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This papar was presented at the SPE/DOE FourthSympmium on EnhancedOil Recovery held in Tulsa, OK, April 15-18, 19S4. The material is subjectto
correctionby the author. Permissionto copy is restrictedto an abstractof not
morethan 300 words.Write SPE, 6200 NorthCentral Expressway, Drswer
S4706, Dallas, Texas 75206 USA. Telex 730989 SPEDAL.
ASSTRACT
The results of laboratory research conducted to fluids are not miscibles on the first contact, but
study displacement of crude oil by high-pressure nit- form two phases, with one of the fluids absorbing
rogen injection are presented in this paper. The components from the other. After sufficient contacts
objectives of this research were to study the effect and exchange of components, the system becomes mis-
. . .
of temperature and orxgiiialqas-~11 ratm .-. in solution cible. Na-light crude oil miscibility phenomenon is
on crude oil recovery and the miscibility process in .L._
complex and depends on the cornposicxunof the zeser-
high-pressure (H-P) nitrogen injection. Also in addi- voir fluid, temperature, pressure, as well as other
tion, the effectiveness of nitrogen injection after factors such as interphase mass transfer, effect of
waterflooding and the effect of nitrogen-driven pro- relative permeability, capillary pressure and gravity2,
pane slugs was examined. Nine experimental tests W2re
p.erfo~nneeGsiRg .VUJa~oil
----- _ of 42.3° API recombined with This research is the continuation of an investi-
natural gas. The experimental tests were made using gation contiuctedby Tazek Ahmed and Donald h!enzie~
two temperatures (70”F and 120”F) and three gas-oil (1983). These researchers studied the displacement
ratios in solution (575 SCF/STB, 400 SCF/STB and 200 of light crude oil by nitrogen at different injection
SCF/STB). The reservoir model used was a stainless pressures at room temperature and using a constant gag
.--.L . a .
n ..-. in diameter,
steel tube Ld> ~eec Loiiqan= A7K iIICheS oil ratio in solution.
packed with sand consolidated to give an average per-
meability of 910 md. The model was provided with five The primary objectives of this research are:
..
sampQng - -1...=+flF
ia.v.. Ilect va.pr
.“ .o----- samples. The vapor
(1) Formulation and preparation of a computer program
samples were analyzed by using a gas chromatography. A to simulate tineheat tramfer process in the physical
temperature control system was built based on the re- model, (2) TO confirm the validity of the data obtain-
sults obtained from a heat transfer mathematical model ed by various researchers using the same physical
specifically prepared for this research. The results model, (3) Injection of nitrogen into the reservoir
obtained in this study suggest very strongly that model at one pressure and different temperatures, (4)
crude oil recovery and miscibility in this kind of oil Injection of nitrogen into the reservoir model at one
depend on temperature and oil-gas ratio in solution. pressure above the miscibility pressure and different
Multiple-regression equations to predict crude oil solution gas-oil ratio to study the effect of the gas-
recovery using temperature and gas-oil ration in solu- oil solution on oil recovery, miscibility and track
tion were developed based on the experimental data. the compositional changes taking place during dis-
placement, (5) Run a regular waterflood and then dis-
INTRODUCTION place nitrogen to study if miscibility is obtained
under those conditions, and (6) Run a nitrogen-driven
A relatively new process of vaporization gas
I
propane slug test to study the Pos=ibili&f fer future
drive, the application of high-pressure nitrogen (l&a) ~-,va=tig=tionOf USiIXI the same laboratory equipment.
injection to increase ultimate production, has been
receiving special attention because of the high cost Literature Review
and limited supply of natural gas.
In 1928, I?ower3performed a laboratory study to
The main goal of injection of N2 is to achieve determine whether air is superior to natural gas as
miscibility with the reservoir fluid. The miscibility a driving medium or vice versa. Power also used
obtained by nitrogen injection in a light crude oil nitrogen in his experiments. He concluded: (1) That
reservoir is a conditional miscibility; where the the volubility of natural gas in oil is snuchgreater
than that of nitrogen at equal temperature and pres-
sure; and that the volubility of nitrogen in oil
References and illustration at end of paper. closely approaches that of air, (2) Volume by volume,
383
2 ENHANCED OIL REC 3RY BY NITROGEN SPE-12709
nitrogen is superior to natural gas as a propulsive solidated sand inside a stainless steel tube 125’
agent at all pressures. long and .435 “ internal diameter. The model was
constructed with 5 sampling valves along the length
In 1958, Koch and Hutchinson4 conducted a labora- of the tube to facilitate the taking of vapor samples
tory study on miscible displacement using flue gas. during the displacement test for chromatographyanaly-
The results confirmed that the composition of the dis- sis. The average porosity of the model was 32% and
placement gas is relatively unimportant in establish- absolute permeability was 910 md. The absolute per-
ing the miscibility pressure for a given reservoir meability was obtained by nitrogen displacement.
fluid. They also reported that above the miscibility
pressure the breakthrough recovery is a constant. The temperature control system used in this work
consisted of heating units, thermostat, insulation
5,6,7 con
Between 1976 and 1977 Rushing, et al. blanket and thermometers. Three commercial heating
ducted experimental works. They mainly studied the units were used with a capacity of 1500 BTU/Hr each.
effect of N2 injection pressure on oil recovery. They
concluded that “the lighter crudes, with some gas in The production and analytical system consisted
solution, have been more responsive to high-pressure of a back-pressure regulator, graduate cylinder, gas
nitrogen injection.” filter, gas metering apparatus, chromatographyand
refractometer. The chromatographyused had a micro-
8
In 1978, Paterson conducted laboratory tests of processor (CPU) that allows the operator to write
crude oil recovery by nitrogen. The model was satur- programs to control gas analysis.
ated with oil and displaced with N2 at 4280 psi at
reservoir temperature. Results showed that miscibil- Material
ity was obtained after multiple contacts and 90% of
the oil recovered after injection of about 90% PV of The oil used was obtained from Noble County,
Na . Oklahoma. Table 1 shows the oil properties and some
PVT characteristics. The gas used to recombine the
In 1975, Hardy and Robertsong reported a field oil was obtained from the same field in Oklahoma.
case history in Block 31 field, Texas. In Block 31 Table 2 shows gas properties and composition.
the miscibility pressure for flue gas (87% N2, 12% C02
and 1% CO) was practically identical to miscibility PROCEDURE OF INVESTIGATION AND TECHNIQUES
pressure for hydrocarbon injection gas.
Separate experimental procedures and techniques
10
In 1980, Vogel and Yarborough conducted labor- were required in this investigation. The procedures
atory tests in which condensate reservoir fluids and involved are: (1) Procedure for recombination process
black oil were contacted by N, at reservoir conditions (2) Procedure for PVT analysis, (3) Procedure for
They concluded that N2 injection into condensate reser –.L .= ~ Precedure of
sam.lra=ioiio~ &@ reservGiF --a-l
.,,”..=- , (4)
voir fluid will significantly increase the dew point nitrogen displacement, (5) Procedure for oil recovery
pressure. When black oil is contacted with Na, the by waterflooding, and (6) Procedure for oil recovery
light and intermediate components will reduce drasti- by propane slug driven by nitrogen. The procedures
cally in the oil. from 1 to 3 were standard procedures for this type of
research. The procedure 4 can be summarized as
In 1980, Ahmed and Menziel conducted laboratory follows:
work using nitrogen injection at high-pressure and
room temperature. The GOR in solution was kept con- After the model had been saturated with water
stant during all of the six tests (575 SCF/STB). The and recombined oil and the temperature of the system
authors determined successfully the miscibility pres- was at the desired test temperature, the equipment
sure for the system. They also, determined the com- was ready to run a displacement by nitrogen.
positional changes taking place during the displace-
ment of crude oil by nitrogen injection. The steps were as follows: Set the pressure
(2000 psi) at the back-pressure regulator, started
11
In December 1981, Carlisle and Crawford nitrogen injection, started collecting information
reported on their laboratory investigation of dead and vapor samples for chromatographic analysis.
crude oil displacement by nitrogen-driven propane Stopped displacement at N2 breakthrough. The most
slugs. They concluded that “nitrogen-driven propane important parameters that were recorded were: (1)
slugs can be very effective in producing oil.” Temperature along the model (“F), (2) Barometric
pressure (nEnHg),(3) Nitrogen injection pressure
.-.— .
EXPERIMENTAL EQUIPMENT (psi), (4) Outlet pressure (pSl), (5) T~e (mm), (6)
Oil recovery (CC), (7) Gas produced (SCF), (8) Water
The experimental equipment available at the saturation at initial condition (fraction of pore
.-.
University of Oklahoma was modified to perform this volume) , (Y) Fore voiume (fractioriof pore volume! ,
research. A schematic diagram of the modified experi- (10) Oil saturation at initial condition (fraction
mental equipment used in this work is shown in Figure of pore volume), (11) GOR in solution in oil (SCF/
.J.. STB), (12) Formation Volume Factor (BBL/STB), (13)
Oil gravity (“API), (14) Room temperature (“F), and
The experimental equipment is divided into the (15) Time and crude oil recovery leveis when the
following systems: (1) PVT-injection system, (2) vapor samples were collected.
Reservoir physical model, (3) Temperature control
System and (4) Production and analytical system. Nitrogen Displacement After Waterflooding:
The reservoir physical model was represented by After crude oil saturation the system was dis-
a linear horizontal core constructed by packing con- Wzter. ~atez iP+jecticfi
piaced tiit?~ wss ~t~pped at
3 ENHANCED OIL RECOVERY BY NITROGEN sPE-12709
A summary of the results of the experiments are The first zone was identified by analyzing the
shown in Table 3. crude oil and gas produced. No compositional change~
3
4 ENHANCED OIL RECOVERY BY NITROGEN SPE-12709
took place in this zone. The second zone is the resul in this study, to conduct the test and evaluate the
of nitrogen being initially immiscible with the reser- data, was followed in this experiment.
voir light crude oil. Analysis of the shapes of the
compositional profiles (Figure 10 and 6) suggested The crude oil recovery obtained in this test was
that vaporization is very strong in the beginning of 66% of the OOIP. Miscibility was not achieved under
the process and at the leading edge of the second the conditions of this test. The lower recovery by
zone. The slopes of straight lines of the composi- itself strongly suggests that the displacement was
tional profiles (Figure 10,6) are a direct consequence an immiscible process. Confirmation of this fact is
of vaporization rates. ebtsined by observing the compositional profiles and
the ternary diagram shown in Figure 13.
In this test, miscibility was postulated after
no change in the composition of the front was detectec Fifth Experiment
In Figure 6, miscibility is present when the slope of
the compositional profile is zero. Miscibility was This test was run at 120”F. The chromatographic
detected at the sampling point D between 76% and 82% analysis, in the form of a compositional profile, for
P.V. of Nz injected (Figure 6). The miscible bank wa: sampling pint “D” is given in Figure 14. The frac-
approximately 6% of the Pv. tional crude oil recovery was 84.5% of OOIP. Compo-
sition profiles confirm miscibility was obtained. The
Figure 11 and 12 are ternary diagrams illustrat- size of the miscible bank was 8% of the P.V. In com-
ing and monitoring the building up of miscibility for parison with all tests run at lower temperature con-
this test. Figure 12 shows the composition of the ditions (70”F), this miscible bank was larger.
miscible bank. BY using this ternary diagram, it is
possible to make a prediction of miscibility during Sixth Experiment
the displacement. Analyzing liquid samples taken
during the displacement would improve this prediction. The objective of this test was to compare the
combined effect of GOR in solution and temperature on
Theoretically, miscibility is reached when all recovery and miscibility with the previous tests.
the intensive properties, such as density and viscos- The sixth test was run at 120°F and used a GOR in
ity in the liquid phase, are similar to density and solution of 200 SCF/STB.
viscosity in the vapor phase and the interracial
tension is zero. In this study the interracial ten- In comparison with experiment No.4, recovery
~i~~ never reaches the theoretical value of zero. at breakthrough (66% of the OOIP) was higher in this
This suggests that miscibility is incomplete or b.ighertemperature conditions (69.4% (’)O1p
teS. .&-,der
partial under these laboratory conditions. No miscibility was achieved during this test. There
was no evidence of miscibility from compositional pro-
The crude oil recovery of 81.1% suggest by it- files or production history.
self that at least partial miscibility was achieved
during displacement. This test result is in agree- Seventh and Eighth Experiment
ment with results reported by previous researchers
(1, 3, 5 and 6). The first two tests showed that the The seventh test was a regular waterflooding at
reservoir physical model is reliable to conduct this 120°F . The injection water was stopped at water
type of research. breakthrough. The eighth test was a tertiary oil
recovery by high pressure nitrogen injection. The
Third Experiment gas-oil ratio in solution was 575 SCF/STB. Vapor
samples from the displacement phase were taken and
This test used a light crude oil displacement by analyzed. This eighth test was designed to observe
high pressure nitrogen injection. Parameters, condi- how the temperature would affect tertiary recovery
tion and production data are shown in Table 6. A with a low saturation of oil and free water in the
gas-oil ratio in a solution of 400 SCF/STB was used. reservoir.
.-
Both the calculatectFVF and the sakzraticm pressure
decreased for this reservoir crude oil. Samples of vapor were very difficzlt to obtain
at the pre-established times during the injection
The fractional recovery of crude oil was 75.4% because only water was obtained at the sampling points
of OOIP. The strong vaporization process at the The few samples that were possible to analyize did
beginning of the test seems to be typical of this not show any compositional change,
type of displacement. Again, miscibility was postu-
lated when no compmitional change was observed in Ninth Experiment
the results of the sample analysis. The miscible
bank formed during this test was approximately 5% In this ninth experiment, a 10% P.V. propane
of the P.V. The same procedure used to treat the slug driven by high pressure nitrogen was used to
second test data was used in this test; i.e. chro- recover crude oil with a GOR in solution of 200 SCF/
matographic analysis of vapor samples and construc- STB . The production data for this test is presented
tion of ternary diagrams. in Table 8. The crude oil recovery obtained in this
test was 88% of the OOIP.
Fourth Experiment
DISCUSSION OF RESULTS
In this test the amount of natural gas dissolved
in the crude oil was reduced to 200 SCF/STB. Hence The evaluation of the production history curves,
the FVF and saturation pressure decreased in rela- ternary diagrams, compositional profiles in all the
tion to the previous tests. Production history data tests in this study showed consistently that three
is shown in Table 7. The routine already established zones exist in the displacement of light crude oil
i
5 ENHANCED OIL RECOVERY BY NITROGEN SPE-12709
by high pressure nitrogen injection. This pattern study . With this limitation in mind, and by using
was observed in all the displacements regardless of the statistical analysis package (sAS) available at
miscible or immiscible conditions. Oklahoma University, a multiple regression equation
was obtained to predict crude oil recovery with both
The secofidzom is the most important one in temperature and GOR in solution as predictors. The
understanding the mechanisms involved in building resulting equaticm is:
up miscibility. The miscible bank may or may not be
developed in the second zone. The displacement is
immiscible until the miscible zone is created. Con- R = 0.5546756 + 0.00053705T + 0.00041454 GOR...(1)
sequently, the amount of reservoir fluid that is
immiscible displaced is primarily a function of the
concentration of intermediate components in the Equation (1) predicts crude oil recoverY when
original crude oil. In this study the miscible dis- the injection pressure is 4000 psi. The correlation
tance was found between 72 and 96 feet. The mis- coefficient for Equation (1) is .99590.
cible distance was observed to decrease with increas
ing temperature and GOR at constant injection pres- As demonstrated in Ahmed and Menzie’s work,
sure. The shape of the compositional profile from crude oil recovery is a function of injection pressur(
tests No.2 to 6 suggest that the vaporization is 1 All the results obtained in this study were put
very strong at the beginning of the process in the together with theirl results (Table 9) to produce a
leading edge of the second zone. This suggests that multiple regression equation to predict crude oil
the original composition of the crude oil is a key recavery. Temperature, pressure and gas-oil ratio
factor for achieving miscibility at an early stage in the reservoir physical model used in this study
of the displacement process. were used as predictors. The resulting equation is
as follows:
The size of the miscible bank is directly
affected by both temperature and GOR in solution
a~~~rdinq to the results of this study. It is R = -0.164 + 0.0294 T + 0.0001198P + 0.000338 GOR
obvious that when the gas-oil ratio in solution ...(2)
increases, the concentration of intermediatecom-
ponents increases since more intermediate components
are available in the crude oil. The temperature Standard deviation of R about regression line
effect could be justified by the kinetic theory of S equals 0.05672. The statistical minitab package
gases. The size of the miscible bank is found to was used to obtain this equation. The coefficient
decrease substantially due to retrograde vaporiza- of determination of equation (2) is 77.3%.
tion when pressure increases.
The increase in crude oil recovery with an
The vaporization process is the most important increase in temperature in high pressure nitrogen
mechanism in the build up of miscibility in this displacement could be explained as follows: Molecular
study . The results analyzed show that the following activity increases with temperature, producing more
actions should be considered to increase the crude interaction between phases. This increase in phase
oil recovery using nitrogen injection. (1) Increas- interaction is translated into a faster vaporization
ing the density of the displacing gas phase, (2) process during nitrogen displacement of crude oil and
Decreasing the density of the displaced oil phase, an increase of equilibrium constants with temperature
(3) Increasing viscosity of the displacing gas That means, theoretically, that miscibility can be
phase, (4) Decreasing viscosity of the displaced obtained faster because vaporization is greater at
oil phase, (5)Reducing the surface tension in the higher temperatures.
system, and (6) Improving the mutual volubility of
both phases at the leading edge of the second zone. On the other hand, liquid viscosity is a strong
function of temperature. The viscosity decreases in
Effect of temperature and gas-oil ratio on high the liquid phase in the second zone will promote
pressure nitrogen injection miscibility at the leading edge of this zone. The
relative permeability for both liquid and vapor
The resuits of ail cxperizva=tsperfwmed in phases is a function of temperature. At least Kro
:.
this study are summarized in Table 3. Figures 16 increases with temperatureL2. TO SUiil~~iZ2f =P.}’
and 17 show the effect of temperature on displace- significant increase in temperature helps the heavy
ment process. The tests where temperature was the ends in the reservoir fluids to be more volatile in
unique independent variable showed that increases contact with the nitrogen.
in temperature produce increases in crude oil
recovery at breakthrough. As can be observed in I?z Injection as a tertiary recovery method after
Figure 17, increments in temperature seem to fol- waterflooding
low a pattern, creating a family of cun?es that
characterize the effect of temperature on crude oil A regular waterflooding was performed in this
recovery in nitrogen displacement. The only con- study . The only observation of merit is that the
clusion that might have merit from Figures 16 and temperature used in this study (120”F) appears not
17 is that a general increase in crude oil recovery to be high enough to cause a significant difference
occurs when temperature and GOR in solution are in crude oil recovery for waterflooding.
increased.
The results obtained from the test where nitro-
There appears to be no basis for assuming a gen was injected after waterflooding suggests that
linear relation between temperature and crude oil when there are low saturations of crude oil and free
recovery beyond the range of temperature in this water in the reservoir model, the efficiency of the
6 —-.. HY
ENHANCED OIL RE( dM-tY. . .. NY1’KJGIiN
---------- --- . .“a -
s.PM-L.z/uY
the displacement phase would be a key factor for tions,” Petroleum Transactions, AIME Vol. 82
earlier miscibility and higher recovery. (1929)
TABLE 1
o
Specific Gravity at 60 F............................. 0.814
389
TABLE ~
Chromatography
run conditions
2CC of sample
65-00-00-65-10
65-200-160
COMPOSITION MOL%
78.32
c1
C* 11.32
4.96
C3
i-c4 .75
N-C4 2.49
i-c5 .’79
N-C5 .98
C6+ .36
99.99
TABLE 3
SUMMARY OF EXPERIOfENTS
(High-pressureN2 Injection)
OIL GRAVITY 42.4° API
= TEMP.°F GOR ‘o
—. ‘w FVF
—— STOIP RECOVERY TYPE PRESSURE
69..5 .-A
8ZW W- 9Z f.? ~Q9 Q(-J
●
66,0% INMISCIBLE 4000
4. II* ~z
SP E12709
TABLE4
HIGH PRESSURE NITROGEN INJECTION
- EXPERIMENT #2
Iniection Pressure : 4000 PSIG
CUMULATIVE OIL CUMULATIVE OUTLET
TIXE ATT
WAJA
mmrq-.
. ..”-” ~~~Qv~RY PRODUCED PRESSURE
(MIN) (cc) GAS
(% OOIP) (SCF) (PSIG)
o -- -- -- 2000
20 21 0.034 .08 2000
30 30 0.048 .11 2000
60 56 0.090 .20 2010
90 83 0.134 .30 2000
120 108 0.174 .39 2005
150 136 0.219 .49 2000
175 160 0.257 .58 2000
200 183 .294 .66 2000
240 220 .354 .80 2010
255 232 .373 .84 2000
300 272 .438 .98 2000
330 303 .487 1.10 2000
345 316 .508 1.14 2005
390 356 .573 1.29 1995
420 384 .618 i.39 2000
450 412 .663 1.49 2000
480. 436 .676 1.57 2000
495 454 .730 1.64 2005
510 480 .766 1.74 2000
540 502 .798 1.87 2000
550 503 .809 1.90 2000
N.
L
BREAKTHROUGH
~g~ %nA
-.. ,811 12.5 2000
c1 30.1 18.06 7.2 45.1 22.1 7.2 ‘40.2 27.2 11.4 52.26 50.3 35 6.I
C2 6.1 4.21 2.8 8.1 7.2 5.~ 13.4 6 1.0 14.3 12.1 8.2 2.1
C3 3.54 2.4 1.1 6.I 5.05 .27 9.5 6.0 4.5 10.8 9.5 6.2 2.3
C4 2.17 .41 ●2 1.2 .8 .05 1.6 1.1 .16 1.8 1.75 1.1 0.35
N-C4 2.25 1.19 .5 1.4 .75 .15 1.6 1.2 .15 1.81 1.70 1.2 0.45
“C5 .58 .35 .1 .61 .25 .01 .8 .57 .00 1.42 f.1 .7 .*5
N-(&j 1.05 .45 .1 .45 .15 .00 .9 .85 .00 1.32 1.25 .5 .15
C6 + 1.91 .95 .3 3.85 2075 .65 5.% .42 ● 18 7.8 7.5 5.1 .85
SP E127U9
TABLE 6 TABLE 7
HIGH PRESSURE NITROGEN INJECTION DATA HIGH PRESSURE NITROGEN INJECTION DATA
EXPERIMENT #3 EXPERIMENT #4
Injection Pressure: 4000—. PSIG Iniection Pressure: 4000 PSIG
CUMULATIVE OIL CUMULATIVE PRESSURE CUMULATIVE OIL CUMULATIVE OUTLET
TIME
TIME OIL RECOVERY PRCIDUCED GAS OUTLET OIL PRODUC. RECOVERY PRODUCED GAS PRESSURE
(MIN) (psIG)
(MIN) PRODUCTION (% OOIP) (SCF) (PSIG) (cc) (% OOIP) (SCF)
(cc) o 0 -- 0 2000
o 0 0 0 2000 39 20 0.02 0.05 2000
38 35 0.0459 .09 2005
73 50 0.06 0.06 2000
49 46 0.0603 .12 2000
65 70 0.0918 .18 2000 97 70 0.09 0.09 2000
87 98 0.12852 .25 2000 135 100 .12 0.13 2000
103 112 0.14689 .28 2000
170 136 .17 0.17 2000
123 132 0.1731 .33 2000
156 172 0.225 .43 2000 227 180 .22 0.23 2000
176 200 0.263 .50 2000 262 220 .27 0.28 2000
214 225 0.295 .57 2000
300 254 .31 0.32 2000
230 245 0.32 .62 2010
261 265 0.347 .67 1995 345 300 .37 0.38 2000
277 280 0.367 .71 2000 .40 2000
370 320 0.40
280 300 0.393 .76 2000
396 338 .42 0.42 2000
218 320 0.4196 .81 2000
340 350 0.459 .88 2000 440 378 .47 0.48 2000
362 360 0.472 .90 2000 2000
480 413 .51 0.52
408 400 0.524 1.01, 2000
521 450 .56 0.56 2000
426 415 0.544 1.051 2000
467 468 0.613 1.17’ 2000 554 480 .59 0.60 2000
488 489 0.641 1.23 2000 .66 2000
611 530 0.66
‘a 2000
508 520 0.681 1.31L
IJ 620 530.1 8.51 2000
539 548 0.178 1.38 2000
-T-I
~ 580 568 0.744 1.4:3 2000 N2 BREAKTHROUGH
Q 590 575 0.754 1.4!5 2000
~ 600 575.5 .- 1.8f8N2 BREAKTHROUGH
3
TABLE 8
TABLE 9
DATA SET USED TO PROPOSED EQUATIONS (1) & (2)
70 000
● 0.590000 5000.00 o.
sPE127ti9
..+..
mum 1: SMN4TIC
0?fWK ==IMUITAL !
Wlmm mm Ill THIS UOSI
OIL RECOVER1
z OOIP
— mum
CUMULATIVEGAS PRODUCEDVS OILFRACTIONRECOVSRY
-mm
ml
4
r
Imwuinlm 72 r
cow 67s m?/slm
2000
I 900
I aoo
A
1700
z
.
; 1600
8
. 1s00
a
g , Uoo
~ 1300
v
= 1200
a
o 1100
*
~ 1000
1
900
000
700
‘“”~
0.0 0.1 0.2 . . . .
mm!
-40M?S.I
OIL RECOVEFI1.
X 00IP
—m78r
GOfi 6’M 8cr/m ncm 5
PRODUCED GOR VS OILRECOVERY
550
I /-
A
5OO
PISUSS 6
./ lb
i
Uso SECONDmERlm
c
:
cOmsITIOs.u PROFILES AT
~ Uoo
; S#MLJNC POINT “D”
: 350
E . N2, Cl, C2 at Scale B
C3, C4, C5, C6+ ac Scale A
: 300
c’ ~
L
n 250
c .
0 1 /
v 200
[
! 150
‘\ /
g.
..
>
‘L!~
0 so 100 150 200 2s0 300 350 ’400 Uso 500 550
1, ~
TIME UI!M1
0
.m .80 .s0
CUMULATIVEOIL?EtOVERY VS TIME %PV N2 lNICCTED
SPE1
.... .
-4000 m
ImPnAm 08.5r
am 176Sc?m
550
go 1 r
‘4s0
1/’’”/
cu
n 400
u
~
1 350
;
E
~ Soo
:
“ 2s0
:
~ 200
:
1 150
i ml /
‘:~ . .... ,.
0 50 100 !50 2;0 250 300 350 UOO ’450 500 550 600
TIME INIMI
?IGLals
FIGURE
7
CUMUIATIVEGAS PRODUCED VS OIL RECOVERY
CUMULATIVE OIL RECOVERY VS TIME
Pm.m..
?mmlmlllm& ammr
CQW678 8cv/m
r
1
Uooo I
“v
35003
I
o J
0.0 0.1 0.2 0.3 O.u
OIL RECOVER,.
Q.5
?. OOIP
0.6 0’7 ‘“a
I n- Ei
FIGURE 11
noms 12
SECOND EXPERU4EWP sm.” KmfaInm
—Y D- REPWCUCINC mwmr DI1OMMRmm=ml w
c.x!TW1TIOBAL CIUWES AT
cD5QoS1T1DKALQIAWES AT sumrmo mm w.
SAUPLINO POIWT “C”
m. PRESSURE: 4oaa F.*$ mmsm.x OP
cRITrciL
mum
TU@ERA=: 69.5° ?
GOR: 515 9CPIST8.
\ lam+”
9****” “ w a . l*e*of.+
FIGOSI 13 B
CSASSES AT
COI4POS1TIONAL IWMFCISITIORLL ~O?lLES AT
cm: 5n Sc?hm
GOR: 200 SCF/STE Llu. FnEssLmE: Cal Pal
a-
lNJ. PSSSSUSJ: 4W0 ?S1
10
% Tmp~Amk ‘~”v”
~,-5
13
80
U2 (scale A)
se
%
C,.5 (s..1. B)
c: ( W,,l. i)
40
so
I .7 .*
1
.0 t.
I
FIGURE 16
I
.s0
.80 -
1 FRACTIONAL
..-~”-::
CRUDE OIL RECOVSRY VS.
It?J . PF03WJRE: 4030 PSI
TStW_m
/-
600
.70 - --
-“”-z==-””
500 /---
.60 -
Uoo
.50-
300
.40-
200
.10-
.#o
to
SP E1270