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 | |
| US28346401P | 2001-04-12 | 2001-04-12 | |
| US28353501P | 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 (44)
| 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 |
| WO2004069900A2 (en) | 2003-01-29 | 2004-08-19 | Greene, Tweed Of Delaware, Inc. | Bisaminophenyl-based curatives and amidine-based curatives and cure accelerators for perfluoroelastomeric compositions |
| RU2380384C2 (ru) | 2003-01-29 | 2010-01-27 | Грин, Твид Оф Делавэр, Инк. | Вулканизирующие агенты на основе бисаминофенила и вулканизирующие агенты и ускорители вулканизации на основе амидина для перфторэластомерных композиций |
| US6956085B2 (en) * | 2003-02-14 | 2005-10-18 | 3M Innovative Properties Company | Fluoroelastomer compositions |
| US7304115B2 (en) * | 2003-12-30 | 2007-12-04 | 3M Innovative Properties Company | Fluoropolymer coagulation method and composition |
| 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 |
| EP1741748A4 (en) * | 2004-04-28 | 2009-07-22 | Daikin Ind Ltd | FLUORELASTOMER COMPOSITION AND FORM BODY THEREOF |
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| 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 |
| WO2009049168A1 (en) * | 2007-10-12 | 2009-04-16 | 3M Innovative Properties Company | Process for manufacturing clean fluoropolymers |
| 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 |
| WO2009111120A2 (en) * | 2008-02-29 | 2009-09-11 | 3M Innovative Properties Company | Perfluoroelastomers with low carbonyl endgroup ratios |
| EP2268679A4 (en) | 2008-04-08 | 2011-10-26 | Greene Tweed Inc | OXYGEN-PLASMA-BASED COMPOSITION WITH LOW-LIABILITY AND CORRESPONDING METHODS |
| WO2010014274A1 (en) | 2008-07-31 | 2010-02-04 | 3M Innovative Properties Company | Fluoropolymer compositions and method of making and using thereof |
| JP5512674B2 (ja) * | 2008-07-31 | 2014-06-04 | スリーエム イノベイティブ プロパティズ カンパニー | アジド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 |
| KR101684719B1 (ko) * | 2009-06-25 | 2016-12-08 | 쓰리엠 이노베이티브 프로퍼티즈 캄파니 | 플루오로중합체를 위한 경화 조성물 |
| CN102597120B (zh) * | 2009-11-11 | 2015-05-27 | 3M创新有限公司 | 聚合物组合物及其制备方法和制品 |
| 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 |
| JP5833657B2 (ja) | 2010-09-24 | 2015-12-16 | 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 | 高温への適用に適したフッ素含有エラストマー組成物 |
| US9365712B2 (en) | 2010-09-24 | 2016-06-14 | 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 |
| WO2013119388A1 (en) | 2012-02-10 | 2013-08-15 | 3M Innovative Properties Company | Anticorrosion coatings |
| WO2014110329A1 (en) * | 2013-01-11 | 2014-07-17 | E. I. Du Pont De Nemours And Company | 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 |
| EP3898835A1 (en) | 2018-12-20 | 2021-10-27 | 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 |
| EP4047055A4 (en) * | 2019-10-17 | 2023-11-15 | Agc Inc. | MOLDED BODY MADE OF PERFLUOREL ELASTOMER AND PROTECTIVE ELEMENT |
| WO2022229752A1 (en) * | 2021-04-30 | 2022-11-03 | 3M Innovative Properties Company | Curable fluoroelastomer compositions containing quaternary phosphonium hydroxybenzoate catalysts |
| WO2024110375A1 (en) * | 2022-11-22 | 2024-05-30 | Dupont Specialty Products Operations Sarl | Perfluoroelastomer compounds |
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| JP5122718B2 (ja) * | 2000-09-18 | 2013-01-16 | スリーエム イノベイティブ プロパティズ カンパニー | イミダート含有フルオロポリマー組成物 |
| US6890995B2 (en) * | 2001-01-31 | 2005-05-10 | 3M Innovative Properties Company | Fluoropolymer compositions |
| US6803425B2 (en) * | 2001-04-12 | 2004-10-12 | 3M Innovative Properties Company | Fluoropolymers having pendant imidate structures |
| US6844388B2 (en) * | 2001-04-12 | 2005-01-18 | 3M Innovative Properties Company | Fluoropolymer compositions containing a nitrogen cure site monomer |
| 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 |
| US6846880B2 (en) * | 2002-10-11 | 2005-01-25 | 3M Innovative Properties Company | Fluoropolymer compositions |
-
2002
- 2002-01-30 US US10/060,690 patent/US6890995B2/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
- 2002-01-31 EP EP02718895.2A patent/EP1366094B1/en not_active Expired - Lifetime
-
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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