JPS59207911A - テトラフルオロエチレン共重合体 - Google Patents
テトラフルオロエチレン共重合体Info
- Publication number
- JPS59207911A JPS59207911A JP59084196A JP8419684A JPS59207911A JP S59207911 A JPS59207911 A JP S59207911A JP 59084196 A JP59084196 A JP 59084196A JP 8419684 A JP8419684 A JP 8419684A JP S59207911 A JPS59207911 A JP S59207911A
- Authority
- JP
- Japan
- Prior art keywords
- copolymer
- formula
- tetrafluoroethylene
- substituted ethylene
- ethylene
- 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 37
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims description 28
- 239000005977 Ethylene Substances 0.000 claims description 23
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 22
- 150000001875 compounds Chemical class 0.000 claims description 12
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 24
- 239000002904 solvent Substances 0.000 description 21
- -1 beta-bromoethyl Chemical group 0.000 description 11
- 239000000203 mixture Substances 0.000 description 10
- 238000009835 boiling Methods 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 8
- 238000004817 gas chromatography Methods 0.000 description 8
- 239000007787 solid Substances 0.000 description 8
- 238000007334 copolymerization reaction Methods 0.000 description 7
- 229920000642 polymer Polymers 0.000 description 7
- 238000006116 polymerization reaction Methods 0.000 description 7
- 229910001220 stainless steel Inorganic materials 0.000 description 7
- 239000010935 stainless steel Substances 0.000 description 7
- 238000005481 NMR spectroscopy Methods 0.000 description 6
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 6
- 239000000178 monomer Substances 0.000 description 6
- 239000002243 precursor Substances 0.000 description 6
- 125000005192 alkyl ethylene group Chemical group 0.000 description 5
- 238000002329 infrared spectrum Methods 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 239000011698 potassium fluoride Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 150000005215 alkyl ethers Chemical class 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 238000003780 insertion Methods 0.000 description 4
- 230000037431 insertion Effects 0.000 description 4
- 150000002978 peroxides Chemical class 0.000 description 4
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 4
- 239000004810 polytetrafluoroethylene Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 238000001228 spectrum Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
- QZRGKCOWNLSUDK-UHFFFAOYSA-N Iodochlorine Chemical compound ICl QZRGKCOWNLSUDK-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 239000003999 initiator Substances 0.000 description 3
- 239000011630 iodine Substances 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000012429 reaction media Substances 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- BOSAWIQFTJIYIS-UHFFFAOYSA-N 1,1,1-trichloro-2,2,2-trifluoroethane Chemical compound FC(F)(F)C(Cl)(Cl)Cl BOSAWIQFTJIYIS-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- BCCOBQSFUDVTJQ-UHFFFAOYSA-N octafluorocyclobutane Chemical compound FC1(F)C(F)(F)C(F)(F)C1(F)F BCCOBQSFUDVTJQ-UHFFFAOYSA-N 0.000 description 2
- 235000019407 octafluorocyclobutane Nutrition 0.000 description 2
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 239000003505 polymerization initiator Substances 0.000 description 2
- NROKBHXJSPEDAR-UHFFFAOYSA-M potassium fluoride Chemical compound [F-].[K+] NROKBHXJSPEDAR-UHFFFAOYSA-M 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 210000003625 skull Anatomy 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000003797 telogen phase Effects 0.000 description 2
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 2
- 229940029284 trichlorofluoromethane Drugs 0.000 description 2
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 2
- CJVROGOPKLYNSX-UHFFFAOYSA-N (4-tert-butylcyclohexyl) carboxyoxy carbonate Chemical compound CC(C)(C)C1CCC(OC(=O)OOC(O)=O)CC1 CJVROGOPKLYNSX-UHFFFAOYSA-N 0.000 description 1
- LVGUZGTVOIAKKC-UHFFFAOYSA-N 1,1,1,2-tetrafluoroethane Chemical compound FCC(F)(F)F LVGUZGTVOIAKKC-UHFFFAOYSA-N 0.000 description 1
- CQPFPFMRZZXKAJ-UHFFFAOYSA-N 1,1,2,2-tetrafluoro-2-(1,1,2,2-tetrafluoro-4-iodobutoxy)ethanesulfonyl fluoride Chemical compound ICCC(F)(F)C(F)(F)OC(F)(F)C(F)(F)S(F)(=O)=O CQPFPFMRZZXKAJ-UHFFFAOYSA-N 0.000 description 1
- BEQKKZICTDFVMG-UHFFFAOYSA-N 1,2,3,4,6-pentaoxepane-5,7-dione Chemical compound O=C1OOOOC(=O)O1 BEQKKZICTDFVMG-UHFFFAOYSA-N 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- DCWQZPJHHVLHSV-UHFFFAOYSA-N 3-ethoxypropanenitrile Chemical compound CCOCCC#N DCWQZPJHHVLHSV-UHFFFAOYSA-N 0.000 description 1
- CONKBQPVFMXDOV-QHCPKHFHSA-N 6-[(5S)-5-[[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]methyl]-2-oxo-1,3-oxazolidin-3-yl]-3H-1,3-benzoxazol-2-one Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C[C@H]1CN(C(O1)=O)C1=CC2=C(NC(O2)=O)C=C1 CONKBQPVFMXDOV-QHCPKHFHSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 150000001265 acyl fluorides Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- INLLPKCGLOXCIV-UHFFFAOYSA-N bromoethene Chemical compound BrC=C INLLPKCGLOXCIV-UHFFFAOYSA-N 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- AFYPFACVUDMOHA-UHFFFAOYSA-N chlorotrifluoromethane Chemical compound FC(F)(F)Cl AFYPFACVUDMOHA-UHFFFAOYSA-N 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000011437 continuous method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- ZFTFAPZRGNKQPU-UHFFFAOYSA-N dicarbonic acid Chemical compound OC(=O)OC(O)=O ZFTFAPZRGNKQPU-UHFFFAOYSA-N 0.000 description 1
- 238000000113 differential scanning calorimetry Methods 0.000 description 1
- 125000000816 ethylene group Chemical class [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- UHCBBWUQDAVSMS-UHFFFAOYSA-N fluoroethane Chemical compound CCF UHCBBWUQDAVSMS-UHFFFAOYSA-N 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- JARKCYVAAOWBJS-UHFFFAOYSA-N hexanal Chemical compound CCCCCC=O JARKCYVAAOWBJS-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000006713 insertion reaction Methods 0.000 description 1
- 125000002346 iodo group Chemical group I* 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 210000003127 knee Anatomy 0.000 description 1
- 230000006651 lactation Effects 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- SNVLJLYUUXKWOJ-UHFFFAOYSA-N methylidenecarbene Chemical compound C=[C] SNVLJLYUUXKWOJ-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- QYSGYZVSCZSLHT-UHFFFAOYSA-N octafluoropropane Chemical compound FC(F)(F)C(F)(F)C(F)(F)F QYSGYZVSCZSLHT-UHFFFAOYSA-N 0.000 description 1
- 239000002939 oilproofing Substances 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 150000002976 peresters Chemical class 0.000 description 1
- 229960004065 perflutren Drugs 0.000 description 1
- 235000003270 potassium fluoride Nutrition 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000646 scanning calorimetry Methods 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
- 238000005303 weighing Methods 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
- C08F214/26—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)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/490,880 US4522995A (en) | 1983-05-02 | 1983-05-02 | Fluorinated alkyl ether-containing ethylenes, precursors thereto, and copolymers thereof with tetrafluoroethylene |
| US490880 | 1995-06-15 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59207911A true JPS59207911A (ja) | 1984-11-26 |
| JPS632964B2 JPS632964B2 (OSRAM) | 1988-01-21 |
Family
ID=23949885
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59084196A Granted JPS59207911A (ja) | 1983-05-02 | 1984-04-27 | テトラフルオロエチレン共重合体 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US4522995A (OSRAM) |
| EP (1) | EP0124378B1 (OSRAM) |
| JP (1) | JPS59207911A (OSRAM) |
| CA (1) | CA1234151A (OSRAM) |
| DE (1) | DE3473282D1 (OSRAM) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60248710A (ja) * | 1984-05-22 | 1985-12-09 | Daikin Ind Ltd | 新規エチレン／テトラフルオロエチレン系共重合体 |
| JPS62106910A (ja) * | 1985-11-01 | 1987-05-18 | Agency Of Ind Science & Technol | 紫外線透過フィルムの製造方法 |
| JP2003518052A (ja) * | 1999-12-22 | 2003-06-03 | ダイネオン リミティド ライアビリティー カンパニー | フッ素含有アリルエーテルおよび高級同族体 |
| JP2013532740A (ja) * | 2010-07-23 | 2013-08-19 | スリーエム イノベイティブ プロパティズ カンパニー | 溶融加工用の高融点ｐｔｆｅポリマー |
| JP2017183166A (ja) * | 2016-03-31 | 2017-10-05 | 株式会社オートネットワーク技術研究所 | 絶縁電線 |
| CN117550999A (zh) * | 2023-11-14 | 2024-02-13 | 四川轻化工大学 | 一种含氟硫化点单体的制备方法 |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5430776A (en) * | 1984-08-09 | 1995-07-04 | Stauffer; J. Christian | Fuel pellets for thermonuclear reactions |
| DE3575566D1 (de) * | 1984-12-19 | 1990-03-01 | Ausimont Usa | Terpolymer aus chlortrifluorethylen oder tetrafluorethylen, ethylen und perfluorisoalkoxyperfluoralkylethylen. |
| WO1990015828A1 (en) * | 1989-06-20 | 1990-12-27 | Raychem Corporation | Thermoplastic fluoropolymers |
| FR2687671B1 (fr) * | 1992-02-21 | 1994-05-20 | Centre Nal Recherc Scientifique | Monomeres derives de sultones perhalogenees et polymeres obtenus a partir de ces monomeres. |
| GB9407886D0 (en) * | 1994-04-21 | 1994-06-15 | Ici Plc | Purification process |
| JP3702468B2 (ja) * | 1995-12-20 | 2005-10-05 | イー・アイ・デユポン・ドウ・ヌムール・アンド・カンパニー | パーフルオロ重合体の製造における連鎖移動剤としてのヨードニトリル |
| US20030069343A1 (en) * | 1998-08-06 | 2003-04-10 | Paul Smith | Melt-processible poly(tetrafluoroethylene) |
| US7276287B2 (en) * | 2003-12-17 | 2007-10-02 | Eidgenössische Technische Hochschule Zürich | Melt-processible poly(tetrafluoroethylene) |
| US6737165B1 (en) | 1998-08-06 | 2004-05-18 | Omlidon Technologies Llc | Melt-processible poly(tetrafluoroethylene) |
| EP2305724A1 (en) * | 1998-08-06 | 2011-04-06 | Omlidon Technologies LLC | Melt-processible poly(tetrafluoroethylene) |
| DE60019925T2 (de) * | 1999-06-16 | 2006-02-16 | E.I. Du Pont De Nemours And Co., Wilmington | Fluorierte ionische polymere |
| GB0027047D0 (en) * | 2000-11-06 | 2000-12-20 | Ici Plc | Process for reducing the concentration of undesired compounds in a composition |
| HUP0303192A2 (hu) * | 2001-01-12 | 2003-12-29 | Amersham Plc | Perfluor-szulfonil-halogenidek és hasonló vegyületek polimerből készült hordozók módosítására |
| US20040039142A1 (en) * | 2001-12-06 | 2004-02-26 | Yang Zhen Yu | Fluorinated ionic polymers |
| US8217126B2 (en) * | 2007-11-09 | 2012-07-10 | E I Du Pont De Nemours And Company | Fluoroolefin monomers and copolymers thereof |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57109811A (en) * | 1980-12-26 | 1982-07-08 | Asahi Glass Co Ltd | Fluorine-containing elastic copolymer |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2732370A (en) * | 1956-01-24 | Polymers | ||
| US3445434A (en) * | 1964-10-30 | 1969-05-20 | Du Pont | Copolymers of tetrafluoroethylene,ethylene and an olefinic acid |
| US3465045A (en) * | 1965-02-18 | 1969-09-02 | Us Agriculture | Fluorinated vinyl ethers and use thereof |
| US3480605A (en) * | 1965-02-18 | 1969-11-25 | Us Agriculture | Fluorinated vinyl ethers and use thereof |
| DE1298514B (de) * | 1965-12-02 | 1969-07-03 | Hoechst Ag | Verfahren zur Herstellung von Perfluoralkyl-alkyl-aethern |
| US3422131A (en) * | 1966-02-10 | 1969-01-14 | Us Agriculture | Fluoroalkoxyalkyl silanes |
| US3420793A (en) * | 1967-03-16 | 1969-01-07 | Us Agriculture | Bis-(fluoroalkoxy)alkyl siloxanes |
| US3577465A (en) * | 1967-04-25 | 1971-05-04 | Allied Chem | Terminally unsaturated fluoroolefins |
| US3758543A (en) * | 1967-04-25 | 1973-09-11 | Allied Chem | Novel sulfates and method for their preparation |
| BE714159A (OSRAM) * | 1967-04-25 | 1968-09-16 | Allied Chem | |
| US3529003A (en) * | 1967-07-17 | 1970-09-15 | Dow Chemical Co | Fluorine containing silicones |
| US3641083A (en) * | 1968-11-01 | 1972-02-08 | Allied Chem | Chromium complexes of fluoroisoalkoxyalkyl carboxylic acids |
| GB1339789A (en) * | 1970-04-20 | 1973-12-05 | Du Pont | Ethylene/chlorotrifluoroethylene or tetrafluoroethylene copolymer glass compositions |
| US3940207A (en) * | 1971-06-11 | 1976-02-24 | E. I. Du Pont De Nemours And Company | Soft, tough low refractive index contact lenses |
| JPS5032098B2 (OSRAM) * | 1972-08-09 | 1975-10-17 | ||
| JPS551351B2 (OSRAM) * | 1974-03-07 | 1980-01-12 | ||
| US4178218A (en) * | 1974-03-07 | 1979-12-11 | Asahi Kasei Kogyo Kabushiki Kaisha | Cation exchange membrane and use thereof in the electrolysis of sodium chloride |
| DE2639109A1 (de) * | 1976-08-31 | 1978-03-09 | Hoechst Ag | Copolymerisate des tetrafluoraethylens und verfahren zu deren herstellung |
| US4281092A (en) * | 1978-11-30 | 1981-07-28 | E. I. Du Pont De Nemours And Company | Vulcanizable fluorinated copolymers |
| US4329435A (en) * | 1979-05-31 | 1982-05-11 | Asahi Kasei Kogyo Kabushiki Kaisha | Novel fluorinated copolymer with tridihydro fluorosulfonyl fluoride pendant groups and preparation thereof |
-
1983
- 1983-05-02 US US06/490,880 patent/US4522995A/en not_active Expired - Fee Related
-
1984
- 1984-04-27 JP JP59084196A patent/JPS59207911A/ja active Granted
- 1984-04-30 DE DE8484302895T patent/DE3473282D1/de not_active Expired
- 1984-04-30 EP EP84302895A patent/EP0124378B1/en not_active Expired
- 1984-05-01 CA CA000453214A patent/CA1234151A/en not_active Expired
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57109811A (en) * | 1980-12-26 | 1982-07-08 | Asahi Glass Co Ltd | Fluorine-containing elastic copolymer |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60248710A (ja) * | 1984-05-22 | 1985-12-09 | Daikin Ind Ltd | 新規エチレン／テトラフルオロエチレン系共重合体 |
| JPS62106910A (ja) * | 1985-11-01 | 1987-05-18 | Agency Of Ind Science & Technol | 紫外線透過フィルムの製造方法 |
| JP2003518052A (ja) * | 1999-12-22 | 2003-06-03 | ダイネオン リミティド ライアビリティー カンパニー | フッ素含有アリルエーテルおよび高級同族体 |
| JP2013532740A (ja) * | 2010-07-23 | 2013-08-19 | スリーエム イノベイティブ プロパティズ カンパニー | 溶融加工用の高融点ｐｔｆｅポリマー |
| JP2017183166A (ja) * | 2016-03-31 | 2017-10-05 | 株式会社オートネットワーク技術研究所 | 絶縁電線 |
| WO2017169679A1 (ja) * | 2016-03-31 | 2017-10-05 | 株式会社オートネットワーク技術研究所 | 絶縁電線 |
| CN109074915A (zh) * | 2016-03-31 | 2018-12-21 | 株式会社自动网络技术研究所 | 绝缘电线 |
| CN117550999A (zh) * | 2023-11-14 | 2024-02-13 | 四川轻化工大学 | 一种含氟硫化点单体的制备方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0124378B1 (en) | 1988-08-10 |
| JPS632964B2 (OSRAM) | 1988-01-21 |
| US4522995A (en) | 1985-06-11 |
| EP0124378A1 (en) | 1984-11-07 |
| CA1234151A (en) | 1988-03-15 |
| DE3473282D1 (en) | 1988-09-15 |
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