JPS6023407A - 含フツ素共重合体及びその製造法 - Google Patents
含フツ素共重合体及びその製造法Info
- Publication number
- JPS6023407A JPS6023407A JP59126534A JP12653484A JPS6023407A JP S6023407 A JPS6023407 A JP S6023407A JP 59126534 A JP59126534 A JP 59126534A JP 12653484 A JP12653484 A JP 12653484A JP S6023407 A JPS6023407 A JP S6023407A
- Authority
- JP
- Japan
- Prior art keywords
- copolymer
- mol
- monomer
- copolymers
- 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.)
- Granted
Links
- 229920001577 copolymer Polymers 0.000 title claims description 70
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 229910052731 fluorine Inorganic materials 0.000 title description 4
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 title description 2
- 239000011737 fluorine Substances 0.000 title description 2
- 239000000178 monomer Substances 0.000 claims description 42
- 239000000203 mixture Substances 0.000 claims description 21
- 229920000570 polyether Polymers 0.000 claims description 18
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 16
- -1 perfluorophenylene Chemical group 0.000 claims description 16
- 238000006116 polymerization reaction Methods 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 15
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims description 13
- 230000009477 glass transition Effects 0.000 claims description 11
- 239000004094 surface-active agent Substances 0.000 claims description 11
- 239000008346 aqueous phase Substances 0.000 claims description 8
- 238000007720 emulsion polymerization reaction Methods 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- 230000008569 process Effects 0.000 claims description 7
- 150000001298 alcohols Chemical class 0.000 claims description 6
- 239000003999 initiator Substances 0.000 claims description 5
- 230000000379 polymerizing effect Effects 0.000 claims description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 4
- 239000012736 aqueous medium Substances 0.000 claims description 4
- RHQDFWAXVIIEBN-UHFFFAOYSA-N Trifluoroethanol Chemical compound OCC(F)(F)F RHQDFWAXVIIEBN-UHFFFAOYSA-N 0.000 claims description 3
- 125000001153 fluoro group Chemical class F* 0.000 claims description 3
- BYEAHWXPCBROCE-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropan-2-ol Chemical compound FC(F)(F)C(O)C(F)(F)F BYEAHWXPCBROCE-UHFFFAOYSA-N 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 239000003995 emulsifying agent Substances 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 238000007334 copolymerization reaction Methods 0.000 claims 2
- 210000003746 feather Anatomy 0.000 claims 1
- 229920000642 polymer Polymers 0.000 description 37
- 239000003921 oil Substances 0.000 description 16
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 15
- 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 9
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 8
- 239000000839 emulsion Substances 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 230000007704 transition Effects 0.000 description 6
- 229960000834 vinyl ether Drugs 0.000 description 6
- 150000002221 fluorine Chemical class 0.000 description 5
- PGFXOWRDDHCDTE-UHFFFAOYSA-N hexafluoropropylene oxide Chemical compound FC(F)(F)C1(F)OC1(F)F PGFXOWRDDHCDTE-UHFFFAOYSA-N 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 238000004587 chromatography analysis Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 3
- AJDIZQLSFPQPEY-UHFFFAOYSA-N 1,1,2-Trichlorotrifluoroethane Chemical compound FC(F)(Cl)C(F)(Cl)Cl AJDIZQLSFPQPEY-UHFFFAOYSA-N 0.000 description 2
- MHNPWFZIRJMRKC-UHFFFAOYSA-N 1,1,2-trifluoroethene Chemical compound F[C]=C(F)F MHNPWFZIRJMRKC-UHFFFAOYSA-N 0.000 description 2
- PPUZXOKAOIOPIE-UHFFFAOYSA-N 1-bromo-2-ethenoxyethane Chemical compound BrCCOC=C PPUZXOKAOIOPIE-UHFFFAOYSA-N 0.000 description 2
- JMGNVALALWCTLC-UHFFFAOYSA-N 1-fluoro-2-(2-fluoroethenoxy)ethene Chemical compound FC=COC=CF JMGNVALALWCTLC-UHFFFAOYSA-N 0.000 description 2
- NHJFHUKLZMQIHN-UHFFFAOYSA-N 2,2,3,3,3-pentafluoropropanoyl 2,2,3,3,3-pentafluoropropaneperoxoate Chemical compound FC(F)(F)C(F)(F)C(=O)OOC(=O)C(F)(F)C(F)(F)F NHJFHUKLZMQIHN-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 2
- HZFDKBPTVOENNB-GAFUQQFSSA-N N-[(2S)-1-[2-[(2R)-2-chloro-2-fluoroacetyl]-2-[[(3S)-2-oxopyrrolidin-3-yl]methyl]hydrazinyl]-3-(1-methylcyclopropyl)-1-oxopropan-2-yl]-5-(difluoromethyl)-1,2-oxazole-3-carboxamide Chemical compound CC1(C[C@@H](C(NN(C[C@H](CCN2)C2=O)C([C@H](F)Cl)=O)=O)NC(C2=NOC(C(F)F)=C2)=O)CC1 HZFDKBPTVOENNB-GAFUQQFSSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- AQYSYJUIMQTRMV-UHFFFAOYSA-N hypofluorous acid Chemical compound FO AQYSYJUIMQTRMV-UHFFFAOYSA-N 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 125000004430 oxygen atom Chemical group O* 0.000 description 2
- 229920001721 polyimide Polymers 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulphite Substances [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- CRHIAMBJMSSNNM-UHFFFAOYSA-N tetraphenylstannane Chemical compound C1=CC=CC=C1[Sn](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 CRHIAMBJMSSNNM-UHFFFAOYSA-N 0.000 description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
- FJSRPVWDOJSWBX-UHFFFAOYSA-N 1-chloro-4-[1-(4-chlorophenyl)-2,2,2-trifluoroethyl]benzene Chemical compound C=1C=C(Cl)C=CC=1C(C(F)(F)F)C1=CC=C(Cl)C=C1 FJSRPVWDOJSWBX-UHFFFAOYSA-N 0.000 description 1
- 238000004293 19F NMR spectroscopy Methods 0.000 description 1
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 241001397173 Kali <angiosperm> Species 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 241000282806 Rhinoceros Species 0.000 description 1
- 229910052776 Thorium Inorganic materials 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 150000001265 acyl fluorides Chemical group 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 239000001099 ammonium carbonate Substances 0.000 description 1
- 235000012501 ammonium carbonate Nutrition 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- YOALFLHFSFEMLP-UHFFFAOYSA-N azane;2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluorooctanoic acid Chemical compound [NH4+].[O-]C(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F YOALFLHFSFEMLP-UHFFFAOYSA-N 0.000 description 1
- 230000036760 body temperature Effects 0.000 description 1
- FAKRSMQSSFJEIM-RQJHMYQMSA-N captopril Chemical compound SC[C@@H](C)C(=O)N1CCC[C@H]1C(O)=O FAKRSMQSSFJEIM-RQJHMYQMSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 235000011089 carbon dioxide Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004581 coalescence Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 229920001198 elastomeric copolymer Polymers 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 229940052303 ethers for general anesthesia Drugs 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 229920001973 fluoroelastomer Polymers 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- 239000002828 fuel tank Substances 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 125000005062 perfluorophenyl group Chemical group FC1=C(C(=C(C(=C1F)F)F)F)* 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 238000012643 polycondensation polymerization Methods 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000012966 redox initiator Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000003303 reheating Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 1
- 235000019801 trisodium phosphate Nutrition 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
- 230000002747 voluntary effect Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F214/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen
- C08F214/18—Monomers containing fluorine
- C08F214/184—Monomers containing fluorine with fluorinated vinyl ethers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F214/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen
- C08F214/18—Monomers containing fluorine
- C08F214/26—Tetrafluoroethene
- C08F214/262—Tetrafluoroethene with fluorinated vinyl ethers
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymerisation Methods In General (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/507,083 US4513128A (en) | 1983-06-23 | 1983-06-23 | Fluorinated vinyl ether copolymers having low glass transition temperatures |
| US507083 | 1995-07-26 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6023407A true JPS6023407A (ja) | 1985-02-06 |
| JPH0481608B2 JPH0481608B2 (enExample) | 1992-12-24 |
Family
ID=24017183
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59126534A Granted JPS6023407A (ja) | 1983-06-23 | 1984-06-21 | 含フツ素共重合体及びその製造法 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US4513128A (enExample) |
| EP (1) | EP0130052B1 (enExample) |
| JP (1) | JPS6023407A (enExample) |
| CA (1) | CA1225195A (enExample) |
| DE (1) | DE3465744D1 (enExample) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6422908A (en) * | 1987-07-17 | 1989-01-25 | Nippon Mektron Kk | Production of fluorine-containing elastic copolymer |
| WO1997024381A1 (en) * | 1995-12-28 | 1997-07-10 | Daikin Industries, Ltd. | Fluorine-containing elastic copolymers, curable composition containing the same and sealant made therefrom |
| JP2006037025A (ja) * | 2004-07-29 | 2006-02-09 | Asahi Glass Co Ltd | 含フッ素エラストマーおよびその製造方法 |
| JP2006052399A (ja) * | 2004-07-30 | 2006-02-23 | Solvay Solexis Spa | パーフルオロエラストマー |
| JP2008266190A (ja) * | 2007-04-19 | 2008-11-06 | Yunimatekku Kk | 含フッ素ビニルエーテル化合物 |
| JP2009516005A (ja) * | 2004-12-21 | 2009-04-16 | スリーエム イノベイティブ プロパティズ カンパニー | フルオロエラストマーを製造するためのフルオロポリマー |
| JP4828783B2 (ja) * | 2001-01-31 | 2011-11-30 | スリーエム イノベイティブ プロパティズ カンパニー | 低いガラス転移温度を有するペルフルオロエラストマーおよびそれらの製造方法 |
| CN105358594A (zh) * | 2013-06-25 | 2016-02-24 | 3M创新有限公司 | 可湿固化的组合物、使用方法以及复合制品 |
Families Citing this family (52)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3662142D1 (en) * | 1985-03-28 | 1989-03-30 | Daikin Ind Ltd | Novel fluorovinyl ether and copolymer comprising the same |
| IT1189092B (it) * | 1986-04-29 | 1988-01-28 | Ausimont Spa | Processo di polimerizzazione in dispersione acquosa di monomeri fluorurati |
| IT1204903B (it) * | 1986-06-26 | 1989-03-10 | Ausimont Spa | Processo di polimerizzazione in dispersione acquosa di monomeri florati |
| EP0290848B1 (en) * | 1987-04-25 | 1991-07-31 | Daikin Industries, Limited | Novel fluorovinyl ether |
| US5349093A (en) * | 1987-04-25 | 1994-09-20 | Daikin Industries, Ltd. | Fluorovinyl ether |
| DE3912148A1 (de) * | 1989-04-13 | 1990-10-18 | Hoechst Ag | Transparente thermoplastische formmasse und ihre verwendung |
| US5152353A (en) * | 1990-12-21 | 1992-10-06 | Smith International, Inc. | High speed rock bit |
| DE4137967A1 (de) * | 1991-11-19 | 1993-05-27 | Bayer Ag | Neue thermoplastische fluorcopolymere und fluormonomere zum einsatz bei deren herstellung |
| IT1264661B1 (it) * | 1993-07-05 | 1996-10-04 | Ausimont Spa | Copolimeri termoprocessabilin del tetrafluoroetilene |
| JP3817757B2 (ja) * | 1994-11-17 | 2006-09-06 | ユニマテック株式会社 | 新規ビニルエーテル化合物、その製造法およびその共重合体の製造法 |
| JP4110736B2 (ja) * | 1998-03-25 | 2008-07-02 | ダイキン工業株式会社 | 含フッ素エラストマーの金属含有量低減化方法 |
| US6255536B1 (en) | 1999-12-22 | 2001-07-03 | Dyneon Llc | Fluorine containing vinyl ethers |
| IT1318488B1 (it) | 2000-04-21 | 2003-08-25 | Ausimont Spa | Fluorovinileteri e polimeri da essi ottenibili. |
| US7534845B2 (en) | 2000-04-21 | 2009-05-19 | Solvay Solexis S.P.A. | Fluorovinyl ethers and polymers obtainable therefrom |
| IT1318487B1 (it) | 2000-04-21 | 2003-08-25 | Ausimont Spa | Fluoroelastomeri. |
| US6730760B2 (en) | 2001-01-31 | 2004-05-04 | 3M Innovative Properties Company | Perfluoroelastomers having a low glass transition temperature and method of making them |
| ATE419287T1 (de) * | 2001-01-31 | 2009-01-15 | 3M Innovative Properties Co | Perfluoroelastomere mit niedriger glasübergangstemperatur und deren herstellungsverfahren |
| ITMI20012164A1 (it) | 2001-10-18 | 2003-04-18 | Ausimont Spa | Fluoroelastomeri |
| ITMI20012165A1 (it) | 2001-10-18 | 2003-04-18 | Ausimont Spa | Perfluoroelastomeri |
| RU2005105936A (ru) * | 2002-09-12 | 2005-10-10 | ЗМ Инновейтив Пропертиз Компани (US) | Фторэластомеры с улучшенным сопротивлением к проницаемости и способ их получения |
| US7150957B2 (en) * | 2003-04-25 | 2006-12-19 | International Business Machines Corporation | Fluorinated vinyl ethers, copolymers thereof, and use in lithographic photoresist compositions |
| ITMI20041573A1 (it) | 2004-07-30 | 2006-01-31 | Solvay Solexis Spa | Fluoroelastomeri |
| US20060135716A1 (en) * | 2004-12-20 | 2006-06-22 | Ming-Hong Hung | Fluoroelastomers having low glass transition temperature |
| US8211964B2 (en) | 2005-07-26 | 2012-07-03 | Daikin Industries, Ltd. | Curable composition, molded article obtained from same and process for production of molded article |
| US20070088143A1 (en) * | 2005-10-19 | 2007-04-19 | Ming-Hong Hung | Alpha, alpha-dihydrofluorovinyl ethers, homopolymers and copolymers thereof |
| EP1995277A4 (en) | 2006-03-15 | 2011-07-06 | Daikin Ind Ltd | COMPOSITE MATERIAL OF FLUOROLE RUBBER, FUEL PERMEATION RESISTANT SEALING ELEMENT, AND METHOD FOR PRODUCING SUCH A COMPOSITE MATERIAL |
| CN101448895B (zh) | 2006-05-19 | 2012-06-20 | 大金工业株式会社 | 含氟弹性体组合物和由该组合物构成的成型品 |
| US20100247913A1 (en) | 2007-05-16 | 2010-09-30 | Daikin Industries, Ltd. | Crosslinked fluorine-containing elastomer fine particles, preparation process of same, and composition |
| EP2344553A1 (en) * | 2008-10-22 | 2011-07-20 | Daikin Industries, Ltd. | Perfluoroelastomer composition |
| KR101352661B1 (ko) | 2008-12-29 | 2014-01-16 | 그린, 트위드 오브 델라웨어, 인코포레이티드 | 가교성 불소 함유 엘라스토머 조성물 및 상기 조성물로 제조된 성형품 |
| EP2409998B1 (en) | 2010-07-23 | 2015-11-25 | 3M Innovative Properties Company | High melting PTFE polymers suitable for melt-processing into shaped articles |
| US9169339B2 (en) | 2010-12-07 | 2015-10-27 | Daikin Industries, Ltd. | Curable composition, molded product and method for producing molded product |
| US9631036B2 (en) | 2012-09-18 | 2017-04-25 | Honeywell International Inc. | Fluoroelastomers |
| US20160311954A1 (en) | 2013-12-26 | 2016-10-27 | Daikin Industries, Ltd. | Processing aid for polyolefins, and polyolefin composition |
| EP2902424B1 (en) | 2014-01-31 | 2020-04-08 | 3M Innovative Properties Company | Tetrafluoroethene polymer dispersions stabilized with aliphatic non-ionic surfactants |
| EP3103836A1 (en) | 2015-06-12 | 2016-12-14 | 3M Innovative Properties Company | Fluoropolymer with improved transparency |
| JP6463474B2 (ja) | 2015-06-19 | 2019-02-06 | ダイキン工業株式会社 | 含フッ素ポリマーからなる組成物及び成形品 |
| US10815369B2 (en) | 2016-08-10 | 2020-10-27 | Akita University | Composition and molded article |
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| WO2018181898A1 (ja) | 2017-03-31 | 2018-10-04 | ダイキン工業株式会社 | フルオロポリマーの製造方法、重合用界面活性剤及び界面活性剤の使用 |
| EP4257638B1 (en) | 2017-03-31 | 2026-07-22 | Daikin Industries, Ltd. | Production method for fluoropolymer, surfactant for polymerization, and use of surfactant |
| WO2018225682A1 (ja) | 2017-06-06 | 2018-12-13 | 国立大学法人東京工業大学 | フルオロエラストマー組成物及びその成形品 |
| WO2018229659A1 (en) | 2017-06-13 | 2018-12-20 | 3M Innovative Properties Company | Modified polytetrafluoroethylene and aqueous dispersion containing the same |
| DE202017003084U1 (de) | 2017-06-13 | 2017-09-19 | 3M Innovative Properties Company | Fluorpolymerdispersion |
| CN114456524B (zh) | 2017-10-18 | 2023-08-11 | 大金工业株式会社 | 交联性弹性体组合物和氟橡胶成型品 |
| KR102365862B1 (ko) | 2017-10-31 | 2022-02-23 | 다이킨 고교 가부시키가이샤 | 웨어러블 단말용 부재 |
| GB201807544D0 (en) | 2018-05-09 | 2018-06-20 | 3M Innovative Properties Co | Fluoropolymers with very low amounts of a fluorinated alkanoic acid or its salts |
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| EP3950725A4 (en) | 2019-05-08 | 2023-07-19 | Daikin Industries, Ltd. | Fluoropolymer production method and fluoropolymer |
| JPWO2022124209A1 (enExample) | 2020-12-10 | 2022-06-16 | ||
| EP4290104A4 (en) | 2021-02-05 | 2025-01-22 | Daikin Industries, Ltd. | Sealing member and battery |
| JP7667493B2 (ja) | 2021-04-27 | 2025-04-23 | ダイキン工業株式会社 | ビスジアミノフェニル化合物、架橋剤、組成物及び成形品 |
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|---|---|---|---|---|
| US3132123A (en) * | 1960-11-25 | 1964-05-05 | Du Pont | Polymers of perfluoroalkoxy perfluorovinyl ethers |
| US3322826A (en) * | 1962-04-11 | 1967-05-30 | Du Pont | Polymerization of hexafluoropropylene epoxide |
| US3450684A (en) * | 1963-07-24 | 1969-06-17 | Du Pont | Fluorocarbon polyethers |
| US3310606A (en) * | 1963-08-28 | 1967-03-21 | Du Pont | Thermosetting perfluorinated divinyl ether resins |
| US3291843A (en) * | 1963-10-08 | 1966-12-13 | Du Pont | Fluorinated vinyl ethers and their preparation |
| US3326984A (en) * | 1965-04-28 | 1967-06-20 | Du Pont | Perfluorodivinyl ether |
| US3397191A (en) * | 1965-06-02 | 1968-08-13 | Du Pont | Fluorocarbon ethers |
| US3467638A (en) * | 1967-03-07 | 1969-09-16 | Du Pont | Fluorinated cure-site monomers and vulcanizable fluorocarbon polymers made therewith |
| CA950923A (en) * | 1971-03-29 | 1974-07-09 | E. I. Du Pont De Nemours And Company | Polymers of perfluorovinyl ethers |
| DE2617829C2 (de) * | 1976-04-23 | 1982-06-03 | Hoechst Ag, 6000 Frankfurt | Verfahren zur Herstellung von Suspensionspolymerisaten des Tetrafluoräthylens |
| GB1550874A (en) * | 1976-10-28 | 1979-08-22 | Asahi Glass Co Ltd | Process for producing fluorinated copolymer having ion-exchange groups |
| US4131740A (en) * | 1977-04-20 | 1978-12-26 | E. I. Du Pont De Nemours And Company | Alkyl perfluoro-ω-fluoroformyl esters and their preparation |
| US4281092A (en) * | 1978-11-30 | 1981-07-28 | E. I. Du Pont De Nemours And Company | Vulcanizable fluorinated copolymers |
| US4330654A (en) * | 1980-06-11 | 1982-05-18 | The Dow Chemical Company | Novel polymers having acid functionality |
| EP0041737B1 (en) * | 1980-06-11 | 1984-08-29 | The Dow Chemical Company | Process to produce novel fluorocarbon vinyl ethers and resulting polymers |
| JPS5718710A (en) * | 1980-07-08 | 1982-01-30 | Asahi Glass Co Ltd | Copolymer capable of giving elastomer containing fluorine having improved cold and oil resistance |
| JPS57109810A (en) * | 1980-12-26 | 1982-07-08 | Asahi Glass Co Ltd | Copolymer giving fluorine-containing elastomer with cold and alcohol resistance |
| JPS5869213A (ja) * | 1981-09-21 | 1983-04-25 | Daikin Ind Ltd | 含フツ素共重合体 |
| JPS5871906A (ja) * | 1981-10-22 | 1983-04-28 | Daikin Ind Ltd | 含フツ素弾性状共重合体の製法 |
| JPS58189210A (ja) * | 1982-04-30 | 1983-11-04 | Daikin Ind Ltd | テトラフルオロエチレン／フルオロ（アルキルビニルエ−テル）共重合体の製法 |
-
1983
- 1983-06-23 US US06/507,083 patent/US4513128A/en not_active Expired - Lifetime
-
1984
- 1984-06-21 DE DE8484304204T patent/DE3465744D1/de not_active Expired
- 1984-06-21 JP JP59126534A patent/JPS6023407A/ja active Granted
- 1984-06-21 EP EP84304204A patent/EP0130052B1/en not_active Expired
- 1984-06-21 CA CA000457081A patent/CA1225195A/en not_active Expired
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6422908A (en) * | 1987-07-17 | 1989-01-25 | Nippon Mektron Kk | Production of fluorine-containing elastic copolymer |
| WO1997024381A1 (en) * | 1995-12-28 | 1997-07-10 | Daikin Industries, Ltd. | Fluorine-containing elastic copolymers, curable composition containing the same and sealant made therefrom |
| US6140437A (en) * | 1995-12-28 | 2000-10-31 | Daikin Industries Ltd. | Fluorine-containing elastic copolymers, curable composition containing the same and sealant made therefrom |
| JP4828783B2 (ja) * | 2001-01-31 | 2011-11-30 | スリーエム イノベイティブ プロパティズ カンパニー | 低いガラス転移温度を有するペルフルオロエラストマーおよびそれらの製造方法 |
| JP2006037025A (ja) * | 2004-07-29 | 2006-02-09 | Asahi Glass Co Ltd | 含フッ素エラストマーおよびその製造方法 |
| JP2006052399A (ja) * | 2004-07-30 | 2006-02-23 | Solvay Solexis Spa | パーフルオロエラストマー |
| JP2009516005A (ja) * | 2004-12-21 | 2009-04-16 | スリーエム イノベイティブ プロパティズ カンパニー | フルオロエラストマーを製造するためのフルオロポリマー |
| JP2008266190A (ja) * | 2007-04-19 | 2008-11-06 | Yunimatekku Kk | 含フッ素ビニルエーテル化合物 |
| CN105358594A (zh) * | 2013-06-25 | 2016-02-24 | 3M创新有限公司 | 可湿固化的组合物、使用方法以及复合制品 |
| US9725546B2 (en) | 2013-06-25 | 2017-08-08 | 3M Innovative Properties Company | Moisture-curable composition, method of using, and composite article |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0481608B2 (enExample) | 1992-12-24 |
| DE3465744D1 (en) | 1987-10-08 |
| CA1225195A (en) | 1987-08-04 |
| EP0130052A1 (en) | 1985-01-02 |
| US4513128A (en) | 1985-04-23 |
| EP0130052B1 (en) | 1987-09-02 |
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