JP2010519399A5 - - Google Patents
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- JP2010519399A5 JP2010519399A5 JP2009551723A JP2009551723A JP2010519399A5 JP 2010519399 A5 JP2010519399 A5 JP 2010519399A5 JP 2009551723 A JP2009551723 A JP 2009551723A JP 2009551723 A JP2009551723 A JP 2009551723A JP 2010519399 A5 JP2010519399 A5 JP 2010519399A5
- Authority
- JP
- Japan
- Prior art keywords
- mol
- site
- fluoroelastomer
- group
- iii
- 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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- 229920001973 fluoroelastomer Polymers 0.000 claims description 42
- 229920001577 copolymer Polymers 0.000 claims description 27
- 239000000178 monomer Substances 0.000 claims description 18
- 229930185605 Bisphenol Natural products 0.000 claims description 10
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 9
- 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 claims description 8
- MIZLGWKEZAPEFJ-UHFFFAOYSA-N 1,1,2-trifluoroethene Chemical group FC=C(F)F MIZLGWKEZAPEFJ-UHFFFAOYSA-N 0.000 claims description 6
- QAERDLQYXMEHEB-UHFFFAOYSA-N 1,1,3,3,3-pentafluoroprop-1-ene Chemical group FC(F)=CC(F)(F)F QAERDLQYXMEHEB-UHFFFAOYSA-N 0.000 claims description 6
- DMUPYMORYHFFCT-UHFFFAOYSA-N 1,2,3,3,3-pentafluoroprop-1-ene Chemical group FC=C(F)C(F)(F)F DMUPYMORYHFFCT-UHFFFAOYSA-N 0.000 claims description 6
- FXRLMCRCYDHQFW-UHFFFAOYSA-N 2,3,3,3-tetrafluoropropene Chemical compound FC(=C)C(F)(F)F FXRLMCRCYDHQFW-UHFFFAOYSA-N 0.000 claims description 6
- 150000004714 phosphonium salts Chemical group 0.000 claims description 5
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 5
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 5
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium group Chemical group [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 238000004073 vulcanization Methods 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 2
- -1 1-bromo-2,2-difluoroethylene, Bromo-trifluoroethylene Chemical group 0.000 description 15
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
- GVCWGFZDSIWLMO-UHFFFAOYSA-N 4-bromo-3,3,4,4-tetrafluorobut-1-ene Chemical compound FC(F)(Br)C(F)(F)C=C GVCWGFZDSIWLMO-UHFFFAOYSA-N 0.000 description 6
- COHBNTMIFZGBGZ-UHFFFAOYSA-N 1,1,1,2,3,3-hexafluoro-2-iodo-3-(1,2,2-trifluoroethenoxy)propane Chemical compound FC(F)=C(F)OC(F)(F)C(F)(I)C(F)(F)F COHBNTMIFZGBGZ-UHFFFAOYSA-N 0.000 description 3
- QFLUCTGSGZFZKK-UHFFFAOYSA-N 1-ethenoxy-1,1,2,2-tetrafluoro-2-iodoethane Chemical compound FC(F)(I)C(F)(F)OC=C QFLUCTGSGZFZKK-UHFFFAOYSA-N 0.000 description 3
- GKFAEUUIDLYIQV-UHFFFAOYSA-N 1-ethenoxy-2-iodoethane Chemical compound ICCOC=C GKFAEUUIDLYIQV-UHFFFAOYSA-N 0.000 description 3
- OUJSWWHXKJQNMJ-UHFFFAOYSA-N 3,3,4,4-tetrafluoro-4-iodobut-1-ene Chemical compound FC(F)(I)C(F)(F)C=C OUJSWWHXKJQNMJ-UHFFFAOYSA-N 0.000 description 3
- LTWXOWGZFQVSKR-UHFFFAOYSA-N 3,3,4,5,5,5-hexafluoro-4-iodopent-1-ene Chemical compound FC(F)(F)C(F)(I)C(F)(F)C=C LTWXOWGZFQVSKR-UHFFFAOYSA-N 0.000 description 3
- BFKBHVSNXIXLCI-UHFFFAOYSA-N 3-chloro-3,4,4-trifluoro-4-iodobut-1-ene Chemical compound FC(F)(I)C(F)(Cl)C=C BFKBHVSNXIXLCI-UHFFFAOYSA-N 0.000 description 3
- GQCQMFYIFUDARF-UHFFFAOYSA-N 4-bromo-1,1,2-trifluorobut-1-ene Chemical compound FC(F)=C(F)CCBr GQCQMFYIFUDARF-UHFFFAOYSA-N 0.000 description 3
- HFEHLDPGIKPNKL-UHFFFAOYSA-N allyl iodide Chemical compound ICC=C HFEHLDPGIKPNKL-UHFFFAOYSA-N 0.000 description 3
- 239000003431 cross linking reagent Substances 0.000 description 3
- GHXZPUGJZVBLGC-UHFFFAOYSA-N iodoethene Chemical group IC=C GHXZPUGJZVBLGC-UHFFFAOYSA-N 0.000 description 3
- PZVZTKFRZJMHEM-UHFFFAOYSA-N iodotrifluoroethylene Chemical group FC(F)=C(F)I PZVZTKFRZJMHEM-UHFFFAOYSA-N 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- OWRCNXZUPFZXOS-UHFFFAOYSA-N 1,3-diphenylguanidine Chemical compound C=1C=CC=CC=1NC(=N)NC1=CC=CC=C1 OWRCNXZUPFZXOS-UHFFFAOYSA-N 0.000 description 2
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 2
- 150000001451 organic peroxides Chemical class 0.000 description 2
- VERMEZLHWFHDLK-UHFFFAOYSA-N tetrahydroxybenzene Natural products OC1=CC=C(O)C(O)=C1O VERMEZLHWFHDLK-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 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 (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/712,250 | 2007-02-27 | ||
| US11/712,250 US7576164B2 (en) | 2007-02-27 | 2007-02-27 | Curable base-resistant fluoroelastomers |
| PCT/US2008/002631 WO2008106189A1 (en) | 2007-02-27 | 2008-02-27 | Curable base-resistant fluoroelastomers |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010519399A JP2010519399A (ja) | 2010-06-03 |
| JP2010519399A5 true JP2010519399A5 (enExample) | 2011-04-07 |
| JP4982781B2 JP4982781B2 (ja) | 2012-07-25 |
Family
ID=39523464
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009551723A Expired - Fee Related JP4982781B2 (ja) | 2007-02-27 | 2008-02-27 | 硬化性の耐塩基性フルオロエラストマー |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US7576164B2 (enExample) |
| EP (1) | EP2125915B1 (enExample) |
| JP (1) | JP4982781B2 (enExample) |
| CN (1) | CN101622285A (enExample) |
| AT (1) | ATE474863T1 (enExample) |
| DE (1) | DE602008001882D1 (enExample) |
| WO (1) | WO2008106189A1 (enExample) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102741304A (zh) * | 2010-01-29 | 2012-10-17 | 旭硝子株式会社 | 含氟弹性共聚物及其制造方法 |
| WO2011125740A1 (ja) * | 2010-03-31 | 2011-10-13 | ダイキン工業株式会社 | 2,3,3,3-テトラフルオロプロペン共重合体 |
| CA2863408C (en) * | 2012-02-03 | 2020-03-24 | Greene, Tweed Technologies, Inc. | Rapid gas decompression-resistant fluoroelastomer compositions and molded articles |
| US9631036B2 (en) | 2012-09-18 | 2017-04-25 | Honeywell International Inc. | Fluoroelastomers |
| EP2968902A1 (en) * | 2013-03-15 | 2016-01-20 | Sanofi-Aventis Deutschland GmbH | Body part and diaphragm materials for medical devices |
| CN106854254A (zh) * | 2016-12-26 | 2017-06-16 | 山东华夏神舟新材料有限公司 | 快速硫化含氟弹性体及其制备方法 |
| WO2020175197A1 (ja) * | 2019-02-26 | 2020-09-03 | Agc株式会社 | 含フッ素共重合体、その製造方法、撥水撥油剤組成物及び物品 |
| EP3950323A4 (en) * | 2019-04-04 | 2022-12-28 | Agc Inc. | LAMINATE MANUFACTURING PROCESS AND LAMINATE |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4035565A (en) * | 1975-03-27 | 1977-07-12 | E. I. Du Pont De Nemours And Company | Fluoropolymer containing a small amount of bromine-containing olefin units |
| US4957975A (en) * | 1988-03-14 | 1990-09-18 | E. I. Du Pont De Nemours And Company | Fluoroelastomer composition with low tendency to foul molds |
| US4912171A (en) * | 1988-04-01 | 1990-03-27 | Minnesota Mining And Manufacturing Company | Fluoroelastomer curing process with phosphonium compound |
| US4882390A (en) * | 1988-04-01 | 1989-11-21 | Minnesota Mining And Manufacturing Company | Fluoroelastomer composition with organo-onium compounds |
| IT1269846B (it) * | 1994-05-27 | 1997-04-15 | Ausimont Spa | Composizioni fluoroelastomeriche vulcanizzabili |
| US6703450B2 (en) * | 2001-05-15 | 2004-03-09 | Dupont Dow Elastomer, L.L.C. | Curable base-resistant fluoroelastomers |
| US6852417B2 (en) * | 2002-05-09 | 2005-02-08 | Dupont Dow Elastomers, Llc | Composition for improving adhesion of base-resistant fluoroelastomers to metal, ceramic or glass substrates |
| US6803435B2 (en) * | 2002-07-18 | 2004-10-12 | 3M Innovative Properties Company | Curable fluoropolymers containing bromine groups having improved compression set |
| JP2006183804A (ja) * | 2004-12-28 | 2006-07-13 | Ntn Corp | アルカリ環境用転がり軸受 |
-
2007
- 2007-02-27 US US11/712,250 patent/US7576164B2/en not_active Expired - Fee Related
-
2008
- 2008-02-27 CN CN200880006466A patent/CN101622285A/zh active Pending
- 2008-02-27 DE DE602008001882T patent/DE602008001882D1/de active Active
- 2008-02-27 JP JP2009551723A patent/JP4982781B2/ja not_active Expired - Fee Related
- 2008-02-27 EP EP08726208A patent/EP2125915B1/en not_active Not-in-force
- 2008-02-27 WO PCT/US2008/002631 patent/WO2008106189A1/en not_active Ceased
- 2008-02-27 AT AT08726208T patent/ATE474863T1/de not_active IP Right Cessation
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