US3490532A - Recovery of low-gravity viscous hydrocarbons - Google Patents
Recovery of low-gravity viscous hydrocarbons Download PDFInfo
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- US3490532A US3490532A US691196A US3490532DA US3490532A US 3490532 A US3490532 A US 3490532A US 691196 A US691196 A US 691196A US 3490532D A US3490532D A US 3490532DA US 3490532 A US3490532 A US 3490532A
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- crude
- recovery
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- aqueous
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- 238000011084 recovery Methods 0.000 title description 32
- 229930195733 hydrocarbon Natural products 0.000 title description 27
- 150000002430 hydrocarbons Chemical class 0.000 title description 21
- 238000000034 method Methods 0.000 description 44
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 36
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 32
- 230000015572 biosynthetic process Effects 0.000 description 30
- 238000005755 formation reaction Methods 0.000 description 30
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 27
- 239000003795 chemical substances by application Substances 0.000 description 26
- 230000008569 process Effects 0.000 description 26
- 239000002904 solvent Substances 0.000 description 22
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 19
- 239000000839 emulsion Substances 0.000 description 18
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 16
- 239000003921 oil Substances 0.000 description 15
- 239000002609 medium Substances 0.000 description 13
- 239000011521 glass Substances 0.000 description 12
- 239000004576 sand Substances 0.000 description 11
- 239000011269 tar Substances 0.000 description 11
- 239000004215 Carbon black (E152) Substances 0.000 description 10
- 239000008365 aqueous carrier Substances 0.000 description 10
- 238000002474 experimental method Methods 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- 239000011275 tar sand Substances 0.000 description 9
- 239000000654 additive Substances 0.000 description 8
- 238000002347 injection Methods 0.000 description 8
- 239000007924 injection Substances 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 8
- 150000001447 alkali salts Chemical class 0.000 description 7
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 7
- 239000007864 aqueous solution Substances 0.000 description 7
- 230000000996 additive effect Effects 0.000 description 6
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 6
- 239000012736 aqueous medium Substances 0.000 description 6
- 239000011280 coal tar Substances 0.000 description 6
- 238000006073 displacement reaction Methods 0.000 description 6
- 125000001183 hydrocarbyl group Chemical group 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 5
- 229920006395 saturated elastomer Polymers 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 239000012153 distilled water Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000000605 extraction Methods 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- 230000009471 action Effects 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 239000012670 alkaline solution Substances 0.000 description 3
- 238000004945 emulsification Methods 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 230000001965 increasing effect Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 150000003222 pyridines Chemical class 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 230000003381 solubilizing effect Effects 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 238000010793 Steam injection (oil industry) Methods 0.000 description 2
- 239000008186 active pharmaceutical agent Substances 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 2
- 239000010779 crude oil Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000005553 drilling Methods 0.000 description 2
- 230000001804 emulsifying effect Effects 0.000 description 2
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000003209 petroleum derivative Substances 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- 241000478345 Afer Species 0.000 description 1
- 241000543381 Cliftonia monophylla Species 0.000 description 1
- 241000237858 Gastropoda Species 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 239000005357 flat glass Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000320 mechanical mixture Substances 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 238000005065 mining Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- -1 steam Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
Classifications
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH DRILLING; MINING
- E21B—EARTH DRILLING, e.g. DEEP DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- E21B43/00—Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
- E21B43/16—Enhanced recovery methods for obtaining hydrocarbons
- E21B43/20—Displacing by water
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/58—Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids
Definitions
- Pateritecl Jan. 20, 1970 2 of water flooding to heavy crudes results in much lower RECOVERY OF fii i f iuvirv viscous remarks HYDROCARBONS The newer development in recovery methods for heavy Joseph T. Carlin, Houston, Tex., assignor to Texaco Inc.,
- This invention relates to an improved process for the in entrapping crude in the pores, thereby reducing rerecovery of petroleum products om hydrocarbon-bean covery.
- Another disadvantage is the tendency of the aqueing formations. More particularly, this invention pertains ous drive fluid to finger, since its viscosity is considerably to a process for increasing the recovery of low-gravity less than that of the crude, thereby reducing the eflipetroleum fluids, including highly viscous crudes, which ciency of the processes.
- a dilute alkaline aquemated oil-in-plac ous solution is known to increase the wetting character- Knewn recovery Processes pp to the recovery of istics of sand surfaces, and promote a leaching action hydrocarbons r tar and are even more ineiiieient and and emulsification of the tarry materials.
- Those solutions m y result in recovery of less than 10% Of the have been used as slugs in conjunction with subsequent p c h yp of hydrocarbon is a Viscous, tarry steam injection processes to force the emulsion thus teiiai, Which has a density 0f PP Y to formed through the formation to a production well.
- the invention comprises contacting the heavy crude in the formation or the oil in tar sands with an aqueous carrier containing an alkaline agent and a solubilizing agent.
- the alkaline agent is selected from the group consisting of anvalkali metal hydroxide, an alkaline earth metal hydroxide, and a basic salt of the alkali or alkaline earth metal which is capable of hydrolyzing in an aqueous medium to give an alkaline solution, the concentration of the alkaline agent being about 0.001 molar to 0.5 molar to give the required alkaline solution.
- solubilizing agents may be used in .the process of the present invention and includes pyridine, quinoline, closely related derivatives of these, coal tar fractions containing at least one member of the group consisting of pyridine and quinoline, and mixtures thereof,
- the solubilizing agent should be present in the aqueous solution in sufficient concentration to effect the emulsification of the hydrocarbon materials and maintain them in this state during passage through the formation. Concentrations in solution of from about 0.1 to about 10.0% by volume are usually sufiicient, although other amounts may be required in some cases.
- the beneficiating results of the aqueous carrier con- I taining the alkaline agent and the solubilizing agent are believed to derive from the wettability-improving characteristics of the alkaline agent and the solubilizing action of the solubilizing agent.
- the solubilizing agent is effective in releasing the crude from the sand surfaces so that the surfaces can be exposed to the alkaline agent, which in turn improves the wettability of the surface, thereby improving the recovery possibility of the crude.
- Emulsions are mechanical mixtures of two immiscible liquids, one of them being dispersed in the other in the form of droplets. Their apparent viscosities are functions of the continuous phase and the interaction of the dispensed droplets. Generally, the viscosity of the emulsion is greater than that of its continuous phase. In the case of a water-in-oil emulsion, the viscosity of the emulsion increases as the volume fraction of the water is increased to about 60-75%. Further increase in water content results in a sharp drop in viscosity to a value comparable with water. This reduction is related to the inversion of the emulsion from a water-in-oil type to an oil-in-water type.
- asphaltenes in cludes the more aromatic and polar materials of moderate molecular weight (-2000-l0,000) dispersed in a lower molecular weight medium, the material together being commonly referred to as asphalt.
- a further demonstration of the effectiveness of treated water to remove a tar sand utilized a series of three glass centrifuge tubes into each of which was placed approximately 20 ml. of the crushed tar sand, An alkaline ysolution containing 0.2 molar NaOH was added to the first centrifuge tube to the ml. mark. A uinoline saturated water was added to the second centrifuge tube to the 100 ml. mark. A quinoline-alkaline water was added to the third tube to the 100 ml. mark.
- one embodiment may consist of drilling an injection wellinto the formation, through which the aqueous carrier with the agents is injected into the formation.
- the injected quality may vary within relatively wide limits, and will depend on a number of conditions, including the thickness of the formation, its charactefistics, and the conditions for the subsequent I injection of the aqueous drive medium.
- the carrier is then pushed through the formation by the drive medium, e.g. H O in the form of either water or steam, the temperature of the water may range up to higher than even 200 F., although in some cases it may be desirable to use even higher temperatures, up to 500 F.', the temperatures being fixed by optimum conditions of operation.
- the drive medium e.g. H O in the form of either water or steam
- hydrocarbons are stripped from the'formation, forming an oil-in-uater emulsion which can then be produced at neighboring fwells. Separation of the hydrocarbons from the 'emulsion is accomplished by one of several emulsion breaking techniques.
- Another embodiment of the invention is the recovery of hydrocarbon materials from tar sands by utilizing the aqueous medium in an extractive technique in combination with Well-known techniques for the mining of the tar sand, arid well-known techniques for the recovery of the oil from the tar sand following its extraction.
- each type of apparatus consisted of a glass tube 7 inches long and V2" in diameter, the top' and bottom of each of these tubes being closed by 100 mesh wire screens.
- Each tube contained a silica sand pack having an initial crude saturation of about 32%, and a pore volume of about 8- ml.
- the properties of the crudes used are shown in Table I.
- a process for recovering hydrocarbons from a subterranean hydrocarbon-bearing formation which comprises contacting said formation with an aqueous alkaline medium containing a solubilizing agent selected from the group consisting of pyridine, quinoline, closely related derivatives of pyridine and quinoline, coal tar fractions containing at least one member of the group consisting of pyridine and quinoline, and mixtures thereof, forming an emulsion in said formation. thereby enhancing the mobility of said hydrocarbons, recovering said emulsion thus formed, and thereafter separating said hydrocarbons from said emulsion.
- a solubilizing agent selected from the group consisting of pyridine, quinoline, closely related derivatives of pyridine and quinoline, coal tar fractions containing at least one member of the group consisting of pyridine and quinoline, and mixtures thereof
- aqueous alkaline medium comprises an aqueous medium containing an alkaline agent selected from the group consisting of alkali metal hydroxides, alkaline earth metal hydroxides, basic salts of alkali metal hydroxides, basic salts of alkaline earth metal hydroxides and mixtures thereof.
- a process for recovering hydrocarbons from a subterranean hydrocarbon-bearing formation penetrated by an injection well and a production well which comprises injecting into said formation through said injection well an aqueous alkaline medium containing a, solubilizing agent selected from the group consisting of pyridine, quinoline, closely related derivatives of pyridine and quinoline, coal tar fractions containing at least one member of the group consisting of pyridine and quinoline, and mixtures thereof, thereafter injecting an aqueous drive medium into said formation through said injection well and driving the same toward said production well.
- a, solubilizing agent selected from the group consisting of pyridine, quinoline, closely related derivatives of pyridine and quinoline, coal tar fractions containing at least one member of the group consisting of pyridine and quinoline, and mixtures thereof
- aqueous alkaline medium comprises an aqueous medium containing an alkaline agent selected from the group consisting of alkali metal hydroxides, alkaline earth metal hydroxides, basic salts of alkali metal hydroxides, basic salts of alkaline earth metal hydroxides and mixtures thereof.
- line medium containing a solubilizing agent selected from the group consisting of pyridine, quinoline, closely related derivatives of pyridine and quinoline, coal tar fractioils containing at least one member of the group consisting of' pyridine and quinoline, and mixtures thereof, thereby emulsifying and extracting said hydrocarbons from said sand matrix in said aqueous alkaline medium, recovering the emulsion thus formed, and separating hydrocarbons from said emulsion.
- a solubilizing agent selected from the group consisting of pyridine, quinoline, closely related derivatives of pyridine and quinoline, coal tar fractioils containing at least one member of the group consisting of' pyridine and quinoline, and mixtures thereof, thereby emulsifying and extracting said hydrocarbons from said sand matrix in said aqueous alkaline medium, recovering the emulsion thus formed, and separating hydrocarbons from said emulsion.
- aqueous alkaline medium comprises an aqueous medium containing an alkaline agent selected from the group consisting of alkali metal hydroxides, alkaline earth metal hydroxides, basic salts of alkali metal hydroxides, basic salts of alkaline earth metal hydroxides and mixtures thereof.
Description
ROOM F 1:? Ii. a a a ii 9 53a GROSS -REFEi-HZNCEv SEARCH on. aim tan ra.-
Pateritecl Jan. 20, 1970 2 of water flooding to heavy crudes results in much lower RECOVERY OF fii i f iuvirv viscous remarks HYDROCARBONS The newer development in recovery methods for heavy Joseph T. Carlin, Houston, Tex., assignor to Texaco Inc.,
carbons left in place. However, generally the application crudes is the use of steam injection which has been ap- New York, N.Y., a corporation of Delaware 5 plied in several modifications, including the push-pull No Drawing. Filed Dec. 18, 1967, Ser. No. 691,196 technique and through-put methods, and has resulted in Int. Cl. E21b 43/16 significant recoveries in some areas of heavy crude reser- 166-266 17 Claims voirs. Crude recovery by this process is enhanced through the beneficial effects of the drastic viscosity reduction that accompanies an increase in temperature which is ABSTRACT OF THE DISCLOSURE characteristic of heavy crudes. This reduction in viscosity A process for the recovery of the low-gravity, viscous facilitates the production of hydrocarbons, since it imud d oil f t nd by contacting h h d proves their mobility, i.e., it increases their ability to flow. carbon-bearing formation or tar sands with an aqueous However, the appiieation Of these Secondary recovery carrier containing an alkaline agent and a solubilizing techniques to depleted formations y 1eave l q agent. tities of oil-in-place, since the crude is tightly bound to the sand particles of the formation, that is, the sorptive FIELD OF THE INVENTION capacity of the sand for the crude is great. In addition, interfacial tensions between the immiscible phases result This invention relates to an improved process for the in entrapping crude in the pores, thereby reducing rerecovery of petroleum products om hydrocarbon-bean covery. Another disadvantage is the tendency of the aqueing formations. More particularly, this invention pertains ous drive fluid to finger, since its viscosity is considerably to a process for increasing the recovery of low-gravity less than that of the crude, thereby reducing the eflipetroleum fluids, including highly viscous crudes, which ciency of the processes. are substantially immobile under ordinary conditions, oils Consequently, process modifications have been defrom tar sands, and residual asphaltic crudes in hydroveloped which may incorporate additives to lessen the carbon-bearing formations, from which varying amounts above cited disadvantages and thereby improve the effiof the more mobile fractions of the original hydrocarciency of these processes. For example, surface-active bons in place have been recovered. agents and miscible liquids are utilized to decrease the DESCRIPTION THE PRIOR ART interfacial tension between the water and the reservoir crude, and thickeners have been developed to ad ust v1s The production of petroleum products is usually accosjty so as to i hibit fingering. complished y drilling into a hydrocarbon-bearing forma- The practiced methods for the injection of additives, tion and utilizing one of the Well-known recovery methods commonly i ts of injection of a slug of additive, confor the recovery of hydrocarbons. However, it is recogmi d i a transporting di e g water, into the titled-that these recovery techniques y recover y a formation and then following this injection with a miner Portion of the Petieieum Products Present in the flood Water to move the additive slug through the formation, Particularly When pp t0 reservoirs of formation. In its ideal effect, the so-called slug moves Viscous efildee, hytimeathons having gravities 1eSS through the formation as an additive bank, thereby imthan Even the use Of'imPTOVed recovery N 40 parting its beneficiating effects to the recovery process. tiees' involving heating, miscible flooding, Water flooding In many hydrocarbon-bearing formations, it is common and Steam Processing y still leaVe p to of to find the oil sands to be preferentially wetted by oil. the'efiginai hydrocarbons in Piece; It is well known in the art to inject into these preferen- Thus, y iaige reserves of Petroleum fluids, tially oil-wetted formations certain chemicals to reverse heavy Crude from Whi h only email recoveries have been the wettability characteristics of the formation, thereby realized by present commercial recovery methods, are increasing the effectiveness of a Water flood to remove yet t Teach a Potential recovery approaching their eSti the residual crude. For example, a dilute alkaline aquemated oil-in-plac ous solution is known to increase the wetting character- Knewn recovery Processes pp to the recovery of istics of sand surfaces, and promote a leaching action hydrocarbons r tar and are even more ineiiieient and and emulsification of the tarry materials. Those solutions m y, result in recovery of less than 10% Of the have been used as slugs in conjunction with subsequent p c h yp of hydrocarbon is a Viscous, tarry steam injection processes to force the emulsion thus teiiai, Which has a density 0f PP Y to formed through the formation to a production well. Since the material in its crude state does not command a Improved recoveries from heavy crudes or tar sands high Price, y recovery Processes are not attractive have been realized also by the use of dilute aqueous alc'omn ercially at the very low estimates of recovery. Herekaline solutions containing an'effective amount of a non tetoie, P p methods involving i g and handling ionic surfactant, whereby extraction is effected by the of the tar sends to recover the hydrocarbons are likewise spontaneous emulsification when the aqueous liquid comes expensive and have not resulted in commercial successes. i Contact ith the tar in the sand. Consequently, the extensive deposits of tar Sands Stiii However, some of the disadvantages .of those additive eweiteemmeteiai Pment. recovery processes include the problem that the additive 1 i well known in the art that improved TeeOVerY may be strongly absorbed in the surfaces of the sand methods include Seeeiied Secondary reeeVerY techniques formation, resulting in a large or excessive amount of hi at e pp after the natural drive of a reservoir additive being required. The costs involved .of these adh been depieted- The appiieatien of these techniques ditives, which may be relatively expensive, may become P m additienai recovery of hydrocarbons froIn P excessive early in the life of the recovery process neces tially depleted f0l'mtitiotissitating its termination. Other disadvantages include the t flooding is one Of the more Widely practiced unfavorable viscosity ratio between the flooding medium secondary recovery methods. A successful water flood and the crude. may result in recovery of 30-50% of the original hydro- Accordingly, it is an object of the present invention to overcome the disadvantages of the prior art by providing a recovery method whereby highly viscous, low-gravity crudes, and oils from tar sands can be recovered by a more efiicient process.
SUMMARY The invention comprises contacting the heavy crude in the formation or the oil in tar sands with an aqueous carrier containing an alkaline agent and a solubilizing agent.
DESCRIPTION OF THE PREFERRED EMBODIMENT More specifically, it has been found that the combination of an alkaline agent and a solubilizing agent results in a beneficial and synergistic effect in the action of the extraction of heavy crudes from sands.
The alkaline agent is selected from the group consisting of anvalkali metal hydroxide, an alkaline earth metal hydroxide, and a basic salt of the alkali or alkaline earth metal which is capable of hydrolyzing in an aqueous medium to give an alkaline solution, the concentration of the alkaline agent being about 0.001 molar to 0.5 molar to give the required alkaline solution.
A variety of solubilizing agents may be used in .the process of the present invention and includes pyridine, quinoline, closely related derivatives of these, coal tar fractions containing at least one member of the group consisting of pyridine and quinoline, and mixtures thereof,
which show a solubilizing and/or emulsifying effect at least upon the asphaltene portions of the crude.
The solubilizing agent should be present in the aqueous solution in sufficient concentration to effect the emulsification of the hydrocarbon materials and maintain them in this state during passage through the formation. Concentrations in solution of from about 0.1 to about 10.0% by volume are usually sufiicient, although other amounts may be required in some cases.
The beneficiating results of the aqueous carrier con- I taining the alkaline agent and the solubilizing agent are believed to derive from the wettability-improving characteristics of the alkaline agent and the solubilizing action of the solubilizing agent. The solubilizing agent is effective in releasing the crude from the sand surfaces so that the surfaces can be exposed to the alkaline agent, which in turn improves the wettability of the surface, thereby improving the recovery possibility of the crude.
A further advantage of the aqueous solution is believed to result from its ability to emulsify the extracted crude to form an oil-in-water emulsion with its attendant benefits including improved mobility. Emulsions are mechanical mixtures of two immiscible liquids, one of them being dispersed in the other in the form of droplets. Their apparent viscosities are functions of the continuous phase and the interaction of the dispensed droplets. Generally, the viscosity of the emulsion is greater than that of its continuous phase. In the case of a water-in-oil emulsion, the viscosity of the emulsion increases as the volume fraction of the water is increased to about 60-75%. Further increase in water content results in a sharp drop in viscosity to a value comparable with water. This reduction is related to the inversion of the emulsion from a water-in-oil type to an oil-in-water type.
Experiments using an emulsion of a crude oil (San Ardo) and an aqueous carrier consisting specifically of an alkaline agent and a solubilizing agent, 0.2 molar sodium hydroxide and 90% quinoline saturated aqueous solution, showed that the viscosities of the emulsion measured when the emulsions were in an agitated state approximated a straight line on a Fisher/Tag blending chart. The results of the viscosity measurements showed that by adding small amounts of an aqueous carrier consisting of an alkaline agent and a solubilizing agent, substantial decreases in viscosity were obtained.
The effectiveness of the aqueous carrier is further believed to result in large part from its action on the heavier, complex hydrocarbon-type materials present in low-gravthese types of viscous crudes have large or relatively large fractions of the heavier compex hydrocarbon-type materials, referred to as asphaltenes. The term asphaltenes in cludes the more aromatic and polar materials of moderate molecular weight (-2000-l0,000) dispersed in a lower molecular weight medium, the material together being commonly referred to as asphalt.
It has been shown that these asphaltene fractions of heavy crudes are responsible in large part for the adhesive force which heavy crudes and tars have for the mineral surfaces of the hydrocarbon-bearing formation. This accounts for the fact that in the comparison of recoveries between two crudes with similar viscosities, the residual hydrocarbon saturation for the crude having the larger asphaltene content will be greater.
Experiments were performed to obtain a general idea of the nature of the adhesive force between various crude oils and a silica surface. Flat glass surfaces cleaned with chromic acid Were chosen for the tests. The tests consisted of putting equal drops of the crudes to 'be examined on the horizontal glass surface, then placing the glass in a vertical position and measuring the distance the drop traveled as a function of time. Although the initial rate of flow of the crudes depends upon viscosity, the total flow length depends upon the amount of crude left on the glass as the drop proceeds down the glass. The total lengths of the crude columns were measured when there was no more flow for a length of time. This distance, called for convenience the equilibrium distance, is an indication of the adhesive force between the respective crudes and the surface. The results of these tests showed that crudes with higher asphaltene contents had a greater tendency to coat the mineral surface.
Further experiments demonstrated the effectiveness of the alkaline solubilizing agent to remove the asphaltene from the silica surface. A glass fiat surface cleaned with chromic acid was covered with a 10 API crude containing 41.5% asphaltenes. The glass was placed in a vertical position and the excess crude was allowed to drain from the glass for a period of one week. Three aqueous solutions and one distilled water standard were then allowed to flow over the crude-covered face of the glass in separate streams at a rate of approximately 0.5 ml. per hour. The three aqueous solutions or treated waters consisted Observations from this demonstration indicated that the distilled water standard and the alkaline water-solution had no apparent effect upon the crude covered sura face. The quinoline saturated water penetrated through the surface and removed minor portions of the crude which were exposed to the treated water. However, the quinoline-alkaline water effectively removed most of the crude from the glass which was exposed to the treated Water. I
This experiment showed that the distilled water standard and the alkaline water solution were ineffective in removing the crude layer on the glass. The quinoline saturated water acted as a solvent and removed some of the crude. The quinoline-alkaline water removed the most of the crude layer because of the incerased wetting ability of the alkaline water.
A further demonstration of the effectiveness of treated water to remove a tar sand (Sunnyside, Okla.) utilized a series of three glass centrifuge tubes into each of which was placed approximately 20 ml. of the crushed tar sand, An alkaline ysolution containing 0.2 molar NaOH was added to the first centrifuge tube to the ml. mark. A uinoline saturated water was added to the second centrifuge tube to the 100 ml. mark. A quinoline-alkaline water was added to the third tube to the 100 ml. mark.
Observations indicated that the tube containing the 0.2 molar NaOH solution showed little or no effective extraction with the tar sand. The tube containing the quinoline saturated water showed some of the oil had been removed from the tar sand. The tube containing the quinoline-alkaline Water showed almost complete removal of the, oil from the tar sand in the form of an emulsion. Fiurther centrifuge tests have demonstrated a sirrlii lar effectiveness of a 5% pyridine-alkaline solution in extracting oil from a tar sand.
Similar tests have demonstrated comparable effectiveness of a coal tar base to remove hydrocarbons from a tar sand in the form of an emulsion when the aqueous carrier contained the coal tar base, thus presenting an attractive commercial possibility.
In utilizing the above disclosed alkaline and solubilizing agents in an aqueous carrier to exploit an underground hydrocarbon-bearing formation, one embodiment may consist of drilling an injection wellinto the formation, through which the aqueous carrier with the agents is injected into the formation. The injected quality may vary within relatively wide limits, and will depend on a number of conditions, including the thickness of the formation, its charactefistics, and the conditions for the subsequent I injection of the aqueous drive medium.
The carrier is then pushed through the formation by the drive medium, e.g. H O in the form of either water or steam, the temperature of the water may range up to higher than even 200 F., although in some cases it may be desirable to use even higher temperatures, up to 500 F.', the temperatures being fixed by optimum conditions of operation.
" In the passage of the carrier through the formation,
hydrocarbons are stripped from the'formation, forming an oil-in-uater emulsion which can then be produced at neighboring fwells. Separation of the hydrocarbons from the 'emulsion is accomplished by one of several emulsion breaking techniques.
Another embodiment of the invention is the recovery of hydrocarbon materials from tar sands by utilizing the aqueous medium in an extractive technique in combination with Well-known techniques for the mining of the tar sand, arid well-known techniques for the recovery of the oil from the tar sand following its extraction. f'In demonstrating the effectiveness of this invention, experiments were performed to measure the displacement efiiiciency of heavy crudes mixed with silica sand and the efficiency of various concentrations of an alkaline agent and a solubilizing agent in water. In these experiments, the alkaline agent was sodium hydroxide and the solubilizing agent was quinoline. Three of each type of apparatus were used and consisted of a glass tube 7 inches long and V2" in diameter, the top' and bottom of each of these tubes being closed by 100 mesh wire screens. Each tube contained a silica sand pack having an initial crude saturation of about 32%, and a pore volume of about 8- ml. The properties of the crudes used are shown in Table I.
TABLE I I I Viscosity (cs.)
Percent; Crude API 100 F. 210 F. asphalteno sand pack. No oil was produced during this phase of the experiment.
h (b) 200 m1. of the treated aqueous solution was passed through the sand pack in the following sequence:
(1) ml; (2) afer 1 hour, 50 ml; (3) after 1 hour, 50 m1.
(c) ml. of distilled water was passed through the pack to remove the aqueous solution.
Additional experiments were performed using a similar set up, but utilizing different concentrations of the said alkaline agent and said solubilizing agent. The results of these displacement experiments are indicated in Table II.
TABLE II CRUDE A [Displacements at; 78 F.]
Cone. of Quinolinc, Vol. percent Percent Oil Revovery Cone. of NaOH Molar:
CRUDE B [Displacements at 78 F.]
Cone. of Quinoline, Vol. percent Percent Oil Revovery Cone. of NaOH Molar:
CRUDE C [Displacements at 78 F.]
Cone. of Quinoline, Vol. percent Percent Oil Revovery The results show that effective maximum displacements can be obtained by utilizing optimum concentrations of the alkaline agent and the solubilizing agent for the type of crude involved. Dilferent crudes require the aqueous medium to have different compositions. The required optimum compositions can be determined prior to field operations by the use of experiments similar to those described above.
Besides the embodiments of the invention described above, others are possible. Thus, the foregoing description is not to be considered as limiting since other variations may be made within the scope of the following claims by one skilled in the art.
I claim:
1. A process for recovering hydrocarbons from a subterranean hydrocarbon-bearing formation which comprises contacting said formation with an aqueous alkaline medium containing a solubilizing agent selected from the group consisting of pyridine, quinoline, closely related derivatives of pyridine and quinoline, coal tar fractions containing at least one member of the group consisting of pyridine and quinoline, and mixtures thereof, forming an emulsion in said formation. thereby enhancing the mobility of said hydrocarbons, recovering said emulsion thus formed, and thereafter separating said hydrocarbons from said emulsion.
2. The process of claim 1 wherein said aqueous alkaline medium comprises an aqueous medium containing an alkaline agent selected from the group consisting of alkali metal hydroxides, alkaline earth metal hydroxides, basic salts of alkali metal hydroxides, basic salts of alkaline earth metal hydroxides and mixtures thereof.
3. The process of claim 2, wherein said alkaline agent is contained in the aqueous carrier in amounts in the range of from about 0.001 molar to 0.5 molar.
4. The process of claim 3 wherein said alkaline agent is sodium hydroxide.
5. The process of claim 1 wherein said solubilizing agent in solution is in the range from about 0.1% to 10.0% by volume.
6. A process for recovering hydrocarbons from a subterranean hydrocarbon-bearing formation penetrated by an injection well and a production well which comprises injecting into said formation through said injection well an aqueous alkaline medium containing a, solubilizing agent selected from the group consisting of pyridine, quinoline, closely related derivatives of pyridine and quinoline, coal tar fractions containing at least one member of the group consisting of pyridine and quinoline, and mixtures thereof, thereafter injecting an aqueous drive medium into said formation through said injection well and driving the same toward said production well.
7. The process of claim 6 wherein said aqueous alkaline medium comprises an aqueous medium containing an alkaline agent selected from the group consisting of alkali metal hydroxides, alkaline earth metal hydroxides, basic salts of alkali metal hydroxides, basic salts of alkaline earth metal hydroxides and mixtures thereof.
8. The process of claim 6, wherein said alkaline agent is contained in the aqueous carrier in amounts in the range of from about'0.001 molar to 0.5 molar;
9. The process of claim 8 wherein said alkaline agent is'sodium hydroxide.
10. The process of claim 6 wherein said solubilizing agent in solution is in the range from about 0.1% to 10.0% by volume.
11. The process of claim 6 wherein said aqueous drive medium is H 0.
12. The process of claim 11 wherein the H is water, steam, and mixtures thereof, the temperatures thereof being fixed by optimum conditions of operation.
line medium containing a solubilizing agent selected from the group consisting of pyridine, quinoline, closely related derivatives of pyridine and quinoline, coal tar fractioils containing at least one member of the group consisting of' pyridine and quinoline, and mixtures thereof, thereby emulsifying and extracting said hydrocarbons from said sand matrix in said aqueous alkaline medium, recovering the emulsion thus formed, and separating hydrocarbons from said emulsion.
14. The process of claim 13 wherein said aqueous alkaline medium comprises an aqueous medium containing an alkaline agent selected from the group consisting of alkali metal hydroxides, alkaline earth metal hydroxides, basic salts of alkali metal hydroxides, basic salts of alkaline earth metal hydroxides and mixtures thereof.
15. The process of claim 14, wherein said alkaline agent is contained in the aqueous mediumin amounts ranging from about 0.001 molar to 0.5 molar.
16. The process of'claim 15 wherein said alkaline agent is sodium hydroxide.
17. The process of claim 13 wherein said solubilizing agent in solution is in the range from about 0.1% to 10.0% by volume.
References Cited UNITED STATES PATENTS 2,356,205 8/1944 Blair et al 252-855 2,813,583 11/1957 Marx et al 166-11 2,910,424 10/1959 Tek et a1 208.11 2,924,566 2/196'0 Vaell et a1 20811 3,108,059 10/1963 Greenwald 20811 3 ,131,759 5/1964 Slusser et al.
3,163,214 12/1964 Csaszar 166--9 3,330,344 7/1967 Reisberg 166-42 X 3,330,757 7/1967 Bichard 208-11 3,338,814 8/1967 Given et a1. 208-11 3,392,105 7/1968 Poettmann et al 208-11 STEPHEN J. NOVOSAD, Primary Examiner US. Cl. X.R. 16 6-272, 274, 275
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US69119667A | 1967-12-18 | 1967-12-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3490532A true US3490532A (en) | 1970-01-20 |
Family
ID=24775535
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US691196A Expired - Lifetime US3490532A (en) | 1967-12-18 | 1967-12-18 | Recovery of low-gravity viscous hydrocarbons |
Country Status (5)
Country | Link |
---|---|
US (1) | US3490532A (en) |
ES (1) | ES361615A1 (en) |
FR (1) | FR1595317A (en) |
GB (1) | GB1217426A (en) |
NL (1) | NL6818239A (en) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3554286A (en) * | 1969-06-19 | 1971-01-12 | Texaco Inc | Recovery of hydrocarbons from subterranean hydrocarbon-bearing formations |
US3581823A (en) * | 1969-06-24 | 1971-06-01 | Texaco Inc | Recovery of hydrocarbons from subterranean hydrocarbon-bearing formations |
US3690376A (en) * | 1970-08-20 | 1972-09-12 | Robert W Zwicky | Oil recovery using steam-chemical drive fluids |
US3706341A (en) * | 1970-08-10 | 1972-12-19 | Canadian Fina Oil Ltd | Process for developing interwell communication in a tar sand |
US3731741A (en) * | 1971-07-06 | 1973-05-08 | Texaco Inc | Secondary oil recovery process using oxyalkylated additives |
US3732926A (en) * | 1971-06-01 | 1973-05-15 | Texaco Inc | Method for recovery of hydrocarbons utilizing steam injection |
US3811506A (en) * | 1973-02-12 | 1974-05-21 | Texaco Inc | Tar sand recovery method |
US3853178A (en) * | 1973-06-06 | 1974-12-10 | Getty Oil Co | Method for recovery of oil |
US3941192A (en) * | 1974-08-26 | 1976-03-02 | Texaco Inc. | Method for recovering high asphaltene content petroleum using surfactants |
US4175618A (en) * | 1978-05-10 | 1979-11-27 | Texaco Inc. | High vertical and horizontal conformance thermal oil recovery process |
US4714113A (en) * | 1986-12-05 | 1987-12-22 | Ppg Industries, Inc. | Alkaline water flooding with a precipitation inhibitor for enhanced oil recovery |
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US2356205A (en) * | 1942-10-21 | 1944-08-22 | Petrolite Corp | Process for increasing productivity of subterranean oil-bearing strata |
US2813583A (en) * | 1954-12-06 | 1957-11-19 | Phillips Petroleum Co | Process for recovery of petroleum from sands and shale |
US2910424A (en) * | 1956-11-19 | 1959-10-27 | Phillips Petroleum Co | Separation and recovery of oil from oil sands |
US2924566A (en) * | 1957-07-26 | 1960-02-09 | Union Oil Co | Treatment of bituminous sands |
US3108059A (en) * | 1961-02-03 | 1963-10-22 | Rohm & Haas | Recovery of oil by strip-mining |
US3131759A (en) * | 1959-06-19 | 1964-05-05 | Socony Mobil Oil Co Inc | Method of treating oil-productive subterranean formations |
US3163214A (en) * | 1961-11-13 | 1964-12-29 | Pure Oil Co | Solvent-waterflood oil recovery process |
US3330344A (en) * | 1964-04-13 | 1967-07-11 | Shell Oil Co | Secondary recovery method |
US3330757A (en) * | 1965-04-02 | 1967-07-11 | Exxon Research Engineering Co | Chemical treatment of athabaska froth |
US3338814A (en) * | 1964-05-08 | 1967-08-29 | Imp Oil Ltd | Process for separating oil from bituminous sand |
US3392105A (en) * | 1965-04-15 | 1968-07-09 | Marathon Oil Co | Use of a soluble oil in the extraction of hydrocarbons from oil sands |
-
1967
- 1967-12-18 US US691196A patent/US3490532A/en not_active Expired - Lifetime
-
1968
- 1968-12-17 GB GB60049/68A patent/GB1217426A/en not_active Expired
- 1968-12-18 FR FR1595317D patent/FR1595317A/fr not_active Expired
- 1968-12-18 ES ES361615A patent/ES361615A1/en not_active Expired
- 1968-12-18 NL NL6818239A patent/NL6818239A/xx unknown
Patent Citations (11)
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US2356205A (en) * | 1942-10-21 | 1944-08-22 | Petrolite Corp | Process for increasing productivity of subterranean oil-bearing strata |
US2813583A (en) * | 1954-12-06 | 1957-11-19 | Phillips Petroleum Co | Process for recovery of petroleum from sands and shale |
US2910424A (en) * | 1956-11-19 | 1959-10-27 | Phillips Petroleum Co | Separation and recovery of oil from oil sands |
US2924566A (en) * | 1957-07-26 | 1960-02-09 | Union Oil Co | Treatment of bituminous sands |
US3131759A (en) * | 1959-06-19 | 1964-05-05 | Socony Mobil Oil Co Inc | Method of treating oil-productive subterranean formations |
US3108059A (en) * | 1961-02-03 | 1963-10-22 | Rohm & Haas | Recovery of oil by strip-mining |
US3163214A (en) * | 1961-11-13 | 1964-12-29 | Pure Oil Co | Solvent-waterflood oil recovery process |
US3330344A (en) * | 1964-04-13 | 1967-07-11 | Shell Oil Co | Secondary recovery method |
US3338814A (en) * | 1964-05-08 | 1967-08-29 | Imp Oil Ltd | Process for separating oil from bituminous sand |
US3330757A (en) * | 1965-04-02 | 1967-07-11 | Exxon Research Engineering Co | Chemical treatment of athabaska froth |
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Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3554286A (en) * | 1969-06-19 | 1971-01-12 | Texaco Inc | Recovery of hydrocarbons from subterranean hydrocarbon-bearing formations |
US3581823A (en) * | 1969-06-24 | 1971-06-01 | Texaco Inc | Recovery of hydrocarbons from subterranean hydrocarbon-bearing formations |
US3706341A (en) * | 1970-08-10 | 1972-12-19 | Canadian Fina Oil Ltd | Process for developing interwell communication in a tar sand |
US3690376A (en) * | 1970-08-20 | 1972-09-12 | Robert W Zwicky | Oil recovery using steam-chemical drive fluids |
US3732926A (en) * | 1971-06-01 | 1973-05-15 | Texaco Inc | Method for recovery of hydrocarbons utilizing steam injection |
US3731741A (en) * | 1971-07-06 | 1973-05-08 | Texaco Inc | Secondary oil recovery process using oxyalkylated additives |
US3811506A (en) * | 1973-02-12 | 1974-05-21 | Texaco Inc | Tar sand recovery method |
US3853178A (en) * | 1973-06-06 | 1974-12-10 | Getty Oil Co | Method for recovery of oil |
US3941192A (en) * | 1974-08-26 | 1976-03-02 | Texaco Inc. | Method for recovering high asphaltene content petroleum using surfactants |
US4175618A (en) * | 1978-05-10 | 1979-11-27 | Texaco Inc. | High vertical and horizontal conformance thermal oil recovery process |
US4714113A (en) * | 1986-12-05 | 1987-12-22 | Ppg Industries, Inc. | Alkaline water flooding with a precipitation inhibitor for enhanced oil recovery |
Also Published As
Publication number | Publication date |
---|---|
ES361615A1 (en) | 1970-09-01 |
DE1815475A1 (en) | 1969-08-21 |
FR1595317A (en) | 1970-06-08 |
NL6818239A (en) | 1969-06-20 |
GB1217426A (en) | 1970-12-31 |
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