ES2554951T5 - Micro-geles polimerizados en dispersión con respuesta frente a tensioactivos - Google Patents
Micro-geles polimerizados en dispersión con respuesta frente a tensioactivos Download PDFInfo
- Publication number
- ES2554951T5 ES2554951T5 ES12766533T ES12766533T ES2554951T5 ES 2554951 T5 ES2554951 T5 ES 2554951T5 ES 12766533 T ES12766533 T ES 12766533T ES 12766533 T ES12766533 T ES 12766533T ES 2554951 T5 ES2554951 T5 ES 2554951T5
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- Prior art keywords
- vinyl
- weight
- alkyl
- monomer
- group
- Prior art date
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- 239000004094 surface-active agent Substances 0.000 title claims description 61
- 239000000499 gel Substances 0.000 title description 22
- 230000004044 response Effects 0.000 title description 7
- 239000000178 monomer Substances 0.000 claims description 162
- 239000000203 mixture Substances 0.000 claims description 143
- -1 poly (allyl ethers Chemical class 0.000 claims description 125
- 229920000642 polymer Polymers 0.000 claims description 95
- 239000012530 fluid Substances 0.000 claims description 85
- 125000000217 alkyl group Chemical group 0.000 claims description 57
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 48
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 38
- 229920002554 vinyl polymer Polymers 0.000 claims description 31
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 28
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 26
- 125000004432 carbon atom Chemical group C* 0.000 claims description 26
- 239000001257 hydrogen Substances 0.000 claims description 25
- 229910052739 hydrogen Inorganic materials 0.000 claims description 25
- 230000002209 hydrophobic effect Effects 0.000 claims description 25
- 238000004132 cross linking Methods 0.000 claims description 23
- 230000015572 biosynthetic process Effects 0.000 claims description 18
- 239000002736 nonionic surfactant Substances 0.000 claims description 18
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 18
- 125000000129 anionic group Chemical group 0.000 claims description 16
- 238000005755 formation reaction Methods 0.000 claims description 16
- 239000003381 stabilizer Substances 0.000 claims description 16
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 14
- 125000002091 cationic group Chemical group 0.000 claims description 14
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 14
- 125000003118 aryl group Chemical group 0.000 claims description 13
- 229920001577 copolymer Polymers 0.000 claims description 13
- 238000005553 drilling Methods 0.000 claims description 13
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 11
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical group C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 10
- 125000002947 alkylene group Chemical group 0.000 claims description 10
- 229920001519 homopolymer Polymers 0.000 claims description 10
- 150000002148 esters Chemical class 0.000 claims description 9
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 9
- 238000006467 substitution reaction Methods 0.000 claims description 9
- 229920001400 block copolymer Polymers 0.000 claims description 8
- 239000004815 dispersion polymer Substances 0.000 claims description 8
- 229940059574 pentaerithrityl Drugs 0.000 claims description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 7
- 229920001567 vinyl ester resin Polymers 0.000 claims description 7
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 6
- 239000007795 chemical reaction product Substances 0.000 claims description 6
- HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 claims description 6
- 229920005862 polyol Polymers 0.000 claims description 6
- 125000001424 substituent group Chemical group 0.000 claims description 6
- 229930006000 Sucrose Natural products 0.000 claims description 5
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims description 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 5
- 235000011187 glycerol Nutrition 0.000 claims description 5
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- 230000006641 stabilisation Effects 0.000 claims description 5
- 238000011105 stabilization Methods 0.000 claims description 5
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- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical class ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 125000000746 allylic group Chemical group 0.000 claims description 4
- 125000000732 arylene group Chemical group 0.000 claims description 4
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical group CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 claims description 4
- KVMGZRHAVFZQQJ-UHFFFAOYSA-N ethenyl 2-methylhexanoate Chemical compound CCCCC(C)C(=O)OC=C KVMGZRHAVFZQQJ-UHFFFAOYSA-N 0.000 claims description 4
- WNMORWGTPVWAIB-UHFFFAOYSA-N ethenyl 2-methylpropanoate Chemical compound CC(C)C(=O)OC=C WNMORWGTPVWAIB-UHFFFAOYSA-N 0.000 claims description 4
- TVFJAZCVMOXQRK-UHFFFAOYSA-N ethenyl 7,7-dimethyloctanoate Chemical compound CC(C)(C)CCCCCC(=O)OC=C TVFJAZCVMOXQRK-UHFFFAOYSA-N 0.000 claims description 4
- MEGHWIAOTJPCHQ-UHFFFAOYSA-N ethenyl butanoate Chemical compound CCCC(=O)OC=C MEGHWIAOTJPCHQ-UHFFFAOYSA-N 0.000 claims description 4
- CMDXMIHZUJPRHG-UHFFFAOYSA-N ethenyl decanoate Chemical compound CCCCCCCCCC(=O)OC=C CMDXMIHZUJPRHG-UHFFFAOYSA-N 0.000 claims description 4
- GLVVKKSPKXTQRB-UHFFFAOYSA-N ethenyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC=C GLVVKKSPKXTQRB-UHFFFAOYSA-N 0.000 claims description 4
- UJRIYYLGNDXVTA-UHFFFAOYSA-N ethenyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OC=C UJRIYYLGNDXVTA-UHFFFAOYSA-N 0.000 claims description 4
- LZWYWAIOTBEZFN-UHFFFAOYSA-N ethenyl hexanoate Chemical compound CCCCCC(=O)OC=C LZWYWAIOTBEZFN-UHFFFAOYSA-N 0.000 claims description 4
- AFSIMBWBBOJPJG-UHFFFAOYSA-N ethenyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC=C AFSIMBWBBOJPJG-UHFFFAOYSA-N 0.000 claims description 4
- BLZSRIYYOIZLJL-UHFFFAOYSA-N ethenyl pentanoate Chemical compound CCCCC(=O)OC=C BLZSRIYYOIZLJL-UHFFFAOYSA-N 0.000 claims description 4
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 claims description 4
- 125000005702 oxyalkylene group Chemical group 0.000 claims description 4
- 229920005604 random copolymer Polymers 0.000 claims description 4
- 229940014800 succinic anhydride Drugs 0.000 claims description 4
- FYRWKWGEFZTOQI-UHFFFAOYSA-N 3-prop-2-enoxy-2,2-bis(prop-2-enoxymethyl)propan-1-ol Chemical compound C=CCOCC(CO)(COCC=C)COCC=C FYRWKWGEFZTOQI-UHFFFAOYSA-N 0.000 claims description 3
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims description 3
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 3
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims description 3
- IGBZOHMCHDADGY-UHFFFAOYSA-N ethenyl 2-ethylhexanoate Chemical compound CCCCC(CC)C(=O)OC=C IGBZOHMCHDADGY-UHFFFAOYSA-N 0.000 claims description 3
- RASNHPFIOGUOOT-UHFFFAOYSA-N ethenyl 6-methylheptanoate Chemical compound CC(C)CCCCC(=O)OC=C RASNHPFIOGUOOT-UHFFFAOYSA-N 0.000 claims description 3
- NWJTZFZQVYJIHU-UHFFFAOYSA-N ethenyl nonanoate Chemical compound CCCCCCCCC(=O)OC=C NWJTZFZQVYJIHU-UHFFFAOYSA-N 0.000 claims description 3
- 229920000223 polyglycerol Polymers 0.000 claims description 3
- 125000005504 styryl group Chemical group 0.000 claims description 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
- SYENVBKSVVOOPS-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)butyl prop-2-enoate Chemical compound CCC(CO)(CO)COC(=O)C=C SYENVBKSVVOOPS-UHFFFAOYSA-N 0.000 claims description 2
- KHOUKKVJOPQVJM-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol;prop-2-enoic acid Chemical compound OC(=O)C=C.OCC(CO)(CO)CO KHOUKKVJOPQVJM-UHFFFAOYSA-N 0.000 claims description 2
- XMHCSVHEBCVIFR-UHFFFAOYSA-N 2-(hydroxymethyl)-2-methylpropane-1,3-diol;prop-2-enoic acid Chemical compound OC(=O)C=C.OCC(C)(CO)CO XMHCSVHEBCVIFR-UHFFFAOYSA-N 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- CMVNWVONJDMTSH-UHFFFAOYSA-N 7-bromo-2-methyl-1h-quinazolin-4-one Chemical compound C1=CC(Br)=CC2=NC(C)=NC(O)=C21 CMVNWVONJDMTSH-UHFFFAOYSA-N 0.000 claims 3
- WHNPOQXWAMXPTA-UHFFFAOYSA-N 3-methylbut-2-enamide Chemical compound CC(C)=CC(N)=O WHNPOQXWAMXPTA-UHFFFAOYSA-N 0.000 claims 1
- GFJVXXWOPWLRNU-UHFFFAOYSA-N ethenyl formate Chemical group C=COC=O GFJVXXWOPWLRNU-UHFFFAOYSA-N 0.000 claims 1
- 125000000524 functional group Chemical group 0.000 claims 1
- 239000002245 particle Substances 0.000 description 29
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- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 24
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- 235000002639 sodium chloride Nutrition 0.000 description 20
- 229920001223 polyethylene glycol Polymers 0.000 description 18
- 239000011324 bead Substances 0.000 description 17
- 229920000831 ionic polymer Polymers 0.000 description 17
- 229910052708 sodium Inorganic materials 0.000 description 17
- 229940083542 sodium Drugs 0.000 description 17
- 235000015424 sodium Nutrition 0.000 description 17
- 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 16
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- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 15
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- 150000003839 salts Chemical class 0.000 description 13
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 12
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 12
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- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 12
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 12
- 239000003999 initiator Substances 0.000 description 12
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- VLKIFCBXANYYCK-GMFCBQQYSA-M sodium;2-[methyl-[(z)-octadec-9-enoyl]amino]acetate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CC([O-])=O VLKIFCBXANYYCK-GMFCBQQYSA-M 0.000 description 1
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- 235000012424 soybean oil Nutrition 0.000 description 1
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- 150000003432 sterols Chemical class 0.000 description 1
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- HCXVJBMSMIARIN-PHZDYDNGSA-N stigmasterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)/C=C/[C@@H](CC)C(C)C)[C@@]1(C)CC2 HCXVJBMSMIARIN-PHZDYDNGSA-N 0.000 description 1
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- RYCLIXPGLDDLTM-UHFFFAOYSA-J tetrapotassium;phosphonato phosphate Chemical compound [K+].[K+].[K+].[K+].[O-]P([O-])(=O)OP([O-])([O-])=O RYCLIXPGLDDLTM-UHFFFAOYSA-J 0.000 description 1
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- JFLKFZNIIQFQBS-FNCQTZNRSA-N trans,trans-1,4-Diphenyl-1,3-butadiene Chemical group C=1C=CC=CC=1\C=C\C=C\C1=CC=CC=C1 JFLKFZNIIQFQBS-FNCQTZNRSA-N 0.000 description 1
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- RKBCYCFRFCNLTO-UHFFFAOYSA-N triisopropylamine Chemical class CC(C)N(C(C)C)C(C)C RKBCYCFRFCNLTO-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 1
- GUIWIPNQQLZJIE-UHFFFAOYSA-K tris[2-(2-hydroxyethoxy)ethyl]-octadecylazanium;phosphate Chemical compound [O-]P([O-])([O-])=O.CCCCCCCCCCCCCCCCCC[N+](CCOCCO)(CCOCCO)CCOCCO GUIWIPNQQLZJIE-UHFFFAOYSA-K 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
- 229940075466 undecylenate Drugs 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 239000004474 valine Substances 0.000 description 1
- ZTWTYVWXUKTLCP-UHFFFAOYSA-N vinylphosphonic acid Chemical compound OP(O)(=O)C=C ZTWTYVWXUKTLCP-UHFFFAOYSA-N 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- QYSXJUFSXHHAJI-YRZJJWOYSA-N vitamin D3 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C\C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-YRZJJWOYSA-N 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
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Classifications
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- 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
- C09K8/70—Compositions for forming crevices or fractures characterised by their form or by the form of their components, e.g. foams
-
- 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
- C09K8/02—Well-drilling compositions
- C09K8/03—Specific additives for general use in well-drilling compositions
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- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
- A61K8/463—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfuric acid derivatives, e.g. sodium lauryl sulfate
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- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/817—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
- A61K8/8182—Copolymers of vinyl-pyrrolidones. Compositions of derivatives of such polymers
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- A61Q5/02—Preparations for cleaning the hair
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F226/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F226/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen
- C08F226/06—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen by a heterocyclic ring containing nitrogen
- C08F226/10—N-Vinyl-pyrrolidone
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- 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
- C09K8/602—Compositions for stimulating production by acting on the underground formation containing surfactants
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
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- 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
- C09K8/602—Compositions for stimulating production by acting on the underground formation containing surfactants
- C09K8/604—Polymeric surfactants
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
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- 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
- C09K8/665—Compositions based on water or polar solvents containing inorganic compounds
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- C—CHEMISTRY; METALLURGY
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- 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
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- 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
- C09K8/685—Compositions based on water or polar solvents containing organic compounds containing cross-linking agents
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- 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
- C09K8/84—Compositions based on water or polar solvents
- C09K8/86—Compositions based on water or polar solvents containing organic compounds
- C09K8/88—Compositions based on water or polar solvents containing organic compounds macromolecular compounds
- C09K8/885—Compositions based on water or polar solvents containing organic compounds macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
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- 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
- C09K8/84—Compositions based on water or polar solvents
- C09K8/86—Compositions based on water or polar solvents containing organic compounds
- C09K8/88—Compositions based on water or polar solvents containing organic compounds macromolecular compounds
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- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/10—General cosmetic use
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- 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
- C09K2208/06—Structured surfactants, i.e. well drilling or treating fluids with a lamellar or spherulitic phase
Landscapes
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- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
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- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
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- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Dermatology (AREA)
- Dispersion Chemistry (AREA)
- Cosmetics (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Polymerisation Methods In General (AREA)
- Colloid Chemistry (AREA)
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161533887P | 2011-09-13 | 2011-09-13 | |
| US201161533884P | 2011-09-13 | 2011-09-13 | |
| US201161533884P | 2011-09-13 | ||
| US201161533887P | 2011-09-13 | ||
| US201161578259P | 2011-12-21 | 2011-12-21 | |
| US201161578259P | 2011-12-21 | ||
| PCT/US2012/055110 WO2013040178A1 (en) | 2011-09-13 | 2012-09-13 | Surfactant responsive dispersion polymerized micro-gels |
Publications (2)
| Publication Number | Publication Date |
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| ES2554951T3 ES2554951T3 (es) | 2015-12-28 |
| ES2554951T5 true ES2554951T5 (es) | 2019-07-18 |
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| Application Number | Title | Priority Date | Filing Date |
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| ES12766533T Active ES2554951T5 (es) | 2011-09-13 | 2012-09-13 | Micro-geles polimerizados en dispersión con respuesta frente a tensioactivos |
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| Country | Link |
|---|---|
| US (1) | US9714376B2 (enExample) |
| EP (1) | EP2756053B2 (enExample) |
| JP (2) | JP6165735B2 (enExample) |
| KR (1) | KR101974993B1 (enExample) |
| CN (1) | CN103917624B (enExample) |
| BR (1) | BR112014005903B1 (enExample) |
| ES (1) | ES2554951T5 (enExample) |
| WO (1) | WO2013040178A1 (enExample) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| ES2554951T5 (es) | 2011-09-13 | 2019-07-18 | Lubrizol Advanced Mat Inc | Micro-geles polimerizados en dispersión con respuesta frente a tensioactivos |
| CN104994836B (zh) * | 2012-12-20 | 2018-10-19 | 路博润先进材料公司 | 刺激性减轻聚合物及其用途 |
| JP6407885B2 (ja) * | 2012-12-20 | 2018-10-17 | ルブリゾル アドバンスド マテリアルズ, インコーポレイテッド | 刺激緩和ポリマーおよびその使用 |
| BR112015021509A2 (pt) * | 2013-03-08 | 2017-07-18 | Lubrizol Advanced Mat Inc | usos de pelo menos um tensoativo aniônico e de um polímero de dispersão não iônico anfifílico |
| KR20150128792A (ko) * | 2013-03-08 | 2015-11-18 | 루브리졸 어드밴스드 머티어리얼스, 인코포레이티드 | 케라틴성 기재로부터 실리콘 침적의 손실을 완화시키는 폴리머 및 방법 |
| WO2014164092A1 (en) * | 2013-03-11 | 2014-10-09 | Lubrizol Advanced Materials, Inc. | Process for preparing surfactant responsive emulsion polymers |
| US11180690B2 (en) | 2013-03-14 | 2021-11-23 | Flotek Chemistry, Llc | Diluted microemulsions with low surface tensions |
| US9868893B2 (en) | 2013-03-14 | 2018-01-16 | Flotek Chemistry, Llc | Methods and compositions for use in oil and/or gas wells |
| US10000693B2 (en) * | 2013-03-14 | 2018-06-19 | Flotek Chemistry, Llc | Methods and compositions for use in oil and/or gas wells |
| US10883037B2 (en) | 2013-06-26 | 2021-01-05 | Halliburton Energy Services, Inc. | Crosslinked n-vinylpyrrolidone polymers for use in subterranean formations and wells |
| US10017680B2 (en) | 2013-06-26 | 2018-07-10 | Halliburton Energy Services, Inc. | Crosslinked N-vinylpyrrolidone polymers for use in subterranean formations and wells |
| US10414963B2 (en) * | 2013-06-26 | 2019-09-17 | Halliburton Energy Services, Inc. | High-temperature crosslinked polymer for use in a well |
| GB2524232A (en) * | 2014-02-19 | 2015-09-23 | Bp Exploration Operating | Process |
| CN104481434A (zh) * | 2014-11-14 | 2015-04-01 | 中国石油大学(华东) | 一种提高钻井液携岩能力的方法 |
| JP2018505252A (ja) * | 2014-12-17 | 2018-02-22 | ルブリゾル アドバンスド マテリアルズ, インコーポレイテッド | 界面活性剤応答性乳化重合マイクロゲル |
| GB2538582B (en) * | 2014-12-22 | 2017-06-14 | M-I L L C | Organic-inorganic hybrid polymer based fluids |
| GB2549658B (en) * | 2015-02-23 | 2021-12-08 | Halliburton Energy Services Inc | Crosslinked polymer compositions and methods for use in subterranean formation operations |
| CA3007790A1 (en) * | 2015-12-08 | 2017-06-15 | Kemira Oyj | Liquid polymer compositions |
| JP7072506B2 (ja) | 2016-07-08 | 2022-05-20 | 株式会社日本触媒 | N-ビニルラクタム系架橋重合体、化粧料、インク用吸収剤及び吸収性複合体 |
| CN107759729B (zh) * | 2016-08-17 | 2020-12-11 | 中国石油化工股份有限公司 | 一种钻井液用耐温耐盐增黏剂、制备方法及应用 |
| BR102016019117B1 (pt) * | 2016-08-17 | 2021-08-17 | Natura Cosméticos S.A. | Composição cosmética antissinais, uso da composição, método para tratamento antissinais e método para recuperação da firmeza e elasticidade da pele do rosto |
| WO2018118679A1 (en) * | 2016-12-19 | 2018-06-28 | Lubrizol Advanced Materials, Inc. | Surfactant responsive emulsion polymerized micro-gels |
| US11584903B2 (en) * | 2017-10-05 | 2023-02-21 | Lubrizol Advanced Materials, Inc. | Structured unit dose cleansing product |
| WO2019182126A1 (ja) | 2018-03-23 | 2019-09-26 | 株式会社 資生堂 | コア-コロナ型ポリマー粒子 |
| CN111886268B (zh) | 2018-03-23 | 2023-05-30 | 株式会社资生堂 | 使用核-壳型聚合物颗粒的化妆品用原料和水包油型乳化化妆品 |
| CN109401746B (zh) * | 2018-10-23 | 2021-05-14 | 中国石油化工股份有限公司 | 乳液自分散相渗调节剂及制备方法 |
| EP3874007A1 (en) * | 2018-11-02 | 2021-09-08 | Rhodia Operations S.A. | Polymer dispersions for wax inhibition during stimulation treatment |
| CN110105928A (zh) * | 2019-05-08 | 2019-08-09 | 成都碧隆双田化工科技有限公司 | 一种油田用低分子量的环保型粘土稳定剂及其制备方法 |
| EP4157987A4 (en) * | 2020-05-29 | 2024-06-19 | ISP Investments LLC | A suspending polymer composition, and method of use thereof |
| WO2025081371A1 (en) * | 2023-10-18 | 2025-04-24 | Saudi Arabian Oil Company | High performance fracturing foam and related methods |
Family Cites Families (72)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US33156A (en) | 1861-08-27 | Improvement in machinery for ringing fog-bells | ||
| US2798053A (en) | 1952-09-03 | 1957-07-02 | Goodrich Co B F | Carboxylic polymers |
| US2858281A (en) | 1954-01-22 | 1958-10-28 | Goodrich Co B F | Insoluble, acid and alkali-resistant carboxylic polymers |
| US3032538A (en) | 1959-04-28 | 1962-05-01 | Goodrich Co B F | Cross-linked carboxylic polymers |
| US3480546A (en) | 1964-02-28 | 1969-11-25 | Dow Chemical Co | Aqueous foam containing a waterswellable polymer flameproofing composition and process of making same |
| DE2514100A1 (de) * | 1975-03-29 | 1976-10-07 | Henkel & Cie Gmbh | Kosmetische emulsionen vom wasser- in-oel-typ und deren herstellung |
| US4282928A (en) * | 1977-07-08 | 1981-08-11 | The Dow Chemical Co. | Method for controlling permeability of subterranean formations |
| EP0019315B1 (en) | 1979-05-16 | 1983-05-25 | Procter & Gamble European Technical Center | Highly concentrated fatty acid containing liquid detergent compositions |
| US4384096A (en) | 1979-08-27 | 1983-05-17 | The Dow Chemical Company | Liquid emulsion polymers useful as pH responsive thickeners for aqueous systems |
| US4284532A (en) | 1979-10-11 | 1981-08-18 | The Procter & Gamble Company | Stable liquid detergent compositions |
| US4375533A (en) | 1981-07-08 | 1983-03-01 | The Bf Goodrich Company | Polymerization process for carboxyl containing polymers |
| US4419502A (en) | 1982-09-29 | 1983-12-06 | The B. F. Goodrich Company | Polymerization process for carboxyl containing polymers |
| US4421902A (en) | 1982-09-30 | 1983-12-20 | Rohm And Haas Company | Alkyl, poly(oxyethylene) poly(carbonyloxyethylene) acrylate emulsion copolymers for thickening purposes |
| US4526937A (en) | 1983-08-31 | 1985-07-02 | The B. F. Goodrich Company | Polycarbonates having plasticizers with fugitive activity |
| US4514552A (en) | 1984-08-23 | 1985-04-30 | Desoto, Inc. | Alkali soluble latex thickeners |
| US4600761A (en) | 1985-04-04 | 1986-07-15 | Alco Chemical Corporation | Acrylic emulsion copolymers for thickening aqueous systems and copolymerizable surfactant monomers for use therein |
| US4616074A (en) | 1985-10-01 | 1986-10-07 | Alco Chemical Corporation | Acrylic-methylene succinic ester emulsion copolymers for thickening aqueous systems |
| US4692502A (en) | 1986-06-09 | 1987-09-08 | The Standard Oil Company | Polymerization process for carboxyl containing polymers utilizing oil soluble ionic surface active agents |
| US4722962A (en) | 1986-06-12 | 1988-02-02 | Desoto, Inc. | Nonionic associative thickeners |
| US4758641A (en) | 1987-02-24 | 1988-07-19 | The B F Goodrich Company | Polycarboxylic acids with small amount of residual monomer |
| US5011978A (en) | 1989-03-02 | 1991-04-30 | National Starch And Chemical Investment Holding Corporation | Copolymers as thickeners and modifiers for latex systems |
| CA2079098A1 (en) | 1990-04-16 | 1991-10-17 | Neil A. Randen | Mildness additives for skin cleansing compositions |
| US5139770A (en) | 1990-12-17 | 1992-08-18 | Isp Investments Inc. | Cosmetic compositions containing strongly swellable, moderately crosslinked polyvinylpyrrolidone |
| US5292843A (en) | 1992-05-29 | 1994-03-08 | Union Carbide Chemicals & Plastics Technology Corporation | Polymers containing macromonomers |
| US5288814A (en) | 1992-08-26 | 1994-02-22 | The B. F. Goodrich Company | Easy to disperse polycarboxylic acid thickeners |
| IT1272109B (it) | 1993-03-19 | 1997-06-11 | Eniricerche Spa | Processo per la preparazione di apg |
| US5294692A (en) | 1993-06-30 | 1994-03-15 | National Starch And Chemical Investment Holding Corporation | Associative monomers and polymers |
| DE4422881A1 (de) * | 1993-10-25 | 1995-04-27 | Bayer Ag | Kolloidal dispergierbare Wirkstoff-Formulierungen |
| US5874495A (en) | 1994-10-03 | 1999-02-23 | Rhodia Inc. | Polymers useful as PH responsive thickeners and monomers therefor |
| US5605685A (en) | 1995-09-13 | 1997-02-25 | Isp Investments Inc. | Non-irritating skin and hair rejuvenating compostion having a pH between 1 and 6.5 |
| US5663258A (en) | 1996-02-20 | 1997-09-02 | Isp Investments Inc. | Strongly swellable, moderately crosslinked copolymers of vinylpyrrolidone and vinyl acetate |
| JPH10121030A (ja) * | 1996-08-16 | 1998-05-12 | Natl Starch & Chem Investment Holding Corp | ポリマーレオロジー調節剤 |
| NZ330278A (en) * | 1996-08-16 | 2000-02-28 | Nat Starch & Chemical Invest H | Aqueous compositions containing an acrylate based polymeric rheology modifier used as a thickener |
| SG67989A1 (en) * | 1996-08-16 | 1999-10-19 | Nat Starch Chem Invest | Thickened personal care composition |
| US5770543A (en) | 1996-09-06 | 1998-06-23 | Henkel Corporation | Agricultural compositions comprising alkyl polyglycosides and fatty acids |
| IT1291520B1 (it) | 1997-04-09 | 1999-01-11 | 3V Sigma Spa | Copolimeri acrilici in emulsione acquosa con miglior potere addesante e sospendente;nuovi monomeri e loro preparazione |
| EP0892039A1 (en) | 1997-07-18 | 1999-01-20 | The Procter & Gamble Company | Liquid cleaning compositions |
| US5985294A (en) * | 1997-11-05 | 1999-11-16 | The Procter & Gamble Company | Personal care compositions |
| GB9903140D0 (en) | 1999-02-12 | 1999-04-07 | Basf Ag | Interpolymers |
| EP1069142B1 (de) | 1999-07-15 | 2010-04-28 | Clariant Produkte (Deutschland) GmbH | Wasserlösliche Polymere und ihre Verwendung in kosmetischen und pharmazeutischen Mitteln |
| US6525129B1 (en) * | 1999-12-20 | 2003-02-25 | Avery Dennison Corporation | Water-soluble pressure-sensitive adhesives |
| US6780209B1 (en) | 2000-01-24 | 2004-08-24 | The Lubrizol Corporation | Partially dehydrated reaction product process for making same, and emulsion containing same |
| US6635702B1 (en) | 2000-04-11 | 2003-10-21 | Noveon Ip Holdings Corp. | Stable aqueous surfactant compositions |
| US7749945B2 (en) * | 2000-06-13 | 2010-07-06 | Baker Hughes Incorporated | Invert emulsion drilling fluid systems comprising an emulsified aqueous phase comprising dispersed integral latex particles |
| US6573375B2 (en) | 2000-12-20 | 2003-06-03 | Union Carbide Chemicals & Plastics Technology Corporation | Liquid thickener for surfactant systems |
| US20030147833A1 (en) * | 2001-12-20 | 2003-08-07 | L'oreal | Reshapable hair styling non-rinse composition comprising (meth)acrylic copolymers |
| US20040057923A9 (en) * | 2001-12-20 | 2004-03-25 | Isabelle Rollat | Reshapable hair styling rinse composition comprising (meth)acrylic copolymers |
| US7378479B2 (en) | 2002-09-13 | 2008-05-27 | Lubrizol Advanced Materials, Inc. | Multi-purpose polymers, methods and compositions |
| DE10243037A1 (de) | 2002-09-17 | 2004-03-25 | Henkel Kgaa | Haarbehandlungsmittel mit festigenden Eigenschaften |
| DE10243038A1 (de) | 2002-09-17 | 2004-03-25 | Henkel Kgaa | Haarbehandlungsmittel mit konditionierenden Eigenschaften |
| US8088404B2 (en) * | 2003-03-20 | 2012-01-03 | Medtronic Vasular, Inc. | Biocompatible controlled release coatings for medical devices and related methods |
| AU2004270669A1 (en) | 2003-08-28 | 2005-03-17 | Irina Ganopolsky | Methods of reducing irritation in personal care compositions |
| US7205271B2 (en) | 2004-10-14 | 2007-04-17 | Isp Investments Inc. | Rheology modifier/hair styling resin |
| US7220713B2 (en) | 2005-04-13 | 2007-05-22 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Low amounts of high molecular weight polymers for enhancing viscosity of aqueous/aqueous biphasic liquids |
| DE102005063376B4 (de) * | 2005-11-26 | 2018-10-11 | Tougas Oilfield Solutions Gmbh | Pfropfcopolymere und deren Verwendung |
| ATE469197T1 (de) * | 2005-12-08 | 2010-06-15 | Hercules Inc | Lösungsmittelfreie verflüssigte polymer- suspensionen für ölfeld-wartungsflüssigkeiten |
| US7786027B2 (en) | 2006-05-05 | 2010-08-31 | The Procter & Gamble Company | Functionalized substrates comprising perfume microcapsules |
| EP2079765B1 (en) | 2006-11-09 | 2016-01-27 | Lubrizol Advanced Materials, Inc. | Irritation mitigating polymers and uses therefor |
| JP5245347B2 (ja) | 2006-11-22 | 2013-07-24 | ライオン株式会社 | 毛髪化粧料 |
| FR2920782B1 (fr) * | 2007-09-07 | 2010-07-30 | Arkema France | Fluide de forage contenant des nanotubes de carbone |
| FR2920978B1 (fr) | 2007-09-14 | 2012-04-27 | Oreal | Composition cosmetique comprenant un copolymere cationique et un amidon et procede de traitement cosmetique. |
| FR2920969B1 (fr) | 2007-09-14 | 2009-12-18 | Oreal | Compositions cosmetiques contenant un copolymere cationique, une silicone aminee et un polymere cationique et leurs utilisations. |
| EP2090295B2 (en) * | 2008-02-11 | 2018-08-22 | The Procter and Gamble Company | Method and composition for reducing the drying time of hair |
| EP2328547B1 (en) | 2008-09-02 | 2014-03-05 | Basf Se | Copolymers useful as rheology modifiers and home and personal care compositions |
| US9089491B2 (en) | 2008-11-26 | 2015-07-28 | L'oréal | Cosmetic compositions with a spongy texture |
| US20100184631A1 (en) | 2009-01-16 | 2010-07-22 | Schlumberger Technology Corporation | Provision of viscous compositions below ground |
| EP2486063B1 (en) | 2009-10-07 | 2018-03-28 | Akzo Nobel Chemicals International B.V. | Superhydrophilic amphiphilic copolymers and processes for making the same |
| BR112012013051A2 (pt) | 2009-12-01 | 2016-11-22 | Lubrizol Advanced Mat Inc | composição e produto |
| KR101963693B1 (ko) * | 2011-09-13 | 2019-03-29 | 루브리졸 어드밴스드 머티어리얼스, 인코포레이티드 | 계면활성제 반응성 마이크로-겔 |
| ES2554951T5 (es) | 2011-09-13 | 2019-07-18 | Lubrizol Advanced Mat Inc | Micro-geles polimerizados en dispersión con respuesta frente a tensioactivos |
| CN103890131A (zh) | 2011-09-13 | 2014-06-25 | 路博润高级材料公司 | 表面活性剂响应性乳液聚合的微凝胶 |
| WO2013054760A1 (ja) | 2011-10-11 | 2013-04-18 | ライオン株式会社 | 化粧料 |
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| BR112014005903A2 (pt) | 2017-04-04 |
| KR20140079403A (ko) | 2014-06-26 |
| EP2756053A1 (en) | 2014-07-23 |
| EP2756053B1 (en) | 2015-11-18 |
| JP2016194091A (ja) | 2016-11-17 |
| BR112014005903B1 (pt) | 2021-03-02 |
| ES2554951T3 (es) | 2015-12-28 |
| CN103917624B (zh) | 2018-11-23 |
| KR101974993B1 (ko) | 2019-05-03 |
| WO2013040178A1 (en) | 2013-03-21 |
| US9714376B2 (en) | 2017-07-25 |
| CN103917624A (zh) | 2014-07-09 |
| JP6165735B2 (ja) | 2017-07-19 |
| US20140341957A1 (en) | 2014-11-20 |
| JP2014532094A (ja) | 2014-12-04 |
| EP2756053B2 (en) | 2019-04-03 |
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