RU2471773C2 - Способ получения акрилового мономера, имеющего одну или более четвертичных аммониевых групп, и его полимеров - Google Patents
Способ получения акрилового мономера, имеющего одну или более четвертичных аммониевых групп, и его полимеров Download PDFInfo
- Publication number
- RU2471773C2 RU2471773C2 RU2009139076/04A RU2009139076A RU2471773C2 RU 2471773 C2 RU2471773 C2 RU 2471773C2 RU 2009139076/04 A RU2009139076/04 A RU 2009139076/04A RU 2009139076 A RU2009139076 A RU 2009139076A RU 2471773 C2 RU2471773 C2 RU 2471773C2
- Authority
- RU
- Russia
- Prior art keywords
- monomer
- aqueous medium
- reaction
- quaternary ammonium
- quaternary
- Prior art date
Links
- 239000000178 monomer Substances 0.000 title claims abstract description 50
- 229920000642 polymer Polymers 0.000 title claims abstract description 16
- 125000001453 quaternary ammonium group Chemical group 0.000 title claims abstract description 14
- 238000000034 method Methods 0.000 title claims abstract description 10
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 title claims abstract description 9
- 238000006243 chemical reaction Methods 0.000 claims abstract description 29
- 239000012736 aqueous medium Substances 0.000 claims abstract description 24
- 239000000376 reactant Substances 0.000 claims abstract description 20
- 239000011541 reaction mixture Substances 0.000 claims abstract description 12
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims abstract description 8
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 5
- 239000000460 chlorine Substances 0.000 claims abstract description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 8
- 150000003839 salts Chemical group 0.000 claims description 8
- 239000003505 polymerization initiator Substances 0.000 claims description 6
- 239000012535 impurity Substances 0.000 abstract description 4
- 125000001309 chloro group Chemical group Cl* 0.000 abstract description 2
- 239000003999 initiator Substances 0.000 abstract description 2
- 238000012544 monitoring process Methods 0.000 abstract 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 150000003254 radicals Chemical class 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 7
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 6
- 125000002947 alkylene group Chemical group 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 238000006116 polymerization reaction Methods 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 5
- CSPHGSFZFWKVDL-UHFFFAOYSA-M (3-chloro-2-hydroxypropyl)-trimethylazanium;chloride Chemical compound [Cl-].C[N+](C)(C)CC(O)CCl CSPHGSFZFWKVDL-UHFFFAOYSA-M 0.000 description 4
- LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
- 230000005587 bubbling Effects 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 150000002430 hydrocarbons Chemical group 0.000 description 4
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 4
- 125000006526 (C1-C2) alkyl group Chemical group 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 239000012153 distilled water Substances 0.000 description 3
- 125000005842 heteroatom Chemical group 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 125000000962 organic group Chemical group 0.000 description 3
- 125000001302 tertiary amino group Chemical group 0.000 description 3
- 150000005208 1,4-dihydroxybenzenes Chemical class 0.000 description 2
- -1 3-chloro-2-hydroxypropyl Chemical group 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 230000000379 polymerizing effect Effects 0.000 description 2
- 239000012429 reaction media Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 229930195734 saturated hydrocarbon Natural products 0.000 description 2
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 2
- 229940001584 sodium metabisulfite Drugs 0.000 description 2
- 235000010262 sodium metabisulphite Nutrition 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- CNHDIAIOKMXOLK-UHFFFAOYSA-N toluquinol Chemical compound CC1=CC(O)=CC=C1O CNHDIAIOKMXOLK-UHFFFAOYSA-N 0.000 description 2
- FLCAEMBIQVZWIF-UHFFFAOYSA-N 6-(dimethylamino)-2-methylhex-2-enamide Chemical compound CN(C)CCCC=C(C)C(N)=O FLCAEMBIQVZWIF-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 125000004103 aminoalkyl group Chemical group 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- NWVVVBRKAWDGAB-UHFFFAOYSA-N hydroquinone methyl ether Natural products COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 238000003402 intramolecular cyclocondensation reaction Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 238000010979 pH adjustment Methods 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- CSMWJXBSXGUPGY-UHFFFAOYSA-L sodium dithionate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)S([O-])(=O)=O CSMWJXBSXGUPGY-UHFFFAOYSA-L 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 125000005208 trialkylammonium group Chemical group 0.000 description 1
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/04—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups
- C07C209/06—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups by substitution of halogen atoms
- C07C209/12—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups by substitution of halogen atoms with formation of quaternary ammonium compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C231/00—Preparation of carboxylic acid amides
- C07C231/12—Preparation of carboxylic acid amides by reactions not involving the formation of carboxamide groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/62—Quaternary ammonium compounds
- C07C211/63—Quaternary ammonium compounds having quaternised nitrogen atoms bound to acyclic carbon atoms
-
- 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
- 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
- C08F220/34—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate
-
- 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
- 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
- C08F220/52—Amides or imides
- C08F220/54—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide
- C08F220/60—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide containing nitrogen in addition to the carbonamido nitrogen
-
- 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
- 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
- C08F220/52—Amides or imides
- C08F220/54—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide
- C08F220/60—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide containing nitrogen in addition to the carbonamido nitrogen
- C08F220/606—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide containing nitrogen in addition to the carbonamido nitrogen and containing other heteroatoms
-
- 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
-
- 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
- C08F226/02—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 single or double bond to nitrogen
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US91970507P | 2007-03-23 | 2007-03-23 | |
| US60/919,705 | 2007-03-23 | ||
| PCT/US2008/003589 WO2008118315A1 (en) | 2007-03-23 | 2008-03-19 | Process for making an acrylic monomer having one or more quaternary ammonium groups and its polymers |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU2009139076A RU2009139076A (ru) | 2011-04-27 |
| RU2471773C2 true RU2471773C2 (ru) | 2013-01-10 |
Family
ID=39775407
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2009139076/04A RU2471773C2 (ru) | 2007-03-23 | 2008-03-19 | Способ получения акрилового мономера, имеющего одну или более четвертичных аммониевых групп, и его полимеров |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US7858722B2 (enExample) |
| EP (1) | EP2139849A4 (enExample) |
| JP (1) | JP5185297B2 (enExample) |
| KR (1) | KR101572596B1 (enExample) |
| CN (1) | CN101687771B (enExample) |
| BR (1) | BRPI0809312A2 (enExample) |
| CA (1) | CA2681763A1 (enExample) |
| RU (1) | RU2471773C2 (enExample) |
| WO (1) | WO2008118315A1 (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8541523B2 (en) | 2010-04-05 | 2013-09-24 | Promerus, Llc | Norbornene-type polymers, compositions thereof and lithographic process using such compositions |
| CN102580607B (zh) * | 2011-12-30 | 2014-02-19 | 武汉理工大学 | 双季铵盐慢裂快凝沥青乳化剂的合成工艺 |
| CN103554526B (zh) * | 2013-10-18 | 2015-03-04 | 辽宁石油化工大学 | 一种引入双季铵阳离子分子的阴离子交换膜及其制备方法 |
| WO2018232115A1 (en) | 2017-06-15 | 2018-12-20 | Ecolab Usa Inc. | Polymer for pitch and stickies deposition control in papermaking |
| CN107619660B (zh) * | 2017-11-02 | 2020-04-14 | 中国石油化工股份有限公司 | 胶凝酸稠化剂及其制备方法 |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU1053758A3 (ru) * | 1978-12-27 | 1983-11-07 | Хемише Фабрик Штокхаузен Унд Ко (Фирма) | Способ получени сополимера на основе азотсодержащего мономера акрилового р да |
| US4495367A (en) * | 1982-07-06 | 1985-01-22 | Celanese Corporation | High charge density, cationic methacrylamide based monomers and their _polymers |
| US4973637A (en) * | 1989-02-23 | 1990-11-27 | Hi-Tek Polymers, Inc. | Polymers made from quaternary ammonium acrylic monomers |
| RU2061679C1 (ru) * | 1993-01-19 | 1996-06-10 | Нижегородский политехнический институт | Соли n-[1,1-r,r-3-диметиламинопропил(поли-1,1-r,r,-7-оксо-4,4-диметил-4,8-диазаоктаметилен)]пропенамидов и способ их получения |
| US6569261B1 (en) * | 1999-07-15 | 2003-05-27 | Rhodia Chimie | Cleaning composition comprising a water-soluble or water-dispersible polymer |
| WO2003101935A1 (en) * | 2002-06-04 | 2003-12-11 | Rhodia Inc. | Monomer compound comprising several cationic groups, process for making the same, and polymers comprising units deriving therefrom |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4387017A (en) * | 1981-12-02 | 1983-06-07 | Texaco Inc. | Demulsification of bitumen emulsions using polymers of diquaternary ammonium monomers containing hydroxyl groups |
| CA1235140A (en) * | 1982-07-06 | 1988-04-12 | Laurence G. Dammann | High charge density, cationic methacrylamide based monomers and their polymers |
| CA1235141A (en) * | 1984-03-28 | 1988-04-12 | Laurence G. Dammann | High charge density, cationic methacrylamide based monomers and their polymers |
| JPH0768678B2 (ja) * | 1985-10-04 | 1995-07-26 | 日本ピー・エム・シー株式会社 | 製紙用添加剤 |
| US6596261B1 (en) | 2000-01-25 | 2003-07-22 | Aeropharm Technology Incorporated | Method of administering a medicinal aerosol formulation |
| WO2003101410A1 (en) | 2002-06-04 | 2003-12-11 | The Procter & Gamble Company | Conditioning shampoo composition containing select cationic conditioning polymers |
| US7064232B2 (en) | 2003-12-08 | 2006-06-20 | Rhodia Inc. | Hydrophobic modified diquaternary monomers and polymers as thickening agents of acidic aqueous compositions |
-
2008
- 2008-03-19 EP EP08726971A patent/EP2139849A4/en not_active Withdrawn
- 2008-03-19 JP JP2009554559A patent/JP5185297B2/ja not_active Expired - Fee Related
- 2008-03-19 US US12/077,326 patent/US7858722B2/en not_active Expired - Fee Related
- 2008-03-19 BR BRPI0809312-1A2A patent/BRPI0809312A2/pt not_active Application Discontinuation
- 2008-03-19 CA CA002681763A patent/CA2681763A1/en not_active Abandoned
- 2008-03-19 WO PCT/US2008/003589 patent/WO2008118315A1/en not_active Ceased
- 2008-03-19 CN CN200880009512.7A patent/CN101687771B/zh not_active Expired - Fee Related
- 2008-03-19 RU RU2009139076/04A patent/RU2471773C2/ru not_active IP Right Cessation
- 2008-03-19 KR KR1020097019448A patent/KR101572596B1/ko not_active Expired - Fee Related
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU1053758A3 (ru) * | 1978-12-27 | 1983-11-07 | Хемише Фабрик Штокхаузен Унд Ко (Фирма) | Способ получени сополимера на основе азотсодержащего мономера акрилового р да |
| US4495367A (en) * | 1982-07-06 | 1985-01-22 | Celanese Corporation | High charge density, cationic methacrylamide based monomers and their _polymers |
| US4973637A (en) * | 1989-02-23 | 1990-11-27 | Hi-Tek Polymers, Inc. | Polymers made from quaternary ammonium acrylic monomers |
| RU2061679C1 (ru) * | 1993-01-19 | 1996-06-10 | Нижегородский политехнический институт | Соли n-[1,1-r,r-3-диметиламинопропил(поли-1,1-r,r,-7-оксо-4,4-диметил-4,8-диазаоктаметилен)]пропенамидов и способ их получения |
| US6569261B1 (en) * | 1999-07-15 | 2003-05-27 | Rhodia Chimie | Cleaning composition comprising a water-soluble or water-dispersible polymer |
| WO2003101935A1 (en) * | 2002-06-04 | 2003-12-11 | Rhodia Inc. | Monomer compound comprising several cationic groups, process for making the same, and polymers comprising units deriving therefrom |
Non-Patent Citations (1)
| Title |
|---|
| VOEFFRAY et. al. 193. L-Camitine. Novel Synthesis and Determination of the Optical Purity, 1987, Helvetica Chimica Acta, vol.70, pp.2058-2064. * |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2010522167A (ja) | 2010-07-01 |
| US20080234432A1 (en) | 2008-09-25 |
| CA2681763A1 (en) | 2008-10-02 |
| US7858722B2 (en) | 2010-12-28 |
| KR20100014452A (ko) | 2010-02-10 |
| CN101687771A (zh) | 2010-03-31 |
| EP2139849A1 (en) | 2010-01-06 |
| JP5185297B2 (ja) | 2013-04-17 |
| RU2009139076A (ru) | 2011-04-27 |
| WO2008118315A1 (en) | 2008-10-02 |
| CN101687771B (zh) | 2014-06-18 |
| EP2139849A4 (en) | 2012-07-04 |
| KR101572596B1 (ko) | 2015-11-27 |
| BRPI0809312A2 (pt) | 2014-10-14 |
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