JP2012507610A5 - - Google Patents
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- JP2012507610A5 JP2012507610A5 JP2011534791A JP2011534791A JP2012507610A5 JP 2012507610 A5 JP2012507610 A5 JP 2012507610A5 JP 2011534791 A JP2011534791 A JP 2011534791A JP 2011534791 A JP2011534791 A JP 2011534791A JP 2012507610 A5 JP2012507610 A5 JP 2012507610A5
- Authority
- JP
- Japan
- Prior art keywords
- ethyl
- bis
- cyclohexyl
- sulfur
- cis
- 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
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- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 29
- 229910052717 sulfur Inorganic materials 0.000 claims description 29
- 239000011593 sulfur Substances 0.000 claims description 29
- 239000000203 mixture Substances 0.000 claims description 28
- 229920001971 elastomer Polymers 0.000 claims description 26
- -1 2-ethylhexyl Chemical group 0.000 claims description 17
- 239000000806 elastomer Substances 0.000 claims description 16
- 150000001334 alicyclic compounds Chemical class 0.000 claims description 11
- 239000000945 filler Substances 0.000 claims description 11
- KOUKXHPPRFNWPP-UHFFFAOYSA-N pyrazine-2,5-dicarboxylic acid;hydrate Chemical compound O.OC(=O)C1=CN=C(C(O)=O)C=N1 KOUKXHPPRFNWPP-UHFFFAOYSA-N 0.000 claims description 11
- 239000005060 rubber Substances 0.000 claims description 10
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 claims description 4
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 claims description 4
- OBEAYGIWBMQVKN-UHFFFAOYSA-N 2-[3,4-bis(2-sulfanylethyl)cyclohexyl]ethanethiol Chemical compound SCCC1CCC(CCS)C(CCS)C1 OBEAYGIWBMQVKN-UHFFFAOYSA-N 0.000 claims description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 3
- VHUAJJUEBGBMFV-UHFFFAOYSA-N s-[2-[3,4-bis(2-acetylsulfanylethyl)cyclohexyl]ethyl] ethanethioate Chemical compound CC(=O)SCCC1CCC(CCSC(C)=O)C(CCSC(C)=O)C1 VHUAJJUEBGBMFV-UHFFFAOYSA-N 0.000 claims description 3
- LGIMTQOWGOYNIL-UHFFFAOYSA-N CCCCCCC1CCC(C(C1)CCCCCCS)CCCCCCS Chemical compound CCCCCCC1CCC(C(C1)CCCCCCS)CCCCCCS LGIMTQOWGOYNIL-UHFFFAOYSA-N 0.000 claims description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- 238000004132 cross linking Methods 0.000 claims description 2
- 239000003431 cross linking reagent Substances 0.000 claims description 2
- 125000002950 monocyclic group Chemical group 0.000 claims description 2
- PMBXCGGQNSVESQ-UHFFFAOYSA-N n-hexyl mercaptan Natural products CCCCCCS PMBXCGGQNSVESQ-UHFFFAOYSA-N 0.000 claims description 2
- AHVREISWKMRAKI-UHFFFAOYSA-N s-[2-[3,5,7-tris(2-acetylsulfanylethyl)cyclooctyl]ethyl] ethanethioate Chemical compound CC(=O)SCCC1CC(CCSC(C)=O)CC(CCSC(C)=O)CC(CCSC(C)=O)C1 AHVREISWKMRAKI-UHFFFAOYSA-N 0.000 claims description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims 7
- 229910000077 silane Inorganic materials 0.000 claims 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 6
- 229940093495 ethanethiol Drugs 0.000 claims 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims 4
- 229920002857 polybutadiene Polymers 0.000 claims 4
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims 3
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims 3
- 229920001577 copolymer Polymers 0.000 claims 3
- 238000007720 emulsion polymerization reaction Methods 0.000 claims 3
- DNJIEGIFACGWOD-UHFFFAOYSA-N ethyl mercaptane Natural products CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 claims 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims 2
- 229920002943 EPDM rubber Polymers 0.000 claims 2
- 239000005062 Polybutadiene Substances 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- 229920001021 polysulfide Polymers 0.000 claims 2
- 239000005077 polysulfide Substances 0.000 claims 2
- 150000008117 polysulfides Polymers 0.000 claims 2
- 239000000377 silicon dioxide Substances 0.000 claims 2
- 229920001897 terpolymer Polymers 0.000 claims 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- 239000005065 High vinyl polybutadiene Substances 0.000 claims 1
- 239000007983 Tris buffer Substances 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- RTACIUYXLGWTAE-UHFFFAOYSA-N buta-1,3-diene;2-methylbuta-1,3-diene;styrene Chemical compound C=CC=C.CC(=C)C=C.C=CC1=CC=CC=C1 RTACIUYXLGWTAE-UHFFFAOYSA-N 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 229920003193 cis-1,4-polybutadiene polymer Polymers 0.000 claims 1
- 229920003211 cis-1,4-polyisoprene Polymers 0.000 claims 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 229930195733 hydrocarbon Natural products 0.000 claims 1
- 150000002430 hydrocarbons Chemical class 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 229920003049 isoprene rubber Polymers 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 125000006178 methyl benzyl group Chemical group 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 229920001195 polyisoprene Polymers 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- PNBWQOOPOMGVSA-UHFFFAOYSA-N s-[2-[3,4-bis(2-acetylsulfanylethyl)cyclopentyl]ethyl] ethanethioate Chemical compound CC(=O)SCCC1CC(CCSC(C)=O)C(CCSC(C)=O)C1 PNBWQOOPOMGVSA-UHFFFAOYSA-N 0.000 claims 1
- NGAHEJQQIIVZTH-UHFFFAOYSA-N s-[3-[3,4-bis(3-acetylsulfanylpropyl)cyclohexyl]propyl] ethanethioate Chemical compound CC(=O)SCCCC1CCC(CCCSC(C)=O)C(CCCSC(C)=O)C1 NGAHEJQQIIVZTH-UHFFFAOYSA-N 0.000 claims 1
- HUDRFGGMCFUAGP-UHFFFAOYSA-N s-[6-[3,4-bis(6-acetylsulfanylhexyl)cyclohexyl]hexyl] ethanethioate Chemical compound CC(=O)SCCCCCCC1CCC(CCCCCCSC(C)=O)C(CCCCCCSC(C)=O)C1 HUDRFGGMCFUAGP-UHFFFAOYSA-N 0.000 claims 1
- 239000000243 solution Substances 0.000 claims 1
- 229920003048 styrene butadiene rubber Polymers 0.000 claims 1
- 238000010059 sulfur vulcanization Methods 0.000 claims 1
- 125000003944 tolyl group Chemical group 0.000 claims 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 1
- 229920002554 vinyl polymer Polymers 0.000 claims 1
- 125000005023 xylyl group Chemical group 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- 125000002723 alicyclic group Chemical group 0.000 description 4
- 238000004821 distillation Methods 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000001924 cycloalkanes Chemical class 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- ZOLLIQAKMYWTBR-MBKAWSJDSA-N (5e,9e)-cyclododeca-1,5,9-triene Chemical compound C1C\C=C\CC\C=C\CCC=C1 ZOLLIQAKMYWTBR-MBKAWSJDSA-N 0.000 description 1
- KTRQRAQRHBLCSQ-UHFFFAOYSA-N 1,2,4-tris(ethenyl)cyclohexane Chemical compound C=CC1CCC(C=C)C(C=C)C1 KTRQRAQRHBLCSQ-UHFFFAOYSA-N 0.000 description 1
- DEDLYXHHUFCCBW-UHFFFAOYSA-N 2-[2,4,6-trimethyl-4,6-bis(2-sulfanylethyl)-1,3,5,2,4,6-trioxatrisilinan-2-yl]ethanethiol Chemical compound SCC[Si]1(C)O[Si](C)(CCS)O[Si](C)(CCS)O1 DEDLYXHHUFCCBW-UHFFFAOYSA-N 0.000 description 1
- CXQFVXUQPAXJKE-UHFFFAOYSA-N 2-[3,4-bis(2-sulfanylethyl)cyclopentyl]ethanethiol Chemical compound SCCC1CC(CCS)C(CCS)C1 CXQFVXUQPAXJKE-UHFFFAOYSA-N 0.000 description 1
- GWELISGQQPRTBJ-UHFFFAOYSA-N 2-[3,5,7-tris(2-sulfanylethyl)cyclooctyl]ethanethiol Chemical compound SCCC1CC(CCS)CC(CCS)CC(CCS)C1 GWELISGQQPRTBJ-UHFFFAOYSA-N 0.000 description 1
- IASIVARBOFVLDM-UHFFFAOYSA-N C1CC(C(CC1CC=O)CCS)CCS Chemical compound C1CC(C(CC1CC=O)CCS)CCS IASIVARBOFVLDM-UHFFFAOYSA-N 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- LMGZGXSXHCMSAA-UHFFFAOYSA-N cyclodecane Chemical compound C1CCCCCCCCC1 LMGZGXSXHCMSAA-UHFFFAOYSA-N 0.000 description 1
- DDTBPAQBQHZRDW-UHFFFAOYSA-N cyclododecane Chemical compound C1CCCCCCCCCCC1 DDTBPAQBQHZRDW-UHFFFAOYSA-N 0.000 description 1
- WJTCGQSWYFHTAC-UHFFFAOYSA-N cyclooctane Chemical compound C1CCCCCCC1 WJTCGQSWYFHTAC-UHFFFAOYSA-N 0.000 description 1
- 239000004914 cyclooctane Substances 0.000 description 1
- HHFAWKCIHAUFRX-UHFFFAOYSA-N ethoxide Chemical compound CC[O-] HHFAWKCIHAUFRX-UHFFFAOYSA-N 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- UDSWPHJWACZZHK-UHFFFAOYSA-N o-[2-[4,6-bis(2-acetylsulfanylethyl)-2,4,6-trimethyl-1,3,5,2,4,6-trioxatrisilinan-2-yl]ethyl] ethanethioate Chemical compound CC(=S)OCC[Si]1(C)O[Si](C)(CCSC(C)=O)O[Si](C)(CCSC(C)=O)O1 UDSWPHJWACZZHK-UHFFFAOYSA-N 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000008707 rearrangement Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- BKNGPSHKIVJZHF-UHFFFAOYSA-N s-[2-[3,5,7,9-tetrakis(2-acetylsulfanylethyl)cyclodecyl]ethyl] ethanethioate Chemical compound CC(=O)SCCC1CC(CCSC(C)=O)CC(CCSC(C)=O)CC(CCSC(C)=O)CC(CCSC(C)=O)C1 BKNGPSHKIVJZHF-UHFFFAOYSA-N 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/290,368 | 2008-10-30 | ||
| US12/290,368 US8124206B2 (en) | 2008-10-30 | 2008-10-30 | Sulfur-containing cycloaliphatic compound, filled sulfur-vulcanizable elastomer composition containing sulfur-containing cycloaliphatic compound and articles fabricated therefrom |
| PCT/US2009/062666 WO2010059402A1 (en) | 2008-10-30 | 2009-10-30 | Sulfur-containing cycloali phatic compound, filled sulfur-vulcanizable elastomer composition containing sulfur-containing cycloaliphatic compound and articles fabricated therefrom |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015030216A Division JP6314096B2 (ja) | 2008-10-30 | 2015-02-19 | 硫黄含有脂環式化合物、硫黄含有脂環式化合物を含有する充填剤入り硫黄加硫可能エラストマー組成物およびそれらより製造される物品 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2012507610A JP2012507610A (ja) | 2012-03-29 |
| JP2012507610A5 true JP2012507610A5 (enExample) | 2015-04-16 |
| JP5827126B2 JP5827126B2 (ja) | 2015-12-02 |
Family
ID=41435459
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011534791A Active JP5827126B2 (ja) | 2008-10-30 | 2009-10-30 | 硫黄含有脂環式化合物、硫黄含有脂環式化合物を含有する充填剤入り硫黄加硫可能エラストマー組成物およびそれらより製造される物品 |
| JP2015030216A Active JP6314096B2 (ja) | 2008-10-30 | 2015-02-19 | 硫黄含有脂環式化合物、硫黄含有脂環式化合物を含有する充填剤入り硫黄加硫可能エラストマー組成物およびそれらより製造される物品 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015030216A Active JP6314096B2 (ja) | 2008-10-30 | 2015-02-19 | 硫黄含有脂環式化合物、硫黄含有脂環式化合物を含有する充填剤入り硫黄加硫可能エラストマー組成物およびそれらより製造される物品 |
Country Status (9)
| Country | Link |
|---|---|
| US (2) | US8124206B2 (enExample) |
| EP (1) | EP2342274B1 (enExample) |
| JP (2) | JP5827126B2 (enExample) |
| KR (1) | KR101659967B1 (enExample) |
| CN (1) | CN102272211B (enExample) |
| BR (1) | BRPI0920618B1 (enExample) |
| CA (1) | CA2740175A1 (enExample) |
| TW (1) | TWI476236B (enExample) |
| WO (1) | WO2010059402A1 (enExample) |
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| KR100996576B1 (ko) | 2003-05-09 | 2010-11-24 | 주식회사 탑 엔지니어링 | 액정적하장치 및 액정적하방법 |
| BR112014000685A2 (pt) * | 2011-07-15 | 2017-11-21 | Momentive Performance Mat Inc | composições estereoisoméricas de trivinil ciclo hexano e processos para a preparação das mesmas |
| EP2853558B1 (de) | 2013-09-27 | 2016-11-09 | Continental Reifen Deutschland GmbH | Schwefelvernetzbare Kautschukmischung |
| CN103756026B (zh) * | 2013-12-04 | 2016-02-17 | 铜陵日兴电子有限公司 | 一种电容器专用混炼胶密封圈及其制备方法 |
| EP2886566B1 (de) | 2013-12-20 | 2016-09-14 | Continental Reifen Deutschland GmbH | Kautschukmischung und Fahrzeugreifen |
| DE102015208813A1 (de) | 2015-05-12 | 2016-11-17 | Continental Reifen Deutschland Gmbh | Monomer zur Copolymerisation mit Alkenen, Dienen, Vinyl-Verbindungen und/oder Vinyliden-Verbindungen, Verfahren zur Herstellung eines Copolymers, Copolymer und Kautschukmischung sowie deren Verwendung |
| US9670379B2 (en) | 2015-07-23 | 2017-06-06 | The Boeing Company | Composites transmissive to visual and infrared radiation and compositions and methods for making the composites |
| US10414870B2 (en) | 2015-07-23 | 2019-09-17 | The Boeing Company | Transparent polymers and methods for making the same |
| JP6328724B2 (ja) * | 2015-10-27 | 2018-05-23 | 住友ゴム工業株式会社 | 空気入りタイヤおよび架橋ゴム組成物 |
| JP6329609B2 (ja) * | 2015-10-27 | 2018-05-23 | 住友ゴム工業株式会社 | 空気入りタイヤおよび架橋ゴム組成物 |
| JP6328723B2 (ja) * | 2015-10-27 | 2018-05-23 | 住友ゴム工業株式会社 | 空気入りタイヤおよび架橋ゴム組成物 |
| CN108349313B (zh) | 2015-10-27 | 2020-10-27 | 住友橡胶工业株式会社 | 充气轮胎和交联橡胶组合物 |
| JP6329610B2 (ja) * | 2015-10-27 | 2018-05-23 | 住友ゴム工業株式会社 | 空気入りタイヤおよび架橋ゴム組成物 |
| CN108136846B (zh) | 2015-10-27 | 2020-11-10 | 住友橡胶工业株式会社 | 充气轮胎和交联橡胶组合物 |
| EP3369588B1 (en) | 2015-10-27 | 2020-08-05 | Sumitomo Rubber Industries, Ltd. | Pneumatic tire and crosslinked rubber composition |
| JP6329612B2 (ja) * | 2015-10-27 | 2018-05-23 | 住友ゴム工業株式会社 | 空気入りタイヤおよび架橋ゴム組成物 |
| EP3348426B1 (en) * | 2015-10-27 | 2020-09-02 | Sumitomo Rubber Industries, Ltd. | Pneumatic tire and crosslinked rubber composition |
| JP6329607B2 (ja) * | 2015-10-27 | 2018-05-23 | 住友ゴム工業株式会社 | 空気入りタイヤおよび架橋ゴム組成物 |
| JP6329608B2 (ja) * | 2015-10-27 | 2018-05-23 | 住友ゴム工業株式会社 | 空気入りタイヤおよび架橋ゴム組成物 |
| JP6329611B2 (ja) * | 2015-10-27 | 2018-05-23 | 住友ゴム工業株式会社 | 空気入りタイヤおよび架橋ゴム組成物 |
| US9611375B1 (en) | 2015-11-03 | 2017-04-04 | The Boeing Company | Rapid curing thiol epoxy resin with improved compression strength performance |
| US10307981B2 (en) * | 2017-02-15 | 2019-06-04 | VF Asia Limited | Methods for making a footwear article |
| US10837947B2 (en) | 2017-04-03 | 2020-11-17 | Eastman Chemical Company | Modified resins and uses thereof |
| ES2952658T3 (es) | 2017-04-03 | 2023-11-03 | Continental Reifen Deutschland Gmbh | Resinas modificadas y usos de las mismas |
| WO2018187243A1 (en) | 2017-04-03 | 2018-10-11 | Eastman Chemical Company | Modified resins and uses thereof |
| ES2966674T3 (es) | 2017-04-03 | 2024-04-23 | Continental Reifen Deutschland Gmbh | Resinas modificadas y usos de las mismas |
| WO2018191187A1 (en) | 2017-04-10 | 2018-10-18 | Continental Reifen Deutschland Gmbh | Functionalized resin having a polar linker |
| PT3609937T (pt) | 2017-04-10 | 2024-02-28 | Synthomer Adhesive Tech Llc | Resina funcionalizada tendo um ligante polar |
| US10815320B2 (en) | 2017-04-10 | 2020-10-27 | Eastman Chemical Company | Functionalized resin having a polar linker |
| EP3609927B1 (en) | 2017-04-10 | 2023-12-13 | Synthomer Adhesive Technologies LLC | Functionalized resin having a polar linker |
| WO2021138417A1 (en) | 2019-12-30 | 2021-07-08 | Bridgestone Corporation | Rubber compositions prepared with a polar polysulfide crosslinking agent |
| JPWO2023032664A1 (enExample) * | 2021-08-30 | 2023-03-09 | ||
| CN113943420B (zh) * | 2021-10-22 | 2022-10-04 | 韦尔通(厦门)科技股份有限公司 | 一种uv光固化树脂组合物及其制备方法和应用 |
| CN113788935B (zh) * | 2021-10-22 | 2022-05-27 | 韦尔通(厦门)科技股份有限公司 | 一种环氧树脂组合物及其制备方法和应用 |
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-
2008
- 2008-10-30 US US12/290,368 patent/US8124206B2/en active Active
-
2009
- 2009-10-26 TW TW098136177A patent/TWI476236B/zh not_active IP Right Cessation
- 2009-10-30 CA CA2740175A patent/CA2740175A1/en not_active Abandoned
- 2009-10-30 JP JP2011534791A patent/JP5827126B2/ja active Active
- 2009-10-30 KR KR1020117012275A patent/KR101659967B1/ko active Active
- 2009-10-30 EP EP09752034.0A patent/EP2342274B1/en active Active
- 2009-10-30 BR BRPI0920618-3A patent/BRPI0920618B1/pt active IP Right Grant
- 2009-10-30 CN CN2009801533833A patent/CN102272211B/zh active Active
- 2009-10-30 WO PCT/US2009/062666 patent/WO2010059402A1/en not_active Ceased
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2012
- 2012-01-17 US US13/351,818 patent/US8846170B2/en active Active
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2015
- 2015-02-19 JP JP2015030216A patent/JP6314096B2/ja active Active
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