CA2547919C - Gels tensioactifs viscoelastiques presentant une concentration reduite en sel - Google Patents
Gels tensioactifs viscoelastiques presentant une concentration reduite en sel Download PDFInfo
- Publication number
- CA2547919C CA2547919C CA2547919A CA2547919A CA2547919C CA 2547919 C CA2547919 C CA 2547919C CA 2547919 A CA2547919 A CA 2547919A CA 2547919 A CA2547919 A CA 2547919A CA 2547919 C CA2547919 C CA 2547919C
- Authority
- CA
- Canada
- Prior art keywords
- fluid
- wellbore fluid
- surfactant
- oleyl
- gel
- 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.)
- Expired - Fee Related
Links
- 150000003839 salts Chemical class 0.000 title claims abstract description 51
- 239000004094 surface-active agent Substances 0.000 title claims abstract description 46
- 239000000499 gel Substances 0.000 title claims description 124
- 239000012530 fluid Substances 0.000 claims abstract description 87
- 238000000034 method Methods 0.000 claims abstract description 7
- 150000002894 organic compounds Chemical class 0.000 claims description 33
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 32
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 32
- 150000001875 compounds Chemical class 0.000 claims description 26
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 claims description 24
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 claims description 19
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 claims description 18
- 150000001412 amines Chemical class 0.000 claims description 18
- 229940055577 oleyl alcohol Drugs 0.000 claims description 18
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 claims description 18
- 230000015572 biosynthetic process Effects 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 12
- 150000007942 carboxylates Chemical group 0.000 claims description 11
- 150000002148 esters Chemical class 0.000 claims description 11
- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 11
- 229940113162 oleylamide Drugs 0.000 claims description 11
- FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 claims description 9
- -1 phosphate ester Chemical class 0.000 claims description 9
- QGLWBTPVKHMVHM-KTKRTIGZSA-N (z)-octadec-9-en-1-amine Chemical compound CCCCCCCC\C=C/CCCCCCCCN QGLWBTPVKHMVHM-KTKRTIGZSA-N 0.000 claims description 8
- CHBBKFAHPLPHBY-KHPPLWFESA-N [(z)-octadec-9-enyl] 2-(methylamino)acetate Chemical compound CCCCCCCC\C=C/CCCCCCCCOC(=O)CNC CHBBKFAHPLPHBY-KHPPLWFESA-N 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 7
- 150000001408 amides Chemical class 0.000 claims description 7
- 229920006395 saturated elastomer Polymers 0.000 claims description 7
- 239000000243 solution Substances 0.000 claims description 7
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 6
- 150000001298 alcohols Chemical class 0.000 claims description 6
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 239000000693 micelle Substances 0.000 claims description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 5
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims description 4
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims description 4
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims description 4
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 claims description 4
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims description 4
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 claims description 4
- 238000009472 formulation Methods 0.000 claims description 4
- 230000002209 hydrophobic effect Effects 0.000 claims description 4
- 238000002347 injection Methods 0.000 claims description 4
- 239000007924 injection Substances 0.000 claims description 4
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims description 4
- 235000020778 linoleic acid Nutrition 0.000 claims description 4
- DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- URXZXNYJPAJJOQ-UHFFFAOYSA-N Erucic acid Natural products CCCCCCC=CCCCCCCCCCCCC(O)=O URXZXNYJPAJJOQ-UHFFFAOYSA-N 0.000 claims description 3
- 239000005642 Oleic acid Substances 0.000 claims description 3
- 229910019142 PO4 Inorganic materials 0.000 claims description 3
- 150000001735 carboxylic acids Chemical class 0.000 claims description 3
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 3
- 150000002009 diols Chemical class 0.000 claims description 3
- DPUOLQHDNGRHBS-KTKRTIGZSA-N erucic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-KTKRTIGZSA-N 0.000 claims description 3
- 239000000194 fatty acid Substances 0.000 claims description 3
- 229930195729 fatty acid Natural products 0.000 claims description 3
- 150000004665 fatty acids Chemical class 0.000 claims description 3
- 150000002576 ketones Chemical class 0.000 claims description 3
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 3
- 150000002889 oleic acids Chemical class 0.000 claims description 3
- 239000010452 phosphate Substances 0.000 claims description 3
- 239000003760 tallow Substances 0.000 claims description 3
- 239000003945 anionic surfactant Substances 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 claims description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 2
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 claims description 2
- 229930195734 saturated hydrocarbon Natural products 0.000 claims description 2
- 230000003019 stabilising effect Effects 0.000 claims description 2
- 229930195735 unsaturated hydrocarbon Natural products 0.000 claims description 2
- 238000011282 treatment Methods 0.000 abstract description 27
- 238000007792 addition Methods 0.000 description 22
- 230000000694 effects Effects 0.000 description 14
- 238000005755 formation reaction Methods 0.000 description 11
- 229960004592 isopropanol Drugs 0.000 description 10
- 239000000654 additive Substances 0.000 description 9
- 229910017053 inorganic salt Inorganic materials 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 230000000996 additive effect Effects 0.000 description 7
- 229930195733 hydrocarbon Natural products 0.000 description 7
- 150000002430 hydrocarbons Chemical class 0.000 description 7
- 150000002888 oleic acid derivatives Chemical class 0.000 description 6
- 239000004215 Carbon black (E152) Substances 0.000 description 5
- 125000003277 amino group Chemical group 0.000 description 5
- 125000000129 anionic group Chemical group 0.000 description 5
- 239000012267 brine Substances 0.000 description 5
- 239000012071 phase Substances 0.000 description 5
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 5
- 230000007423 decrease Effects 0.000 description 4
- 235000021313 oleic acid Nutrition 0.000 description 4
- GIIGBNLFBXYUEF-GMFCBQQYSA-M [(z)-docos-13-enyl]-bis(2-hydroxyethyl)-methylazanium;chloride Chemical compound [Cl-].CCCCCCCC\C=C/CCCCCCCCCCCC[N+](C)(CCO)CCO GIIGBNLFBXYUEF-GMFCBQQYSA-M 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 229940096992 potassium oleate Drugs 0.000 description 3
- MLICVSDCCDDWMD-KVVVOXFISA-M potassium;(z)-octadec-9-enoate Chemical compound [K+].CCCCCCCC\C=C/CCCCCCCC([O-])=O MLICVSDCCDDWMD-KVVVOXFISA-M 0.000 description 3
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 2
- LPMBTLLQQJBUOO-KTKRTIGZSA-N (z)-n,n-bis(2-hydroxyethyl)octadec-9-enamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)N(CCO)CCO LPMBTLLQQJBUOO-KTKRTIGZSA-N 0.000 description 2
- HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 description 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 2
- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 2
- FKLJPTJMIBLJAV-UHFFFAOYSA-N Compound IV Chemical compound O1N=C(C)C=C1CCCCCCCOC1=CC=C(C=2OCCN=2)C=C1 FKLJPTJMIBLJAV-UHFFFAOYSA-N 0.000 description 2
- IZWSFJTYBVKZNK-UHFFFAOYSA-O N-dodecyl-N,N-dimethyl-3-ammonio-1-propanesulfonic acid Chemical compound CCCCCCCCCCCC[N+](C)(C)CCCS(O)(=O)=O IZWSFJTYBVKZNK-UHFFFAOYSA-O 0.000 description 2
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 229960003237 betaine Drugs 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 239000000539 dimer Substances 0.000 description 2
- UAUDZVJPLUQNMU-KTKRTIGZSA-N erucamide Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-KTKRTIGZSA-N 0.000 description 2
- NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 238000005191 phase separation Methods 0.000 description 2
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 2
- 239000012266 salt solution Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- KLSLBUSXWBJMEC-UHFFFAOYSA-N 4-Propylphenol Chemical compound CCCC1=CC=C(O)C=C1 KLSLBUSXWBJMEC-UHFFFAOYSA-N 0.000 description 1
- FCSKOFQQCWLGMV-UHFFFAOYSA-N 5-{5-[2-chloro-4-(4,5-dihydro-1,3-oxazol-2-yl)phenoxy]pentyl}-3-methylisoxazole Chemical compound O1N=C(C)C=C1CCCCCOC1=CC=C(C=2OCCN=2)C=C1Cl FCSKOFQQCWLGMV-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 241001012508 Carpiodes cyprinus Species 0.000 description 1
- KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical compound C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 description 1
- 108091006629 SLC13A2 Proteins 0.000 description 1
- BCKXLBQYZLBQEK-KVVVOXFISA-M Sodium oleate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC([O-])=O BCKXLBQYZLBQEK-KVVVOXFISA-M 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 229940027983 antiseptic and disinfectant quaternary ammonium compound Drugs 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 229910001570 bauxite Inorganic materials 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- YMKDRGPMQRFJGP-UHFFFAOYSA-M cetylpyridinium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 YMKDRGPMQRFJGP-UHFFFAOYSA-M 0.000 description 1
- 229960001927 cetylpyridinium chloride Drugs 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N glutaric acid Chemical compound OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- CQDGTJPVBWZJAZ-UHFFFAOYSA-N monoethyl carbonate Chemical class CCOC(O)=O CQDGTJPVBWZJAZ-UHFFFAOYSA-N 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000002691 unilamellar liposome Substances 0.000 description 1
- 239000002888 zwitterionic surfactant Substances 0.000 description 1
Classifications
-
- 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
- C09K8/584—Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids characterised by the use of specific surfactants
-
- 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
- C09K8/588—Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids characterised by the use of specific polymers
-
- 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
- C09K8/60—Compositions for stimulating production by acting on the underground formation
- C09K8/62—Compositions for forming crevices or fractures
-
- 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
- C09K8/60—Compositions for stimulating production by acting on the underground formation
- C09K8/62—Compositions for forming crevices or fractures
- C09K8/66—Compositions based on water or polar solvents
- C09K8/68—Compositions based on water or polar solvents containing organic compounds
-
- 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
- C09K8/60—Compositions for stimulating production by acting on the underground formation
- C09K8/62—Compositions for forming crevices or fractures
- C09K8/72—Eroding chemicals, e.g. acids
- C09K8/74—Eroding chemicals, e.g. acids combined with additives added for specific purposes
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21B—EARTH OR ROCK 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
- E21B43/25—Methods for stimulating production
- E21B43/26—Methods for stimulating production by forming crevices or fractures
-
- 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
- C09K2208/00—Aspects relating to compositions of drilling or well treatment fluids
- C09K2208/30—Viscoelastic surfactants [VES]
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Geology (AREA)
- Mining & Mineral Resources (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- General Chemical & Material Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Fluid Mechanics (AREA)
- Environmental & Geological Engineering (AREA)
- Colloid Chemistry (AREA)
- Cosmetics (AREA)
- Detergent Compositions (AREA)
- Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0323916A GB2406864A (en) | 2003-10-11 | 2003-10-11 | Viscoelastic fluid with increased thermal stability and reduced salt concentration |
GB0323916.7 | 2003-10-11 | ||
PCT/GB2004/004280 WO2005040554A1 (fr) | 2003-10-11 | 2004-10-11 | Gels tensioactifs viscoelastiques presentant une concentration reduite en sel |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2547919A1 CA2547919A1 (fr) | 2005-05-06 |
CA2547919C true CA2547919C (fr) | 2013-08-27 |
Family
ID=29433781
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA2547919A Expired - Fee Related CA2547919C (fr) | 2003-10-11 | 2004-10-11 | Gels tensioactifs viscoelastiques presentant une concentration reduite en sel |
Country Status (5)
Country | Link |
---|---|
US (1) | US20070213232A1 (fr) |
CA (1) | CA2547919C (fr) |
EA (1) | EA014308B1 (fr) |
GB (2) | GB2406864A (fr) |
WO (1) | WO2005040554A1 (fr) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2001270798A1 (en) | 2000-08-07 | 2002-02-18 | Schlumberger Canada Limited | Viscoelastic wellbore treatment fluid |
US7261160B2 (en) | 2005-09-13 | 2007-08-28 | Halliburton Energy Services, Inc. | Methods and compositions for controlling the viscosity of viscoelastic surfactant fluids |
CA2669617C (fr) | 2006-11-30 | 2015-11-10 | Basf Se | Systeme epaississant a ph commutable |
US7997342B2 (en) * | 2006-12-29 | 2011-08-16 | Halliburton Energy Services, Inc. | Subterranean treatment fluids comprising viscoelastic surfactant gels |
US7727935B2 (en) * | 2006-12-29 | 2010-06-01 | Halliburton Energy Services, Inc. | Dual-function additives for enhancing fluid loss control and stabilizing viscoelastic surfactant fluids |
US7718584B2 (en) * | 2006-12-29 | 2010-05-18 | Halliburton Energy Services, Inc. | Dual-function additives for enhancing fluid loss control and stabilizing viscoelastic surfactant fluids |
US8815785B2 (en) * | 2006-12-29 | 2014-08-26 | Halliburton Energy Services, Inc. | Utilization of surfactant as conformance materials |
US7939471B2 (en) * | 2006-12-29 | 2011-05-10 | Halliburton Energy Services, Inc. | Subterranean treatment fluids comprising viscoelastic surfactant gels |
GB2446801B (en) | 2007-02-23 | 2011-06-29 | Schlumberger Holdings | Wellbore treatment fluid |
US8193127B2 (en) * | 2008-02-04 | 2012-06-05 | Sanjel Corporation | Low residue fluid fracturing system and method of use |
US9315712B2 (en) * | 2009-04-07 | 2016-04-19 | Halliburton Energy Services, Inc. | Viscoelastic surfactants and methods of making and using same |
US8728990B2 (en) | 2009-12-04 | 2014-05-20 | Elementis Specialties, Inc. | Phosphate ester oil gellant |
FR3013055B1 (fr) | 2013-11-14 | 2020-05-15 | Arkema France | Composition fluide pour la stimulation dans le domaine de la production de petrole et de gaz |
US10017682B2 (en) * | 2014-01-17 | 2018-07-10 | Elevance Renewable Sciences, Inc. | Natural oil-derived wellbore compositions and methods of use |
US9670397B2 (en) | 2014-02-21 | 2017-06-06 | Halliburton Energy Services Inc. | Amido-functionalized gemini surfactant for fluid control in subterranean formations |
CN110819332B (zh) * | 2019-11-19 | 2022-03-15 | 西安石油大学 | 一种基于小分子凝胶对油水识别的智能驱油剂及其制备方法 |
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Publication number | Priority date | Publication date | Assignee | Title |
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CA1023239A (en) * | 1973-05-01 | 1977-12-27 | Leroy L. Carney | Water-in-oil emulsions and emulsifiers for preparing the same |
US5258137A (en) * | 1984-12-24 | 1993-11-02 | The Dow Chemical Company | Viscoelastic surfactant based foam fluids |
US5551516A (en) * | 1995-02-17 | 1996-09-03 | Dowell, A Division Of Schlumberger Technology Corporation | Hydraulic fracturing process and compositions |
US6435277B1 (en) * | 1996-10-09 | 2002-08-20 | Schlumberger Technology Corporation | Compositions containing aqueous viscosifying surfactants and methods for applying such compositions in subterranean formations |
US5964295A (en) * | 1996-10-09 | 1999-10-12 | Schlumberger Technology Corporation, Dowell Division | Methods and compositions for testing subterranean formations |
US5981446A (en) * | 1997-07-09 | 1999-11-09 | Schlumberger Technology Corporation | Apparatus, compositions, and methods of employing particulates as fracturing fluid compositions in subterranean formations |
US6302209B1 (en) * | 1997-09-10 | 2001-10-16 | Bj Services Company | Surfactant compositions and uses therefor |
US6035936A (en) * | 1997-11-06 | 2000-03-14 | Whalen; Robert T. | Viscoelastic surfactant fracturing fluids and a method for fracturing subterranean formations |
US5979555A (en) * | 1997-12-02 | 1999-11-09 | Akzo Nobel Nv | Surfactants for hydraulic fractoring compositions |
US6239183B1 (en) * | 1997-12-19 | 2001-05-29 | Akzo Nobel Nv | Method for controlling the rheology of an aqueous fluid and gelling agent therefor |
US6509301B1 (en) * | 1999-08-26 | 2003-01-21 | Daniel Patrick Vollmer | Well treatment fluids and methods for the use thereof |
CA2329600A1 (fr) * | 2000-12-22 | 2002-06-22 | Kewei Zhang | Fluide de fracturation |
AU2001270798A1 (en) * | 2000-08-07 | 2002-02-18 | Schlumberger Canada Limited | Viscoelastic wellbore treatment fluid |
GB2393722A (en) * | 2001-02-13 | 2004-04-07 | Schlumberger Holdings | Cleavable surfactants which may be useful in viscoelastic compositions for oil-field applications |
US7119050B2 (en) * | 2001-12-21 | 2006-10-10 | Schlumberger Technology Corporation | Fluid system having controllable reversible viscosity |
-
2003
- 2003-10-11 GB GB0323916A patent/GB2406864A/en not_active Withdrawn
-
2004
- 2004-10-11 GB GB0606698A patent/GB2422167B/en not_active Expired - Fee Related
- 2004-10-11 EA EA200600753A patent/EA014308B1/ru not_active IP Right Cessation
- 2004-10-11 CA CA2547919A patent/CA2547919C/fr not_active Expired - Fee Related
- 2004-10-11 WO PCT/GB2004/004280 patent/WO2005040554A1/fr active Application Filing
- 2004-10-11 US US10/574,592 patent/US20070213232A1/en not_active Abandoned
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GB0606698D0 (en) | 2006-05-10 |
GB2422167A (en) | 2006-07-19 |
EA200600753A1 (ru) | 2006-10-27 |
US20070213232A1 (en) | 2007-09-13 |
WO2005040554A1 (fr) | 2005-05-06 |
GB0323916D0 (en) | 2003-11-12 |
GB2422167B (en) | 2007-11-07 |
GB2406864A (en) | 2005-04-13 |
CA2547919A1 (fr) | 2005-05-06 |
EA014308B1 (ru) | 2010-10-29 |
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