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Mansour2013 PDF
Mansour2013 PDF
a
Egyptian Petroleum Research Institute, Cairo, Egypt
b
Chemistry Department, Faculty of Science, Helwan University, Egypt
KEYWORDS Abstract The study aims to predict the physical properties of Egyptian crude oils using modified
PVT properties; Soave–Redlich–Kowng equation of state. The modification was theoretically developed and then
Gas–liquid equilibrium; performed by using data of 43 black oil samples representing all active oil producing areas of Egypt.
Soave–Redlich–Kowng The equation enables to predict the bubble-point pressure, oil formation volume factor, gas–oil
equation of state; ratio, oil density, crude oil gravity, gas gravity and gas formation volume factor of black oils with
Constant mass depletion; average relative errors ranging from 0.01% to 10.713%.
Differential liberation Calculation sensitivity of the proposed MSRKE is determined by testing four oil samples col-
lected from different locations in Egypt and comparing the measured PVT properties with those cal-
culated from MSRKE. These evaluations show an excellent agreement between the measured
properties and calculated ones.
The estimation of reservoir liquid and gas properties from MSRKE is often needed when detailed
laboratory PVT data are not available.
ª 2012 Egyptian Petroleum Research Institute. Production and hosting by Elsevier B.V.
Open access under CC BY-NC-ND license.
1110-0621 ª 2012 Egyptian Petroleum Research Institute. Production and hosting by Elsevier B.V. Open access under CC BY-NC-ND license.
http://dx.doi.org/10.1016/j.ejpe.2012.09.005
138 E.M. Mansour et al.
Nomenclature
P
List of symbols summation
EOS equation of state m parameter in Soave–Redlich–Kwong equation of
BWR Benedict–Webb–Rubin state
RK Redlich–Kwong API American Petroleum Institute ()
SRK Soave–Redlich–Kwong MWo molecular weight of stock tank oil
MSRKE modified Soave–Redlich–Kwong equation of BP bubble point (psia)
state GOR gas oil ratio (SCF/STB)
p system pressure (psia) Er average percent relative error
T system temperature (F) nd number of data points
Tc critical temperature S standard deviation
Tr reduced temperature r the correlation coefficient
Pc critical pressure w.s. well stream
R gas constant (10.73 psi-ft3/lb-mol) psi pound/square inch
Vm volume (ft3/mol) psia pound/square inch absolute
a equation of state attraction parameter
b equation of state co-volume parameter Greek letters
C third virial coefficient q density
B second virial coefficient £V i fugacity coefficient of component i in the vapor
a, b, c, A0, B0 constants in Beattie and Bridgeman equation phase
of state £Li fugacity coefficient of component i in the liquid
a, b, c, A0, B0, C0 constants in Benedict–Webb–Rubin phase
equation x a centric factor
fVi fugacity of component i in the gas phase c constant in Benedict–Webb–Rubin equation
fLi fugacity of component j in the liquid phase cg flashed gas gravity
x mole fraction of gas phase co flashed oil gravity
y mole fraction of liquid phase
k equilibrium ratio for the component Superscripts
kij unlike interaction parameter L liquid phase
A, B parameter in Soave–Redlich–Kwong equation of V gas phase
state
a non-sphericity parameter in various equations of Subscripts
state i component in the gas phase
aT temperature-dependent coefficient in Soave–Red- j component in the liquid phase
lich–Kowng equation of state 0 denotes component; reference system
ac constant coefficient in Soave–Redlich–Kowng c critical
equation m mixture
aTi temperature dependent coefficient of component i g gas
aTj temperature dependent coefficient of component j o oil
Z compressibility factor res reservoir
samples of crude oils, but, sometimes because of lack of which they were originally developed and the geographical
experimental data, the values of reservoir fluid properties area with similar fluid compositions and API oil gravity. Fur-
would be necessary. Actual data unavailability may be because thermore, PVT correlations are based on easily measured field
of sampling cost, uncertainty of measurements or obtained data, such as reservoir pressure, reservoir temperature, and
data, inaccessibility of fluid samples of reservoir hydrocarbon oil and gas specific gravity. The currently available PVT sim-
or disability of samples obtaining [7]. Therefore, in case of the ulator predicts the physical properties of the reservoir fluids
absence of the experimental measurements of PVT properties, with varying degree of accuracy based on the type of the used
it is necessary to use the empirically derived correlation or equa- model, the nature of fluid and the prevailing conditions [11].
tion of state (EOS) [8,9]. Theoretical computations, collectively Petroleum engineers have traditionally used EOS to predict
known as oil-system correlations (or PVT correlations), based the volumetric and phase behavior of a wide variety of reser-
on easily measurable parameters, are used for the prediction voir fluids.
of reservoir fluid properties. Such parameters include tempera- This predictive tool is of great importance during the eval-
ture, pressure, solubility, and API and gas gravity [10]. The uation of newly discovered reservoirs, in the design and the
development of correlations for PVT calculations has been the management of oil recovery projects during the various stages
subject of extensive research, resulting in a large volume of pub- of the reservoir exploitation [12]. The Soave–Redlich–Kowng
lications. The successes of such correlations are not reliable equation of state becomes one of the most widely used and ac-
predictions and they depend mainly on the range of data at cepted models for petroleum fluid properties prediction. Many
Predicting PVT properties of Egyptian crude oils by a modified Soave–Redlich–Kowng equation of state 139
articles in the literature discussed the use of EOS models for satisfactory representation of volumetric properties except in
predicting PVT reservoir fluid properties. the critical region [15].
RT c b Aoð1a=VM Þ
1.1. Equations of state P¼ 1 3
VM þ Bo 1 ð8Þ
VM2 VM T VM VM
Extensive efforts had been made in the past two decades to im- Benedict suggested a multi-parameter equation of state, known
prove the performance of EOS. These include the move from as the Benedict–Webb–Rubin (BWR) equation:
two-constant to three-constant equations to enhance the accu- RT Bo RT Ao Co =T2 bRT a aa
racy of volumetric calculations. P¼ þ þ þ 6
VM V2M V3M VM
One of the earliest attempts to represent the behavior of
real gases by an equation was that of van der Waals who pro- c c c
þ 2 3 1 þ 2 exp ð9Þ
posed the following expression for PVT relationship [13]. T VM VM V2M
a This equation may be considered a modification of the Beat-
p þ 2 ðVM bÞ ¼ RT ð1Þ tie–Bridgeman equation of state, where A0, B0, C0, a, b, c, a,
VM
and c are eight adjustable parameters. The BWR equation
where p is the system pressure (psi), T is the system tempera- suffers from disadvantages [16,17,12]. Perhaps, the most
ture, R is the gas constant (10.73 psi-ft3/lb-mol), V is the vol- important model for the modification of the van der
ume (ft3/mol), a is the attraction parameter and b is the Waals equation of state is the Redlich–Kwong (RK) equa-
repulsion parameter. The symbol a is considered a measure tion. The Redlich–Kwong cubic equation of state is the first
of the intermolecular attractive forces between the molecules. equation which has been successfully applied to the predic-
b is known as the co-volume and considered to reflect the vol- tion of the vapor phase properties [18,19]. It is the precursor
ume of molecules [6]. Other researchers began attempts to im- of a family of simple and relatively precise equations of
prove van der Waals equation of state. These attempts have state.
continued for over 100 years. Clausius proposed that the
molecular attraction term is inversely proportional to RT a
q¼ pffiffiffiffi ð10Þ
temperature. V b VðV þ bÞ T
" #
a where P is the pressure, T is the temperature, V is the molar
pþ ðVM bÞ ¼ RT ð2Þ volume, R is the gas constant. a and b are the Redlich–Kwong
TðVM þ cÞ2
parameters. One of the most commonly and widely applied cu-
The addition of the fourth constant, c enables better agreement bic equations of state was reported by Soave–Redlich–Kwong
with data. However, mathematical manipulations required in (SRK). Soave replaced the term (a/T0.5) in Eq. (10) with a
the thermodynamic calculations are more difficult. So Berthe- more general temperature-dependent term, denoted by aa(T),
lot removed the constant c, resulting in Eq. (2). to give [6]
RT aaðTÞ
a q¼ ð11Þ
pþ ðVM bÞ ¼ RT ð3Þ V b VðV þ bÞ
TV2M
Dieterici handled the temperature dependence of the molecular where the correction parameter a(T) is defined by the following
attraction term in a different manner as follows. relationship:
pffiffiffiffiffi
a a ¼ ½1 þ mð1 Tr Þ2 ð12Þ
P exp ðVM bÞ ¼ RT ð4Þ
VM RT Soave correlated the parameter m with the centric factor, x, to
Lorentz addressed the molecular volume term as follows. give
a bVM m ¼ 0:480m þ 1:574- 0:176-2 ð13Þ
pþ 2 VM ¼ RT ð5Þ
VM VM þ b # For pure substances the equation parameters a and b are
Wohl considered the effect of temperature on the molecular usually expressed as
attraction term. b ¼ 0:08664RTc =Pc ð14Þ
a c
Pþ ðVM bÞ ¼ RT ð6Þ a ¼ 0:42747R2 T2c =Pc ð15Þ
TVM ðVM bÞ T2 V3M
The constants a, b, and c in the equations above have different ðaaÞP
A¼ ð16Þ
values for different substances. Several investigations proposed RT2
virial-type of EOS. Kammerlingh-Onnes proposed the virial
equation of state as the following [14]. bP
B¼ ð17Þ
RT
B C
PVM ¼ RT 1 þ þ 2 þ ð7Þ # For mixtures the equation parameters a and b are usually ex-
VM VM
pressed as am and bm.
And are called the second, third, etc. virial coefficients. Beattie Calculate am and bm for a hydrocarbon liquid mixture with
and Bridgeman published a five constant equation that gives a a composition of xi
140 E.M. Mansour et al.
XX qffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffi
ðaaÞm ¼ ½Xi Xj ai aj ai aj ð1 kij Þ ð18Þ Groboski and Daubert proposed a new expression for cal-
i j culating parameter m. The proposed relationship, originated
from analyzing extensive experimental data for pure hydrocar-
X
bm ¼ ½Xi bi ð19Þ bons, has the following form.
i
m ¼ 0:48508 þ 1:55171- 0:15613-2 ð32Þ
Calculate am and bm for a hydrocarbon gas mixture with a
Sim and Daubert pointed out that, because the coefficients
composition of yi
qffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffi of equation (32) were determined by analyzing vapor pressure
XX
ðaaÞm ¼ ½yi yj ai aj ai aj ð1 kij Þ ð20Þ data of low-molecular-weight hydrocarbons, it is unlikely that
i j Eq. (32) will suffice for high-molecular-weight petroleum frac-
tions. Realizing that the centric factors for the heavy petro-
X
bm ¼ ½yi bi ð21Þ leum fractions are calculated from an equation such as the
i Edmister correlation or the Lee and Kesler correlation, the
authors proposed the following expressions for determining
bm p parameter m, as follows [6].
B¼ ð22Þ
RT
m ¼ 0:431 þ 1:57- 0:161-2 ð33Þ
ðaaÞm P
A¼ ð23Þ
ðRTÞ2 1.2. Determining the accuracy of Soave–Redlich–Kwong
Replacing the molar volume, V, in the equation with (ZRT/p) equation of state
and rearranging give the compressibility factor of gas and li-
quid phases. In order to determine the accuracy of SRKE along with m-
parameter formula, data of 43 PVT crude oils analysis stud-
Z3 Z2 þ ðA B B2 ÞZ AB ð24Þ ies (13 surface crude oil samples and 30 bottom hole crude
The equilibrium ratio, Ki that is, Ki = yi/xi, can be redefined in oil samples) were employed. These data were collected from
terms of the fugacity of component. the literature for different oil well locations in Egypt and
L plotted in Fig. 1. This figure shows a very big variation in
f =ðXi PÞ UL data ranges of bubble point, gas oil ratio, oil gravities,
Ki ¼ iV ¼ Vi ð25Þ
½fi =ðyi PÞ Ui C7+, reservoir pressures, reservoir temperatures, molecular
Soave proposed the following expression for the fugacity coef- weights of well stream, gas specific gravities and oil specific
ficient of component i in the liquid phase. gravities.
L The data were statistically treated and the results are given
fi in Table 1. It shows the basic characteristics of the collected
ln ¼ lnðULi Þ
Xi P Egyptian black oils, which comprise the values of arithmetic
bi ðZl 1Þ mean, maximum, minimum and standard deviation for the
¼ lnðZL BÞ 43 crude oil sample.
bm
The above data were used to determine the accuracy of the
A 2wi bi B
ln 1 þ L ð26Þ SRKE, and results are plotted in Fig. 1.
P ðaaÞm bm Z This figure shows that the average relative errors between
where: experimental K-values and the calculated ones are ranged from
X qffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffi 111% to 55%. This error cannot be accepted to simulate
wi ¼ ½Xi ai aj ai aj ð1 kij Þ ð27Þ PVT data.
i
10000
BP
GOR
1000
API
C7+
100 ResT,Fo
Res P,psi
MW well stream
10
g
o
1
0 10 20 30 40 50 60
0.1
Figure 1 Variations in the physical properties of the 43 Egyptian PVT-studied crude oils.
80
Error, % SRK Eq=
60
40
20
0
Error, %
1 5 9 13 17 21 25 29 33 37 41
-20
-40
-60
-80
-100
-120
Sample ID
Figure 2 Error % between experimental K-value and calculated K-value from SRKE.
a1 ¼ b1 þ b2 X þ b3 X2 ð35Þ The resulting average relative errors are plotted in Fig. 3, from
which the errors were ranged from 0.01% to 10.713%.
where X is a function of pressure and temperature and defined
by
2. Experimental
X ¼ logðP=TÞ3 ð36Þ
Four different oil samples were obtained from different Egyp-
Fitting of the data listed in Fig. 2 with Eqs. (33)–(35) values tian oil companies. The physical properties of the samples are
of the constants b1, b2, b3, a2 and a3 are. given in Table 2.
The PVT analysis consists of (1) sample validation test, (2)
b1 ¼ 0:07578; b2 ¼ 2:28353; b3 ¼ 0:86057; a2 primary test, (3) constant mass depletion (CMD) and (4) dif-
¼ 0:10827; a3 ¼ 0:1104 ð37Þ ferential liberation.
142 E.M. Mansour et al.
12
Error, % MSRK E=
10
Error, %
6
0
1 5 9 13 17 21 25 29 33 37 41
Sample ID
gas–oil ratio, gas gravity, gas formation volume factor, oil den- 3.1. Oil relative volume
sity and oil formation volume factor below bubble point
pressure. Fig. 5a–d shows the results of the reservoir oil relative volume
versus pressure at reservoir temperature for the studied four
2.5. Statistical error analysis wells X1, X2, X3 and X4, respectively.
This property is determined from constant-mass (or con-
The accuracy of MSRKE is determined by studying the stant-composition) depletion stage. In each figure, dot-line rep-
statistical errors. The error analysis comprises the average per- resents oil relative volume from experimental data and the
cent relative error, standard deviation and correlation solid-line represents oil relative volume predicted using the
coefficient. MSRE. The plots show an excellent agreement between the
measured data and calculated ones. In addition, the bubble
2.5.1. Average percent relative error (Er) point pressure was determined from each data plot (Table 3).
The average percent relative error is an identification of rela- The relative volume is equal to 1 at the bubble point pres-
tive deviation of the predicted value from the experimental va- sure. It can also be observed that, the bubble point pressure is
lue in percent, as Eq. (36) strongly affected by changing temperature, gas oil ratio and
1X
nd composition of gas and oil. It should be noted that no hydro-
Er ¼ Ei ð38Þ carbon material is removed from the cell; therefore, the com-
nd 1
position of the total hydrocarbon mixture in the cell remains
where constant as the original composition.
By applying the statistical error analysis technique, the
Xexp Xcst resulting average percent relative error, standard deviation,
Ei ¼ 100 ði ¼ 1; 2; . . . ; nd Þ ð39Þ
Xexp i and correlation coefficient of the oil relative volume for the
The lower the value the more equally distributed is the error four samples above and below bubble point pressure are given
between positive and negative values. in Appendix A. These values ensure the accuracy of the
MSRE.
2.5.2. Standard deviation (s)
3.2. Oil formation volume factor
The standard deviation is a measure of dispersion of predicted
errors by a correlation, and it is expressed as Eq. (38).
rffiffiffiffiffiffiffiffiffiffiffiffiffiffi nd Fig. 6 shows the results of the oil formation volume factor
1 X above and below bubble point pressure versus pressure for
S¼ ðEi Er Þ2 ð40Þ
nd 1 1 the four wells X1, X2, X3 and X4.
The oil formation volume factor above bubble point pres-
A lower value implies a smaller degree of scatter around the sure was measured from constant-mass depletion stage while
average calculated errors. below bubble point pressure measured from differential liber-
ation stage. In each figure, dot-line represents oil formation
2.5.3. Correlation coefficient (r)
volume factor from experimental data and the solid-line repre-
The correlation coefficient, r, represents the degree of success in sents oil formation volume factor predicted using the MSRE.
reducing the standard deviation by regression analysis. The cor- It is indicated that, the oil formation volume factor above bub-
relation coefficient lies between 0 and 1. A value of 1 indicates a ble point pressure increases as the pressure deceased due to the
perfect correlation whereas a value of 0 implies no correlation at oil expansion. Continuous decreasing pressure leads to gas
all among the given variables. The larger the value of r, the great- releasing. Below bubble point pressure, a decrease in oil forma-
er is the reduction in the sum of squares of errors, and the stron- tion volume factor with decreasing pressure is related to the
ger is the relationship between the independent variable and the liberation of gas. The amount of gas dissolved in the oil de-
dependent ones. It is expressed as Eq. (39). creases with decreasing pressure till reaching standard condi-
tions, at which oil formation volume factor is equal to 1.
pffiffiffi X
nd X
nd
r¼ 1 ½Xexp Xcst 2i = ½Xexp X
2 ð41Þ The statistical error analysis results as given in Appendix A
i
1 1 for the four samples above and below bubble point pressures
ensure a good agreement between the measured data and cal-
where
culated ones, and consequently emphasize the accuracy of the
1X nd MSRE.
X ¼ ½Xexp i ð42Þ
nd 1
3.3. Density
3. Results and discussion Fig. 7 shows the results of the densities versus pressures above
and below bubble point pressure for the studied four wells X1,
The accuracy of the proposed MSRKE is determined from the X2, X3 and X4.
comparison between the results of experimental work and cor- The density above bubble point pressure was measured
responding values calculated from MSRKE. Four oil samples from constant-mass depletion stage and below bubble point
were tested to PVT analysis (2-bottom hole samples and 2-sur- pressure from differential liberation stage. The dot-lines repre-
face samples). They were collected from different locations in sent density measurements and the solid-lines represent density
Egypt. Discussions are given here below: predicted using the MSRE. The figure indicates that, the
144 E.M. Mansour et al.
(a) 7
Well ID=X1 (Experimental)
6
Well ID=X1 (Simulated)
Relative volume of
Reservoir Oil
5
4
3 BP=3654.79 BP=3659 PSI
2
1
0
0 1000 2000 3000 4000 5000 6000
Pressure,Psi
(b) 8
Well ID=X2 (Experimental)
7
Well ID=X2 (Simulated)
Relative volume of
6
Reservoir Oil
5
4 BP=1622.5 PSI BP=1667.5 PSI
3
2
1
0
0 1000 2000 3000 4000 5000 6000
Pressure,Psi
(c) 4
Well ID=X3 (Experimental)
Well ID=X3 (Simulated)
Relative volume of
3
Reservoir Oil
BP=318.7 PSI
2
BP=348PSI
0
0 500 1000 1500 2000 2500
Pressure,Psi
(d) 10
Well ID=X4 (Experimental)
8 Well ID=X4 (Simulated)
Relative volume of
Reservoir Oil
0
0 1000 2000 3000 4000 5000
Pressure,Psi
densities decreases as the pressure increased above bubble standard condition (p = 14.7 psia and T = 60 F), the oil
point pressure. At any pressure below the bubble point pres- remaining is called residual oil. The density of this oil is mea-
sure, the amount of gas dissolved in the oil will release with sured by density meter then API gravity is calculated. This API
further decreasing pressure. This will result in increase density gravity which is measured during differential liberation stage is
as shown in Fig. 8. By continuously deceasing the pressure to usually smaller than that of flashed stage. It is important to
Predicting PVT properties of Egyptian crude oils by a modified Soave–Redlich–Kowng equation of state 145
2.200
Oil Formation Volume Factor ,Bob
1.400
1.200
1.000
0 1000 2000 3000 4000 5000 6000 7000 8000 9000
Pressure,Psi
0.9000
Well ID=X1 (Experimental)
Well ID=X1 (Simulated)
0.8500 Well ID=X2 (Experimental)
Well ID=X2 (Simulated)
Well ID=X3 (Experimental)
0.8000 Well ID=X3 (Simulated)
o
0.7000
0.6500
0.6000
0 1000 2000 3000 4000 5000 6000 7000 8000
Pressure,Psi
2000
Well ID=X1 (Experimental)
Well ID=X1 (Simulated)
Well ID=X2 (Experimental)
Well ID=X2 (Simulated)
1500
Gas/Oil Ratio ,Rsb
500
0
0 1000 2000 3000 4000 5000 6000 7000 8000 9000 10000
Pressure,Psi
note here that flashing operation is conducted through one fore more gas was liberated from each stage. Accordingly, the
step, while in case of differential liberation stage, separation density of oil from differential liberation stage is greater than
of oil must be passed through multi-pressure stages and there- that obtained from flashing operation.
146 E.M. Mansour et al.
0.4000
0.2000
0.1000
0.0000
0 500 1000 1500 2000 2500 3000 3500
Pressure,Psi
The average percentage relative error, standard deviation Above the bubble point pressure, gas/oil ratios are constant
and correlation coefficient are given in Appendix A for the because the composition of the produced reservoir fluid is con-
studied sample values above and below bubble point pressure. stant until the bubble point pressure is reached.
The evaluation ensures that, the measured data are well agreed An excellent agreement between the measured data and
with the calculated ones. calculated ones was obtained. The values of statistical tools
(average percentage relative error, standard deviation, and cor-
3.4. Gas/oil ratio relation coefficient) are listed in Appendix A, from which it can
be observed that the data of well: X1 results in good evalua-
Fig. 8 shows the results of gas/oil ratio versus pressure for the tion. It shows an average percentage relative error ranging
four wells X1, X2, X3 and X4. from 4.09 to 6.18 and standard deviation ranged from 1.65
Gas/oil ratio is measured from differential liberation stage. to 8.20. All the values of correlation coefficient are close to 1.
For each well, dot-line represents gas/oil ratio from experimen-
tal data and the solid-line represents gas/oil ratio predicted by 3.5. Gas formation volume factor
the MSRE. Gas/oil ratios increase with increasing pressure at a
constant temperature. The gas/oil ratio which is measured dur- Fig. 9 shows the results of the gas formation volume factor
ing differential liberation stage is greater than that of flashed versus pressure for the four wells X1, X2, X3 and X4.
gas/oil ratio. This is because the gas/oil ratio in a differential The gas/oil ratios are measured in differential liberation
liberation stage is calculated by summing the standard volumes stage. In each figure, dot-line represents gas formation volume
of the gas that is liberated in each pressure. Following this, at factor from excremental data and the solid-line represents gas
each pressure interval, the sum of the gas volumes was divided formation volume factor predicted using the MSRE. The gas
by the residual oil volume to get differential gas/oil ratio. In formation volume factor is a measure of how much the gas vol-
case of calculating flashed gas/oil ratios, the gas and oil are ume increases from reservoir to standard conditions. The
flashed at standard conditions (p = 14.7 psia and changes in gas volume during production are larger than the
T = 60 F). According to the following equation changes in oil volume. The gas volume increases approximately
as much as the pressure decreases. Above the bubble point pres-
volume of gas standard condition sure, gas formation volume factor is constant because no gas is
flashed gas=oil ratio ¼
volume of oil standard condition librated. It can also be observed that there is an excellent agree-
ð43Þ ment between the measured data and calculated ones.
1.0000
0.7000
0 500 1000 1500 2000 2500 3000 3500
Pressure,Psi
The statistical error analysis results are given in Appendix proposing a new formula for m-parameter and the con-
A, which clarify the compatibility between the measured data stants were calculated from the real data of the different
and calculated ones. types of Egyptian black oils.
2. Our modification of Soave–Redlich–Kowng equation
3.6. Gas gravity reduces the errors from (111% to 55%) to (0.01–
10.713%) and consequently has better overall accuracy
Fig. 10 shows the results of the gas gravity versus pressure for than the modified Soave–Redlich–Kowng equation for all
the four wells X1, X2, X3 and X4. the data considered in this study.
These results were calculated from differential study test. 3. Calculation sensitivity of the proposed MSRKE is deter-
For each well, dot-line represents gas gravity from excremental mined by testing four oil samples collected from differ-
data and the solid-line represents gas gravity predicted using ent locations in Egypt and comparing the measured
the MSRE. As the pressure is further decreased, the content PVT properties with those calculated from the pro-
of heavier compounds in the gas will increase. This is reflected posed MSRKE. The evaluation shows an excellent
in increasing gas gravity with decreasing pressure. agreement between the measured properties and calcu-
lated ones.
4. Conclusion
Soave–Redlich–Kowng equation of state is the most com- Appendix A. The following statistical error analysis of oil rel-
mon method for predicting PVT properties of oil fluid prop- ative volume, oil formation volume factor, density, gas oil ra-
erties at different reservoir conditions. Application of this tio, gas formation volume factor and gas gravity is used to
equation to 43 Egyptian black oil samples collected from determine the accuracy of the MSRKE.
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