JP2008502789A5 - - Google Patents
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- Publication number
- JP2008502789A5 JP2008502789A5 JP2007527756A JP2007527756A JP2008502789A5 JP 2008502789 A5 JP2008502789 A5 JP 2008502789A5 JP 2007527756 A JP2007527756 A JP 2007527756A JP 2007527756 A JP2007527756 A JP 2007527756A JP 2008502789 A5 JP2008502789 A5 JP 2008502789A5
- Authority
- JP
- Japan
- Prior art keywords
- fluoroelastomer
- grafted
- substantially free
- composition
- monophenol
- 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
- 229920001973 fluoroelastomer Polymers 0.000 claims description 58
- 239000000203 mixture Substances 0.000 claims description 21
- 238000000034 method Methods 0.000 claims description 16
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 15
- 239000002253 acid Substances 0.000 claims description 14
- 230000000269 nucleophilic effect Effects 0.000 claims description 14
- 239000000370 acceptor Substances 0.000 claims description 11
- 229920001971 elastomer Polymers 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 238000010438 heat treatment Methods 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 229920001577 copolymer Polymers 0.000 description 15
- 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
- -1 perfluoro Chemical group 0.000 description 8
- FDMFUZHCIRHGRG-UHFFFAOYSA-N 3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)C=C FDMFUZHCIRHGRG-UHFFFAOYSA-N 0.000 description 7
- 150000002148 esters Chemical class 0.000 description 6
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 6
- FUGYGGDSWSUORM-UHFFFAOYSA-N 4-hydroxystyrene Chemical compound OC1=CC=C(C=C)C=C1 FUGYGGDSWSUORM-UHFFFAOYSA-N 0.000 description 4
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical group COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 3
- ZFVMWEVVKGLCIJ-UHFFFAOYSA-N bisphenol AF Chemical compound C1=CC(O)=CC=C1C(C(F)(F)F)(C(F)(F)F)C1=CC=C(O)C=C1 ZFVMWEVVKGLCIJ-UHFFFAOYSA-N 0.000 description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- 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 2
- QIRNGVVZBINFMX-UHFFFAOYSA-N 2-allylphenol Chemical compound OC1=CC=CC=C1CC=C QIRNGVVZBINFMX-UHFFFAOYSA-N 0.000 description 2
- ATVJXMYDOSMEPO-UHFFFAOYSA-N 3-prop-2-enoxyprop-1-ene Chemical compound C=CCOCC=C ATVJXMYDOSMEPO-UHFFFAOYSA-N 0.000 description 2
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 2
- 229930185605 Bisphenol Natural products 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 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 2
- XGZGQQDTACZODX-UHFFFAOYSA-N n-(3-hydroxyphenyl)-n-methylacetamide Chemical compound CC(=O)N(C)C1=CC=CC(O)=C1 XGZGQQDTACZODX-UHFFFAOYSA-N 0.000 description 2
- NXPPAOGUKPJVDI-UHFFFAOYSA-N naphthalene-1,2-diol Chemical compound C1=CC=CC2=C(O)C(O)=CC=C21 NXPPAOGUKPJVDI-UHFFFAOYSA-N 0.000 description 2
- SRMZHGJLSDITLO-UHFFFAOYSA-N phenyl 3-hydroxynaphthalene-2-carboxylate Chemical compound OC1=CC2=CC=CC=C2C=C1C(=O)OC1=CC=CC=C1 SRMZHGJLSDITLO-UHFFFAOYSA-N 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001733 carboxylic acid esters Chemical class 0.000 description 1
- 125000002843 carboxylic acid group Chemical group 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical group 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- GHUWFVHVFLBXBR-UHFFFAOYSA-N phenyl 4-(hydroxymethyl)benzoate Chemical compound C1=CC(CO)=CC=C1C(=O)OC1=CC=CC=C1 GHUWFVHVFLBXBR-UHFFFAOYSA-N 0.000 description 1
- FCJSHPDYVMKCHI-UHFFFAOYSA-N phenyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OC1=CC=CC=C1 FCJSHPDYVMKCHI-UHFFFAOYSA-N 0.000 description 1
- ZQBAKBUEJOMQEX-UHFFFAOYSA-N phenyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 description 1
- 150000004714 phosphonium salts Chemical group 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium group Chemical group [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US57859204P | 2004-06-10 | 2004-06-10 | |
| US60/578,592 | 2004-06-10 | ||
| US11/134,098 US7253236B2 (en) | 2004-06-10 | 2005-05-20 | Grafted fluoroelastomers |
| US11/134,098 | 2005-05-20 | ||
| PCT/US2005/020409 WO2005123786A1 (en) | 2004-06-10 | 2005-06-08 | Grafted fluoroelastomers |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2008502789A JP2008502789A (ja) | 2008-01-31 |
| JP2008502789A5 true JP2008502789A5 (enExample) | 2008-07-31 |
| JP4980908B2 JP4980908B2 (ja) | 2012-07-18 |
Family
ID=34981452
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007527756A Expired - Fee Related JP4980908B2 (ja) | 2004-06-10 | 2005-06-08 | グラフト化したフルオロエラストマー |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US7253236B2 (enExample) |
| EP (1) | EP1753788B1 (enExample) |
| JP (1) | JP4980908B2 (enExample) |
| KR (1) | KR101176676B1 (enExample) |
| DE (1) | DE602005008239D1 (enExample) |
| WO (1) | WO2005123786A1 (enExample) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5179502B2 (ja) * | 2006-10-13 | 2013-04-10 | スリーエム イノベイティブ プロパティズ カンパニー | モノヒドロキシ芳香族材料を含有する粉末コーティングフルオロポリマー組成物 |
| US8125060B2 (en) | 2006-12-08 | 2012-02-28 | Infineon Technologies Ag | Electronic component with layered frame |
| US7803890B2 (en) * | 2006-12-20 | 2010-09-28 | Honeywell International Inc. | Fluorocopolymers |
| US7767758B2 (en) * | 2007-02-28 | 2010-08-03 | Xerox Corporation | Silane functionalized fluoropolymers |
| US7955659B2 (en) * | 2007-03-01 | 2011-06-07 | Xerox Corporation | Silane functionalized fluoropolymers |
| US20090197028A1 (en) * | 2008-01-31 | 2009-08-06 | Lyons Donald F | Fluoropolymers of tetrafluoroethylene and 3,3,3-trifluoropropylene |
| EP3234011A4 (en) * | 2014-12-19 | 2018-08-01 | 3M Innovative Properties Company | Curable partially fluorinated polymer compositions |
| CA2971217A1 (en) * | 2014-12-19 | 2016-06-23 | 3M Innovative Properties Company | Curable partially fluorinated polymer compositions |
| WO2017043448A1 (ja) * | 2015-09-08 | 2017-03-16 | 旭硝子株式会社 | 変性ポリテトラフルオロエチレンファインパウダー、その製造方法、およびチューブまたはホースの製造方法 |
| CN106632795B (zh) * | 2016-12-06 | 2019-02-19 | 哈尔滨工业大学无锡新材料研究院 | Uv自交联型氟橡胶及其制备方法 |
| WO2018125790A1 (en) | 2016-12-28 | 2018-07-05 | 3M Innovative Properties Company | Silicon-containing halogenated elastomers |
| CN111511777B (zh) | 2017-12-22 | 2024-01-30 | 3M创新有限公司 | 具有含硅表面层的过氧化物固化的卤化弹性体 |
| WO2024090559A1 (ja) * | 2022-10-27 | 2024-05-02 | ダイキン工業株式会社 | フッ素ゴム架橋用組成物および成形品 |
| JP2024064171A (ja) * | 2022-10-27 | 2024-05-14 | ダイキン工業株式会社 | フッ素ゴム架橋用組成物および成形品 |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4916740A (enExample) * | 1972-06-03 | 1974-02-14 | ||
| JPS53125491A (en) * | 1977-04-08 | 1978-11-01 | Daikin Ind Ltd | Fluorine-containing polymer easily curable and its curable composition |
| CA1231496A (en) | 1982-11-22 | 1988-01-12 | Richard A. Guenthner | Vulcanizing fluorocarbon elastomer with allyl ethers of aromatic polyhydroxy compounds |
| JPS6197347A (ja) * | 1984-10-18 | 1986-05-15 | Asahi Glass Co Ltd | 加硫可能な組成物 |
| IT1212111B (it) * | 1985-03-06 | 1989-11-08 | Montefluos Spa | Procedimento per preparare fluoroelastomeri insaturi. |
| US4985520A (en) * | 1988-07-29 | 1991-01-15 | Asahi Kasei Kogyo Kabushiki Kaisha | Fluoroelastomer having excellent processability |
| TW222650B (enExample) * | 1991-04-01 | 1994-04-21 | Dow Corning | |
| DE69622560T2 (de) * | 1995-06-22 | 2003-04-03 | Dyneon Llc, Oakdale | Verbesserte scorch-sicherheit von härtbaren fluorelastomerzusammensetzungen |
| US5654375A (en) * | 1996-05-24 | 1997-08-05 | Minnesota Mining And Manufacturing Company | Fluoroelastomer compositions containing organo-onium compounds |
| JPH10139968A (ja) * | 1996-11-06 | 1998-05-26 | Jsr Corp | フッ素ゴム組成物 |
| US5936060A (en) * | 1996-11-25 | 1999-08-10 | E. I. Du Pont De Nemours And Company | Perfluoroelastomer composition having improved processability |
| US6020440A (en) * | 1997-09-29 | 2000-02-01 | Dupont Dow Elastomers, L.L.C. | Process for curing elastomeric vinylidene fluoride copolymers |
| US6423784B1 (en) * | 1999-12-15 | 2002-07-23 | 3M Innovative Properties Company | Acid functional fluoropolymer membranes and method of manufacture |
| US6664339B2 (en) * | 2001-05-15 | 2003-12-16 | Dupont Dow Elastomers Llc | Curable base-resistant fluoroelastomers |
| US6703450B2 (en) * | 2001-05-15 | 2004-03-09 | Dupont Dow Elastomer, L.L.C. | Curable base-resistant fluoroelastomers |
| US6838407B2 (en) * | 2001-11-30 | 2005-01-04 | Lord Corporation | Room temperature curable fluoropolymer coating |
| WO2004000896A1 (en) | 2002-06-21 | 2003-12-31 | 3M Innovative Properties Company | Process for producing fluoropolymers having a reduced amount of polar end groups |
-
2005
- 2005-05-20 US US11/134,098 patent/US7253236B2/en not_active Expired - Fee Related
- 2005-06-08 DE DE602005008239T patent/DE602005008239D1/de not_active Expired - Lifetime
- 2005-06-08 EP EP05760401A patent/EP1753788B1/en not_active Expired - Lifetime
- 2005-06-08 JP JP2007527756A patent/JP4980908B2/ja not_active Expired - Fee Related
- 2005-06-08 WO PCT/US2005/020409 patent/WO2005123786A1/en not_active Ceased
- 2005-06-08 KR KR1020077000577A patent/KR101176676B1/ko not_active Expired - Fee Related
-
2007
- 2007-06-12 US US11/811,755 patent/US7342074B2/en not_active Expired - Fee Related
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