JP2003519261A5 - - Google Patents
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- Publication number
- JP2003519261A5 JP2003519261A5 JP2001550300A JP2001550300A JP2003519261A5 JP 2003519261 A5 JP2003519261 A5 JP 2003519261A5 JP 2001550300 A JP2001550300 A JP 2001550300A JP 2001550300 A JP2001550300 A JP 2001550300A JP 2003519261 A5 JP2003519261 A5 JP 2003519261A5
- Authority
- JP
- Japan
- Prior art keywords
- polymerization
- solvent
- carried out
- copolymerization
- alkyl
- 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
- 238000000034 method Methods 0.000 description 23
- 239000002904 solvent Substances 0.000 description 8
- 238000007334 copolymerization reaction Methods 0.000 description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- 229920001971 elastomer Polymers 0.000 description 4
- 239000000806 elastomer Substances 0.000 description 4
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical compound FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 4
- 239000003999 initiator Substances 0.000 description 4
- -1 perfluorosulfonyl Chemical group 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 2
- GAZFDPSEEIVCEX-UHFFFAOYSA-N dimethyl 2-(2-methylpropyl)propanedioate Chemical compound COC(=O)C(CC(C)C)C(=O)OC GAZFDPSEEIVCEX-UHFFFAOYSA-N 0.000 description 2
- 238000007720 emulsion polymerization reaction Methods 0.000 description 2
- CBYABTHXYJJUTO-UHFFFAOYSA-N (1-tert-butylcyclohexyl) carboxyoxy carbonate Chemical compound OC(=O)OOC(=O)OC1(C(C)(C)C)CCCCC1 CBYABTHXYJJUTO-UHFFFAOYSA-N 0.000 description 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- JGZVUTYDEVUNMK-UHFFFAOYSA-N 5-carboxy-2',7'-dichlorofluorescein Chemical compound C12=CC(Cl)=C(O)C=C2OC2=CC(O)=C(Cl)C=C2C21OC(=O)C1=CC(C(=O)O)=CC=C21 JGZVUTYDEVUNMK-UHFFFAOYSA-N 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- NUCLHURQSPMEMR-UHFFFAOYSA-N CCOCCCOC=C.F Chemical compound CCOCCCOC=C.F NUCLHURQSPMEMR-UHFFFAOYSA-N 0.000 description 1
- 150000003863 ammonium salts Chemical group 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- KVNRLNFWIYMESJ-UHFFFAOYSA-N butyronitrile Chemical compound CCCC#N KVNRLNFWIYMESJ-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 210000003850 cellular structure Anatomy 0.000 description 1
- 239000012986 chain transfer agent Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- BSVQJWUUZCXSOL-UHFFFAOYSA-N cyclohexylsulfonyl ethaneperoxoate Chemical compound CC(=O)OOS(=O)(=O)C1CCCCC1 BSVQJWUUZCXSOL-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- CWINGZLCRSDKCL-UHFFFAOYSA-N ethoxycarbonyloxy ethyl carbonate Chemical compound CCOC(=O)OOC(=O)OCC CWINGZLCRSDKCL-UHFFFAOYSA-N 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- UQSQSQZYBQSBJZ-UHFFFAOYSA-N fluorosulfonic acid Chemical class OS(F)(=O)=O UQSQSQZYBQSBJZ-UHFFFAOYSA-N 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 229920000554 ionomer Polymers 0.000 description 1
- 238000012703 microemulsion polymerization Methods 0.000 description 1
- 238000005065 mining Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- WPPLKRDOKPISSC-UHFFFAOYSA-N pentyl 2,2-dimethylpropaneperoxoate Chemical compound CCCCCOOC(=O)C(C)(C)C WPPLKRDOKPISSC-UHFFFAOYSA-N 0.000 description 1
- FYJQJMIEZVMYSD-UHFFFAOYSA-N perfluoro-2-butyltetrahydrofuran Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C1(F)OC(F)(F)C(F)(F)C1(F)F FYJQJMIEZVMYSD-UHFFFAOYSA-N 0.000 description 1
- ZJIJAJXFLBMLCK-UHFFFAOYSA-N perfluorohexane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F ZJIJAJXFLBMLCK-UHFFFAOYSA-N 0.000 description 1
- 125000005634 peroxydicarbonate group Chemical group 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000005518 polymer electrolyte Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- BWJUFXUULUEGMA-UHFFFAOYSA-N propan-2-yl propan-2-yloxycarbonyloxy carbonate Chemical compound CC(C)OC(=O)OOC(=O)OC(C)C BWJUFXUULUEGMA-UHFFFAOYSA-N 0.000 description 1
- 125000005373 siloxane group Chemical group [SiH2](O*)* 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- OPQYOFWUFGEMRZ-UHFFFAOYSA-N tert-butyl 2,2-dimethylpropaneperoxoate Chemical compound CC(C)(C)OOC(=O)C(C)(C)C OPQYOFWUFGEMRZ-UHFFFAOYSA-N 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA002293845A CA2293845A1 (fr) | 1999-12-29 | 1999-12-29 | Elastomeres fluorosulfones a faible tg a base d'hexafluoropropene et ne contenant ni du tetrafluoroethylene, ni de groupement siloxane |
| CA2,293,845 | 1999-12-29 | ||
| CA2,299,621 | 2000-02-24 | ||
| CA002299621A CA2299621A1 (fr) | 2000-02-24 | 2000-02-24 | Elastomeres fluorosulfones a faible tg a base d'hexafluoropropene et ne contenant ni du tetrafluoroethylene, ni de groupement siloxane |
| PCT/CA2000/001589 WO2001049760A1 (fr) | 1999-12-29 | 2000-12-29 | ELASTOMERES FLUOROSULFONES A FAIBLE Tg A BASE D'HEXAFLUOROPROPENE ET NE CONTENANT NI DU TETRAFLUOROETHYLENE, NI DE GROUPEMENT SILOXANE |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2003519261A JP2003519261A (ja) | 2003-06-17 |
| JP2003519261A5 true JP2003519261A5 (cg-RX-API-DMAC10.html) | 2012-05-31 |
| JP5007009B2 JP5007009B2 (ja) | 2012-08-22 |
Family
ID=25681439
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001550300A Expired - Fee Related JP5007009B2 (ja) | 1999-12-29 | 2000-12-29 | 低いＴｇを有し、ヘキサフルオロプロペンを主成分とし、テトラフルオロエチレンも、シロキサン基も含まない、フルオロスルホン化エラストマー |
Country Status (7)
| Country | Link |
|---|---|
| US (5) | US20030153699A1 (cg-RX-API-DMAC10.html) |
| EP (1) | EP1242486B1 (cg-RX-API-DMAC10.html) |
| JP (1) | JP5007009B2 (cg-RX-API-DMAC10.html) |
| AT (1) | ATE282649T1 (cg-RX-API-DMAC10.html) |
| AU (1) | AU2338301A (cg-RX-API-DMAC10.html) |
| DE (1) | DE60016030T2 (cg-RX-API-DMAC10.html) |
| WO (1) | WO2001049760A1 (cg-RX-API-DMAC10.html) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE60018476T2 (de) * | 1999-12-29 | 2006-02-16 | Hydro-Québec, Montréal | Fluorosulfoneelastomere mit niedrigem tg basierend auf vinylidenfluorit |
| JP5007009B2 (ja) * | 1999-12-29 | 2012-08-22 | ハイドロ−ケベック | 低いＴｇを有し、ヘキサフルオロプロペンを主成分とし、テトラフルオロエチレンも、シロキサン基も含まない、フルオロスルホン化エラストマー |
| CA2312194A1 (fr) * | 2000-06-13 | 2001-12-13 | Mario Boucher | Elastomeres reticulables fluores bromosulfones a faible tg a base de fluorure de vinylidene et ne contenant ni du tetrafluoroethylene ni de groupement siloxane |
| CA2328433A1 (fr) * | 2000-12-20 | 2002-06-20 | Hydro-Quebec | Elastomeres nitriles fluorosulfones reticulables a faible tg a base de fluorure de vinylidene et ne contenant ni du tetrafluoroethylene ni de groupement siloxane |
| US6861489B2 (en) * | 2001-12-06 | 2005-03-01 | Gore Enterprise Holdings, Inc. | Low equivalent weight ionomer |
| US7094851B2 (en) * | 2001-12-06 | 2006-08-22 | Gore Enterprise Holdings, Inc. | Low equivalent weight ionomer |
| US7425601B2 (en) | 2002-12-20 | 2008-09-16 | Exxonmobil Chemical Patents Inc. | Polymers with new sequence distributions |
| JP4426527B2 (ja) | 2002-12-20 | 2010-03-03 | エクソンモービル・ケミカル・パテンツ・インク | 重合プロセス |
| ATE471950T1 (de) | 2002-12-20 | 2010-07-15 | Exxonmobil Chem Patents Inc | Polymerisationsverfahren |
| WO2006009942A1 (en) | 2004-06-21 | 2006-01-26 | Exxonmobil Chemical Patents Inc. | Polymerization process |
| US20100093878A1 (en) * | 2007-12-27 | 2010-04-15 | E.I. Du Pont De Nemours And Company | Crosslinkable fluoropolymer, crosslinked fluoropolymers and crosslinked fluoropolymer membranes |
| WO2009083451A1 (en) * | 2007-12-28 | 2009-07-09 | Solvay Solexis S.P.A. | Addition reaction to fluoroallylfluorosulfate |
| US8765217B2 (en) * | 2008-11-04 | 2014-07-01 | Entrotech, Inc. | Method for continuous production of (meth)acrylate syrup and adhesives therefrom |
| US8329079B2 (en) | 2009-04-20 | 2012-12-11 | Entrochem, Inc. | Method and apparatus for continuous production of partially polymerized compositions and polymers therefrom |
| US20130090439A1 (en) * | 2011-10-05 | 2013-04-11 | Honeywell International Inc. | Polymerization Of 2,3,3,3-Tetrafluoropropene And Polymers Formed From 2,3,3,3-Tetrafluoropropene |
| US9234062B2 (en) | 2011-12-14 | 2016-01-12 | Honeywell International Inc. | Process, properties, and applications of graft copolymers |
| CN107406550A (zh) | 2015-02-12 | 2017-11-28 | 3M创新有限公司 | 具有磺酰基基团的四氟乙烯共聚物 |
| DK3256501T3 (en) | 2015-02-12 | 2019-03-18 | 3M Innovative Properties Co | TETRAFLUORETHYLEN / HEXAFLUORPROPYLEN COPOLYMERS INCLUDING PERFLUORAL COXYALKYL GROUPS AS PREPARATIONS AND METHODS OF PRODUCTION AND USE PROCEDURES |
| US10730980B2 (en) | 2015-02-12 | 2020-08-04 | 3M Innovative Properties Company | Tetrafluoroethylene/hexafluoropropylene copolymers including perfluoroalkoxyalkyl pendant groups |
| CN108503738B (zh) * | 2018-04-16 | 2020-06-26 | 中国海洋石油集团有限公司 | 一种聚偏氟乙烯树脂及其制备方法与应用 |
| CN112174855B (zh) * | 2020-11-16 | 2021-09-24 | 福州大学 | 一种磺酰氟类产物的制备方法 |
| WO2023017701A1 (ja) * | 2021-08-10 | 2023-02-16 | ダイキン工業株式会社 | 低粘度含フッ素エラストマーの製造方法 |
| JPWO2024014400A1 (cg-RX-API-DMAC10.html) * | 2022-07-13 | 2024-01-18 |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3041317A (en) * | 1960-05-02 | 1962-06-26 | Du Pont | Fluorocarbon sulfonyl fluorides |
| US3282875A (en) * | 1964-07-22 | 1966-11-01 | Du Pont | Fluorocarbon vinyl ether polymers |
| JPS57109810A (en) * | 1980-12-26 | 1982-07-08 | Asahi Glass Co Ltd | Copolymer giving fluorine-containing elastomer with cold and alcohol resistance |
| JPS5837187A (ja) * | 1981-01-16 | 1983-03-04 | イ−・アイ・デユポン・デ・ニモアス・アンド・カンパニ− | 膜 |
| US4604323A (en) * | 1985-02-22 | 1986-08-05 | E. I. Du Pont De Nemours And Company | Multilayer cation exchange membrane |
| US5478905A (en) * | 1995-02-06 | 1995-12-26 | E. I. Du Pont De Nemours And Company | Amorphous tetrafluoroethylene/hexafluoropropylene copolymers |
| US5674957A (en) * | 1995-03-10 | 1997-10-07 | The University Of North Carolina At Chapel Hill | Nonaqueous polymerization of fluoromonomers |
| JPH10279634A (ja) * | 1997-04-02 | 1998-10-20 | Toagosei Co Ltd | 含フッ素共重合体の製造方法 |
| US6288187B1 (en) * | 1997-07-25 | 2001-09-11 | Acep Inc. | Perfluorovinyl ionic compounds and their use in conductive materials |
| US6025092A (en) * | 1998-02-13 | 2000-02-15 | E. I. Du Pont De Nemours And Company | Fluorinated ionomers and their uses |
| IL137932A0 (en) * | 1998-03-03 | 2001-10-31 | Du Pont | Substantially fluorinated ionomers |
| EP1082389B1 (en) * | 1998-05-29 | 2004-03-24 | E.I. Du Pont De Nemours And Company | Dyeable fluoropolymer fibers |
| DE60018476T2 (de) * | 1999-12-29 | 2006-02-16 | Hydro-Québec, Montréal | Fluorosulfoneelastomere mit niedrigem tg basierend auf vinylidenfluorit |
| JP5007009B2 (ja) * | 1999-12-29 | 2012-08-22 | ハイドロ−ケベック | 低いＴｇを有し、ヘキサフルオロプロペンを主成分とし、テトラフルオロエチレンも、シロキサン基も含まない、フルオロスルホン化エラストマー |
-
2000
- 2000-12-29 JP JP2001550300A patent/JP5007009B2/ja not_active Expired - Fee Related
- 2000-12-29 EP EP00986958A patent/EP1242486B1/fr not_active Expired - Lifetime
- 2000-12-29 WO PCT/CA2000/001589 patent/WO2001049760A1/fr not_active Ceased
- 2000-12-29 US US10/168,525 patent/US20030153699A1/en not_active Abandoned
- 2000-12-29 DE DE60016030T patent/DE60016030T2/de not_active Expired - Lifetime
- 2000-12-29 AT AT00986958T patent/ATE282649T1/de not_active IP Right Cessation
- 2000-12-29 AU AU23383/01A patent/AU2338301A/en not_active Abandoned
-
2005
- 2005-07-18 US US11/182,858 patent/US20050282986A1/en not_active Abandoned
-
2007
- 2007-07-18 US US11/779,551 patent/US20070293643A1/en not_active Abandoned
-
2010
- 2010-09-09 US US12/878,444 patent/US20100330317A1/en not_active Abandoned
-
2012
- 2012-04-18 US US13/450,074 patent/US20120231369A1/en not_active Abandoned
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