JP2005506391A5 - - Google Patents
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- JP2005506391A5 JP2005506391A5 JP2002561535A JP2002561535A JP2005506391A5 JP 2005506391 A5 JP2005506391 A5 JP 2005506391A5 JP 2002561535 A JP2002561535 A JP 2002561535A JP 2002561535 A JP2002561535 A JP 2002561535A JP 2005506391 A5 JP2005506391 A5 JP 2005506391A5
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- JP
- Japan
- Prior art keywords
- composition
- optionally
- fluoropolymer
- group
- alkyl
- 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.)
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- 239000000203 mixture Substances 0.000 claims 39
- 229920002313 fluoropolymer Polymers 0.000 claims 16
- 239000004811 fluoropolymer Substances 0.000 claims 16
- 125000000217 alkyl group Chemical group 0.000 claims 12
- 239000000178 monomer Substances 0.000 claims 12
- 229910052757 nitrogen Inorganic materials 0.000 claims 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 9
- 125000003118 aryl group Chemical group 0.000 claims 9
- 238000001723 curing Methods 0.000 claims 9
- 150000001875 compounds Chemical class 0.000 claims 8
- 229910052739 hydrogen Inorganic materials 0.000 claims 8
- 239000001257 hydrogen Substances 0.000 claims 8
- 125000003342 alkenyl group Chemical group 0.000 claims 7
- 150000001450 anions Chemical class 0.000 claims 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 claims 6
- 239000002253 acid Substances 0.000 claims 6
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 6
- 150000001336 alkenes Chemical class 0.000 claims 5
- 125000004432 carbon atom Chemical group C* 0.000 claims 5
- 239000002243 precursor Substances 0.000 claims 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 4
- 125000003710 aryl alkyl group Chemical group 0.000 claims 4
- 239000003054 catalyst Substances 0.000 claims 4
- 229910052801 chlorine Chemical group 0.000 claims 4
- 239000000460 chlorine Chemical group 0.000 claims 4
- 229910052731 fluorine Inorganic materials 0.000 claims 4
- 238000000465 moulding Methods 0.000 claims 4
- -1 oxy, carbonyl Chemical group 0.000 claims 4
- BJQWBACJIAKDTJ-UHFFFAOYSA-N tetrabutylphosphanium Chemical compound CCCC[P+](CCCC)(CCCC)CCCC BJQWBACJIAKDTJ-UHFFFAOYSA-N 0.000 claims 4
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical group [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 3
- 125000002877 alkyl aryl group Chemical group 0.000 claims 3
- 229910052787 antimony Chemical group 0.000 claims 3
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical group [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims 3
- 229910052785 arsenic Inorganic materials 0.000 claims 3
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical group [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 claims 3
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims 3
- 239000011737 fluorine Chemical group 0.000 claims 3
- 150000002431 hydrogen Chemical group 0.000 claims 3
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims 3
- 238000000034 method Methods 0.000 claims 3
- 125000002560 nitrile group Chemical group 0.000 claims 3
- 229910052698 phosphorus Inorganic materials 0.000 claims 3
- 239000011574 phosphorus Substances 0.000 claims 3
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims 3
- 229910052717 sulfur Inorganic materials 0.000 claims 3
- 239000011593 sulfur Chemical group 0.000 claims 3
- 229920001897 terpolymer Polymers 0.000 claims 3
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical class FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 claims 2
- BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 claims 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims 2
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical group [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims 2
- 230000032683 aging Effects 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 claims 2
- 230000000052 comparative effect Effects 0.000 claims 2
- 125000001153 fluoro group Chemical group F* 0.000 claims 2
- 230000006698 induction Effects 0.000 claims 2
- 239000000463 material Substances 0.000 claims 2
- 150000002825 nitriles Chemical class 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 150000002978 peroxides Chemical class 0.000 claims 2
- 239000004848 polyfunctional curative Substances 0.000 claims 2
- 238000011417 postcuring Methods 0.000 claims 2
- 150000003918 triazines Chemical class 0.000 claims 2
- BTMIENSZKMNLRR-UHFFFAOYSA-N tributyl(2-methoxypropyl)phosphanium Chemical compound CCCC[P+](CCCC)(CCCC)CC(C)OC BTMIENSZKMNLRR-UHFFFAOYSA-N 0.000 claims 2
- GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 claims 2
- 125000006737 (C6-C20) arylalkyl group Chemical group 0.000 claims 1
- YCMPCPHVHGPYHB-UHFFFAOYSA-N 1,1-diethyl-2,2-diphenylhydrazine Chemical compound C=1C=CC=CC=1N(N(CC)CC)C1=CC=CC=C1 YCMPCPHVHGPYHB-UHFFFAOYSA-N 0.000 claims 1
- 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 claims 1
- HWCLMKDWXUGDKL-UHFFFAOYSA-N 1-ethenoxy-2-ethoxyethane Chemical compound CCOCCOC=C HWCLMKDWXUGDKL-UHFFFAOYSA-N 0.000 claims 1
- PCAXITAPTVOLGL-UHFFFAOYSA-N 2,3-diaminophenol Chemical class NC1=CC=CC(O)=C1N PCAXITAPTVOLGL-UHFFFAOYSA-N 0.000 claims 1
- DJLHOEYSQWJYMT-UHFFFAOYSA-N 2-methoxypropylphosphane Chemical compound COC(C)CP DJLHOEYSQWJYMT-UHFFFAOYSA-N 0.000 claims 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- 125000006725 C1-C10 alkenyl group Chemical group 0.000 claims 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- 239000007983 Tris buffer Substances 0.000 claims 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims 1
- 125000002252 acyl group Chemical group 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 229910052783 alkali metal Chemical group 0.000 claims 1
- 150000001340 alkali metals Chemical group 0.000 claims 1
- 229910052784 alkaline earth metal Chemical group 0.000 claims 1
- 150000001342 alkaline earth metals Chemical group 0.000 claims 1
- 229910021529 ammonia Inorganic materials 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 239000012752 auxiliary agent Substances 0.000 claims 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 1
- UZCPNEBHTFYJNY-UHFFFAOYSA-N benzyl(diphenyl)phosphane Chemical compound C=1C=CC=CC=1CP(C=1C=CC=CC=1)C1=CC=CC=C1 UZCPNEBHTFYJNY-UHFFFAOYSA-N 0.000 claims 1
- QSRFYFHZPSGRQX-UHFFFAOYSA-N benzyl(tributyl)azanium Chemical compound CCCC[N+](CCCC)(CCCC)CC1=CC=CC=C1 QSRFYFHZPSGRQX-UHFFFAOYSA-N 0.000 claims 1
- QUCVNPJIPOQRLJ-UHFFFAOYSA-N benzyl(triphenyl)azanium Chemical compound C=1C=CC=CC=1[N+](C=1C=CC=CC=1)(C=1C=CC=CC=1)CC1=CC=CC=C1 QUCVNPJIPOQRLJ-UHFFFAOYSA-N 0.000 claims 1
- BNQRPLGZFADFGA-UHFFFAOYSA-N benzyl(triphenyl)phosphanium Chemical compound C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)CC1=CC=CC=C1 BNQRPLGZFADFGA-UHFFFAOYSA-N 0.000 claims 1
- JGTUMZJDTJDJJR-UHFFFAOYSA-N benzyl-tris(dimethylamino)phosphanium Chemical compound CN(C)[P+](N(C)C)(N(C)C)CC1=CC=CC=C1 JGTUMZJDTJDJJR-UHFFFAOYSA-N 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 239000012018 catalyst precursor Substances 0.000 claims 1
- 230000003197 catalytic effect Effects 0.000 claims 1
- DMSZORWOGDLWGN-UHFFFAOYSA-N ctk1a3526 Chemical compound NP(N)(N)=O DMSZORWOGDLWGN-UHFFFAOYSA-N 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 235000010299 hexamethylene tetramine Nutrition 0.000 claims 1
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 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 claims 1
- DYUWTXWIYMHBQS-UHFFFAOYSA-N n-prop-2-enylprop-2-en-1-amine Chemical compound C=CCNCC=C DYUWTXWIYMHBQS-UHFFFAOYSA-N 0.000 claims 1
- 125000006551 perfluoro alkylene group Chemical group 0.000 claims 1
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- NNOBHPBYUHDMQF-UHFFFAOYSA-N propylphosphine Chemical compound CCCP NNOBHPBYUHDMQF-UHFFFAOYSA-N 0.000 claims 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims 1
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 1
- OSWMMVUHYHQYCV-UHFFFAOYSA-N tetrabenzylazanium Chemical compound C=1C=CC=CC=1C[N+](CC=1C=CC=CC=1)(CC=1C=CC=CC=1)CC1=CC=CC=C1 OSWMMVUHYHQYCV-UHFFFAOYSA-N 0.000 claims 1
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical compound CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 claims 1
- YFZDLRVCXDBOPH-UHFFFAOYSA-N tetraheptylazanium Chemical compound CCCCCCC[N+](CCCCCCC)(CCCCCCC)CCCCCCC YFZDLRVCXDBOPH-UHFFFAOYSA-N 0.000 claims 1
- DTIFFPXSSXFQCJ-UHFFFAOYSA-N tetrahexylazanium Chemical compound CCCCCC[N+](CCCCCC)(CCCCCC)CCCCCC DTIFFPXSSXFQCJ-UHFFFAOYSA-N 0.000 claims 1
- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 claims 1
- BXYHVFRRNNWPMB-UHFFFAOYSA-N tetramethylphosphanium Chemical group C[P+](C)(C)C BXYHVFRRNNWPMB-UHFFFAOYSA-N 0.000 claims 1
- GJSGYPDDPQRWPK-UHFFFAOYSA-N tetrapentylammonium Chemical compound CCCCC[N+](CCCCC)(CCCCC)CCCCC GJSGYPDDPQRWPK-UHFFFAOYSA-N 0.000 claims 1
- CZMILNXHOAKSBR-UHFFFAOYSA-N tetraphenylazanium Chemical compound C1=CC=CC=C1[N+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 CZMILNXHOAKSBR-UHFFFAOYSA-N 0.000 claims 1
- USFPINLPPFWTJW-UHFFFAOYSA-N tetraphenylphosphonium Chemical compound C1=CC=CC=C1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 USFPINLPPFWTJW-UHFFFAOYSA-N 0.000 claims 1
- OSBSFAARYOCBHB-UHFFFAOYSA-N tetrapropylammonium Chemical compound CCC[N+](CCC)(CCC)CCC OSBSFAARYOCBHB-UHFFFAOYSA-N 0.000 claims 1
- ZNEOHLHCKGUAEB-UHFFFAOYSA-N trimethylphenylammonium Chemical compound C[N+](C)(C)C1=CC=CC=C1 ZNEOHLHCKGUAEB-UHFFFAOYSA-N 0.000 claims 1
- KJWHEZXBZQXVSA-UHFFFAOYSA-N tris(prop-2-enyl) phosphite Chemical compound C=CCOP(OCC=C)OCC=C KJWHEZXBZQXVSA-UHFFFAOYSA-N 0.000 claims 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US26549801P | 2001-01-31 | 2001-01-31 | |
| US28353501P | 2001-04-12 | 2001-04-12 | |
| US28346401P | 2001-04-12 | 2001-04-12 | |
| US10/060,690 US6890995B2 (en) | 2001-01-31 | 2002-01-30 | Fluoropolymer compositions |
| PCT/US2002/003099 WO2002060969A1 (en) | 2001-01-31 | 2002-01-31 | Fluoropolymer compositions |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008120997A Division JP5460974B2 (ja) | 2001-01-31 | 2008-05-07 | フルオロポリマー組成物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005506391A JP2005506391A (ja) | 2005-03-03 |
| JP2005506391A5 true JP2005506391A5 (enExample) | 2005-12-22 |
Family
ID=27490136
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002561535A Pending JP2005506391A (ja) | 2001-01-31 | 2002-01-31 | フルオロポリマー組成物 |
| JP2008120997A Expired - Lifetime JP5460974B2 (ja) | 2001-01-31 | 2008-05-07 | フルオロポリマー組成物 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008120997A Expired - Lifetime JP5460974B2 (ja) | 2001-01-31 | 2008-05-07 | フルオロポリマー組成物 |
Country Status (5)
| Country | Link |
|---|---|
| US (2) | US6890995B2 (enExample) |
| EP (1) | EP1366094B1 (enExample) |
| JP (2) | JP2005506391A (enExample) |
| CA (1) | CA2433554A1 (enExample) |
| WO (1) | WO2002060969A1 (enExample) |
Families Citing this family (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6720360B1 (en) * | 2000-02-01 | 2004-04-13 | 3M Innovative Properties Company | Ultra-clean fluoropolymers |
| US6638999B2 (en) * | 2000-02-08 | 2003-10-28 | Dupont Dow Elastomers Llc. | Curable perfluoroelastomer composition |
| US6890995B2 (en) * | 2001-01-31 | 2005-05-10 | 3M Innovative Properties Company | Fluoropolymer compositions |
| US6844388B2 (en) * | 2001-04-12 | 2005-01-18 | 3M Innovative Properties Company | Fluoropolymer compositions containing a nitrogen cure site monomer |
| US6803425B2 (en) * | 2001-04-12 | 2004-10-12 | 3M Innovative Properties Company | Fluoropolymers having pendant imidate structures |
| US6794457B2 (en) | 2001-04-30 | 2004-09-21 | 3M Innovative Properties Company | Fluoropolymer curing system containing a nitrogen cure site monomer |
| US6887927B2 (en) | 2002-08-27 | 2005-05-03 | 3M Innovative Properties Company | Fluoropolymer compositions containing a nitrogen cure site monomer and a sulfone or sulfoxide compound |
| US6794455B2 (en) * | 2002-12-12 | 2004-09-21 | Dupont Dow Elastomers | Coagents for fluoroelastomer free radical-curable compositions |
| WO2005000917A1 (en) | 2003-01-29 | 2005-01-06 | Greene, Tweed Of Delaware, Inc. | Bisaminopehnyl-based curatives curatives and amidine-based curatives and cure accelerators for perfluoroelastomeric compositions. |
| US20040214956A1 (en) | 2003-01-29 | 2004-10-28 | Greene, Tweed Of Delaware, Inc. | Bisaminophenyl-based curatives and amidine-based curatives and cure accelerators for perfluoroelastomeric compositions |
| US6956085B2 (en) * | 2003-02-14 | 2005-10-18 | 3M Innovative Properties Company | Fluoroelastomer compositions |
| KR20070012640A (ko) * | 2003-12-30 | 2007-01-26 | 쓰리엠 이노베이티브 프로퍼티즈 캄파니 | 플루오로중합체 응집 방법 및 조성물 |
| 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 |
| JP4687650B2 (ja) * | 2004-04-28 | 2011-05-25 | ダイキン工業株式会社 | 含フッ素エラストマー組成物およびそれからなる成形品 |
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| US7294677B2 (en) * | 2005-08-25 | 2007-11-13 | 3M Innovative Properties Company | Catalyst for making fluoroelastomer compositions and methods of using the same |
| US7589140B2 (en) * | 2005-09-29 | 2009-09-15 | 3M Innovative Properties Company | Fluoropolymer bonding compositions |
| US7388054B2 (en) * | 2005-12-23 | 2008-06-17 | 3M Innovative Properties Company | Fluoropolymer curing co-agent compositions |
| US20070208142A1 (en) * | 2006-03-03 | 2007-09-06 | Adair Eric W | Fluoropolymer curing compositions |
| JP2008266368A (ja) * | 2007-04-16 | 2008-11-06 | Daikin Ind Ltd | 含フッ素エラストマー組成物およびそれからなるシール材 |
| CN101821301B (zh) * | 2007-10-12 | 2012-06-27 | 3M创新有限公司 | 制备纯净含氟聚合物的方法 |
| JP4571197B2 (ja) * | 2008-02-28 | 2010-10-27 | ニチアス株式会社 | パーフルオロエラストマー組成物及びその成形体 |
| JP5452508B2 (ja) * | 2008-02-29 | 2014-03-26 | スリーエム イノベイティブ プロパティズ カンパニー | 低カルボニル末端基率を有するペルフルオロエラストマー |
| JP2011516693A (ja) | 2008-04-08 | 2011-05-26 | グリーン， ツイード オブ デラウェア， インコーポレイテッド | 低粘性を特徴とする耐酸素プラズマ組成物およびそれに関連する方法 |
| WO2010014276A1 (en) * | 2008-07-31 | 2010-02-04 | 3M Innovative Properties Company | Azide compositions and methods of making and using thereof |
| JP2011529977A (ja) | 2008-07-31 | 2011-12-15 | スリーエム イノベイティブ プロパティズ カンパニー | フルオロポリマー組成物並びにその製造及び使用方法 |
| TWI394787B (zh) * | 2008-10-16 | 2013-05-01 | Greene Tweed Of Delaware | 全氟彈性體組成物以及彼之製造方法 |
| EP2445939B1 (en) * | 2009-06-25 | 2020-09-23 | 3M Innovative Properties Company | Curing compositions for fluoropolymers |
| WO2011059994A2 (en) * | 2009-11-11 | 2011-05-19 | 3M Innovative Properties Company | Polymeric compositions and method of making and articles thereof |
| US20110143138A1 (en) * | 2009-12-10 | 2011-06-16 | 3M Properties Company | Perfluoroelastomer bonding |
| US20110152487A1 (en) * | 2009-12-17 | 2011-06-23 | 3M Innovative Properties Company | Peroxide cured partially fluorinated elastomers |
| US9365712B2 (en) | 2010-09-24 | 2016-06-14 | Greene, Tweed Technologies, Inc. | Fluorine-containing elastomer compositions suitable for high temperature applications |
| US9018309B2 (en) | 2010-09-24 | 2015-04-28 | Greene, Tweed Technologies, Inc. | Fluorine-containing elastomer compositions suitable for high temperature applications |
| EP2776498B1 (en) | 2011-11-09 | 2018-12-26 | 3M Innovative Properties Company | Curing compositions for fluoropolymers |
| JP6143798B2 (ja) | 2012-02-10 | 2017-06-07 | スリーエム イノベイティブ プロパティズ カンパニー | 耐食コーティング |
| EP2943456B1 (en) * | 2013-01-11 | 2018-06-13 | The Chemours Company FC, LLC | Quarternary ammonium perfluoroalkoxy salts for preparation of perfluoropolyethers |
| US9169393B2 (en) | 2013-07-25 | 2015-10-27 | 3M Innovative Properties Company | Anticorrosion coatings |
| WO2017222812A1 (en) | 2016-06-20 | 2017-12-28 | 3M Innovative Properties Company | Self-priming adhesive |
| CN109912908B (zh) | 2017-12-13 | 2021-05-18 | 财团法人工业技术研究院 | 基板组合物及由其所制备的基板 |
| WO2020132213A1 (en) | 2018-12-20 | 2020-06-25 | 3M Innovative Properties Company | Latex blends of amorphous perfluorinated polymers and articles derived therefrom |
| JP7706367B2 (ja) | 2018-12-20 | 2025-07-11 | スリーエム イノベイティブ プロパティズ カンパニー | 非晶質全フッ素化ポリマーの乾燥粉末ブレンド、その製造方法、及び乾燥粉末ブレンドから誘導される物品 |
| WO2021075431A1 (ja) * | 2019-10-17 | 2021-04-22 | Ａｇｃ株式会社 | パーフルオロエラストマー成形体及び保護部材 |
| WO2022229752A1 (en) * | 2021-04-30 | 2022-11-03 | 3M Innovative Properties Company | Curable fluoroelastomer compositions containing quaternary phosphonium hydroxybenzoate catalysts |
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-
2002
- 2002-01-30 US US10/060,690 patent/US6890995B2/en not_active Expired - Lifetime
- 2002-01-31 EP EP02718895.2A patent/EP1366094B1/en not_active Expired - Lifetime
- 2002-01-31 CA CA002433554A patent/CA2433554A1/en not_active Abandoned
- 2002-01-31 WO PCT/US2002/003099 patent/WO2002060969A1/en not_active Ceased
- 2002-01-31 JP JP2002561535A patent/JP2005506391A/ja active Pending
-
2005
- 2005-02-28 US US11/067,799 patent/US20050154145A1/en not_active Abandoned
-
2008
- 2008-05-07 JP JP2008120997A patent/JP5460974B2/ja not_active Expired - Lifetime
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