CA1266600A - Epaississement reversible d'un liquide - Google Patents

Epaississement reversible d'un liquide

Info

Publication number: CA1266600A
Authority: CA; Canada
Prior art keywords: liquid; surfactant; viscosity; viscoelastic; viscoelastic surfactant
Prior art date: 1986-06-16
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

Application number

CA000511639A

Other languages

English (en)

Inventor

Gene D. Rose

Arthur S. Teot

Peter A. Doty

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Dow Chemical Co

Original Assignee

Dow Chemical Co

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1986-06-16

Filing date

1986-06-16

Publication date

1990-03-13

1986-06-16 Application filed by Dow Chemical Co filed Critical Dow Chemical Co

1986-06-16 Priority to CA000511639A priority Critical patent/CA1266600A/fr

1990-03-13 Application granted granted Critical

1990-03-13 Publication of CA1266600A publication Critical patent/CA1266600A/fr

2007-03-13 Anticipated expiration legal-status Critical

Status Expired - Fee Related legal-status Critical Current

Links

239000007788 liquid Substances 0.000 title claims abstract description 187
238000000034 method Methods 0.000 title claims abstract description 48
230000008719 thickening Effects 0.000 title claims description 6
230000008569 process Effects 0.000 title description 11
230000002441 reversible effect Effects 0.000 title description 4
239000004094 surface-active agent Substances 0.000 claims abstract description 135
239000007787 solid Substances 0.000 claims abstract description 32
229930195733 hydrocarbon Natural products 0.000 claims abstract description 29
150000002430 hydrocarbons Chemical class 0.000 claims abstract description 29
239000004215 Carbon black (E152) Substances 0.000 claims abstract description 28
239000000203 mixture Substances 0.000 claims abstract description 19
239000003792 electrolyte Substances 0.000 claims description 22
125000000129 anionic group Chemical group 0.000 claims description 19
125000002091 cationic group Chemical group 0.000 claims description 18
230000002209 hydrophobic effect Effects 0.000 claims description 11
125000004432 carbon atom Chemical group C* 0.000 claims description 10
230000003381 solubilizing effect Effects 0.000 claims description 7
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 6
150000001875 compounds Chemical class 0.000 claims description 6
239000011358 absorbing material Substances 0.000 claims description 3
239000002562 thickening agent Substances 0.000 abstract 1
150000002500 ions Chemical class 0.000 description 35
-1 hydrocarbyl radicals Chemical class 0.000 description 21
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
125000000217 alkyl group Chemical group 0.000 description 13
239000000243 solution Substances 0.000 description 11
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
239000003945 anionic surfactant Substances 0.000 description 7
238000005553 drilling Methods 0.000 description 7
239000005486 organic electrolyte Substances 0.000 description 7
239000011368 organic material Substances 0.000 description 7
229920000642 polymer Polymers 0.000 description 7
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
229910052783 alkali metal Inorganic materials 0.000 description 6
239000012267 brine Substances 0.000 description 6
239000004927 clay Substances 0.000 description 6
125000001183 hydrocarbyl group Chemical group 0.000 description 6
YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 6
HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 6
239000003093 cationic surfactant Substances 0.000 description 5
230000000694 effects Effects 0.000 description 5
239000003921 oil Substances 0.000 description 5
229960001860 salicylate Drugs 0.000 description 5
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
150000001298 alcohols Chemical class 0.000 description 4
238000010494 dissociation reaction Methods 0.000 description 4
230000005593 dissociations Effects 0.000 description 4
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
239000002736 nonionic surfactant Substances 0.000 description 4
150000004010 onium ions Chemical class 0.000 description 4
238000005086 pumping Methods 0.000 description 4
241000894007 species Species 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 3
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical group OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
230000002378 acidificating effect Effects 0.000 description 3
239000000654 additive Substances 0.000 description 3
125000003342 alkenyl group Chemical group 0.000 description 3
125000003118 aryl group Chemical group 0.000 description 3
239000011324 bead Substances 0.000 description 3
150000007942 carboxylates Chemical group 0.000 description 3
238000005520 cutting process Methods 0.000 description 3
125000003438 dodecyl group Chemical group [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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
238000009472 formulation Methods 0.000 description 3
238000000227 grinding Methods 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
229960004592 isopropanol Drugs 0.000 description 3
125000001421 myristyl 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])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
239000003129 oil well Substances 0.000 description 3
125000000913 palmityl 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])([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 3
238000005498 polishing Methods 0.000 description 3
125000001453 quaternary ammonium group Chemical group 0.000 description 3
239000002002 slurry Substances 0.000 description 3
GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
235000010469 Glycine max Nutrition 0.000 description 2
244000068988 Glycine max Species 0.000 description 2
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 2
RSPISYXLHRIGJD-UHFFFAOYSA-N OOOO Chemical compound OOOO RSPISYXLHRIGJD-UHFFFAOYSA-N 0.000 description 2
ABBQHOQBGMUPJH-UHFFFAOYSA-M Sodium salicylate Chemical compound [Na+].OC1=CC=CC=C1C([O-])=O ABBQHOQBGMUPJH-UHFFFAOYSA-M 0.000 description 2
XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 2
230000002730 additional effect Effects 0.000 description 2
125000005211 alkyl trimethyl ammonium group Chemical group 0.000 description 2
150000001412 amines Chemical group 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
150000001450 anions Chemical class 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
229910001622 calcium bromide Inorganic materials 0.000 description 2
WGEFECGEFUFIQW-UHFFFAOYSA-L calcium dibromide Chemical compound [Ca+2].[Br-].[Br-] WGEFECGEFUFIQW-UHFFFAOYSA-L 0.000 description 2
230000015556 catabolic process Effects 0.000 description 2
150000001768 cations Chemical class 0.000 description 2
230000008602 contraction Effects 0.000 description 2
238000001816 cooling Methods 0.000 description 2
PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
238000006731 degradation reaction Methods 0.000 description 2
230000001419 dependent effect Effects 0.000 description 2
239000000428 dust Substances 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
238000001914 filtration Methods 0.000 description 2
150000002334 glycols Chemical class 0.000 description 2
229920006158 high molecular weight polymer Polymers 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
229910052739 hydrogen Inorganic materials 0.000 description 2
125000002768 hydroxyalkyl group Chemical group 0.000 description 2
230000002427 irreversible effect Effects 0.000 description 2
239000006193 liquid solution Substances 0.000 description 2
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 2
239000000693 micelle Substances 0.000 description 2
IXQGCWUGDFDQMF-UHFFFAOYSA-N o-Hydroxyethylbenzene Natural products CCC1=CC=CC=C1O IXQGCWUGDFDQMF-UHFFFAOYSA-N 0.000 description 2
125000005064 octadecenyl group Chemical group C(=CCCCCCCCCCCCCCCCC)* 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
239000010453 quartz Substances 0.000 description 2
239000012266 salt solution Substances 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
239000011734 sodium Substances 0.000 description 2
229960004025 sodium salicylate Drugs 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-L sulfate group Chemical group S(=O)(=O)([O-])[O-] QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
239000003760 tallow Substances 0.000 description 2
150000003512 tertiary amines Chemical class 0.000 description 2
238000010998 test method Methods 0.000 description 2
TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 description 2
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 2
LHJGJYXLEPZJPM-UHFFFAOYSA-N 2,4,5-trichlorophenol Chemical compound OC1=CC(Cl)=C(Cl)C=C1Cl LHJGJYXLEPZJPM-UHFFFAOYSA-N 0.000 description 1
MGUMZJAQENFQKN-UHFFFAOYSA-N 2-(cyclohexylamino)ethanol Chemical compound OCCNC1CCCCC1 MGUMZJAQENFQKN-UHFFFAOYSA-N 0.000 description 1
JFLDCETXOKFEJC-UHFFFAOYSA-M 2-carboxyphenolate;hexadecyl(trimethyl)azanium Chemical compound OC1=CC=CC=C1C([O-])=O.CCCCCCCCCCCCCCCC[N+](C)(C)C JFLDCETXOKFEJC-UHFFFAOYSA-M 0.000 description 1
MPNXSZJPSVBLHP-UHFFFAOYSA-N 2-chloro-n-phenylpyridine-3-carboxamide Chemical compound ClC1=NC=CC=C1C(=O)NC1=CC=CC=C1 MPNXSZJPSVBLHP-UHFFFAOYSA-N 0.000 description 1
LULAYUGMBFYYEX-UHFFFAOYSA-M 3-chlorobenzoate Chemical compound [O-]C(=O)C1=CC=CC(Cl)=C1 LULAYUGMBFYYEX-UHFFFAOYSA-M 0.000 description 1
JIGUICYYOYEXFS-UHFFFAOYSA-N 3-tert-butylbenzene-1,2-diol Chemical compound CC(C)(C)C1=CC=CC(O)=C1O JIGUICYYOYEXFS-UHFFFAOYSA-N 0.000 description 1
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical group OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
239000003929 acidic solution Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
239000002585 base Substances 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
YOUGRGFIHBUKRS-UHFFFAOYSA-N benzyl(trimethyl)azanium Chemical compound C[N+](C)(C)CC1=CC=CC=C1 YOUGRGFIHBUKRS-UHFFFAOYSA-N 0.000 description 1
KXHPPCXNWTUNSB-UHFFFAOYSA-M benzyl(trimethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CC1=CC=CC=C1 KXHPPCXNWTUNSB-UHFFFAOYSA-M 0.000 description 1
239000001110 calcium chloride Substances 0.000 description 1
229910001628 calcium chloride Inorganic materials 0.000 description 1
235000011089 carbon dioxide Nutrition 0.000 description 1
NEUSVAOJNUQRTM-UHFFFAOYSA-N cetylpyridinium Chemical compound CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 NEUSVAOJNUQRTM-UHFFFAOYSA-N 0.000 description 1
229960004830 cetylpyridinium Drugs 0.000 description 1
WOWHHFRSBJGXCM-UHFFFAOYSA-M cetyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)C WOWHHFRSBJGXCM-UHFFFAOYSA-M 0.000 description 1
RLGQACBPNDBWTB-UHFFFAOYSA-N cetyltrimethylammonium ion Chemical compound CCCCCCCCCCCCCCCC[N+](C)(C)C RLGQACBPNDBWTB-UHFFFAOYSA-N 0.000 description 1
150000001805 chlorine compounds Chemical group 0.000 description 1
239000008119 colloidal silica Substances 0.000 description 1
229940000425 combination drug Drugs 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
235000019628 coolness Nutrition 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
230000006378 damage Effects 0.000 description 1
125000002704 decyl group Chemical group [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])C([H])([H])C([H])([H])* 0.000 description 1
230000007812 deficiency Effects 0.000 description 1
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
229910001873 dinitrogen Inorganic materials 0.000 description 1
IGHFVKIBHWMEFC-UHFFFAOYSA-L disodium;2-[(2-carboxylatophenoxy)methoxy]benzoate Chemical compound [Na+].[Na+].[O-]C(=O)C1=CC=CC=C1OCOC1=CC=CC=C1C([O-])=O IGHFVKIBHWMEFC-UHFFFAOYSA-L 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
230000001747 exhibiting effect Effects 0.000 description 1
239000012530 fluid Substances 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
229940083124 ganglion-blocking antiadrenergic secondary and tertiary amines Drugs 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical group C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
229910017053 inorganic salt Inorganic materials 0.000 description 1
239000002198 insoluble material Substances 0.000 description 1
239000002563 ionic surfactant Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
239000011707 mineral Substances 0.000 description 1
239000002480 mineral oil Substances 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
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
125000002347 octyl 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])[H] 0.000 description 1
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 1
150000002894 organic compounds Chemical class 0.000 description 1
239000002245 particle Substances 0.000 description 1
239000011236 particulate material Substances 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-M phenolate Chemical group [O-]C1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-M 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
125000005496 phosphonium group Chemical group 0.000 description 1
NQQVFXUMIDALNH-UHFFFAOYSA-N picloram Chemical compound NC1=C(Cl)C(Cl)=NC(C(O)=O)=C1Cl NQQVFXUMIDALNH-UHFFFAOYSA-N 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
FRMWBRPWYBNAFB-UHFFFAOYSA-M potassium salicylate Chemical compound [K+].OC1=CC=CC=C1C([O-])=O FRMWBRPWYBNAFB-UHFFFAOYSA-M 0.000 description 1
229960003629 potassium salicylate Drugs 0.000 description 1
YENGGBGPRNEVGP-UHFFFAOYSA-M potassium;3,5-dichlorobenzoate Chemical compound [K+].[O-]C(=O)C1=CC(Cl)=CC(Cl)=C1 YENGGBGPRNEVGP-UHFFFAOYSA-M 0.000 description 1
150000003141 primary amines Chemical class 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
239000004576 sand Substances 0.000 description 1
238000000926 separation method Methods 0.000 description 1
229910052710 silicon Inorganic materials 0.000 description 1
239000010703 silicon Substances 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
XVYLSIXULOLXJR-UHFFFAOYSA-M sodium;2,4-dichlorobenzoate Chemical compound [Na+].[O-]C(=O)C1=CC=C(Cl)C=C1Cl XVYLSIXULOLXJR-UHFFFAOYSA-M 0.000 description 1
239000002195 soluble material Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium group Chemical group [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
239000000725 suspension Substances 0.000 description 1
MQAYPFVXSPHGJM-UHFFFAOYSA-M trimethyl(phenyl)azanium;chloride Chemical group [Cl-].C[N+](C)(C)C1=CC=CC=C1 MQAYPFVXSPHGJM-UHFFFAOYSA-M 0.000 description 1
QYWVQMLYIXYLRE-SEYXRHQNSA-N trimethyl-[(z)-octadec-9-enyl]azanium Chemical compound CCCCCCCC\C=C/CCCCCCCC[N+](C)(C)C QYWVQMLYIXYLRE-SEYXRHQNSA-N 0.000 description 1
125000004417 unsaturated alkyl group Chemical group 0.000 description 1
239000008096 xylene Substances 0.000 description 1
150000003738 xylenes Chemical class 0.000 description 1

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Detergent Compositions (AREA)
Colloid Chemistry (AREA)
Lubricants (AREA)

CA000511639A 1986-06-16 1986-06-16 Epaississement reversible d'un liquide Expired - Fee Related CA1266600A (fr)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CA000511639A CA1266600A (fr)	1986-06-16	1986-06-16	Epaississement reversible d'un liquide

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CA000511639A CA1266600A (fr)	1986-06-16	1986-06-16	Epaississement reversible d'un liquide

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Publication Number	Publication Date
CA1266600A true CA1266600A (fr)	1990-03-13

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ID=4133356

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CA000511639A Expired - Fee Related CA1266600A (fr)	1986-06-16	1986-06-16	Epaississement reversible d'un liquide

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CA (1)	CA1266600A (fr)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6410489B1 (en)	1998-12-31	2002-06-25	Bj Services Company Canada	Foam-fluid for fracturing subterranean formations
US6468945B1 (en)	1998-12-31	2002-10-22	Bj Services Company Canada	Fluids for fracturing subterranean formations
US6875728B2 (en)	1999-12-29	2005-04-05	Bj Services Company Canada	Method for fracturing subterranean formations

1986
- 1986-06-16 CA CA000511639A patent/CA1266600A/fr not_active Expired - Fee Related

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6410489B1 (en)	1998-12-31	2002-06-25	Bj Services Company Canada	Foam-fluid for fracturing subterranean formations
US6468945B1 (en)	1998-12-31	2002-10-22	Bj Services Company Canada	Fluids for fracturing subterranean formations
US6875728B2 (en)	1999-12-29	2005-04-05	Bj Services Company Canada	Method for fracturing subterranean formations

Legal Events

Date	Code	Title	Description
1999-03-15	MKLA	Lapsed

Publication	Publication Date	Title
US4735731A (en)	1988-04-05	Process for reversible thickening of a liquid
CA2148583C (fr)	2001-01-30	Fluides expanses a base de surfactif viscoelastique
Hill et al.	1973	Aqueous surfactant systems for oil recovery
CA1097052A (fr)	1981-03-10	Systemes tensio-actifs aqueux formant in situ des micro-emulsions multiphases
CA2030694C (fr)	1998-04-07	Fluides fonctionnels
US5807810A (en)	1998-09-15	Functional fluids and liquid cleaning compositions and suspending media
EP0835983B1 (fr)	2003-12-17	Méthodes pour fracturer des formations souterraines
US5964692A (en)	1999-10-12	Functional fluids and liquid cleaning compositions and suspending media
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Ahmadali et al.	1993	Reducing surfactant adsorption in carbonate reservoirs
US3348611A (en)	1967-10-24	Surfactants for oil recovery by waterfloods
US4596662A (en)	1986-06-24	Compositions for use in drilling, completion and workover fluids
US20030019627A1 (en)	2003-01-30	Compositions containing aqueous viscosifying surfactants and methods for applying such compositions in subterranean formations
US20110021388A1 (en)	2011-01-27	Microemulsifiers and methods of making and using same
US20020033260A1 (en)	2002-03-21	Viscoelastic surfactant fluids stable at high brine concentrations
EP1634938A1 (fr)	2006-03-15	Fluides viscoélastiques pour utilisation dans les puits de pétrole
US3500923A (en)	1970-03-17	Use of highly saline ethoxylated surfactant system for oil recovery
US4017405A (en)	1977-04-12	Soluble oil composition
WO2016083322A1 (fr)	2016-06-02	Agent de rupture à action retardée pour fluides à base d'un tensioactif viscoélastique
EP0032072B1 (fr)	1983-05-18	Compositions de tensides pour l'amélioration des procédés de récupération d'huile
CA1230960A (fr)	1988-01-05	Methode modifiee d'extraction par injection d'eau des hydrocarbures contenus dans des gisements souterrains argileux
EP0037699A2 (fr)	1981-10-14	Complexes de polymères en microémulsion et leur utilisation pour la récupération d'huile
US3422890A (en)	1969-01-21	Treatment of subsurface oil-bearing formations with oil-wetting cationic emulsions
US3515214A (en)	1970-06-02	Chemical waterflooding techniques using complex surfactants
GB2114190A (en)	1983-08-17	Esters of sulfonic acids as anti-sludge agents and their use during the acidizing of formations containing sludging crude oils

CA1266600A - Epaississement reversible d'un liquide - Google Patents

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Priority Applications (1)

Applications Claiming Priority (1)

Publications (1)

Family

ID=4133356

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Cited By (3)

Cited By (3)

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