Dodson 1953
Dodson 1953
Dodson 1953
3710
tory techniques of Lindsly12~l. led to the present methods of ing conditions may change as well as the nature of the reservoir
reservoir fluid analysis. Such improved techniques make pos- fluid: thus, new PVT analyses will take into account these
sible the quantitative inve~tjgation of re~ervoir prohlem~ now factnr~ which were not anticipated in prior tests.
taking place.
Modern laboratory procedures still do not truly represent
reservoir behavior. This paper will present some proposals to
help correct these discrepancies. Bottom-H ole Samples
Many types of bottom-hole samplers have been devised and
de,cribed in the literature.",]·"·,24,25,,. The mechanical nature of
the devices introduces some error into the sampling operation;
however, these errors are probably of less importance than
those resulting from the other difficulties.
RESERVOIR TEMPERATURE AND PRESSURE
It is often questionable whether the fluids in the tubing at
SURVEYS, SAMPLING OF RESERVOIR FLUIDS
the point where a bottom-hole sample is taken are representa-
The applicability of the results of laboratory PVT deter- tive of the reservoir hydrocarbons. This is particularly true if
minations to problems in reservoir behavior depends upon there has been considerable drawdown of the well prior to
field information. To use the laboratory results in reservoir sampling, if several zones containing fluids of dissimilar prop-
studies it is necessary to have accurate field temperature, pres- erties are produced together, if the gas and liquid are not
sure, and production information, and to know the samples homogeneously mixed in the proportions in which they existed
tested are representative of the reservoir fluid. in the formation, and if both gas cap and oil zones of a reser·
voir are open simultaneously to the well bore.
Allowing the well to stand shut-in for a short time prior to
sampling usually assures a fairly representative reservoir
liquid sample, lacking only the gas formerly associated with
Temperature Surveys
it. Only in the case where the reservoir fluid was under-
Bi-metallis,17 maximum recording," and electrical resistance saturated initially and during production would the sample
thermometers"; thermocouples; and other methods" are avail· be truly representative.
able to obtain bottom-hole temperatures. It is essential that
the fluid within the well bore through which the measuring
device passes be in thermal equilibrium with the forma-
tion and that the recording instrument come to thermal equili. Recombined Samples
brium with the well fluids readily. For these reasons, static Often sampling of the fluids produced from a well is a
or shut-in temperature measurements are considered the most satisfactory and accurate method for obtaining a representa-
representative. tive reservoir fluid sample. Both the produced liquids and gas
are sampled, usually at the high pressure separator. These
two samples are then combined in the same proportion as the
two ph:tses are produced from the well. The liquid and gas
Pressure Surveys also may be combined in other ratios to give samples rep-
resentative of other reservoirs or of the originating reservoir
The merits and limitations of the various sub· surface pres-
as it existed at some previous time.
sure measuring devices are adequately discussed in liter-
ature.'·~23
There are also some inaccuracies possible in using this
method, and they must be corrected for if the results obtained
from the recombination are to be representative. Relative per-
meability conditions in the formation may allow unequal flow
rates of liquid and its formerly associated gas to the well bore;
t~~~-~ -~
such a condition would obviously render a sample combined
on the basis of the primary trap gas-oil ratio inaccurate. The
necessity for accurate gauging and steady-state well conditions _ u un--+----
is immediately apparent. (If the well is producing both gas
from a gas cap and gas released from solution, the proper
combination of the fluid samples will depend on other infor-
;60oL--:--_______
a: I
I ______
I :
~
f L-- ~
mation besides the primary separator gas-oil ratio. General
correlations concerning the properties of reservoir fluids may
be useful in this regard"-30).
The economy resulting from the use of recombined well fluid
V t,
:3
a:
400
COMPOSITE UBERATION-
SEPARATOR
I
CONDITIONS 100 PStG, eOOF~
TANK CONDITIONS
.~ I
I 0 PSIG:, 80 0 r
I
i
all the fluid entering the flow-string must be removed from
it at the surface and there is sufficien~ agitation in the flow-
SEPA~A -I
::J
<.> string to induce equilibrium. There are several differences,
w
::; FLASH TlON however, between this flow·string liberation and a laboratory
-~
::J
..J
i TEMPERATURE 140·
flash liberation. The laboratory flash liberation allows only the
o I
> II gas liberated from the sample to stay in contact with the re-
<.>
i;: .0300 maining liquid until certain conditions are reached. This is
'\
<3
w usually done under isothermal condition". In the well bore,
Q. I
I
27TI gas from oil other than that in the well bore may be present,
en I
~ 1
/BUBBLE TINT PSIG AND ,
0.02241 CU FT/LB
resulting in differences from the laboratory results in both
the gas and oil characteristics. This is particularly true in
.0200
i I 'I gas injection where part of the injected gas is by. passin•
1000 2000 3000 4000 5000 through partially depleted pores. Also separation of some gas
PRESSURE CPSIG)
from the liquid hydrocarbons at th~ tubing shoe may occur.
This gas may then be produced from the casing-tubing annulus
RIG. 3 - PRESSURE·VOLUME RELATIONS OF RESERVOIR FLUID. thus rendering more inaccurate the oil and gas characteristics
predicted from the laboratory flash liberation. And if a well
flows by heads, equilibrium between all produced fluids will
not be attained. Currently, however, the liberation process in
the tubing and casing is rei!arded as more nearly flash in
nature than differential.
a true laboratory differential liberation because the gas is con-
stantly in contact with oil on its trip to the well bore, and
the oil the gas is in contact with is not its originating liquid.
Whether there is sufficient agitation to allow the traveling gas Fluid Separator Gas Liberation
to come to equilibrium with the oil it by-passes is unknown.
It is probable that complete equilibrium between the gas and It is generally agreed that flash vaporization best represents
oil is never attained. the separator type liberation. When entering the separator the
It is also possible at this stage to have a combination of fluids are probably in equilibrium due to the agitation occur·
the differential and flash liberation in the reservoir due to the ring in the flow-string. During separation in the trap, a certain
pore size variance. When the larger pore spaces have attained amount of oil always remains inside the trap in contact with
gas equilibrium, there may be smaller pore spaces or capil· a constant volume of gas. Each unit volume of oil-gas mixture
laries where an equilibrium gas saturation has not been entering the separator is of approximately the same composi.
reached. These small capillaries probably contribute little to tion as the previous unit volume; thus homogeneous flow is
the total production of the field. and the dual liber'ttion effect essentially attained under conditions of ~teady well flow. Each
may therefore be neglected. subsequent separator results in another flash liberation with the
final flash liberation occurring in the stock tanks.
During gas injection it is known that very little of the gas
returned to the formation goes into solution in the remaining The variance between the laboratory and separator flash
reservoir oil due to lack of agitation. The gas goes either into liberation results from the laboratory flash being carried out at
the gas cap or by-passes through the larger, already depleted, a constant temperature for each trap, while the field separator
pores of the formation. The injected gas, mainly comprised of liberation may occur at greatly differing temperatures through-
methane and ethane due to prior recovery of the heavier con· out the year. However, this discrepancy between laboratory
stitutents, is of different composition than the gas that would and field results is slight in most cases.
be evolved by the oil remaining in the by-pass channels if the
reservoir pressure were allowed to decline. The volatile injected
gas will pick up some of the heavier constituents of the oil
and will mix with the liberated gases; the oil in turn will Composite Gas Liberation Method
dissolve some of the injected gas. This enrichment of rapidly In the previous discussion the reservoir liberation, after
moving gas will not produce complete equilibrium an:l is gas equilibrium was reached, was described as a declining-
not represented either by the flash or differential-type labora- pressure, relatively-constant-temperature, differential libera-
tory liberation. However, since the gas is moving rapidly past tion; the flowstring liberation was described as a declining-
the remaining oil, differential liberation is considered to afford pressure, declining-temperature, flash liberation; the separator
the best representation of the formation process. This non· and stock tank liberation was described as a reduced-pressure,
attainment of equilibrium causes computations involved in variable·temperature, flash liberation. To better approximate
gas injection operations to be in error if baeed on the assump- this reservoir and producing liberation cycle a composite type
tion that equilibrium is attained between the oil and injected liberation can be run in the laboratory. A differential libera-
gas. tion represents the reservoir vaporization; a series of flash lib-
Miller" believes the formation liberation to be an adiabatic erations represents the behavior of the oil passing up the flow-
rather than isothermal process as it is generally regarded. string, through the surface separators, and into the storage
Under certain conditions the use of isothermal laboratory data tanks. The limitations and errors involved in these approxima-
to approximate adiabatic reEervoir conditions might cause tions have been previously discussed.
errors of a measurable magnitude. However. Miller reports The laboratory procedure for this composite liberation fol-
that in most cases this error is slight. lows. A representative fluid sample is charged into the main test
~
The differential liberation of tile oil in the main test cell
Q.
Ul· ---....,
is continued with removal of portiulls of the differentially lib- 0 0
I---.,
0.6
erated oil at selected pressures. Each portion removed is Hashed 1000 2000 ~OOO 4000
PRESSURE (PSIG)
through what approximates the surface trapping arrangement.
Near the end of the composite liberation process the main
cell pressure may drop below the initial assumed trap pressure fIG. 5 - GAS SPECIFIC GRAVITY.
>- 36,5
I- may then be compared to the deviation factors as determined
:>
<t by the Brown'" or some other similar method." A formation
a: ,
'" volullle factor for the gas (space in barrels (.ccupied in the
36~4 - ----- , -t---·--·~------+------- --- reservoir at a certain pressure bv one standard cubic foot of
gas that is not in solution') mav he computed using the devia-
tion information and gas laws. Use of the gas formation vol-
363
0 1000 2000 3000 lime factor. ,olution gas·oil ratio. and li(plid volume factor
PRESSURE (PSIG)
readilv gives the two.phase formation \'olume farto]'. To be of
"ignifican('(~ this two.phase factor must he romputed from the
FIG. 6 - GRAVITY OF COMPOSITE-LIBERATION TANK OIl. ('ompositt- liberation data and should not he obtained from
flash lilwration informatioll.
The thermal expansibilit\ and collipres"ihilit\ of the "at 11-
ratt"d nudt" sll<luld lw obtaint"d so that the obsened data may
he rt"vised to allY datllm. Slirface and interfacial tensiono.;
of Table 6. The material balance equation ~Iwwn in Table 6 ,hould ht" determilwd. The method of Hocutt" is typical.
was simplified before u~e by assuming: (1) No gas in solution :\11 data regarding field sampling methods. field sampling
in re'ervoir or encroached water. (2) The water compression conditions. and field tt'sls should he induded in the final report.
and thermal expansion are negligible or of compensating mag-
nitude, (3) No pore volume reduction due to sand compaction.
(4) TI'e water initially in place equals zero as it is inter-
The ""Minimum" PVT Requirements
,t:t;al and thus is assumed to be both immobile and to undergo
110 volumetric change.
Such a "miniIlItJlll" analysis would he one in which only the
1II0st important physical properties were measured. Other prop-
In pooh where the oil is highly volatile and the gas produced
('nies wOlild he approximated hy using the ha,.;ie test data.
contains considerable amounts of liquefiable constituents. con-
production information. and various corrt'lations.
o.;:deration mw't be given in material balance calculations to
Ca"-oil ratios and formation volume fa('tors a~ dett'rmined
the amounts of LPG and casinghead gasoline recoverable from
hy the composite and differential methods are important. The
both tl~e gas in solution in the oil produced and from the gas
gravity of the liberated gas can be obtained from this informa-
coming from the gas cap or residual reservoir oil.'" The solution
tion using the correlations of Standing" or Borden and Rzasa."
gas produced by the composite liberation can be analyzed for
From the test cell information and the liquid viscosity at one
Equid content. The method of Cook, Spencer, and Bobrowski'"
set of conditions the correlations of Beal'" will allow approxi-
;:lIows the liquids contained in the other produced gas to be
mation of reservoir liquid viscosities at other conditions. Esti-
computed. The formation volume factors for the liquids pro-
mated gas gravities will allow approximation of the viscosity of
duced will be obtained hy the composite liberation method.
the liberated gas through the correlations of Bicher and Katz.""
Estimated liberated gas deviation factors and gravities per-
mit computation of gas formation volume and two-phase forma-
tion volume factors as descrihed under "ideal"' PVT require-
ments.
REQUIREMENTS FOR PVT DETERMINATIONS Again the field sampling and field testing information are
an integral part of the report.
Evaluation of various producing methods or future produc·
tion possibilities may be gained through the combined use of
PVT information and operating data. The "ideal," "minimum."
and "no reservoir sample" PVT requirements are discussed. The '"No Reservoir Sample" PVT Requirements
With a knowledge of the gravity of the produced gas, grav-
ity of the tank oil, instantaneolls gas-oil ratio (assumed equal
to the solution gas-oil ratio or corrected to an estimated solu-
tioll ratio by other means), and bottom hole temperature and
Table 2 -_. Well Sampling Data ,ite methud were 100 psig and /:lO°F for the oeparator, and
Total Dppth: S,:JHO fl. I'lu,.:,.:t'd to: S.2:-lh 1'1.
o psig and 80°F for the tank.
Compj P tiol1: Date: ])PI·. I. 11)42. From tlH~ dat a (Tahles I through 4 J curves were constructed
( :a~i ng ~iZf~: hllt If!. (I-'i/-!:,. I Ihrollgh 61. It is to he noted that only three poinls
ll .. pth: S,:'7:1 fl. ',('n' ddt'rllli" .. d hy tlw composite method. The general form
I't~rlo,.aliofl: Clln pt"rforatl·(1.
Intpr\,al: S.II7·S.IS1 1'1.
of till' ,'.omposil(~ liheration curves was dictated hy the three
Tuhin,.: Size: 21f2 in. poinls ohtaine!1 and the shape of the differential curves. The
ll"pt It of tubi 11": ;;IJOe: :-;.1 ()O I!. shape of Ihe composite curves in the under-saturated area
Packer: S,074 ft. wa" determined hy the linear relationship of the differential
Commenb: Pack!'r "PI to i"olatt' IIl'l'er 1\ att'r ,allik
Samplin,.: Date: ,\1ay I, 19S1. ('urve; an offset was made to allow for the different final
I'rodlll'tion Data: (Durin,.: "amplin,.: I properties, The symhols, abhreviations, and suhscripts used are
Tuhin~ Prf's~tlrt': 480 I'sig Ihose given in the appendix.
(:asin,.: Pressure: Not recorded
~"parator Data
\faterial halance techniques were used in conjunction with
Pn"':-.:--lIn-· T'-llIperature the PVT data to calculate the tank oil uriginally in place in
Fi rst Sta~~: "l01lf' \j,,",- Ihe reservoir. The equation employed, production clata used,
Second Sta,.: .. : 'iOIlt' \jOlW
and rt";ults obtained are shown in Table 6. Note that at a
Tank: ~flt n-'(·ordt·d 'iot rPI'ord"d
Oil and (;a, Halt' pre.;surt' of 2,070 ]>~ig the tank oil initially in place for the
Fir,t Sta,.:": \Ollt' composite data was 292.9 x 10'; bbl against 231.8 x 10" bbl for
St'('ond Sta,.:!': \on!' Ihe difft'rential dala. at a pressure of 1.560 p~ig a similar differ-
Tank: \jot rf'I'orded
ellce was noted. The magnitude of the difference obtained
Ca,,·Oil Hatin: S.Mh I'll ft lI!'r bhl
Tank Oil Cravity: ::I4.:·\" .-\1'1 between the two types of calculations shows the necessity of
\Vat .. r: Tra('!' using liberation data that approximates conditions cluring the
(:ommf'nts: Produ(,tion rates durin:! ~ampling pf'riod: production sequence.
Gro.'>' Fluids - 74.4 HI D
Total Gas - 420 Mcf!D
Table 5 - Compressibility and Specific Velume Data regard to gas-cap properties may be quite inaccurate. partic-
Type of Sample: Recombined ularly where gas injection operations are occurring.
Specific Volume No determination of the physical behavior of a reservoir fluid
At Bubble Point Conditions: 2,730 poig and 140°F as far as the authors know has considered the effect of gas
Measured: 0.02241 eu ftjlb injection on the results of the analysis. An answer to the ques-
Calculated by Composition: 0.02190 cu ftjlh
Calculated by Flash Vaporization: Not Run tion of whether the present methods of approximating reservoir
Calculated by Stage Separations gas liberations are applicable when gas of non-equilibrium
at 100 psig and 0 psig 0.02119 cu ftjlb composition is coming in contact with the oil (i.e., by-passing)
Unsaturated Oil Above Bubble Point Pressure would be extremely helpful in laboratory work and in the
Specific Volume at 4964 psig and 140°F: 0.02188 cu ftjlb
Thermal Expansion: Not run application of the results of laboratory tests.
Compressibility at 140°F:
from 2,730 psig b) 3,414 psig. 10.937 x lO- G hhl
per bbl per psi
from 3,414 psig to 4,002 psig. 11.880 x 10-· bbl
per bbl per psi
from 4,002 psig to 4,964 psig. 9.815 x 10- 6 bbl
per bbl per psi
NOMENCLATURE
Symbols
Quantity Units Symbol
Table 6 - Material Balance Computations Using
Composite and Differential Liberation Data Cumulative production Barrels Op
of stock tank oil
Equations used (all symbols are defined in the appendix) :
Cumulative production Barrels
of water
Deviation factor for gas None z
llV. d
(l) Formation volume factor
(2)
1. Single phase Barrels reservoir space B
UiW =B iw • • • • (3)
per stock tank barrel
Vo = Bo + (5'0-50) B•. (4)
Vw =
Bw + (Sw' -Sw) B. (5) 2. Two phase Barrels reservoir space U
B-~~_Z_ (6) per stock tank barrel
• - P R • 520 • 5.62
Gas-oil ratio
Pressures 1. Cumulative produced Standard cubic feet per
QUANTITY* 2070 psig 1560 psig UNITS
gas-oil ratio barrel stock tank oil
acre feet.
III 0.1770 0.1770
acre feeto 2. Solution gas-oil Standard cubic feet per
0,. 11.20 x 10' 18.50 X 106 bbho ratio barrel stock tank oil
WF. 0 0 bbl
34.26 x 10" 67.08 X 10' std cu ft Pressure - absolute Pounds per square inch p
G"
Sf' 3059 3626 cu ftjbbho Ratio of original reservoir gas Barrels of gas at reser- m
W p 0.7950 x lOG 1.249 x 106 bbl cap volume to original vol- voir conditions per
Tank Oil 0 1** ume of reservoir oil barrel of oil at reser-
( calculated) 292.9 x lOG 275.6 X lOG bbho
voir conditions
Differential **
0, (calculated) 231.8 x 106 229.2 x 10' bbl' •• 'ri Change in reservoir pore vol- Barrels II Vsd*
*All PVT data used in computations are obtained from Tables 1 ,to ume due to rock compaction
5 and Figs. 1 to 5.
**For this material balance V,w =
1, Sw =
0, Vw 1, = Solution ratio of Standard cubic feet per S ..
Sw' = 0, llV,d = 0, W, = 0 gas in water volume of water at
standard conditions
Space occupied in the reser- Barrels reservoir space
voir by 1 volume of gas at per standard cubic foot
and phase behavior studies would give much valuable informa- standard conditions
tion in this regard. These studies may show that reservoir
evaluation can be made on the basis that thermodynamic Stock tank oil volume in place Barrels o
equilibrium attains in the reservoir; or conversely they may at any time
permit the magnitude of the error involved in this assump- Temperature - absolute Degrees Rankine T
tion to be approximated if equilibrium does not occur.
That the properties ef reservoir oil vary with structural posi- Volume Barrels, standard cubic V
tion has been pointed out. Further studies of this condition feet
would be valuable to the industry. Whether this variation Water encroachment - gross Barrels
represents a condition of equilibrium or non-equilibrium also
should be investigated. Water at standard conditions Barrels If'
Properties of the vapor phase existing in the gas caps of in place at any time
various reservoirs should be studied. Present assumptions in • A negative numerical value in most cases as a reduction is shown.
39. Standing, M. B., and Katz, D. L.: "Density of Natural liberation method during approximately the first third of
Gases," Trans. AIME, (1942) 146, 140. pressure depletion below the bubble point, breaking up toward
40. Hocott, C. R.: "Interfacial Tension Between Water and the differential liberation curve during the second third of
Oil Under Reservoir Conditions," Trans. AIME, (1939) pressure depletion where gas is being removed approximately
132, 184. as fast as it is liberated in the reservoir, and during the
41. Espach and Fry, J.: "Variable Characteristics of the Oil last third, the formation-volume probably would remain well
in the Tensleep Sandstone Reservoir, Elk Basin Field, above the composite liberation curve and probably closer to
Wyoming and Montana," Trans. AIME, (1951) 192, 75. the differential liberation curve since large quantities of com-
42. Graybeal, O. A.: "California's Prolific Potrero Oil Field," paratively dry (largely methane) reservoir gas would be pass-
Oil and Gas Jour., (1951) 50, (10), 80. ing through the surface separators in intimate contact with
43. Cupps, c. Q., Lipstate, P. H., Jr., and Fry, J.: "Variance the oil, causing an abnormal amount of shrinkage of the
in Characteristics of the Oil in the Weber Sandstone Res· separator oil. There is no discussion in the paper of this
ervoir, Rangely Field, Colo." R.I. 4761, USBM, (1951). last effect (large amounts of excess gas production above
44. Sage, B. H., and Lacey, W. N.: "Gravitational Concentra- the solution GOR) on the formation-volume factor of the
tion Gradients in Static Columns of Hydrocarbon Fluid," oil during the last stages of depletion; in fact, it is neglected
Trans. AIME, (1939) 132, 120. in the laboratory method.
45. Burtchaell, E. P.: "Reservoir Performance of a High Since the formation volume factor is by definition a ratio
Relief Pool," Trans. AIME, (1949) 186, 171. of an end product (either tank oil or residual oil) to a
46. Muskat, M., and Taylor, M. 0.: "Effect of Reservoir reservoir volume of oil, it is difficult even to theorize on
Fluid and Rock Characteristics on Production Histories of the shape of the curve throughout the true liberation sequence
Gas-Drive Reservoirs," Trans. AIME, (1946) 165, 78. as the absolute values depend upon an exact duplication of
47. Babson, E. C.: "Prediction of Reservoir Behavior from the reservoir production process. At least the composite libera-
Laboratory Data," Trans. AIME, (1944) 155, 120. tion method proposed by Dodson, et ai, goes a step further
48. Patton, E. c., Jr.: "Evaluation of Pressure Maintenance along this line in that it considers the tank oil as a variable
by Internal Gas Injection in Volumetrically Controlled instead of a constant which is the manner in which the
Reservoirs," Trans. AIME (1947) 170, 112. residual oil is used in the differential liberation method.
49. Tarner, J.: "How Different Size Gas Caps and Pressure It should be well to remember that neither of the laboratory
Maintenance Programs Affect the Amount of Recoverable methods can exactly duplicate the actual behavior of the
Oil," Oil Weekly, (June 12, 1944) 114, (2),32. solution-gas drive reservoir and the limitations of both of
50. Muskat, M.: Physical Principles of Oil Production, Mc- these methods should be kept in mind.
Graw-Hill Book Co., Inc., New York, (1949).
With reference to Fig. 2 of the paper (solution GOR
curve), the curve obtained by the composite liberation gives
the solution GOR at surface conditions, however, only 20 to
DISCUSSION 25 per cent of this oil ever experiences these conditions. The
By William L. Boyd, Continental Oil Co., Ponca City, Okla. remaining 75 to 80 per cent of the oil remains in the reservoir
It is generally acknowledged that little is known concerning and is best represented by the differential curve, i.e., gas
the exact nature of gas liberation from a solution-gas drive in solution at reservoir pressure and temperatures instead of
oil reservoir. The composite liberation as suggested by Dodson, separating conditions which are at much lower pressures
et al, and the standard differential liberation are laboratory and temperatures.
methods to approximate the true liberation sequence as it It should be mentioned also that there can be no com-
actually occurs in the production process. In applying these parison between the two curves illustrated in Fig. 5. Naturally,
data to reservoir engineering calculations, one would prefer the specific gravity of the composite liberation gas is higher
to use the laboratory data which more nearly approximates than the differentially liberated gas because the pressure-
the true liberation sequence. temperature conditions are entirely unrelated. Without close
Differential liberation as performed in the PVT labora- inspection, the graph would lead one to believed that the
tory is approached by the true liberation sequence only in composite liberation gas specific gravity was 0.73 in the
the intermediate stage of pressure depletion after the relative reservoir at 200 Ib, whereas, it is really the specific gravity
permeability to the reservoir gas is such to allow the flow of of the solution gas liberated at 100 Ib to 0 Ib at 80°F
gas along with the oil so that the rate of gas production equals from the oil which was removed from the reservoir at 2000 lb.
rate of gas liberation in the reservoir. Even this is not entirely As such, these data could not be used in the conventional
correct, as the flowing gas in the reservoir is the gas which material balance calculation.
was in equilibrium with its originating oil and not necessarily The foregoing comments are not meant to detract from
the oil flowing toward the well bore. the data as presented in this paper, but to point out some
On the other hand, the composite liberation makes the of the difficulties in applying correctly these, or any other
assumption of differential liberation in the reservoir plus a set, of laboratory PVT data to reservoir engineering problems.
flash liberation of the oil through the flow string and sep-
arating equipment. This method assumes that the flowing gas
from the primary or secondary gas cap (the differentially
liberated gas) never comes in contact with the produced oil
and its solution gas.· This type of reservoir behavior is AUTHORS' REPLY TO MR. BOYD
obtained in the primary stages of depletion of a solution- Boyd's discussion is appreciated by the authors.
gas drive reservoir where gas saturations are not large enough The section of the paper titled "Types of Gas Liberation
to permit the flow of gas. and Application of Data Obtained from These Liberations to
One could, therefore, reason that in actual reservoir Reservoir Problems" discusses the formation liberations occur-
behavior, the formation volume factor curve for the true ring at various conditions of gas saturation. The differential
liberation sequence would follow the laboratory composite vaporization has been considered most representative of the
formation liberation. However, before equilibrium gas satura· A flashing of the produced oil will occur during the flow up
tion is reached, where the oil is of a highly volatile nature, the tubing and through the separators and tanks. If large
or where the producing gas-oil ratio is in excess of the amounts of gas are produced with the oil in the field, make-up
solution gas-oil ratio, the differential process is not completely gas can be injected into the auxiliary cell in the laboratory
representative of the formation liberation. along with the differentially liberated oil to make the flash
At conditions below the equilibruim gas saturation, a flash trapping stage of the composite liberation more representative.
liberation best represents the formation process. Special tech· The liberation to which any produced oil is subjected i~ a
niques must be used to simulate the formation liberation composite of the vaporization in the formation and that
when the re'3ervoir contains oil of high volatility; the paper occurring from well bore to stock tank. This dual process
of Cook, Spencer and Bobrowski (ref. 34 above) outlines a of vaporization occurring during production must be con-
method that will approximate the formation vaporization under sidered in any laboratory technique seeking to similate actual
,;nch circumstances. production.
Conservation of reservoir energy usually dictates that no It is recognized that the oil residual in the reservoir does
well or pool will be produced at gas·oil ratios greatly exceed· not undergo the composite vaporization. However, material
ing the solution gas·oil ratio. However, during production of' balance techniques commonly involve the tank oil in place
depletion type pools and when gas is being injected into ~t any time despite the fact that all this oil in place actually
the reservoir, the gas-oil ratio sometimes may be high. Under will not be produced to the ~tock tanks. Such balance cal-
these circumstances the differential vaporization is not en- culations, therefore. must use volume data that is hased
tirely repre~entative of the formation liberation because a on tank oil.
unit volume of oil produced or remaining in the reservoir Boyd is correct in his statements about Fig. 5_ It also
comes in contact with amounts of gas that are in excess of is to be pointed out that the gas formation volume factoL
those which the volume of oil would evolve during pressure B., used in the material balance is calculated using differential
decline. The gas under such circumstances generally is moving gas gravity data only. B. enters the "Schilthius" type material
much more rapidly than the oil and there is probably in- balance equation only in conversion of the volume of the
sufficient flow agitation to allow attainment of equilibrium. gas cap to surface conditions. Since the gas cap is composed
While the differential liberation is not completely repre· of differentially liberated gas and the original free gas
sentative of the reservoir process in such instances, it rep· (except under circumstances of gas injection), it is felt the
resents the formation vaporization more closely than any volumetric behavior of the gas cap is best represented by
other type. differential data.