JP5703231B2 - 非ヒドロカルビル疎水性変性ポリカルボン酸ポリマー - Google Patents
非ヒドロカルビル疎水性変性ポリカルボン酸ポリマー Download PDFInfo
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- JP5703231B2 JP5703231B2 JP2011537598A JP2011537598A JP5703231B2 JP 5703231 B2 JP5703231 B2 JP 5703231B2 JP 2011537598 A JP2011537598 A JP 2011537598A JP 2011537598 A JP2011537598 A JP 2011537598A JP 5703231 B2 JP5703231 B2 JP 5703231B2
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- carboxylic acid
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- 239000002253 acid Substances 0.000 title claims description 13
- 229920000642 polymer Polymers 0.000 title description 33
- 239000000178 monomer Substances 0.000 claims description 65
- 229920001577 copolymer Polymers 0.000 claims description 48
- 230000002209 hydrophobic effect Effects 0.000 claims description 39
- -1 poly (dimethylsiloxane) group Polymers 0.000 claims description 38
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 22
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 20
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims description 16
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 claims description 16
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 15
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 14
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 claims description 10
- 150000001735 carboxylic acids Chemical class 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 9
- JQGGYGKXKWTXTF-UHFFFAOYSA-N 1-ethenoxy-3-prop-2-enoxy-2,2-bis(prop-2-enoxymethyl)propane Chemical compound C=CCOCC(COCC=C)(COCC=C)COC=C JQGGYGKXKWTXTF-UHFFFAOYSA-N 0.000 claims description 8
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 8
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 8
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 6
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 6
- JQRRFDWXQOQICD-UHFFFAOYSA-N biphenylen-1-ylboronic acid Chemical compound C12=CC=CC=C2C2=C1C=CC=C2B(O)O JQRRFDWXQOQICD-UHFFFAOYSA-N 0.000 claims description 6
- KAKZBPTYRLMSJV-UHFFFAOYSA-N butadiene group Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 6
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 6
- 239000011976 maleic acid Substances 0.000 claims description 6
- 229940086737 allyl sucrose Drugs 0.000 claims description 5
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 claims description 4
- RFIMISVNSAUMBU-UHFFFAOYSA-N 2-(hydroxymethyl)-2-(prop-2-enoxymethyl)propane-1,3-diol Chemical group OCC(CO)(CO)COCC=C RFIMISVNSAUMBU-UHFFFAOYSA-N 0.000 claims description 4
- MUZDXNQOSGWMJJ-UHFFFAOYSA-N 2-methylprop-2-enoic acid;prop-2-enoic acid Chemical compound OC(=O)C=C.CC(=C)C(O)=O MUZDXNQOSGWMJJ-UHFFFAOYSA-N 0.000 claims description 4
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 4
- 150000003926 acrylamides Chemical class 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims description 4
- SZTBMYHIYNGYIA-UHFFFAOYSA-N 2-chloroacrylic acid Chemical compound OC(=O)C(Cl)=C SZTBMYHIYNGYIA-UHFFFAOYSA-N 0.000 claims description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 3
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 125000004386 diacrylate group Chemical group 0.000 claims description 3
- 239000001530 fumaric acid Substances 0.000 claims description 3
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- ZINGPVGWKVTAAC-IAROGAJJSA-N (2z,4e)-2-chlorohexa-2,4-dienoic acid Chemical compound C\C=C\C=C(/Cl)C(O)=O ZINGPVGWKVTAAC-IAROGAJJSA-N 0.000 claims description 2
- XVOUMQNXTGKGMA-OWOJBTEDSA-N (E)-glutaconic acid Chemical compound OC(=O)C\C=C\C(O)=O XVOUMQNXTGKGMA-OWOJBTEDSA-N 0.000 claims description 2
- 239000001124 (E)-prop-1-ene-1,2,3-tricarboxylic acid Substances 0.000 claims description 2
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 claims description 2
- QLLUAUADIMPKIH-UHFFFAOYSA-N 1,2-bis(ethenyl)naphthalene Chemical compound C1=CC=CC2=C(C=C)C(C=C)=CC=C21 QLLUAUADIMPKIH-UHFFFAOYSA-N 0.000 claims description 2
- IJVRPNIWWODHHA-UHFFFAOYSA-N 2-cyanoprop-2-enoic acid Chemical compound OC(=O)C(=C)C#N IJVRPNIWWODHHA-UHFFFAOYSA-N 0.000 claims description 2
- WROUWQQRXUBECT-UHFFFAOYSA-N 2-ethylacrylic acid Chemical compound CCC(=C)C(O)=O WROUWQQRXUBECT-UHFFFAOYSA-N 0.000 claims description 2
- ONPJWQSDZCGSQM-UHFFFAOYSA-N 2-phenylprop-2-enoic acid Chemical compound OC(=O)C(=C)C1=CC=CC=C1 ONPJWQSDZCGSQM-UHFFFAOYSA-N 0.000 claims description 2
- GXLIFJYFGMHYDY-ZZXKWVIFSA-N 4-chlorocinnamic acid Chemical compound OC(=O)\C=C\C1=CC=C(Cl)C=C1 GXLIFJYFGMHYDY-ZZXKWVIFSA-N 0.000 claims description 2
- UIERETOOQGIECD-UHFFFAOYSA-N Angelic acid Natural products CC=C(C)C(O)=O UIERETOOQGIECD-UHFFFAOYSA-N 0.000 claims description 2
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 claims description 2
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- 229940091181 aconitic acid Drugs 0.000 claims description 2
- 125000005037 alkyl phenyl group Chemical group 0.000 claims description 2
- UIERETOOQGIECD-ARJAWSKDSA-N angelic acid Chemical compound C\C=C(\C)C(O)=O UIERETOOQGIECD-ARJAWSKDSA-N 0.000 claims description 2
- RLYNGYDVXRKEOO-SQQVDAMQSA-N but-2-enoic acid;(e)-but-2-enoic acid Chemical compound CC=CC(O)=O.C\C=C\C(O)=O RLYNGYDVXRKEOO-SQQVDAMQSA-N 0.000 claims description 2
- 229930016911 cinnamic acid Natural products 0.000 claims description 2
- 235000013985 cinnamic acid Nutrition 0.000 claims description 2
- GTZCVFVGUGFEME-IWQZZHSRSA-N cis-aconitic acid Chemical compound OC(=O)C\C(C(O)=O)=C\C(O)=O GTZCVFVGUGFEME-IWQZZHSRSA-N 0.000 claims description 2
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 claims description 2
- 229940018557 citraconic acid Drugs 0.000 claims description 2
- BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 claims description 2
- HNEGQIOMVPPMNR-NSCUHMNNSA-N mesaconic acid Chemical compound OC(=O)C(/C)=C/C(O)=O HNEGQIOMVPPMNR-NSCUHMNNSA-N 0.000 claims description 2
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 claims description 2
- HNEGQIOMVPPMNR-UHFFFAOYSA-N methylfumaric acid Natural products OC(=O)C(C)=CC(O)=O HNEGQIOMVPPMNR-UHFFFAOYSA-N 0.000 claims description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 2
- 239000010452 phosphate Substances 0.000 claims description 2
- QTECDUFMBMSHKR-UHFFFAOYSA-N prop-2-enyl prop-2-enoate Chemical compound C=CCOC(=O)C=C QTECDUFMBMSHKR-UHFFFAOYSA-N 0.000 claims description 2
- 239000004334 sorbic acid Substances 0.000 claims description 2
- 235000010199 sorbic acid Nutrition 0.000 claims description 2
- 229940075582 sorbic acid Drugs 0.000 claims description 2
- UFHILTCGAOPTOV-UHFFFAOYSA-N tetrakis(ethenyl)silane Chemical compound C=C[Si](C=C)(C=C)C=C UFHILTCGAOPTOV-UHFFFAOYSA-N 0.000 claims description 2
- XJPKDRJZNZMJQM-UHFFFAOYSA-N tetrakis(prop-2-enyl)stannane Chemical compound C=CC[Sn](CC=C)(CC=C)CC=C XJPKDRJZNZMJQM-UHFFFAOYSA-N 0.000 claims description 2
- GTZCVFVGUGFEME-UHFFFAOYSA-N trans-aconitic acid Natural products OC(=O)CC(C(O)=O)=CC(O)=O GTZCVFVGUGFEME-UHFFFAOYSA-N 0.000 claims description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 2
- DUKJZYZDOKKAMU-UHFFFAOYSA-N 1-chloronaphthalene-2-carbaldehyde Chemical compound C1=CC=C2C(Cl)=C(C=O)C=CC2=C1 DUKJZYZDOKKAMU-UHFFFAOYSA-N 0.000 claims 1
- HVVPYFQMCGANJX-UHFFFAOYSA-N 2-methylprop-2-enyl prop-2-enoate Chemical compound CC(=C)COC(=O)C=C HVVPYFQMCGANJX-UHFFFAOYSA-N 0.000 claims 1
- FEIQOMCWGDNMHM-UHFFFAOYSA-N 5-phenylpenta-2,4-dienoic acid Chemical compound OC(=O)C=CC=CC1=CC=CC=C1 FEIQOMCWGDNMHM-UHFFFAOYSA-N 0.000 claims 1
- 235000019260 propionic acid Nutrition 0.000 claims 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 claims 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 42
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 39
- 229920002125 Sokalan® Polymers 0.000 description 27
- 230000000052 comparative effect Effects 0.000 description 27
- 229910052757 nitrogen Inorganic materials 0.000 description 21
- 239000004094 surface-active agent Substances 0.000 description 19
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 17
- 239000000203 mixture Substances 0.000 description 14
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 13
- 125000004432 carbon atom Chemical group C* 0.000 description 12
- 239000000463 material Substances 0.000 description 11
- 230000008719 thickening Effects 0.000 description 11
- 238000010926 purge Methods 0.000 description 10
- 230000000694 effects Effects 0.000 description 9
- 238000005259 measurement Methods 0.000 description 9
- 239000003999 initiator Substances 0.000 description 8
- IIEWJVIFRVWJOD-UHFFFAOYSA-N ethyl cyclohexane Natural products CCC1CCCCC1 IIEWJVIFRVWJOD-UHFFFAOYSA-N 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 6
- 238000006116 polymerization reaction Methods 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 6
- 229920002554 vinyl polymer Polymers 0.000 description 6
- BEQKKZICTDFVMG-UHFFFAOYSA-N 1,2,3,4,6-pentaoxepane-5,7-dione Chemical compound O=C1OOOOC(=O)O1 BEQKKZICTDFVMG-UHFFFAOYSA-N 0.000 description 5
- 239000004971 Cross linker Substances 0.000 description 5
- 150000001408 amides Chemical class 0.000 description 5
- 150000008064 anhydrides Chemical class 0.000 description 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 230000015784 hyperosmotic salinity response Effects 0.000 description 5
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 5
- 229920000570 polyether Polymers 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
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- 125000004093 cyano group Chemical group *C#N 0.000 description 4
- 239000004205 dimethyl polysiloxane Substances 0.000 description 4
- 125000001033 ether group Chemical group 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
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- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
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- NOBYOEQUFMGXBP-UHFFFAOYSA-N (4-tert-butylcyclohexyl) (4-tert-butylcyclohexyl)oxycarbonyloxy carbonate Chemical compound C1CC(C(C)(C)C)CCC1OC(=O)OOC(=O)OC1CCC(C(C)(C)C)CC1 NOBYOEQUFMGXBP-UHFFFAOYSA-N 0.000 description 3
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical group [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 3
- 239000004721 Polyphenylene oxide Substances 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 125000003342 alkenyl group Chemical group 0.000 description 3
- 125000005907 alkyl ester group Chemical group 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 229960001631 carbomer Drugs 0.000 description 3
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- 229940057404 di-(4-tert-butylcyclohexyl)peroxydicarbonate Drugs 0.000 description 3
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- 239000000499 gel Substances 0.000 description 3
- 150000002431 hydrogen Chemical class 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- LEJBBGNFPAFPKQ-UHFFFAOYSA-N 2-(2-prop-2-enoyloxyethoxy)ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOC(=O)C=C LEJBBGNFPAFPKQ-UHFFFAOYSA-N 0.000 description 2
- JTHZUSWLNCPZLX-UHFFFAOYSA-N 6-fluoro-3-methyl-2h-indazole Chemical compound FC1=CC=C2C(C)=NNC2=C1 JTHZUSWLNCPZLX-UHFFFAOYSA-N 0.000 description 2
- COCLLEMEIJQBAG-UHFFFAOYSA-N 8-methylnonyl 2-methylprop-2-enoate Chemical compound CC(C)CCCCCCCOC(=O)C(C)=C COCLLEMEIJQBAG-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
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- HXNZTJULPKRNPR-UHFFFAOYSA-N borinine Chemical compound B1=CC=CC=C1 HXNZTJULPKRNPR-UHFFFAOYSA-N 0.000 description 2
- FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 2
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- 238000006243 chemical reaction Methods 0.000 description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 229940052303 ethers for general anesthesia Drugs 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
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- DNTMQTKDNSEIFO-UHFFFAOYSA-N n-(hydroxymethyl)-2-methylprop-2-enamide Chemical compound CC(=C)C(=O)NCO DNTMQTKDNSEIFO-UHFFFAOYSA-N 0.000 description 2
- 150000002825 nitriles Chemical class 0.000 description 2
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- 229910000027 potassium carbonate Inorganic materials 0.000 description 2
- 238000000518 rheometry Methods 0.000 description 2
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- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- FONWXYJNYDZEEY-UPHRSURJSA-N (z)-4-(hydroxymethylamino)-4-oxobut-2-enoic acid Chemical compound OCNC(=O)\C=C/C(O)=O FONWXYJNYDZEEY-UPHRSURJSA-N 0.000 description 1
- YLYDRLOKLHJOQR-UPHRSURJSA-N (z)-n'-(hydroxymethyl)but-2-enediamide Chemical compound NC(=O)\C=C/C(=O)NCO YLYDRLOKLHJOQR-UPHRSURJSA-N 0.000 description 1
- BHPDNFUVYQFFNK-UHFFFAOYSA-N 1-(hydroxymethyl)pyrrole-2,5-dione Chemical compound OCN1C(=O)C=CC1=O BHPDNFUVYQFFNK-UHFFFAOYSA-N 0.000 description 1
- LHHMNJZNWUJFOC-UHFFFAOYSA-N 1-chloro-2-[2-chloroethoxy(ethenyl)phosphoryl]oxyethane Chemical compound ClCCOP(=O)(C=C)OCCCl LHHMNJZNWUJFOC-UHFFFAOYSA-N 0.000 description 1
- SLBOQBILGNEPEB-UHFFFAOYSA-N 1-chloroprop-2-enylbenzene Chemical class C=CC(Cl)C1=CC=CC=C1 SLBOQBILGNEPEB-UHFFFAOYSA-N 0.000 description 1
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/12—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polysiloxanes
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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
- C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
- C08F290/02—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated end groups
- C08F290/06—Polymers provided for in subclass C08G
- C08F290/068—Polysiloxanes
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- 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
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- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
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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
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- C08F236/02—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
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- C08F236/06—Butadiene
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
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- 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
- C09K3/00—Materials not provided for elsewhere
- C09K3/20—Materials not provided for elsewhere as substitutes for glycerol in its non-chemical uses, e.g. as a base in toiletry creams or ointments
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- 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
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- C08F216/12—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 an alcohol, ether, aldehydo, ketonic, acetal or ketal radical by an ether radical
- C08F216/125—Monomers containing two or more unsaturated aliphatic radicals, e.g. trimethylolpropane triallyl ether or pentaerythritol triallyl ether
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- 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
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
- C08F220/1818—C13or longer chain (meth)acrylate, e.g. stearyl (meth)acrylate
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- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/22—Esters containing halogen
- C08F220/24—Esters containing halogen containing perhaloalkyl radicals
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- C08F222/00—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 carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
- C08F222/10—Esters
- C08F222/1006—Esters of polyhydric alcohols or polyhydric phenols
- C08F222/103—Esters of polyhydric alcohols or polyhydric phenols of trialcohols, e.g. trimethylolpropane tri(meth)acrylate
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- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Description
本出願は、2008年11月21日に出願された米国仮出願番号第61/199,960号の利益を主張し、その全体を参照により援用する。
カーボマー製品を目的とする。
として存在することによって、重合において容易に機能するオレフィン二重結合を含む酸である。この群のオレフィン性不飽和酸には、アクリル酸自体に代表されるアクリル酸類、アクリル酸、メタクリル酸、エタクリル酸、α−クロロアクリル酸、α−シアノアクリル酸、β−メチルアクリル酸(クロトン酸)、α−フェニルアクリル酸、β−アクリロキシプロピオン酸、ソルビン酸、α−クロロソルビン酸、アンゲリカ酸、桂皮酸、p−クロロ桂皮酸、β−スチリル酸(1−カルボキシル−4−フェニル−1,3−ブタジエン)、イタコン酸、シトラコン酸、メサコン酸、グルタコン酸、アコニット酸、マレイン酸、フマル酸、及びトリカルボキシエチレンなどの物質が含まれる。
を有する。
を有するモノオレフィン性アクリル酸類である。この群のうち、アクリル酸及びメタクリル酸が最も好ましい。別の有用なカルボン酸モノマーは無水マレイン酸又はマレイン酸である。
で表されるアクリル酸の誘導体などが含まれる。
を有するものである。
に基づいて通常約5質量%以下またはそれ以上の架橋性モノマーを含む。
レオメトリック・サイエンティフィックRFSIII(RFS)と、ボーリン・インスツルメンツCVO120HR(ボーリン、Bohlin)を使用して、レオロジー測定を行った。RFS(ひずみ制御レオメーター)を用いて、サンプルの線形粘弾性特性を測定した。直径40mmの平行プレートを1mmのギャップで用いた。ボーリン(ひずみ制御レオメーター)を使用してフロー曲線と降伏応力を測定した。フロー曲線のためには、直径40mmの形状の平行プレートを1mmのギャップで用いた。降伏応力のためには、直径25mmの形状の縁にのこぎり状切れ込みのある平行プレートを1mmのギャップで用いた。全ての測定は温度コントローラーを用いて25℃で行った。
最初に、サンプルを2枚の平行プレートの間のすき間に装填した。過装填したサンプルを次に取り除いた。歪み掃引を、線形性測定の目的で、1ラジアン/秒の振動数で、0.1%から20%までの傾斜歪みで行った。最大の線形歪みにて、周期掃引を0.1ラジアン/秒から100ラジアン/秒まで行った。貯蔵弾性率と損失弾性率の両方を、解析のために記録した。
最初にサンプルを2枚の平行プレートの間のすき間に充填した。過充填したサンプルを次に取り除いた。制御した速度のひずみ掃引での剪断の表を、0.01Paから200Paまで行った。粘度と剪断速度の両方を解析のために記録した。
最初にサンプルを2枚の縁に切り込みのある平行プレートの間のすき間に装填した。過装填したサンプルを次に取り除いた。制御したひずみ掃引でのひずみ傾斜を、0.01Paから500Paまで行った。応力とひずみの両方を解析のために記録した。
一度に、0.25gの乾燥ポリマーを、80mlビーカー中の50gの水の表面に置くように添加した。ポリマーを投入したときに時間の計測を始める。乾燥ポリマーが、水の表面又は水中のいずれにも見えなくなった時間を記録する。
モデル界面活性剤配合物を用いて、本発明のポリマーを含む様々な組成物の気泡安定性を試験した。
非イオン性界面活性剤を添加した。
アクリル酸、炭酸カリウム、シクロヘキサン、及び酢酸エチルは、アルドリッチ社から入手した。テトラアリルペンタエリスリトールエーテル(TAPE)は、Monomer-Polymer Dajac Labs社から得た。ジ−2−エチルへキシルパーオキシジカーボネート(Trignox EHP C-75)は、ミネラルオイル中の75%溶液としてアクゾノーベル社から入手した。α−ブチルジメチルシロキシ−ω−(3−メタクリルオキシプロピル)ポリジメチルシロキサンは、チッソ社から入手した。パーフルオロアルキルメタクリレート(ZONYL(登録商標)TN-A界面活性剤)は、E.I. du Pont de Nemours and Companyから入手した。HYPERMER(登録商標)B 246 SF 界面活性剤はユニケマ社から入手した。全ての化学品はさらに精製することなく用いた。
〔疎水性物質で変性したポリ(アクリル酸)の調製、比較例1〕
酢酸エチル(91.0g)、シクロヘキサン(78.0g)、炭酸カリウム(0.96g)、テトラアリルペンタエリスリトールエーテル(0.24g)、HYPERMER(登録商標)B 246 SF 界面活性剤(0.23g)、ステアリルメタクリレート(0.69g)、及びアクリル酸(23.0g)を、機械式撹拌機、凝縮器(コンデンサー)、及び窒素の入口/出口を備えた三ツ口の500mlの丸底フラスコに入れた。この混合物を窒素パージしながら20分間撹拌した。温度を、連続窒素パージしながら50℃に挙げ、次に窒素のオーバーフローに切り替えた。ジ−2−エチルへキシルパーオキシジカーボネート(上の割合の酢酸エチル/シクロヘキサン36ml中に0.165g)をシリンジポンプによって6時間で添加した。開始剤の添加後、温度を50℃に30分間保ってから室温まで冷やした。溶媒を、Rotavaporを使用して105〜110℃で6時間蒸発させた。
酢酸エチル(182.0g)、シクロヘキサン(156.0g)、テトラアリルペンタエリスリトールエーテル(0.51g)、HYPERMER(登録商標)B 246 SF界面活性剤、α−ブチルジメチルシロキシ−ω−(3−メタクリロキシプロピル)ポリジメチルシロキサン(Silaplane(登録商標)FM-0711シロキサン、チッソ社から入手できる)(1.44g)、及びアクリル酸(46.0g)を、機械式撹拌機、凝縮器、及び窒素の入口/出口を備えた1リットルの樹脂製釜に入れた。この混合物を窒素パージしながら20分間かき混ぜた。温度を、連続窒素パージしながら50℃に昇温し、次に窒素オーバーフローに切り替えた。ジ−2−エチルへキシルパーオキシジカーボネート(上の割合の酢酸エチル/シクロヘキサン27ml中に0.33g)をシリンジポンプによって6時間で添加した。開始剤の添加後、温度を50℃に30分間保ってから室温まで冷やした。溶媒を、Rotavaporを使用して105〜110℃で6時間蒸発させた。
酢酸エチル(182.0g)、シクロヘキサン(156.0g)、テトラアリルペンタエリスリトールエーテル(0.56g)、HYPERMER(登録商標)B 246 SF界面活性剤(0.46g)、パーフルオロアルキルメタクリレート(ZONYL(登録商標)TN-A、フルオロカーボン系界面活性剤)(1.50g)、及びアクリル酸(46.0g)を、機械式撹拌機、凝縮器、及び窒素の入口/出口を備えた1リットルの樹脂製釜に入れた。この混合物を窒素パージしながら20分間かき混ぜた。温度を、連続窒素パージしながら50℃に昇温し、次に窒素オーバーフローに切り替えた。ジ−2−エチルへキシルパーオキシジカーボネート(上の割合の酢酸エチル/シクロヘキサン27ml中に0.33g)をシリンジポンプによって6時間で添加した。開始剤の添加後、温度を50℃に30分間保ってから室温まで冷やした。溶媒を、Rotavaporを使用して105〜110℃で6時間蒸発させた。
酢酸エチル(273.0g)、シクロヘキサン(234.0g)、トリメチロールプロパンジアリルエーテル(1.90g)、HYPERMER(登録商標)B 246 SF界面活性剤(0.69g)、ブチルジメチルシロキシ−ω−(3−メタクリロキシプロピル)ポリジメチルシロキサン(Silaplane(登録商標)FM-0711シロキサン、チッソ社から入手可能)(2.16g)、及びアクリル酸(69.0g)を、機械式撹拌機、凝縮器、及び窒素の入口/出口を備えた1リットルの樹脂製釜に入れた。この混合物を窒素パージしながら60分間かき混ぜた。温度を、連続窒素パージしながら50℃に昇温し、次に窒素オーバーフローに切り替えた。ジ(4-tert-ブチルシクロへキシル)パーオキシジカーボネート(上の割合の酢酸エチル/シクロヘキサン20ml中に0.45g)をシリンジポンプによって6時間で添加した。最初の添加剤の添加後、第二の添加剤(上の割合の酢酸エチル/シクロヘキサン2m中に0.045g)を一度に添加し、温度を50℃に60分間保ってから室温まで冷やした。溶媒を、Rotavaporを使用して70〜80℃で3時間、115〜120℃で6時間、約10Torrの減圧下で蒸発させた。
酢酸エチル(273.0g)、シクロヘキサン(234.0g)、トリメチロールプロパントリメタクリレート(1.04g)、HYPERMER(登録商標)B 246 SF界面活性剤(0.69g)、ブチルジメチルシロキシ−ω−(3−メタクリロキシプロピル)ポリジメチルシロキサン(Silaplane(登録商標)FM-0711シロキサン、チッソ社から入手可能)(2.16g)、及びアクリル酸(69.0g)を、機械式撹拌機、凝縮器、及び窒素の入口/出口を備えた1リットルの樹脂製釜に入れた。この混合物を窒素パージしながら60分間かき混ぜた。温度を、連続窒素パージしながら50℃に昇温し、次に窒素オーバーフローに切り替えた。ジ(4-tert-ブチルシクロへキシル)パーオキシジカーボネート(上の割合の酢酸エチル/シクロヘキサン20ml中に0.45g)をシリンジポンプによって6時間で添加した。この最初の開始剤の添加後、第二の開始剤(上の割合の酢酸エチル/シクロヘキサン2ml中に0.045g)を一度に添加し、温度を50℃に60分間保ってから室温まで冷やした。溶媒を、Rotavaporを使用して70〜80℃で3時間、115〜120℃で6時間、約10Torrの減圧下で蒸発させた。
比較例1、Si-又はF-変性ポリ(アクリル酸)についての濡れ時間は、それぞれ、1時間、5分、及び2時間超だった。
図3及び表7に示すように、0.3〜0.7質量%の間の濃度における水性ゲルの増粘効果及び透明性を試験した。
Claims (14)
- a)オレフィン性不飽和カルボン酸の繰り返し単位と、
b)架橋されたカルボン酸コポリマーの1〜10質量%の量で存在する、非ヒドロカルビル基含有疎水性モノマーの繰り返し単位とを含む、架橋されたカルボン酸コポリマーであって、
前記コポリマーが、少なくとも2つの末端CH2=C<基を含む多官能ビニリデンモノマーで架橋されており、
前記非ヒドロカルビル基含有疎水性モノマーが、Mw500〜50,000の範囲の分子量を有するシロキサン疎水性モノマーまたはフッ素化された疎水性のモノマーを含み、
前記シロキサン疎水性モノマーが、モノメタクリレート(アクリレート)末端又はモノメタクリレート(アクリレート)官能性のポリ(ジアルキルシロキサン)基を含む、
架橋されたカルボン酸コポリマー。 - 非ヒドロカルビル基含有疎水性モノマーの前記繰り返し単位が、架橋されたカルボン酸コポリマーの3〜5質量%の量で存在する、請求項1に記載の架橋されたカルボン酸コポリマー。
- 非ヒドロカルビル基含有疎水性モノマーの前記繰り返し単位が、架橋されたカルボン酸コポリマーの3質量%の量で存在する、請求項1に記載の架橋されたカルボン酸コポリマー。
- 前記シロキサン疎水性モノマーがCH3〜C4H9の範囲のアルキル基を含む、請求項1に記載の架橋されたカルボン酸コポリマー。
- 前記シロキサン疎水性モノマーがフェニル又はアルキルフェニルから選択されたアリール基を含む、請求項1に記載の架橋されたカルボン酸コポリマー。
- 前記シロキサン疎水性モノマーが、モノビニル末端またはモノビニル官能性のポリ(ジアルキルシロキサン)及びポリ(ジアリールシロキサン)からなる群から選択される、請求項1に記載の架橋されたカルボン酸コポリマー。
- 前記シロキサン疎水性モノマーがポリ(ジメチルシロキサン)基を含む、請求項1に記載の架橋されたカルボン酸コポリマー。
- 前記オレフィン性不飽和カルボン酸が、アクリル酸、メタクリル酸、エタクリル酸、α−クロロアクリル酸、α−シアノアクリル酸、β−メチルアクリル酸(クロトン酸)、α−フェニルアクリル酸、β−アクリロキシプロピオン酸、ソルビン酸、α−クロロソルビン酸、アンゲリカ酸、桂皮酸、p−クロロ桂皮酸、β−スチリル酸(1−カルボキシル−4−フェニル−1,3−ブタジエン)、イタコン酸、シトラコン酸、メサコン酸、グルタコン酸、アコニット酸、マレイン酸、フマル酸、及びトリカルボキシエチレンからなる群から選択される、請求項1に記載の架橋されたカルボン酸コポリマー。
- 前記多官能ビニリデンモノマーが、ブタジエン、イソプレン、ジビニルベンゼン、ジビニルナフタレン、アリルアクリレート、トリメチロールプロパンジアリルエーテル、トリメチロールプロパントリアクリレート、アリルスクロース、及びテトラアリルペンタエリスリトールエーテルからなる群から選択される、請求項1に記載の架橋されたカルボン酸コポリマー。
- 前記多官能ビニリデンモノマーが、ジアリルエステル、ジメタリルエーテル、アリル又はメタリルアクリレート及びアクリルアミド類、テトラアリル錫、テトラビニルシラン、ポリアルケニルメタン、ジアクリレート類、及びジメタクリレート類、ジビニル化合物、例えば、ジビニルベンゼン、ポリアリルホスフェート、及びジアリルオキシ化合物からなる群から選択される、請求項1に記載の架橋されたカルボン酸コポリマー。
- 前記の多官能ビニリデンモノマーが、アリルペンタエリスリトール、トリメチロールプロパンジアリルエーテル、及びアリルスクロースからなる群から選択される、請求項1に記載の架橋されたカルボン酸コポリマー。
- 前記非ヒドロカルビル基含有疎水性モノマーが、フッ素化されたアルキルメタクリレートを含む、請求項1に記載の架橋されたカルボン酸コポリマー。
- 前記のオレフィン性不飽和カルボン酸がアクリル酸を含み、前記多官能ビニリデンモノマーがテトラアリルペンタエリスリトールエーテルを含み、且つ前記ポリ(ジメチルシロキサン)が、架橋されたカルボン酸コポリマーの3〜5質量%の量で存在する、請求項7に記載の架橋されたカルボン酸コポリマー。
- 前記オレフィン性不飽和カルボン酸がアクリル酸を含み、前記多官能ビニリデンモノマーがテトラアリルペンタエリスリトールエーテルを含み、且つ前記フッ素化されたアルキルメタクリレートが、架橋されたカルボン酸コポリマーの3〜5質量%の量で存在する、請求項12に記載の架橋されたカルボン酸コポリマー。
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RU2531996C2 (ru) | 2014-10-27 |
US20100130711A1 (en) | 2010-05-27 |
RU2011124513A (ru) | 2012-12-27 |
BRPI0922802A2 (pt) | 2015-12-22 |
KR101622803B1 (ko) | 2016-05-19 |
ES2523722T3 (es) | 2014-12-01 |
EP2403884A1 (en) | 2012-01-11 |
CN102224175A (zh) | 2011-10-19 |
BRPI0922802B1 (pt) | 2019-09-17 |
EP2403884B1 (en) | 2014-09-10 |
US8623977B2 (en) | 2014-01-07 |
KR20110097860A (ko) | 2011-08-31 |
WO2010059765A1 (en) | 2010-05-27 |
JP2012509959A (ja) | 2012-04-26 |
MX2011005226A (es) | 2011-06-16 |
CN102224175B (zh) | 2013-11-06 |
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