JP2003531255A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2003531255A5 JP2003531255A5 JP2001578383A JP2001578383A JP2003531255A5 JP 2003531255 A5 JP2003531255 A5 JP 2003531255A5 JP 2001578383 A JP2001578383 A JP 2001578383A JP 2001578383 A JP2001578383 A JP 2001578383A JP 2003531255 A5 JP2003531255 A5 JP 2003531255A5
- Authority
- JP
- Japan
- Prior art keywords
- monomer
- ether
- item
- group
- copolymerized unit
- 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.)
- Withdrawn
Links
- 239000000178 monomer Substances 0.000 description 41
- 238000000034 method Methods 0.000 description 21
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 18
- 229920001973 fluoroelastomer Polymers 0.000 description 15
- -1 hydrocarbon olefin Chemical class 0.000 description 14
- 239000000203 mixture Substances 0.000 description 14
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 12
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 10
- 238000004073 vulcanization Methods 0.000 description 10
- 229920002554 vinyl polymer Polymers 0.000 description 8
- 239000003431 cross linking reagent Substances 0.000 description 7
- 229920001774 Perfluoroether Polymers 0.000 description 6
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 6
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 5
- BLTXWCKMNMYXEA-UHFFFAOYSA-N 1,1,2-trifluoro-2-(trifluoromethoxy)ethene Chemical group FC(F)=C(F)OC(F)(F)F BLTXWCKMNMYXEA-UHFFFAOYSA-N 0.000 description 4
- JMGNVALALWCTLC-UHFFFAOYSA-N 1-fluoro-2-(2-fluoroethenoxy)ethene Chemical compound FC=COC=CF JMGNVALALWCTLC-UHFFFAOYSA-N 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- 239000000010 aprotic solvent Substances 0.000 description 4
- 238000007334 copolymerization reaction Methods 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
- 229930195733 hydrocarbon Natural products 0.000 description 4
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 4
- 229930185605 Bisphenol Natural products 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical group CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 150000004714 phosphonium salts Chemical group 0.000 description 3
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 3
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium group Chemical group [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 3
- JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical class OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 238000006298 dechlorination reaction Methods 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 229910000000 metal hydroxide Inorganic materials 0.000 description 2
- 150000004692 metal hydroxides Chemical class 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- VERMEZLHWFHDLK-UHFFFAOYSA-N tetrahydroxybenzene Natural products OC1=CC=C(O)C(O)=C1O VERMEZLHWFHDLK-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical group [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical group [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- WQGWDDDVZFFDIG-UHFFFAOYSA-N trihydroxybenzene Natural products OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US19835100P | 2000-04-19 | 2000-04-19 | |
| US60/198,351 | 2000-04-19 | ||
| US09/815,737 | 2001-03-23 | ||
| US09/815,737 US6630244B1 (en) | 2001-03-23 | 2001-03-23 | Carbon resistant surface coating |
| PCT/US2001/012511 WO2001081285A2 (fr) | 2000-04-19 | 2001-04-18 | Nouveaux monomeres de site de traitement d'ether fluorovinylique et compositions copolymeres fluoroelastomeres |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2003531255A JP2003531255A (ja) | 2003-10-21 |
| JP2003531255A5 true JP2003531255A5 (fr) | 2008-03-21 |
Family
ID=26893695
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001578383A Withdrawn JP2003531255A (ja) | 2000-04-19 | 2001-04-18 | フルオロビニルエーテルおよびそのコポリマー組成物 |
Country Status (2)
| Country | Link |
|---|---|
| JP (1) | JP2003531255A (fr) |
| WO (1) | WO2001081285A2 (fr) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ITMI20020598A1 (it) * | 2002-03-22 | 2003-09-22 | Ausimont Spa | Fluoroelastomeri vulcanizzabili |
| US6927259B2 (en) | 2002-05-02 | 2005-08-09 | Dupont Dow Elastomers Llc | Curable base-resistant fluoroelastomers |
| JP4528713B2 (ja) * | 2005-11-16 | 2010-08-18 | Ｎｏｋ株式会社 | フッ素ゴム組成物及びフッ素ゴム架橋体の製造方法 |
| EP4306506A1 (fr) * | 2021-03-09 | 2024-01-17 | Daikin Industries, Ltd. | Éther halogéné, procédé de production de celui-ci, éther vinylique et procédé de production de celui-ci |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3207143A1 (de) * | 1982-02-27 | 1983-09-08 | Hoechst Ag, 6230 Frankfurt | Perfluorierte vinylether mit einem sekundaeren wasserstoffatom, polymere daraus, sowie verfahren zur herstellung der monomeren |
| DE3662142D1 (en) * | 1985-03-28 | 1989-03-30 | Daikin Ind Ltd | Novel fluorovinyl ether and copolymer comprising the same |
| US4982009A (en) * | 1990-01-31 | 1991-01-01 | E. I. Du Pont De Nemours And Company | Hydroxy containing fluorovinyl compounds and polymers thereof |
| CA2084092A1 (fr) * | 1990-06-04 | 1991-12-05 | Ming-Hong Hung | Ethers de trifluorovinyle a groupes fonctionnels et polymeres derives |
-
2001
- 2001-04-18 JP JP2001578383A patent/JP2003531255A/ja not_active Withdrawn
- 2001-04-18 WO PCT/US2001/012511 patent/WO2001081285A2/fr active IP Right Grant
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR101205569B1 (ko) | 플루오로엘라스토머 | |
| TWI432463B (zh) | 含氟彈性體 | |
| US7160967B2 (en) | Fluorovinyl ethers and polymers obtainable therefrom | |
| JP5404054B2 (ja) | フルオロエラストマー | |
| JP2008506834A5 (fr) | ||
| JP2004514757A5 (fr) | ||
| JP2006009010A (ja) | パーフルオロエラストマー組成物 | |
| JP4801311B2 (ja) | フルオロエラストマー | |
| JP2007502359A5 (fr) | ||
| JP5744902B2 (ja) | フルオロエラストマーの製造方法 | |
| JP2007517964A5 (fr) | ||
| EP1294666B1 (fr) | Nouveaux monomeres de site de traitement d'ether fluorovinylique et compositions copolymeres fluoroelastomeres | |
| JP3719749B2 (ja) | 熱加工性テトラフルオロエチレンコポリマー | |
| JP2003531263A5 (fr) | ||
| TWI405777B (zh) | 含氟彈性體 | |
| JP2003531255A5 (fr) | ||
| EP1629043B1 (fr) | Composition de fluoroelastomere presentant d'excellentes proprietes a basse temperature | |
| JP2002249522A (ja) | カルボキシル基含有含フッ素共重合体 | |
| JP2003531255A (ja) | フルオロビニルエーテルおよびそのコポリマー組成物 | |
| US20230357172A1 (en) | Perfluorinated Allyl Ethers and Perfluorinated Allyl Amines and Methods of Making and Using the Same |