certain authigenic clays. σLV and interfacial tension to water. P Laboratory. Table 6.8 27. together with contact angles and interfacial tensions [8].4 27. P Reservoir.8 21.6.

6. Table 6. r Oil h R θ Water θ Rock Figure 6.4 Contact Angle and Interfacial Tension With two immisible fluids (oil and water) present in the reservoir. . surrounded by oil. and in order to reveal the relationship between them a "gedanken" experiment is carried out on a droplet of water. 6.86 Chapter 6. there are three interfacial tension parameters to be assessed.3 and in Fig. Contact angle values 0 – 30 30 – 90 90 90 – 150 150 – 180 Wettability preference Strongly water wet Preferentially water wet Neutral wettability Preferentially oil wet Strongly oil wet o o w s θ=0 w s θ = 90 o w s θ ~ 180 Figure 6.3.3: Wettability preference expressed by contact angle. placed in a contact with a water-wet reservoir rock.3: Geometry of the water droplet in oil. σos .2 [19]. Wettability and Capillary Pressure can be illustrated by the following rule of thumb presented in Table 6. placed in a contact with a water-wet reservoir rock. σws and σwo . 6. The three interfacial tension are not independent parameters. The following definitions will be used: • surface tension between the oil and solid.2: Example of wetting preference. σos . as seen in Fig.

6.4) . 2rh dr. A small deformation of the surface area. which is known as the Young-Dupre equation [15]. θ .4 Contact Angle and Interfacial Tension 87 • surface tension between the water and solid. (6. (6.3). • contact angle at the oil-water-solid interface measured through the water. As = π r 2 Aw = π (r2 + h2 ) Vw = π6h (3r2 + h2 ) Incompressible liquids give. (6. • surface area of the water droplet. The deformation is described by the equilibrium equation. σow . σws dAs + (−σos dAs ) + σow dAd = 0 Elaborating on Eq. ∂r ∂h σws − σos + σow 1 − and taking into account that (see Fig. Eq.2) ∂ Vw ∂ Vw dr + dh = 0.As . 6. dVw = which leads to dh = − Using these results. • interfacial tension between the oil and water phases. 2h2 h2 + r2 ) = cos θ . σos − σws = σow cos θ . the following relationships are valid (see also Fig.3) R sin θ = r R cos θ = R − h and (1 − a final result is obtained. The water droplet is assumed to be in equilibrium with the surrounding medium. expressing the change in energy due to the change in area.3).6. • area of the reservoir rock occupied by the water droplet. Ad .2). h2 + r2 ⇒ ⇒ dAs = 2π rdr dAw = 2π (rdr + hdh) (6.2) is rewritten. 2h2 h2 + r2 = 0. (6. σws . will deform the droplet slightly and force the droplet to expand on the solid surface.

i.e. one we successively obtain. Normally. a curved surface is characterised by two radii of curvature.4: Pressure difference across a curved (spherical) interface.5 Capillary Pressure Capillary pressure may be defined as the pressure difference across a curved interface between two immiscible fluids. the droplet takes the form of a perfect sphere. ** Pw Po Water Oil Figure 6. the capillary pressure can be obtained by the following evaluation: r ∼ 1µ m and σow = 0. If the droplet is small. is described by an equation taking into account the energy change due to the volume and the surface change. where Pc is defined as the pressure difference between the non. Pc = σow dA dA = σow dV dr dV dr −1 = σow 8π r 2 = σow .4.R1 and R2 . 6. .5. Substituting definition of the capillary pressure pc . The equilibrium condition is ecpressed as the change in potential and surface energy. one may assume the interfacial tension to be far more important than the gravitational force acting on the droplet and thus. a small reduction of the sphere volume. the Pc term is positive for unconfined immiscible fluid pairs. Wettability and Capillary Pressure 6. Taking typical values of a pore radius and an interfacial tension of oil and water. since this is the energy needed to form a droplet that can pass through a porous channel . A small perturbation. in the latter equation.1 Capillary Pressure Across Curved Surfaces For two immiscible liquids as part of a real physical system.025 N ⇒ Pc m N = 0. since the surface area is minimised. By convention. 2 4π r r Capillary pressure can be of significant magnitude. Using an example with an oil drop floating in water where the density of oil and water are assumed similar.wetting and the wetting phase.5 bar m2 ·104 6.5. as seen in Fig 6. pw dV + σow dA = po dV. a spherical interface is an odd observation. Pc = po − pw .88 Chapter 6. as seen in Fig. the capillary pressure is written.

which can be expressed by Eq. a potential energy equal to about 0. .5: Curved surface and radii of curvature.073 mN/m? The energy in question. when the surface tension of water to vapor is 0. Example: Surface tension and surface energy The process of displacing water through a porous medium is comparable to the formation of droplets of sizes equal to the capillary pore throats.5 Capillary Pressure 89 R2 R1 Figure 6. the interface will show a net curvature with the larger pressure on the concave side. + R1 R2 (6. Since the increased area ∆A is directly proportional to the increase in potential energy ∆E p . What is then the energy needed to transform 1 cm3 of pure water to droplets with an average radius of 1 µ m. ∆E p = σair. The area increase is. Ad and volume . ∆A = N · Ad − A = V 3 Ad − A = V − A. of the initial volume V to N number of droplets with area. r If the initial water area is considered to be small (or negligible) to the area of the droplets. The relationship between the pressure difference ∆p = Pc and the curvature is given by Laplace equation. With a pressure difference across the interface in the two phases.6.w ∆A = σair. For a spherical droplet R1 = R2 = r and ∆p = 2σ /r. Across a planar interface/surface R1 = R2 = ∞ and ∆p = 0. 4π r2 and (4/3)π r3 .1). is the energy needed to increase the initial water surface A. Vd r where the droplet area and volume are respectively.22J is found. (6.w 3 V −A .Vd .5) where R1 and R2 are the principal radii of curvature and σ is the interfacial tension. Pc = σ 1 1 .

The surface against the second type of molecules is minimised and in the case of small droplets. σ < 0. We may observe a chemical reaction where the final state is stable in time. the interfacial tension and the radius in a cylindrical tube. two immiscible fluids (oil + water) are confined in a cylindrical capillary of radiusrc .6: Formation of interface as function of the sign of the interfacial tension in pairs of immicsible unconfined fluids. molecules of one type will prefer (have affinity for) the company of the second type of molecules. Wettability and Capillary Pressure . Using the Eq. 6. a curved interface is formed in the capillary tube. • When the surface tension is positive.5.2 Interfacial Tension Assuming pairs of immicsible unconfined fluids the following phenomena.5. depending on the sign of interfacial tension: σ>0 σ~0 σ<0 Figure 6.5) for the pressure difference between the two sides of the interface. In these cases no preference with respect to mixing of the two fluids is observed. 6.90 Chapter 6.) • When the surface tension is negative. have a preference for keeping their own company. 6. diffusion will lead to mixing of the two fluids. To reveal the relation between the capillary pressure. .3 Capillary Pressure in a Cylindrical Tube When a non-wetting fluid is displacing a wetting fluid. as illustrated in Fig.7. spherical interfaces are formed. 6. confined molecules. (6. An example of such a process is the hydrophilic ability of pure ethanol to mix with air more or less instantaneously. σ > 0. as shown in Fig. • In the cases when σ ≈ 0. liquids are classified as "truely" miscible.6 can be observed. as is the case when oil is displacing water in a water-wet porous rock. (However.

6. + R1 R2 where R1 and R2 are main radii of the curvature. Example: Oil .and capillary forces. the process by which oil displaces water in a cylindrical tube is considered in analogy with the production of oil from a water-wet reservoir where oil is forced through capillary pores which initially contained water. In this example. The pressure drop along the cylindrical tube is partly the viscous pressure drop ∆po + ∆pw . Pc = po − pw = σow 1 1 + R1 R2 = 2σow · cos θc . r q [µo x + µw (L − x)] .water displacement in a capillary tube Displacement processes in porous media are very often a competition between viscous.6) rc .8 where the oil front has reached a position x in to the cylinder (pore). in the oil.6. cos θc where Eq. (6. rc (6. Ak Pc = .5 Capillary Pressure 91 θc rc Water θc R Oil Figure 6. expressing the radius of the interfacial surface R by means of the contact angle θc and the capillary radius rc in the cylindrical tube. as sketch in Fig. po − pw = σow 1 1 . When R1 = R2 = R and R= the capillary pressure is written. Consider a dynamical situation.7: Idealised model of a pore channel filled with two immiscible fluids forming a curved interface between them.and water zone and partly the capillary pressure drop. Pc across the oil-water interface: ∆pV = ∆po + ∆pw = 2σow cos θ .6) is the capillary pressure in a cylindrical tube of radiusr.

capillary forces are totally predominant and that viscous forces play a minor role when microscopic flow pattern is considered. Wettability and Capillary Pressure ∆po ∆pc ∆pw Oil 0 x Water L Figure 6. where A and v is respectively the cross-section area and the pore velocity. Pc σow cos θ r σow cos θ r In the equation above. a set of "typical values" could be chosen and the average pore velocity is found. ∆pv /Pc ∼ 1. it is obvious (even when the appropriate bulk velocity u = v pore /(φ (1 − Sr ) cos2 α ) is taken into account) that under reservoir flow conditions. describes the competition between the viscous.8: Cross-section view of a cylindrical "pore channel". which is equal to 3.  ∆pV /Pc = 1     θ = 60o  L/r = 5 v pore ≈ 1. In analogy with the definition of Reynolds number.and the capillary force. the relation vµ /(σ · cos θ ) is the only term containing dynamical parameters.e.   µo ≈ µw = 1 mPa · s    σow = 50 mN/m Reservoir flow is commonly considered to be of the order of 1 foot pr. The strength between the two forces is considered by simply comparing their pressure drops.5 · 10−5 (using the numbers above). . ∆pV vµo x vµw L − x =4 + . a dimension-less number could be defined. and r is the tube radius. σ cos θ The Capillary number Nc .92 Chapter 6. Nc = vµ . This means that the capillary forces alone decide which pore channels are going to be swept and which are not. in the reservoir. The Capillary number for reservoir flow becomes Nc = 1. day. i. while the Capillary number at the "breaking point" when the viscous force becomes equally important to the capillary force is 8· 10−3 .k = r2 /8. From this comparison . The flow rate is q = Av.3 m/s. The permeability of the tube is known as.5 µ m/s. In a situation where the two forces are assumed to be equally important.

Sw and Sw Oil σow Oil θc Water σws Water-wet σow σos σos θc Water σws Oil-wet Figure 6. mentioned above. So = 1 − Sw .6. k. σos . (6.9): • surface tensions. θc . 6. σow · cos θc . • contact angle measured through the water phase.8) A dimensional analysis of Eq.9: Wettability of oil-water-solid system. Pc = f (φ . (6.7) σos − σws = σow · cos θc . • rock permeability.6 Capillary Pressure and Fluid Saturation 93 The capillary number for field water-floods ranges from 10−6 to 10−4 . The task is to define (if possible) a correlation between capillary pressurePc and the parameters. So . . Relying upon the data obtained. the following dependency can be expressed. σow . Laboratory studies have shown that the value of the Capillary number is directly related to the ultimate recovery of oil.8) can be carried out using the following notation for dimensions.6 Capillary Pressure and Fluid Saturation Results from drainage and imbibiation laboratory experiments have shown that the capillary pressure Pc = po − pw is dependent on the following parameters (see Fig. 6. σws and σow . σws . the list of independent parameters is shortened and Eq.7) is written. θc . (6. k. • fluid saturations. φ . k. Pc = f (φ . The Capillary number is generally varied by increasing the flow rate (pore velocity) and/or lowering the interfacial tension. . where an increase in the Capillary number implies an increase in the oil recovery. Sw ) (6. σos . • rock porosity. being responsible for the numeric variation of the capillary pressure in the experiments. Sw ) Since some of the parameters are dependent on others.

Wettability and Capillary Pressure M – mass. a dimension-less parameter F can be composed. [Sw ] = 1 (6. T : −2 = −2β .8) can be rewritten in dimension-less form. Sw ). Sw ). Pc = Pc = σow · cos θc · J(Sw ). [φ ] = 1.. F= √ Pc · k.9). This means that dimension of the capillary pressure can be defined through dimensions of those parameters. σow · cos θc and by making use of this result. . can only appear in correlations where they form a product. i. Eq. the number of independent variable parameters is reduced and an almost exact form of the correlation between the capillary pressure Pc .8). which gives the following dimensions for all the parameters in Eq. (6.94 Chapter 6. [σow · cos θc ] = M · T −2 . the last relation is written in the form. 15]. (6. ⇒ α = −1/2 and β = 1. or using the initial notation. F = F(φ .e. [Pc ] = [k]α · [σow · cos θc ]β . Thus. fluids and rock parameters is obtained.10) · F1 (φ ) · F2 (Sw ) k Thus by using the dimension analysis (the π -theorem) [11]. The following correlation is widely used for reservoir simulation tasks [13.9) Comparing all the parameters of the right-hand side of Eq. k It can be shown that parameters φ and Sw and their functions. which is followed by. Pc = σow · cos θc √ · F(φ . [k] = L2 . it appears that both dimension parameters k and σow have independent dimensions. (k/φ ) (6. M · L−1 · T −2 = L2α · M β · T −2β . and T – time.8): [Pc ] = M · L−1 · T −2 . (6. L : −1 = 2α . Using notation (6. M: 1 = β.11) where J(Sw ) is known as the J-function (after Leverett). L – length. σow · cos θc √ (6.

10: Illustration of imbibition process in an idealised model of porous medium. r + dr) .7 Pore Size Distribution 95 6. where all pore channels have the same type of wettability and. The capillary pressure does also represent the response of interfacial tensions and rock wettability. as shown in Fig. Pc ≥ ∆po (t). Generally. To reveal the relation between the capillary pressure and the microscopic heterogeneity of the reservoir. is the capillary pressure characteristic of the reservoir heterogeneity. Rock Water Oil Figure 6. represented by the 1/r relationship. Hence. i. 6. Let Vi be the pore volume of a single capillary with radiusri and V be the total pore volume of the porous medium considered. as a consequence. that a certain invariant distribution-function χ (r) defines a fraction of pore channels with capillary radii belonging to the interval (r. . which satisfy the condition.6. χ (r) = n(r. V = ∑ Vi .e. the water will invade the pores. It is also assumed. a fixed contact angle θc . r + dr) as. the pressure in the oil phase po . at a certain time only those channels will be filled with water.7 Pore Size Distribution It is obvious that the capillary pressure is strongly affected by the distribution of pore channel sizes. i=1 N Now let us consider a process of imbibition for a strongly water-wet rock initially saturated with oil. N where N is the total number of pore channels.10. It is quite obvious that the water enters only those capillary channels with capillary pressurePc . is high enough to protect the water invading the pore channels. exceeding the difference between the outlet and inlet pressure ∆po (t). the following example is considered: An idealised model of the porous medium consisting of cylindrical capillaries with different radii ri . Assume that at the starting point. Then gradually decreasing the outlet pressure (pressure in the oil phase)..

by using a mercury injection technique. is Vc = V rc 2 0 χ (r)r dr . Wettability and Capillary Pressure or. r . before it is sealed in a mercury pycnometer. A series ofN + 1. it will be shown how data from a mercury drainage experiment could be used to produce a capillary pressure curve and how these data could be used further. substituting Eq. on core samples taken from different elevations in the same well. is recorded inside the pycnometer and the injection volume Vi is read as the pore sample is invaded by more and more mercury. Defining the total pore volume as. it is expected that the capillary pressure curve shape will also vary from layer to layer. Example: Pore size distribution and capillary pressure curve In this example.96 Chapter 6. rc Vc = N 0 χ (r)π r2 ldr. representative pressure measurements pi .6) into the last inequality. the core sample is properly cleaned. The experimental data is as follows: pHg VHg p0 V0 p1 V1 p2 V2 p3 V3 ··· ··· pN VN The capillary pressure Pc . (6. to define the pore size distribution for the core sample tested. rc ≤ 2σow cos θc . the relations between the water saturation Sw . Pc = pHg − pg = 2σ cos θ . is here the pressure difference between the mercury pressure pHg . rc (6. First. ∆po (t) Then the volume of water which has invaded the porous medium can be defined as. ∞ 2 0 χ (r)r dr Sw = Pc = and 2σow · cos θc . ∞ V =N 0 χ (r)π r2 ldr. and the gas pressure in the core sample pg . Since the pore size distribution varies between the different layers in a reservoir. where l is the length of a single pore channel. dried and placed in vacuum for some time.12) which explicitly indicates that microscopic reservoir heterogeneity strongly affects the capillary pressure. This phenomenon is frequently observed in laboratory tests. and the capillary pressure Pc .

one may write. D(r) = 1 dPc . 6. one gets. D(r) = − 1 1 ∂V ∂ S dPc . D(r) = − Pc 1 .0 S1 r1 Pc.1 S2 r2 Pc. gives dPc = ∂ Pc Pc dr = − dr. ∆V dr where ∆V = VN −V0 and dV = Vi −Vi−1 . one gets. The wetting saturation is therefore written.3 ··· ··· ··· 0 rN Pc. Sg r Pc 1 r0 Pc.2 S3 r3 Pc. When Pc (Sg ) is known.7 Pore Size Distribution 97 The gas is the wetting phase since mercury definitely does not wet any core sample. the corresponding capillary pressure Pc (Sg ) is calculated. ∂S 1 =− ∂V ∆V ⇒ ∂V = −∆V. taken from the above tabulated data. respectively.N The pore size distribution D(r) is representing the relative increase in pore volume as function of the pore throat radius. r (∂ Pc /∂ S) Fig. The minus sign "-" is added due to convenience. Sg = 1 − SHg = VN −Vi . dr (∂ Pc /∂ S) Using the definition of the capillary pressure Pc = 2σ cos θ /r. D(r) = − de f 1 dV . . then D(r) can be calculated. ∂S and by substituting in the pore size distribution equation. VN −V0 Based on the data in the table above. using the following steps. ∆V dr ∂ S ∂ Pc Remembering the definition of the wetting phase saturation Sg = (VN −V )/(VN −V0 ).6. 1. the following parameters are calculated. For a certain gas saturation Sg . ∂r r Substituting this last expression into the pore size distribution.11 shows the two curves for the capillary pressure and the pore size distribution. The pore size distribution is then rewritten.

Wettability and Capillary Pressure Pore radius distribution. 6. The tangent to the curve Pc (Sg ) through the co-ordinate (Sg . The FWL is a property of the reservoir system.8 Saturation Distribution in Reservoirs The equilibrium fluid saturation distribution in a petroleum reservoir. Pc = gρw h. The threshold capillary pressure. where a 100% water saturation is found.11 the pore size distribution is drawn in accordance with the enumerated list. 6. entering pore space initially occupied by the wetting fluid. .11: Capillary pressure curve and corresponding pore size distribution [8]. the following relation exist. A pressure differential is required for the non-wetting phase to displace wetting phase and this is equivalent to a minimum threshold capillary pressure and is dependent on pore size. The physical significance of threshold pressure in an oil reservoir may be appreciated by the analogy with a capillary rise of water in different vertical glass tubes suspended in an open tray of water. . 2. prior to production is governed by the pore space characteristics. while an oil-water contact observed in a particular well will depend on the threshold pressure of the rock type present in the vicinity of the well. Pc (Sg )) gives the slope defined by ∂ Pc /∂ S. Pc Incremental Mercury Injection P d Sw D(r) = rc d Pc Pore radius. D(r) Capillary Pressure. For a water-air system. The pore radius related to this pressure is r = 2σ cos θ /Pc . during migration of hydrocarbons from a source rock region into a reservoir trap. Since Pc ∝ 1/r it is observed that entry of the non-wetting phase should be most difficult in the smallest tube (highest threshold pressure). normally hydrocarbons. found in reservoir is proportional to the height above the free water level (FWL). In Fig. This is as a result of the non-wetting phase. as seen in Fig. r Water saturation. Sw Figure 6.98 Chapter 6. ⇒ Pc(3) > Pc(2) > Pc(1) where r3 < r2 < r1 . normally water.12. 6. 3.

6. At some height h. In a particular rock type. ht = Pct . this height is given.6. above FWL. hSw = 2σow cos θc . which indicated that saturation at height h. one obtains. rg(ρw − ρo ) Similarly. The relation between height above the free water level and the capillary pressure is derived from consideration of the gravity-capillary pressure force equilibrium. the capillary pressure at a depth equivalent toh above the FWL is.13. Pc(FW L) = po − pw = 0. will depend on both the water saturation and the pore radius (see example: "Equilibrium in a capillary channel"). Each unit can have its own capillary pressure characteristic and the static saturation distribution in the reservoir will be a superposition of all units. the pressures are.12: Capillary water elevation in cylindrical tubes as function of tube radii. the threshold height ht is equivalent to the height of an observed water-oil contact above FWL. g(ρw − ρo ) In real reservoir systems it is expected that a number of rock type units or layers will be encountered. r). . as seen in Fig.8 Saturation Distribution in Reservoirs 99 h3 h2 h1 Figure 6. Using a free water level as the datum plane and defining its position in the reservoir as the place where the oil phase pressure po equals the water phase pressure pw . Pc = po − pw = (pFW L − ρo gh) − (pFW L − ρw gh) = gh(ρw − ρo ) Since Pc = Pc (Sw . r) there exist a dependence. po = pFW L − ρo gh pw = pFW L − ρw gh Therefore. h = h(Sw .

when oil is replacing water as being the contact fluid. For a small perturbation ∆h. . as shown in Fig. the relation between elevation of water above FWL in reservoirs is coupled to the pore dimension (pore radius).14). is related to the saturation of water in a reservoir.100 Chapter 6. Equilibrium in a vertical water wet capillary tube. ∆Es = 2π r(σos − σws )∆h. Example: Equilibrium in a capillary tube In this example. 6. r Oil o ∆h h w Water Figure 6. where oil is the non-wetting fluid. 6. The change in surface energy. a small part of the tube surface will experience a change in fluid coverage. caused by oil displacing water in a small fraction of the capillary tube (see close up in Fig.14: Perturbation around equilibrium in a water-wet capillary tube.13: Observed water-oil contacts and their relationship with free water level (FWL) in a layered reservoir with a common aquifer [8]. is given by the difference in surface tension (or surface energy).14. Wettability and Capillary Pressure k1 Well k2 k3 OWC OWC OWC k4 OWC FWL k1 > k 4 > k 3 > k 2 Figure 6.

6. From the above consideration.brine in the laboratory. The relationship for the reservoir oil-brine pair capillary pressure is obtained using the appropriate value of (σ cos θc )res =26 dynes/cm. and at the same time. (σ cos θc )lab . the surface.lab (σ cos θc )res .9 Laboratory Measurements of Capillary Pressure Laboratory measurements of capillary pressure are based on the fact thatPc ∝ σ cos θ /r. where r characterizes the porous medium with respect to the pore throats and the pore size distribution . where.6. due to change in elevation is written. the following relation is given. This dual characteristic of the capillary pressure gives the condition for the coexistence of oil and water in porous rock. i. If small perturbations close to equilibrium are considered. (σ cos θc )1 (σ cos θc )2 Practical use is made of this relationship in conducting laboratory tests with fluids other than reservoir condition fluids. r where the capillary pressure is the pressure difference between oil. Using the Young.and the potential energy changes is expected to be equal.e.res = Pc. the capillary pressure has a "dual" characteristic. the pore radiusr and the height above FWL h are reciprocal variables.and water phase at a certain elevation h in the reservoir. This means that the saturation of initial water present in the reservoir above a certain height h is localised in those pores having a radii less than r.Dupre equation. ∆E p = π r2 ∆h(ρw − ρo )gh.water interfacial tension are known parameters. the pressure difference across a curved surface in inside a pore channel of radiusr. air and brine with a (σ cos θc )lab value of 72 dynes/cm may be used to measure capillary pressure for air. This implies that for any given porous medium and any pairs of fluids. Pc1 Pc2 = . Pc = g(ρw − ρo )h = 2σow cos θ .9 Laboratory Measurements of Capillary Pressure 101 The corresponding potential energy change. g σow cos θ = (ρw − ρo )rh. Pc. . For example. the following relationship is valid. ∆Es = ∆E p . where the densities and the oil. 2 In a oil reservoir where the fluids are well defined . i.e.

The pore size distribution in a given rock type is usually determined by a mercury injection test. Example: Height of water . where mercury. and the displacement is affected by increasing air pressure in a series of discrete steps in water saturated core plugs sitting on a semi-permeable porous diaphragm. Liquid saturation measured after equilibrium saturation has been reached. and measuring the quantity of any produced wetting phase. A laboratory air-brine capillary pressure of 1.102 Chapter 6.15: Gas-liquid drainage capillary pressure measurement. Wettability and Capillary Pressure The migration of hydrocarbons into an initially water filled reservoir rock and subsequent equilibrium vertical saturation distribution is modelled in the laboratory by a non-wetting phase displacing a wetting phase (drainage capillary pressure test). Air and brine are frequently used as the pseudo reservoir fluids. it has the advantage that high pressures can be attained.070 N/m and the brine-oil interfacial tension for the reservoir fluids is 0. Air pressure Capillary contact powder Core plug Neoprene diaphragm Screen Porous plate Figure 6. Portion of liquid in saturated core is displaced at a particular pressure level by either gas or liquid. . The air-brine interfacial tension is 0. As a result of an increase in pressure (equivalent to Pc since Pc = pair − pbrine ) the water saturation decreases and its value is established by weighting the core plugs. the non-wetting phase with respect to air. The height of the water-oil transition zone is the height from FWL and up to the point in the reservoir where connate water saturation is reached. 6. The apparatus layout is shown in Fig. in the sense that the sample cannot be used again.oil transition zone.25 bar has been measured in a reservoir core sample at residual water saturation. In laboratory tests the final irreducible wetting phase saturation value is often beyond the breakdown pressure of the porous plate and is sometimes obtained by centrifuge spinning at a rotational force equivalent to about 150 psi (10.15.022 N/m. can be forced into very small pores. Repetition for several successive pressure levels [8].34 bar). Although this test is destructive.

res .res = Pc. the height of the transition zone is found.10 Drainage and Imbibition Processes. the phase pressures pi . Pc. hres = which gives. Pc. σlab Combining these two equation. In the case of identical wetting preferences for the core sample and the reservoir.lab σres .10 Drainage and Imbibition Processes. as illustrated in Fig. The difference between the phase pressures of two coexisting phases is defined as the capillary pressure.5 m. 103 hres = Pc. which is usually dominated by the smallest local curvature (radius) of the interface.16. hres = 12. When two or more fluids flow through a porous medium simultaneously. An idealised permeable medium is considered by the arrangements of decreasing pore sizes (a single pore bounded by the decreasing sizes sphere assemblage) and initially saturated with a wetting phase (w) into which a non-wetting phase (nw) is alternatively injected and then . rock water r R oil Figure 6.lab σres . . generally speaking. 6.16: Local curvature of the interface of two coexisting liquids.res is the capillary pressure in the reservoir at this water saturation. σlab g(ρbrine − ρoil ) 6. are not identical. one may assume proportionality between capillary pressure and the interfacial tension in the two situations. g(ρbrine − ρoil ) where Pc. ρbrine and ρoil is respectively 1074 kg/m3 and 752 kg/m3 .6. The capillary pressure is inversely proportional to a generalised interfacial curvature.

is first considered. and a higher trapped non-wetting phase saturation after imbibition (condition).17. that results in even higher non-wetting saturation. When the wetting fluid is introduced into the pore from the right. At static conditions. The reverse (wetting saturation increasing) is animbibition process.wetting phase. the pressure difference between the exit and entrance of the assemblage is the capillary pressure at that saturation. At the static condition 2. Wettability and Capillary Pressure withdrawn. being quite simple. a higher capillary pressure. the non-wetting fluid disconnects leaving a trapped or non-flowing glob in the largest pore (condition 2). but the difference shrinks at high non-wetting phase saturations where more of the originally disconnected globs . explains many features of actual capillary pressure curves.imbibition trapped saturation is maximum. and a post . that the termination of any imbibition curve is at zero capillary pressure. The forcing of a non-wetting phase into a pore (non-wetting saturation increasing) is a drainage process.17: The distribution of a non-wetting phase at various saturations. The capillary pressure curve going from the largest non-wetting phase saturation to the largest trapped non-wetting phase saturation is the imbibition curve ( ondition c 6). Beginning at zero non-wetting saturation. Imbibition curves are generally different from drainage curves. Note. 1 2 5 Oil 3 Water Capillary pressure 4 Rock 5 6 3 1 6 4 2 Non-wetting phase saturation Figure 6. This representation.104 Chapter 6. Going from condition 2 to condition 3 is a second drainage process. the entrance . At the highest capillary pressure (condition 5).exit pressure difference is zero since both pressures are being measured in the same wetting phase. We imagine the pores have an exit for the wetting fluid somewhere on the right. injection up to the saturation shown incondition 1 in Fig. all pores of the subtracted volume contain the non. The capillary pressure curve from condition 1 to condition 2 is an imbibition curve that is different from the drainage curve because it terminates (Pc = 0) at a different saturation. 6.

• The second effect is related to the dissipation of energy towards the capillary walls. The hysterisis is detected by measuring the advancing θa . over the same surface.18: Measurement of hysterics in contact angle. which then becomes practically immobile. The effect of this dissipation of energy is experienced as a resistance towards flow and is often materialised through "rip off" of small droplets.10. . The test is repeated after some time. where the receding angle is smaller than the advancing angle. 105 are connected.2 Capillary Hysterisis It is seen that capillary pressure depends both on wetting phase saturation and the direction of its variation. This phenomenon is called trapping hysteresis or drag hysteresis and is caused by differences in advancing and receding contact angles. When the mobile plate is moved. when the interface is advancing through the pore. typical for non-reversible systems. unless a finite capillary pressure difference is imposed. when the two angles have stabilised.10 Drainage and Imbibition Processes. This effect is called the hysterisis in contact angle and has to do with the inherent memory of a physical system. In practical terms this means that the back and forth movement is energy dependent. 6. it has been experimental proven that the contact angle is smaller than in the case when water is replacing oil.19.18. One plate is fixed and the other can move smoothly to either side. is shown in the Fig. The oil drop is left to age between the plates for some time. and residing θr contact angles of an oil drop suspended between two horizontal plates (made of polished rock material. as shown in Fig. is an expression of the fact that energy is lost in cyclic systems. θr oil water θa s Figure 6.1 Hysterisis in Contact Angle When oil is moving to cover a rock surface which previously has been wetted by water. the hysterics has two important effects: • One is to stabilise the capillary surfaces (interfaces) between the fluids in the pore system. quartz or calcite) submerged in water. 6. which relates prehistoric events to present experience. until the two contact angles are equal. A typical curve of the capillary pressure in case of two-phase flow. 6. In relation to multiphase flow in porous media. such as to preserve the fluid distribution in the reservoir. The hysterics observed. the two contact angles are measured.10. 6.6.

which is different from the curve 1. The presence of two different curves of imbibition and displacement is called capillary hysteresis. .19: Typical type of capillary pressure curve for a two-phase flow problem: 1 drainage. Two ways in which one phase can be substituted by the other in a porous medium are usually considered. The hysteresis effect i demonstrated by the two curves 2 and 3 in Fig. If displacement is preceded by imbibition the capillary pressure curve is as the curve 3 in the Fig. 6.0 3 Snc Pcb 1. 6. The first is the process of displacement where the wetting phase is displaced by the non-wetting one.19. 2 imbibition and 3 secondary drainage. where the non-wetting phase is displaced by the wetting one. The presence of the negative capillary pressure near the saturation pointSw = Snc was first discovered by Welge (1949).19. and the second is the process of imbibition.0 Sw Figure 6. Wettability and Capillary Pressure P (Sw ) c 1 Swc 2 0. The value Pcb is defined as threshold capillary pressure which should be exceeded to provide displacement.106 Chapter 6.

air will displace some of the water in the sample. At a rotation frequency ω . 5. r 1 1 . A capillary glass-cylinder is positioned vertically in a cup of water.6. r. Calculate the energy needed to transform 1 cm3 of water into droplets with an average radius of 1 µ m.11 Exercises 107 6. A core sample is placed in a core holder in a centrifuge. corresponds to the threshold pressure Pd at that particular rotation frequency.025 N/m. filled with oil. See the figure below. The length of the sample is therefore. The advancing contact angle is 40o and the receding angle is 20o .2 . What is the pressure drop along the cylinder. assuming the same flow velocity as above. 2. and the water is assumed to wet the glass 100 %. Define the parameters.1 cm.1 m long and has a inner diameter of 0. a pressure of 25 psig is needed.01mm/s ? An equal amount of water and oil is pumped through the cylinder and the water and oil is assumed to move through the tube as droplets. A horizontal cylinder. 4. 3. droplet. Find the diameter. + R1 R2 for a cylindrical tube. with an average length of 0. The oil has a viscosity similar to water. given in µ m. a) Show that the pressure difference for one phase is given by: 1 2 2 P2 − P1 = ρω 2 (r2 − r1 ). Calculate the height of water inside the cylinder when the inner diameter is 0. assume an interfacial tension σo.11 Exercises 1.w = 0. of the largest pore channel disconnecting the porous plate. 1 m Pa · s. In analogy with displacement processes in porous media. The radial distance rd . r2 − r1 . In order to displace water by air form a porous plate. θ and σ . when the average flow velocity is found to be 0.03mm pr. The surface tension between water and air is 72 dyn/cm.w is 72 dyn/cm. 6. Show that the general expression for capillary pressure Pc = σ could be written Pc = 2σ cos θ . The radial distance to the core sample is given by the two position vectors r1 and r2 . R1. Calculate the pressure drop through the tube. The interfacial tension between water and oil is 25 mN/m.01 mm. 2 b) Show that 1 2 Pc(r) = ∆ρω 2 (r2 − r2 ) 2 when P2 = P(r2 ). P1 = P(r1 ) . is 0. when the surface tension σair.

assuming the length of core sample to be short compared to the radius of rotation. r1 = r2 = ∆ρ = Vp = RPM∗ ∆V [cm3 ] RPM ∆V [cm3 ] 415 0.30 3135 4. Sw1 = Sw (r1 ) = d(S¯w Pc1 ) dPc1 when r1 ∼ r2 .75 RPM∗ : Rotation pr.0 r rd when its known that 1 2 2 Pc1 = Pc(r1 ) = ∆ρω 2 (r2 − r1 ) 2 and when 1 2 2 Pd = ∆ρω 2 (r2 − rd ) 2 It is assumed that Pc2 = Pc (r2 ) = 0.00 1550 2.09 g/cm3 8.108 Chapter 6. (This is an approximation.21 1005 0.) Use the equations above to derive the a formula giving the capillary pressure as function of the water saturation (Pc –curve). Minute and ∆V : produced volume.20 765 0. .38 cm 1. c) The water saturation can be written. when the capillary pressure is given in kPa.0 Sw 0.24 1305 1.90 4. The following data is given for a core sample. saturated with sea-water and rotated in air.23 cm3 850 0.50 3920 5.00 1835 2.72 1110 0.10 2200 3. only partly true.15 2655 4.61 915 0.46 cm 9.10 4850 5. Wettability and Capillary Pressure r2 r1 ω 1.

water capillary pressure curve for laboratory conditions.0 0.12 5. Calculate the corresponding height above the OWC in the reservoir from where the core originates. when the following information is given (assume capillary pressure at the OWC to be zero). determine Sw as function hight in the reservoir. So .60 4.2 0.6.90 4.30 5.0 1. capillary data from two water saturated core samples was obtained by using air as the displacing fluid.6 0.18 Calculate the distribution of vertical water saturation in the stratified reservoir given by the figure below.18 10.20 7.0 0.11 Exercises 109 7. Additional data: . 12 ft 4 ft 6 ft 3 ft 4 ft 5 ft FWL Additional data: Laboratory: Reservoir: σw/air = 50 dyn/cm σo/w = 23 dyn/cm ρo = 0. In the laboratory.e.8 0.00 1.13 4. Use the air . Sg and Sw at the reservoir level (hight) 120 f t above the oil-water contact (assume Pc = 0 at this level).5 0.0 0.0 0.00 3. a capillary pressure difference of 5 psi has been measured between water and air in a core sample.0 0. 1000 mD core sample Pc [psi] Sw 1.0 0. i. below.0 g/cm3 Reservoir σ = 25 dyn/cm ∆ρo/w = 0.5 0. The distance between the contacts (OWC and GOC) is 70 f t.2 g/cm3 8.01 g/cm3 9.5 0.20 3.81 g/cm3 ρw = 1.12 200 mD core sample Pc [psi] Sw 3. Laboratory σ = 75dyn/cm ∆ρw/air = 1.40 2. to calculate the saturations. In a laboratory experiment.0 1.80 1.

Sg = 0. 7. h = 3 cm.36.5 µ m.6 82. An oil water capillary pressure experiment on a core sample gives the following results: Pc. what is the average water saturation over this interval? (ρw = 64 lbs/ f t 3 and ρo = 45 lbs/ f t 3 ) 11.3 90.8 m.o/w [psi] Sw [%] 0 100 4. ∆p = 29bar. σ cos θ = 25 dyn/cm and a permeability and porosity respectively 100 mD and 18 %.110 Chapter 6. Wettability and Capillary Pressure Laboratory: Reservoir: σw/air = 72 dyn/cm σo/g = 50 dyn/cm σw/o = 25 dyn/cm ρo = 53 lb/ f t 3 ρw = 68 lb/ f t 3 ρg = 7 lb/ f t 3 90 80 70 Capillary pressure [psi] 60 50 40 30 20 10 0 20 30 40 50 60 70 80 90 100 Water saturation [%] 10. we may construct the capillary curve for a laboratory experiment using mercury as non-wetting phase.2. in the exercise above. 9.0 29. 11. 4.1 5. So = 0.075J. h = 5.2 m bar. Sw = 0. In the laboratory experiments one assume the lithology to be unchanged.4 100 5. Answers to questions: 1. but the permeability and porosity to be respectively 25 mD and 13 %.2 35.8 Given that the sample was taken from a point 100 ft above the oil-water contact. Sw = 0. d = 0. If we assume an interfacial tension.5 43. Find laboratory capillary curve when the interfacial tension to mercury is 370 dyne/cm.7 15.4 10.62 . ∆E = 0. 3. ∆p = 3. . 5.7 32. what is the expected water saturation at that elevation? If the hydrocarbon bearing thickness from the crest (top) of the structure to the oil-water contact in 175 ft.41.

e. S2 . Sn . A pj In a vast number of laboratory experiments it has been observed that a sum of effective permeability’s is less than the total or absolute permeability. i. j=1 n Moreover. . For 100% saturation. q j = k je A µj pj . . k je = f (k. and reservoir conditions (pressure. ke = k. x where j denotes a fluid phase j.. temperature). A p Here ke is called effective permeability. such as: fluid saturation. . T. and k je is called the effective (phase) permeability. the effective permeability is identical to the absolute permeability. According to the last equation we can obtain. µ x and qµ x ke = . rock property.Chapter 7 Relative Permeability 7. i. absolute permeability. When measuring a flow-rate of a fluid versus the pressure difference in a core sample. ∑ k je < k. . we can obtain (single phase flow). p. n]. k je = qj µj x . fluid property. ke A p q= .) j ∈ [1. 111 . S1 . .e. In multiphase flow a generalisation of Darcy law has been accepted [12]. to the effective permeability of a particular fluid in the system. effective (phase) permeability was noticed to be a function of quite a number of parameters. when that fluid occupies only a fraction of the total pore volume. . .1 Definitions Relative permeability is a concept used to relate the absolute permeability (100% saturation with a single fluid) of a porous system.

interfacial tension) change drastically. However in mathematical modelling of two-phase and multi-phase flow it is conventional to assume that relative permeabilities are the functions of saturation only. 7. in general. ke j = kr j · k. This implicates that it is important to keep definitions of mobility.perm. a strong correlation between relative permeability and fluid properties.-curves should be emphasised. This assumption considerably simplifies the task of laboratory experiments carried out in order to determine relative permeabilities. One important feature in the behaviour of the rel. the typical curves of relative permeability are as shown in Fig. Though there have been attempts to calculate relative permeability on theoretical grounds.0 kw Snc Sw 1. the functionality between kr j and S j is also a function of rock properties (e.0 0.112 Chapter 7.1. It is not. Being a rockfluid property.0 kc Swc 0. 1. This means that continuity of the phase is broken or disturbed and the phase . It is important to note that the phase permeability is a tensorial function (as the absolute permeability) and that the relative permeability is not.0 Figure 7. then the corresponding relative permeability for that phase becomes zero and the phase becomes immobile. by far the most common source of them. phase permeability and relative permeability separate and clear. The relative permeability is a strong function of the saturation of phaseS j . The effective permeability can be decomposed into the absolute permeability and the relative permeability. has been experimental measurements. pore size distribution) and wettability. Relative Permeability In two phase systems the latter relationship is expressed as functions of a single (by convention. as shown below. wetting) saturation. where Sw is the wetting phase and Sn is the non-wetting phase. Functions k j (S j ) depend both on the structure of the porous medium and on the saturation distribution of the phases. In the presence of two coexisting phases.g.g.1: Typical type of relative permeability characteristics for a two-phase flow. If saturation of one of the phases becomes less than some definite value: Sw < Swc or Sn < Snc . relative permeability can be affected [40]. though when certain properties (e.

respectively. . Let us note that those values depend on thermodynamic condition of the reservoir (reservoir pressure.4 0.2 Rock Wettability and Relative Permeabilities It should be noted that evaluations of phase. 7. we would expect micro-heterogeneity and rock wettability to have a certain influence on relative (phase) permeability.0 Water 0.8 0. The difference in the flow properties that indicates different wettability preferences can be illustrated by the following rule of thumb [29]: 1 Here w and n denote wetting and non-wetting phase.2 0.0 Oil kr 1.6 0. number of phases. temperature. respectively.0 Water 0.4 0.4 0.2 (left) and 7. etc.0 0.7.0 Figure 7. The values S jc . 1. Because of certain links between them. where n1 are defined as residual saturation of the i-th phase. j = w.8 1.2 0.6 0.2 (right). Typical water-oil relative permeabilities are presented for strongly water-wet and oil-wet formations in Fig. which shows the evidence of strong correlation between them.8 Oil 0.4 Sw 0.2 0.2: Characteristics of typical relative permeability for a twophase flow.6 kr 0.6 Sw 0.and relative permeabilities can be done through measurements of capillary pressure. where Sw is the wetting phase and Sn is the non-wetting phase (left: a water-wet formation and right: an oil-wet formations).0 0. type of rock.0 0.2 0. 7.2 Rock Wettability and Relative Permeabilities 113 remains in a passive or loose state.0 0.).8 1.

Others view the crossover saturation (kr2 = kr1 ). 7. Trapped wetting phase. Thus we would expect the trapped non-wetting phase to be a bigger obstacle to the wetting phase. Movement of an oil zone into receding depleting gas cap. the endpoint relative permeability to the wetting phase can be 0. be smaller than the non-wetting phase endpoint. The non-wetting phase occurs in isolated globules.05 or less. as the process can represent a drainage process. on the other hand. 2. therefore. which is always present in the reservoir. For extreme cases of preferential wetting.3 Drainage/Imbibition Relative Permeability Curves In a gas-oil systems. perhaps because it is less sensitive to the value of the residual saturations (see the rule of thumb. . SL = So + Sw = 1 − Sg . such as: 1.114 Chapter 7.e. i. the direction of displacement is particularly important. The ratio of wetting to non-wetting endpoints proves to be a good qualitative measure of the wettability of the medium. Relative Permeability Water-wet Connate water saturation Saturation at which oil and water permeabilities are equal (crossover saturation) Relative permeabilities to water at maximum water saturation. such as gas drive (gas displacing oil immiscibily) or an imbibition process. above). is considered to stay at irreducible saturation and play no part in the displacement processes. The wetting phase endpoint relative permeability will. then the trapped wetting phase is to the non-wetting phase. flood-out Usually greater than 20 to 25 percent PV Greater than 50 percent water saturation Oil-wet Generally less than 15 percent PV. frequently less than 10 percent Less than 50 percent water saturation Generally less than 30 percent Greater than 50 percent and approaching 100 percent Let us note that the endpoint values of the relative permeabilities are usually (if not always) less than 1 and which are measures of wettability. that occupy the center of the pores. occupies the cavities between rock the grains and coats the rock surfaces. It is therefore argued that experiments in the laboratory can be conducted with or without irreducible water present and that effective permeabilities could be correlated to total liquid saturation (SL ). Movement of an aquifer into receding depleting gas cap. rather than gas saturation. several pore diameters in length. of the relative permeabilities is a more appropriate indicator of wettability. water. In gas-oil systems the third phase. The relation is based on a definition of liquid saturation.

In a system where gas saturation increases from zero. increasing pressure gradients force the non-wetting phase into the pore channels. The residual non-wetting phase is trapped in the large pores in globules several pore diameters in length. the wetting phase approaches mono-layer coverage and a low saturation. This relationship is called the capillary de-saturation curve (CDC). and can be variously defined. Repeated experimental evidence has shown that under most conditions. 7.0 Sgc Sg Sgmax 1. The capillary number Nc is a dimension-less ratio of viscous forces to local capillary forces. these curves are plots of percent residual (non-flowing) saturation for the non-wetting ( nwr ) or wetting (Swr ) phases S on the y axis versus a capillary number on a logarithmic x axis. One of the examples is shown below (after Dombrovsky and Brownell): Nc = k | ∇Φ | σow · cos θc . At very high pressure differences.0 kr = k o / k kr = k o / k kro krg krg kro 0. the Snwr could be as large as Swr .3. In liquid imbibition processes (gas saturation decreasing from a maximum initial value) the gas permeability goes to zero when the residual or trapped gas saturation (Sgr ) is reached. 7.3: Gas-oil relative permeabilities [8]. Typically. it is observed that gas does not flow until some critical gas saturation (Sgc ) has been attained. as a condition for gas flow.0 Figure 7.0 0. See Fig.0 1. as in a liquid drainage process.4 Residual Phase Saturations As we know from the previous discussion. This is attributed to the physical process of the gas phase becoming continuous through the system.7.4 Residual Phase Saturations 115 1.0 Sgr Sg Sgmax 1. According to experimental observations there is a strict evidence of a relationship between residual non-wetting or wetting phase saturations and the so-called local capillary number. causing the wetting phase to retreat into the concave contacts between the rock grains and other cavities in the pore body.

Different equipment arrangements for those test are shown in Figs.5 Laboratory Determination of Relative Permeability Data Laboratory determination of effective permeability is generally conducted as a special core analysis test on representative and carefully preserved core plug samples. and severe errors can occur with heterogeneous samples. 7. or steady state conditions. The displacement theory of Buckley and Leverett is combined with that of Weldge in a technique described by Johnson. For reservoirs with more core-scale heterogeneity and with mixed wettability. Unsteady state rel. The reduction of interfacial tension at the interface allows the trapped oil to become mobile and be displaced by the water. It is important to mention that chemical additives reduce capillary forces at the interface of the oil/water system.116 Chapter 7. Bossler and Naumann [38]. test simulate the flooding of a reservoir with an immiscible fluid (gas or water). The detection of the breakthrough time of the displacing phase at the outlet core face is critical in the representation of relative permeability. and with homogeneous samples. The unsteady state or dynamic displacement test is most frequently applied in reservoir analysis of strong wetting preference.4: Schematic capillary de-saturation curve [40].6. The determination of rel. resulting in increased capillary number Nc and reduced residual oil saturation. Such reservoir condition tests may model displacement under unsteady state. 7. At each . Flow rates are determined according to the method of Rappoport and Leas in order to minimize the effect of capillary pressure forces in retaining wetting phase fluid at the outlet end face discontinuity. the steady state laboratory test is preferred. % 30 Wetting phase 20 Nonwetting phase 10 Nonwetting critical Nc -6 Wetting critical Nc 10 -5 010-7 10 10 -4 10 -3 10 -2 Capillary number Nc Figure 7. A reservoir condition test is conducted at reservoir pore pressure conditions and reservoir temperatures with real or simulated reservoir fluids. Relative Permeability where Φ is the potential of flow.perm. is based on observation of the fractional flow of displacing phase fluid from the outlet end of the core plug and its relationship with saturation. perm. being either wetting or non-wetting phase. The steady state process provides simultaneous flow of displacing and displaced fluids through the core sample at a number of equilibrium ratios. Normal range waterfloods Residual non-wetting or wetting saturation.5 and 7.

Ruska pump Brine Oil Chart recorder Hg Oil colector Hg Oil Soltrol Hg Soltrol 1000 cc Oil Brine Sample Brine colector 0 . and at which the pressure difference between inlet and outlet is constant. .7. Between five and ten stages are usually needed to establish rel.5: Unsteady state relative permeability measurement at constant rate (above) and at constant pressure (below). curves.perm. At such a condition the Darcy law equation is applied to each phase to calculate effective permeability at the given steady state saturation.5 Laboratory Determination of Relative Permeability Data 117 Oil colector 3 way valve Sample Brine colector Hg res.50 psig Transducer Chart recorder 3 way valve 300 cc 300 cc Figure 7. ratio from 100% displaced phase to 100% displacing phase an equilibrium condition must be reached at which the inflow ratio of fluids equals to the outflow ratio. Capillary pressure tends to be ignored and a major difficulty is the determination of saturation at each stage.

can be written: qw 1 fw = = qw + qo 1 + kro µw /krw µo Assume the capillary forces to be negligible and dPo /dr = dPw/dr.00 krw 1.0 ∞ ρo = 0. = 22dyn/cm σlab = 75dyn/cm µo = 15. Oil Pressure transducer Chart recorder Oil res.70 0. fw .7 8.60 0.90 0.04 0.23 0.39 0.00 lab Pc [psi] 1.50 0.00g/cm3 σres.85g/cm3 ρw = 1. Relative Permeability Oil Hg Sample Hg res.00 0.6: Steady state relative permeability measurement [8]. The following laboratory data is given: Sw 1.14 0. Constant displacement Ruska pumps Brine Figure 7.00 0.05 and the data above to construct a graph showing the water fraction as function of height above the WOC.5 5.30 kro 0.78 0.00 0.80 0.09 0. 7. Soc = 0. Use Darcy’s law for radial flow and show that the fractional flow for water.4 3.00 0.40 0.0cp Use critical oil saturation.73 1.9 4.0 3.118 Chapter 7.29 0. What is the water fraction at 15 m above the WOC ? .49 0.0cp µw = 1.6 Exercises 1.58 0.00 1.4 18.

87 3.05 164.1 cp length of core sample Oil viscosity Porosity 9 cm 2.65 5.and water rate through the sample.93 7.52 123.30 137. respectively. determined by weighing. curves for kro and krw using the data above. qo and qw is the oil.2 cm 1.6 Exercises 119 2. qo [cm3 /time] 90 75 60 45 30 15 0 qw [cm3 /time] 0 5 9 20 34 85 122 ∆P [psi] 49. 25% .17 2.20 Draw the rel.7 mD 3. Answers to questions: 1.7.29 109.25 91. Additional data is given: Absolute permeability Diameter of core sample Water viscosity 1 atm. The laboratory data below is recorded at stationary conditions. ∆P is the pressure drop.perm. equals 14. measuring the relative permeability for a oil-water injection experiment.86 Vw is the volume of water in the core sample.63 4.95 9.65 psi 16.30 147.0 cp 0.00 Vw [cm3 ] 2.

Relative Permeability .120 Chapter 7.

8. since the reservoir temperature changes slightly or remain constant in most cases. i. It is necessary to study the physical properties of these naturally existing HC and in particular. as physical phenomenon. In the case of formation rock and the saturation of fluids contained therein.2 Compressibility of Solids.Chapter 8 Compressibility of Reservoir Rock and Fluids 8. Compressibility is therefore an important "drive mechanism" in underground petroleum production. gas and initial water from the reservoir. their variation with pressure and temperature. Oil and gas are naturally existing hydrocarbon (HC) mixtures. plays a key role in general underground petroleum production. When produced to the surface.e. The state of equilibrium is defined by these two parameters and consequently also the phase behaviour of the fluid. Liquids and Gases For a mixture of HC it is quite obvious that pressure and temperature are essential parameters. where the state of the HC mixture at the surface depends upon the composition of the HC fluid found in the reservoir. in order to fully understand and control the production process.1 Introduction Compressibility is a universal phenomenon. The fluid remaining in the reservoir at any stage of depletion undergoes physical changes as the pressure is reduced due to removal of quantities of oil. the temperature and pressure of the mixture are reduced. the fractional volume of oil and gas. responsabile for reservoir fluid production. pore volume and fluid changes due to the pressure decline is the dominating phenomenon. of significant importance where all substances are compressible. Nearly all production of oil. Volumes of reservoir fluid brought to the surface will experience change in both 121 . gas and formation water is related to volume expansion when the reservoir pressure decreases due to removeal of reservoir fluids. some more compressible than others. This information is important in estimating the performance of the fluids in the reservoir. Compressibility. quite complex in chemical composition which exist at elevated temperatures and pressures in the reservoir.

8. The stress tensor is often written in matrix form. the final state of oil and gas is characterised by volume changes due to both drop in pressure and in temperature.1 Rock Stresses and Compressibility When rocks are subjected to external load or force. In relation to reservoir production. σy and σz and 3 tangential (shear stresses): τxy .1) (8. The general stress condition may be characterised by a stress tensor. Underground gas and oil reservoirs experience stresses due to the overload of rock material and water and the lateral confinement stresses exerted on the reservoir from the surrounding rock masses. i. cr . The stresses on any plane surface through a rock sample under in situ. cg . co and cw . which means that τxy = τyx and so on. c ≥ 0 and β is the isobaric thermal expansion. ∂p T ∂V .1. In practice. with nine components as shown in Fig. conditions are composed of a normal stress vector (perpendicular to the plane) and two shear stresses. • Rock bulk compressibility. • Gas compressibility. β ≥ 0.2.2.122 Chapter 8. it is normal to use an average compressibility factor of the different HC components. cb . see Fig. ∂T p (8.2) where c is the isothermal compressibility. The general behaviour of materials can be described by the compressibility and expansion terms. 8. it is common practise to distinguish between the following definitions of compressibility: • Rock matrix compressibility. 1 V c = − β = 1 V ∂V . τzx . There are thus only six independent stress components in the stress tensor: 3 normal stresses: σx . Compressibility of Reservoir Rock and Fluids pressure and temperature. It is possible to show that there exist one set of ortogonal axis with . internal stresses are developed and if the stresses are sufficiently strong. 8.   σx τxy τxz  τyx σy τyz  τzx τzy σz Due to the general conditions of equilibrium.e. τyz . • Liquid compressibility (oil or initial water). deformation such as volume and shape changes of the rock will be the result. parallel to the plane surface. the stress tensor will be symmetric around the diagonal.

the type of cementing material. (In case of non-zero shear stresses. the principal normal stresses are orientated as shown in Fig. Liquids and Gases 123 σz z τzx τzx τxy τzy τzy σy τxy y x σx Figure 8.8. εi = ∆li li − li = .2.3) 3 The collective action of the principal stresses will cause the rock material to deform.g. The average normal stress is generally defined by. where i = x. (8. while the two lateral stresses σx and σy are acting in the horizontal plane. σy .strain relationship is dependent on several parameters of which the following are the most important.4) where li is the initial length of the rock in the i’th direction. σz > σx . li li (8. the compressibility of the rock matrix.) The stress . 8.1: Stress conditions of formation rock media. e. l is the length after deformation. These stresses are called the principal stresses For most reservoirs. a displacement or rotation of the rock may be experienced. The sum of principal strains will give the relative volume change∆ε = (εx + εy + εz ).2: Principal stresses on reservoir rock. the porosity of the rock material and the pressure and temperature in the reservoir. . The relative longitudinal deformation is given by theprincipal strain. the composition and lithology of the rocks. 1 σ = (σx + σy + σz ). where the major principle stress σz is acting parallel to the force of gravity. respect to which all shear stresses are zero and the normal stresses have their extreme values. where εV = ∆V /V . z.2 Compressibility of Solids. the degree of cementation of the rock material. y. σz σy σx Figure 8..

124 Chapter 8.8) (8. In that case srain are refered to the initial conditions. σ1 . ∆σx etc.11) In introducing cr . ε . (8. it will shorten. Compressibility of Reservoir Rock and Fluids In the following. This observation is presented in Hooke’s law in three dimensions: E εx = σx − ν (σy + σz ). The significance of Poisson’s ratio. σ2 and σ3 are the principar stress directions. . (8. E εy = σy − ν (σx + σz ). which means equal properties in all directions.9). If the transverse strain is defined by ε2 and ε3 . Within the elastic limit of volume deformation of any rock material. For simplicity. (8. σ 1 = E ε1 . coupling axial and transverse strain. (8. The ratio of transverse strain to the axial strain is expressed by the Poisson ratio ν . If a cylindrical rock sample is subjected to a compressive stress. ∆V 3σ (1 − 2ν ) = V E (8.10) and Eq. one assumes that the rock is completely solid with no pores or cracks within it.1) on differential from. Combining equation Eq. parallel to its long axis. (8. the strains are reddered to the condition of zero stresses.5) where E is the Young’s modulus of elasticity and the subscript indicate change in stress and strain in the same direction and where the stresses normal to this direction are constant. Hooke’s law states that there exist a proportionality between stress. ε1 and the diameter will increase. the relative volume change is given. E εz = σz − ν (σx + σy ).10) Relative volume deformation of the rock is also described by the compressibility Eq. ∆V = cr ∆σ . Using Hooke’s law. then the transverse deformation is given. (8. it is also assumed that the stresses are refered to the principal stress directions.9) In writing Hooke’s law this way. indicates that deformation along one principal axis is caused by a combination of all three principal stresses.6) where ε1 is the principal strain direction.11) proves that the compressibility and the elasticity are "two sides of the same case". V (8. the rock will be assumed to be isotropic. It is often convenient to write Hooke’s law in changes of stresses. where σ1 .7) (8. The total deformation due to all three principal stresses acting on the rock material is given by ∆V = (εx + εy + εz )V . σ and strain. ν= ε2 ε3 = . ε1 ε1 (8. Eqs.7) to (8.

e. 8.e.(8. the compressibility is.(8. Under the assumption that the deformation of the rock is within the range of the elasticity (see Fig. Within the elastic limit of the liquid. following the same chain of arguments as seen for solid (rock) material. i. V = V0 e−cr (σ −σ0 ) V0 [1 − cr (σ − σ0 )]. 8.2 Compressibility of Solids.5 · 10−6 bar−1 .3). one can expect the compressibility to be constant and in accordance to Eq.(8. compressibility is constant.1) and in analogy with Eq. Vl = Vl0 e−cl (p−p0 ) Vl0 [1 − cl (p − p0 )]. cr (σ − σ0 ) V V0 Within the range of elasticity 0 p0 p Figure 8.15) . V according to Eq.cquarts ∼ 2. dV = −cr d σ .3: Deformation of rock bulk volume under conditions of elastic behaviour (constant compressibility factor).2 Compressibility of Liquids Deformation of liquids can be explained. (8. Liquids and Gases 125 3(1 − 2ν ) .(8. refer to the solid rock material. The dimension of compressibility cr is reciprocal pressure.e.1) or (8. 1.14). E where also the elastic constants E and ν . cr = (8. (8. as follows from Eq.14) The approximation is valid when cr ∆σ is small.8.(8.13) (8.14). i.1) the deformed volumeV is equal to.12) In Eq.12) the important relation between the compressibility and the elastic properties of the rock material is established. [cr ] = [σ ]−1 For normal reservoir rock like quarts.2. i.

depending on the content of the solution gas. In the case of a perfect gas. expressing the non-ideal deviation from perfect gas behaviour. pV = znRT. Differentiation of the volum function.3 Compressibility of Gases Experience tells us that gases are very compressible.16) p: V: T: where n: R: Combining Eqs. may have a varying compressibility factor. the mixture of light and heavy HC and the amount of gas contained in the oil. depending on the composition of oil.(8.(8. Black oils may have a compressibility ∼ 25 · 10−5 bar−1 . ∂p ∂T ∂z V V V = − d p + dT + dz. (8.6 · 10−5 bar−1 . Gas compressibility can be defined equally to solids and liquids. pV = nRT.2.e. also valid for gases. Oil. z). 1 ∂V 1 = .1). using the definition in Eq.17) V ∂p p Form this deduction it must be conclude that compressibility of gases is notconstant. Water is not particularly compressible and has a compressibility factorcw ∼ 4. dV ∂V ∂V ∂V dp+ dT + dz. in an attempt to consistently describe the nature of compressibility as a universal characteristic. 8. cg = − Example: Compressibility of real gas The real gas law is. (8. i. temperature and a non-ideal factor.e. on the other hand. we may assume the volume to be a function of pressure. Compressibility of Reservoir Rock and Fluids where the last approximation is valid when cl (p − po ) 1. volume which it occupies. Various liquids may behave quite differently depending on the composition of that liquid. where z is the deviation factor. absolute temperature of gas. i. while light oils can have substantially higher compressibility. but varies as the reciprocal pressure (under the assumption of constant temperature). V = V (p.1) and (8. number of moles of gas equal to its mass divided by its gaseous molecular weight and the gas constant. p T z = . absolute pressure of the gas phase. Since compressibility describes the volume deformation.126 Chapter 8. T.16) one obtain.

0 n 1 Tpr 0 ppr Figure 8. i m where pci and Tci are critical pressure and temperature of the different HC components and ni is the volume fraction or the mole fraction of each component given by Avogadro’s law. Z Tpr Tpr 1. . . The z-factor is usually expressed as a function of the so-called pseudo reduced pressure ppr and pseudo reduced temperature Tpr . Critical pressure and temperature for a mixture of m numbers of HC components are defined.e. p pc = ∑ ni pci . p z dp The deviaton factor z.2 Compressibility of Solids. i m Tpc = ∑ ni Tci .4: z-factor as a function of pseudo reduced pressure p pr and temperature Tpr . T is constant and consequently.4.8. p pr = p . 8. Liquids and Gases 127 At reservoir condition. is a non-trivial function of pressure and temperature. i. V dp p z dp Compressibility for real gases in the reservoir is then given by. − 1 dV 1 1 dz = − . Tpc where p pc and Tpc are pseudo critical pressure and pseudo critical temperature. as seen in Fig. cg = 1 1 dz − . Tpr ). where pseudo reduced pressure and temperature are defined as. z = z(p pr . respectively. p pc Tpr = T .

The total external stress acting on the porous rock is partly counterbalanced by the pore presssure and the forces acting through the rock matrix. acting on the surface of the pore walls. (8. the stresses in Hooke’s law should be replaced by effective stresses. The horizontal stresses may also change with pore pressure and the development of complete stress conditions may be difficult to determine. later the defineition of effective stress has been generalized to. Experience in rock and soil mechanics has shown that the deformation of porous and premeable materials depend on the effective stress which is the difference between the applied total stress and the pore pressure. It should be noted however that the consept of effective stress does not follow from strictly theoretical considerations. For reservoir engineering. and in addition to an internal pore pressure p. while the pore pressure and the forces acting through the rock matrix are the counteracting pressures [62]. . causing compaction of the reservoir rock.18) σ = σ − α p. where the total stress will be the pressure acting on the outer surface. This is depicted in Fig. The overburden load will however remain more or less constant and thus the vertical effective stress will increase. σ p p σ σ Figure 8. but must be regarded as a close approximation. For porous rocks.128 Chapter 8. Effective stress was originally introduced by Terzaghi and is defined as. When a reservoir is produced the reservoir pressure will in most cases be reduced. Compressibility of Reservoir Rock and Fluids 8.5: Stresses working on a porous rock.3 Deformation of Porous Rock The elastic deformation or compressibility of porous rock is complicated by the fact that it is subjected to an external confining stress σ . often called the Biot constant is a number equal or less than one. α ≤ 1. it is first of all the volumetric behaviour that is important. The volumetric changes are given by the average applied stress and one will therefore for simplicity in the following assume a hydrostatic applied stress field on the porous rock. where the constant α .5. For most reservoir rocks α will become close to one and may be neglected. 8. σ = σ − p.

Eqs.3. (8.e.19) gives the relative volume change. If a porous rock sample is brought to the laboratory and the external stress σ . left. dVb = −cbσ d σ . dVb Vb dVp Vp = −cbσ d σ + cbp d p. (8. c p = c p (cb . .21) is written.21) where the "minus" sign demonstrates the fact that when σ increases. 8. Differentiation of Eqs. such that d σ = d p. The four compressibilites defined in Eqs. gas or initial water) will cause deformation in the bulk volumeVb . then the bulk and pore volume will increase.20) Using Eq.22) Since cbσ depends on the elastic moduli of the matrix rock material and the geometry of the pore space. on the other hand. i.e.19) ∂ Vb 1 ∂ Vb dσ + d p. while when p increases. then Eqs. (8. ∂σ Vp ∂ p (8. it must in general be considered to be an independent parameter. (8. If.8. p).3 Deformation of Porous Rock 129 Variation of the effective stress on the rock due to withdrawal of reservoir fluid (oil. both the external stress σ and the pore pressure p may provoke changes in the bulk or/and pore volume.21) gives. a set of four compressibilities may be defined and Eq. 8. Generally. (8. the rock sample is exposed to an external stress equal to the internal pressure. Vp = Vp (σ . dVb Vb dVp Vp 1 Vb 1 = Vp = (8. right. as seen in Fig.6.20) is written. as well as deformation in the pore volume Vp . cr ).21) are all not independent and through elastic theory it is possible to resolve the relation between them.1 Compressibility Measurements. = −c pσ d σ + c pp d p. 8. see Fig. Vb (8. i. on the sample is increase while the pore pressure is kept constant d p = 0. cbσ = cb . ∂σ Vb ∂ p ∂ Vp 1 ∂ Vp dσ + d p. The purpose of this process is to express the pore compressibility as function of the compressibilities of bulk volume and rock material. (8.1) the definition of isothermal compressibility. The bulk and pore volume are therefore defined as function of both external stress and pore pressure. (8. characterised as the bulk compressibility. Vb = Vb (σ .6. both the bulk and pore volume will decrease. p).

(8. the compressibility of the rock sample is equal to the compressibility of the rock material cr . i. then the bulk and pore volume are deformed accordingly. is only related to the rock matrix material itself. (8. is equal to the work given by the volume expansion of the pore volume due to the external stressdVp (σ ) times the change in the pore pressure d p.130 Chapter 8. Under these condition.e. dVb = dVb (σ ) + dVb (p).23). Betti’s theorem states that the hypothetical work given by the volume expansion of the bulk volume due to the pore pressure dVb (p) times the change in the external stress d σ . (8. Seen from the outside the material would behave as a completly solid rock. −cb + cbp = −cr . = (−c pσ + c pp )d σ . When the pore pressure increases/decreases equally to the confining stress. dVb Vb dVp Vp = (−cb + cbp )d σ .24) where the minus sign for cr reflects the fact that the rock will compress under these conditions.2 Betti’s Reciprocal Theorem of Elasticity. . the following relation between compressibilities are deduced. 8. −c pσ + c pp = −cr .6: Stresses working on a porous rock.25) where dV (σ ) is the volume change relative to the external stress and dV (p) is the volume change relative to the pore pressure.23) where d σ = d p and where cbσ = cb . then the effect of the pores with respect to the deformation of the porous rock.3. (8. If both the external stress and the pore pressure are changing. Compressibility of Reservoir Rock and Fluids σ dp = 0 σ=p Figure 8. From Eqs. dVp = dVp (σ ) + dVp (p).

4 Compressibility for Reservoir Rock Saturated with Fluids 131 dVb (p) · d σ = dVp (σ ) · d p. (8. gives c= 1 ∆V V ∆p ⇒ ∆V = cV ∆p.28) on gets.26). Vp Vp Vp = cw Sw + co So + cg Sg . like in experiments sketched in Fig.21) in Eq. This compressibility accounts for the expansion of fluid.27) where cbp = cb . Vg Vw Vo = cw + co + cg . developed by Geertsma [31]. (8.26) (8. where the pressure drop ∆p is sufficiently small. Using Eqs. one gets. relates the pore compressibility to the bulk and rock compressibilities which are the parameters normally measured. The fluid compressibility is written. co and cg . (8. cbp = φ c pσ Combining Eqs. φ (8. oil.4 Compressibility for Reservoir Rock Saturated with Fluids Compressibility of homogenous matter like the rock material cr and the contained saturations of fluids.31) where S is the fluid phase saturation (Sw + So + Sg = 1).28) where c pp = c p is the pore volume compressibility. (8. cw . are all defined by Eq.1). e.29) (8. ∆V f cf = ∆Vw + ∆Vo + ∆Vg . −Vb cbp d p · d σ = −Vp c pσ d σ · d p. . 8. the bulk compressibility is given. cp = cb − (1 + φ )cr . This formula. (8. (8.24 and Eq. water and/or gas. given by c p in Eq. (8. given by the fluid compressibility c f and the reduction of the pore volume when the pore pressure is reduced. (8. Since porosity is defined φ = Vp /Vb . Since the pore volume is expanded by the fluid phase volumes: V f = Vw + Vo + Vg . Of interest in relation to the production of oil and gas.g.6.fluid system.29). 8. A discrete version of this definition. (8. a change in the pore pressure will cause the fluid volume to change.30) The compressibility of the fluids c f contained in the pore volume is defined by the compressibility of the different phases. is the total compressibility of the rock .8. The minus sign for the first term reflects that the force and displacement are in opposite directions.

cr (8. An equally important term is the effective compressibility responsible for the expansion of initial water and reduction of the pore volume.132 Chapter 8. cnon−HC = cb − (1 + φ )cr + φ cw Sw . the dependence on the effective stress is an exact theoretical result.29) with Eq.21) in Eq.e. dVp dVb dφ = − . the equilibrium of stresses in the reservoir is changed. when pressure is released as a result of HC production. i. φ (8. φ Vp Vb (8. (8.24) and Eq. φ 1 = [cb − (1 + φ )cr + φ (cw Sw + co So + cg Sg )]. cb − (1 + φ )cr = + cw Sw + co So + cg Sg . (8. (8. d φ = −cb (1 − φ ) − cr d(σ − p).34) gives. This term.36) where the pressure drop ∆p. ∆φ = cr cb (1 − φ ) − 1 ∆p.34) where the porosity change d φ is proportional to the change in the effective stress. cHC = co So + cg Sg . due to fluid production from the reservoir is small enough to keep the material within the elastic limit.32) The effective HC compressibility is a useful term. .35) (8. related to the pore space occupied by the hydrocarbons.33) and remembering that c pp is the pore compressibility c p and cbσ is the bulk compressibility cb . due to oil or gas production. By differentiation the porosity one gets. d σ = 0 and thus the change in porosity is. φ Combining Eqs. Compressibility of Reservoir Rock and Fluids ct = cp + c f . a non-HC compressibility is defined. This change in the effective stress on the rock material will cause the porosity φ = Vp /Vb to change. (8. dφ = (c p d p − c pσ d σ ) − (cbp d p − cb d σ ). the confinement stress is constant. φ Example: Porosity variation in the reservoir When the reservoir pore pressure is reduced. It should be noted that in this case. (8. (8.33) Substituting Eqs. Under reservoir conditions.

the confinement pressure and the pore pressure will be close to equal. .e. the porosity will increase when the rock sample is brought to the surface. p1 Vp : φ1 p2 φ2 Figure 8. Eq. which then define the lower bound.e.4 Compressibility for Reservoir Rock Saturated with Fluids 133 In a non-porous rock. is one of the very few direct sources of information available regarding reservoir characteristics. . i. the ratio cb /cr is often found to be between 4 to 100. where the bulk and rock matrix compressibilities are such that (cb (1 − φ ) − cr ) > o. . At initial conditions in the reservoir. i.8. the porosity is reduced in the reservoir when the pressure is reduced. p1 > p2 (Fig. which is the case for practically all porous rock materials.e. cb = cr . which is an important drive mechanism for undersaturated oil reservoirs. When the pore pressure is reduced. the terms in the bracket in Eq.7). φR < φL . In the laboratory or at normal atmospheric condition. (σ − p)L = 0. (σ − p)R > 0.35) gives the porosity change relative to the change in the pressure difference (σ − p). a porosity deformation is observed. For sandstone reservoirs with a typical porosity larger than 5-10 %.7: Constant confinement pressure and reduced pore pressure leads to a reduction in the pore volume. i. when φ → 0. under the assumption of constant confinement stress. i. In typical sandstone porous rocks. φ1 > φ2 . i. (8. For a porous rock sample.36) will always be positive.e. the pressure difference is normally such that the confinement pressure is larger than the pore pressure.e. What about the porosity change in rock samples which are brought to the surface for further experimental investigations? This question is quite important since laboratory measurements on core material from wells. where by cb /cr ≥ 1. Example: Porosity variation in formation core samples Reservoir porosity is seen to decrease with the pore pressure. 8. the bulk compressibility will be equal to the rock matrix compressibility. (8.

6 %.86 2000 0. 8.80 3000 0. 2200 psia and 4000 psia.8: Variation of bulk volume during surfacing of core material.4 · 10−6 psi−1 . A gas reservoir has a gas deviation factor (at 150 o F). 0. co = 10 ×10−6 psi−1 . Then.6 · 10−6 psi−1 .00 Plot z versus p and graphically determine the slope at 1000 psia. 18.92 1000 0. p [psia] z 0 1.82 4000 0. Find the formation porosity when the field is abandoned? 3.00 500 0.24 and gas saturation is 0. Bulk compressibility is 3.45 · 10−3 psi−1 . The reservoir pressure is 1923 psi. find the gas compressibility at these pressures.89 5000 1. Compressibility of Reservoir Rock and Fluids pR φR pL φL Figure 8. Find the total compressibility and the effective hydrocarbon compressibility when the following fluid and formation compressibility are known.14 · 10−3 psi−1 . 0. and estimated abandonment pressure is 500 psia.134 Chapter 8. Answers to questions: 1. cg = 1/p psi−1 and cr = cb = 5 ×10−6 psi−1 . 2. A reservoir with an initial pressure of 6500 psia has an average porosity of 19 %. 1.11 · 10−3 psi−1 . 224.8×10−6 psi−1 . 2.31.5 Exercises 1. cw = 3 ×10−6 psi−1 . 171. connate water saturation is 0. 3.

Primary reservoir production takes place without any temperature change. During this process both pressure and temperature are significantly changed. see Fig.1: Volume transformation of oil and gas.1 Introduction Production of oil and gas can be compared to a process where volumes of the reservoir fluids are transformed to the stock tank volumes of oil and gas.1. while the reservoir pressure drops substantially near the well. 9. The composition of oil and/or gas will therefore changed slightly during production.Chapter 9 Properties of Reservoir Fluids 9. Qgn=∆V /∆t gn Qon=∆Von /∆t Sea Reservoir Qg=∆V /∆t g Qo=∆Vo /∆t Figure 9. In an oil reservoir we may experience the shrinkage of oil due to the solution gas liberation near the well and in a rich gas reservoir we expect condensa135 . The reservoir production rates of oil and gas will in the event of continuously decreasing pressure and temperature transform. where the phase ratio of oil and gas is changed as well as the gas-oil ratio and the composition of both phases.

The number 2 accounts for the intensive properties p. and vapour pressure line) No degrees of freedom – a single triple point in the phase diagram When NP = 3 NF = 0 We know that water may appear in different phases like ice. NF = NC − NP + 2 − NR. the critical temperature is 374. for temperatures T > TC and pressures p > pC . pressure is further reduced through different stages of separation.1 oC and the critical pressure is 218. The different regions are separated by phase boundaries. (For pure water. number of phases NP . hence we call this state the fluid state. melting point line. T)-plot reflecting this occurrence (sublimation line. liquid and vapour. When the reservoir fluid is produced and brought to the surface. For pure components the phase rule says that no more than three phases can form at any temperature and pressure. In this chapter focus is put on some characteristic aspects of hydrocarbon mixtures and the separation of oil and gas as function of pressure and temperature.e.3 atm. Properties of Reservoir Fluids tion of liquid hydrocarbons (oil) when the pressure is reduced. i. 9. 9. H2 O. and NC − NR defines the number of independent components. The co-existence of different phases. all depending on temperature and pressure.2. is shown in Fig. For a pure component (like H2 O). In these processes.2 Definitions The process by which the different hydrocarbon (HC) components form phases through various chemical reactions is governed by a natural (entropy driven) development towards equilibrium or the lowest energy level. We will look at how oil and gas behave in the reservoir and their expansion to stock tank condition. then NC − NR = 1 and NF = 3 − NP. When NP = 1 When NP = 2 NF = 2 NF = 1 Both intensive properties can be changed arbitrarily Only one intensive property can be independent – there are three lines on a (p. where. number of chemical reactions NR . temperature is also reduced and consequently the composition of oil and gas undergoes significant change. Beyond this point. This could be expressed more precisely referring to the Gibbs phase rule.) . i.136 Chapter 9. and degrees of freedom NF . there is no distinct difference between water and vapour. The Gibbs phase rule shows a relationship among the number of componentsNC . The phase boundary between water and vapour ends in a critical point where the two phases cease to co-exist. T .e.

typically light components likeC1 . + Components C7 are heavy and in most interesting cases of petroleum engineering. say. 9. For pure components of oil.9. Some of the components in the paraffin series are listed below: Methane Ethane Propane Butane Pentane Hexane CH4 C2 H6 C3 H8 C4 H10 C5 H12 C6 H14 C1 C2 C3 C4 C5 C6 Heptane Octane Nonane Decane C7 H16 C8 H18 C9 H20 C10 H22 Some typical non-hydrocarbon impurities are represented by. C4 .3 Representation of hydrocarbons Naturally occurring HC are complex in composition and contain a great many members of paraffins (alkanes).3. However. In gases. it is quite common to write C7 . the phase boundaries form a closed boundary . When two or more HC components are mixed. naphthenes (cyclo-alkanes) and aromatic series and often some non-hydrocarbon impurities. C5 and C6 are the important components and for heavier oils the presence of various decanes and asfaltenes are quit common. Water Critical point Vapour 100 °C Tc Figure 9. 9. shown in Fig. For light oils. The C7 characteristic is then the average for all components higher then C6 .3 Representation of hydrocarbons 137 pc Ice 1 atm.2: PT-diagram for H2 O. and their mixture (50% of C2 H6 and 50% of C7 H16 ) the phase PT-diagram is shown in Fig. mean+ ing all component in the series.2. 9. intermediate components like C4 − C5 can be in both gaseous and liquid state depending on prevailing pressure and temperature. The PTcharacteristics of the pure components are somewhat similar to theH2 O case. can not be evaporized. Ethane (C2 H6 ) and Heptane (C7 H16 ). C2 and C3 dominate the composition. C7 H16 and higher. Nitrogen Carbon Dioxide Hydrogen Sulphide N2 CO2 H2 S + For mixtures of HC components.

138 Chapter 9. These relations between pressure. a) 100% Ethane p p b) 100% Heptane c) 50% Ethane 50% Heptane p Liquid C Liquid C Gas T Liquid C Liquid + Gas Gas T Gas T Figure 9. The equilibrium state is defined as function of p and T and consequently also the volume ratio of oil and gas is PT-dependent.4: PVT diagram for a mixed component system.4.4 (lower right). For a mixture of hydrocarbons. Liqu id u tc rv e Pressure poi n t cu Bu bb rve p le oi n Vo lu G as l tica Cri int po uid orVap sure s Pre rve Cu me Pressure Liq Dew s Ga re atu per Tem Figure 9. 9. This area is called the two-phase region and has a characteristic shape for that particular composition. The PV-diagram (upper left) shows how the oil volume is increasing when pressure is . Properties of Reservoir Fluids area in the PT-diagram. a PVT-diagram can be drawn. Volume is therefore a dependent function of p and T . volume and temperature are often referred to as PVT-relations. as shown by the law of real gases. where the two phases of oil and gas co-exists.3: PT-diargam for Ethane. Heptane and their mixture. as shown in Fig. is seen in the PT-diagram in Fig. The existence of a super critical fluid region to the right of the critical point where phases can not be distinguished. 9.

then oil will gradually drop out of the gas both in the reservoir and on the way to location x. 9. Molar volume is equal to volume occupied by one mole of a substance.6. only gas is produced.e. At this pressure the volume continues to increase by separation into co-existing oil . 9. above which a gas can not be condensed. A reservoir with initial conditions as indicated by position 1 in Fig.6 is what we would call a gas reservoir. in Fig.5. 9. the production follows the dotted line from 1 to x. For temperatures higher than T3 . where the heavier components are condensed. Another way of representing the PVT discontinuity.and gas phases. above which a liquid can not be vaporised. with the following definitions: CP: Cricondenbar – a pressure point. represented by the two-phase region. It is important to notice that the shape of an envelope A-CP-CT-B depends on the composition of HC mixture. on the other hand.3 Representation of hydrocarbons 139 decreasing. from1 to 2. CT: Cricondentherm – a temperature point. Continued volume increase means gradually increased gas-oil ratio at constant pressure. is to present the intensive property of specific . . see Fig. lines which defines the fractional oil-gas ratio. there is no phase change when pressure is decreased. a phase transformation will pass through a twophase region confined by a bubble point locus and a dew point locus where the oil and gas are in equilibrium.e. at which two phases become identical.5: Pressure-specific volume diagram for mixed component system. [Vm ] = m3 /kg-mole or cm3 /g-mole (ft3 /lb-mole). For a given temperature. Specific volume is volume occupied by a unit of mass of a substance. 9. [Vs ] = m3 /kg (ft3 /lb). i. For lower temperatures.or molar volume. no phase boundary is crossed. The composition of the gas will have changed. C: Critical Point – a pressure and temperature point. i. we observe a monotonously volume increase or swelling of the oil phase down to a certain pressure level. however. If. T1 T2 T3 T4 Liquid Liquid Pressure Critical point Gas T4 T3 T2 T1 Gas Two-phase region Specific volume Temperature Figure 9.5. The PT-diagram for a more complex mixtures is presented in Fig. All the quality lines merge at this point.e. When this reservoir is produced at constant temperature.9. i. The two-phase region is left when the pressure starts to decrease again and further volume increase is due to gas expansion only.

140 Chapter 9. At this time.1 Ternary diagrams Binary diagrams are often used for representing an overall behaviour of hydrocarbons and for detailed analysis of phase behaviour when the number of components or groups of pure components. 9. condensation of gas in the reservoir starts as soon as the two-phase region is entered. no change in the composition will occur. 1 CP p Liquid C 3 4 CT A 80% 60% 40% 20% x 5 B Gas T 2 Figure 9. do not exceed three .6. Form that point onwards. 3 . 9. As we have mentioned before. i = 1. Natural hydrocarbons are complex mixtures of different components and are usually represented by pseudo-components (normally 2 or 3).6.3. 9. at point 4. When this reservoir is produced at constant temperature. we can imagine that an oil reservoir is located somewhere in the upper left corner in Fig. When this reservoir is produced at constant temperature.6: PT. see Figs. Ci = Ci1 S1 +Ci2 S2 . 9. In order to predict phase behaviour for such compositions ternary diagrams are often used. Let us assume that the overall composition is represented by point M. Then the overall compositions Ci can be expressed through the phase compositions Ci j . One of the advantages of ternary diagrams is that they enable us to represent both the phase compositions and the overall composition of mixture. from 1 to 5. such that an oil reservoir would have a different shaped two-phase region than seen in Fig. vaporisation of residual oil can happen and the gas composition may become richer until the dew point line is crossed.diagram for a complex HC mixture. Properties of Reservoir Fluids A reservoir located at point 3 in Fig. 9. Having said this.7 and 9.6. 2. solution gas will slowly build up to a continuous phase and flow towards the well with a considerably higher mobility than the oil itself. should be called a gas condensate reservoir.8. the two-phase region is characterising the reservoir fluid. When the pressure continues to decrease. no gas will exist in the reservoir until the bubbel point line is crossed. and the dew point line is approached.

8 shows the case when the composition has a 3-phase region which is indicated by the embedded smaller triangle. Using the fact that S1 + S2 = 1.invariant point 2-phase region a b e C3 d C2 3-phase region Figure 9. The lever rule enables us to calculate the relative amounts of these phases. 9.7: Two-phase ternary diagram. All sides of this triangle are surrounded by 2. Fig.9. the system has only one degree of freedom. Ci2 −Ci1 which is called "the lever rule". Note that the fraction of each component is 1 at their apex and 0 at the opposite edge. Any total composition M within this triangle gives three phases with the same overall composition.8: Three-phase ternary diagram. This means that if one of the parameters is specified all the other can be easily evaluated. Moving inside the triangle we can only change the fraction of phases and not the overall composition. It means that the compositions of the three phases are given by the apexes of the 3 phase triangle (invariant points). weight.3 Representation of hydrocarbons 141 C1 1-phase region Plait point Tie line C3 Binodal curve 2-phase region C2 Figure 9. where (p and T are expected to be known). Ci1 −Ci2 S2 = Ci −Ci1 .or volume fraction). . we can obtain the following expression for the relative amounts of phases Si j in the overall composition. C1 1-phase region Plait point Tie line f c .phase regions. There is no degrees of freedom in the three phase region. It follows from the Gibbs phase rule that in case of 3 (pseudo) components and 2 phases. S1 = Ci −Ci2 . Any unit can be used (mole-.

When producing the gas to the surface. Starting at point 3 in Fig. in practical field developments this is not easily accomplished. Let us imagine initial pressure and temperature at point 3 in Fig. thus inhibiting re-vaporisation. 9.4 Natural gas and gas condensate fields In a dry gas field. i. this does not occur because once the pressure falls below point 4 the overall composition and hence. the position of the point being dependent on surface separation. If initial conditions in the reservoir coincide with point 1 in Fig. During isothermal depletion liquid will start to condense in the reservoir when the pressure has fallen below the dew point at 4. the injection is terminated and the remaining dry gas produced. that the phase envelope moves to the left and upwards. this represents a loss of a valuable part of the hydrocarbon mixture. the reservoir temperature is always larger than the critical temperature of the same gas. c+d S3 = e .7 and 9. Sometimes it is economically advantageous to produce a gas condensate field by the process of gas re-cycling.9 and separating the liquid condensate from the dry gas at the surface and re-injecting the latter into the reservoir in such a way that the dry gas displaces the wet gas towards the producing wells. The objective of the gas re-cycling process is to keep reservoir conditions above/or to the right from the dew point curve. the molecular weight of the HC remaining in the reservoir increases and is left behind in the reservoir as retrograde condensate while the light components are mobile and will be produce. Continued pressure depletion below the point of maximum condensation would lead to revaporisation of the liquid condensate.e. .142 Chapter 9. However. 9. however. which is usually the case for surfactant+oil+brine systems. The condensation is generally rather small and frequently below the critical saturation which must be exceeded before the liquid becomes mobile. since the heavier components tend to condense first. Properties of Reservoir Fluids S1 = a . a+b S2 = c . as seen in Fig.8 both triangles have a common baseline. Tr > TCT . both p and T will decrease and the final state will be at some point x within the two-phase envelope. The process of condensation is called retrograde liquid condensation. The composite phase envelope for the reservoir fluids tends to move downwards and to the right. than the dew point line will never be crossed and only dry gas will exist in the reservoir at any pressure. However. After breakthrough of the dry gas occurs. 9. 9. the following initial condition is important.6 and gas recovery is performed in such a way that the pressure will decline from1 to 2. The maximum liquid saturation deposited in the reservoir is when the pressure is between points 4 and 5 in the two-phase region.6. where the retrograde liquid condensate is not recovered and. e+ f In Figs. 9. The reservoir pressure is kept almost at the initial level but the composition of the reservoir gas is gradually changed in such a way.9. 9.

there will be only one phase present.5 Oil fields Since the oil contains more of the heavier HC components.10: Development of the oil field.10. namely liquid oil containing dissolved gas. 9.9: Development of the gas field by the gas re-cycling process. .10. a phase diagram for oil will be more elongated in horizontal direction. • liquid oil. If initial conditions in the reservoir coincide with pointA in Fig. containing an amount of dissolved gas which commensurate with the pressure and • liberated gas. originally dissolved in the oil.5 Oil fields 143 3 p Initial composition Intermediate composition Final composition T Figure 9. Further reduction in pressure will lead to solution gas production and the presence of two phases in the reservoir.9. 9. as compared with gas fields and as shown in Fig. 9. Unfavourable conditions of production p A B X Initial composition Intermediate composition Final composition T Figure 9. Reducing the pressure isothermally will eventually bring the oil to the bubble point B.

10. will flow with a much greater velocity than the oil towards the well. 9. gas injection or other enhanced oil recovery methods. Volumes defined at reservoir conditions (or at the surface) are transformed to surface volumes (or reservoir volumes) by use of volume factors. and the shape of the phase diagram will change towards more and more unfavourable conditions for oil production. 9. Properties of Reservoir Fluids Keeping production at point X below the bubble point. Rs and R.12. the overall reservoir HC composition will change due to the fact that the gas. or above the bubble point by using water flooding. The volume factors are defined by laboratory experiments performed on samples taken from the reservoir oil or gas. It is therefore preferable to maintain oil production close to. which is the number of standard cubic meters (feet) of gas which will dissolve in one stock tank cubic meter (barrel) of oil when both are measured at surface conditions. Bo . These factors are defined in accordance to Fig. The composition will change to such an extent.144 Chapter 9. measured in standard volume quantities (at normal pressure and temperature) are converted to reservoir volumes by the use of volume factors. in Fig. Reservoir gas p A Reservoir fluid Reservoir oil Initial reservoir conditions T Figure 9. The relative content of heavier components in oil will increase. The phase diagram for an oil reservoir with a gas cap must necessarily have a phase envelope which is characterised by both the gas and oil contained in the reservoir.11: Phase diagram for the oil reservoir with a gas cap. The definition of these factors are [21]: Rs : The solution gas-oil ratio.11. that the liquid phase is finally becoming less and less mobile. Vogn Sm3 Rs = . 9. 9.6 Relation between reservoir and surface volumes The amount of oil and gas produced form the reservoir. The two-phase area of the reservoir fluid is overlapping the appropriate oil and gas reservoir. Bg . as shown in Fig. being more mobile. Von Sm3 .

6 Relation between reservoir and surface volumes 145 Reservoir: p. 9. Sm3 Bg : The gas formation volume factor is defined as the volume of gas in cubic meters (or barrels) in the reservoir divided by the volume of the same gas at standard cubic meter (foot).3) .2) (9. simply using Fig. Vg Rm3 Bg = . Bo = Vo Von Rm3 .12: Vgn = RVon Vg = Bg (R − Rs)Von Vo +Vg = [Bo + (R − Rs)Bg ]Von (9. R= Vgn Von Sm3 .1) (9.9. Tn Vg Vp Vo Vggn Vgn Vogn Von Von Figure 9. Bo : The oil formation volume factor is defined as the volume of oil in cubic meters (or barrels) occupied in the reservoir at the prevailing p and T divided by the volume of oil in stock tank cubic meter (barrel). Vggn Sm3 R: The gas-oil ratio (GOR). is the volume of gas in standard cubic meters (feet) produced divided by volume of stock tank cubic meter (barrel) of oil at surface conditions.T Surface: pn .12: Stock tank production through expansion of reservoir oil and -gas from an oil reservoir. Sm3 The following useful relationships between the volume factors can be deduced.

This increase in Bo is directly linked to the oil compressibility.146 Chapter 9. Rs . all free gas will be dissolve in the oil. .13: Dependency of PVT volum parameters on pressure.e. This process continues until standard condition is reached.13.13. the volume of gas will expand as the reciprocal pressure. The solution gas-oil ratio Rs is constant for pressures higher than the bubble point pressure. Finally all gas will evaporate and the oil is said to be dead and Bo ≈ 1. In order to explain the characteristic behaviour of the different volume factors it is natural to follow a decreasing pressure development. 9. Bo Rs pb p R pb p Bg pb p pb p Figure 9. gas in equilibrium with oil can only exist up to its bubble point pressure. A unit sample of oil at different pressures (p > pb ) will therefore contain the same amount of gas and oil at standard condition. from right to left in Fig. solution gas is gradually leaving the oil phase which leads to a shrinking volume of oil.e. when pressure is released. The oil volume factor Bo is seen to increase linearly when pressure is decreasing towards the bubble point pressure pb . In the case of the volum factor for gas. Properties of Reservoir Fluids Vg = Bg (1 − Rs )Vgn R (9. For pressure higher than pb . For pressures lower than the bubble point pressure. i. as seen from Fig. For decreasing pressure lower than the bubble point pressure. 9. we will find a decreasing amount of gas in the reservoir oil sample because some gas has already evaporated and been produced as gas. i. Bg and R are all pressure dependent functions. then volume is increased. For pressure lower then the bubble point.4) The volume factors Bo . since no gas is produced in the reservoir.

and the reservoir gas-oil flow ratio is written. Qgn = RQon. R= Vgn Qgn = . not only because it gives the gas-oil ratio as function of pressure and time. i. The minimum gas-oil ratio is reached as the gas saturation becomes continuous and starts to flow. Example: Importance of the GOR The GOR is an important parameter.and gas flow. where Qg is the gas rate in the reservoir. both for oil. no change is observed in the gas-oil ratio at surface condition. we may express the GOR in terms of reservoir parameters. but also because it carries important information about the mobility ratio of gas and oil in the reservoir. The presence of discontinuous gas will block some of the path ways for the oil and consequently oil with less gas are being produced. first near the wellbore.(9.9. When pressure is further decreased. Using the relations Eqs. With reference to Figs. with a reservoir pressure lower than bubble point pressure. .6 Relation between reservoir and surface volumes 147 The gas-oil ratio R.1) . Qon = Qg /[Bg (R − Rs)].4) we find.e.12 we may define the gas-oil ratio for a saturated oil reservoir. more gas than oil is produced than initially. we may safely neglect all capillary effects. Shortly after the reservoir pressure has dropped below the bubble point pressure. we may write the following expression for the GOR factor. i. Qo µg ko Substituting this ratio in the GOR equation. Qg kg µo = . 9. g. When the pressure is above the bubble point pressure. where Qi are the reservoir flow rates. µi dr i = o. Qi = ki d pi A . the gas is not mobile due to gas saturation below critical gas saturation. Von Qon where Qon = Qo /Bo and where Qo is the oil rate in the reservoir. is given as a function of decreasing reservoir pressure. since gas liberated in the reservoir is more mobile and therefore is produced faster than the oil it originally evaporated from.(9. and the two relations giving the gas. we assume Darcy’s law to be valid.13.1 and 9. 9. shown in Fig. For reservoir flow in the vicinity of the well. the process of solution gas vaporisation will take place. defined above. R= Qg Bo + Rs . Bg Qo For reservoir flow. Using the GOR.and oil rate.e. For a short while.

Solution gas-oil ratio. shown in Fig.7 Determination of the basic PVT parameters Conventional analysis of basic PVT parameters follow well established procedures by which the different volume factors are measured: • Flash expansion of the fluid sample is used to determine the bubble point pressure pb . and i = o. Bg and Rs are known from laboratory measurements. λi = ki /µi . 9. . OIIP = GIIP/Rs . Rs and Bg . Oil reserves: Gas reserves: OIIP = HCPV /Bo .and flash expansion.14. is important in defining the reserves in an oil reservoir. • Differential expansion of the fluid sample is used to determine the basic parametersBo . Properties of Reservoir Fluids R= kg µo Bo + Rs . µg ko Bg (9. The reserves coming from a gas reservoir is defined.and gas reservoirs.5) where the mobility of oil.(9. For a general reservoir we may define the following parameters. The process differential . Formation factor.5) gives the relation between gas . GIIP = OIIP · Rs . • Flash expansion of fluid samples through various separator combinations is used to enable the modification of laboratory derived PVT data to match field separator conditions.(9. Example: Initial reservoir fluids The definition of initial in place volumes are somewhat different for oil. The hydrocarbon pore volume. HCPV = VR · φ .5) gives a idealized approximation of reservoir dependence and should therefore be interpretated with care. g.and oil mobility in the reservoir and the observed gas-oil ration.and gas is defined. VR φ Bo . where the volume factors Bo . Gas reserves: Oil reserves: GIIP = HCPV /Bg . The GOR as presented in Eq. Bg Rs Reservoir bulk volume.148 Chapter 9. 9. Porosity. illustrates the difference between flash and differential expansion of the fluid sample. Eq.

9. Therefore. Consequently flash expansion leaves smaller oil volumes then differential expansion. there is a continous compositional change in the PVT-cell. where multi-stage separation at the surface is commonly used because differential liberation will normally yield a larger final volume of equilibrium oil than the corresponding flash expansion. depletion gas is liberated physically and removed from the cell.14: Flash and differential expansion of fluid samples. . Note that the flash expansion experiment does not change the overall hydrocarbon composition in the cell while in the differential liberation experiment. The remaining hydrocarbones are becoming progressively richer in heavier components and the average molecular weight is increasing.7 Determination of the basic PVT parameters 149 pi > pb pb p < pb pb pb new Oil Oil Gas Oil Oil Gas Oil Oil Hg 1 p 2 3 p 1 2 3 Flash expansion 1 2 3 Differential expansion 1 2 Initial composition Final composition 3 T T Figure 9. Reservoir production is most likely reproduced by a non-isothermal differential expansion. at each stage.

480 SCF/STB Elevation [ft] -5420 -5424 -5426 -5428 . 0. 1. The pressure is increased isothermally until two phases appear. Estimate the following PVT parameters.1 Gas specific gravity.18 RB/STB Gas formation volume factor.7.150 Chapter 9. Properties of Reservoir Fluids 9. as above. The contained liquid volume is 388 cm3 and the measured gas volume (at 1 atm. Calculate the density expressed in SI-units. The following data are obtained in a PVT analysis at 900C. Bo factor at 207 bar. when water density is 1000 kg/m3 at standard condition (1 atm. 45. 4.65 Oil formation volume factor. Pressure [bar] Celle (system) volume [cm3 ] 276 404 207 408 172 410 138 430 103 450 a) Estimate the bubble point pressure.8 Exercises 1.2 and – for a natural gas API gravity of 70. and residual liquid volume is found to be 295 cm3 and the liberated gas volume is 21 litres.60C) is 5. A gas consists of 50% – 50% mixture by weight of two hydrocarbons. What are the weight functions of the liquid and the vapour phase? 3. b) c) d) e) co .0025 RB/SCF Solution gas-oil ratio. 2. 0. The system is re-compressed. Calculate the gas-oil capillary pressure for the following reservoir: Gas saturation [%] 75 50 25 0 Additional data: Oil API gravity. – for a crude oil API gravity of 57.275 litres. The liquid phase consists of 40% by weight of the more volatile component and the vapour phase 65% by weight of this component. and 15. and 200C). liquid compressibility at 207 bar. expanded to 138 bar and the free gas is removed at constant pressure and then measured by further expansion to standard condition. The pressure is reduced to normal condition. Bo and Rs at 172 bar and 138 bar and Bg and z at 138 bar.

0. . 3. b) 14. 699. ρo = 735.1 · 10−5 bar−1 . 1. e) 0.5 kg/Rm3 .0079 Rm3 /Sm3 .7 kg/Rm3 . 749.3898 Rm3 /Sm3 .8 kg/m3 .383 Rm3 /Sm3 .2 Sm3 /Sm3 . c) 1. ρg = 55. a) 172 bar. 71. 2.887 4. d)1.9. 2/3. 89.5 kg/m3 .315 Rm3 /Sm3 .8 Exercises 151 Answers to questions: 1.07 Sm3 /Sm3 .

152 Chapter 9. Properties of Reservoir Fluids .

Part II Reservoir Parameter Estimation Methods 153 .

.

• History matching. i. where Expansion = Production. i. p= 1 Vi pdV. Even though material balance techniques use crude approximations of the reservoir.e.e.Chapter 10 Material Balance Equation 10. If we assume the fluid density in the reservoir to be constant during the depletion process. water and gas (production decline curve analysis). The pressure in this tank is defined by the volumetric average pressure.1 Introduction The basic principle behind the Material Balance Equation is very fundamental: The mass of hydrocarbons (HC) initially in place is equal to sum of the mass produced and the mass still remaining in the reservoir. methods based on the material balance equation are commonly used in the following cases: • Extrapolation of production curves for oil.(10. Vi −V = ∆V when pi → p. 155 (10. Vi where Vi is the initial hydrocarbone volume. Being simple in principle. In material balance calculations we implicitly consider the reservoir as being a tank of constant volume. ρ ∼ constant.1) is often referred to as the golden principle. we may write the mass conservation law in terms of volume conservation. In this chapter we will develop the Material Balance Equation for a general oil and gas reservoir and illustrate the use of the equation by various examples. Eq. their application and use have proven to be of great importance in various situations. • Identification of the drive mechanism.1) . Mi = ∆M + M. with limited reference to local information. the hydrocarbon pore volume (HCPV).

[Sm3 /Rm3 ] and Bg : gas formation volume factor at current reservoir pressure.2) that. The material balance equation given by Eq.1) is slightly redefined where the volumeof gas in the reservoir initially in place is obviously equal to the volumeof gas in the reservoir at a given pressure p. Bgi = Vi = Vn p zT · n zT p and i . where the purpose is to visualise the transformation of gas volume under reservoir condition to surface conditions. Material Balance Equation 10.(10.(10. in standard units.3) Using the equation of state for a real gas pV = znRT . G: resources of gas initially in place. [Sm3 /Rm3 ]. the volume occupied by the gas in the reservoir.1.2) is illustrated in Fig.e Eq. When a surface volume of G p has been produced. Bgi Gp = 1− .156 Chapter 10. and assuming isothermal conditions of production one can obtain the relations. G · Bgi = (G − G p )Bg . the volume of gas left in the reservoir is G − G p . Bgi : initial gas formation volume factor. At a reservoir pressure p.(10.2). The relation presented in Eq. Bg G (10. i. 10. It follows from Eq. [Sm3 ]. is equal to (G − G p )Bgp . The production of gas at surface conditions is G p .(10. p G Bgi pn G [Sm ] 3 (10.2 Dry gas expansion Let us consider a dry gas reservoir where the production is modelled using material balance calculations.1: Volume transformation using volume formation factors. where the following definitions are used. The HCPV is constant in absence of water influx. [Sm3 ]. G p : cumulative volume of gas produced.2) (G-Gp)Bg G-Gp Gp Figure 10.

the intersection point with the x-axis gives us an estimate for initial gas in place. G (10.3) can now be written. this serves as a proof for the assumption of no or negligible water influx during gas production and that the main driving force behind the production is gas expansion. 10.4) Using Eq. p where the indices i and p refer to the initial and current pressures respectively .2: Gas reservoir exhibiting a straight line trend in p/z vs.3. When the data follows a linear trend.2. G. p z = p z 1− i Gp .4). 10.3 A general oil reservoir In a general oil reservoir. Two important characteristics are displayed by plotting the data as shown in the figure.3 A general oil reservoir 157 Bg = Vp = Vn p zT · n zT p .10. (p) z i G 0 Gp Figure 10. p/z vs. there may exist a gas cap above the oil zone. . allowing us to estimate the resources of gas. hydrocarbons will be represented as oil and/or gas. m: Ratio between the resources of gas in the gas cap and resources of oil in the oil zone measured at reservoir conditions.(10.(10. The gas in the gas cap is in equilibrium with the oil in the oil zone and the volume part of the reservoir occupied by gas relative to oil is constant. as shown in Fig. as schematically indicated in Fig. reservoir temperature and initial pressure. The following nomenclature is used in the derivation of the material balance equation: HCPV : Part of pore volume occupied by hydrocarbons. Dependent on the composition of the fluid. cumulative gas production. 10. when a straight line is fitted through the data. cumulative gas production exhibits a straight line trend. Secondly. Eq. N: Resources of oil (initial oil in place) in Sm3 .

B.3. N p : Volume of oil produced in Sm3 . C . A1: Expansion of oil. Production from the oil reservoir (with a gas cap.3) is explained as expansion of the oil zone.produced volumes Figure 10. expansion of the gas cap. Reservoir expansion is equal to production. Here Vo (pi ) is the oil volume at initial conditions and Vo (p) is the volume of the oil initial in place at pressure p. 10. see Fig. .4. mNBoi: Resources of gas (initial gas in place) in Rm3 . it is therefore convenient to break up the expansion term into its components. B: Expansion of gas cap gas. Note that we are here considering underground withdrawal of hydrocarbon fluids. Vo (p) −Vo (pi ) = ∆Vo (p).A.3: Oil reservoir with a gas cap: Illustration of material balance. 10. see Fig. volume . measured in Rm3 . ∆Vo is the volume oil produced at reservoir pressure p. 10. C: Reduction in HCPV due to expansion of connate water and reduction of pore volume. A2: Expansion of originally dissolved gas. In dealing with the development of the material balance equation. Material Balance Equation Initial reservoir conditions Current reservoir conditions Gas cap 3 mNBoi (Rm ) Gas cap B Oil zone NBoi (Rm ) 3 C Oil zone A A. hence: ∆Vprod = A1 + A2 + B + C. volume . volume .C.158 Chapter 10.B and as expansion of initial water present plus reduction of pore volume due to expansion of reservoir formation matrix and possible reduction of bulk volume.1 A1: Expansion of oil The oil (liquid phase) expansion at reservoir condition can be defined as.

GBgi = (G − G p )Bg .3 A general oil reservoir 159 pi p ∆Vo Vo Figure 10. but since we want to express all expanded volumes at reservoir condition. ∆Vo = N · Bo − N · Boi = N(Bo − Boi). measured in surface volumes. we have to multiply the surface volume by the volume factor for gas at reservoir pressure. i.4: Expansion of oil at reservoir pressure.10. The amount of gas still dissolved in the oil at current reservoir pressure and temperature isNRs . N = Vp (1 − Sw )/Boi .3. Reducing the pressure below the bubble point pressure. where Sw is the average water saturation andVp the pore volume.5) where ∆Vo is measured in Rm3 . The total volume of the gas cap as part of the oil volume in the reservoir.2). pb will cause the liberation of solution gas.e.3. also in surface volumes. . GBgi = mNBoi. frompi to p.(10. the gas volume liberated during the pressure drop. Oil expansion is written. The total amount of solution gas in the oil is NRsi. N is the initial oil in place [Sm3 ] and is defined. (10. (10. is. NRsi − NRs = N(Rsi − Rs ).6) 10.2 A2: Expansion of originally dissolved gas At initial conditions oil and gas in the gas cap are in mutual equilibrium . Therefore. 10. measured at reservoir condition. The gas production at current reservoir pressure is then. ∆Vog = N(Rsi − Rs)Bg . This gas volume is measured at surface condition.3 B: Expansion of gas cap gas The expansion of gas cap gas follows the same principle as observed for the expansion/production of dry gas given by Eq. Bg .

c p = (cb − (1 + φ )cr )/φ and VHCPV = Vo +Vg = NBoi + mNBoi = (1 + m)NBoi. i.3. c= 1 ∆V V ∆p ⇒ ∆V = cV ∆p. we found that: Vw = SwVp and Vp = VHCPV /(1 − Sw ) and we get. ∆VHCPV = cwVw ∆p + c pVp ∆p.8) . where the absolute volume change in the HC pore space due to expansion of connate water and reduction of pore volume is. we get. The volume expansion due to initial water and reduction in the pore volume. Expansion of connate water and reduction of pore volume are controlled by the compressibility of water and pore volumes. ∆VHCPV = (1 + m)NBoi cw Sw + c p ∆p. Bgi The expansion of the gas cap (in reservoir volumes) is therefore written. The HCPV compressibility as the compressibility for connate water and formation matrix are defined in accordance with the general law of thermal compressibility. ∆VHCPV = VHCPV cw Sw + c p ∆p. Material Balance Equation G p Bg = mNBoi (Bg − Bgi ).e. respectively. From previous considerations. 1 − Sw (10. Using the definition of compressibility. 1 − Sw where the pore volume compressibility is. Bgi (10.4 C: Reduction in HCPV due to expansion of connate water and reduction of pore volume Reduction in HCPV due to expansion of connate water and reduction of pore volume is in practice equal to the increased production by the same volume. cw and c p . gives the expansion of the HCPV or volume -C.7) 10.160 Chapter 10. ∆Vgg = mNBoi Bg −1 . ∆VHCPV = ∆Vw + ∆Vp . ∆Vw and ∆Vp are the volume changes due to expansion of connate water and that due to reduction in pore volume.

In order to compare the two types of volumes. ∆Vprod = N p [Bo + (R − Rs)Bg ].(10. A2.N p Bo + G p Bg .4 The material balance equation 161 10.5) to (10. N p + G p .10) (We −Wp )Bw on the right-hand side of Eq. i. Using the relation between gas and oil produced at standard condition. we have to transform the production volumes to reservoir volumes. G p = (R − Rs)N p . • Eq. The equation gives a static representation of the reservoir and does not include any terms describing the energy loss in the reservoir due to fluid flow behaviour. are measured at reservoir conditions. It is important to notice under which circumstances the material balance equation is developed.(10.9) we can write the material balance equation for a general oil reservoir.4).4 The material balance equation Combining Eqs. B and C. Bgi 1 − Sw N p [Bo + (R − Rs)Bg ] = NBoi (10.9) 10. The water influx is also pressure dependent. Results published in 1963-64 by Havlena and Odeh opened a wide range .(9. We can now write the overall production term as. The expansion volumes. • Although the pressure only appears explicitly in the water and pore volume compressibility terms. it is implicit in all the other terms of Eq. 10.10) accounts for water influx into the reservoir and production of water.(10. The following features of the MBE should be noted: • MBE generally exhibits a lack of time dependence although the water influx has a time dependence. by comparing the current volumes at pressure p to the original volumes at pi . (10. (Bo − Boi ) + (Rsi − Rs )Bg + Boi Bg cwSw + c p m( − 1) + (1 + m)( )∆p + (We −Wp )Bw .10. where R is the gas-oil ratio (GOR) and Rs is the solution gas-oil ratio.1) to (9.e. Note that the material balance equation is not evaluated in a step-wise or differential fashion.3.10) is evaluated.10) since the PVT parameters Bo . in the way it was derived.5 Linearized material balance equation The linearized material balance equation is particular interesting in connection with reservoir parameter estimation. A1. respectively. Rs and Bg are functions of pressure. Eqs.(10.5 Production terms The production of oil and gas at surface conditions is.

as undersaturated oil.e. Production is driven by expansion of undersaturated oil. i. Rsi = Rs = R. No gas cap can exist. 34].10) is.(10. where the following definitions are used: The underground withdrawal: F = N p [Bo + (R − Rs)Bg ] +Wp Bw Expansion of oil and its originally dissolved gas: Eo = (Bo − Boi) + (Rsi − Rs )Bg Expansion of the gas cap gas: Eg = Boi Bg −1 Bgi (10. indicate a reservoir pressure larger than the bubble point pressure. The reservoir fluid exists in only one phase. i. . 5. The linear form of equation (10. All produced gas comes from the oil. 4. N p Bo = NBoi Bo − Boi cw Sw + c p + ∆p . From this information alone. is described by the law of compressibility.6 Dissolved gas expansion drive Fluid samples taken from an oil reservoir.11) Expansion of the connate water and reduction of pore volume: Ec = (1 + m) cw Sw + c p Boi ∆p 1 − Sw Eq. -water and -formation. p > pb . Boi 1 − Sw We have seen earlier that the slow decline of the volume factorBo . 10. 3. important deductions are made: 1.11) is especially important for revealing the drive mechanism of the reservoir and for estimation of initial oil and gas. Production of oil is controlled by compressibility of oil. for increasing pressures higher than the bubble point pressure. Material Balance Equation of applications of the MBE to reservoir engineering [33. With these restrictions in mind.162 Chapter 10. a simplified material balance equation is written. F = N(Eo + mEg + Ec ) +We Bw . 2.e.

1 − Sw By introducing a total compressibility. Vo = Von Boi and ∆Vo = Von (Bo − Boi). 10.10. in accordance with Fig. N p Bo = NBoi co So + cw Sw + c p ∆p .13) and by introducing the reservoir pore volume using the expression. we may find a simple relation between produced oil.6 Dissolved gas expansion drive 163 co = 1 ∆Vo . Vo ∆p where we may use the definitions. ∆p given by. 9. Oil compressibility is therefore written.5 shows a linear representation of the data. N p and observed pressure drop. Np ∆p Figure 10.5: Reservoir parameter estimation for dissolved gas expansion data. used to determineVp and ct . Bo The linear relationship between oil production N p and pressure drop ∆p can be used to estimate unknown reservoir parameters such as pore volume Vp or total compressibility ct . N p · Bo = N · Boi ct ∆p. Note the notation: N = Von .12) and the simplified material balance equation above is therefore. Np = Vp ct ∆p. Von Boi ∆p Boi ∆p (10. ct = co So + cw Sw + c p . . 1 − Sw (10.12. ∆p = pi − p. Fig. we may write the equation above. co = 1 Von (Bo − Boi) Bo − Boi 1 = .Vp So = N · Boi .

= N Bob 1 − Sw where ct = co So + cw Sw + c p . 10.2 pi = 4000 psi pb = 3330 psi Boi = 1. we may assume the gas expansion to be gradually more important than the expansion due to compressibility of initial water and the formation. When this happens. 3330psi which gives an oil recovery at the bubble point pressure equal to 1. ct = 18. After some time with continuous production.24 · 10−6 psi−1 .5%. For reservoir pressures p < pb . N p [Bo + (R − Rs)Bg ] = N (Bo − Boi) + (Rsi − Rs )Bg + cw Sw + c p ∆p . What is the oil recovery at this time when the following parameters are given? From Eq. .12) we have the total compressibility. Using Eq. we find the total compressibility.(10.14) The use of this approximate equation is justified through a comparison of the different volumes A and C in Fig. we will find that A C in all practical cases. Np Boi ct ∆p . ct = Bob − Boi (1 − Sw ) + cw Sw + c p . 1 − Sw When we consider the significance of the different expansion factors. (10. we may neglect the compressibility term and write the simplified material balance equation as. Np N = 0.2417 RB/STB Bob = 1. Boi ∆p Inserting for the numbers from the table above. . the reservoir pressure will finally decrease below bubble point pressure. The material balance equation Eq. Consequently. gas is produced in the reservoir and the expansion of this gas will become increasingly important for the process of oil production.3.2511 RB/STB Example: Oil recovery factor at bubble point pressure An undersaturated oil reservoir has been produced down to its bubble point pressure.01516.(10. Material Balance Equation cw = 3 · 10−6 psi−1 c p = 8.(10.164 Chapter 10. N p [Bo + (R − Rs)Bg ] ≈ N[(Bo − Boi ) + (Rsi − Rs )Bg ].10) can now be expressed as. and the relative production becomes.6 · 10−6 psi−1 Sw = 0.13) we may write.

we find the oil recovery equal to. As learned from the example above. but the oil will also be smeared out due to the withdrawal of the gas zone. This is about 15 times larger than the total compressibility at pressures above the bubble point pressure.(10. to be negligible compared to the solution gas compressibility. The formula for gas compressibility can be given by cg = 1/V (∆V /∆p). . N p (Bo − Boi) + (Rsi − Rs )Bg . On the other hand it is quite obvious that oil recovery is maximised when R is kept as small as possible. i.where the volume factors are given: The solution gas produced in the reservoir will change the compressibility in the reservoir drastically.4 . information about the GOR is necessary. = N Bo + (R − Rs)Bg where R is the gas-oil ratio (GOR).00339 RB/SCF Bo (900psi) = 1.14). is most probably lost. 10. it should.7 Gas cap expansion drive The presence of a gas cap at initial conditions indicates a saturated oil in equilibrium with the gas.10). production of gas should be minimised since gas acts as the driving force behind oil production. If the gas is produced first. we will not only loose some of the driving force.7 Gas cap expansion drive 165 Rsi (4000psi) = 510 SCF/STB Rs (900psi) = 122 SCF/STB Bg (900psi) = 0. Since the gas is considered as the driving force in the reservoir production.7 (10.(10. R + 200. we can now calculate the oil recovery down to a pressure p = 900psi. Using the numbers from the tables above. namely that: All production should come from the oil zone. if possible be produced after the oil is produced. gas should remain in the reservoir if oil production is to be optimized. From the example above we may state an improtant production strategy for oil reservoirs. This oil.10. Np N = 900psi 344. We may therefore use the approximation Eq.0940 RB/STB Example: Oil recovery below the bubble point pressure Using the same example as above. due to capillary effects.e. The wells should therefore be drilled and . From this simple consideration we may assume all compressibility terms in the material balance equation.15) In order to numerically define the oil recovery. Eq. indicating a gas compressibility of cg 300 · 10−6 psi−1 .

(10. Bgi where we assume no water production or water influx. In the case of gas cap expansion drive we therefore get the somewhat simplified material balance equation. F = N(Eo + mEg ) +We Bw .(10. i. and the size of the gas cap mN. When a gas cap is discovered in connection with an oil reservoir. The linearized terms used in Eq.(10. We = 0. F = N p [Bo + (R − Rs)Bg ]. Eq. where mN is the slope and N is the constant term (N is the intersection point with the y-axis). (10. unless the aquifer size is large compared to the oil reservoir. Example: Linearization of material balance equation The pressure decline in a saturated oil reservoir with a gas cap is driven by expansion of liberated solution gas Eo . Eo = (Bo − Boi ) + (Rsi − Rs )Bg . we can safely neglect all terms in the material balance equation. we have the following data. The data in the table above is plotted in Fig. Further information is also acquired with respect to the different volume factors Bo . like produced oil volume at surface condition N p .16) are defined as below. we need to know the production data. containing expansion of connate water or formation matrix. Boi Bgi where the linearized material balance equation is. Bg and Rs . N p [Bo + (R − Rs)Bg ] = (Bo − Boi ) + (Rsi − Rs )Bg Bg NBoi + m( − 1) + (We −Wp )Bw . For an oil reservoir with a gas cap.166 Chapter 10. If we could assume no water influx during oil production. and gas cap expansion Eg .16). Material Balance Equation completed with the purposed of optimising oil production. in addition to the gas-oil ratio R. In order to estimate initial oil in place N. Bg Eg = Boi ( − 1).10).16) Eo Eo which clearly indicates the advantage with linearization. 10. Eg F = N + mN .e. keeping as much gas in the reservoir as possible.6 which shows a linearization fit taking into account all data points. The assumption of negligible water influx is rather plausible for reservoirs with a gas cap since the expansion of initial water and formation matrix is small compared to the expansion of gas cap gas. as presented in Eq. the linearized material balance equation could then be written. From the figure we find the initial oil volume .

94 4.25 3.8 Water influx 167 p [psia] 3150 3000 2850 2700 2550 2400 F/Eo · 106 [ST B] 398.93 F/E o 450 [STB] 400 350 300 250 200 150 100 50 0 0 1 2 3 4 5 Measurements Linear fit E g/E o Figure 10. 10.29 4.e.54. .99 3. We = f (p. Note that the units on the y. . indicating a fractional gas cap size of m = 0.8 371.8 Water influx Water influx is more the rule. where f is some function which will depend on the reservoir and the extent and volume of the aquifer itself.axis (F/Eo ) is given in 106 ST B.7 · 106 STB.6: Extrapolation of lineraized gas cap expansion data. Generally we may expect the influx of water to be both time and pressure dependent and we write. we expect some influx of water to be present in all situations where reservoir production takes place over some period of time.6 340. than the exception for normal oil and gas production.5 355.t). i.7 340.51 4. to be N = 109.7 Eg /Eo 4.10.8 368.5 · 106 STB and the slope or gas cap size mN = 58.

10. Injection water rate will be proportional to the oil production rate and the following simplified material balance equation is applied.7: Water influx from external aquifer. The use of this equation is important when real data is supposed to be fitted in accordance with a material balance model.2002 RB/STB Bg = 0. i i In the equation above we move from a continuous case to a discrete case by summing over all pressure drops ∆p for all time periods ∆t. will then cause water to flow into the reservoir volume. The constant C is adjusted in such a way as to secure the match between the model and the real data. as shown in Fig. p qw qw qw re pe qw qw Figure 10. t We = 0 qw dt ∑ qi ∆ti = C ∑ ∆pi∆ti. This flow will obey Darcy’s law. N p = 10000 STB Bo = 1. where C is a constant depending on the various reservoir parameters. Material Balance Equation This picture could be clarified by considering a reservoir model.00107 RB/SCF R = 3000 SCF/STB Rs = 401 SCF/STB . qw = C(pe − p). N p [Bo + (R − Rs)Bg ] = Wp Bw . The cumulative water influx can be found by integrating over the time this process takes place. The pressure difference induced. where the periphery pressure (pressure near the boundary) in the aquifer zone is equal tope . Key data for a typical oil reservoir is. Example: Pressure maintenance through water injection In an attempt to maintain the reservoir pressure we may inject water into the reservoir.168 Chapter 10.7.

measured in [STB].10.0N p . Wp = 4.8 Water influx 169 If pressure is maintained. . . we can conclude from the data above that the relation between produced oil and injected water has to be.

2.2417 1. p = pb .1115 1. What is the injection water rate necessary to maintain the production at p=2700 psia ? Use Bw = 1.170 Chapter 10. Material Balance Equation 10.1450 1. The boiling point pressure is 1850 psia.2222 1.0940 1. The following PVT-data is used in material balance calculations.0 RB/ST B. .9 Exercises 1. b) Calculate the recovery N p /N for declining pressure. c p = 8. the water injection rate is not known. For an oil reservoir with gas cap.1633 1. when R = 1000 SCF/STB ? c) The oil rate is 10000 STB/d at pressure p = 2700 psia and the gas-oil ratio is R = 3000SCF /ST B.2022 1. from pi = 4000 psia to p = 600 psia.2480 1.00519 0. p [psia] 4000 3500 3330 3000 2700 2400 2100 1800 1500 1200 900 600 300 Bo 1. Compressibility is given.6 · 10−6 psi−1 and connate water saturation is Swc = 0.1822 1.00161 0. N p [Bt + Bg (R − Rsi)] −Wi Bw . What is the gas saturation at 600psia.0583 Rs 510 510 510 450 401 352 304 257 214 167 122 78 35 Bg – – 0.00339 0.0763 1. cw = 3.01066 a) Find the recovery N p /N.00096 0. 2. (Bt − Boi) + (Bg − Bgi )mBoi /Bgi N= where Bt = Bo + (Rsi − Rs )Bg and Wi is the water volume injected given in STB.00249 0.00119 0.00107 0.0940 1. The material balance equation with no water production is.00137 0.2511 1. a) Calculate the initial oil in place and the size of the gas cap when the following PVTand production data is given. when the pressure decreases from pi = 4000 psia to the bubble point.00196 0.00087 0.0 · 10−6 psi−1 .

Calculate the height of the cone when the pressure at the bottom level of the oil zone (cone) is 1919 psia ( –the water-oil contact).363 RB/STB Bg =0.12 · 108 Water saturation is 0.3049 3.928 – R [SCF/STB] – 1050 1060 1160 – Bo [RB/STB] 1. 3.300 0.2122 1. p [psia] 3330 3150 3000 2850 2700 Np [106 STB] – 1.333 0. calculated from the material balance equation and secondly calculated from the GOR– equation (as done in Exercise 1).3090 5. The data in the table below is taken form an oil reservoir.17 and the water volume factor is approximately 1. Estimate the initial oil volume in the reservoir.2222 1. assume there is no gas cap present and the production mechanism is dissolved gas drive. [Volume of a right circular cone is π r2 h/3].1 · 108 1100 1.5 · 108 1350 2.3014 – – – 1600 621 1.10.3132 5.00092 0.748 0.9 · 108 1800 3.947 2. b) Geological information indicates that the reservoir could be approximated to a right circular cone.594 · 108 1300 535 1.0 RB/STB.00107 a) First.00087 0.2511 1.00096 0.00124 1.018 cp ko =1000 mD kg =96 mD Bo =1.8 cp µg =0.363 0. porosity is 0.024 1.2353 1.00190 1.24.001162 RB/SCF Rs = 500 SCF/STB 4. µo =0.614 · 108 1000 494 1.00250 1.594 0. by a method of comparing R. GOR [SCF/STB] in a reservoir with supercritical gas saturation.437 0. b) Estimate oil production at p = 2700 psia. R = Rs + kg Bo µo .2022 Rs [SCF/STB] 510 477 450 425 401 Bg [RB/SCF] 0.9 Exercises 171 p [psia] Rs [SCF/STB] Bo [RB/STB] Bg [RB/SCF] Bt [RB/STB] ρo [psi/ft] N p [STB] R [SCF/STB] Wi [STB] 1850 690 1. Find the GOR using the following data. ko Bg µg A relation kg /ko exists experimentaly and the gas saturation dependency has been established: .363 0.00150 1. Define an expression giving the gas-oil ratio.00101 0.258 0.

30. a) 2. 4. 0.172 Chapter 10. Calculate the initial oil volume. b) 738 ft. 3.1 cp.43. 0. a) 122.8 · 106 STB.0 cp and µg =0. Material Balance Equation log(kg /ko ) = 34. b) 46%. where Swc =0. µo =1. 5505 SCF/STB.22 · 109 STB. b) by iteration c) 108.54. a) 1.52%.5 · Sg − 2. in view of this new information. Answer to questions: 1.6 · 106 STB .49. c) 39830 STB/d 2. c) Data from an other well indicates the existence of a small gas cap.

only well testing data provide information on dynamic reservoir response. While seismic data and well logs provide a static description of the reservoir. cuttings.) and from interpreted data (surface seismic. Measurement Geophysics Electric Log Well Test PVT. well tests. PVT analysis.11. etc. Such a model is constructed using geological. geophysical and well data.1 Introduction In order to optimise a development strategy for an oil or gas field. well logs.1. A brief understanding of the fundamental aspects of well testing is necessary in order to incorporate dynamic well test data into the reservoir model and it is the function of the reservoir engineer to incorporate these 173 .1: Stages of reservoir modelling. we have to consider a reservoir model capable of realistically predicting the dynamic behaviour of the field in terms of production rate and fluid recovery. formation fluid samples. The necessary parameters are obtained from direct measurements (cores. The well test data is therefore a key element in the reservoir model construction. etc. the petrophysicist and well analyst think the reservoir looks like).).Chapter 11 Well Test Analysis 11. Interpretation of these data leads to individual "models" (what the geophysicist. Core Interpretation Geophysical Model Log Model Reservoir Engineering Well Test Model Reservoir Model Figure 11. see Fig.

created by the start-up of production. Then. Well Test Analysis individual models into a cohesive reservoir model [50]. explaining reservoir behaviour on basis of the well test data. as the fluid moves it will. • horizontal radial flow paths (no cross flow) and • constant flow rate.1. . Some conversion factors mostly used in well test analysis are listed below: . Production from the wellbore and nearby cavities. in turn. Production from an infinite acting reservoir where no boundary effects are observed. the average pressure in the reservoir will decrease in a way similar to emptying a confined volume.174 Chapter 11. c∇p · ∇p is small (compressibility times pressure gradient squared) .1. the fluid near the well expands and moves towards the area of lower pressure. Production from a confined reservoir (closed volume) where the interference from the boundary dominates pressure decline. each describing characteristic well and reservoir pressure response profile: 1. Semi steady state period. 2. fluid contained in the wellbore and its direct connected volumes are produced. In this chapter we will develop simple models that can explain the measured well test data. Semi logarithmic period. as presented in Table 11. In the initial phase of well tests. is affected by the interference from other wells or by boundary effects such as those that occur when the pressure disturbance reaches the edge of a reservoir. like a tank of gas.e. The tail portion of the well test data for the test of sufficient duration. as the production of the reservoir fluid starts. The wellbore pressure data is subdivided into three different production periods. • test production with relative small pressure gradients.1 Systems of Uunits Used in Well Test Analysis The following systems of units are traditionally used in well test analysis: SI-Units and Field Units. i.absolute permeability. is dissipated throughout the reservoir. characterised by: • isotropic and homogenous reservoir volume. create a pressure imbalance and this will induce neighbouring fluid to move towards the well.viscosity and . From this time and onwards. pressure measurements are dominated by wellbore storage effects. This movement will be retarded by friction against the pore walls and the fluid’s own inertia and viscosity.reservoir height (reservoir thickness). During this time. Wellbore storage period. The models give a rather simplified and idealistic view of the reservoir. . Even though these items place tight restrictions on the reservoir itself. This process continues until the drop in pressure. • constant porosity. 3. However. some important information can be extracted from the models. 11.

c f Vw (11. (B is the wellbore fluid volume factor. c f and the well storage volume.1: System of units used in well test analysis Parameter Nomenclature SI-units Field units Flow rate Volume factor Thickness Permeability Viscosity Pressure Radial distance Compressibility Time q B h k µ p r c t Sm3 /d Rm3 /Sm3 m µ m2 mPa·s kPa m (kPa)−1 hrs STB/d RB/STB ft mD cp psia ft psi−1 hrs 1 STB/d 1 ft 1 mD 1 cp 1 psi = = = = = 0. Vw . standard volume.895 kPa 11. The definition of the wellbore fluid compressibility is c f = ∆Vw /(Vw ∆p) and the well flowrate is qB = ∆Vw /∆t. ∆p. Example: Wellbore storage effect A well has a certain volume capacity for fluids. at a well depth of H = 2000m has a volume Vw .2 Wellbore Storage Period 175 Table 11. where the pressure drop in the well is.2 Wellbore Storage Period Let us consider the initiation of well production at a constant rate at timet0 = 0. cws = c f Vw is used to characterise particular wells. First. with an average well radius of rw = 0. This production is characterised by the expansion of oil and gas in the well. .1m. measured in reservoir volume pr. accessible to fluids close to 17 m3 . A real well.1) where ∆p = pi − pw (t) is the difference between initial and wellbore pressure.159 Sm3 /d 0.987·10−3 µ m2 1 mPa·s 6. The compressibility is often redefined. where the wellbore storage.3048 m 0.) ∆p = qB t. the fluids contained in the wellbore itself and its continuous cavities will be produced.11. defined by the fluid compressibility.

exhibits the linear relation between time and pressure drop. hrs Figure 11.e. (11. The technique of using log-log plots is commonly used in well test analysis for model recognition. This straight line behaviour seen in Fig. . day [Sm3 /d] and time in hours [hr]. This effect must be incorporated into the interpretation model of the pressure test data.2) 24(pi − pw (1hr)) with pw (1 hr) picked from the unit slope line. in a logarithmic scale. as seen in Fig. has a slope equal to unity. 24cws and the logarithmic pressure difference can be given by.2. but also as here. where the well itself contains a certain volume of compressible fluid. there is a delay in a flow-rate response at the sand-face (bottom of the well). the well pressure is then given by. log(pi − pw (t)) = log(t) + log qB 24cws . in the wellbore storage period If well production is measured in standard cubic meter pr. When the well is opened (shut-in) to flow.2: Logarithmic analysis of the pressure drawdown data at early times of well testing. Well Test Analysis log( pi . Due to the wellbore storage.3. i.176 Chapter 11. for estimation of the wellbore storage constant cws : qB cws = . 11. pi − pw = qB t. 11. The latter equation. it is opened at the surface. . where pw is the wellbore pressure.pwf ) Slope = 1 10 -3 10 -2 10 -1 10 0 t.

Using an independent co-ordinate system. If we consider a volume element. dt k v = − ∇p.11. The production profile in this period is characterised by a semi logarithmic pressure dependence. d(ρ vx ) dx vx = − ∂ (φ ρ ) . µ Substituting these two equations gives us. µ dx where ρ is density. We shall develop a theory for fluid flow in a cylindrical and somewhat idealistic reservoir (see introductory remarks). 11. µ ∂t (11. k is permeability and vx is flow velocity in x-direction. ∇ · (ρ v) = − ∂ (φ ρ ) .3.3: The wellbore storage effect on flow-rate during the drawdown (left) and build. 11.1 Diffusivity Equation Transport of oil in porous media is generally described by the law of continuity and Darcy’s law.3) . we may write the same equations as. φ is porosity. as shown in Fig.3 Semi Logarithmic Period 177 q Surface flow rate q Surface flow rate Sandface flow rate ∆t ∆t t tp Sandface flow rate ∆t t Figure 11.3 Semi Logarithmic Period In this section we will focus our attention on what happens in the reservoir when the fluid is drawn towards the well due to the pressure drop in the wellbore. µ is viscosity.4. ∂t k dp = − . k ∂ (φ ρ ) ∇ · ρ ∇p = .up tests (right). we may define the flow of oil in the x-direction by the equations. hence the title of this section.11.

(11.7) 11. In case of a constant flow rate the following Initialand Boundary condition are defined. Well Test Analysis px vx px+∆x vx+∆x x x+∆x x Figure 11. while oil density and reservoir porosity may vary with pressure. η ∂t (11.6) (11.178 Chapter 11. ρ ∂p φ ∂p Eq. η ∂t The diffusitivity equation in cylindrical co-ordinates gives. and we write. as mentioned above. 1 ∂ ∂p r r ∂r ∂r = 1 ∂p .e. while the boundary condition is deduced from Darcy’s law. we can write the Diffusitivity equation (independent of co-ordinate systems). With this last simplification in mind. From these relations we can define the liquid compressibility as well as the matrix compressibility as. ρ = ρ (p) and φ = φ (p).5) (11.4) where η = k/(φ cµ ) and c = cl + cm .2 Solution of the Diffusitivity Equation The solution of the diffusivity equation can be simplified by using the linear source approximation implicating a zero wellbore radius. Initial conditions are described by the pressure start-up conditions in the reservoir. In accordance with an idealistic view of the reservoir.4: Flow of oil in the x-direction through a volume element.3) is further developed using the newly defined compressibilities. 1 ∂p . i.3. cl ∇p∇p + ∇2 p = 1 ∂p . cl = 1 ∂ρ 1 ∂φ and cm = . where c is the total compressibility.cl and cm . we will consider both permeability and viscosity to be constant. ∇2 p = 1 ∂ ∂p ∂2 1 ∂p r + 2= . Further simplification of Eq. .4) rests on the assumption that cl ∇p∇p |∇2 p|. which is the case in almost all real cases. η ∂t (11.(11. the linearized diffusitivity equation is written. r ∂r ∂r ∂z η ∂t With no crossflow in the reservoir.

Eq.(11.7). When the Boltzmann transformation is applied to Eq. . ∀r. Second integration of Eq.9) 4π hk r2 /(4η t) s The integral in Eq. pi − p(r.(11. 0) = pi .8). ∀t > 0. Values of the function −Ei(−ξ ) is tabulated in Table 11. gives the following expression. ∀t.11.8).e. pi − p(r.8) ∂p 2 = K3 e−r /(4η t) .2. 4t which gives the following partial derivatives: ∂ r = (r/2y)∂ y and ∂ t = −(t/y)∂ y. K3 = (qBµ )/(4π hk). (11.7) we may use the well known Boltzmann transformation. limr→∞ = pi .10) where η = k/(φ µ c).t) = qBµ r2 −Ei − 4π hk 4η t . y (11. can then be presented as.3 Semi Logarithmic Period 179 Initial condition: i) ii) Boundary condition: r∂p ∂r r=rw p(r. using the boundary condition for the line-source solution. > 0 2π hk = In solving the linear diffusitivity Eq.(11. (11. e−s qBµ ∞ ds. 2π hk qBµ = .9) is known as the Exponential integral and is originally defined as. −∞ s ∞ e−s ds. i.(11. ∂y ∂y η ∂y We may solve Eq. ∂ ∂p y ∂p y = . Line-source solution: limr→∞ r ∂ p ∂r qBµ . r2 y= .t) = Ei(ξ ) ≡ −Ei(−ξ ) = es ds. by direct integration and we get.(11. ∂y where K3 is a constant that could be defined. ∀t.7).(11. the variable of time is made implicit and the diffusivity equation is reduced to only one variable. s ξ ξ The general solution of the linear diffusitivity equation.

0269 1.50 0.07 0. This fact is commonly used in a gas well test analysis.00 4. In the case of more compressible fluids.11) where pb is an arbitrary (datum) pressure.6813 2. Well Test Analysis Table 11. ξ 0.40 0. replaced the dependent variable p by the real gas pseudo pressure m(p) in the following manner.11) they derived a simplified linear equation for a real gas flow: 1 ∂ ∂ m(p) 1 ∂ m(p) (r )= .00 2.1508 2.9057 ξ 0.7024 0.3403 0.80 [−Ei(−ξ )] 0. some modifications are necessary in order to use the diffusivity equation.12) which is precisely the same as Eq.7942 0.9187 1.90 1.1454 1.01 ≤ ξ ≤ 10.28 0.180 Chapter 11.02 0.10 [−Ei(−ξ )] 4.12 0.3.00 7.0762 1. Attempting to obtain a linear type of the diffusivity equation for a highly compressible gas flow.7).04 0.3098 1.6253 0.6595 1.0001 0.0249 0.30 [−Ei(−ξ )] 1.0139 0.70 0.9591 2.4092 1.45 0.50 3.12) that the behaviour of m(p) vs.4544 0. Using the equation of state for a real gas. .1000 0.0011 0.00 [−Ei(−ξ )] 0. It follows from Eq.(11.60 0.65 0.3 Gas Reservoir The general form of the basic (material balance) equation.26 0.22 0.2227 1. is valid for both liquid and gas flow. zRT and a pseudo pressure function m(p) from Eq.8229 ξ 0.0038 0.55 0.2: Table of the function Ei(ξ ) for 0.2602 0.0379 3.06 0. time in gas well testing should have identical trends as pressure vs. Al-Hussainy. given by Eq.14 0.3738 0.4115 0.(11. (11.2953 2.3106 ξ 0.2194 0.0489 0. r ∂r ∂r η ∂t (11.08 0.50 2.35 0. p m(p) = 2 pb p d p.(11.0130 0.3547 2.05 0.7) where the term p is replaced by a pseudo pressure function m(p).18 0.00 10. Ramey and Crawford (1966).20 0.09 0.4679 2.9573 0. time in oil well testing. like gases.24 0.00 5. ρ= Mp .03 0.01 0.5241 1.00 1.5598 0.5034 0. µz (11.0000 11.75 0.16 0.

13) where the factor 1/2 in front of the exponential function is of purely historical reasons.or field units. we get.14) +γ . 1 1 1 1 pwD (tD ) = − Ei − ≈− (11. standard.units: rD = Field units: rD = π hk r 0.5772157 is Euler’s constant.4 The Solution of the Diffusitivity Equation in Dimensionless Form In connection with model recognition and practical application of the well test data it is quite often advantageous to plot the measured data in such a way as to initially compare it with a standard and well known function. (11.3. 2 rw φ µ crw 141. r rD = . 2 · 2! 3 · 3! where γ 0. The interesting question now is related to the validity of the approximation: −Ei(−ξ ) ≈ − ln ξ − γ . the above normalisation can be written. 2 φ µ crw 2π hk pD = [pi − p(r. 2 4tD From mathematical tables we have the following approximation. 11. such as. i. qBµ Depending on the units preferred.11.3 Semi Logarithmic Period 181 11.000264kt .t)].t)].0036kt . It is therefore convenient to introduce dimensionless variables.3. as presented in Eq. related to the presentation of semi logarithmic data. SI.5 Wellbore Pressure for Semi Logarithmic Data The wellbore pressure (rD = 1) is given by.842qBµ π hk r 0.e. ln 2 4tD 2 4tD . tD = and pD = [pi − p(r.10). 2 rw φ µ crw 1.t)]. rw kt tD = .tD ) = − Ei − D 2 4tD . tD = and pD = [pi − p(r.(11. 1 r2 pD (rD .2qBµ Using dimensionless variables for the solution of the linear diffusivity equation. −Ei(−ξ ) = ∞ e−s ξ s ds ≈ (− ln ξ − γ ) + ξ − ξ2 ξ3 + −···. 1 −1 pwD (tD ) = − Ei .

0 cP Using the definition of the dimensionless time in field units from above.tD ) = 2 with the restriction of tD /rD ≥ 25. ln 2 2π hk 2 φ µ crw Rewriting this equation using log term instead of ln and standard units. is not more than 0. Generally we may therefore use the following approximation.80907 . for a "typical" oil reservoir with the following parameters (in field units). 2 rD (11. k = 100 mD c = 5 ·10−6 psi−1 φ = 25 % rw = 1 ft µ = 1. i.16) Example: Semi logarithmic analysis of pressure drawdown data The wellbore pressure is given by the approximation (in dimensionless form).182 Chapter 11. In order to illustrate the implication of the restrictiontD ≥ 25. (11. lntD + 0. In cases where the pressure drop observed in one well is induced by an other well a certain lateral distance apart from the observation well. .e. Error = 1/(4tD ) . is 1/(4tD ).14). we may write. In order to check the accuracy of this approximation we may look at the relative importance of the next term not included in the approximation Eq. tD ≥ 25. 1 pwD (tD ) = (lntD + 0.25 %. Well Test Analysis We may write the dimensionless wellbore pressure as. pi − pw (t) = qBµ 1 kt + 0.15) If we assume the dimensionless time. or 4. pwD (rD .(11. is insignificant for all practical purposes. We therefore conclude that the error done in applying the approximation in Eq. is thought to be insignificant. In these cases the approximation may usually not hold.(11. 1 pwD (tD ) ≈ − (ln 1 − ln 4 − lntD + γ ).80907 .3 seconds. 1 tD ln 2 + 0.14).80907 (11.80907) 2 Using the definition of dimensionless variables.(11. 2 where the next term in the series expansion of Eq. then we would expect the Error always to be less then 0. we can consider the constraint on time (in hours). Eq.14) is valid.0012 hrs. we find that the real time that passes before the approximation.14). given above.80907). we have to consider the restriction imposed above very carefully. 2 1 ≈ (lntD + 0.

.1208qBµ hk logt + log k − 2. 2 φ µ crw 162.units).2275 . k could be estimated when information about reservoir height. kPa Wellbore storage effect Slope m Outer boundary effect 10 -3 10 -2 10 -1 10 0 10 1 10 2 t. oil viscosity.1208 qBµ . The straight line through the semi logarithmic data points in Figure 11. This line is compared with the model above.0923 . These data does not comply with the straight line and should therefore be disregarded when the semi logarithmic data is matched. hrs Figure 11. and from this comparison we get the following equality (using SI . . p(t) ∼ −m logt. is defined by the equation. we may use one of the two equations above in order to extract vital information about the reservoir. where m is the slope of the straight line. pi − pw (t) = 2. m = 2.5. p. some early data originates from the wellbore storage period and some late data originates from the period when boundary effects starts to mask the pressure data.11.5.6qBµ hk logt + log k − 3. In the figure.3 Semi Logarithmic Period 183 pi − pw (t) = and in field units. oil volume factor and oil rate are known. hk The reservoir permeability. 2 φ µ crw When the well test data is presented in a semi logarithmic plot as shown in Figure 11.5: Pressure drawdown data.

but in addition we have assumed that the pressure profile does not significantly vary after the reservoir boundary limit is reached.184 Chapter 11. At this limit. The boundary conditions in the semi steady state are partly defined as for the case of the logarithmic period. the pressure profile in the reservoir is maintained unchanged.17) where K2 is also a constant.6: Steady state pressure profiles. Integration of the time independent diffusivity equation gives. In Figure 11. the reservoir pressure is steadily decreasing while the pressure profile is conserved.e. At constant well production. i. It should be emphasised that this is an idealised model of how we think the reservoir responds to boundaries effects. the drawdown pressure profile is assumed to be constant.e. Well Test Analysis 11. we expect the diffusitivity equation to be time independent. p pe rw Figure 11. there comes a period of production where the influence from neighbouring wells or reservoir boundaries. prudent interpretation of steady state data is highly recommendable. i. . faults or sands thinning out. Simultaneously. in the reservoir. ∂r 2 (11. such as lateral extension. and as such.6.4 Semi Steady State Period After a period of reservoir production from an infinite reservoir. r ∂p 1 = K1 r2 + K2 . several pressure profiles are plotted. a constant K1 balances the diffusitivity equation. are going to play an increasingly important role. ∂ p(r)/∂ t = constant. re Since the pressure profile is assumed to be constant. This period is called the semi steady state period and a steadily decreasing reservoir pressure is observed (decreased average pressure in a confined reservoir volume). 1 ∂ ∂p r r ∂r ∂r = K1 .

(11.19) Eq.6206 (Dietz. Substituting for p given by Eq. find the shape-factor CA 4π e . 11.18) rw and so where re is the radial distance to the boundary of the confined reservoir. however.20) where γ is Euler’s constant. the reservoir shape is seldom cylindrical and more so.19) gives the average pressure in a cylindrical reservoir with an outer radius equal to re and where the well is located in the centre. p(r) = p(rw ) + qBµ 1 r2 r ln − 2 2π hk rw 2 re . re rw /re → 0. i. A = π (re − rw ). with a centred well location.11.18) and integrating. (11.4. we find the average reservoir pressure. p = p(rw ) + qBµ 2π hk 1 4A ln γ 2 2 e CA rw . and integrating Eq. In these real cases we may not use Eq.e. 2π hk Boundary condition at infinite reservoir radius: r ∂p ∂r = 0. gives.(11. The average pressure for a general reservoir is then written.19) directly. 2π hk rw 4 (11.1 Average Reservoir Pressure The average reservoir pressure is not an observable quantity. Instead a slight modified version given by Eq.17) from the well (r = rw ).20) is used. we (3/2−γ ) = 31.(11. r=re Using the boundary conditions to define the constantsK1 and K2 . p= re rw pdV re rw dV .e. p = p(rw ) + qBµ re 3 ln − .4 Semi Steady State Period 185 Boundary condition in the well: r ∂p ∂r = r=rw qBµ . In real cases. The average pressure is a weighted function of the pressure in the whole reservoir and could be defined as.(11. (11. i.(11. where A is the top area of the reservoir and CA is a parameter characterising the shape and relative position of the well. the well position is most frequently off centred. 2 2 In the case of a cylindrical reservoir.1965).

some of the drilling fluid penetrates the formation and particles suspended in the mud can partially penetrate the pore spaces. pe − pw = k rs − 1) ln . Well Test Analysis 11. as stated for formation beds in series. Consequently. and within the rest of the reservoir (rs < r < re ) is k.7: Skin effect caused by formation damage.2 Well Skin Factor When a well is drilled it is always necessary to have a positive differential pressure acting from the wellbore to the formation to prevent inflow of the reservoir fluids (blow-out). The total pressure drop from the wellbore through the reservoir is given by. 2π kh rs ps − pw ≈ Note the approximation made due to the fact that re rw and re rs . ks rw qBµ re (ln + S). pe − pw = pe − ps + ps − pw = qBµ k rs re .7. For the steady state inflow we can write the following equations for a cylindrical reservoir with a centred well. pwf ps pe rw rs re Figure 11.21) where the last term is called the mechanical skin factor S. reducing permeability. Assuming modification of the permeability in the damaged zone (rw < r < rs ) is ks .4. 2π kh rw (11. as shown in Fig.186 Chapter 11. and creating a so-calleddamaged zone next to the wellbore. 2π ks h rw qBµ re pe − ps ≈ ln . S=( Hence.23) . qBµ rs ln . ln + ( − 1) ln 2π kh rw ks rw (11.22) (11. 11.

27) In tDA dimensionless time is referenced to the reservoir drainage areaA. Dimensionless variables are introduced. following the same definitions as for the case of semi steady state. due to drilling or well treatments.(11. pi − p(rw ) = qBµ 2π hk qB 1 4A +S + t ln γ 2 2 e CA rw cV (11. pi to the average pressure p and we get the following simple relation between reservoir pressure and time. ∆pskin = • Skin factor is positive. which can be rewritten as.3 Wellbore Pressure at Semi Steady State The reservoir pressure development in a closed reservoir could be compared to the production from a pressurised closed tank of oil. we pi − p(t) = get.4. qBµ S. As seen from Eq. accounting for a partly damaged zone around the well.11. c = −dV /(V d p).(11. Skin is associated with the condition of reservoir permeability in the closed volume next to the well. If the well. qB t. 11. on the other hand. is the important parameter. Production is maintained through volume expansion where the combined compressibility of oil and reservoir rock . then the well will experience an increased pressure drop in this region while the skin is positive.4 Semi Steady State Period 187 where the skin is a number characterising the cylindrical volume next to the wellbore. we may integrate from initial pressure. with Eq.25) cV Combining Eq. . S > 0 when ks < k and • Skin factor is negative.e. φ Acµ (11. then the skin is negative. If the permeability in the skin zone is reduced. while when S is negative the pressure drop is less than expected. At constant reservoir flow rate. i. an increased pressure drop towards the well is observed.(11. has a permeability higher than expected. dp qB =− . dt cV where qB is the oil flow in the reservoir and V = φ Ah is the reservoir pore volume.25).19) which describes the semi steady state analysis.26) have introduced the skin S as an extra term in the equation.26) Note that we in Eq. (11.c. (11.(11. tDA = kt .23). The total compressibility of oil and reservoir rock is defined by.24) 2π kh From this equation it is evident that when the skin S is positive. with the exception of the dimensionless timetDA . the skin may be associated with a characteristic pressure drop ∆pskin caused by the reduction in permeability in the skin zone. which is defined. S < 0 when ks > k.

0036kt hk . cws Using the following set of dimensionless variables. rw φ Acµ 141. In reality.2qBµ r 0.(11. Well Test Analysis Hence.28) 11. 2 2 e CA rw (11.t). ln 2 2π hk 2 φ µ crw qB t.t)). rw φ Acµ 1. Summing up what we already know. Eq.units: rD = Field units: rD = r 0. tDA = . as if they were independent sequences reservoir production. wD 2 2 e CA rw 1 4A ln 2 γ tDA + 2S . 2 rw e A cst tDA .000264kt hk . 1 4A pwD = 2π tDA + ln γ +S .26) can be rewritten using dimensionless variables and we get.5 Wellbore Pressure Solutions To this time we have developed the pressure function for the three periods of reservoir production. the semi logarithmic period and the semi steady state period. pD = (pi − p(r.80907 + 2S . 2 φ Acµ 2 e CA rw qBµ 1 kt + 0. Well storage period: pi − pw = Semi logarithmic period: pi − pw = Semi steady state period: pi − pw = qBµ 2π hk 1 2π k 4A t + ln γ +S . originating from the different periods are not easily distinguishable and quite a lot of effort is spent identifying which data belongs to which period of production. pD = (pi − p(r. tDA = . well test data. where cD = . we may write the following three pressure equations.188 Chapter 11. Well storage period: pW S = wD Semi logarithmic period: pSL = wD Semi steady state period: 1 4A pSS = 2π tDA + ln γ +S . SI.842qBµ we get the three wellbore pressure equations in dimensionless form. referring to the wellbore storage period. cD 2π hφ c .

For real data.11. such that wD wD d(pSS (tDA ) − pSL (tDA )) wD wD = 0. we may define the transient time when one period is followed by the other.e. 11. Since the wellbore pressure development in the two periods are principally different. i. as seen in the Fig. we can get important reservoir information. The semi logarithmic data is plotted as a straight line and from the slope of this line. changes from being semi logarithmic to being semi steady state dominated.8.9. .1 Transition Time Between Semi Logarithmic Period and Semi Steady State Period The difficulties in recognising the semi logarithmic data is primarily related to identification of the time when the wellbore pressure. data plotted as a straight line. This analysis is mainly performed by plotting the interesting data linearly. pwD SS pwD SL pwD semi semi logaritmic state steady state tDA Figure 11. The purpose of plotting data is partly to be able to identify the different production periods. in a linear-log plot. to facilitate quantitative data analysis. by the minimum pressure difference min{pSS − pSL }.5. which can be transferred to real time by using the definition of dimenisonless time.2 Recognition of Semi Logarithmic Data Appropriate plotting of the well test data is an important tool in the process of differentiating the different reservoir production periods.10 where we have plotted the semi logarithmic data as shown in Fig. This technique is shown in Fig.5. we can identify the semi logarithmic data. 11. 11.8: Transition between semi logarithmic period and semi steady state period.9. following a non linear time development. such identification could be rather difficult to perform and therefore of less practical importance. dtDA Carrying out the derivation we find the transition time.5 Wellbore Pressure Solutions 189 11. 11.11. but equally important. In a linear-linear plot as shown in Fig.tDA = 1/(4π ).

1 D b) with data: φ . Claculate the dimensionless time tD for the following cases.12 µ = 0. Well Test Analysis pwD WS pwD SL pwD SS pwD 1/4π Figure 11.7 cp c = 10 · 10−5 atm−1 h = 2400cm r = 10cm t = 1s k = 0.01D 2. a) with data: φ = 0. µ and c as above and r = 10 cm t = 1000s k = 0. 11.9: Linear-linear plot of well test data.10: Linear-log plot of well test data.05 D q = 10000cm3 /s ..190 Chapter 11.3 cp t = 10 s c = 15 · 10−5 atm−1 k = 0. tDA pwD WS pwD SL pwD SS pwD 1/4π log(tDA) Figure 11.6 Exercises 1.15 r = 10cm µ = 0. Find the exponential intergrals and pressure drops for the following cases. a) with data: φ = 0.

0 cp c= 10 ·10−6 psi−1 Bo = 1. c and h as above and r = 30000cm t = 24h 3.0 ·10−6 psi−1 cw = 3.5 ft φ = 0. In a reservoir at initial pressure. i=1 ∑ dxi 3 d ρ dp dxi = φ µ dρ . µ . c= 1 dρ . after the shut-in. at constant flow rate. k dt and the expression for the compressibility at constant temperature.20 rw = 0. . Use the diffusivity equation. b) What is the pressure draw-down in the well after 3 hours of production? c) For how long must the well produce. a well with a flow rate of 400 STB/D is shut-in.0 ·10−6 psi−1 Use the total compressibility ct = So co + Sw cw + c f in the calculations. The reservoir is characterised by the following parameters: k= 50 mD h= 30 ft rw = 0.25 RB/STB a) At what time. the following data is given: Pi = 4483 psia ko = 7.80 Sw = 0.5 mD µo = 1.3 µ = 3.5772.15 RB/STB So = 0. A pressure drop of 4439 psi is observed in well W1 after 1600 hours of production at a constant flow rate of 190 STB/D from well W2 and after 1550 hours of production of 80 STB/D from W3.11. i=1 dxi 3 5. For a reservoir at initial pressure with 3 wells (W1. Estimate the average reservoir porosity between the wells. Well W2 is located 2000 f t north of W1 and W3 is 1900 f t west of W1. until a pressure drop of 1 psi is observed in a neighbouring well 2000 f t away? 4. W2 and W3) where W1 is an observation well. will the approximation Ei(−x) = − ln(xeγ ) be valid ? (Eulers constant γ =0.276 ft h=30 ft co = 8.) Show that: d2 p φ µ c d p ∑ 2 = k dt . (Assume the liquid compressibility to be small and constant for the pressures in mind.6 Exercises 191 b) with data: φ .0 ·10−6 psi−1 Bo = 1. ρ dp to derive the diffusivity equation for one phase liquid flow.15 cp c f = 4.

62. a) 4. a) 1481. b) 14815.895. 3.4 s.192 Chapter 11. 5. b) 0. c) 227 hr. 0.175 .3 bar. 2. a) 15. Well Test Analysis Answers to questions: 1. b) 51.

Analysis of pressure trends enables us to evaluate several important reservoir parameters and to appraise the drainage zone. • Pressure drawdown test (Fig.1. This is followed by a shut-in period. which again lasts until the pressure stabilises. fluid segregation and gas liberation.lower left): Injecting at constant rate and injection well shut-in. Pressure tests are classified in accordance with their operation. 12. and then opened and produced at a steady rate while the pressure decrease within the well bore is monitored. The development of well testing has accelerated from rudimentary productivity tests into a powerful technique which is strengthening the understanding of complex reservoir characteristics. • Multiple rate (Fig. the well is first shut-in until wellbore pressures stabilise. 12. This poses a problem as well testing theory requires downhole flow rates. causing pressure build-up. Unfortunately. A drawdown test simply involves flow rate measurements and pressure decline in a flowing well. 12.1.upper right): Production of constant flow rate well is shut-in. • Falloff test (Fig. Build-up tests are basically the opposite of drawdown tests.1. each lasting until the flowing pressure stabilises. the well is shut-in and the increase or build-up in 193 .1 Pressure Tests Well testing has become a widely used tool for reservoir characterisation and parameter identification. 12.lower right): Well tested at different flow rates. causing pressure falloff.upper left): The well is opened to flow at a constant rate causing pressure drawdown.1. flow rates are still measured at the surface in most well tests. Such flow rates do not reflect the true downhole conditions as they are considerably affected by wellbore storage. • Pressure build-up test (Fig. Drawdown and build-up tests are the two most common types of well tests and the selection of which one to use depends on the practical field requirements. as in drawdown testing. In a conventional drawdown test.Chapter 12 Methods of Well Testing 12. Instead of measuring pressures in a flowing well.

incorporates all the pressure transient effects caused by every previous step-change in production rate. multiple rate tests are not as simple as it might appear. within a given time. pressure is monitored. Methods of Well Testing q q 0 t 0 t p p 0 q t 0 q t 0 t 0 t p p 0 t 0 t Figure 12.1: Methods of well testing. In practice. Therefore pressure readings taken from the beginning of the test has to be ignored and all analysis is done on the later part of the pressure response. However. it is not so easy to carry out a "pure" drawdown or build-up test as the production schedule prior to the test. is usually complex.2 Pressure Drawdown Test Drawdown test analysis are done by direct application of the wellbore pressure solutions. a Drill-Stem Test (DST) is performed by carrying out a series of build-up and drawdown tests in relatively quick succession. while it relies on additional reservoir information as well as complex interpretation of pressure data using analysis based on theoretical models. The observed pressure build-up/drawdown response. presented in the previous chapter. build-up tests are still affected by wellbore storage effects during the initial stages or "early time"-part of the test.194 Chapter 12. Nevertheless. 12. as with drawdown tests. For example. even though it has been realised that this discarded early time data contains a considerable amount of information. .

An alternative straight line could be the signature of a fault located near the well. The early portion of the data is unfortunately. Well tests have therefore to be made long enough to overcome both effects and to produce a straight line in a semi logaritmic plot.2: Semi-logarithmic plot of pressure drawdown test data.6 qBµ S k − 3. we may formulate the semi logarithmic pressure solutions in SI-units and Field-units as: SI-units: pw = pi − 2.2. will show the radial flow solution as a straight line. log(t)). 12. kPa Wellbore storage effect Slope m Outer boundary effect 10 -3 10 -2 10 -1 10 0 10 1 10 2 t. This fact provides us with an easy and seemingly precise graphical procedure for interpretation of the pressure data. 12.1 Pressure Drawdown Test Under Semi Logarithmic Conditions From the previous chapter in section "Wellbore pressure solutions". distorted by wellbore storage and skin effects as indicated in Fig.1) Field-units: pw = pi − 162. 2 kh φ µ crw 1.2. But even this approach presents drawbacks. The slope and intercept of the portion of the curve forming a straight line is used for permeability and skin factor calculations.2.151 (12.1208 qBµ S k − 2. The latter portion of the pressure transient is affected by the interference from other wells or by boundary effects such as those that occur when the pressure response reaches the edge of the reservoir. see Fig.12. hrs Figure 12. 2 kh φ µ crw 1. Sometimes more than one "apparent" straight line appears and analysis finds it difficult to decide which one to use.0923 + (logt + log ).2275 + (logt + log ).2 Pressure Drawdown Test 195 A plot of pressure versus the log of time (p.151 (12. . 12.2) p.

0923 . SI-units: Field-units: 2 ]. see Fig.2) and the skin is directly calculated. k= [µ m mh 2.6qB µ [mD].151 pi − pw (1hr) k + 3. where the well is producing from its own drained area.3) . The known m-value yields a permeability value.151 Field-units: S = 1. k. These effects can completely mask the all-important pressure response such that proper pressure analysis becomes impossible. k = 162.196 Chapter 12. If we define the slope as a positive number. (Note that pw (1hr) in the equations below.2 we recognise the semi logarithmic data. pw (t) = pi − qBµ 2π kh 2π kt 1 4A +S .) SI-units: S = 1. Semi steady state tests are therefore normally not preferred when typical reservoir parameters like permeability. 12.2.2275 . is a data point on the straight line which needs not necessarily correspond to an observed pressure. neighbouring sealing faults or other pressure disturbing zones. The linear pressure at time t = 1 hr is used in Eqs. productivity and skin are estimated.1) or (12. log(t1 ) − log(t2 ) we may use Eqs.1208qB µ mh The skin factor S is conventionally identified from the same plot. as the data points being plotted on a straight line. m= (pi − pw (t1 )) − (pi − pw (t2 )) > 0.2 Pressure Drawdown Test Under Semi Steady State Conditions When the pressure transient is affected by the interference from boundary effects or other wells. Under semi steady state test conditions we are investigating a sealed-off reservoir. 12. where m is the slope of the straight line. the pressure curve deviates downwards from the straight line behaviour. The semi steady state equation is written. (12. (12.2. Methods of Well Testing In Fig. At these late times in the development of the well test procedure we may likely observe complicated pressure data which is masked by several effects.2).1) or (12. The analysis of semi steady state data is more rigorous than might possible be interpreted by the wellbore pressure equation. to define the reservoir permeability. − log 2 m φ µ crw pi − pw (1hr) k + 2. − log 2 m φ µ crw 12. Sometimes such disturbances overlap with other kinds of "early time" effects like large scale reservoir inhomogeneity. + ln γ 2 φ cµ A 2 e CA rw (12.

3 Pressure Build-Up Test 197 where the pressure is a linear function of time. enables us to define the Dietz shape factor CA . If a well is shut-in at a certain time t. the no-flow conditions.4. the bottomhole pressure drawdown is. The technique of superposition is depicted in Fig. hrs Figure 12. the wellbore pressure is influenced by the continuos production at positive rate +q causing the pressure to decrease. At timet when the well is shut-in.3 Pressure Build-Up Test In analysing drawdown data. when the well is closed. psi po 0 t. the build-up pressure data is considered to be more reliable than the pressure drawdown data.4. the no-flow condition can be described by adding the pressure solutions for the positive flow rate and the pressure solution for the negative flow rate.4) pwf .3) can re-written. For times greater than t. we will observe a combined pressure development caused . γ r2 e w 1. As a theoretical assumption we may consider the wellbore rate to be both positive. the same equations can be applied since the process. as seen in Fig. as indicated in Fig. in the figure.12. can be described by a superposition technique. In the case of pressure build-up. Consequently. 12. The influence by the negative rate −q is to increase the wellbore pressure.151 (12. 12. Fortunately. the "Wellbore pressure solutions" may not be used directly. In Field Units. as shown in Fig. using the "Wellbore pressure solutions" (drawdown pressure analysis). (12.e. Semi steady state data is plotted as a straight line in a line-line plot.5.3: Semi steady state analysis of pressure drawdown data. p0 = pi − 162. we could directly apply the "Wellbore pressure solutions" from the previous chapter. i.6qBµ kh log S 4A − logCA + . Normally. Eq. in principle. 12. −q.3. similar too the process of pressure build-up. at constant wellbore rate. 12. The asymptotic pressure value p0 = pw (t = 0). since the influence from dynamical effects near the well is of lesser importance. (+q) + (−q) = 0. The no-flow condition is obtained when the positive and negative well rate are summed. +q and negative. since pressure is decreasing with time. 12.

198

Chapter 12. Methods of Well Testing

q +q

q=0

0

t

∆t

time

-q

Figure 12.4: Pressure build-up test. Representation of a non-flowing well performance by a superposition technique.

by a decreasing pressure due to the positive well rate (−q) and a increasing pressure due to the negative well rate (−q).

pi
pw(∆t)

A B" ∆t B ∆t A"

pw(t+∆t)

0

t 0

t+∆t ∆t

t ∆t

Figure 12.5: Pressure formation by superposition in build-up tests. Using wellbore pressure, we define, pw (∆t): pw (t + ∆t): pi − pw (∆t): Pressure in the well after shut-in. Pressure in the well given by continuos production at positive well rate. Pressure in the well given by start-up of continuos production at negative well rate (increasing pressure contribution).

12.4 Pressure Test Analysis

199

The superposition principle gives, pw (∆t) = pw (t + ∆t) + pi − pw (∆t), where pw on the left side of the equallity is the well shut-in pressure, while pw on the right side is the well flow pressure. Using dimensionless pressures, the well shut-in pressure is given, pi − pw (∆t) = qBµ [pwD (tD + ∆tD ) − pwD (∆tD )]. 2π hk

If skin is included and the wellbore pressure at shut-in is pw (∆tD = 0) = pws , we have pi − pws = qBµ [pwD (tD ) + S]. 2π hk

From the above equations, we may derive the following expressions for the wellbore pressure. qBµ [pwD (tD + ∆tD ) − pwD (∆tD )], 2π hk qBµ pw (∆t) = pws + [pwD (tD ) − pwD (tD + ∆tD ) + pwD (∆tD ) + S], 2π hk qBµ pw (∆t) = p − [pwD (tD + ∆tD ) − pwD (∆tD ) − 2π tDA ]. 2π hk

pw (∆t) = pi −

(12.5) (12.6) (12.7)

Pressure build-up data is analysed using the three equations above, where Eq. (12.6) is applied to estimate the reservoir permeability and skin, while Eq. (12.7) is used to determine the average pressure p. Eq. (12.7) is derived on the basis of average pressure development, where pi − p = qB k qBµ t. t= 2π tDA , tDA = ct V 2π hk φ Acµ

It is important to notice that the dimensionless pressures pD in Eqs. (12.5) to (12.7) could represent the equations describing both semi logarithmic period as well as semi steady state period, i.e. depending on the analysis to be performed, we may chose which set of equations we think will fit the data best.

12.4 Pressure Test Analysis
Based on Eqs. (12.5) to (12.7), we may perform different analysis, where certain assumptions are made about the nature of pressure test data. In the following, two examples are give on how pressure build-up data might be analysed.

12.4.1 Miller - Dyes - Hutchinson (MDH) Analysis
In this analysis [43] we will assume that the semi logarithmic period is long enough to recognise a straight line behaviour in a semi logarithmic plot, i.e. we need to be able to differentiate between the three different periods, described in the previous chapter.

200

Chapter 12. Methods of Well Testing

pi

p(t+∆t)~ p(t) t t+∆t

Figure 12.6: Pressure approximation in MDH-analysis. Shortly after the well is shut-in, at time t, we start to monitor the wellbore pressure pw (∆t). For some period of time we may assume t ∆t and during this period the dimensional pressure approximation pwD (tD + ∆tD ) pwD (tD ) is valid, as depicted in Fig. 12.6. Combining Eq. (12.6) and the above assumption, gives the wellbore pressure qBµ (12.8) [pwD (∆tD ) + S]. 2π hk If the pressure development is assumed to have reached the semi logarithmic state, after shut-in of the well, we may write: pwD (∆t) = pSL (∆tD ), with reference to the definitions of wD semi logarithmic solutions in the previous chapter. Using the definitions of dimensionless time and pressure for semi logarithmic data, we get the following pressure expression, pw (∆t) = pws + pw (∆t) = pws + m log ∆t + log k S − 2.0923 + , 2 φ µ crw 1.151

where m is the slope of the linearized semi logarithmic data (see Fig. 12.7) and the number 2.0923 is a conversion factor to SI-units. SI-units or Field units depends on preference and the following definitions. SI-units: m= Field units: m =
2.1208qB µ hk 162.6qB µ hk

and −2.0923 and −3.2275

From Eq. (12.8), we find the skin factor by direct substitution, see also Fig. 12.7, S = 1.151 pw (∆t = 1hr) − pws k + 2.0923 . − log 2 m φ µ crw

The average reservoir pressure p, could be evaluated on the basis of Eq. (12.7), using the same approximation as above, namely; pwD (tD + ∆tD ) pwD (tD ). pw (∆t) = p − m [pwD (tD ) − pwD (∆tD ) − 2π tDA ]. 1.151

12.4 Pressure Test Analysis

201

pw
p

pw (∆t=1hr)

∆t =

φµcA 0.0036 k CA

0.1

1

10

100

∆t

Figure 12.7: MDH analysis of semi logarithmic pressure data. We shall now assume that the reservoir had reached its semi steady state period before or shortly after the well was shut-in. The interpretation of the different dimensionless pressures are accordingly, pwD (tD ) = pSS (tD ) wD and pwD (∆tD ) = pSL (∆tD ), wD

and the wellbore pressure is the written, pw (∆t) = p − m [pSS (tD ) − pSL (∆tD ) − 2π tDA ], wD 1.151 wD m 1 1 4∆tD 4A = p− − ln γ − 2π tDA , 2π tDA + ln γ 2 1.151 2 e CA rw 2 e m 1 A = p− . ln 2 1.151 2 CA rw ∆tD

Using SI-units we get, pw (∆t) = p −

φ µ cA m 1 ln . 1.151 2 0.0036kCA ∆t

If the reservoir has reached its semi steady state period before (or shortly after) the well was shut-in, the average reservoir pressure p is found by following the semi logarithmic line to the time ∆t = φ µ cA/(0.0036kCA ), as shown in Fig. 12.7, where the average pressure is, p = pw ∆t =

φ µ cA 0.0036kCA

.

12.4.2 Matthews - Brons - Hazebroek (MBH) Analysis (Horner plot)
Following the same approach as in the above section, we have assumed the pressure difference pwD (tD + ∆tD ) − pwD (tD ) to be small but finite, i.e.,

9) and the wellbore pressure solution Eq.8: Wellbore pressure difference at the shut-in time. The slope of the linear data is m and hence k or kh are found by substitution.10) where pwD (∆tD ) = pSL (∆tD ).151 2 t (12. which points out that the time of shut-in tD . . The skin is calculated at the time ∆t = 1.8. (12.0923 + + logt + log . S = 1.0923 .0923 + + log∆t + log .9) 2 t In practical terms. 12. as indicated by Eq.analysis [36].151 pw (∆t = 1hr) − pws k + 2. as shown in Fig. − log 2 m φ µ crw The pressure pw (∆t = 1) is read directly from the plot.202 Chapter 12.. 2 t φ µ crw 1. Combining the approximation given by Eq. wD Using SI-units this gives.11) 2 t + ∆t φ µ crw 1. Methods of Well Testing 1 t + ∆t ln . where t + 1 t is assumed. 12. In Fig. (12. i.151 ∆t S k = pws + m log − 2. in MBH . is considered to be in the semi logarithmic period.analysis. (12. (12. 1. (12. while for dimension less pressures pwD (tD + ∆tD ) ≥ pwD (tD ). since pwD ∝ (pi − pw ).6). 12.11).e. compared to MDH . The pressure difference is depicted in Fig. may come earlier and further up on the pressure decline curve. we get pw (∆t) = pws + m 1 t + ∆t − ln + pwD (∆tD ) + S .analysis. t + ∆t S k − 2. pwD (tD + ∆tD ) − pwD (tD ) = pi p(t) p(t+∆t) t t+∆t Figure 12.8 we have pw (t) ≥ pw (t + ∆t).151 pw (∆t) = pws + m − log Permeability and skin are estimated by plotting the build-up pressures pw (∆t) against the time function ∆t/(t + ∆t) on a semi logarithmic plot.9. this means that the well could be closed somewhat earlier in the MBH .

wD . (12.12). = 2t t + ∆t CA rw D CAtDA If we now assume that the well is in its semi logarithmic state at the time of shut-in.e.12) pw (∆t) = p − If we then assume that the well is in its semi steady state at the time of shut-in. 2 + pwD (tD ) − pSL (tD ) − 2π tDA .151 2 ∆t 2 e 2 e CA rw t + ∆t A 1 = p − m log . wD (12. for defining the average reservoir pressure p. the we get wD pw (∆t) = p − m 1 1 t + ∆t 1 4tD 4A − 2π tDA . 1 + pwD (tD ) − (ln ∆tD + 0. (12.80907) − 2π tDA . (12. ln − ln γ + 2π tDA + ln γ 2 1.13) is a well defined time (time of shut-in). we may estimate the average reservoir pressure as the pressure on the straight line (see Fig. pwD (tD ) = pSL (tD ).9) in Eq. 2 1 + pwD (tD ) − (lntD + 0.151 m = p− 1.4 Pressure Test Analysis 203 pw p pi pw (∆t=1) 1 ∆t = t+∆t CA tDA 10 -4 10 -3 10 -2 10 -1 1 ∆t t+∆t Figure 12. we then get by substitution into Eq.151 1 t + ∆t ln 2 t 1 t + ∆t ln 2 t 1 t + ∆t ln 2 ∆t 1 t + ∆t ln 2 ∆t + −pwD (∆tD ) − 2π tDA . i. we get m 1. i.13) 2 ∆t CA rw tD Since tD in Eq.9) may be applied in a similar way as done above. ∆t 1 A = . 12. (12. pwD (tD ) = pSS (tD ).151 m = p− 1.7). (12.e.9) at the time. Wellbore pressure data plotted for MBH analysis. Substituting Eq.12. The pressure approximation Eq.80907) − 2π tDA . (12.9: Horner plot.151 m = p− 1.

204

Chapter 12. Methods of Well Testing

pw (∆t) = p

m 1 t + ∆t ln − 2π tDA 1.151 2 ∆t

At the time ∆t/(t + ∆t) = 1, we get ∆t =1 t + ∆t m [2π tDA ], 1.151 kt qBµ = p , 2π 2π hk φ Acµ qBt = p+ , where V = φ Ah Vc

pw

= p+

(12.14)

Under semi steady state conditions we have seen that, pi − p = and consequently we may write, pw ∆t = 1 = p + (pi − p) = pi . t + ∆t qBt , Vc

The initial reservoir pressure is defined in Fig. 12.9 on the straight line at time∆t/(t +∆t) = 1.

12.5 Exercises

205

12.5 Exercises
1. A well is tested by exploiting it at a constant rate of 1500 STB/d for a period of 100 hours. It is suspected, from seismic and geological evidence, that the well is draining an isolated reservoir block which has approximately a 2:1 rectangular geometrical shape and the extended drawdown test is intended to confirm this. The reservoir data and the flowing bottom hole pressures recorded during the test are detailed below. h = 20 f t rw = 0.33 f t φ = 0.18 Time (hours) 0 1 2 3 4 5 pw (psi) 3500 (pi ) 2917 2900 2888 2879 2869 c = 15 · 10−6 psi−1 µo = 1 cp Bo = 1.20 RB/ST B Time (hours) 7.5 10 15 20 30 40 pw (psi) 2848 2830 2794 2762 2703 2650 Time (hours) 50 60 70 80 90 100 pw (psi) 2597 2545 2495 2443 2392 2341

a) Calculate the effective permeability and skin factor of the well. b) Make an estimate of the area being drained by the well and the Dietz shape factor. (after L.P.Dake) 2. A discovery well is produced for a period of approximately 100 hours proir to closure for an initial pressure buildup survey. The production data and estimated reservoir and fluid properties are listed below. q = 123ST B/d N p = 500ST B h = 20 f t rw = 0.3 f t A = 300 acers Time (hours) 0.0 0.5 0.66 1.0 pw (psi) 4506 4675 4705 4733

φ = 0.2 µ = 1 cp Boi = 1.22 RB/ST B c = 20 · 10−6 psi−1 (co So + cw Sw + c f )

Time (hours) 1.5 2.0 2.5 3.0

pw (psi) 4750 4757 4761 4763

Time (hours) 4.0 6.0 8.0 10.0

pw (psi) 4766 4770 4773 4775

a) What is the initial reservoir pressure? b) If the well is completed across the entire formation thickness, calculated the effective permeability.

206

Chapter 12. Methods of Well Testing

c) Calculate the value of the mechanical skin factor. d) What is the additional pressure drop in the wellbore due to the skin? e) If it is initially assumed that the well is draining from the centre of a circle, is it valid to equate pi to the asymptotic value log(t + ∆t)/(∆t) = 0? (after L.P.Dake) 3. A reservoir has 3 wells; W1, W2 and W3. Well W1 has been producing at a constant flow rate of 120 STB/D for 70 hours and is then converted to an observation well. Well W2, located 2500 f t straight north of well W1, is producing at a flow rate of 190 STB/D. Well W3, located 1900 f t west of W1, is producing at a rate of 80 STB/D. At the time when well W1 was shut-down, well W2 had produced for 100 hours and well W3 for 50 hours. Pressure data from well W1 is given in the table: ∆t [hours] Pws [psia] ∆t Pws 0 4213 200 4473 5 4380 250 4474 10 4413 300 4478 20 4433 400 4480 30 4443 500 4470 40 4450 800 4461 50 4455 1200 4448 100 4466 1500 4439 150 4472 – –

Additional reservoir data:

µo = 0.8 cp So = 0.80 h = 30 ft

Bo = 1.15 RB/STB Sw = 0.20 rw = 0.276 ft

c f = 4.0 ·10−6 psi−1 co = 8.0 ·10−6 psi−1 cw = 3.0 ·10−6 psi−1

Assume that the pressure development in well W1 can be expressed by the formula below: Pws = Pi − 162.6 where Q1 µ B t1 + ∆t log kh ∆t − 70.6 Q3 Q1 µ B Q2 Ei(x1 ) + Ei(x2 ) kh Q1 Q1

2 2 φ µ ct d13 φ µ ct d12 x2 = 0.00105kt2 0.00105kt3 and where d12 and d13 is the distance between W1 and W2 and W1 and W3, respectively. t1 is the time of production for well W1.

x1 =

a) Calculate the average reservoir compressibility ct . b) Estimate the initial pressure Pi, assuming the interference between well W2 and W3 is negligible for early pressure data. c) Calculate the average reservoir oil permeability ,ko . d) Calculate the mechanical skin, S. e) Use the pressure observation form ∆t = 1500 hours to find the average reservoir porosity between the wells.

12.5 Exercises

207

4. An oil well has been producing 1484 STB at a flow rate of 124 STB/D, when it was shut down. The pressure build-up data is given in the table below: ∆t [hours] Pws [psia] ∆t Pws Additional reservoir data: 4 2857 28 3308 8 3027 32 3315 12 3144 36 3323 16 3252 40 3331 20 3283 44 3338 24 3298 48 3342

µ = 3.2 cp h = 8.4 ft φ = 0.02

Bo = 1.21 RB/STB ct = 12 ·10−6 psia−1

a) Find the reservoir pressure at the outer boundary, Pe . b) Calculate the average reservoir oil permeability, ko . Answers to questions: 1. a) 240 mD, b) 4.5, 2. a) 4800 psi, b) 50 mD, c) 6.0, d) 128 psi, 3. a) 11· 10−6 psi−1 , b) 4485 psi, c) 7.6 mD, d) -3.5, e) 0.135, 4. a) 3475 psi, b)58 mD.

Methods of Well Testing .208 Chapter 12.

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