JP2005537359A5 - - Google Patents
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- JP2005537359A5 JP2005537359A5 JP2004532595A JP2004532595A JP2005537359A5 JP 2005537359 A5 JP2005537359 A5 JP 2005537359A5 JP 2004532595 A JP2004532595 A JP 2004532595A JP 2004532595 A JP2004532595 A JP 2004532595A JP 2005537359 A5 JP2005537359 A5 JP 2005537359A5
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- JP
- Japan
- Prior art keywords
- group
- fluorinated
- alkyl
- aryl
- formula
- 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 description 20
- 125000003118 aryl group Chemical group 0.000 claims description 13
- 125000000217 alkyl group Chemical group 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 11
- 229910052739 hydrogen Inorganic materials 0.000 claims description 11
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 10
- 239000000178 monomer Substances 0.000 claims description 10
- 229910052757 nitrogen Inorganic materials 0.000 claims description 10
- 229920002313 fluoropolymer Polymers 0.000 claims description 9
- 239000004811 fluoropolymer Substances 0.000 claims description 9
- 239000001257 hydrogen Substances 0.000 claims description 9
- 125000003342 alkenyl group Chemical group 0.000 claims description 8
- 125000000129 anionic group Chemical group 0.000 claims description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 7
- 125000000524 functional group Chemical group 0.000 claims description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 239000003054 catalyst Substances 0.000 claims description 5
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 5
- 230000002378 acidificating effect Effects 0.000 claims description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
- 125000000623 heterocyclic group Chemical group 0.000 claims description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
- 229910052787 antimony Chemical group 0.000 claims description 3
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical group [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims description 3
- 229910052785 arsenic Inorganic materials 0.000 claims description 3
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical group [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 claims description 3
- 125000002091 cationic group Chemical group 0.000 claims description 3
- 125000004122 cyclic group Chemical group 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- 239000011593 sulfur Chemical group 0.000 claims description 3
- RRZIJNVZMJUGTK-UHFFFAOYSA-N 1,1,2-trifluoro-2-(1,2,2-trifluoroethenoxy)ethene Chemical class FC(F)=C(F)OC(F)=C(F)F RRZIJNVZMJUGTK-UHFFFAOYSA-N 0.000 claims description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical group [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 2
- 125000004450 alkenylene group Chemical group 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 229910052698 phosphorus Inorganic materials 0.000 claims description 2
- 239000011574 phosphorus Substances 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims 4
- 229910052731 fluorine Inorganic materials 0.000 claims 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 3
- 150000001450 anions Chemical class 0.000 claims 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- 150000001336 alkenes Chemical class 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 claims 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims 2
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 2
- 125000001153 fluoro group Chemical group F* 0.000 claims 2
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims 2
- -1 oxy, carbonyl Chemical group 0.000 claims 2
- 239000002243 precursor Substances 0.000 claims 2
- CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical compound OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 claims 2
- 150000003457 sulfones Chemical class 0.000 claims 2
- HHVIBTZHLRERCL-UHFFFAOYSA-N sulfonyldimethane Chemical compound CS(C)(=O)=O HHVIBTZHLRERCL-UHFFFAOYSA-N 0.000 claims 2
- 150000003462 sulfoxides Chemical class 0.000 claims 2
- BJQWBACJIAKDTJ-UHFFFAOYSA-N tetrabutylphosphanium Chemical compound CCCC[P+](CCCC)(CCCC)CCCC BJQWBACJIAKDTJ-UHFFFAOYSA-N 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
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 claims 1
- 125000006737 (C6-C20) arylalkyl group Chemical group 0.000 claims 1
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical class FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 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
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 claims 1
- AXRSOGFYDSXLQX-UHFFFAOYSA-N 2,2,3,3,4,4,5,5-octafluorohexanedioic acid Chemical compound OC(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(O)=O AXRSOGFYDSXLQX-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
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims 1
- 125000006725 C1-C10 alkenyl group Chemical group 0.000 claims 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 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
- 125000002252 acyl group Chemical group 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 125000002877 alkyl aryl group Chemical group 0.000 claims 1
- 150000001412 amines Chemical class 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
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 229920001577 copolymer Polymers 0.000 claims 1
- 239000011737 fluorine Substances 0.000 claims 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical group [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 150000007522 mineralic acids Chemical class 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
- 150000007524 organic acids Chemical class 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 229920005548 perfluoropolymer Polymers 0.000 claims 1
- 150000002978 peroxides Chemical class 0.000 claims 1
- 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 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims 1
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 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
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-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
- ISXOBTBCNRIIQO-UHFFFAOYSA-N tetrahydrothiophene 1-oxide Chemical compound O=S1CCCC1 ISXOBTBCNRIIQO-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 compound 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
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 2
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical compound FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 description 1
- 150000002463 imidates Chemical class 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/228,507 US6887927B2 (en) | 2002-08-27 | 2002-08-27 | Fluoropolymer compositions containing a nitrogen cure site monomer and a sulfone or sulfoxide compound |
| PCT/US2003/021673 WO2004020513A1 (en) | 2002-08-27 | 2003-07-11 | Fluoropolymer compositions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005537359A JP2005537359A (ja) | 2005-12-08 |
| JP2005537359A5 true JP2005537359A5 (enExample) | 2008-12-25 |
Family
ID=31976043
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004532595A Ceased JP2005537359A (ja) | 2002-08-27 | 2003-07-11 | フルオロポリマー組成物 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US6887927B2 (enExample) |
| EP (1) | EP1551915B1 (enExample) |
| JP (1) | JP2005537359A (enExample) |
| KR (1) | KR101019432B1 (enExample) |
| CN (1) | CN1678672B (enExample) |
| AT (1) | ATE373040T1 (enExample) |
| AU (1) | AU2003249037A1 (enExample) |
| DE (1) | DE60316331T2 (enExample) |
| HK (1) | HK1080880A1 (enExample) |
| RU (1) | RU2005103393A (enExample) |
| WO (1) | WO2004020513A1 (enExample) |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6890995B2 (en) * | 2001-01-31 | 2005-05-10 | 3M Innovative Properties Company | Fluoropolymer compositions |
| US6794457B2 (en) * | 2001-04-30 | 2004-09-21 | 3M Innovative Properties Company | Fluoropolymer curing system containing a nitrogen cure site monomer |
| ATE496951T1 (de) * | 2002-12-23 | 2011-02-15 | 3M Innovative Properties Co | Flourpolymere mit stickstoff-enthaltenden vernetzungsstellen |
| EP1587784B1 (en) | 2003-01-29 | 2014-10-15 | Greene, Tweed Of Delaware, Inc. | Bisaminophenyl-based curatives and amidine-based curatives and cure accelerators for perfluoroelastomeric compositions |
| CN100410278C (zh) * | 2003-01-29 | 2008-08-13 | 特拉华特威德·格林公司 | 用于全氟弹性体组合物的基于双氨基苯基的固化剂和基于脒的固化剂以及固化促进剂 |
| US6992143B2 (en) * | 2003-08-15 | 2006-01-31 | Dupont Dow Elastomers Llc | Curable perfluoroelastomer composition |
| CN100471877C (zh) * | 2003-12-30 | 2009-03-25 | 3M创新有限公司 | 含氟聚合物的凝聚方法及组合物 |
| 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 |
| US8039681B2 (en) * | 2004-08-20 | 2011-10-18 | E. I. Du Pont De Nemours And Company | Functionalized carbon materials |
| US8785013B2 (en) * | 2004-08-20 | 2014-07-22 | E I Du Pont De Nemours And Company | Compositions containing modified fullerenes |
| JP2008532567A (ja) * | 2004-12-15 | 2008-08-21 | スリーエム イノベイティブ プロパティズ カンパニー | 医療用エアロゾル装置に用いるエラストマーシール |
| US7402630B2 (en) * | 2004-12-16 | 2008-07-22 | 3M Innovative Properties Company | Curing compositions for fluoropolymers |
| US7294677B2 (en) * | 2005-08-25 | 2007-11-13 | 3M Innovative Properties Company | Catalyst for making fluoroelastomer compositions and methods of using the same |
| US20080021148A1 (en) * | 2006-07-24 | 2008-01-24 | 3M Innovative Properties Company | Scorch safe fluoropolymer compositions |
| JP2010514913A (ja) * | 2007-01-03 | 2010-05-06 | ソルヴェイ・ソレクシス・インコーポレーテッド | フルオロエラストマー組成物 |
| GB0712191D0 (en) * | 2007-06-25 | 2007-08-01 | 3M Innovative Properties Co | Process for removing fluorinated compounds for an aqueous phase originating from the preparation of fluoropolymers |
| WO2009045993A2 (en) * | 2007-10-01 | 2009-04-09 | 3M Innovative Properties Company | Compositions comprising cationic fluorinated ether, silanes, and related methods |
| US8080170B2 (en) * | 2007-10-01 | 2011-12-20 | 3M Innovative Properties Company | Cationic fluorinated ether silane compositions and related methods |
| JP2011505488A (ja) | 2007-12-03 | 2011-02-24 | スリーエム イノベイティブ プロパティズ カンパニー | カチオン性ポリマー系フッ素化エーテルシラン組成物及び使用方法 |
| WO2009073537A2 (en) * | 2007-12-03 | 2009-06-11 | 3M Innovative Properties Company | Cationic polymeric fluorinated ether silane compositions and methods of use |
| 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 |
| US20090270573A1 (en) * | 2008-04-29 | 2009-10-29 | Christopher John Bish | Process for coagulating perfluoroelastomers |
| US20100069554A1 (en) * | 2008-09-18 | 2010-03-18 | Dupont Performance Elastomers L.L.C. | Curable fluoropolymer compositions |
| US8906821B2 (en) | 2009-06-25 | 2014-12-09 | 3M Innovative Properties Company | Curing compositions for fluoropolymers |
| US20110152487A1 (en) * | 2009-12-17 | 2011-06-23 | 3M Innovative Properties Company | Peroxide cured partially fluorinated elastomers |
| TWI627192B (zh) * | 2015-03-13 | 2018-06-21 | Murata Manufacturing Co., Ltd. | 原子層堆積抑制材料 |
| KR102609833B1 (ko) * | 2017-03-31 | 2023-12-07 | 솔베이 스페셜티 폴리머스 이태리 에스.피.에이. | 경화 부품을 제조하는 방법 |
| JP7248402B2 (ja) * | 2018-09-26 | 2023-03-29 | スリーエム イノベイティブ プロパティズ カンパニー | 硬化性フッ素系エラストマーコンポジット及びその硬化物 |
| TWI918597B (zh) * | 2018-12-17 | 2026-03-21 | 美商3M新設資產公司 | 包括可固化氟聚合物及固化劑之組成物及製造及使用其之方法 |
| WO2020261089A1 (en) * | 2019-06-28 | 2020-12-30 | 3M Innovative Properties Company | Functionalized triazine compounds, compositions comprising such compounds and cured fluoropolymer articles |
| CN115403984B (zh) * | 2021-05-27 | 2023-08-18 | 常州正洁智造科技有限公司 | 一种阳离子型可固化组合物 |
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| JPH08104789A (ja) * | 1994-10-04 | 1996-04-23 | Nippon Mektron Ltd | 含フッ素エラストマー組成物 |
| JP2833645B2 (ja) | 1994-10-21 | 1998-12-09 | 日本メクトロン株式会社 | 含フッ素エラストマー組成物 |
| JP3398492B2 (ja) | 1994-10-21 | 2003-04-21 | 日本メクトロン株式会社 | 含フッ素エラストマー組成物 |
| JP2770769B2 (ja) | 1995-02-16 | 1998-07-02 | 日本メクトロン株式会社 | ビスアミドキシム化合物、その製造法およびそれを含有する含フッ素エラストマー組成物 |
| JP3223776B2 (ja) | 1995-03-31 | 2001-10-29 | 日本メクトロン株式会社 | 含フッ素エラストマー組成物 |
| IT1276979B1 (it) | 1995-10-20 | 1997-11-03 | Ausimont Spa | Composizioni fluoroelastomeriche |
| US5728773A (en) | 1997-02-21 | 1998-03-17 | Minnesota Mining And Manufacturing Company | Fluoroelastomer composition with organo-onium and blocked-carbonate compounds |
| US6191208B1 (en) * | 1998-05-20 | 2001-02-20 | Dupont Dow Elastomers L.L.S. | Thermally stable perfluoroelastomer composition |
| WO2001002448A1 (en) | 1999-07-02 | 2001-01-11 | Dyneon Llc | Fluoroelastomer compositions and articles made therefrom |
| US6593416B2 (en) * | 2000-02-01 | 2003-07-15 | 3M Innovative Properties Company | Fluoropolymers |
| US6638999B2 (en) | 2000-02-08 | 2003-10-28 | Dupont Dow Elastomers Llc. | Curable perfluoroelastomer composition |
| KR100800954B1 (ko) | 2000-12-14 | 2008-02-04 | 듀폰 퍼포먼스 엘라스토머스 엘.엘.씨. | 고순도 반투명 퍼플루오로엘라스토머 물품의 제조 방법 |
| US6890995B2 (en) | 2001-01-31 | 2005-05-10 | 3M Innovative Properties Company | Fluoropolymer compositions |
-
2002
- 2002-08-27 US US10/228,507 patent/US6887927B2/en not_active Expired - Fee Related
-
2003
- 2003-07-11 RU RU2005103393/04A patent/RU2005103393A/ru not_active Application Discontinuation
- 2003-07-11 CN CN03820147XA patent/CN1678672B/zh not_active Expired - Fee Related
- 2003-07-11 AT AT03791572T patent/ATE373040T1/de not_active IP Right Cessation
- 2003-07-11 EP EP03791572A patent/EP1551915B1/en not_active Expired - Lifetime
- 2003-07-11 WO PCT/US2003/021673 patent/WO2004020513A1/en not_active Ceased
- 2003-07-11 KR KR1020057003239A patent/KR101019432B1/ko not_active Expired - Fee Related
- 2003-07-11 DE DE60316331T patent/DE60316331T2/de not_active Expired - Lifetime
- 2003-07-11 JP JP2004532595A patent/JP2005537359A/ja not_active Ceased
- 2003-07-11 AU AU2003249037A patent/AU2003249037A1/en not_active Abandoned
- 2003-07-11 HK HK06100242.0A patent/HK1080880A1/zh unknown
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