JP2020514436A5 - - Google Patents
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- JP2020514436A5 JP2020514436A5 JP2019532721A JP2019532721A JP2020514436A5 JP 2020514436 A5 JP2020514436 A5 JP 2020514436A5 JP 2019532721 A JP2019532721 A JP 2019532721A JP 2019532721 A JP2019532721 A JP 2019532721A JP 2020514436 A5 JP2020514436 A5 JP 2020514436A5
- Authority
- JP
- Japan
- Prior art keywords
- weight
- acrylate
- meth
- monomer
- poly
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000178 monomer Substances 0.000 claims description 62
- 239000000203 mixture Substances 0.000 claims description 52
- 239000004908 Emulsion polymer Substances 0.000 claims description 43
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 41
- 239000000654 additive Substances 0.000 claims description 24
- 230000000996 additive effect Effects 0.000 claims description 23
- 125000000217 alkyl group Polymers 0.000 claims description 22
- 229920000642 polymer Polymers 0.000 claims description 21
- 229920006395 saturated elastomer Polymers 0.000 claims description 16
- 239000003431 cross linking reagent Substances 0.000 claims description 15
- 239000004094 surface-active agent Substances 0.000 claims description 14
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 12
- 229920001223 polyethylene glycol Polymers 0.000 claims description 11
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical group OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 10
- -1 glucoside ester Chemical class 0.000 claims description 8
- 239000012530 fluid Substances 0.000 claims description 7
- 239000004971 Cross linker Substances 0.000 claims description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical group CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 6
- 229930195729 fatty acid Natural products 0.000 claims description 6
- 239000000194 fatty acid Substances 0.000 claims description 6
- 150000004665 fatty acids Chemical class 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- 229920001451 polypropylene glycol Chemical group 0.000 claims description 6
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims description 4
- 229920000464 Poly(propylene glycol)-block-poly(ethylene glycol)-block-poly(propylene glycol) Polymers 0.000 claims description 4
- 125000002252 acyl group Chemical group 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 125000002511 behenyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- 229920001400 block copolymer Polymers 0.000 claims description 4
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims description 4
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
- 229930182478 glucoside Natural products 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims description 4
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims description 2
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 claims description 2
- TYMYJUHDFROXOO-UHFFFAOYSA-N 1,3-bis(prop-2-enoxy)-2,2-bis(prop-2-enoxymethyl)propane Chemical compound C=CCOCC(COCC=C)(COCC=C)COCC=C TYMYJUHDFROXOO-UHFFFAOYSA-N 0.000 claims description 2
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical group CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 claims description 2
- JHSWSKVODYPNDV-UHFFFAOYSA-N 2,2-bis(prop-2-enoxymethyl)propane-1,3-diol Chemical compound C=CCOCC(CO)(CO)COCC=C JHSWSKVODYPNDV-UHFFFAOYSA-N 0.000 claims description 2
- 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 2
- 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 2
- 229930006000 Sucrose Natural products 0.000 claims description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims description 2
- 125000003342 alkenyl group Chemical group 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- 239000000084 colloidal system Substances 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 150000005690 diesters Chemical class 0.000 claims description 2
- 150000008131 glucosides Chemical class 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 125000002819 montanyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical group CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims description 2
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 2
- 230000000379 polymerizing effect Effects 0.000 claims description 2
- 150000003077 polyols Chemical group 0.000 claims description 2
- 229920002689 polyvinyl acetate Polymers 0.000 claims description 2
- 239000011118 polyvinyl acetate Substances 0.000 claims description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 2
- 230000001681 protective effect Effects 0.000 claims description 2
- 125000005504 styryl group Chemical group 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 239000005720 sucrose Substances 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- 239000005977 Ethylene Substances 0.000 claims 1
- 235000021355 Stearic acid Nutrition 0.000 claims 1
- 125000001204 arachidyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- SCFQUKBBGYTJNC-UHFFFAOYSA-N heptyl prop-2-enoate Chemical compound CCCCCCCOC(=O)C=C SCFQUKBBGYTJNC-UHFFFAOYSA-N 0.000 claims 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims 1
- 239000008117 stearic acid Substances 0.000 claims 1
- 239000002280 amphoteric surfactant Substances 0.000 description 3
- 239000003945 anionic surfactant Substances 0.000 description 3
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical group [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 239000003205 fragrance Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- MRUAUOIMASANKQ-UHFFFAOYSA-N cocamidopropyl betaine Chemical group CCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC([O-])=O MRUAUOIMASANKQ-UHFFFAOYSA-N 0.000 description 1
- 229940073507 cocamidopropyl betaine Drugs 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- OGQYPPBGSLZBEG-UHFFFAOYSA-N dimethyl(dioctadecyl)azanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC OGQYPPBGSLZBEG-UHFFFAOYSA-N 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229940057950 sodium laureth sulfate Drugs 0.000 description 1
- SXHLENDCVBIJFO-UHFFFAOYSA-M sodium;2-[2-(2-dodecoxyethoxy)ethoxy]ethyl sulfate Chemical compound [Na+].CCCCCCCCCCCCOCCOCCOCCOS([O-])(=O)=O SXHLENDCVBIJFO-UHFFFAOYSA-M 0.000 description 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2023107188A JP2023120438A (ja) | 2016-12-19 | 2023-06-29 | 界面活性剤応答性乳化重合マイクロゲル |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662435968P | 2016-12-19 | 2016-12-19 | |
| US62/435,968 | 2016-12-19 | ||
| PCT/US2017/066655 WO2018118679A1 (en) | 2016-12-19 | 2017-12-15 | Surfactant responsive emulsion polymerized micro-gels |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2023107188A Division JP2023120438A (ja) | 2016-12-19 | 2023-06-29 | 界面活性剤応答性乳化重合マイクロゲル |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2020514436A JP2020514436A (ja) | 2020-05-21 |
| JP2020514436A5 true JP2020514436A5 (enExample) | 2021-01-28 |
| JP7328893B2 JP7328893B2 (ja) | 2023-08-17 |
Family
ID=61132887
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019532721A Active JP7328893B2 (ja) | 2016-12-19 | 2017-12-15 | 界面活性剤応答性乳化重合マイクロゲル |
| JP2023107188A Withdrawn JP2023120438A (ja) | 2016-12-19 | 2023-06-29 | 界面活性剤応答性乳化重合マイクロゲル |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2023107188A Withdrawn JP2023120438A (ja) | 2016-12-19 | 2023-06-29 | 界面活性剤応答性乳化重合マイクロゲル |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US11254766B2 (enExample) |
| EP (1) | EP3555147B1 (enExample) |
| JP (2) | JP7328893B2 (enExample) |
| KR (1) | KR102529819B1 (enExample) |
| CN (1) | CN110446724B (enExample) |
| ES (1) | ES2867394T3 (enExample) |
| WO (1) | WO2018118679A1 (enExample) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11912871B2 (en) * | 2018-07-12 | 2024-02-27 | Dow Global Technologies Llc | Aqueous polymer dispersion and process of making the same |
| WO2021126453A1 (en) * | 2019-12-18 | 2021-06-24 | Dow Global Technologies Llc | Aqueous dispersion of occluded polymer particles |
| EP4005599A1 (en) * | 2020-11-30 | 2022-06-01 | Elkem Silicones France SAS | Method for manufacturing a silicone elastomer article using a 3d printer |
| CN114989551A (zh) * | 2022-06-30 | 2022-09-02 | 芜湖美的智能厨电制造有限公司 | 可再生干燥材料及其制备方法、洗碗机 |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| 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 |
| DE3063434D1 (en) | 1979-05-16 | 1983-07-07 | Procter & Gamble Europ | 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 |
| US4421902A (en) | 1982-09-30 | 1983-12-20 | Rohm And Haas Company | Alkyl, poly(oxyethylene) poly(carbonyloxyethylene) acrylate emulsion copolymers for thickening purposes |
| 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 |
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| 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 |
| 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 |
| 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 |
| US5874495A (en) | 1994-10-03 | 1999-02-23 | Rhodia Inc. | Polymers useful as PH responsive thickeners and monomers therefor |
| US5663258A (en) | 1996-02-20 | 1997-09-02 | Isp Investments Inc. | Strongly swellable, moderately crosslinked copolymers of vinylpyrrolidone and vinyl acetate |
| US5770543A (en) | 1996-09-06 | 1998-06-23 | Henkel Corporation | Agricultural compositions comprising alkyl polyglycosides and fatty acids |
| DE50015912D1 (de) | 1999-07-15 | 2010-06-10 | Clariant Produkte Deutschland | Wasserlösliche Polymere und ihre Verwendung in kosmetischen und pharmazeutischen Mitteln |
| US6533873B1 (en) | 1999-09-10 | 2003-03-18 | Unilever Home & Personal Care Usa Division Of Conopco, Inc. | Suspending clear cleansing formulation |
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| US6573375B2 (en) | 2000-12-20 | 2003-06-03 | Union Carbide Chemicals & Plastics Technology Corporation | Liquid thickener for surfactant systems |
| US7378479B2 (en) | 2002-09-13 | 2008-05-27 | Lubrizol Advanced Materials, Inc. | Multi-purpose polymers, methods and compositions |
| EP1690878B1 (en) | 2005-02-14 | 2007-09-12 | Rohm and Haas Company | Thickener for aqueous systems |
| US7786027B2 (en) | 2006-05-05 | 2010-08-31 | The Procter & Gamble Company | Functionalized substrates comprising perfume microcapsules |
| BR112012013051A2 (pt) * | 2009-12-01 | 2016-11-22 | Lubrizol Advanced Mat Inc | composição e produto |
| MX356505B (es) | 2011-08-29 | 2018-05-31 | Ethox Chemicals Llc | Nuevos tensioactivos reactivos para polimerizacion de emulsion, dispersion de pigmento, y recubrimientos utravioleta (uv). |
| US9096755B2 (en) * | 2011-09-13 | 2015-08-04 | Lubrizol Advanced Materials, Inc. | Surfactant responsive micro-gels |
| ES2554951T5 (es) * | 2011-09-13 | 2019-07-18 | Lubrizol Advanced Mat Inc | Micro-geles polimerizados en dispersión con respuesta frente a tensioactivos |
| US10934393B2 (en) | 2011-10-21 | 2021-03-02 | Ethox Chemicals, Llc | Reactive surfactants for freeze-thaw stable emulsion polymers and coatings thereof |
| JP6184484B2 (ja) * | 2012-06-15 | 2017-08-23 | 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 | 界面活性剤系のためのアルキルグリコシドベースのミセル増粘剤 |
| WO2015095286A1 (en) * | 2013-12-17 | 2015-06-25 | Lubrizol Advanced Materials, Inc. | Surfactant responsive emulsion polymerization micro-gels |
| WO2016033012A1 (en) | 2014-08-28 | 2016-03-03 | Lubrizol Advanced Materials, Inc. | Conditioning compositions |
| KR20170096170A (ko) | 2014-12-17 | 2017-08-23 | 루브리졸 어드밴스드 머티어리얼스, 인코포레이티드 | 계면활성제 반응성 에멀젼 중합 마이크로-겔 |
-
2017
- 2017-12-15 EP EP17837921.0A patent/EP3555147B1/en not_active Not-in-force
- 2017-12-15 KR KR1020197020917A patent/KR102529819B1/ko active Active
- 2017-12-15 US US16/470,788 patent/US11254766B2/en active Active
- 2017-12-15 ES ES17837921T patent/ES2867394T3/es active Active
- 2017-12-15 CN CN201780086565.8A patent/CN110446724B/zh active Active
- 2017-12-15 JP JP2019532721A patent/JP7328893B2/ja active Active
- 2017-12-15 WO PCT/US2017/066655 patent/WO2018118679A1/en not_active Ceased
-
2023
- 2023-06-29 JP JP2023107188A patent/JP2023120438A/ja not_active Withdrawn
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