JP2004514776A5 - - Google Patents
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- Publication number
- JP2004514776A5 JP2004514776A5 JP2002546624A JP2002546624A JP2004514776A5 JP 2004514776 A5 JP2004514776 A5 JP 2004514776A5 JP 2002546624 A JP2002546624 A JP 2002546624A JP 2002546624 A JP2002546624 A JP 2002546624A JP 2004514776 A5 JP2004514776 A5 JP 2004514776A5
- Authority
- JP
- Japan
- Prior art keywords
- weight percent
- group
- composition according
- bisphenol
- curable composition
- 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- Withdrawn
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- 239000000203 mixture Substances 0.000 description 24
- 229930185605 Bisphenol Natural products 0.000 description 10
- 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 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- 229920001973 fluoroelastomer Polymers 0.000 description 8
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 6
- 150000001451 organic peroxides Chemical class 0.000 description 6
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 4
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 4
- WPXLSICRBPNKEI-UHFFFAOYSA-N OC(=O)OC(C)CC(C)(C)OOC(C)(C)C Chemical compound OC(=O)OC(C)CC(C)(C)OOC(C)(C)C WPXLSICRBPNKEI-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 239000011630 iodine Substances 0.000 description 4
- 229910052740 iodine Inorganic materials 0.000 description 4
- 229910000000 metal hydroxide Inorganic materials 0.000 description 4
- 150000004692 metal hydroxides Chemical class 0.000 description 4
- 229910044991 metal oxide Inorganic materials 0.000 description 4
- 150000004706 metal oxides Chemical class 0.000 description 4
- 239000012764 mineral filler Substances 0.000 description 4
- -1 perfluoro Chemical group 0.000 description 4
- 150000004714 phosphonium salts Chemical group 0.000 description 4
- 150000004756 silanes Chemical class 0.000 description 4
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium group Chemical group [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 4
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- 239000010456 wollastonite Substances 0.000 description 4
- 229910052882 wollastonite Inorganic materials 0.000 description 4
- 239000003431 cross linking reagent Substances 0.000 description 3
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 3
- KOMNUTZXSVSERR-UHFFFAOYSA-N 1,3,5-tris(prop-2-enyl)-1,3,5-triazinane-2,4,6-trione Chemical compound C=CCN1C(=O)N(CC=C)C(=O)N(CC=C)C1=O KOMNUTZXSVSERR-UHFFFAOYSA-N 0.000 description 2
- BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical group C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 description 2
- DMWVYCCGCQPJEA-UHFFFAOYSA-N 2,5-bis(tert-butylperoxy)-2,5-dimethylhexane Chemical compound CC(C)(C)OOC(C)(C)CCC(C)(C)OOC(C)(C)C DMWVYCCGCQPJEA-UHFFFAOYSA-N 0.000 description 2
- YKTNISGZEGZHIS-UHFFFAOYSA-N 2-$l^{1}-oxidanyloxy-2-methylpropane Chemical group CC(C)(C)O[O] YKTNISGZEGZHIS-UHFFFAOYSA-N 0.000 description 2
- 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 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- 229910021536 Zeolite Inorganic materials 0.000 description 2
- 239000012752 auxiliary agent Substances 0.000 description 2
- 235000019400 benzoyl peroxide Nutrition 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 2
- 125000005394 methallyl group Chemical group 0.000 description 2
- 239000002808 molecular sieve Substances 0.000 description 2
- BLYOHBPLFYXHQA-UHFFFAOYSA-N n,n-bis(prop-2-enyl)prop-2-enamide Chemical compound C=CCN(CC=C)C(=O)C=C BLYOHBPLFYXHQA-UHFFFAOYSA-N 0.000 description 2
- DYUWTXWIYMHBQS-UHFFFAOYSA-N n-prop-2-enylprop-2-en-1-amine Chemical compound C=CCNCC=C DYUWTXWIYMHBQS-UHFFFAOYSA-N 0.000 description 2
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 2
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 2
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 2
- VERMEZLHWFHDLK-UHFFFAOYSA-N tetrahydroxybenzene Natural products OC1=CC=C(O)C(O)=C1O VERMEZLHWFHDLK-UHFFFAOYSA-N 0.000 description 2
- KJWHEZXBZQXVSA-UHFFFAOYSA-N tris(prop-2-enyl) phosphite Chemical compound C=CCOP(OCC=C)OCC=C KJWHEZXBZQXVSA-UHFFFAOYSA-N 0.000 description 2
- 239000010457 zeolite Substances 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910000077 silane Inorganic materials 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 (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/US2000/032674 WO2002044263A1 (en) | 2000-12-01 | 2000-12-01 | Fluoroelastomer composition having excellent processability and low temperature properties |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2004514776A JP2004514776A (ja) | 2004-05-20 |
| JP2004514776A5 true JP2004514776A5 (https=) | 2007-12-27 |
Family
ID=21742041
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002546624A Withdrawn JP2004514776A (ja) | 2000-12-01 | 2000-12-01 | 優れた加工性および低温特性を有するフルオロエラストマー組成物 |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP1337583B1 (https=) |
| JP (1) | JP2004514776A (https=) |
| KR (1) | KR20030057566A (https=) |
| DE (1) | DE60021289T2 (https=) |
| WO (1) | WO2002044263A1 (https=) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6921796B2 (en) * | 2002-07-29 | 2005-07-26 | Illinois Tool Works, Inc. | Fluoroelastomer compositions, their preparation, and their use |
| KR101022727B1 (ko) * | 2002-09-12 | 2011-03-22 | 쓰리엠 이노베이티브 프로퍼티즈 캄파니 | 내투과성이 향상된 플루오로엘라스토머 및 이의 제조 방법 |
| US7514506B2 (en) * | 2004-03-31 | 2009-04-07 | Greene, Tweed Of Delaware, Inc. | Fast curing fluoroelastomeric compositions, adhesive fluoroelastomeric compositions and methods for bonding fluoroelastomeric compositions |
| JP2007169511A (ja) * | 2005-12-22 | 2007-07-05 | Nok Corp | ゴム組成物及びフッ素ゴム架橋体の製造方法 |
| WO2008019068A2 (en) * | 2006-08-03 | 2008-02-14 | Great Lakes Chemical Corporation | Compositions and chemical production processes |
| CA2671991A1 (en) * | 2006-12-21 | 2008-07-03 | E. I. Du Pont De Nemours And Company | Crosslinkable vinyl fluoride copolymers |
| WO2011096477A1 (ja) * | 2010-02-08 | 2011-08-11 | 日本化成株式会社 | 架橋性エラストマー用架橋剤およびその応用 |
| US8227535B2 (en) * | 2010-12-07 | 2012-07-24 | E I Du Pont De Nemours And Company | Polyhydroxy curable fluoroelastomer compositions |
| US9074074B2 (en) * | 2011-12-15 | 2015-07-07 | The Chemours Company Fc, Llc | Polyhydroxy curable fluoroelastomer compositions |
| EP2873687B1 (en) * | 2013-11-13 | 2018-06-06 | GVK Coating Technology Oy | A polymer composition and a method for its preparation |
| CN117683308A (zh) * | 2015-04-24 | 2024-03-12 | Nok株式会社 | 氟橡胶组合物 |
| DE102021002431A1 (de) | 2021-05-04 | 2022-11-10 | Kaco Gmbh + Co. Kg | Fluorkautschukmischung, Dichtung aus einer solchen Fluorkautschukmischung sowie Wellendichtring mit einem Dichtkörper |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE69914923T2 (de) * | 1998-08-21 | 2004-12-09 | Dupont Dow Elastomers L.L.C., Wilmington | Fluoroelastomerzusammensetzung mit exzellenter verarbeitbarkeit und gute eigenschaften bei niedrigen temperaturen |
| US6291576B1 (en) * | 1998-08-21 | 2001-09-18 | Dupont Dow Elastomers L.L.C. | Crosslinkable fluoroelastomer composition |
-
2000
- 2000-12-01 WO PCT/US2000/032674 patent/WO2002044263A1/en not_active Ceased
- 2000-12-01 EP EP00983844A patent/EP1337583B1/en not_active Expired - Lifetime
- 2000-12-01 DE DE60021289T patent/DE60021289T2/de not_active Expired - Fee Related
- 2000-12-01 JP JP2002546624A patent/JP2004514776A/ja not_active Withdrawn
- 2000-12-01 KR KR10-2003-7007285A patent/KR20030057566A/ko not_active Withdrawn
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