JP2003519259A5 - - Google Patents
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- Publication number
- JP2003519259A5 JP2003519259A5 JP2001550297A JP2001550297A JP2003519259A5 JP 2003519259 A5 JP2003519259 A5 JP 2003519259A5 JP 2001550297 A JP2001550297 A JP 2001550297A JP 2001550297 A JP2001550297 A JP 2001550297A JP 2003519259 A5 JP2003519259 A5 JP 2003519259A5
- Authority
- JP
- Japan
- Prior art keywords
- fluoride
- perfluoro
- vinyl ether
- ether
- solvent
- 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.)
- Pending
Links
- 238000000034 method Methods 0.000 description 28
- -1 fluoro (4-methyl-3,6-dioxaoct-7-ene) sulfonyl fluoride Chemical compound 0.000 description 16
- 238000007334 copolymerization reaction Methods 0.000 description 8
- 239000002904 solvent Substances 0.000 description 8
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 7
- RRZIJNVZMJUGTK-UHFFFAOYSA-N 1,1,2-trifluoro-2-(1,2,2-trifluoroethenoxy)ethene Chemical compound FC(F)=C(F)OC(F)=C(F)F RRZIJNVZMJUGTK-UHFFFAOYSA-N 0.000 description 6
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- 229920001971 elastomer Polymers 0.000 description 6
- 239000000806 elastomer Substances 0.000 description 6
- 239000003999 initiator Substances 0.000 description 4
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- UPVJEODAZWTJKZ-OWOJBTEDSA-N (e)-1,2-dichloro-1,2-difluoroethene Chemical group F\C(Cl)=C(\F)Cl UPVJEODAZWTJKZ-OWOJBTEDSA-N 0.000 description 2
- BZPCMSSQHRAJCC-UHFFFAOYSA-N 1,2,3,3,4,4,5,5,5-nonafluoro-1-(1,2,3,3,4,4,5,5,5-nonafluoropent-1-enoxy)pent-1-ene Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)=C(F)OC(F)=C(F)C(F)(F)C(F)(F)C(F)(F)F BZPCMSSQHRAJCC-UHFFFAOYSA-N 0.000 description 2
- HTHNTJCVPNKCPZ-UHFFFAOYSA-N 2-chloro-1,1-difluoroethene Chemical group FC(F)=CCl HTHNTJCVPNKCPZ-UHFFFAOYSA-N 0.000 description 2
- QMIWYOZFFSLIAK-UHFFFAOYSA-N 3,3,3-trifluoro-2-(trifluoromethyl)prop-1-ene Chemical group FC(F)(F)C(=C)C(F)(F)F QMIWYOZFFSLIAK-UHFFFAOYSA-N 0.000 description 2
- FDMFUZHCIRHGRG-UHFFFAOYSA-N 3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)C=C FDMFUZHCIRHGRG-UHFFFAOYSA-N 0.000 description 2
- 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
- 229920001577 copolymer Polymers 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
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical group FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000006116 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
- BLTXWCKMNMYXEA-UHFFFAOYSA-N 1,1,2-trifluoro-2-(trifluoromethoxy)ethene Chemical compound FC(F)=C(F)OC(F)(F)F BLTXWCKMNMYXEA-UHFFFAOYSA-N 0.000 description 1
- WUMVZXWBOFOYAW-UHFFFAOYSA-N 1,2,3,3,4,4,4-heptafluoro-1-(1,2,3,3,4,4,4-heptafluorobut-1-enoxy)but-1-ene Chemical compound FC(F)(F)C(F)(F)C(F)=C(F)OC(F)=C(F)C(F)(F)C(F)(F)F WUMVZXWBOFOYAW-UHFFFAOYSA-N 0.000 description 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- WFJINAXLTGKWLB-UHFFFAOYSA-N 1-ethenoxy-1,1,2,2,3,3-hexafluoro-3-(trifluoromethoxy)propane Chemical compound FC(F)(F)OC(F)(F)C(F)(F)C(F)(F)OC=C WFJINAXLTGKWLB-UHFFFAOYSA-N 0.000 description 1
- ZLFSOCVJMGQPTE-UHFFFAOYSA-N 1-ethenoxy-1,1,2,2-tetrafluoro-2-(trifluoromethoxy)ethane Chemical compound FC(F)(F)OC(F)(F)C(F)(F)OC=C ZLFSOCVJMGQPTE-UHFFFAOYSA-N 0.000 description 1
- ODCNTFOJYJYLPH-UHFFFAOYSA-N 1-ethenoxy-1,1,2,3,3,3-hexafluoro-2-(trifluoromethoxy)propane Chemical compound FC(F)(F)OC(F)(C(F)(F)F)C(F)(F)OC=C ODCNTFOJYJYLPH-UHFFFAOYSA-N 0.000 description 1
- JMGNVALALWCTLC-UHFFFAOYSA-N 1-fluoro-2-(2-fluoroethenoxy)ethene Chemical compound FC=COC=CF JMGNVALALWCTLC-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
- XRYWSOJOSFWGLH-UHFFFAOYSA-N 2-(3-ethenoxy-1,1,2,2,3,3-hexafluoropropoxy)-1,1,1,2,3,3,3-heptafluoropropane Chemical compound FC(F)(F)C(F)(C(F)(F)F)OC(F)(F)C(F)(F)C(F)(F)OC=C XRYWSOJOSFWGLH-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
- 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
- 150000001875 compounds Chemical class 0.000 description 1
- BSVQJWUUZCXSOL-UHFFFAOYSA-N cyclohexylsulfonyl ethaneperoxoate Chemical group CC(=O)OOS(=O)(=O)C1CCCCC1 BSVQJWUUZCXSOL-UHFFFAOYSA-N 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 150000002148 esters Chemical group 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
- 229920001973 fluoroelastomer Polymers 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
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical compound FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 1
- 229920000554 ionomer Polymers 0.000 description 1
- 238000004519 manufacturing process Methods 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
- CSJWOWRPMBXQLD-UHFFFAOYSA-N perfluoromethylvinylether group Chemical group FC(=C(C(F)(F)F)F)OC(=C(F)C(F)(F)F)F CSJWOWRPMBXQLD-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 |
|---|---|---|---|
| CA2,293,846 | 1999-12-29 | ||
| CA 2293846 CA2293846A1 (fr) | 1999-12-29 | 1999-12-29 | Elastomeres fluorosulfones a faible tg a base de fluorure de vinylidene et ne contenant ni du tetrafluoroethylene, ni de l'hexafluoropropene, ni de groupement siloxane |
| CA2,299,622 | 2000-02-24 | ||
| CA002299622A CA2299622A1 (fr) | 2000-02-24 | 2000-02-24 | Elastomeres fluorosulfones a faible tg a base de fluorure de vinylidene et ne contenant ni du tetrafluoroethylene, ni de l'hexafluoropropene, ni de groupement siloxane |
| PCT/CA2000/001585 WO2001049757A1 (fr) | 1999-12-29 | 2000-12-29 | Elastomeres fluorosulfones a faible tg a base de fluorure de vinylidene |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2003519259A JP2003519259A (ja) | 2003-06-17 |
| JP2003519259A5 true JP2003519259A5 (https=) | 2012-05-31 |
Family
ID=25681440
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001550297A Pending JP2003519259A (ja) | 1999-12-29 | 2000-12-29 | 低いＴｇを有し、ビニリデンフルオライドを主成分とし、かつテトラフルオロエチレンもヘキサフルオロプロペ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 (4) | US20030148158A1 (https=) |
| EP (1) | EP1252205B1 (https=) |
| JP (1) | JP2003519259A (https=) |
| AT (1) | ATE290026T1 (https=) |
| AU (1) | AU2496101A (https=) |
| DE (1) | DE60018476T2 (https=) |
| WO (1) | WO2001049757A1 (https=) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001049760A1 (fr) * | 1999-12-29 | 2001-07-12 | HYDRO-QUéBEC | ELASTOMERES FLUOROSULFONES A FAIBLE Tg A BASE D'HEXAFLUOROPROPENE ET NE CONTENANT NI DU TETRAFLUOROETHYLENE, NI DE GROUPEMENT SILOXANE |
| US20030148158A1 (en) * | 1999-12-29 | 2003-08-07 | Ameduri Bruno Michel | Fluorosulphonated elastomers with low glass transition based on vinylidene fluoride |
| 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 |
| IT1318594B1 (it) * | 2000-06-23 | 2003-08-27 | Ausimont Spa | Processo di polimerizzazione di monomeri solfonici. |
| 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 |
| US6777515B2 (en) * | 2001-07-13 | 2004-08-17 | I. Du Pont De Nemours And Company | Functional fluorine-containing polymers and ionomers derived therefrom |
| 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 |
| US7332554B2 (en) | 2002-12-20 | 2008-02-19 | Exxonmobil Chemical Patents Inc. | Polymers with new sequence distributions |
| CA2510860C (en) | 2002-12-20 | 2012-10-09 | Exxonmobil Chemical Patents Inc. | Polymerization process utilizing hydrofluorocarbons as diluents |
| WO2006009942A1 (en) | 2004-06-21 | 2006-01-26 | Exxonmobil Chemical Patents Inc. | Polymerization process |
| US20070100101A1 (en) * | 2005-10-28 | 2007-05-03 | Ming-Hong Hung | Fluoroelastomers containing copolymerized units of vinyl esters |
| EP2046430B1 (en) * | 2006-07-28 | 2016-04-20 | ResMed Ltd. | Delivery of respiratory therapy |
| JP4720734B2 (ja) * | 2006-12-08 | 2011-07-13 | ダイキン工業株式会社 | フルオロモノマーの回収方法 |
| WO2011051168A1 (en) * | 2009-10-29 | 2011-05-05 | Solvay Solexis S.P.A. | Process for the isolation of sulfonyl fluoride polymers and polymers obtained therefrom |
| US11059922B2 (en) * | 2016-10-28 | 2021-07-13 | Solvay Specialty Polymers Italy S.P.A. | Method for cross-linking polymers |
| WO2018192368A1 (zh) * | 2017-04-18 | 2018-10-25 | 浙江汉丞科技有限公司 | 一种含氟含氯导电高分子树脂的制备方法及其制备的单面或双面填充复合薄膜和制备方法 |
| WO2022059271A1 (ja) * | 2020-09-17 | 2022-03-24 | ダイキン工業株式会社 | 含フッ素重合体及びその製造方法 |
Family Cites Families (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US367085A (en) * | 1887-07-26 | Wire-barbing machine | ||
| US303082A (en) * | 1884-08-05 | Balanced door for stoves | ||
| 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 |
| US3291843A (en) * | 1963-10-08 | 1966-12-13 | Du Pont | Fluorinated vinyl ethers and their preparation |
| US3876654A (en) * | 1970-12-23 | 1975-04-08 | Du Pont | Fluoroelastomer composition |
| SE426839B (sv) * | 1977-12-14 | 1983-02-14 | Montedison Spa | Vulkbara kompositioner av vinylidenfluoridelaster samt forfarande for vulkning herav |
| 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 |
| IT1189092B (it) * | 1986-04-29 | 1988-01-28 | Ausimont Spa | Processo di polimerizzazione in dispersione acquosa di monomeri fluorurati |
| US4948853A (en) * | 1989-05-19 | 1990-08-14 | E. I. Du Pont De Nemours And Company | Bromo-containing perfluoropolymers having iodine curesites |
| JPH10279634A (ja) * | 1997-04-02 | 1998-10-20 | Toagosei Co Ltd | 含フッ素共重合体の製造方法 |
| WO1999005126A1 (fr) * | 1997-07-25 | 1999-02-04 | Acep Inc. | Composes ioniques perfluorovinyliques et leur utilisation dans des materiaux conducteurs |
| US6025092A (en) * | 1998-02-13 | 2000-02-15 | E. I. Du Pont De Nemours And Company | Fluorinated ionomers and their uses |
| JP4417554B2 (ja) * | 1998-03-03 | 2010-02-17 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 相当にフッ素化されたイオノマー |
| DE69915824T2 (de) * | 1998-05-29 | 2005-02-03 | E.I. Du Pont De Nemours And Co., Wilmington | Färbbare fluorpolymer-fasern |
| KR20010103035A (ko) * | 1999-03-02 | 2001-11-17 | 메리 이. 보울러 | 플루오르화 공중합체를 위한 자유 라디칼 중합 방법 |
| US20030148158A1 (en) * | 1999-12-29 | 2003-08-07 | Ameduri Bruno Michel | Fluorosulphonated elastomers with low glass transition based on vinylidene fluoride |
| WO2001049760A1 (fr) * | 1999-12-29 | 2001-07-12 | HYDRO-QUéBEC | ELASTOMERES FLUOROSULFONES A FAIBLE Tg A BASE D'HEXAFLUOROPROPENE ET NE CONTENANT NI DU TETRAFLUOROETHYLENE, NI DE GROUPEMENT SILOXANE |
| WO2001049758A1 (fr) * | 1999-12-29 | 2001-07-12 | HYDRO-QUéBEC | ELASTOMERES FLUORES A FAIBLE Tg A BASE DE FLUORURE DE VINYLIDENE ET NE CONTENANT NI DU TETRAFLUOROETHYLENE, NI DE GROUPEMENT SILOXANE |
| 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 |
| CA2352417A1 (fr) * | 2001-07-05 | 2003-01-05 | Hydro-Quebec | Procede de synthese de monomeres fluorosulfones et leur copolymerisation avec des alcenes fluores |
| US7422795B2 (en) * | 2004-06-21 | 2008-09-09 | E.I. Du Pont De Nemours And Company | Polytrimethylene ether ester elastomer flexible films |
-
2000
- 2000-12-29 US US10/168,524 patent/US20030148158A1/en not_active Abandoned
- 2000-12-29 WO PCT/CA2000/001585 patent/WO2001049757A1/fr not_active Ceased
- 2000-12-29 DE DE60018476T patent/DE60018476T2/de not_active Expired - Lifetime
- 2000-12-29 JP JP2001550297A patent/JP2003519259A/ja active Pending
- 2000-12-29 EP EP00988537A patent/EP1252205B1/fr not_active Expired - Lifetime
- 2000-12-29 AU AU24961/01A patent/AU2496101A/en not_active Abandoned
- 2000-12-29 AT AT00988537T patent/ATE290026T1/de not_active IP Right Cessation
-
2005
- 2005-07-12 US US11/178,786 patent/US20060014889A1/en not_active Abandoned
-
2007
- 2007-02-02 US US11/670,826 patent/US20070185293A1/en not_active Abandoned
-
2011
- 2011-01-24 US US13/012,636 patent/US20110117306A1/en not_active Abandoned
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