Interrelation of Crude Oil and Rock Properties With the Recovery of Oil by Caustic Waterflooding

1977 ◽  
Vol 17 (04) ◽  
pp. 263-270 ◽  
Author(s):  
Robert Ehrlich ◽  
Robert J. Wygal

Abstract This paper describes a series of laboratory caustic (NaOH) waterfloods and related measurements using crude oils from 19 oil reservoirs. These were light (mostly,>30 degrees API) crudes mainly from South Louisiana and Texas, although crude oils from other areas also were tested. The waterfloods held core material (Berea sandstone), connate water (2-percent-NaCl brine) and other conditions (temperature, flow rate, aging time before flood) constant, and determined increased production due to NaOH injection for each crude oil. Relative permeability end-points before and after flooding were used to estimate initial and final wettabilities and, together with crude-oil acid numbers and interfacial tensions against NaOH solution, to infer the probable mechanism by which increased recovery was obtained. A series of laboratory NaOH depletion measurements by static and dynamic methods in core material from several oil-producing formations and in Berea sandstone is also described. Results are compared with those from similar measurements using pure clays and other minerals and with X-ray diffraction analysis of the core material. The following are observations from these tests.Crude oils with acid numbers greater than about 0.1 to a 0.2 mg KOH per gm of oil or interfacial tension against 0.1 percent NaOH less than about 0.5 dyne/cm gave significant caustic-waterflood increased production. There was no further correlation of increased production at higher acid numbers or lower interfacial tensions nor was there a correlation with the apparent initial rock wettability.Regardless of initial wettability or increased production, the cores are indicated to be water-wet production, the cores are indicated to be water-wet following NaOH waterflooding to a high water-oil ratio (WOR).Caustic consumption by reservoir rock is predictable from the formation mineral composition predictable from the formation mineral composition as determined by X-ray methods. Exceptions are noted where clay content is high and where trace amounts of gypsum are present. Introduction Crude oils containing naturally occurring organic acids will react with aqueous caustic solution to produce surface-active materials. These surfactants, produce surface-active materials. These surfactants, when generated during a caustic waterflood, can improve oil recovery over that of a normal waterflood by a number of mechanisms related to changes occurring at the oil-water and liquid-solid interfaces: interfacial-tension lowering, wettability change, changes in interface rheology, etc. The extent to which any of these mechanisms will be operative and the recovery improvement obtainable depends on, among other things, the amount and type of acids present, the initial formation wettability, the reservoir-rock pore geometry, and the extent to which it consumes caustic. The available literature describing mechanisms proposed for caustic-waterflooding improved recovery, proposed for caustic-waterflooding improved recovery, the conditions required for applicability, and the results of various laboratory and field studies have been surveyed most recently by Johnson. Some common currents of thought or implication in this literature and some common areas of uncertainty related to the effects of crude oil and reservoir rock properties on recovery mechanisms are listed below. properties on recovery mechanisms are listed below.The presence of acids in crude oil at some minimum level is an obvious necessary condition for improved recovery. Where emulsification is involved, minimum acid numbers ranging from 0.5 to 1.5 mg KOH per gm of oil have been suggested. No minimum has been stated for other recovery mechanisms. One might not expect such minimum requirements to be absolute since the quality of surfactants generated from these acids can vary widely among crude oils.Improved recovery by wettability alteration generally has been discussed in terms of a reversal from oil-wet to water-wet or vice versa. It has been implied that wettability reversal is required since capillary forces trapping oil are eliminated as the neutral wettability condition is traversed. SPEJ P. 263

1982 ◽  
Vol 22 (02) ◽  
pp. 245-258 ◽  
Author(s):  
E.F. deZabala ◽  
J.M. Vislocky ◽  
E. Rubin ◽  
C.J. Radke

Abstract A simple equilibrium chemical model is presented for continuous, linear, alkaline waterflooding of acid oils. The unique feature of the theory is that the chemistry of the acid hydrolysis to produce surfactants is included, but only for a single acid species. The in-situ produced surfactant is presumed to alter the oil/water fractional flow curves depending on its local concentration. Alkali adsorption lag is accounted for by base ion exchange with the reservoir rock. The effect of varying acid number, mobility ratio, and injected pH is investigated for secondary and tertiary alkaline flooding. Since the surface-active agent is produced in-situ, a continuous alkaline flood behaves similar to a displacement with a surfactant pulse. This surfactant-pulse behavior strands otherwise mobile oil. It also leads to delayed and reduced enhanced oil recovery for adverse mobility ratios, especially in the tertiary mode. Caustic ion exchange significantly delays enhanced oil production at low injected pH. New, experimental tertiary caustic displacements are presented for Ranger-zone oil in Wilmington sands. Tertiary oil recovery is observed once mobility control is established. Qualitative agreement is found between the chemical displacement model and the experimental displacement results. Introduction Use of alkaline agents to enhance oil recovery has considerable economic impetus. Hence, significant effort has been directed toward understanding and applying the process. To date, however, little progress has been made toward quantifying the alkaline flooding technique with a chemical displacement model. Part of the reason why simulation models have not been forthcoming for alkali recovery schemes is the wide divergence of opinion on the governing principles. Currently, there are at least eight postulated recovery mechanisms. As classified by Johnson and Radke and Somerton, these include emulsification with entrainment, emulsification with entrapment, emulsification (i.e., spontaneous or shear induced) with coalescence, wettability reversal (i.e., oil-wet to water-wet or water-wet to oil-wet), wettability gradients, oil-phase swelling (i.e., from water-in-oil emulsions), disruption of rigid films, and low interfacial tensions. The contradictions among these mechanisms apparently reside in the chemical sensitivity of the crude oil and the reservoir rock to reaction with hydroxide. Different crude oils in different reservoir rock can lead to widely disparate behavior upon contact with alkali under varying environments such as temperature, salinity, hardness concentration, and pH. The alkaline process remains one of the most complicated and least understood. It is not surprising that there is no consensus on how to design a high-pH flood for successful oil recovery. One theme, however, does unify all present understanding. The crude oil must contain acidic components, so that a finite acid number (i.e., the milligrams of potassium hydroxide required to neutralize 1 gram of oil) is necessary. Acid species in the oil react with hydroxide to produce salts, which must be surface active. It is not alkali per se that enhances oil recovery, but rather the hydrolyzed surfactant products. Therefore, a high acid number is not a sufficient recovery criterion, because not all the hydrolyzed acid species will be interfacially active. That acid crude oils can produce surfactants upon contact with alkali is well documented. The alkali technique must be distinguished from all others by the fundamental basis that the chemicals promoting oil recovery are generated in situ by saponification. SPEJ P. 245^


1981 ◽  
Vol 21 (04) ◽  
pp. 493-499 ◽  
Author(s):  
J.H. Runnels ◽  
C.J. Engel

Abstract An procedure is given for separating surfactant precursors that occur in some crude oils. The effect of the precursors on the properties of the oils are described also. The separations were made by silica gel chromatography on crude oil from which the asphaltenes had been removed. The effect of the precursors on the properties of the crude was evaluated by blending the surfactant precursors into the original oil, a modified oil, or a hydrocarbon solvent such as benzene. Precursors activated and converted to surface active materials by a strong base such as sodium hydroxide are effective in reducing the interfacial tension between the oil and aqueous phase. Occurrence of precursors in crude oils is essential for improved oil recovery by the causticflood process. The procedure for separating the precursors should provide a viable means for evaluating the applicability of a causticflood tertiary oil recovery process to a particular crude or reservoir. Introduction Tertiary oil recovery by the causticflood process is inherently dependent on naturally occurring surfactant precursors in the crude. The surfactant precursors react with the caustic (base) in the floodwater to form surface active compounds that reduce the interfacial tension between the crude and aqueous phase, alter the wettability of the mineral surfaces, or reduce rigid film formation at the crude/aqueous interface. In laboratory oil-recovery tests, these mechanisms stimulate oil production characterized by increased production at caustic breakthrough and a high oil/water ratio after breakthrough. An early effort to identify the surfactant precursors in a Rio Bravo (CA) crude concluded that the surfactant precursors were related closely to the asphaltene and resin fractions of the crude. Subsequent studies using an Eichlingen Niedersachen (West German) crude and a Ventura (CA) crude concluded that the surfactant precursors were acids and phenols, respectively. The extensive work of Seifert established that the surfactant precursors of a Ventura crude were carboxylic acids and that the phenolic components of the crude were interfacially inactive. The purpose of our study was to develop a simple and practical method of separating surfactant precursors from crude oil and to evaluate their effect on the interfacial tension, acid number, and other properties of the crude. The separation technique was developed using Smackover Nacatoch crude and the surfactant precursors evaluated were obtained from the same crude. Description of Smackover Nacatoch Crude The Smackover reservoir is located in southern Arkansas, and the Nacatoch pay zone is the shallowest of five pay zones. The crude has an API gravity of 21 degrees, a viscosity of 160 cp at room temperature, and is produced from an unconsolidated sand formation about 2,000 ft deep. Preliminary studies showed that the interfacial tension between the crude and an aqueous phase was reduced from about 12 to 0.02 dyne/cm when the pH of the aqueous phase was increased from 7.0 to 12.5 with sodium hydroxide. The significant reduction in interfacial tension at higher pH's indicated that the crude contained a relatively high concentration of surfactant precursors that were converted to surface active materials by sodium hydroxide. SPEJ P. 493^


SPE Journal ◽  
2021 ◽  
pp. 1-6
Author(s):  
Lee Yeh Seng ◽  
Berna Hascakir

Summary This study investigates the role of polar fractions of heavy oil in the surfactant-steamflooding process. Performance analyses of this process were done by examination of the dipole-dipole and ion-ion interactions between the polar head group of surfactants and the charged polar fraction of crude oil, namely, asphaltenes. Surfactants are designed to reduce the interfacial tension (IFT) between two immiscible fluids (such as oil and water) and effectively used for oil recovery. They reduce the IFT by aligning themselves at the interface of these two immiscible fluids; this way, their polar head group can stay in water and nonpolar tail can stay in the oil phase. However, in heavy oil, the crude oil itself has a high number of polar components (mainly asphaltenes). Moreover, the polar head group in surfactants is charged, and the asphaltene fraction of crude oils carries reservoir rock components with charges. The impact of these intermolecular forces on the surfactant-steam process performance was investigated with 10 coreflood experiments on an extraheavy crude oil. Nine surfactants (three anionic, three cationic, and three nonionic surfactants) were tested. Results of each coreflood test were analyzed through cumulative oil recovery and residual oil content. The performance differences were evaluated by polarity determination through dielectric constant measurements and by ionic charges through zeta potential measurements on asphaltene fractions of produced oil and residual oil samples. The differences in each group of surfactants tested in this study are the tail length. Results indicate that a longer hydrocarbon tail yielded higher cumulative oil recovery. Based on the charge groups present in the polar head of anionic surfactants resulted in higher oil recovery. Further examinations on asphaltenes from produced and residual oils show that the dielectric constants of asphaltenes originated from the produced oil, giving higher polarity for surfactant-steam experiments conducted with longer tail length, which provide information on the polarity of asphaltenes. The ion-ion interaction between produced oil asphaltenes and surfactant head groups were determined through zeta potential measurements. For the most successful surfactant-steam processes, these results showed that the changes on asphaltene surface charges were becoming lower with the increase in oil recovery, which indicates that once asphaltenes are interacting more with the polar head of surfactants, then the recovery rate increases. Our study shows that the surfactant-steamflooding performance in heavy oil reservoirs is controlled by the interaction between asphaltenes and the polar head group of surfactants. Accordingly, the main mechanism that controls the effectiveness of the process is the ion-ion interaction between the charges in asphaltene surfaces and the polar head group of crude oils. Because crude oils carry mostly negatively charged reservoir rock particles, our study suggests the use of anionic surfactants for the extraction of heavy oils.


1975 ◽  
Vol 15 (03) ◽  
pp. 197-202 ◽  
Author(s):  
Harley Y. Jenning

Abstract This paper presents the results of a study of caustic solution-crude oil interfacial tension measurements on 164 crude oils from 78 fields. Of these crude oils 131 showed marked surface activity against caustic solutions. Surface activity of crude oil against caustic solution correlates with the acid number, gravity, and viscosity. Almost all crude oils with gravities of 20 degrees API or lower produced a caustic solution-crude oil interfacial produced a caustic solution-crude oil interfacial tension less than 0.01 dyne/cm. Of the interfacially active samples, 90 percent reached maximum measurable surface activity at a caustic concentration of close to 0.1 percent by weight. The dissolved solids content of the water bas a marked influence on the surface activity. Sodium chloride in solution reduces the caustic concentration required to give maximum surface activity. Conversely, calcium chloride in solution suppresses surface activity. Introduction The oil-production technology literature contains a number of papers that indicate that the addition of sodium hydroxide to the flood water beneficially affects oil recovery. Although the proposed recovery mechanisms differ in detail, a variable common to almost all is the interfacial tension between caustic solutions and crude oil. A study of the factors influencing caustic solution-crude oil interfacial tensions is fundamental to an understanding of the proposed mechanisms and their optimum utilization. proposed mechanisms and their optimum utilization. We have obtained interfacial tensions against caustic solutions of 164 crudes. These crudes come from all major oil-producing areas in the free world. In addition to determining the correlation of interfacial tension with crude oil properties of acid number, gravity, and viscosity, we have also determined the effect of certain dissolved solids in the water. We define acid number as the number of milligrams of potassium hydroxide required to neutralize the acid in one gram of sample. The interfacial tension data were obtained by the pendent-drop method. pendent-drop method. EXPERIMENTAL PROCEDURE The caustic solutions used in this study were prepared by adding reagent-grade sodium hydroxide prepared by adding reagent-grade sodium hydroxide to laboratory distilled water. Our standard solutions were made from a 50 percent by weight reagent-grade sodium hydroxide solution. For convenience in relating our laboratory data to possible field application, the data were recorded and plotted in terms of weight percent sodium hydroxide. The pH of the caustic solutions was determined experimentally using a Coming expanded-scale pH meter; and the densities of the caustic solutions were measured experimentally using a Chainomatic Westphal balance. CRUDE OILS The crude oils were protected from the atmosphere and were collected in carefully cleaned glass or, when practicable, in plastic-lined containers. The crude oil samples were free of chemical additives, such as emulsion breakers and corrosion inhibitors. If the oil contained suspended solid material it was dehydrated and filtered. The densities were determined by the Westphal balance; and the viscosities were determined as a function of temperature using a glass capillary viscometer. APPARATUS AND EXPERIMENTAL PROCEDURE The interfacial tension measurements described in this study were made by the pendent-drop method. The pendent-drop method is based on the formation of a drop of liquid on a tip, the drop being slightly smaller than that which will spontaneously detach itself from the tip. The profile of this drop is magnified by projection and can be recorded on a photosensitive emulsion. The interfacial tension is photosensitive emulsion. The interfacial tension is calculated from the dimensions of the drop profile, a knowledge of be densities of the liquid forming. the drop, and the bulk phase surrounding the drop. All interfacial tensions described in this paper were recorded at a temperature of 74 degrees F and at an interface age of 10 seconds. Most systems were studied as a function of temperature; but temperature was found to be a second-order effect, so we selected 74 degrees F in order that all correlations would be at constant temperature. We selected 10 seconds because a study of the time variable showed that most of the decay of interfacial tension with time in these systems had occurred by the end of 10 seconds. SPEJ P. 197


1976 ◽  
Vol 16 (06) ◽  
pp. 351-357 ◽  
Author(s):  
J.L. Cayias ◽  
R.S. Schechter ◽  
W.H. Wade

American Institute of Mining, Metallurgical, and Petroleum Engineers, Inc. Abstract Using the correlation between interfacial-tension behavior for three homologous series of hydrocarbons and a simple, mole-fraction averaging procedure, it was found possible to predict interracial tensions for complex hydrocarbon oil phases/aqueous surfactant Phases. This leads to an extension of the equivalent alkane carbon-number (EACN) concept to a mixed hydrocarbon oil phase. The EACN for eight crude oils was determined and it was found that the interfacial tension of crudes can be best modeled by alkanes in the range of hexane to nonane. Introduction Previous publications, have demonstrated that low interfacial tensions can be attained with pure hydrocarbons as the oil phase. The aqueous phase contained surfactants that were proposed as candidates for tertiary oil recovery of crude oils, namely petroleum sulfonates and alkyl xylene sulfonates. These observations demonstrate that complex hydrocarbon mixtures are not a necessary requirement for low tensions and, as can be attested by any worker in the field, are certainly not a sufficient requirement for attaining low tensions. The question is, then, how can tensions for complex hydrocarbon mixtures (crude oils) be modeled given the tension of their components? Systematic trends in the tension have been observed for various hydrocarbon homologous series. It was found, for example, that an alkyl benzene gave the same interfacial tension as an alkane having the same number of carbon atoms as the alkyl side chain. The alkyl side chain is therefore the only contributor to the tension. Likewise, it was found that a cyclohexyl ring was approximately equivalent to four carbons. The hydrocarbon giving minimal tension can be varied by changing either the salinity or the surfactant concentration, but the above-mentioned scaling rules were found to apply. These observations have resulted in the concept of an equivalent alkane carbon number (EACN) for binary mixtures of alkanes, alkyl benzenes, and alkyl cyclohexanes. Hydrocarbon behavior was found to be additive and mole-fraction weighted by the simple relationship, (1) where the Ci are EACN values for the individual components, the Xi are mole fractions, and Cavg is the EACN for the mixture. For example, an equimolar mixture of butylcyclohexane (C1 = 4 for butyl groups + 4 for cyclohexyl = 8, X1 = 0.5) and propylbenzene (C2 = 3 for the propyl group + 0 for propylbenzene (C2 = 3 for the propyl group + 0 for benzene, X2 = 0.5) has a Cavg of 5.5. This mixture then would be predicted to yield a minimum interfacial tension against a surfactant solution that gives low tensions against pure alkanes intermediate between pentane and hexane. Eq. 1 has been verified for a wide variety of binary mixtures. Crude-oil behavior could be predicted by expanding Eq. 1 to the general form, (2) where the running index i extends over all the crude oil components. Of course, this cannot be accomplished in practice since all the components of a specific crude oil have never been identified. However, if Eq. 2 applies to complex but known-composition hydrocarbon mixtures, then applicability to crude oils can be inferred. Tests verifying Eq. 2 are reported in this paper. Eq. 2, in a variety of situations, requires that effects resulting from alkane isomerization be investigated. In addition, the role of sulfur compounds needs to be assessed. These studies also are reported. Finally, two different experimental techniques are used to validate the EACN concept as applied to crude oils, and values for eight samples are reported. EXPERIMENTAL PROCEDURE All interfacial tensions were measured without pre-equilibration at 27 degrees C using the spinning drop pre-equilibration at 27 degrees C using the spinning drop technique. Five sodium sulfonate surfactants were used: Witco TRS 10-80, Shell Martinez 380 and Martinez 470, and Exxon Chemical Dodecyl and Pentadecyl Xylene sulfonates. Pentadecyl Xylene sulfonates. SPEJ P. 351


1982 ◽  
Vol 22 (03) ◽  
pp. 350-352
Author(s):  
G.E. Kellerhals

Abstract In surfactant flooding, low interfacial tensions (IFT's) are required for recovery of additional significant quantities of crude oil from a reservoir rock. This paper indicates the usefulness of perspective plots to facilitate comparison of sets of IFT data. Such perspective plots simplify the process of screening various surfactant systems for enhanced oil recovery. Introduction Numerous articles have been written about the effects and/or importance of IFT between oil and aqueous phases in determining ultimate oil recovery during a phases in determining ultimate oil recovery during a secondary (waterflooding) or tertiary oil-recovery process. In the area of micellar/polymer or surfactant process. In the area of micellar/polymer or surfactant flooding, IFT has been studied extensively both by industrial and by academic investigators. A simplistic summary of this work is that low IFT's (generally corresponding to high capillary numbers ( are required for recovery of additional significant quantities of crude oil from a reservoir rock. Method Development Several variables influence between an oil-rich phase and a surfactant-containing aqueous phase. During phase and a surfactant-containing aqueous phase. During a surfactant flood, variations in surfactant concentration and salt concentration will occur as a result of mixing of the chemical slug with the pre flush (or formation brine) and polymer drive (" rear mixing" ). Nelson investigated salt concentrations required during a chemical flood to achieve efficient oil displacement. Since these variables (and others) change during the progress of a flood, it is desirable to determine the impact of these changes on the IFT between the oil- and water-rich phases. To assess the importance of changes in these two key variables (surfactant concentration and salinity) on IFT, an x-y plot may be constructed with values of each variable along the axes. The IFT for a particular surfactant concentration and salinity then is obtained experimentally and the numerical value placed at the corresponding (x, y) point on the plot. The resultant figure/table can be referred to as an IFT map. Points of equal, or about equal, IFT can be connected to produce an IFT contour map. In the investigation of the effect(s) of temperature on a given surfactant system and crude oil, IFT maps might be constructed for each of the pertinent temperatures. IFT's might be determined at six different sodium chloride concentrations (e.g., 1.0, 1.5, 2.0, 3.0, 4.0, and 5.0 wt%) and four surfactant concentrations (e.g., 0.085, 0.064, 0.042, and 0.021 meq/mL), resulting in IFT maps (for each temperature) each consisting of 24 IFT values. A comparison of the values of one map to the values of a second map (measurements made at different temperature) then is required to determine the impact of the temperature change. A single value for IFT for a given salinity and surfactant concentration assumes that the system is two-phase, because two IFT's can be measured for a three-phase system consisting of an oil-rich phase, a water-rich phase, and a microemulsion phase. phase. A method to allow easier comparison for the relatively large number of IFT data points that may be obtained during the study/screening of various surfactant systems at various conditions is described in this paper. The technique consists of interpolating between IFT values and then plotting the data with a perspective plotting routine. The method allows comparisons of IFT values for different crude oils, temperatures, cosolvent types, surfactant types, hardness ion concentrations, etc., through visual scanning of a perspective plot ranter than through trying to judge or compare numerical IFT values of an IFT map. SPEJ p. 350


1982 ◽  
Vol 22 (01) ◽  
pp. 87-98 ◽  
Author(s):  
LeRoy W. Holm ◽  
Virgil A. Josendal

Abstract This paper presents additional data related to the correlation between minimum miscibility pressure (MMP) for CO2 flooding and to the composition of the crude oil to be displaced. Yellig and Metcalfe have stated that there is little or no effect of oil composition on the MMP. However, their conclusion was based on experiments with one type of reservoir oil that was varied in C through C6 content and in the amount of C7 + present but not varied in composition of the C7 + fraction. We have found that the Holm-Josendal correlation, which is based on temperature and C5 + molecular weight, predicts the general trend of the MMP's required for CO2 flooding of various crude oils. MMP's were predicted with this correlation and then tested for several crude oils using oil recovery of 80% at CO2 break through and 94% ultimate recovery as the criteria. We now have data showing that miscible-type displacement is also correlatable with the amount of C5 through C3O hydrocarbons present in the crude oil and with the solvency of the CO2 as indicated by its density. Variations from such a correlation are shown to be related to the C5 through C 12 content and to the type of these hydrocarbons. The MMP data were obtained from slim-tube floods with crude oils having gravities between 28 and 44 degrees API (0.88 and 0.80 g/cm3) and C5 + molecular weights between 171 and 267. The crude oils used varied in carbon residue between 1 and 4 wt% and in waxy hydrocarbon content between 1 and 17%. The required MMP for these crude oils at 165 degrees F (74 degrees C) varied between 2,450 and 4,400 psi (16.9 and 30.3 MPa) for an oil recovery of 94% OIP. The MMP was found to be a linear function of the amount of C5 through C30 hydrocarbons present and of the density of the CO2. Introduction Our 1974 paper, "Mechanisms of Oil Displacement by Carbon Dioxide," discussed the various mechanisms by which oil is displaced from reservoir rock using CO2. One conclusion of this study was that multiple-contact, miscible-type displacement of oil occurs through extraction of C5 through C30 hydrocarbons from the reservoir oil by COB when a certain pressure is maintained at a given flood temperature. The mechanism of oil recovery was described as follows. The CO2 vaporizes or extracts hydrocarbons from the reservoir oil until a sufficient quantity of these hydrocarbons exists at the displacement front to cause the oil to be miscibly displaced. At that point, the vaporization or extraction mechanism stops until the miscible front that has been developed breaks down through the dispersion mechanism. When miscibility does not exist, the vaporization or extraction mechanism again occurs to re-establish miscibility. The miscible bank is formed, dispersed, and reformed throughout the displacement path; a small amount of residual oil remains behind all along the displacement path. Also, an optimal flooding pressure at a given temperature for a given oil was defined in that paper as when oil recovery of about 94% OIP was achieved and above which point essentially no additional oil was recovered. This pressure has since been termed the "minimum miscibility pressure" by others. We further determined in our previous study thatthis miscible-type displacement does not depend on the presence of C2 through C4 in the reservoir oil and thatthe presence of methane in the reservoir oil does not change the MMP appreciably. Those findings have been confirmed by Yellig and Metcalfe with the qualification that the CO2 MMP must be greater than or equal to the bubble-point pressure of the reservoir oil. SPEJ P. 87^


Energies ◽  
2021 ◽  
Vol 14 (16) ◽  
pp. 5103
Author(s):  
Irena Viktorovna Yazynina ◽  
Evgeny Vladimirovich Shelyago ◽  
Andrey Andreevich Abrosimov ◽  
Vladimir Stanislavovich Yakushev

This paper considers a new method for “pore scale” oil reservoir rock quantitative estimation. The method is based on core sample X-ray tomography data analysis and can be directly used to both classify rocks by heterogeneity and assess representativeness of the core material collection. The proposed heterogeneity criteria consider the heterogeneity of pore size and heterogeneity of pore arrangement in the sample void and can thus be related to the drainage effectiveness. The classification of rocks by heterogeneity at the pore scale is also proposed when choosing a reservoir engineering method and may help us to find formations that are similar at pore scale. We analyzed a set of reservoir rocks of different lithologies using the new method that considers only tomographic images and clearly distributes samples over the structure of their pore space.


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