WO2002064945A1 - Viscoelastic compositions - Google Patents
Viscoelastic compositions Download PDFInfo
- Publication number
- WO2002064945A1 WO2002064945A1 PCT/GB2002/000587 GB0200587W WO02064945A1 WO 2002064945 A1 WO2002064945 A1 WO 2002064945A1 GB 0200587 W GB0200587 W GB 0200587W WO 02064945 A1 WO02064945 A1 WO 02064945A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- cleavable
- surfactant
- formula
- viscoelastic
- aqueous
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 105
- 239000004094 surface-active agent Substances 0.000 claims abstract description 144
- 239000012530 fluid Substances 0.000 claims abstract description 80
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 50
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 28
- 239000003792 electrolyte Substances 0.000 claims abstract description 19
- 238000000034 method Methods 0.000 claims abstract description 16
- 239000000126 substance Substances 0.000 claims abstract description 13
- -1 ester chloride Chemical class 0.000 claims description 30
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- 150000003839 salts Chemical class 0.000 claims description 12
- 150000001450 anions Chemical class 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 108010065338 N-ethylglycine Proteins 0.000 claims description 9
- 125000001931 aliphatic group Chemical group 0.000 claims description 9
- 150000001408 amides Chemical class 0.000 claims description 9
- XACKAZKMZQZZDT-KTKRTIGZSA-N 2-[(z)-octadec-9-enyl]butanedioic acid Chemical group CCCCCCCC\C=C/CCCCCCCCC(C(O)=O)CC(O)=O XACKAZKMZQZZDT-KTKRTIGZSA-N 0.000 claims description 7
- 229910052799 carbon Inorganic materials 0.000 claims description 7
- 125000002091 cationic group Chemical group 0.000 claims description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
- 229920006395 saturated elastomer Polymers 0.000 claims description 6
- 125000000129 anionic group Chemical group 0.000 claims description 5
- 125000004185 ester group Chemical group 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims description 4
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 claims description 4
- 150000001768 cations Chemical class 0.000 claims description 4
- 125000001165 hydrophobic group Chemical group 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 238000005086 pumping Methods 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 2
- 238000005755 formation reaction Methods 0.000 abstract description 41
- 238000003776 cleavage reaction Methods 0.000 abstract description 8
- 230000007017 scission Effects 0.000 abstract description 8
- 230000008030 elimination Effects 0.000 abstract description 2
- 238000003379 elimination reaction Methods 0.000 abstract description 2
- 239000000499 gel Substances 0.000 description 77
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 45
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 35
- UAUDZVJPLUQNMU-KTKRTIGZSA-N erucamide Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-KTKRTIGZSA-N 0.000 description 28
- 239000000047 product Substances 0.000 description 28
- 239000000243 solution Substances 0.000 description 25
- 150000002148 esters Chemical class 0.000 description 24
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 22
- 150000002430 hydrocarbons Chemical class 0.000 description 22
- 239000001103 potassium chloride Substances 0.000 description 22
- 235000011164 potassium chloride Nutrition 0.000 description 22
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 20
- 230000006870 function Effects 0.000 description 19
- 229930195733 hydrocarbon Natural products 0.000 description 19
- 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 description 19
- 239000003921 oil Substances 0.000 description 17
- 239000004215 Carbon black (E152) Substances 0.000 description 16
- 238000006243 chemical reaction Methods 0.000 description 15
- JFCQEDHGNNZCLN-UHFFFAOYSA-N glutaric acid Chemical compound OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 15
- 208000010392 Bone Fractures Diseases 0.000 description 13
- 206010017076 Fracture Diseases 0.000 description 13
- 150000001412 amines Chemical class 0.000 description 13
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 13
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- 239000000693 micelle Substances 0.000 description 11
- FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 description 11
- 229940113162 oleylamide Drugs 0.000 description 11
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- 239000000839 emulsion Substances 0.000 description 9
- CFOQKXQWGLAKSK-KTKRTIGZSA-N (13Z)-docosen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCCO CFOQKXQWGLAKSK-KTKRTIGZSA-N 0.000 description 8
- 238000000354 decomposition reaction Methods 0.000 description 8
- 239000007864 aqueous solution Substances 0.000 description 7
- 235000011056 potassium acetate Nutrition 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 6
- 238000003786 synthesis reaction Methods 0.000 description 6
- SNPIXHALJNCKOI-KTKRTIGZSA-N [(z)-docos-13-enyl] 2-chloroacetate Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCCOC(=O)CCl SNPIXHALJNCKOI-KTKRTIGZSA-N 0.000 description 5
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 5
- 239000012044 organic layer Substances 0.000 description 5
- 239000003208 petroleum Substances 0.000 description 5
- 239000011148 porous material Substances 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 230000035882 stress Effects 0.000 description 5
- CFOQKXQWGLAKSK-UHFFFAOYSA-N 13-docosen-1-ol Natural products CCCCCCCCC=CCCCCCCCCCCCCO CFOQKXQWGLAKSK-UHFFFAOYSA-N 0.000 description 4
- 241001012508 Carpiodes cyprinus Species 0.000 description 4
- 230000002378 acidificating effect Effects 0.000 description 4
- 230000015556 catabolic process Effects 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- DPUOLQHDNGRHBS-KTKRTIGZSA-N erucic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-KTKRTIGZSA-N 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 230000003534 oscillatory effect Effects 0.000 description 4
- 230000035699 permeability Effects 0.000 description 4
- 238000000518 rheometry Methods 0.000 description 4
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 4
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 3
- DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 3
- URXZXNYJPAJJOQ-UHFFFAOYSA-N Erucic acid Natural products CCCCCCC=CCCCCCCCCCCCC(O)=O URXZXNYJPAJJOQ-UHFFFAOYSA-N 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 238000013459 approach Methods 0.000 description 3
- CMPOVQUVPYXEBN-UHFFFAOYSA-N bis(2-hydroxyethyl)-methylazanium;chloride Chemical compound Cl.OCCN(C)CCO CMPOVQUVPYXEBN-UHFFFAOYSA-N 0.000 description 3
- 229910002092 carbon dioxide Inorganic materials 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- 230000008878 coupling Effects 0.000 description 3
- 238000010168 coupling process Methods 0.000 description 3
- 238000005859 coupling reaction Methods 0.000 description 3
- 230000001419 dependent effect Effects 0.000 description 3
- 239000006260 foam Substances 0.000 description 3
- 230000001965 increasing effect Effects 0.000 description 3
- 230000003993 interaction Effects 0.000 description 3
- 239000000543 intermediate Substances 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 238000004949 mass spectrometry Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 230000002829 reductive effect Effects 0.000 description 3
- 239000011435 rock Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 239000001384 succinic acid Substances 0.000 description 3
- 229940014800 succinic anhydride Drugs 0.000 description 3
- 239000002562 thickening agent Substances 0.000 description 3
- 238000004809 thin layer chromatography Methods 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 2
- BRRUPRMXQXEZAR-KTKRTIGZSA-N 4-[(z)-octadec-9-enoxy]-4-oxobutanoic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCOC(=O)CCC(O)=O BRRUPRMXQXEZAR-KTKRTIGZSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- 208000005156 Dehydration Diseases 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 125000003368 amide group Chemical group 0.000 description 2
- UCMIRNVEIXFBKS-UHFFFAOYSA-N beta-alanine Chemical compound NCCC(O)=O UCMIRNVEIXFBKS-UHFFFAOYSA-N 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- VILAVOFMIJHSJA-UHFFFAOYSA-N dicarbon monoxide Chemical group [C]=C=O VILAVOFMIJHSJA-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 230000000670 limiting effect Effects 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- DAZXVJBJRMWXJP-UHFFFAOYSA-N n,n-dimethylethylamine Chemical compound CCN(C)C DAZXVJBJRMWXJP-UHFFFAOYSA-N 0.000 description 2
- 230000036961 partial effect Effects 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 230000002441 reversible effect Effects 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 230000000638 stimulation Effects 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- QGLWBTPVKHMVHM-KTKRTIGZSA-N (z)-octadec-9-en-1-amine Chemical compound CCCCCCCC\C=C/CCCCCCCCN QGLWBTPVKHMVHM-KTKRTIGZSA-N 0.000 description 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- KEWNKZNZRIAIAK-UHFFFAOYSA-N 2,3,5,6-tetrachlorophenol Chemical compound OC1=C(Cl)C(Cl)=CC(Cl)=C1Cl KEWNKZNZRIAIAK-UHFFFAOYSA-N 0.000 description 1
- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 1
- ATCRIUVQKHMXSH-UHFFFAOYSA-N 2,4-dichlorobenzoic acid Chemical class OC(=O)C1=CC=C(Cl)C=C1Cl ATCRIUVQKHMXSH-UHFFFAOYSA-N 0.000 description 1
- 229940087195 2,4-dichlorophenoxyacetate Drugs 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- LBLYYCQCTBFVLH-UHFFFAOYSA-M 2-methylbenzenesulfonate Chemical compound CC1=CC=CC=C1S([O-])(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-M 0.000 description 1
- TVMKSGXYTVKNRK-UHFFFAOYSA-N 3,5,6-trichloropyridine-2-carboxylic acid Chemical compound OC(=O)C1=NC(Cl)=C(Cl)C=C1Cl TVMKSGXYTVKNRK-UHFFFAOYSA-N 0.000 description 1
- LULAYUGMBFYYEX-UHFFFAOYSA-N 3-chlorobenzoic acid Chemical class OC(=O)C1=CC=CC(Cl)=C1 LULAYUGMBFYYEX-UHFFFAOYSA-N 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- VGCXGMAHQTYDJK-UHFFFAOYSA-N Chloroacetyl chloride Chemical compound ClCC(Cl)=O VGCXGMAHQTYDJK-UHFFFAOYSA-N 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- 229910017741 MH2O Inorganic materials 0.000 description 1
- 208000006670 Multiple fractures Diseases 0.000 description 1
- OKIZCWYLBDKLSU-UHFFFAOYSA-M N,N,N-Trimethylmethanaminium chloride Chemical compound [Cl-].C[N+](C)(C)C OKIZCWYLBDKLSU-UHFFFAOYSA-M 0.000 description 1
- YPIGGYHFMKJNKV-UHFFFAOYSA-N N-ethylglycine Chemical compound CC[NH2+]CC([O-])=O YPIGGYHFMKJNKV-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 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 1
- JNGWKQJZIUZUPR-UHFFFAOYSA-N [3-(dodecanoylamino)propyl](hydroxy)dimethylammonium Chemical compound CCCCCCCCCCCC(=O)NCCC[N+](C)(C)[O-] JNGWKQJZIUZUPR-UHFFFAOYSA-N 0.000 description 1
- 150000001266 acyl halides Chemical class 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 239000003570 air Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910001413 alkali metal ion Inorganic materials 0.000 description 1
- 229910001615 alkaline earth metal halide Inorganic materials 0.000 description 1
- 159000000013 aluminium salts Chemical class 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 229940000635 beta-alanine Drugs 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 229910001622 calcium bromide Inorganic materials 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- WGEFECGEFUFIQW-UHFFFAOYSA-L calcium dibromide Chemical compound [Ca+2].[Br-].[Br-] WGEFECGEFUFIQW-UHFFFAOYSA-L 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000007806 chemical reaction intermediate Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 230000005595 deprotonation Effects 0.000 description 1
- 238000010537 deprotonation reaction Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000002979 fabric softener Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000007667 floating Methods 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000008398 formation water Substances 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- VANNPISTIUFMLH-UHFFFAOYSA-N glutaric anhydride Chemical compound O=C1CCCC(=O)O1 VANNPISTIUFMLH-UHFFFAOYSA-N 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-M naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-M 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 150000002891 organic anions Chemical class 0.000 description 1
- 230000010355 oscillation Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000000246 remedial effect Effects 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
- 229960001860 salicylate Drugs 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 230000003019 stabilising effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000006277 sulfonation reaction Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 150000003754 zirconium Chemical class 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
- C09K8/60—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
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C229/04—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C229/06—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton
- C07C229/10—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton the nitrogen atom of the amino group being further bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings
- C07C229/12—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton the nitrogen atom of the amino group being further bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings to carbon atoms of acyclic carbon skeletons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/34—Esters of acyclic saturated polycarboxylic acids having an esterified carboxyl group bound to an acyclic carbon atom
- C07C69/40—Succinic acid esters
-
- 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
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/18—Quaternary ammonium 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
-
- 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)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Detergent Compositions (AREA)
- Lubricants (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Liquid Carbonaceous Fuels (AREA)
- Colloid Chemistry (AREA)
Abstract
Description
Claims
Priority Applications (10)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EA200300896A EA006450B1 (en) | 2001-02-13 | 2002-02-13 | Viscoelastic compositions |
MXPA03007219A MXPA03007219A (en) | 2001-02-13 | 2002-02-13 | Viscoelastic compositions. |
EP02712051A EP1360395A1 (en) | 2001-02-13 | 2002-02-13 | Viscoelastic compositions |
CA2434613A CA2434613C (en) | 2001-02-13 | 2002-02-13 | Viscoelastic compositions |
US10/250,415 US7704926B2 (en) | 2001-02-13 | 2002-02-13 | Viscoelastic compositions |
BRPI0207484-2A BR0207484B1 (en) | 2001-02-13 | 2002-02-13 | well drilling service fluid and method for fracturing an underground formation. |
AU2002231958A AU2002231958C1 (en) | 2001-02-13 | 2002-02-13 | Viscoelastic compositions |
NO20033572A NO20033572L (en) | 2001-02-13 | 2003-08-12 | Viscoelastic mixtures |
US12/466,411 US8785355B2 (en) | 2001-02-13 | 2009-05-15 | Viscoelastic compositions |
US14/303,196 US20150072905A1 (en) | 2001-02-13 | 2014-06-12 | Viscoelastic compositions |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0103449.5 | 2001-02-13 | ||
GB0103449A GB2372058B (en) | 2001-02-13 | 2001-02-13 | Viscoelastic compositions |
Related Child Applications (4)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10250415 A-371-Of-International | 2002-02-12 | ||
US10/250,415 A-371-Of-International US7704926B2 (en) | 2001-02-13 | 2002-02-13 | Viscoelastic compositions |
US10/993,985 Continuation-In-Part US20050124525A1 (en) | 2001-02-13 | 2004-11-19 | Anionic viscoelastic surfactant |
US12/466,411 Continuation-In-Part US8785355B2 (en) | 2001-02-13 | 2009-05-15 | Viscoelastic compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2002064945A1 true WO2002064945A1 (en) | 2002-08-22 |
Family
ID=9908579
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/GB2002/000606 WO2002064947A1 (en) | 2001-02-13 | 2002-02-13 | Aqueous viscoelastic fluid |
PCT/GB2002/000587 WO2002064945A1 (en) | 2001-02-13 | 2002-02-13 | Viscoelastic compositions |
PCT/GB2002/000589 WO2002064946A1 (en) | 2001-02-13 | 2002-02-13 | Aqueous viscoelastic fluid |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/GB2002/000606 WO2002064947A1 (en) | 2001-02-13 | 2002-02-13 | Aqueous viscoelastic fluid |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/GB2002/000589 WO2002064946A1 (en) | 2001-02-13 | 2002-02-13 | Aqueous viscoelastic fluid |
Country Status (12)
Country | Link |
---|---|
US (4) | US7410934B2 (en) |
EP (2) | EP1360394A1 (en) |
CN (2) | CN1606654B (en) |
AU (2) | AU2002229950B2 (en) |
BR (2) | BR0207483B1 (en) |
CA (3) | CA2434613C (en) |
EA (3) | EA006450B1 (en) |
GB (4) | GB2393722A (en) |
MX (2) | MXPA03007219A (en) |
NO (2) | NO20033573L (en) |
OA (2) | OA12446A (en) |
WO (3) | WO2002064947A1 (en) |
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7022861B1 (en) | 2004-06-10 | 2006-04-04 | Sandia National Laboratories | Thermally cleavable surfactants |
US7081439B2 (en) | 2003-11-13 | 2006-07-25 | Schlumberger Technology Corporation | Methods for controlling the fluid loss properties of viscoelastic surfactant based fluids |
US7287590B1 (en) | 2006-09-18 | 2007-10-30 | Schlumberger Technology Corporation | Internal breaker for oilfield fluids |
WO2008117222A1 (en) * | 2007-03-26 | 2008-10-02 | Schlumberger Canada Limited | Method for treating subterranean formation |
US7635028B2 (en) | 2006-09-18 | 2009-12-22 | Schlumberger Technology Corporation | Acidic internal breaker for viscoelastic surfactant fluids in brine |
US7677311B2 (en) | 2002-08-26 | 2010-03-16 | Schlumberger Technology Corporation | Internal breaker for oilfield treatments |
US7728044B2 (en) * | 2005-03-16 | 2010-06-01 | Baker Hughes Incorporated | Saponified fatty acids as breakers for viscoelastic surfactant-gelled fluids |
US7772164B2 (en) | 2004-06-02 | 2010-08-10 | Rhodia, Inc. | Multicomponent viscoelastic surfactant fluid and method of using as a fracturing fluid |
US7776798B2 (en) | 1999-09-07 | 2010-08-17 | Akzo Nobel Surface Chemistry Llc | Quaternary ammonium salts as thickening agents for aqueous systems |
US7879770B2 (en) | 2006-09-18 | 2011-02-01 | Schlumberger Technology Corporation | Oxidative internal breaker for viscoelastic surfactant fluids |
US8044106B2 (en) * | 2005-03-16 | 2011-10-25 | Baker Hughes Incorporated | Saponified fatty acids as viscosity modifiers for viscoelastic surfactant-gelled fluids |
US8067342B2 (en) | 2006-09-18 | 2011-11-29 | Schlumberger Technology Corporation | Internal breakers for viscoelastic surfactant fluids |
US8141637B2 (en) | 2009-08-11 | 2012-03-27 | Schlumberger Technology Corporation | Manipulation of flow underground |
US8143197B2 (en) | 2001-12-22 | 2012-03-27 | Schlumberger Technology Corporation | Aqueous fracturing fluid |
JP2012529663A (en) * | 2009-06-11 | 2012-11-22 | エシロール アテルナジオナール カンパニー ジェネラーレ デ オプティック | Curable coating composition modified with a cleavable surfactant to improve adhesion of multilayer coating stacks |
US8481462B2 (en) | 2006-09-18 | 2013-07-09 | Schlumberger Technology Corporation | Oxidative internal breaker system with breaking activators for viscoelastic surfactant fluids |
US8695708B2 (en) | 2007-03-26 | 2014-04-15 | Schlumberger Technology Corporation | Method for treating subterranean formation with degradable material |
US8785355B2 (en) | 2001-02-13 | 2014-07-22 | Schlumberger Technology Corporation | Viscoelastic compositions |
Families Citing this family (106)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002011874A1 (en) | 2000-08-07 | 2002-02-14 | Sofitech N.V. | 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 |
GB2408506B (en) * | 2003-11-29 | 2007-06-13 | Schlumberger Holdings | Anionic viscoelastic surfactant |
US6908888B2 (en) * | 2001-04-04 | 2005-06-21 | Schlumberger Technology Corporation | Viscosity reduction of viscoelastic surfactant based fluids |
US7168489B2 (en) * | 2001-06-11 | 2007-01-30 | Halliburton Energy Services, Inc. | Orthoester compositions and methods for reducing the viscosified treatment fluids |
US8273693B2 (en) | 2001-12-12 | 2012-09-25 | Clearwater International Llc | Polymeric gel system and methods for making and using same in hydrocarbon recovery |
US6929070B2 (en) | 2001-12-21 | 2005-08-16 | Schlumberger Technology Corporation | Compositions and methods for treating a subterranean formation |
US7066260B2 (en) * | 2002-08-26 | 2006-06-27 | Schlumberger Technology Corporation | Dissolving filter cake |
US7219731B2 (en) * | 2002-08-26 | 2007-05-22 | Schlumberger Technology Corporation | Degradable additive for viscoelastic surfactant based fluid systems |
US7157409B2 (en) | 2002-09-25 | 2007-01-02 | M-I Llc | Surfactant-polymer compositions for enhancing the stability of viscoelastic-surfactant based fluid |
CA2501318A1 (en) * | 2002-10-10 | 2004-04-22 | Yeda Research And Development Co. Ltd | Basic esters of fatty alcohols and their use as anti-inflammatory or immunomodulatory agents |
US7345012B2 (en) | 2004-12-15 | 2008-03-18 | Schlumberger Technology Corporation | Foamed viscoelastic surfactants |
US6959588B2 (en) * | 2003-06-19 | 2005-11-01 | Schlumberger Technology Corporation | Couette device and method to study solids deposition from flowing fluids |
US7303018B2 (en) | 2003-07-22 | 2007-12-04 | Bj Services Company | Method of acidizing a subterranean formation with diverting foam or fluid |
US7148184B2 (en) | 2003-07-22 | 2006-12-12 | Schlumberger Technology Corporation | Self-diverting foamed system |
GB2406864A (en) * | 2003-10-11 | 2005-04-13 | Schlumberger Holdings | Viscoelastic fluid with increased thermal stability and reduced salt concentration |
US7073588B2 (en) * | 2004-02-27 | 2006-07-11 | Halliburton Energy Services, Inc. | Esterquat acidic subterranean treatment fluids and methods of using esterquats acidic subterranean treatment fluids |
US7534745B2 (en) * | 2004-05-05 | 2009-05-19 | Halliburton Energy Services, Inc. | Gelled invert emulsion compositions comprising polyvalent metal salts of an organophosphonic acid ester or an organophosphinic acid and methods of use and manufacture |
US7703531B2 (en) * | 2004-05-13 | 2010-04-27 | Baker Hughes Incorporated | Multifunctional nanoparticles for downhole formation treatments |
US8499832B2 (en) * | 2004-05-13 | 2013-08-06 | Baker Hughes Incorporated | Re-use of surfactant-containing fluids |
US8196659B2 (en) * | 2004-05-13 | 2012-06-12 | Baker Hughes Incorporated | Multifunctional particles for downhole formation treatments |
US7723272B2 (en) * | 2007-02-26 | 2010-05-25 | Baker Hughes Incorporated | Methods and compositions for fracturing subterranean formations |
US8567502B2 (en) * | 2004-05-13 | 2013-10-29 | Baker Hughes Incorporated | Filtration of dangerous or undesirable contaminants |
US8226830B2 (en) | 2008-04-29 | 2012-07-24 | Baker Hughes Incorporated | Wastewater purification with nanoparticle-treated bed |
AU2005269800B8 (en) | 2004-07-19 | 2011-12-01 | Celator Pharmaceuticals, Inc. | Particulate constructs for release of active agents |
US7237608B2 (en) | 2004-10-20 | 2007-07-03 | Schlumberger Technology Corporation | Self diverting matrix acid |
US7303019B2 (en) | 2005-02-15 | 2007-12-04 | Halliburton Energy Services, Inc. | Viscoelastic surfactant fluids and associated diverting methods |
US7299874B2 (en) | 2005-02-15 | 2007-11-27 | Halliburton Energy Services, Inc. | Viscoelastic surfactant fluids and associated methods |
US7159659B2 (en) | 2005-02-15 | 2007-01-09 | Halliburton Energy Services, Inc. | Viscoelastic surfactant fluids and associated acidizing methods |
US7696135B2 (en) | 2005-03-16 | 2010-04-13 | Baker Hughes Incorporated | Use of oil-soluble surfactants as breaker enhancers for VES-gelled fluids |
US7645724B2 (en) * | 2005-03-16 | 2010-01-12 | Baker Hughes Incorporated | Compositions and use of mono- and polyenoic acids for breaking VES-gelled fluids |
US7696134B2 (en) | 2005-03-16 | 2010-04-13 | Baker Hughes Incorporated | Unsaturated fatty acids and mineral oils as internal breakers for VES-gelled fluids |
US7662753B2 (en) * | 2005-05-12 | 2010-02-16 | Halliburton Energy Services, Inc. | Degradable surfactants and methods for use |
US7677315B2 (en) * | 2005-05-12 | 2010-03-16 | Halliburton Energy Services, Inc. | Degradable surfactants and methods for use |
US7608567B2 (en) * | 2005-05-12 | 2009-10-27 | Halliburton Energy Services, Inc. | Degradable surfactants and methods for use |
US7261160B2 (en) * | 2005-09-13 | 2007-08-28 | Halliburton Energy Services, Inc. | Methods and compositions for controlling the viscosity of viscoelastic surfactant fluids |
US20070060482A1 (en) * | 2005-09-13 | 2007-03-15 | Halliburton Energy Services, Inc. | Methods and compositions for controlling the viscosity of viscoelastic surfactant fluids |
US7713916B2 (en) | 2005-09-22 | 2010-05-11 | Halliburton Energy Services, Inc. | Orthoester-based surfactants and associated methods |
US20070066493A1 (en) * | 2005-09-22 | 2007-03-22 | Halliburton Energy Services, Inc. | Orthoester-based surfactants and associated methods |
CA2628498C (en) | 2005-11-07 | 2015-03-31 | Paul W. Knox | Viscoelastic compositions comprising polycationic quaternary ammonium compounds |
EP2256175B1 (en) | 2005-11-14 | 2017-01-18 | Stepan Company | Viscoelastic cationic carbohydrate ether compositions |
US20070125542A1 (en) * | 2005-12-07 | 2007-06-07 | Akzo Nobel N.V. | High temperature gellant in low and high density brines |
US20070287301A1 (en) * | 2006-03-31 | 2007-12-13 | Huiwen Xu | Method to minimize wet etch undercuts and provide pore sealing of extreme low k (k<2.5) dielectrics |
US9120964B2 (en) | 2006-08-04 | 2015-09-01 | Halliburton Energy Services, Inc. | Treatment fluids containing biodegradable chelating agents and methods for use thereof |
US9127194B2 (en) | 2006-08-04 | 2015-09-08 | Halliburton Energy Services, Inc. | Treatment fluids containing a boron trifluoride complex and methods for use thereof |
US9027647B2 (en) | 2006-08-04 | 2015-05-12 | Halliburton Energy Services, Inc. | Treatment fluids containing a biodegradable chelating agent and methods for use thereof |
US8567504B2 (en) | 2006-08-04 | 2013-10-29 | Halliburton Energy Services, Inc. | Composition and method relating to the prevention and remediation of surfactant gel damage |
US8567503B2 (en) * | 2006-08-04 | 2013-10-29 | Halliburton Energy Services, Inc. | Composition and method relating to the prevention and remediation of surfactant gel damage |
US8008236B2 (en) | 2006-10-27 | 2011-08-30 | Halliburton Energy Services, Inc. | Ortho ester breakers for viscoelastic surfactant gels and associated methods |
US8012914B2 (en) | 2006-10-27 | 2011-09-06 | Halliburton Energy Services, Inc. | Ortho ester breakers for viscoelastic surfactant gels and associated methods |
US9018146B2 (en) * | 2006-11-22 | 2015-04-28 | Baker Hughes Incorporated | Method of treating a well with viscoelastic surfactant and viscosification activator |
US8220548B2 (en) * | 2007-01-12 | 2012-07-17 | Halliburton Energy Services Inc. | Surfactant wash treatment fluids and associated methods |
US20080169103A1 (en) * | 2007-01-12 | 2008-07-17 | Carbajal David L | Surfactant Wash Treatment Fluids and Associated Methods |
US7699106B2 (en) * | 2007-02-13 | 2010-04-20 | Bj Services Company | Method for reducing fluid loss during hydraulic fracturing or sand control treatment |
GB2446801B (en) | 2007-02-23 | 2011-06-29 | Schlumberger Holdings | Wellbore treatment fluid |
US9428684B2 (en) * | 2007-10-31 | 2016-08-30 | Rhodia Operation | Addition of zwitterionic surfactant to water soluble polymer to increase the stability of the polymers in aqueous solutions containing salt and/or surfactants |
US7789160B2 (en) * | 2007-10-31 | 2010-09-07 | Rhodia Inc. | Addition of nonionic surfactants to water soluble block copolymers to increase the stability of the copolymer in aqueous solutions containing salt and/or surfactants |
DE102007059844A1 (en) * | 2007-12-12 | 2009-06-25 | Basf Construction Polymers Gmbh | Copolymer based on a sulfonic acid-containing compound |
WO2009097189A1 (en) * | 2008-01-28 | 2009-08-06 | Schlumberger Canada Limited | Well thermal insulation for formation sampling of viscous fluids |
JP5101324B2 (en) * | 2008-02-07 | 2012-12-19 | 日立建機株式会社 | Arrangement structure of NOx reduction device for construction machinery |
US7906464B2 (en) | 2008-05-13 | 2011-03-15 | Halliburton Energy Services, Inc. | Compositions and methods for the removal of oil-based filtercakes |
CN102170781B (en) * | 2008-09-04 | 2015-04-08 | 阿克佐诺贝尔股份有限公司 | Viscoelastic system for drift reduction |
US7833943B2 (en) | 2008-09-26 | 2010-11-16 | Halliburton Energy Services Inc. | Microemulsifiers and methods of making and using same |
US9315712B2 (en) * | 2009-04-07 | 2016-04-19 | Halliburton Energy Services, Inc. | Viscoelastic surfactants and methods of making and using same |
US7846877B1 (en) * | 2009-05-20 | 2010-12-07 | Halliburton Energy Services, Inc. | Methods for treating a well using a treatment fluid containing a water-soluble polysaccharide, a water-soluble salt, and urea |
US20110009299A1 (en) * | 2009-07-10 | 2011-01-13 | Van Zanten Ryan | Emulsion stabilizing agents for drilling and completion fluids |
US8459360B2 (en) * | 2009-09-02 | 2013-06-11 | Board Of Regents, The University Of Texas System | Di-functional surfactants for enhanced oil recovery |
US20110077311A1 (en) * | 2009-09-25 | 2011-03-31 | Chevron U.S.A. Inc. | Method for handling viscous liquid crude hydrocarbons |
US20110105369A1 (en) * | 2009-10-30 | 2011-05-05 | Halliburton Energy Services, Inc. | Well treatment fluids containing a viscoelastic surfactant and a cross-linking agent comprising a water-soluble transition metal complex |
US8347960B2 (en) * | 2010-01-25 | 2013-01-08 | Water Tectonics, Inc. | Method for using electrocoagulation in hydraulic fracturing |
US20130048283A1 (en) * | 2010-04-27 | 2013-02-28 | Schlumberger Technology Corporation | Subterranean Reservoir Treatment Method |
US8448706B2 (en) | 2010-08-25 | 2013-05-28 | Schlumberger Technology Corporation | Delivery of particulate material below ground |
US9234415B2 (en) | 2010-08-25 | 2016-01-12 | Schlumberger Technology Corporation | Delivery of particulate material below ground |
US8714248B2 (en) | 2010-08-25 | 2014-05-06 | Schlumberger Technology Corporation | Method of gravel packing |
US8459353B2 (en) | 2010-08-25 | 2013-06-11 | Schlumberger Technology Corporation | Delivery of particulate material below ground |
US8524639B2 (en) | 2010-09-17 | 2013-09-03 | Clearwater International Llc | Complementary surfactant compositions and methods for making and using same |
US8618025B2 (en) * | 2010-12-16 | 2013-12-31 | Nalco Company | Composition and method for reducing hydrate agglomeration |
US8881823B2 (en) | 2011-05-03 | 2014-11-11 | Halliburton Energy Services, Inc. | Environmentally friendly low temperature breaker systems and related methods |
US9334716B2 (en) | 2012-04-12 | 2016-05-10 | Halliburton Energy Services, Inc. | Treatment fluids comprising a hydroxypyridinecarboxylic acid and methods for use thereof |
AU2013245868A1 (en) * | 2012-04-12 | 2014-10-30 | Baker Hughes Incorporated | Method of increasing the permeability of a subterranean formation by creating a multiple fracture network |
JP6183039B2 (en) * | 2012-12-12 | 2017-08-23 | 東洋製罐株式会社 | Dispersion liquid for excavation and mining method using the same |
CN103071424B (en) * | 2013-02-16 | 2015-05-20 | 中国石油大学(华东) | Medium-high temperature resistant viscoelasticity surfactant, clean fracturing fluid and preparation method |
US9670399B2 (en) | 2013-03-15 | 2017-06-06 | Halliburton Energy Services, Inc. | Methods for acidizing a subterranean formation using a stabilized microemulsion carrier fluid |
WO2014167374A1 (en) * | 2013-04-09 | 2014-10-16 | Services Petroliers Schlumberger (Sps) | Compositions and methods for completing subterranean wells |
CN103272524B (en) * | 2013-06-21 | 2014-11-26 | 山东大学 | Preparation method for fluid of increasing viscoelasticity of anionic/cationic surfactant through polymer |
CA2921813C (en) * | 2013-08-26 | 2021-07-13 | Sasol Chemicals (Usa) Llc | Aliphatic polycarbonate-based surface active agents |
US10017682B2 (en) * | 2014-01-17 | 2018-07-10 | Elevance Renewable Sciences, Inc. | Natural oil-derived wellbore compositions and methods of use |
US9932511B2 (en) | 2014-01-17 | 2018-04-03 | Elevance Renewable Sciences, Inc. | Natural oil-derived wellbore compositions and methods of use |
CN104028163A (en) * | 2014-06-24 | 2014-09-10 | 江苏万淇生物科技有限公司 | Method for synthesizing cardanol quaternary ammonium surfactant |
US10161222B2 (en) | 2014-11-05 | 2018-12-25 | Schlumberger Technology Corporation | Compositions and methods for servicing subterranean wells |
WO2016083322A1 (en) * | 2014-11-24 | 2016-06-02 | Akzo Nobel Chemicals International B.V. | Delayed breaker for viscoelastic surfactant-based fluids |
CN104645875B (en) * | 2014-12-16 | 2016-09-07 | 江南大学 | Viscoelastic system that a kind of functionalization Gemini surface active is constructed and preparation method |
CN104549077B (en) * | 2014-12-25 | 2016-08-17 | 中国石油大学(北京) | A kind of cationic and anionic surfactant mixed system gel and preparation method thereof |
WO2017010983A1 (en) * | 2015-07-13 | 2017-01-19 | Elevance Renewable Sciences, Inc. | Natural oil-derived wellbore compositions and methods of use |
CN106946743B (en) * | 2017-05-02 | 2019-06-21 | 中国科学技术大学 | A kind of gemini cationic surfactant and preparation method thereof and fracturing fluid |
CN109111906B (en) * | 2018-09-19 | 2020-10-13 | 中国石油化工股份有限公司 | Thick oil emulsifying viscosity reducer |
CN109135709B (en) * | 2018-09-19 | 2020-10-13 | 中国石油化工股份有限公司 | Viscosity-reducing oil displacement agent and oil displacement system suitable for heavy oil reservoir |
GB2583070B (en) | 2019-03-20 | 2023-09-13 | Schlumberger Technology Bv | Viscosification of aqueous solutions |
US11505503B2 (en) | 2019-04-18 | 2022-11-22 | Corning Incorporated | Ceramic honeycomb bodies and manufacture |
AU2020306004A1 (en) * | 2019-06-27 | 2022-01-06 | Schlumberger Technology B.V. | Additives to temporarily reduce viscosities in oil-based fluids |
CN113621361B (en) * | 2021-08-09 | 2022-10-21 | 中国石油天然气股份有限公司 | Cationic viscoelastic surfactant, preparation method and application thereof, and fracturing fluid |
US11814570B2 (en) | 2021-08-19 | 2023-11-14 | Schlumberger Technology Corporation | Amide emulsifier for high-temperature oil-based drilling fluid |
US11713412B2 (en) | 2021-11-12 | 2023-08-01 | Saudi Arabian Oil Company | Piperazine-based viscoelastic surfactants for hydraulic fracturing applications |
US11739255B2 (en) | 2021-11-12 | 2023-08-29 | Saudi Arabian Oil Company | Methods and compositions of piperazine-based viscoelastic surfactants as diversion agents |
US11746279B2 (en) | 2021-11-12 | 2023-09-05 | Saudi Arabian Oil Company | Fracturing fluids based on viscoelastic surfactants |
US11643590B1 (en) | 2021-11-12 | 2023-05-09 | Saudi Arabian Oil Company | Methods and compositions of using viscoelastic surfactants as diversion agents |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5258137A (en) * | 1984-12-24 | 1993-11-02 | The Dow Chemical Company | Viscoelastic surfactant based foam fluids |
WO1998056497A1 (en) * | 1997-06-10 | 1998-12-17 | Rhodia Inc. | Fluids containing viscoelastic surfactant and methods for using the same |
WO2001018147A1 (en) * | 1999-09-07 | 2001-03-15 | Crompton Corporation | Quaternary ammonium salts as thickening agents for aqueous systems |
Family Cites Families (34)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE519671A (en) * | 1952-05-06 | |||
NL198202A (en) * | 1954-06-21 | |||
US2836560A (en) * | 1955-05-02 | 1958-05-27 | Shell Dev | Water- and corrosion-resistant lubricating greases gelled with inorganic colloids |
US3302711A (en) * | 1964-09-22 | 1967-02-07 | Shell Oil Co | Petroleum recovery with chemical interacting floods forming organic sulfonates |
US3762932A (en) * | 1967-06-21 | 1973-10-02 | Paniplus Co | Bakery products containing emulsification and improving agents |
US3886293A (en) * | 1971-04-01 | 1975-05-27 | Ici America Inc | Food products containing surfactants |
US4806256A (en) * | 1984-06-18 | 1989-02-21 | The Dow Chemical Company | Water-based hydraulic fluids |
WO1994009852A1 (en) | 1992-03-09 | 1994-05-11 | The Dow Chemical Company | Viscoelastic surfactant based foam fluids |
US4853138A (en) * | 1987-08-05 | 1989-08-01 | The Standard Oil Company | C-branched zwitterionic surfactants and enhanced oil recovery method using same |
DE3929866A1 (en) * | 1989-09-08 | 1991-03-21 | Bayer Ag | FISSILE SURFACES, METHOD FOR THEIR PRODUCTION AND THEIR USE |
JPH04327570A (en) * | 1991-02-12 | 1992-11-17 | Hoechst Ag | Alkyl ether carboxylic acid tauride |
ATE150481T1 (en) | 1992-06-10 | 1997-04-15 | Procter & Gamble | STABLE, BIODEGRADABLE TISSUE PLASTICIZER COMPOSITIONS |
US5466396A (en) * | 1993-11-19 | 1995-11-14 | Lever Brothers Company | Isethionate esters of alkyl alkoxy carboxylic acid |
DE4435495C2 (en) * | 1994-10-04 | 1997-08-14 | Henkel Kgaa | Pumpable aqueous surfactant concentrates |
US5551516A (en) * | 1995-02-17 | 1996-09-03 | Dowell, A Division Of Schlumberger Technology Corporation | Hydraulic fracturing process and compositions |
DE19520884A1 (en) * | 1995-06-08 | 1996-12-12 | Wella Ag | Hydrous fabric softener for the treatment of textiles |
US5922663A (en) * | 1996-10-04 | 1999-07-13 | Rhodia Inc. | Enhancement of soil release with gemini surfactants |
US5964295A (en) * | 1996-10-09 | 1999-10-12 | Schlumberger Technology Corporation, Dowell Division | Methods and compositions for testing subterranean formations |
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 |
US5979555A (en) * | 1997-12-02 | 1999-11-09 | Akzo Nobel Nv | Surfactants for hydraulic fractoring compositions |
US6506710B1 (en) | 1997-12-19 | 2003-01-14 | Akzo Nobel N.V. | Viscoelastic surfactants and compositions containing same |
US7060661B2 (en) * | 1997-12-19 | 2006-06-13 | Akzo Nobel N.V. | Acid thickeners and uses thereof |
US6239183B1 (en) * | 1997-12-19 | 2001-05-29 | Akzo Nobel Nv | Method for controlling the rheology of an aqueous fluid and gelling agent therefor |
US6211120B1 (en) * | 1998-02-11 | 2001-04-03 | Baker Hughes Incorporated | Application of aluminum chlorohydrate in viscosifying brine for carrying proppants in gravel packing |
GB2335679B (en) * | 1998-03-27 | 2000-09-13 | Sofitech Nv | Gelling composition based on monomeric viscoelastic surfactants for wellbore service fluids |
GB2335680B (en) * | 1998-03-27 | 2000-05-17 | Sofitech Nv | Method for water control |
DE19914989C2 (en) * | 1999-04-01 | 2002-04-18 | Siemens Ag | Magnetic antenna |
US6767869B2 (en) * | 2000-02-29 | 2004-07-27 | Bj Services Company | Well service fluid and method of making and using the same |
US6455483B1 (en) * | 2000-03-28 | 2002-09-24 | Charles C. Carey | Well stimulation and formation purging composition |
CA2405256C (en) * | 2000-04-05 | 2009-06-02 | Schlumberger Canada Limited | Viscosity reduction of viscoelastic surfactant based fluids |
US6727196B2 (en) * | 2000-12-08 | 2004-04-27 | Kimberly-Clark Worldwide, Inc. | Surfactant systems for personal care products |
GB2393722A (en) | 2001-02-13 | 2004-04-07 | Schlumberger Holdings | Cleavable surfactants which may be useful in viscoelastic compositions for oil-field applications |
US8785355B2 (en) * | 2001-02-13 | 2014-07-22 | Schlumberger Technology Corporation | Viscoelastic compositions |
US6908888B2 (en) * | 2001-04-04 | 2005-06-21 | Schlumberger Technology Corporation | Viscosity reduction of viscoelastic surfactant based fluids |
-
2001
- 2001-02-13 GB GB0325742A patent/GB2393722A/en not_active Withdrawn
- 2001-02-13 GB GB0103449A patent/GB2372058B/en not_active Expired - Fee Related
-
2002
- 2002-02-13 CA CA2434613A patent/CA2434613C/en not_active Expired - Fee Related
- 2002-02-13 CA CA002434345A patent/CA2434345C/en not_active Expired - Fee Related
- 2002-02-13 EP EP02711056A patent/EP1360394A1/en not_active Withdrawn
- 2002-02-13 GB GB0315146A patent/GB2389603B/en not_active Expired - Fee Related
- 2002-02-13 WO PCT/GB2002/000606 patent/WO2002064947A1/en not_active Application Discontinuation
- 2002-02-13 EP EP02712051A patent/EP1360395A1/en not_active Withdrawn
- 2002-02-13 AU AU2002229950A patent/AU2002229950B2/en not_active Ceased
- 2002-02-13 MX MXPA03007219A patent/MXPA03007219A/en active IP Right Grant
- 2002-02-13 US US10/250,416 patent/US7410934B2/en not_active Expired - Fee Related
- 2002-02-13 BR BRPI0207483-4B1A patent/BR0207483B1/en not_active IP Right Cessation
- 2002-02-13 WO PCT/GB2002/000587 patent/WO2002064945A1/en active IP Right Grant
- 2002-02-13 EA EA200300896A patent/EA006450B1/en not_active IP Right Cessation
- 2002-02-13 EA EA200300894A patent/EA006867B1/en not_active IP Right Cessation
- 2002-02-13 CN CN028049268A patent/CN1606654B/en not_active Expired - Fee Related
- 2002-02-13 CN CNB028049276A patent/CN100510316C/en not_active Expired - Fee Related
- 2002-02-13 EA EA200300893A patent/EA006142B1/en not_active IP Right Cessation
- 2002-02-13 US US10/250,417 patent/US7036585B2/en not_active Expired - Lifetime
- 2002-02-13 GB GB0315173A patent/GB2389604B/en not_active Expired - Fee Related
- 2002-02-13 MX MXPA03007164A patent/MXPA03007164A/en active IP Right Grant
- 2002-02-13 OA OA1200300208A patent/OA12446A/en unknown
- 2002-02-13 US US10/250,415 patent/US7704926B2/en not_active Expired - Lifetime
- 2002-02-13 CA CA2434357A patent/CA2434357C/en not_active Expired - Fee Related
- 2002-02-13 BR BRPI0207484-2A patent/BR0207484B1/en not_active IP Right Cessation
- 2002-02-13 WO PCT/GB2002/000589 patent/WO2002064946A1/en active IP Right Grant
- 2002-02-13 AU AU2002231958A patent/AU2002231958C1/en not_active Ceased
- 2002-02-13 OA OA1200300207A patent/OA12445A/en unknown
-
2003
- 2003-08-12 NO NO20033573A patent/NO20033573L/en not_active Application Discontinuation
- 2003-08-12 NO NO20033572A patent/NO20033572L/en not_active Application Discontinuation
-
2014
- 2014-06-12 US US14/303,196 patent/US20150072905A1/en not_active Abandoned
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5258137A (en) * | 1984-12-24 | 1993-11-02 | The Dow Chemical Company | Viscoelastic surfactant based foam fluids |
WO1998056497A1 (en) * | 1997-06-10 | 1998-12-17 | Rhodia Inc. | Fluids containing viscoelastic surfactant and methods for using the same |
WO2001018147A1 (en) * | 1999-09-07 | 2001-03-15 | Crompton Corporation | Quaternary ammonium salts as thickening agents for aqueous systems |
Cited By (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7776798B2 (en) | 1999-09-07 | 2010-08-17 | Akzo Nobel Surface Chemistry Llc | Quaternary ammonium salts as thickening agents for aqueous systems |
US8785355B2 (en) | 2001-02-13 | 2014-07-22 | Schlumberger Technology Corporation | Viscoelastic compositions |
US8143197B2 (en) | 2001-12-22 | 2012-03-27 | Schlumberger Technology Corporation | Aqueous fracturing fluid |
US7677311B2 (en) | 2002-08-26 | 2010-03-16 | Schlumberger Technology Corporation | Internal breaker for oilfield treatments |
US7081439B2 (en) | 2003-11-13 | 2006-07-25 | Schlumberger Technology Corporation | Methods for controlling the fluid loss properties of viscoelastic surfactant based fluids |
US8524642B2 (en) | 2004-06-02 | 2013-09-03 | Rhodia Operations | Multicomponent viscoelastic surfactant fluid and method of using as a fracturing fluid |
US7772164B2 (en) | 2004-06-02 | 2010-08-10 | Rhodia, Inc. | Multicomponent viscoelastic surfactant fluid and method of using as a fracturing fluid |
US9732268B2 (en) | 2004-06-02 | 2017-08-15 | Rhodia Operations | Multicomponent viscoelastic surfactant fluid and method of using as a fracturing fluid |
US8022016B2 (en) | 2004-06-02 | 2011-09-20 | Rhodia, Inc. | Multicomponent viscoelastic surfactant fluid and method of using as a fracturing fluid |
US8124570B2 (en) | 2004-06-02 | 2012-02-28 | Rhodia, Inc. | Multicomponent viscoelastic surfactant fluid and method of using as a fracturing fluid |
US7022861B1 (en) | 2004-06-10 | 2006-04-04 | Sandia National Laboratories | Thermally cleavable surfactants |
US7378533B1 (en) | 2004-06-10 | 2008-05-27 | Sandia Corporation | Method for preparing thermally cleavable surfactants without deprotonation |
US7351837B1 (en) | 2004-06-10 | 2008-04-01 | Sandia Corporation | Thermally cleavable surfactants without deprotonation |
US8633255B2 (en) | 2005-03-16 | 2014-01-21 | Baker Hughes Incorporated | Saponified fatty acids as breakers for viscoelastic surfactant-gelled fluids |
US7728044B2 (en) * | 2005-03-16 | 2010-06-01 | Baker Hughes Incorporated | Saponified fatty acids as breakers for viscoelastic surfactant-gelled fluids |
US8044106B2 (en) * | 2005-03-16 | 2011-10-25 | Baker Hughes Incorporated | Saponified fatty acids as viscosity modifiers for viscoelastic surfactant-gelled fluids |
US8236864B2 (en) | 2005-03-16 | 2012-08-07 | Baker Hughes Incorporated | Saponified fatty acids as breakers for viscoelastic surfactant-gelled fluids |
US7635028B2 (en) | 2006-09-18 | 2009-12-22 | Schlumberger Technology Corporation | Acidic internal breaker for viscoelastic surfactant fluids in brine |
US8067342B2 (en) | 2006-09-18 | 2011-11-29 | Schlumberger Technology Corporation | Internal breakers for viscoelastic surfactant fluids |
US8481462B2 (en) | 2006-09-18 | 2013-07-09 | Schlumberger Technology Corporation | Oxidative internal breaker system with breaking activators for viscoelastic surfactant fluids |
US7879770B2 (en) | 2006-09-18 | 2011-02-01 | Schlumberger Technology Corporation | Oxidative internal breaker for viscoelastic surfactant fluids |
US7431087B2 (en) | 2006-09-18 | 2008-10-07 | Schlumberger Technology Corporation | Internal breaker for oilfield fluids |
US9006153B2 (en) | 2006-09-18 | 2015-04-14 | Schlumberger Technology Corporation | Oxidative internal breaker system with breaking activators for viscoelastic surfactant fluids |
US9284482B2 (en) | 2006-09-18 | 2016-03-15 | Schlumberger Technology Corporation | Acidic internal breaker for viscoelastic surfactant fluids in brine |
US7287590B1 (en) | 2006-09-18 | 2007-10-30 | Schlumberger Technology Corporation | Internal breaker for oilfield fluids |
US8695708B2 (en) | 2007-03-26 | 2014-04-15 | Schlumberger Technology Corporation | Method for treating subterranean formation with degradable material |
WO2008117222A1 (en) * | 2007-03-26 | 2008-10-02 | Schlumberger Canada Limited | Method for treating subterranean formation |
JP2012529663A (en) * | 2009-06-11 | 2012-11-22 | エシロール アテルナジオナール カンパニー ジェネラーレ デ オプティック | Curable coating composition modified with a cleavable surfactant to improve adhesion of multilayer coating stacks |
US9103969B2 (en) | 2009-06-11 | 2015-08-11 | Essilor International (Compagnie Generale D'optique) | Curable coating composition modified with a cleavable surfactant for improving adhesion in multilayered coating stacks |
US8141637B2 (en) | 2009-08-11 | 2012-03-27 | Schlumberger Technology Corporation | Manipulation of flow underground |
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AU2002231958C1 (en) | Viscoelastic compositions | |
AU2002231958A1 (en) | Viscoelastic compositions | |
US7125825B2 (en) | Amidoamine salt-based viscosifying agents and methods of use | |
CA2384108C (en) | Quaternary ammonium salts as thickening agents for aqueous systems | |
US6762154B2 (en) | Viscoelastic surfactant fluids stable at high brine concentrations | |
US7947633B2 (en) | Polycationic viscoelastic compositions | |
CA2437285C (en) | Viscoelastic wellbore treatment fluids comprising oligomeric surfactants | |
AU2002229950A1 (en) | Aqueous viscoelastic fluid | |
US8785355B2 (en) | Viscoelastic compositions | |
CN101326259A (en) | High temperature gellant for viscosity modification of low and high density brines | |
WO2023094434A1 (en) | Surfactant composition |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ PL PT RO RU SD SE SG SI SK SL TJ TM TR TT TZ UA UG US UZ VN YU ZA ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG |
|
DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
WWE | Wipo information: entry into national phase |
Ref document number: 2434613 Country of ref document: CA |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2002231958 Country of ref document: AU |
|
WWE | Wipo information: entry into national phase |
Ref document number: DZP2003000173 Country of ref document: DZ |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1244/CHENP/2003 Country of ref document: IN |
|
WWE | Wipo information: entry into national phase |
Ref document number: PA/a/2003/007219 Country of ref document: MX Ref document number: 028049276 Country of ref document: CN |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2002712051 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 200300896 Country of ref document: EA |
|
WWP | Wipo information: published in national office |
Ref document number: 2002712051 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 10250415 Country of ref document: US |
|
REG | Reference to national code |
Ref country code: DE Ref legal event code: 8642 |
|
NENP | Non-entry into the national phase |
Ref country code: JP |
|
WWW | Wipo information: withdrawn in national office |
Ref document number: JP |
|
WWG | Wipo information: grant in national office |
Ref document number: 2002231958 Country of ref document: AU |