GB2156400A - Steam foam process - Google Patents

Steam foam process Download PDF

Info

Publication number
GB2156400A
GB2156400A GB08407747A GB8407747A GB2156400A GB 2156400 A GB2156400 A GB 2156400A GB 08407747 A GB08407747 A GB 08407747A GB 8407747 A GB8407747 A GB 8407747A GB 2156400 A GB2156400 A GB 2156400A
Authority
GB
United Kingdom
Prior art keywords
steam
reservoir
foam
oil
fluid
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
GB08407747A
Other versions
GB2156400B (en
GB8407747D0 (en
Inventor
Rosmalen Renee Janssen Van
Paulus Petrus Maria Keijzer
Herman Mathieu Muijs
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shell Internationale Research Maatschappij BV
Original Assignee
Shell Internationale Research Maatschappij BV
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Shell Internationale Research Maatschappij BV filed Critical Shell Internationale Research Maatschappij BV
Priority to GB08407747A priority Critical patent/GB2156400B/en
Publication of GB8407747D0 publication Critical patent/GB8407747D0/en
Priority to CA000474601A priority patent/CA1247850A/en
Priority to NO851186A priority patent/NO851186L/en
Priority to BR8501321A priority patent/BR8501321A/en
Priority to DE19853510765 priority patent/DE3510765C2/en
Priority to NL8500877A priority patent/NL192394C/en
Publication of GB2156400A publication Critical patent/GB2156400A/en
Application granted granted Critical
Publication of GB2156400B publication Critical patent/GB2156400B/en
Expired legal-status Critical Current

Links

Classifications

    • EFIXED CONSTRUCTIONS
    • E21EARTH DRILLING; MINING
    • E21BEARTH DRILLING, e.g. DEEP DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
    • E21B43/00Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
    • E21B43/16Enhanced recovery methods for obtaining hydrocarbons
    • E21B43/24Enhanced recovery methods for obtaining hydrocarbons using heat, e.g. steam injection
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/58Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids
    • C09K8/592Compositions used in combination with generated heat, e.g. by steam injection

Abstract

A steam foam process for diverting steam within a subterranean reservoir and improving oil displacement is carried out by injecting into the reservoir a steam-foam-forming mixture comprising steam and a linear C18-alkylaryl sulphonate surfactant and preferably a non-condensable gas.

Description

SPECIFICATION Steam foam process The invention relates to a steam foam process for producing oil from, or displacing oil within, a subterranean reservoir.
In certain respects, this invention is an improvement in the steam-channel-expanding steam foam drive process described in U.S.A. patent specification 4,086,964 (inventors: R.E. Dilgren, G.J. Hirasaki, H.J. Hill, D.G. Whitten; filed 27th May, 1977; published 2nd May 1978).
The invention is particularly useful in an oil producing process of the type described in the above patent specification. In this process steam in injected into, and fluid is produced from, horizontally spaced locations within a portion of an oil reservoir in which the disposition of a steam flow path is determined by gravity and/or oil distribution.
After a steam channel has been formed the composition of the fluid being injected is changed from steam to a steam-foam-forming mixture. The com position of the mixture is correlated with the properties of the rocks and the fluids in the reservoir so that the pressure required to inject the mixture and to move it through the steam channel exceeds that required for steam alone but is less than the reservoir fracturing pressure. The composition and rate of injecting the mixture is subsequently adjusted to the extent required to maintain a flow of steam foam within the channel at a relatively high pressure gradient at which the oil-displacing and chan nel-expanding effects are significantly greater than those provided by the steam alone. Oil is recovered from the fluid produced from the r'eservoir.
The present invention also relates to an improve ment in an oil recovery process in which steam is cyclically injected into the fluid is backflowed from a heavy oil reservoir which is susceptible to a gravity override that causes an oil layer to become adjacent to a gas or vapour-containing substantially oil-desaturated zone in which there is an undesirable intake and retention of the injection fluid within the desaturated zone.In such a process, the steam to be injected is premixed with surfactant components arranged to form a steam foam within the reservoir having physical and chemical properties such that is (a) is capable of being injected into the reservoir without plugging any portion of the reservoir at a pressure which exceeds that required for injecting steam but is less than the reservoir fracturing pressure and (b) is chemically weakened by contact with the reservoir oil so that it is more mobile in sand containing that oil than in sand which is substantially free of that oil. The surfactant-containing steam is injected into the reservoir at a rate slow enough to be conducive to displacing a front of the steam foam along the oil-contain ing edge portions of the oil-desaturated zone than along the central portion of that zone.And, fluid is backflowed from the reservoir at a time at which part or all of the steam is condensed within the steam foam in the reservoir.
As used herein the following terms have the following meanings: "steam foam" refers to a foam i.e. gas-liquid dispersion which (a) is capable of both reducing the effective mobility, or ease with which a fluid containing such a foam or dispersion will flow within a permeable porous medium and (b) has steam in the gas phase thereof. "Mobility" or "permeability" refers to an effective mobility or ease of flow of a fluid within a permeable porous medium. A "permeability reduction" or "mobility reduction" refers to reducing the ease of such a fluid flow due to an increase in the effective viscosity of the fluid and/or a decrease in the effective permeability of the porous medium.A reduction in such a mobility or permeability can be detected and/or determined by measuring differences in internal pressures within a column of permeable porous material during a steady state flow of fluid through a column of such material. "Steam quality" as used regarding any steam-containing fluid refers to the weight percent of the water in that fluid which is in the vapour phase of the fluid at the boiling temperature of that water at the pressure of the fluid.For example: in a mono-component steam-containing fluid which consists entirely of water and has a steam quality of 50%, one-half of the weight of the water is in the vapour phase; and, in a multicomponent steam-containing fluid which contains nitrogen in the vapour phase and dissolved or dispersed surfactant and electrolyte in the liquid phase and has a steam quality of 50%, one-half the weight of the weight of the water in the multicomponent steam-containing fluid is in the vapour phase.Thus, the steam quality of a steam-containing fluid can be calculated as, for example, 100 times the mass (or mass flow rate) of the water vapour in that fluid divided by the sum of the mass (or mass flow rate) of both the water vapour and the liquid water in that fluid. "Steam foamforming mixture" (or composition) refers to a mixture of steam and aqueous liquid solution (or dispersion) or surfactant, with some or all, of the steam being present in the gas phase of a steam foam. The gas phase may include noncondensable gas(es) such as nitrogen.
Object of the invention is an improved process for displacing oil within an oil-containing subterranean reservoir by flowing a steam-containing fluid in conjunction with a surfactant component through a relatively steam permeable zone within said reservoir.
According to the invention the surfactant component comprises in substantial part at least one sulphonate of the formula RSO3X in which R is alkylaryl including benzene or toluene having attached thereto a linear alkyl group containing 18 carbon atoms in the alkyl chain and ". is sodium, potassium, lithium or ammonium.
The alkylaryl sulphonate-containino steam-foamforming mixture suitably includes an aqueous solution of electrolyte and advantageously further also includes a substantially noncondensable gas; with each of the surfactant, ele,c rolyte and gas components being present in propo--t-ions effective for steam-form-formation in the pre-sence of the reservoir oil. The invention also relates to the alkylaryl sulphonate-containing steam-foam-forming mixtures which are described herein.
The invention is useful where it is desirable to remove oil from, or displace oil within, a subterranean reservoir. For example, the invention can be used to move oil or an emulsion of oil and water away from a well borehole in a well-cleaning type of operation, and/or to displace oil into a producing location in an oil-recovery operation.
In particular, the present invention relates to a process for recovering oil from a subterranean reservoir, comprising: injecting steam and producing fluid at horizontally spaced locations within a portion of an oil reservoir in which the disposition of a steam flow path is determined by the effect of gravity and/or oil distribution, rather than being substantially confined within at least the one most permeable layer of reservoir rocks; advantageously maintaining rates of steam injecting and fluid production such that a steam channel has been extended from the injection location; changing the composition of the fluid being injected from steam to a steam-foam-forming mixture including steam and an aqueous, electrolytecontaining solution or dispersion of an alkylaryl sulphonate-containing surfactant, whilst continuing to product fluid from the reservoir;; correlating the composition of the steam-foamforming mixture with the properties of the rocks and fluids in the reservoir so that the pressure required to inject the mixture and the foam it forms or comprises into and through the steam channel exceeds that required for steam alone but Is less than the reservoir fracturing pressure; and adjusting the composition of the fluid being injected into the steam channel to the extent required to maintain a flow of both steam and foam within the channel in response to a relatively high pressure gradient at which the oil-displacing and channelexpanding effects are significantly greater than those provided by steam alone, without plugging the channel.
The invention also relates to an oil recovery process in which steam is cyclically injected into and fluid is backflowed from a subterranean heavy oil reservoir which is susceptible to gravity override and tends to intake and retain undesirably large proportions of the injected fluid. This process comprises:: (1) injecting steam mixed with a linear C,,-alky- larylsulphonate-containing steam-foam-forming compound which is arranged for forming a steam foam which (a) can be displaced through the pores of the reservoir, without plugging any portion of the reservoir, in response to a pressure which exceeds that required for displacing steam through the reservoir but is less than the fracturing pressure of the reservoir, and (b) can be chemically weakened by contact with the reservoir oil to an extent such that the weakened foam is significantly more mobile in reservoir oil-containing pores of a porous medium than in oil-free pores of that medium;; (2) injecting the steam-foam-forming mixture at a rate equivalent to one which is siow enough to cause the foam formed by that mixture to advance more rapidly through the pores of a reservoir oilcontaining permeable medium than through the pores of a substantially oil-free permeable medium; and (3) backflowing fluid from the reservoir after a steam soak time sufficient to condense part of all of the steam in the injected steam-foam-forming mixture. The steam-foam-forming mixture preferably comprises steam, a noncondensible gas, a linear C,8-alkylarylsulphonate surfactant and an electrolyte.
The invention provides unobvious and beneficial advantages in oil displacement procedures by the use of the alkylaryl sulphonate surfactant in the steam-foam-forming compositions. For example, where a steam-foam-forming mixture contains such a surfactant and an electrolyte in proportions near optimum for foam formation, the present surfactant components provide exceptionally strong steam foams using other surfactants. In addition, significant reductions are reached in the mobilities of the steam foams at concentrations which are much less than those required for equal mobility reductions by the surfactants which were previously considered to be the best available for such a purpose. The use of the present alkylaryl sulphonate surfactant components involves no problems with respect to thermal and hydrolytic stability.No chemical or physical deterioration has been detectable in the present alkylaryl sulphonate surfactants that were recovered along with the fluids produced during productions of oil from subterranean reservoirs. In each of those types of sulphonate surfactants the sulphur atoms of the sulphonate groups are bonded directly to carbon atoms. The surfactants which were recovered and tested during the production of oil had travelled through the reservoirs at steam temperatures for significant times and distances.
The present C18-alkylaryl sulphonate-containing steam foams have been found to represent a substantial improvement in mobility reduction over foams based on the C12-C1 > -alkylaryl sulphonates e.g. dodecylbenzene sulphonates. The foams to be used according to the present invention represent also substantial improvement over the C16-Cl8 alpha-olefinsulphonate-containing foams.
The present invention further relates to compositions containing at least one C,8-alkylaryl sulphonate, and steam, optionally electrolyte, and optionally noncondensable gas, that are suitable for use in oil-displacing and/or producing processes. Of particular interest in this respect are steam-foam-forming compositions consisting essentially of (a) water, which is present in the composition, at a temperature substantially equalling its boiling temperature, at the pressure of the composition, in both a liquid phase and a vapour phase; (b) a surfactant component present in the liquid phase of the composition in an amount between 0.01 and 10 percent by weight, calculated on the weight of the liquid phase, said surfactant component comprising in substantial part at least one C,8-alkylaryl sulphonate; (c) an electrolyte present in the liquid phase of the composition in an amount between 0.001 percent by weight (calculated on the weight of the liquid phase) and an amount tending to partition the surfactant into a separate liquid phase; and (d) a noncondensable gas present in the vapour phase in an amount between about 0.0001 and 0.3 percent by mol, calculated on total mols in the vapour phase.
Illustrative of the alkylaryl sulphonate surfactants suitably employed in steam-foam drive processes of enhanced performance, according to the invention, are the alkylaryl sulphonates obtained by reacting a linear Cl8-alkylbenzene and/or linear C13- alkyltoluene with sulphurtrioxide followed by neutralization of the sulphonic acid. Particularly suitable for purposes of the invention is a sulphonate derived from substantially linear C,8-alkyltoluene.
Different reservoir materials have different debilitating effects on the strength of a steam foam.
Tests should therefore be carried out to determine the sulphonates or sulphonate-containing steamfoam-forming compositions that perform optimally in a given reservoir. This is preferably done by testing the influence of specific sulphonates on the mobility of a steam-containing fluid having the steam quality selected for use in the reservoir in the presence of the reservoir material.
Such tests are preferably conducted by flowing steam-containing fluids sand pack. The permeability of the sand pack and foam-debilitating properties of the oil in the sand pack should be at least substantially equivalent to those of the reservoir to be treated. Comparisons are made of the rhobility of the steam-containing fluid with and without the surfactant component. The mobility is indicated by the substantially steady-state pressure drop between a pair of points located between the inlet and outlet portions of the sand pack in positions which are substantially free of end effects on the pressures.
Some laboratory tests to determine steam mobility will now be described with reference to Figures 1 and 2.
Figure 1 shows schematically a sand pack test apparatus which can be made of currently available apparatus components. The apparatus consists of a cylindrical tube 1 that is 400 mm long and has a cross-sectional area of 8 cm2. Such a tube is preferably arranged for a horizontal flow of fluid from an inlet 2 to an outlet 3. The tube is preferably provided with 5 pressure taps 4, 5, 6, 7 and 8. The location of the first pressure tap 4 is at a distance of 150mm from the inlet 2. The locations of the other taps are chosen so as to divide the part of the tube 1 situated behind tap 4 into equal parts of 50 mm. The tube 1 contains a permeable and porous column of suitable material, such as a sand pack, which is capable of providing an adequately realistic laboratory model of a subterranean reservoir.
At the inlet end 2, the sand pack or equivalent column of permeable material is arranged to re ceive separate streams of steam, noncondensable gas such as nitrogen, and one or more aqueous liquid solutions or dispersions containing a surfactant to be tested and/or a dissolved or dispersed electrolyte. Some or all of those components are injected at constant mass flow rates proportioned so that steam of a selected quality, or a selected steam-containing fluid or composition, or a steamfoam-forming mixture of a selected steam quality can be injected and will be substantially homoge neous substantially as soon as it enters the face of the sand pack.
In the tests, steam-foam-forming mixtures are compared with and without surfactant components added thereto, by measuring pressure gradients formed within a sand pack during flows through the pack at the same substantially constant mass flow rate.
Numerous tests have been made of different steam-foam-forming mixtures using sand packs composed of a reservoir sand and having a high permeability, such as 10 darcys. The pressures were measured with pressure detectors (not shown) (such as piezo-electric devices) installed at the inlet 2 and at the taps 4, 5, 6, 7 and 8 of the tube 1. The results of such tests have proven to be generally comparable with the results obtained in the field.
In the laboratory tests, the steam-foam-forming components were injected at constant mass rates until substantially steady-state pressures were obtained at the inlet and at the taps. The ratio between the steady-state pressures at the taps during flow of steam mixed with the foam-forming surfactant component and the steady-state pressure at the taps during flow of the steam by itself are indicative for the mobility reduction. The higher this ratio, the stronger the steam foam and the higher the mobility reduction caused by the steam-foamforming mixture.
Figure 2 illustrates the results of comparative tests with steam and various steam-foam-forming mixtures in sand packs containing Venezuelan Reservoir sand having a permeability of 10 darcys. The backpressure was 21 bar, corresponding with a temperature of 215 C. The injection rate was 900 cm3/min. The figure shows the variation of the pressure in bar (Y-axis) with distance in centimetres (X-axis) from the pack inlet 2. The pressures were measured at the inlet 2, a. the taps 4, 5, 6, 7 and 8, and at the outlet 3 -or the pipe 1 of Figure 1. Curve A relates to the difplacement wherein a mixture of 90% quality steam wac used as a displacing composition.
Curve B relates to using a steam-containing fluid having a steam quality of 90% and a water phase which contains 1% by weight sodium chloride and 0.25%: by weight of a surfactant. In the Curve B test, the surfactant was a branched side-chain C1 C,8-alkyltoluene sodium sulphonate available from Sun Refining Company under the trademark SUN TECH IV-1015.
Curve C relates to using the mixture used for Curve B except that the surEact3n- was a linear side-chain octadecylbenzene sor um sulphonate.
In the tests represented by Curve D the formulation was the same as those used in the tests represented by Curves B and C except that the sulphonate component was linear side-chain octadecyltoluene sulphonate.
The greatly improved steam permeability reduction performance of the presently described C18-alkylaryl sulphonate-containing surfactant component is clear from the Curves C and D as compared to the Curves A and B in Figure 2.
Compositions and procedures suitable for use in the present invention For purposes of the present invention, the surfactant component of the steam-foam-forming mixture is necessarily comprised in substantial part of linear C,3-alkylaryl sulphonate. Materials of this class but with a much shorter alkyl chain have heretofore found commercial utility, for example, in detergent formulations for industrial, household and personal care application.
A class of alkylaryl sulphonates very suitable for use in the present invention is that derived from a particular class of olefins, which may be defined for present purposes in terms of the configuration and number of carbon atoms in their molecular structure. These olefins have a carbon number of 18.
In terms of molecular structure, these olefins are aliphatic and linear. Either alpha- or internal olefins are considered suitable for the alkylation route chosen to produce the products to be used according to the invention. For purposes of derivation of the alkylaryl sulphonates for use in the process according to the invention, olefins are advantageously applied in which at least 90% of the molecules are alpha-olefins.
Particularly attractive are sulphonates derived from the Neodene alpha-olefins (trademark) sold by Shell Chemical Company, in part for their linear structure and high alpha-olefin content, i.e., greater than 95% in each case. The Neodene alpha-olefins are prepared by ethylene oligomerization. products having a high content of internal C13-olefins are also commercially manufactured, for instance, by the chlorination-dehydrochlorination of paraffins or by paraffin dehydrogenation, and can also be prepared by isomerization of alpha-olefins. Internal olefin-rich products are manufactured and sold, for example, by Shell Chemical Company.
For preparations of alkylaryl sulphonates, the olefins as described above are subjected to reaction with benzene or toluene. Reaction conditions and catalyst type are chosen in such a way that preferably para alkyltoluene is formed. The alkylbenzene or alkyltoluene isomers are reacted with sulphur trioxide. The term "sulphur trioxide" as used in the present specification and claims is intended to include any compounds or complexes which contain or yield SO3 for a sulphonation reaction as well as S03 per se.This reaction may be conducted according to methods well known in the chemical arts, typically by contact of a flow of dilute SO, vapour with a thin film of liquid alkylate at a temperature in the range of about 5 to 50"C. The reaction between S03 and the alkylate yields a sulphonic acid which is neutralized by reaction with a base, preferably an alkali metal hydroxide, oxide, or carbonate.
The specific composition of alkylaryl sulphonates prepared as described above (and also, for instance, the methods used for sulphonation, hydrolysis, and neutralization of the specified olefins) have not been found to be a critical factor to the performance of the surfactant in the steam foam process according to this invention. in this regard, it is observed that factors which have conventionally governed the choice of sulphonation conditions, e.g., product colour, clarity, odour, etc., do not carry with same weight in the preparation of alkylaryl sulphonates for purposes of use in the process according to the invention that they have been accorded in detergent manufacture.Consequently, reaction conditions outside of those heretofore considered desirable for alkylate sulphonation are still suitably applied in the preparation of surfactant components suitable for use in the steam-foam-forming mixture.
For purposes related to maintaining product stability, conventional manufacture typically yields a dilute solution or dispersion of the alkylaryl sulphonates, for instance, products with a 15-30 %wt active matter content in water. Such products may be directly applied to the preparation of steamfoam-forming mixtures for purposes of this invention.
Suitable alkylaryl sulphonates, generally prepared by methods such as described above, are themselves commercially available products.
The strength of the foam formed by the steamfoam-forming composition including alkylaryl sulphonate tends to increase with increases in the proportion of the surfactant andfor electrolyte components of the composition. Also, there tends to be an optimum ratio of surfactant and electrolyte components at which the surface activity of the composition is maximized.
The steam-foam-forming composition according to the present invention can form a steam-foam capable of reducing the effective mobility of the steam to less than about 1110to and even to 1/50th1/75th of the mobility it would have within a permeable porous medium in the absence of the surfactant.
The steam used in the present process andfor compositions can be generated and supplied in the form of substantially any dry, wet, superheated, or low grade steam in which the steam condensate and/or liquid components are compatible with, and do not inhibit, the foam-forming properties of the foam-forming components of a steam-foam-forming mixture according to the present invention. The steam quality of the steam as generated and/or amount of aqueous liquid with which it is mixed be such that the steam quality of the resulting mixture is preferably from 10 to 90%. The desired steam-foam is advantageously prepared by mixing the steam with aqueous solution(s) o-r the surfactant component and optionally, and lectrnlyte.
The water content of these aqueous solutions must, of course, be taken into account .1 determin ing the steam quality of the mixture being formed.
Suitably, the noncondensable gas advantageously used in a steam-foam-forming mixture according to the present invention can comprise substantially any gas which (a) undergoes little or no condensation at the temperatures (100-350 C) and pressures (1-100 bar) at which the steamfoam-forming mixture is preferably injected into and displaced through the reservoir to be treated and (b) is substantially inert to and compatible with the foam-forming surfactant and other components of that mixture. Such a gas is preferably nitrogen but can comprise other substantially inert gases, such as air, ethane, methane, flue gas, fuel gas, or the like.Suitable concentrations of noncondensable gas in the steam-foam mixture fall in the range of from 0.001 to 0.3 mole percent such as 0.001 and 0.2 mole percent, or between 0.003 and 0.1 mole percent of the gas phase of the mixture.
Suitably, the electrolyte used should have a composition similar to and should be used in a proportion similar to those described as suitable alkali metal salt electrolytes in the above-mentioned USA patent specification 4,086,964. An aqueous solution may be applied that contains an amount of electrolyte substantially equivalent in salting-out effect to a sodium chloride concentration of from 0.001 to 10% (but less than enough to cause significant salting out) of the liquid-phase of the steam. Some or all of the electrolyte can comprise an inorganic salt, such as an alkali metal salt, an alkali metal halide, and sodium chloride. Other inorganic salts, for example, halides, sulphonates, carbonates, nitrates and phosphates, in the form of salts of alkaline earth metals, can be used.
Generally stated, an electrolyte concentration may be applied which has approximately the same effect on mobility reduction of the foam as does a sodium chloride concentration of between 0.001 and 5 percent by weight (but less than a salting out-inducing proportion) of the liquid phase of the steam-foam-forming mixture. The electrolyte concentration may be between 0.001 and 10 percent calculated on the same basis.
In compounding a steam-foam-forming mixture or composition in accordance with the present invention, the steam can be generated by means of substantially any of the commercially available device and techniques for steam generation. A stream of the steam being injected into the reservoir is preferably generated and mixed, in substantially any surface or downhole location, with selected proportions of substantially noncondensable gas, aqueous electrolyte solution, and foamforming surfactant. For example, in such a mixture, the quality of the steam which is generated and the concentration of the electrolyte and surfactantcontaining aqueous liquid with which it is mixed are preferably arranged so that (1) the proportion of aqueous liquid mixed with a dry steam which is injected into the reservoir is sufficient to provide a steam-containing fluid have a steam quality of from 10-90% (preferably from 30-80%); (2) the weight proportion of surfactant dissolved or dispersed in the aqueous liquid is from 0.01 to 10.0 (preferably from 1.0 to 4.0); and (3) the amount of noncondensable gas is from 0.0003 to 0.3 mole fraction of the gas phase of the mixture.

Claims (8)

1. A process for displacing oil within an oil-containing subterranean reservoir by flowing a steamcontaining fluid in conjunction with a surfactant component through a relatively steam-permeable zone within said reservoir, characterized in that a surfactant component is employed which comprises in substantial part at least one sulphonate of the formula RSO3X in which R is alkylaryl including benzene or toluene having attached thereto a linear alkyl group containing 18 carbon atoms in the alkyl chain and X is sodium, lithium, potassium or ammonium.
2. A process according to claim 1, characterized in that an electrolyte is employed in the flow within the reservoir in conjunction with the steamcontaining fluid.
3. A process according to claim 1 or 2, characterized in that a substantially noncondensable gas is employed in the flow within the reservoir in conjunction with the steam-containing fluid.
4. A process according to any one or more of the preceding claims, characterized in that the surfactant component comprises in substantial part sulphonate obtained by reacting a linear C,8-alkylbenzene and/or linear C18-alkyltoluene with sulphur trioxide followed by neutralization of the sulphonic acid.
5. A process according to claim 4, characterized in that the sulphonate is derived from linear C,8-al- kyltoluene.
6. A process according to any one or more of the preceding claims, characterized in that the aqueous liquid phase of the steam-foam-forming composition contains between about 0.01 and 10 percent by weight of alkylaryl sulphonate.
7. A process according to any one or more of the preceding claims, characterized in that in addition to or instead of nitrogen or another non-condensable gas electrolyte is used up to 10 % in the liquid phase to enhance the performance of the surfactant.
8. A process for displacing oil within an oil-containing subterranean reservoir according to claim 1 substantially as hereinbefore particularly described.
GB08407747A 1984-03-26 1984-03-26 Steam foam process Expired GB2156400B (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
GB08407747A GB2156400B (en) 1984-03-26 1984-03-26 Steam foam process
CA000474601A CA1247850A (en) 1984-03-26 1985-02-19 Steam foam process
NO851186A NO851186L (en) 1984-03-26 1985-03-25 PROCEDURE FOR AA REPLACING OIL IN AN OIL RESERVE
BR8501321A BR8501321A (en) 1984-03-26 1985-03-25 PROCESS FOR DISPLACING OIL INSIDE A RESERVOIR CONTAINING OIL
DE19853510765 DE3510765C2 (en) 1984-03-26 1985-03-25 Process for displacing oil in an oil-bearing underground deposit
NL8500877A NL192394C (en) 1984-03-26 1985-03-26 Method for recovering oil using steam foam.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB08407747A GB2156400B (en) 1984-03-26 1984-03-26 Steam foam process

Publications (3)

Publication Number Publication Date
GB8407747D0 GB8407747D0 (en) 1984-05-02
GB2156400A true GB2156400A (en) 1985-10-09
GB2156400B GB2156400B (en) 1987-08-26

Family

ID=10558667

Family Applications (1)

Application Number Title Priority Date Filing Date
GB08407747A Expired GB2156400B (en) 1984-03-26 1984-03-26 Steam foam process

Country Status (1)

Country Link
GB (1) GB2156400B (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2164978A (en) * 1984-09-26 1986-04-03 Shell Int Research Steam foam process
NL8702293A (en) * 1986-10-10 1988-05-02 Shell Int Research METHOD FOR EXTRACTING OIL USING STEAM FOAM
US5005644A (en) * 1987-05-28 1991-04-09 Chevron Research Company Steam enhanced oil recovery method using branched alkyl aromatic sulfonates
US10487636B2 (en) 2017-07-27 2019-11-26 Exxonmobil Upstream Research Company Enhanced methods for recovering viscous hydrocarbons from a subterranean formation as a follow-up to thermal recovery processes
US11002123B2 (en) 2017-08-31 2021-05-11 Exxonmobil Upstream Research Company Thermal recovery methods for recovering viscous hydrocarbons from a subterranean formation
US11142681B2 (en) 2017-06-29 2021-10-12 Exxonmobil Upstream Research Company Chasing solvent for enhanced recovery processes
US11261725B2 (en) 2017-10-24 2022-03-01 Exxonmobil Upstream Research Company Systems and methods for estimating and controlling liquid level using periodic shut-ins

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7809538B2 (en) 2006-01-13 2010-10-05 Halliburton Energy Services, Inc. Real time monitoring and control of thermal recovery operations for heavy oil reservoirs
US7770643B2 (en) 2006-10-10 2010-08-10 Halliburton Energy Services, Inc. Hydrocarbon recovery using fluids
US7832482B2 (en) 2006-10-10 2010-11-16 Halliburton Energy Services, Inc. Producing resources using steam injection

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2164978A (en) * 1984-09-26 1986-04-03 Shell Int Research Steam foam process
NL8702293A (en) * 1986-10-10 1988-05-02 Shell Int Research METHOD FOR EXTRACTING OIL USING STEAM FOAM
US5005644A (en) * 1987-05-28 1991-04-09 Chevron Research Company Steam enhanced oil recovery method using branched alkyl aromatic sulfonates
US11142681B2 (en) 2017-06-29 2021-10-12 Exxonmobil Upstream Research Company Chasing solvent for enhanced recovery processes
US10487636B2 (en) 2017-07-27 2019-11-26 Exxonmobil Upstream Research Company Enhanced methods for recovering viscous hydrocarbons from a subterranean formation as a follow-up to thermal recovery processes
US11002123B2 (en) 2017-08-31 2021-05-11 Exxonmobil Upstream Research Company Thermal recovery methods for recovering viscous hydrocarbons from a subterranean formation
US11261725B2 (en) 2017-10-24 2022-03-01 Exxonmobil Upstream Research Company Systems and methods for estimating and controlling liquid level using periodic shut-ins

Also Published As

Publication number Publication date
GB2156400B (en) 1987-08-26
GB8407747D0 (en) 1984-05-02

Similar Documents

Publication Publication Date Title
CA1172160A (en) Steam foam drive process
US3981361A (en) Oil recovery method using microemulsions
EP0003183B1 (en) Propoxylated ethoxylated surfactants and method of recovering oil therewith
US4113011A (en) Enhanced oil recovery process
US4016932A (en) Surfactant oil recovery method for use in high temperature formations containing water having high salinity and hardness
CN1989313B (en) Alkylxylene sulfonates for enhanced oil recovery processes
US5363915A (en) Enhanced oil recovery technique employing nonionic surfactants
CA2039965C (en) Foaming agents for carbon dioxide and steam floods
US9441148B2 (en) Method and composition for enhanced hydrocarbon recovery
BRPI0908071B1 (en) METHOD FOR TREATING A FORMATION CONTAINING HYDROCARBONS
US4733728A (en) Micellar slug for oil recovery
BRPI0908063B1 (en) METHOD FOR TREATING A FORMATION CONTAINING HYDROCARBONS, AND, COMPOSITION OF RECOVERY OF HYDROCARBONS
US4693311A (en) Steam foam process
US20160215200A1 (en) Composition and method for enhanced hydrocarbon recovery
GB2156400A (en) Steam foam process
US20140005082A1 (en) Method and composition for enhanced hydrocarbons recovery from a formation containing a crude oil
Mannhardt et al. Adsorption of foam-forming surfactants in Berea sandstone
CA1295118C (en) Steam foam process
US5031698A (en) Steam foam surfactants enriched in alpha olefin disulfonates for enhanced oil recovery
US4203491A (en) Chemical flood oil recovery with highly saline reservoir water
BR112020000589A2 (en) methods for the production of crude oil and for the manufacture of a surfactant composition, aqueous surfactant composition, and, use of a solubility intensifier.
GB2164978A (en) Steam foam process
US4773484A (en) Enhanced oil recovery process with reduced gas drive mobility
CA1316681C (en) Process for recovering oil
US3994342A (en) Microemulsion flooding process

Legal Events

Date Code Title Description
PCNP Patent ceased through non-payment of renewal fee

Effective date: 20010326