Compurers them. Engng, Vol. 18, No. 2. pp. 75-81, Printed in Great Britain. All rights reserved
0098-I 354/94 56.00 + 0.00 Copyright 0 1994 Pergamon Press L:d
1994
COMPOSITIONAL SIMULATION PERFORMANCE BY A THERMODYNAMIC P. WANG Engineering
Research
Center,
(Received
4 December
and
E.
H.
OF RESERVOIR REDUCED MODEL
STENsYt
IVC-SEP. Department of Chemical Engineering. of Denmark, Building 229, DK-2800, Lyngby
1992, final revision received
The Technical
I7 June 1993: received for publication
University
I July
1993)
Abstract-In compositional reservoir simulations, it is usually assumed that a local thermodynamic equilibrium between all phases exists throughout the reservoir within each time step. Phase behavior calculations are conducted based on an equation of state (EOS) in each block. This computation normally takes a very significant percentage of the total CPU time. In this work, an extension of the reduced thermodynamic model (Wang and Stenby, Compurers &em. Engng 16, 5449-5456, 1992) to the processes vary is demonstrated. This modified model has been tested in which both pressure and feed composition against the experimental data of gas condensates and the PVT data computed from the EOS. The results indicate that the new model can well represent the influences of changes in the feed composition and the pressure on the K-values. The new model has been implemented into a compositional reservoir simulator, UTCOMP (Chang Ph.D. Thesis, Univ. of Texas, Austin, 1990). Simulations of natural depletion for three well-defined mixtures and of a dry gas recycle process for a gas condensate in the North Sea are performed. The results simulated with the new method are comparable to those computed by the PR EOS. But the CPU time is reduced by approximately 50% by means of the new method compared to the one required by the PR EOS. In addition, this work shows that the CPU time can be further decreased by using the newly suggested procedure (Leibovici and Neoschil, Fluid Phase E9uil. 74, 303-308, 1992) for solving the Rachford-Rice equation for phase split.
assumption Two
types
of
reservoir
reservoirs
are
industry;
black
simulators.
being oil
The
components
the
equilibria
pseudo-oil
dependent
of the reservoir
solubility
mixture sitions,
gas
constant
no volatility
solubility
of
a
simple
in the oil of
function
pressure
processes
dependent
techniques
where
and
This
the fluid
on composition,
properties
however,
treated
the reser-
as
a
separate
in the water phase,
between
water
and
and no
oil or gas
ture. The
best predictive of state (EOS) behavior
pressure.
Once
are
For
the number 10’.
to whom all correspondence should be addressed.
by
methods
simulator
behavior
of
hydrocarbon may
of hydrocarbon
the mix-
be based
on
are usually description
mixtures
is employed,
at high the com-
very slow since the fluid properties iteration.
For
a
usual
in which the compositional of isothermal
It is generaily
has strongly 75
PVT
since cubic EOS
this approach
becomes
obtained
simulation
oil
of
to be able to give an accurate
of phase putation
as a
in the compositional
prediction
equations
simulation tAuthor
occurs
and the thermodynthroughout
fluid which is a complex
considered
are also
the black
efficient
reservoir
oil model
pressure.
only
The major difficulty
in the reservoirs
saturation
transfer
is an
and zero
can be expressed
normally
present
to describe
phases.
and
Based on these
it may be said that the black
voir. mass
pressure-
phase.
is required
In both models it is assumed
is isothermal
is
gas
model
the reservoir fluid with more than
state prevails
Water
immiscible
compositional
amic equilibrium component
oil and gas phase compo-
the fluid properties of
the
A
components
that the reservoir
the hydrocarbon
of oil in the gas phase,
is used to study recovery for which
two
fluid/rock
by a pseudo-gas
of gas and oil in the water.
assumptions,
some
with
representation
presumes
how
composition,
is invalid.
these recovery processes.
The black oil model charac-
component
two-component
and
of constant
phases
two hydrocarbon
of appropriately
process,
terizes the reservoir fluid simply a
these
oil
which characterizes
compositional
between
as a means
system are characterized.
isothermal
arises from how many
displacement
thermodynamic
for
in the petroleum
and
difference
essentially
are chosen
describing
used
simulators
main
types of simulators
simulators
widely
and
flashes is often
true that
time is spent
over
50%
reservoir
model
is used,
as high as of the total
on these calculations.
restricted the practical
application
This of the
P.
16
WANG
and E. H.
EOS compositional simulator. In order to reduce the computation time, many attempts have been made in literature to improve the existing flash calculation algorithm or develop new flash routines. The objective of this work is to develop a reduced model to determine the distribution of components between phases of hydrocarbon mixtures in order to save computation time in the reservoir simulations. The phase fraction is then obtained by simply solving the Rachford-Rice equation. The parameters of the reduced mode1 are fluid-dependent and easily estimated by fitting the experimental K-values or those computed from the EOS.
STENBY
The K-value changes caused by the variations of the feed composition, which is the second term of equation (6) can be presented by means of the following way:
By a material balancing and elimination of phase fraction variation, we may reach: InKy=
1
2 j=18(Kj-11)+
REDUCED
THERMODYNAMIC
One of the most fundamental relationships dealing with the thermodynamic properties of a substance in a two-phase region is the Clapeyron equation, which may be expressed as: dP=’ dT=-’
1
MODEL
AH T-AV
Assuming that gas phase is ideal gas and AH constant at low pressure, we may have:
(1)
is
x
aIn&:
(I--@--
NC
zi(Ki -
SF, (K, -
p”’ K!d,_L_ P’
where
C~=ln(P.)(j&--f) , ---1 1 . Tai
(5)
Tci
For the real component K-values of a mixture under reservoir conditions, the following equation can be written if the temperature is assumed to be constant: lnKi=lnK~+InK~.
(6)
The first term of the right-hand side of the above equation accounts for the contribution of the pressure variation to the K-values. It is found in this work that this term can be well described by: lnK:=(a+bP-lnP)+(c+dP)C,.
(7)
(9)
1)
(10)
1)e + 1 = ‘*
(11)
(3)
(4)
dn,.
The composition of the liquid and vapor phases is then computed by means of the equations below:
y; = K;xi.
By application of equation (2), we may reach the equation below (P, = 1 atm): In Kid I = C I - In P 3
1
This term was neglected in our earlier work (Wang and Stenby, 1992) since the pressure term is dominating in a natural depletion process of a reservoir where the feed compositions vary slightly during the displacement compared to a gas injection process. Once the K-values of each component are known, the fraction of vapor phase can readily be obtained by solving the Rachford-Rice equation:
In PsaL= In P, + where P, is the vapor pressure. The term In P, goes to zero if the boiling temperature is evaluated at 1 atm. For a mixture, the ideal K-value for component i is defined as:
8Kaln4: J any
an)
[
VALIDATION I.
Experimental
OF
THE
K-values
(12) REDUCED
from
a CVD
MODEL
process
The K-values at each pressure stage of a constantvolume depletion [(CVD), Moses and Donohoe, 19891 process for the gas condensates can be obtained by a mass-balance calculation based on the measured PVT data. These K-values may be considered as the experimental data. In Fig. 1 the typical result of the K-values correlated by equation (6) is shown for a gas condensate (Kenyon and Behie, 1987). The estimations of the critical properties and acentric factors of C,, fractions required by equation (6) are given in the next section. 2. K-values calculated from
an EOS
It is generally accepted that the cubic EOS can be used for high-pressure PVT calculations of hydrocarbon fluids. Therefore, investigation of the Kvalues computed from an EOS is also the way of
77
Simulation of reservoir performance .
pressure at which the above equation is satisfied can be found. The K-value at the dew point can also be obtained from the above equation. The liquid dropout at each pressure stage is evaluated from:
Expl.
-
Calc.
(14)
c = 0.824559 d = -0.002827 0.01
0
I
I
I
I
I
50
100
150
200
250
Pressure (atm) Fig. 1. Comparison between experimentalK-values and computed ones for a gas condensate(Kenyon and Behie, 1987). testing the validity of equation (6). Many hydrocarbon mixtures with defined components (Yarborough, 1972) have been used for this test. A typical comparison of the K-values computed from the PR (Peng and Robinson, 1976) EOS and the reduced model is shown in Fig. 2. It appears from Figs 1 and 2 that the K-values measured and computed from the EOS can be well represented by the reduced model with a single set of parameters
in both
high-
REGENERATION
and low-pressure
regions.
[$,$=
A l-._.-.-•
nC5
*r-*-,/r
(15)
T, = 0.556 exp(4.2009i?~“6’SSG0.046’4),
(16)
e
1.
I
(1 - T,sIT,)CT
p =exp
(13)
By adjusting the pressure in equation (6) at the given composition zi and the temperature, the dew point
fz: c3
T, = 169.43822MW”~45534SGo~~2*‘,
OF THE PVT DATA
The above well-defined mixtures and gas condensates are also used to test the capability of the reduced model to reproduce the PVT data. Phase volumes are estimated from the PR EOS. The dew point pressure is estimated from:
10
are calculated from The phase compositions equations (11) and (12). The 0 -value is obtained from equation (10) at the given pressure. Since C,+ fractions are involved in the gas condensates, the critical properties (T, and P,) and acentric factor (w) of the plus fractions have to be known in advance, namely plus fraction characterization. In this work, the following procedure is used: (a) by extrapolation of equation (6) the Ci values of the C,+ fractions can be found as the K-values of the C,+ fractions at each pressure stage are known from the mass-balance calculations; (b) the Ta value in equation (5) is found from the Whitson-relation (Whitson, 1983). The critical temperature T, is obtained from the Winn-relation (Winn, 1957). The PC is then estimated from equation (5) as follows:
T -
TB
;
(17)
1
(c) by consideration of each of the C,+ fractions as a pure component, the acentric factor (w) may be found by fitting the T, values estimated by means of the EOS to those obtained from equation (15). Figures 3 and 4 demonstrate the comparisons of the liquid dropout curves computed from the reduced model and the PR EOS for the mixtures examined. The evaluation of the K-values is EOS-independent in this work. The EOS is only used to estimate the phase volumes. This may slightly affect the feed mole number in the next stage. It appears from these two figures that the reduced model can reproduce the
i--_-a ,-:
2 _,
10-I
r/
;i M
lc7 10-Z
nCl0
--
.‘/ ,. a = -0.1247893
/*
b = 0.0210786
/-
E = 0.8817808
l
d = -0.0032097 10-j
. 0
I 50
l
-
I
I
I
I
100
150
200
250
Pressure
(atm)
Fig. 2. Comparison between experimental K-values and computed ones for a well-defined mixture (Yarborough, 1972).
f,l
Expl. Reduced
model \
0
I
I
I
50
100
150
I\,, 200
250
Pressure (atm) Fig. 3. Liquid dropout curve of the gas condensate.
78
and E. H.
P. WANG
STENBY
reservoir gas condensate, constituent cycling
of
of
gas.
in order
variations element
during
the
A 3-D Pressure (atm)
reservoir.
produced
mixture.
An
dropout
Besides,
with
satisfactory
accuracy.
the dew point pressure is obtained
extrapolation dew
curves of equation
point
balance
pressure
cannot
calculations.
lated dew points
from
(6) since the K-values be
obtained
by
Table
the
well
the upper
from
with the measured
the reduced
model
given
from
the
PR EOS. COMPOSlTlONAL SIMULATION REDUCED MODEL
reduced model proposed
The
implemented reservoir
in
a newly
simulator,
simulations
of
have
been
flow
rate well model For
to estimate
with
reduced
model.
Simulation
developed
by
the
1990).
of
The
three
well-
UTCOMP
with
the
results
of the fluids in order to
from
the
runs
with
the
The same runs as made in our earlier work (Wang 1992) are performed
new reduced the fluid work.
apparent
made
observed. K-values be
to those difference
in this
This
in this work with the
The reservoir
are identical
No
lations
model.
work
implies
used
system and
in the earlier
between
and
that
block
the
the
previous
simu-
work
influence
on
of small change in the feed composition
neglected
in
the
natural
depletion
of
the
is the can gas
condensates. Simulation Part
of
of gas cychg
process
the produced
gas
reservoir to maintain minimize
the injected
gas.
into
the
the reservoir pressure. This can
the amount
sation and vaporize
is re-injected
of retrograde
liquid
the in situ condensed
Dry
gas
is usually
conden-
liquid into
miscible
For rate
with
the
to 5%
proposed
to characterize
initial
from
the PR
the dew point volume Reservoir
well,
a total is
per annum.
by Pedersen
et ai. (1988)
the reservoir fluid for the curve estimated
is compared
EOS
as shown
to the one in Fig.
liquid volumes
’
Layer I 2 3
5. It
relative to
by both the reduced
rock propertics. well for the 3-D run
Permeability
gas
specified,
data
NX=lS, NY=5, NZ=3 DX(ft) = 52.72, 13 x 105.45, 52.72: DY(ft) = 5 x 32.08 Datum (subsurface, ft) Capillary pressure Initial reservoir pressure (atm) Experimental dew point pressure (atm) Calculated dew point pressure (atm, PR EOS) Calculated dew point pressure (am, reduced model) Formation properties Temperature (“F) Compressibility, Psi Injection well Radius (ft) Permeability (md) Constanr bottomhole pressure (atm) Production well Radius (ft) Permeability (md) Constant production rate (lb-mol day-‘) Thickness
pressure
of the injected fluid
depletion
calculated
grid data, conditions
bottomhole
reservoir
The liquid dropout model
well
for the production
908.6 lb-mol/day
appears that the retrograde
I.
The
is also
pressure
well the flowing
the production of
the simplified
computed
Table
of natural depletion
and Stenby,
is employed
in
well, while a constant
atm), and the composition
The procedure
from
fluid are listed.
is applied
equals
EOS calculations.
the
The PR EOS is also used in these runs behavior
that
production
is
block
of the initial
bottomhole
the injection
which is equivalent
compositional
(Chang,
and gas cycling of a gas condensate
the PVT
compare
(289.6
corner,
for the EOS calculation
flowing
well.
are specified.
depletions
conducted
reduced model.
THE
in this work has been
UTCOMP
natural
defined mixtures
FROM
the
gas
initial water saturation
is used for the injection
pressure
in
wet
2.
constant
model
the
of each layer are presented
fluid and the injected
in Table
and
2 the compositions
mass-
agree well
ones or those computed
1. In Table
is located
right hand
porosity,
necessary information A
to large
displacement,
(1,1,3)
at the
It can be seen that the extrapo-
cycling
block
Thickness,
reservoir
Due
in each small volume
(15 x 5 x 3) is used to describe
and rock permeability liquid
recovery.
injection
comer, from
(15,5,1).
be a
of such a process.
grid model
bottom-left
Fig. 4. Liquid dropout curve of the well-defined
gas
may
of hydrocarbon
term, lnKF, has to be taken into account
in the simulation the
displacement
to improve
the dry gas
reservoir
in feed compositions
composition
is the primary
Therefore,
the gas condensate
special case of miscible fluids
and methane
the dry
Porosity
(fi)
(md)
(%)
47.5 78.5 33.0
3.17 I .48 6.39
41.47 33.52 40.86
and
initial
6500.0 0.0 289.6 289.6 291.6 2X9.6 160.0 I+.-6 16 lCUKl.0 289.6 16
1000.0 908.6
water saturation 30.0 30.0 30.0
(%)
Simulation of 2.
Table
model
and
imental
C,
C,
EOS
agree well with
by using the reduced of liquid
reduction. the
supports
would
not
in the estimation permeability,
the liquid
it is
vertical
horizontal
the gas-relative
phase
on
one.
permeability
The
is esti-
(18)
is set to be equal
capillary
pressures
in the simulation
is assumed
simulations
of
model
voir pressure average
reservoir
between
are not accounted
a period
MW
0.016 0.098 0. I52 0.176 0.193 0.274 0.462 0.503 0.597 0.792
16.44 30.07 44.09 58.12 58.12 80.04 94.00 108.00 139.57 211.34
production
since only the
the earlier production is mainly
caused
in Fig. 6 as a function
progress,
significantly
of
during
period because the production
by the expansion
fluid within this period.
of the reservoir
As the dry gas injection
more and more condensed
condensation
is in
oil is evaporated.
mated are
by both
almost
profiles
of
those blocks
Figure
esti-
and the PR EOS
7 shows
the
pressure
layer in X-direction
pre-
It appears that the pressure is nearly linear, except
close to the production
profile
The
average
reduced model As
indicated
dicted
estimated
from
well. Again,
both
models
in the
agree
oil
the initial
model,
saturations
computed
in Fig.
5, the dew point
EOS
reservoir
is around
the
pressure.
of 0.001
pre-
higher
than
Therefore,
the initial
state with an oil
for the simulation
while,
pressure
2 atm
fluid is in the two-phase EOS,
from
and the PR EOS are shown in Fig. 8.
by the PR
the PR
at the
model
region.
behaviors
well
saturation
the pressure
identical.
drop in most of the blocks
been
and
the reduced
dicted by the two models.
ther-
runs. The
that the pressure
of the production
15 yr have
An initial reser-
pressure,
if the fluid is in the retrograde
it appears
reservoir
atm is used in both
pressure
well are plotted
time. Both pressures are reduced
with the reduced
and the PR EOS.
of 289.4
to the
to be mobile.
out by the UTCOMP
modynamic
0
46.31 48.20 41.90 36.00 37.50 30.90 29.55 27.10 23.88 21.36
pressure
for. But it does not pose any problem gas phase The
the
way as:
permeability
phases appearing
carried
only
Due to the
k,, = s, The
of
of the gas phase and no relative permeability in the simplest
(2) 194.3 305.4 369.8 408.1 425.2 490.6 526.2 552.8 605.3 696.8
as seen in the graph, which can also reduce the liquid
impact
mated
gas
This results in the increase of the reservoir
relative
of
dry
PC Wm)
Besides,
of the presence
injected
also
made
of
the
pro-
that the water and oil are not mobile,
available,
and
the
during
to be mobile.
data
in
fluid
This observation
be large
the gas phase is considered mobility
the
permeability. calculation
assumed
small
and
that the liquid condensation
the assumption
In the
can be
Besides,
are found
with a dry gas cycling.
gas-relative
the exper-
curve is not steep during the pressure
reservoir
duction
model.
condensation
It induces
reservoir
4.86 2.08 0.39 0.70 0.00 0.82 0.00 0.00 0.00
It seems that the better match
achieved
initial
91.14
5.133 2.275 0.502 1.014 I .929 0.659 0.379 0.541 0.439
amounts
liquid dropout
the
87.130
the PR
values.
of
79
performance
Injection fluid mole (%)
Reservoir fluid mole (%)
Compound N,, CO,. C, C, LC, nC, ic,, ncs. C, C, C, 12 C13+
Compositions
reservoir
in the study
conducted
with
with
the reduced
the reservoir fluid is initially at the dew point.
This leads to the oil saturations
estimated
run with the reduced model being around
T 5
o .
PR EOS
-
Reduced
from
0.001
the
lower
model
-~._,_.-.-.--r--r--r-. ;
:
Ave.
res.
P.
CJ l-
-
” 50
Fig. 5. CME
Reduced
Prod.
model
I
I
I
I
I
100
150
200
250
300
Pressure
(atm)
liquid dropout curve of the North Sea gas condensate.
I
270 0
1000
well
I
I
I
2000
3000
4000
Time
P. I 5000
I 6000
(day)
Fig. 6. Production well and average reservoir pressures a function of time.
as
P. WANG
80
and
E. H.
STENBY
r
. *r
.
l
_
.I
-Reducedmodel
.
.
..
.
PR (EOS)
Reduced model
. 270
0
I
I
I
I
I
I
I
I
2
4
6
8
10
12
14
16
0
I 1000
I 2000
Block number in X-direction Fig. 7. Pressure profiles in the block different times.
(1 :I 5,5,1)
I 5000
I 4000
I 6000
Time (day) at three
than those from the PR EOS. However, almost no difference of the pressure profiles simulated by the two models is observed. It may be concluded that the pressure estimation is not sensitive to the saturation in the cases where the S,, is very small. Figure 9 shows the ratio of cumulative gas injection to cumulative oil production simulated from the two models. In the later stages, the increase of this ratio means that the injected dry gas has probably reached the production well (breakthrough). The oil recovery estimated from the reduced model and the PR EOS is, as shown in Fig. 10, also agreed well. The purpose of introducing the reduced model is to see how much computation time can be saved. For the simulations performed in this study, 55% of the CPU time is saved by using the reduced model compared to the one required by the simulation with the PR EOS. TRANSFORMATION
I 3000
Fig. 9. Ratio of cumulative gas injected to oil produced.
inal equation was transformed into the following form:
WJ- %.)(cra -
8),$* ,;y;, ‘1 t 1
0,
(19)
where OLL = --_1, K -1 cfR= --.
1
(20)
1 r&,-l
(21)
The bounds of the phase split 8 in equation (19) are defined as below instead of (0,l):
(22) for Ki> 1, ea=min(-$+),
OF THE RACHFORD-RICE EQUATION
(23)
for K.<
A newly developed technique for solving the phase split suggested by Leibovici and Neoschil (1992) has been employed in our work as a tool of saving computational expense. In this procedure, the orig-
=
1.
80 O I60 -
PR EOS Reduced model
0.5
E .Ig z ;: 3 .s 0
0.4
-0. .
._
l
.
0.3 0.2 .
0.1
,
-
PR EOS Reduced model
I 0
I
0
I 1000
I 2000
I 3000
I 4000
I 5000
I
0
2000
6000
Time (day) Fig. 8. Average oil saturationas a functionof time.
4000
I 6000
Time (day) Fig. 10. Oil recovery computed by the runs with the PR EOS
and the reduced model.
Simulation
It is found (22)
that this technique
is helpful.
and (23) can often provide
aries within
which
this range,
(19)
solution
like
can thus generally
iterations, ations
in most
are
in
this
Rachford-Rice 2,069,533
For
and Neoschil,
a linear
function.
be reached
within
the for
work,
equation
cycling
example,
[equation
the three
only two iter-
gas
process
the
(lo)]
times flash calculations.
form,
equation
by only 610,004 iterations equation.
(19),
original
is solved
This
by
the
results
by
to be solved of the
Rachford-Rice
in a further
reduction
of the
time spent on the phase behavior
is analogous
to IMPES
tation
procedure
each
time
an
fully implicit
around
of the CPU
compu-
and noniterative
additional
is only
larger reduction
calcu-
of the UTCOMP
type and the overall
is sequential
step,
(19)
scheme
to
the trans-
is just one-third
original
Since the solution
equation
While
is required
times, which
needed
computation lations.
Within
times for the phase split corresponding
the 290,612 formed
is searched.
of the calculations
required.
simulated
bound-
by Leibovici
behaves
saving
2.5%.
over
by
using
A considerably
time can be expected
for
simulators. CONCLUSION
The results in this work may lead to the following conclusions: model
calculations
of carrying
out the P-T
for the hydrocarbon
been developed.
The impacts
feed composition
variations
model.
the parameters
which
are
flash
mixtures
has
of the pressure and are included
in the
of the reduced
fluid-dependent,
are
model,
easily
deter-
mined; 2. The K-values EOS
can
model.
measured
be
well
When
reduced
involved
can be simulated
results
are
by the simulation
However,
around
schil could
the
natural of
the
by the reduced
to
those
with the PR EOS.
half of the computation technique
suggested
time
of the Rachford-
by Leibovici
time for fully-implicit
5. The pressures
estimated
simulator
saturation
in
processes
and Neo-
be efficient for the reduction
computation sitional
the
be saved;
The transformation Rice equation
the
reproduce
comparable
computed
can generally
reduced EOS,
data;
behavior
The
from the
the
the PR
and the gas cycling
gas condensates model.
with
by
can satisfactorily
PVT
phase
depletions
and computed
correlated
coupled
model
experimental
4.
81 NOMENCLATURE
a,b,c,d
=
Parameters of equation (3)
C, = Characteristic constant of component i defined in equation (4) dni = Variation of the feed mole number for component F = AH = K, = = K KII = L., = MW = N, = nF = rz! = Pe = P = P, = SG = T = T, = T, = Vo = V, = X, = y, = z, = Greek
i Feed mole number Latent heat Equilibrium constant
of component
i
Maximum one of the K, values Maximum one of the K, values Liquid volume % of dew point volume Molecular weight Number of components Mole number of component i in liquid phase Mole number of component i in vapor phase Vapor pressure Pressure, atm Critical pressure, atm Specific gravity Temperature, K True boiling point, K Critical temperature, K Dew point volume Liquid volume Liquid composition of component i Vapor composition of component i Feed composition of component i
letters
aL = 0~~= 8 = 4 F= 4:’ =
Left bound of 0 Right bound of 0 Mole fraction of vapor phase to the feed Fugacity coefficient of component i in liquid phase Fugacity coefficient of component i in vapor phase REFERENCES
1. A reduced
3. The
performance
Equations
very narrow
the solution
as mentioned
equation
of reservoir
by the IMPES
are not sensitive
of the order
of magnitude
of the
simulators; compo-
to the low of 10e3.
Chang Y. B. Development of an equation of state compositional simulator. Ph.D Thesis. The University of Texas at Austin (1990). Kenyon D. E. and G. A. Behie, Third SPE comparative solution project: gas cycling of retrograde condensate reservoirs. J. Petrol. Technol. 981-997 (1987). Leibovici C. F. and J. Neoschil, A new look at the Rachford-Rice equation. Ffuid Phase Equil. 74, 303-308 (1992). Moses P. L. and C. W. Donohoe, Gas-condensate rescrvoirs, Chap. 39. Petroleum Engineering Handbook (H. B. Bradley, Ed.) SPE (1989). Pedersen K. S., P. Thomassen and A. Fredenslund, Characterization of gas condensate mixtures. paper presented at the 1988 AIChE Spring National Meeting, New Orleans (1988). Peng D.-Y. and D. B. Robinson, A new two-constant equation of state. ind Engng Chem. Fundam. f5, 5964 (1976). Turek E. A., R. S. Metcalfe, L. Yarborough and R. L. Robinson, Phase equilibria in CO,-multicomponent hydrocarbon systems: experimental data and improved prediction technique. Sot. Petrol. Engrs J. Jun 308423 (1984). Yarborough L., Vapor-liquid equilibrium data for multicomponent mixtures containing hydrocarbon and nonhydrocarbon components. f. Chem. Engng. Data 17, 129-133 (1972). Wang P. and E. Stenby, Phase equilibrium calculation in compositional reservoir simulation. Computers them. Engng 16, s449-S456 (1992). Whitson C. H., Characterizing hydrocarbon plus fractions. Sot. Petrol Engrs. J. 683494 (1983). Winn F. W., Petrol. Refiner. 36, 157-162 (1957).