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ABSTRACT
This paper will describe the evaluation of a horizontal gascondensate well using numerical pressure transient analysis
techniques. The reservoir contains near critical fluid which
exhibits significant liquid dropout when subjected to
depletion. The paper will describe the experimental work
performed, its mathematical characterization and the matching
of both a well test and long-term production data with an
extended black-oil reservoir simulation model. The focus of
the work was to determine how the multiphase flow effects
impact test interpretation and how liquid dropout would affect
the long-term production performance of the well.
One of the important practical aspects was resolving
production data at different separator conditions. The
difficulties in characterizing near critical fluids and their
impact on the test interpretation will also be reviewed.
Introduction
Gas-condensate systems are becoming increasingly important
as higher pressure and temperature reservoirs are exploited. In
many instances, the economic value of the condensate
production far outweighs that of the gas. As a result, it is vital
to accurately characterize the reservoir and reservoir fluids in
order to maximize fluid recoveries and to accurately project
future cash flows.
This paper examines techniques to analyze gas-condensate
systems using the extended black-oil model suggested by
Coats1. To this end, a discussion of methods to convert
laboratory PVT data (constant volume depletion and constant
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experiments were performed to characterize the gascondensate fluid. These experiments consisted of:
the fluid system, was used to analyze the well test. The general
model developed from the well test analysis was then
incorporated into an extended black-oil simulator to history
match the historical long-term production data.
The laboratory CVD experiments were used to derive
extended black oil PVT properties as detailed in the
Background section of this paper. Separator conditions during
the well test were 3,500 kPa and 35 oC. These calculations
resulted in the PVT properties shown in Table 3 and
illustrated in Fig. 4. Since the PVT representation consisted of
a two pseudo-component system, a standard phase envelope
versus gas mole fraction was constructed, as illustrated in Fig.
5. The initial composition of the fluid is the dew point entry at
the 31,717 kPa. The dew and bubble point lines converge at
the critical point. As can be seen from the phase envelope the
fluid system is within a few mole percent of being classified as
a volatile oil. At separator conditions, a solution gas-oil ratio
(GOR) of 653.0 m3/m3 and a condensate-gas ratio (CGR) of
1.1101 m3/m3 at the dew point pressure of 31,717 kPa was
obtained.
Daily oil and gas rates for the long-term production period
were recorded at conditions that did not represent standard
conditions of either the gas or oil. Liquid rates from the first
stage separator were metered and reported without regard to
further flashing of this liquid to surface conditions. The gas
volumes reported were metered values from the first stage
separator, corrected to surface conditions using standard
orifice correction factors. The actual field separator
configuration is schematically illustrated in Fig. 6.
Unfortunately, the numerical model required volumes input at
standard conditions. As a result, it was necessary to convert
the reported volumes to standard conditions using the PVT
characterization. To compute actual surface volumes of gas
and oil, gas volumes were first re-converted to volumes at first
stage separator pressure and temperature. This was
accomplished by inverting the pressure and temperature
corrections of the standard orifice calculation. The oil and gas
rates at first stage separator pressure and temperature were
then known. This mixture was flashed using the known PVT
properties of the fluid to give oil and gas rates at standard
conditions. This last step must be accomplished using either a
mathematically characterized EOS package or the extended
black oil properties previously described. The flow rates,
corrected to standard conditions as previously outlined, are
shown in Table 4.
Unfortunately, special core analysis was not available for
this well. Therefore, relative permeability characteristics were
estimated using typical values for a gas-condensate system. Of
note was the low residual oil saturation in the presence of gas
(Sorg), also referred to as the critical condensate saturation. A
value of 10 percent was initially chosen for the residual oil
saturation. In a conventional gas-oil-water system, the residual
oil saturation is typically much higher, often in the range of 25
to 50 percent. Recent studies4, have suggested that low critical
condensate saturations, ranging from 7 to 15 percent, are
reasonable in gas-condensate systems. The low residual oil
saturation is further supported by the history match.
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Bo
1 rs R s
1 rs R s
B g
B o
where the prime denotes the derivative with respect
pressure.
gSTC
oSTC
3.
4.
5.
to
(A-1)
References
2.
Basic Notation
The starting point for deriving expressions relating the black
oil to compositional properties is to partition the total
hydrocarbon mass into four parts. But first define the ratio of
the stock tank density of gas to the stock tank density of oil as
1.
..(A-2)
..(A-3)
gSTC
m oo
oSTC
1 m go
.
m oo
..(A-4)
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m og
rs =
m og
oSTC
=
.
m gg
m gg
yg =
..(A-5)
yo =
gSTC
For the oil formation volume factor, consider a given
volume of the oil phase at reservoir conditions. When that
volume to taken to stock tank conditions, the volume generally
will have shrunk due to the evolution of gas. The oil formation
volume factor Bo is, by definition, the above volume at
reservoir conditions divided by the volume at stock tank
conditions. The thing to keep in mind here is that the
composition has changed, and that the density, a phase
property, includes that change in composition. So the oil
formation volume factor is
mTo
oSTC + R s gSTC
o
Bo =
= oSTC (1 + R s ) =
.
m oo
o
O
oSTC
(A-6)
R s m oo
R s m oo + m oo
R s
R + 1
s
m oo
m oo
1
xo =
=
=
m go + m oo R s m oo + m oo R s + 1
m Tg
m og
m Tg
=
=
+ rs
rs
(A-9)
+ rs
xg
R s + rs
R s + rs
.
y o rs R s + 1
(1 rs R s )
=
= 1
Ko =
xo
+ rs
+ rs
Kg =
yg
)
)
...(A-10)
xg =
m gg
.(A-8)
Rs =
rs R s =
1 1 Ko
K g 1
Ko
Kg
Critical Point
It is a well-known property that at the critical point, the K
values must be 1. From equations (A-10), it is clear that the K
values become 1 when
...(A-11)
1 rs R s = 0
+ rsc
1 + R sc
1
R sc
= rsc ,
..(A-12)
Flash Calculation
If the K values are known for a given total composition, then it
is possible to determine the amount of material in each phase
by doing a flash calculation. The general flash equation is
z c (1 K c )
=0,
K c + (1 K c ) f L
(A-13)
+ rs 1 + R s
fL .
m oT = oSTC VoSTC
(A-15)
V gSTC
VoSTC
m oT
..(A-17)
and
zg =
m gT
m gT + m oT
.
1 +
..(A-18)
r
s m gT m go
rs
m gT R s m oo
= m oT
...(A-14)
m gT = gSTC V gSTC
m gT
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= m oT
= m oT
..(A-19)
(A-20)
and similarly
m gg
m gT
1 Rs
.
1 rs R s
(A-21)
mTg
g
(m gg + rs m gg )B g
gSTC + rs oSTC
m gg B g
gSTC
= V gSTC
...(A-22)
1 Rs
Bg
1 rs R s
..(A-16)
m oo Bo
1 rs
= VoSTC
Bo .
oSTC
1 rs R s
...(A-23)
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( R s )B g + (1 rs )Bo
1 rs R s
...(A-24)
(1 rs )Bo
( R s )B g + (1 rs )Bo
S g Bo + S o B g R s
S o B g + S g Bo rs
(A-26)
S g Bo (1 rs R s )
..(A-27)
S o B g + S g Bo rs
1 V
.
V P
cT =
.
1 rs =
S o B g (1 rs R s )
S o B g + S g Bo rs
..(A-28)
Sg
rs Bo B g R s S o
R s B g Bo rs
B g
Bo
B g
1 rs R s
1 rs R s
B o
...(A-31)
and
..(A-30)
..(A-25)
Sg
So
B o B g R s
B g ,
Bo
Bg
Sg
So
B o
B g Bo rs ,
Bo
Bb
10
Discussion
Based on the familiar saturation weighted average concept,
the individual phase compressibilities can clearly be identified
in equation (A-31) as
Bo B g R s
B g rs
1 rs R s
B g B o rs
1
co =
Bo R s
Bo
1 rs R s
cg =
1
Bg
..(A-32)
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44.010
34.080
28.013
16.043
30.070
44.097
58.124
58.124
72.151
72.151
86.200
84.160
78.110
82.150
100.200
98.190
92.140
3.375
9.745
2.903
23.022
4.540
3.925
1.454
2.964
1.705
1.836
3.159
0.644
0.228
0.535
3.365
1.160
0.965
34.475
2.971
11.078
4.015
55.595
5.850
3.449
0.969
1.976
0.916
0.986
1.420
0.296
0.113
0.252
1.301
0.458
0.406
7.949
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Pressure
11
Displaced
Vapor Density
(g/cm3)
(psia)
4600
(kPaa)
31717
4000
27580
48.713
24.673
73.386
5.346
0.3291
3250
22409
52.184
25.707
77.891
9.852
0.2403
2750
18961
53.370
24.585
77.955
10.076
0.1883
2000
13790
68.391
22.413
90.804
22.829
0.1275
1500
10343
69.065
20.761
89.826
21.868
0.0935
1000
6895
83.478
18.958
102.436
34.478
0.0600
562
3875
110.700
17.226
127.926
59.887
0.0324
4000
(kPaa)
27580
(gmol) (1)
0.0548
3250
22409
2750
Res Relative %
Liquid (2)
(Vol%)
7.42
(gmol) (1)
0.0548
7.42
0.8421
36.26
0.5096
0.0837
11.33
0.1384
18.75
0.8252
37.78
0.5565
18961
0.0724
9.81
0.2108
28.55
0.8250
36.22
0.5868
2000
13790
0.1188
16.09
0.3296
44.64
0.8286
32.97
0.6184
1000
6895
0.0870
11.79
0.5016
67.94
0.8542
27.90
0.6655
562
3875
0.0757
10.26
0.5774
78.20
0.9581
25.32
0.6948
(psia)
(%) (1)
Vapor Z Factor
12
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775.20
Stage 1 Press
3500 kPa
Stage 2 Press
101 kPa
0.9782
Stage 1 Temp
35 oC
Stage 2 Temp
15.6 oC
Pressure
(kPa)
3875
Gas expansion
factor, Eg
(st m3/res m3)
30.9610
Oil viscosity
(mPa-s)
0.892
Gas Viscosity
(mPa-s)
0.01400
Oil density
(kg/m3)
694.80
Gas density
(kg/m3)
32.40
60.00
6895
51.05
0.01432
1.2399
60.6491
0.620
0.01510
665.50
10343
103.33
0.06694
1.3769
90.7686
0.425
0.01670
636.40
93.50
13790
151.13
0.08754
1.4926
121.8865
0.304
0.01880
618.40
127.50
18961
159.43
0.02838
1.5868
188.2627
0.196
0.02350
586.80
188.30
22409
331.29
0.34247
1.9753
193.2173
0.150
0.02820
556.50
240.30
27580
445.68
0.62305
2.3767
225.2276
0.100
0.03990
509.60
329.10
31717
653.03
1.11001
2.6000
250.0000
0.060
0.05670
543.84
459.67
33000
717.34
1.20000
2.6200
257.6826
0.048
0.06191
563.70
491.77
35000
817.58
1.30000
2.6300
269.6587
0.028
0.07003
598.84
535.53
775.20
Stage 1 Press
9000 kPa
Stage 2 Press
101 kPa
0.9782
Stage 1 Temp
38 oC
Stage 2 Temp
15.6 oC
Pressure
(kPa)
3875
Gas expansion
factor, Eg
(st m3/res m3)
31.8210
Oil viscosity
(mPa-s)
0.892
Gas Viscosity
(mPa-s)
0.01400
Oil density
(kg/m3)
694.80
Gas density
(kg/m3)
32.40
60.00
6895
92.04
0.00207
1.3001
61.2368
0.620
0.01510
665.50
10343
145.32
0.04385
1.4415
92.3738
0.425
0.01670
636.40
93.50
13790
195.94
0.06215
1.5635
124.2237
0.304
0.01880
618.40
127.50
18961
316.63
0.21739
1.8489
164.2075
0.196
0.02350
586.80
188.30
22409
354.34
0.29351
2.0158
199.2984
0.150
0.02820
556.50
240.30
27580
477.09
0.56306
2.4370
232.6314
0.100
0.03990
509.60
329.10
31717
600.00
1.02712
2.6000
250.0000
0.060
0.05670
523.89
443.60
33000
638.12
1.20000
2.6200
255.3865
0.048
0.06191
534.12
487.39
35000
697.54
1.30000
2.6300
263.7832
0.028
0.07003
554.19
523.86
Flow
Period
1
Duration
(hours)
0.917
Wtr Rate
(m3/d)
0.000
17.500
100.527
112.800
1.083
11
720.000
42.749
35.930
0.000
26.000
113.776
127.500
0.822
12
744.000
41.565
40.102
0.000
65.000
80.237
93.000
0.491
13
744.000
44.923
59.177
0.000
863.750
0.000
0.000
0.000
14
720.000
42.426
58.481
0.000
468.250
57.523
77.659
0.000
15
744.000
35.300
40.217
0.000
744.000
51.859
52.496
0.000
16
720.000
53.779
55.881
0.000
192.000
0.000
0.000
0.000
17
744.000
50.929
45.682
0.000
528.000
34.530
33.522
0.000
18
552.000
50.810
40.475
0.000
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Parameter
Ultimate gas recovery
Ultimate C5+ recovery
Gas recovery factor
C5+ recovery factor
Gas influx into inner region at
01/01/2018
Well shut-in date
16.2
01/01/13
106m3
103m3
percent
percent
13
Units
106m3
14
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15
16
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Fig. 11 - Long-term production history match for the limited reservoir case. Model generated results are presented as solid lines while
observed data is presented as symbols.
Fig. 12 Long-term production history match for the recharge case. Model generated results are presented as solid lines while observed data
is presented as symbols.
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