JPH11509244A - 含フッ素重合体の製造方法 - Google Patents
含フッ素重合体の製造方法Info
- Publication number
- JPH11509244A JPH11509244A JP9505149A JP50514997A JPH11509244A JP H11509244 A JPH11509244 A JP H11509244A JP 9505149 A JP9505149 A JP 9505149A JP 50514997 A JP50514997 A JP 50514997A JP H11509244 A JPH11509244 A JP H11509244A
- Authority
- JP
- Japan
- Prior art keywords
- tetrafluoroethylene
- perfluoro
- hexafluoropropylene
- vinyl ether
- fluorine
- 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
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 229920002313 fluoropolymer Polymers 0.000 title description 8
- 239000004811 fluoropolymer Substances 0.000 title description 8
- 229920000642 polymer Polymers 0.000 claims abstract description 102
- -1 fluorinated aliphatic sulfinic acid salt Chemical class 0.000 claims abstract description 69
- 238000000034 method Methods 0.000 claims abstract description 44
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 41
- 239000011737 fluorine Substances 0.000 claims abstract description 34
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims abstract description 32
- 150000001336 alkenes Chemical class 0.000 claims abstract description 29
- BUUPQKDIAURBJP-UHFFFAOYSA-N sulfinic acid Chemical compound OS=O BUUPQKDIAURBJP-UHFFFAOYSA-N 0.000 claims abstract description 29
- 239000003999 initiator Substances 0.000 claims abstract description 25
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims abstract description 19
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Inorganic materials Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 claims abstract description 16
- SXDBWCPKPHAZSM-UHFFFAOYSA-M bromate Inorganic materials [O-]Br(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-M 0.000 claims abstract description 10
- SXDBWCPKPHAZSM-UHFFFAOYSA-N bromic acid Chemical compound OBr(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-N 0.000 claims abstract description 6
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims description 93
- 238000006116 polymerization reaction Methods 0.000 claims description 61
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 claims description 50
- 239000000178 monomer Substances 0.000 claims description 40
- 239000007800 oxidant agent Substances 0.000 claims description 38
- 239000011734 sodium Substances 0.000 claims description 31
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 27
- 125000001931 aliphatic group Chemical group 0.000 claims description 22
- 125000004432 carbon atom Chemical group C* 0.000 claims description 20
- 125000000217 alkyl group Chemical group 0.000 claims description 16
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 claims description 15
- DOUHZFSGSXMPIE-UHFFFAOYSA-N hydroxidooxidosulfur(.) Chemical compound [O]SO DOUHZFSGSXMPIE-UHFFFAOYSA-N 0.000 claims description 15
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 14
- 239000005977 Ethylene Substances 0.000 claims description 14
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 claims description 14
- 150000002500 ions Chemical class 0.000 claims description 14
- 229910021529 ammonia Inorganic materials 0.000 claims description 11
- 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 claims description 10
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 claims description 10
- 229910052708 sodium Inorganic materials 0.000 claims description 10
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 claims description 9
- YSYRISKCBOPJRG-UHFFFAOYSA-N 4,5-difluoro-2,2-bis(trifluoromethyl)-1,3-dioxole Chemical compound FC1=C(F)OC(C(F)(F)F)(C(F)(F)F)O1 YSYRISKCBOPJRG-UHFFFAOYSA-N 0.000 claims description 8
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 8
- 229910052783 alkali metal Inorganic materials 0.000 claims description 7
- OVGRCEFMXPHEBL-UHFFFAOYSA-N 1-ethenoxypropane Chemical compound CCCOC=C OVGRCEFMXPHEBL-UHFFFAOYSA-N 0.000 claims description 6
- XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical group [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 claims description 6
- 150000001768 cations Chemical class 0.000 claims description 4
- 239000000460 chlorine Substances 0.000 claims description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 claims description 3
- 150000001340 alkali metals Chemical group 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 claims 2
- 241001061127 Thione Species 0.000 claims 2
- 239000003513 alkali Substances 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims 1
- 239000010931 gold Substances 0.000 claims 1
- 229910052737 gold Inorganic materials 0.000 claims 1
- 229920001169 thermoplastic Polymers 0.000 abstract description 8
- 239000000806 elastomer Substances 0.000 abstract description 7
- 229920001971 elastomer Polymers 0.000 abstract description 5
- XTEGARKTQYYJKE-UHFFFAOYSA-N chloric acid Chemical compound OCl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-N 0.000 abstract 1
- 229940005991 chloric acid Drugs 0.000 abstract 1
- 230000000379 polymerizing effect Effects 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 84
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 62
- 239000000243 solution Substances 0.000 description 55
- 239000000203 mixture Substances 0.000 description 39
- 239000012153 distilled water Substances 0.000 description 35
- 229910052757 nitrogen Inorganic materials 0.000 description 31
- 239000007787 solid Substances 0.000 description 29
- 239000007789 gas Substances 0.000 description 26
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 24
- 238000004458 analytical method Methods 0.000 description 22
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 16
- 239000000155 melt Substances 0.000 description 16
- 238000002360 preparation method Methods 0.000 description 16
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 15
- 239000000047 product Substances 0.000 description 15
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 14
- 150000001875 compounds Chemical class 0.000 description 14
- 229910001220 stainless steel Inorganic materials 0.000 description 13
- 239000010935 stainless steel Substances 0.000 description 13
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 12
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 12
- 239000011347 resin Substances 0.000 description 12
- 229920005989 resin Polymers 0.000 description 12
- 239000002904 solvent Substances 0.000 description 12
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 11
- 239000005708 Sodium hypochlorite Substances 0.000 description 11
- 229910052799 carbon Inorganic materials 0.000 description 11
- 235000011089 carbon dioxide Nutrition 0.000 description 11
- 238000002474 experimental method Methods 0.000 description 11
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 11
- 238000005481 NMR spectroscopy Methods 0.000 description 10
- 239000007864 aqueous solution Substances 0.000 description 10
- 239000007900 aqueous suspension Substances 0.000 description 10
- 238000010926 purge Methods 0.000 description 10
- 150000003254 radicals Chemical class 0.000 description 10
- 238000004293 19F NMR spectroscopy Methods 0.000 description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 9
- 238000001125 extrusion Methods 0.000 description 9
- 239000001301 oxygen Substances 0.000 description 9
- 229910052760 oxygen Inorganic materials 0.000 description 9
- 239000000843 powder Substances 0.000 description 9
- 239000004094 surface-active agent Substances 0.000 description 9
- BZSXEZOLBIJVQK-UHFFFAOYSA-N 2-methylsulfonylbenzoic acid Chemical compound CS(=O)(=O)C1=CC=CC=C1C(O)=O BZSXEZOLBIJVQK-UHFFFAOYSA-N 0.000 description 8
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 8
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 8
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 8
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 8
- 229920001577 copolymer Polymers 0.000 description 8
- 239000000839 emulsion Substances 0.000 description 8
- 125000001153 fluoro group Chemical group F* 0.000 description 8
- 239000004816 latex Substances 0.000 description 8
- 229920000126 latex Polymers 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 239000000725 suspension Substances 0.000 description 7
- TWIYDBQRYCWOAU-UHFFFAOYSA-N 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfinic acid Chemical compound OS(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F TWIYDBQRYCWOAU-UHFFFAOYSA-N 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
- 238000010526 radical polymerization reaction Methods 0.000 description 6
- 230000035484 reaction time Effects 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 229910052717 sulfur Inorganic materials 0.000 description 6
- 238000005160 1H NMR spectroscopy Methods 0.000 description 5
- 230000009102 absorption Effects 0.000 description 5
- 238000010521 absorption reaction Methods 0.000 description 5
- 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 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000012634 fragment Substances 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- XUXNAKZDHHEHPC-UHFFFAOYSA-M sodium bromate Chemical compound [Na+].[O-]Br(=O)=O XUXNAKZDHHEHPC-UHFFFAOYSA-M 0.000 description 5
- CRWJEUDFKNYSBX-UHFFFAOYSA-N sodium;hypobromite Chemical compound [Na+].Br[O-] CRWJEUDFKNYSBX-UHFFFAOYSA-N 0.000 description 5
- 239000004416 thermosoftening plastic Substances 0.000 description 5
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 5
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 4
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 239000000908 ammonium hydroxide Substances 0.000 description 4
- 150000001450 anions Chemical class 0.000 description 4
- 239000008346 aqueous phase Substances 0.000 description 4
- 229910052786 argon Inorganic materials 0.000 description 4
- 238000007865 diluting Methods 0.000 description 4
- 238000004821 distillation Methods 0.000 description 4
- 238000000921 elemental analysis Methods 0.000 description 4
- 238000007720 emulsion polymerization reaction Methods 0.000 description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
- 239000003456 ion exchange resin Substances 0.000 description 4
- 229920003303 ion-exchange polymer Polymers 0.000 description 4
- YVBBRRALBYAZBM-UHFFFAOYSA-N perfluorooctane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F YVBBRRALBYAZBM-UHFFFAOYSA-N 0.000 description 4
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 4
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 4
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 4
- 150000003839 salts Chemical group 0.000 description 4
- 229920006395 saturated elastomer Polymers 0.000 description 4
- 235000017557 sodium bicarbonate Nutrition 0.000 description 4
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 4
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 4
- 125000000626 sulfinic acid group Chemical group 0.000 description 4
- 150000003455 sulfinic acids Chemical class 0.000 description 4
- 238000012546 transfer Methods 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- DFCYBFLXCKGZML-UHFFFAOYSA-N 1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctane-1-sulfinic acid Chemical compound OS(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F DFCYBFLXCKGZML-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000001721 carbon Chemical group 0.000 description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000000284 extract Substances 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 3
- 230000000977 initiatory effect Effects 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- CSMWJXBSXGUPGY-UHFFFAOYSA-L sodium dithionate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)S([O-])(=O)=O CSMWJXBSXGUPGY-UHFFFAOYSA-L 0.000 description 3
- 229940075931 sodium dithionate Drugs 0.000 description 3
- 238000001291 vacuum drying Methods 0.000 description 3
- MIZLGWKEZAPEFJ-UHFFFAOYSA-N 1,1,2-trifluoroethene Chemical group FC=C(F)F MIZLGWKEZAPEFJ-UHFFFAOYSA-N 0.000 description 2
- QGHDLJAZIIFENW-UHFFFAOYSA-N 4-[1,1,1,3,3,3-hexafluoro-2-(4-hydroxy-3-prop-2-enylphenyl)propan-2-yl]-2-prop-2-enylphenol Chemical group C1=C(CC=C)C(O)=CC=C1C(C(F)(F)F)(C(F)(F)F)C1=CC=C(O)C(CC=C)=C1 QGHDLJAZIIFENW-UHFFFAOYSA-N 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 2
- 238000004566 IR spectroscopy Methods 0.000 description 2
- BHFJBHMTEDLICO-UHFFFAOYSA-N Perfluorooctylsulfonyl fluoride Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)S(F)(=O)=O BHFJBHMTEDLICO-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 229910052770 Uranium Inorganic materials 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 125000002947 alkylene group Chemical group 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
- 239000012736 aqueous medium Substances 0.000 description 2
- UAWBWGUIUMQJIT-UHFFFAOYSA-N azanium;1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctane-1-sulfonate Chemical compound N.OS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F UAWBWGUIUMQJIT-UHFFFAOYSA-N 0.000 description 2
- 150000007514 bases Chemical class 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 238000007872 degassing Methods 0.000 description 2
- 239000007857 degradation product Substances 0.000 description 2
- 238000001938 differential scanning calorimetry curve Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 125000001033 ether group Chemical group 0.000 description 2
- 125000003709 fluoroalkyl group Chemical group 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 150000008040 ionic compounds Chemical class 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- WYURNTSHIVDZCO-SVYQBANQSA-N oxolane-d8 Chemical compound [2H]C1([2H])OC([2H])([2H])C([2H])([2H])C1([2H])[2H] WYURNTSHIVDZCO-SVYQBANQSA-N 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 2
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 description 2
- 235000010265 sodium sulphite Nutrition 0.000 description 2
- KSGPZCLVYJGMFY-UHFFFAOYSA-M sodium;1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfinate Chemical compound [Na+].[O-]S(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F KSGPZCLVYJGMFY-UHFFFAOYSA-M 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 229920002725 thermoplastic elastomer Polymers 0.000 description 2
- 238000006276 transfer reaction Methods 0.000 description 2
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- BULLJMKUVKYZDJ-UHFFFAOYSA-N 1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluoro-6-iodohexane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)I BULLJMKUVKYZDJ-UHFFFAOYSA-N 0.000 description 1
- XJSRKJAHJGCPGC-UHFFFAOYSA-N 1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluorohexane Chemical compound FC(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F XJSRKJAHJGCPGC-UHFFFAOYSA-N 0.000 description 1
- PGRFXXCKHGIFSV-UHFFFAOYSA-N 1,1,1,2,2,3,3,4,4-nonafluoro-4-iodobutane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)I PGRFXXCKHGIFSV-UHFFFAOYSA-N 0.000 description 1
- AJDIZQLSFPQPEY-UHFFFAOYSA-N 1,1,2-Trichlorotrifluoroethane Chemical group FC(F)(Cl)C(F)(Cl)Cl AJDIZQLSFPQPEY-UHFFFAOYSA-N 0.000 description 1
- CIKVTYVSUSJJAA-UHFFFAOYSA-N 1,1-difluoroethene;fluoroethene Chemical compound FC=C.FC(F)=C CIKVTYVSUSJJAA-UHFFFAOYSA-N 0.000 description 1
- ZNEMGFATAVGQSF-UHFFFAOYSA-N 1-(2-amino-6,7-dihydro-4H-[1,3]thiazolo[4,5-c]pyridin-5-yl)-2-[5-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-1,3,4-oxadiazol-2-yl]ethanone Chemical compound NC=1SC2=C(CN(CC2)C(CC=2OC(=NN=2)C=2C=NC(=NC=2)NC2CC3=CC=CC=C3C2)=O)N=1 ZNEMGFATAVGQSF-UHFFFAOYSA-N 0.000 description 1
- AYCANDRGVPTASA-UHFFFAOYSA-N 1-bromo-1,2,2-trifluoroethene Chemical group FC(F)=C(F)Br AYCANDRGVPTASA-UHFFFAOYSA-N 0.000 description 1
- FDMFUZHCIRHGRG-UHFFFAOYSA-N 3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)C=C FDMFUZHCIRHGRG-UHFFFAOYSA-N 0.000 description 1
- 229910000619 316 stainless steel Inorganic materials 0.000 description 1
- KYARBIJYVGJZLB-UHFFFAOYSA-N 7-amino-4-hydroxy-2-naphthalenesulfonic acid Chemical compound OC1=CC(S(O)(=O)=O)=CC2=CC(N)=CC=C21 KYARBIJYVGJZLB-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- VUGHUBKRIVNEJQ-UHFFFAOYSA-N FC=C(F)F.[Cl] Chemical group FC=C(F)F.[Cl] VUGHUBKRIVNEJQ-UHFFFAOYSA-N 0.000 description 1
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical group [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 description 1
- 241001072332 Monia Species 0.000 description 1
- TZRXHJWUDPFEEY-UHFFFAOYSA-N Pentaerythritol Tetranitrate Chemical compound [O-][N+](=O)OCC(CO[N+]([O-])=O)(CO[N+]([O-])=O)CO[N+]([O-])=O TZRXHJWUDPFEEY-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 229920002253 Tannate Polymers 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- UCGPQTPYONQEOB-UHFFFAOYSA-L [Li+].[Li+].O.[O-]S([O-])=O Chemical compound [Li+].[Li+].O.[O-]S([O-])=O UCGPQTPYONQEOB-UHFFFAOYSA-L 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 150000001733 carboxylic acid esters Chemical class 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
- 239000012259 ether extract Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 229910000856 hastalloy Inorganic materials 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- CUILPNURFADTPE-UHFFFAOYSA-N hypobromous acid Chemical compound BrO CUILPNURFADTPE-UHFFFAOYSA-N 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 150000004694 iodide salts Chemical class 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229940006487 lithium cation Drugs 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- FOKCKXCUQFKNLD-UHFFFAOYSA-N pent-1-enyl hypofluorite Chemical compound C(CC)C=COF FOKCKXCUQFKNLD-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000005375 photometry Methods 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
- 150000004053 quinones Chemical class 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000012966 redox initiator Substances 0.000 description 1
- 238000006479 redox reaction Methods 0.000 description 1
- 238000001226 reprecipitation Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 125000006337 tetrafluoro ethyl group Chemical group 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- JFALSRSLKYAFGM-UHFFFAOYSA-N uranium(0) Chemical compound [U] JFALSRSLKYAFGM-UHFFFAOYSA-N 0.000 description 1
- 238000010792 warming 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
- C08F14/00—Homopolymers and 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
- C08F14/18—Monomers containing fluorine
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)
- Polymerization Catalysts (AREA)
Abstract
Description
Claims (1)
- 【特許請求の範囲】 1.開始剤が、含フッ素脂肪族スルフィン酸塩又はスルフィン酸と、塩素酸イオ ン、臭素酸イオン及び次亜塩素酸イオンからなる群から選ばれた酸化剤との組み 合わせであり、該含フッ素脂肪族スルフィン酸塩又は該含フッ素脂肪族スルフィ ン酸及び該酸化剤が水溶性であり、フッ素含有オレフィンを水性の乳化又は懸濁 状態で重合させることを特徴とするフッ素含有重合体の製造方法。 2.アンモニアが共存する請求項1に記載の方法。 3.該フッ素含有オレフィンが、テトラフルオルエチレン、フッ化ビニル、フッ 化ビニリデン、ヘキサフルオルプロピレン、クロルトリフルオルエチレン、又は ペルフルオル(2,2−ジメチル−1,3−ジオキソール)である請求項1に記 載の方法。 4.該フッ素含有オレフィンがテトラフルオルエチレンである請求項1に記載の 方法。 5.該フッ素含有オレフィンが、テトラフルオルエチレン、フッ化ビニル、フッ 化ビニリデン、ヘキサフルオルプロピレン、クロルトリフルオルエチレン、又は ペルフルオル(2,2−ジメチル−1,3−ジオキソール)である請求項2に記 載の方法。 6.該フッ素含有オレフィンがテトラフルオルエチレンである請求項2に記載の 方法。 7.該フッ素含有オレフィンと他の単量体が、以下の組み合わせ: テトラフルオルエチレン; テトラフルオルエチレン/ヘキサフルオルプロピレン; テトラフルオルエチレン/ペルフルオル(メチルビニルエーテル); テトラフルオルエチレン/ペルフルオル(エチルビニルエーテル); テトラフルオルエチレン/ペルフルオル(n-プロピルビニルエーテル); テトラフルオルエチレン/ペルフルオル(2,2−ジメチルジオキソール) ; フッ化ビニル; テトラフルオルエチレン/エチレン; クロルトリフルオルエチレン/エチレン; テトラフルオルエチレン/ヘキサフルオルプロピレン/ペルフルオル(アル キルビニルエーテル)(アルキル基は1〜5個の炭素原子を含有する); ヘキサフルオルプロピレン/フッ化ビニリデン; テトラフルオルエチレン/ヘキサフルオルプロピレン/フッ化ビニリデン; テトラフルオルエチレン/フッ化ビニリデン; テトラフルオルエチレン/ペルフルオル(メチルビニルエーテル)/ペルフ ルオル化キュアサイトモノマー;及び クロルトリフルオルエチレン で存在する請求項1に記載の方法。 8.アンモニアが共存する請求項7に記載の方法。 9.該スルフィン酸塩又はスルフィン酸が式 [(R1SO2)n]qMr (式中、R1は自由原子価nを持つ含フッ素脂肪族であり、 Mは電荷がsであるカチオンであり、 sは1又は2であり、 nは1又は2であり、 r及びqは1または2であり、 但し、q・n=r・s である) を有する請求項1に記載の方法。 10.Mガアルカリ金属カチオン又はNH4 +である請求項9に記載の方法。 11.工程温度が、約20℃〜約150℃である請求項1に記載の方法。 12.アンモニアが共存する請求項10に記載の方法。 13.存在する該スルフィン酸塩又はスルフィン酸1モル当たりに少なくとも約 1モルのアンモニアが存在する請求項2に記載の方法。 14.R1がペルフルオル-n-アルキルである請求項10に記載の方法。 15.Mがナトリウムである請求項10に記載の方法。 16.該酸化剤が臭素酸塩であり、該酸化剤に対する対イオンがアルカリ金属カ チオンである請求項9に記載の方法。 17.該酸化剤が塩素酸塩であり、該酸化剤に対する対イオンがアルカリ金属カ チオンである請求項9に記載の方法。 18.該酸化剤が次亜塩素酸塩であり、該酸化剤に対する対イオンがアルカリ金 属カチオンである請求項9に記載の方法。 19.該フッ素含有オレフィンと任意成分である他の単量体が、以下の組み合わ せ: テトラフルオルエチレン; テトラフルオルエチレン/ヘキサフルオルプロピレン; テトラフルオルエチレン/ペルフルオル(メチルビニルエーテル); テトラフルオルエチレン/ペルフルオル(エチルビニルエーテル); テトラフルオルエチレン/ペルフルオル(n-プロピルビニルエーテル); テトラフルオルエチレン/ペルフルオル(2,2−ジメチルジオキソール) ; フッ化ビニル; テトラフルオルエチレン/エチレン; クロルトリフルオルエチレン/エチレン; テトラフルオルエチレン/ヘキサフルオルプロピレン/ペルフルオル(アル キルビニルエーテル)(アルキル基は1〜5個の炭素原子を含有する); ヘキサフルオルプロピレン/フッ化ビニリデン; テトラフルオルエチレン/ヘキサフルオルプロピレン/フッ化ビニリデン; テトラフルオルエチレン/フッ化ビニリデン; テトラフルオルエチレン/ペルフルオル(メチルビニルエーテル)/ペルフ ルオル化キュアサイトモノマー;及び クロルトリフルオルエチレン で存在する請求項10に記載の方法。 20.該フッ素含有オレフィンと他の単量体が、以下の組み合わせ: テトラフルオルエチレン; テトラフルオルエチレン/ヘキサフルオルプロピレン; テトラフルオルエチレン/ペルフルオル(メチルビニルエーテル); テトラフルオルエチレン/ペルフルオル(エチルビニルエーテル); テトラフルオルエチレン/ペルフルオル(n-プロピルビニルエーテル); テトラフルオルエチレン/ペルフルオル(2,2−ジメチルジオキソール) ; フッ化ビニル; テトラフルオルエチレン/エチレン; クロルトリフルオルエチレン/エチレン; テトラフルオルエチレン/ヘキサフルオルプロピレン/ペルフルオル(アル キルビニルエーテル)(アルキル基は1〜5個の炭素原子を含有する); ヘキサフルオルプロピレン/フッ化ビニリデン; テトラフルオルエチレン/ヘキサフルオルプロピレン/フッ化ビニリデン; テトラフルオルエチレン/フッ化ビニリデン; テトラフルオルエチレン/ペルフルオル(メチルビニルエーテル)/ペルフ ルオル化キュアサイトモノマー;及び クロルトリフルオルエチレン で存在する請求項12に記載の方法。
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US73595P | 1995-06-30 | 1995-06-30 | |
US60/000,735 | 1995-06-30 | ||
US08/658,676 US5639837A (en) | 1996-06-04 | 1996-06-04 | Process for making fluoropolymers |
US08/658,676 | 1996-06-04 | ||
PCT/US1996/010265 WO1997002300A1 (en) | 1995-06-30 | 1996-06-13 | Process for making fluoropolymers |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH11509244A true JPH11509244A (ja) | 1999-08-17 |
JP3806941B2 JP3806941B2 (ja) | 2006-08-09 |
Family
ID=26668075
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP50514997A Expired - Fee Related JP3806941B2 (ja) | 1995-06-30 | 1996-06-13 | 含フッ素重合体の製造方法 |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0835270B1 (ja) |
JP (1) | JP3806941B2 (ja) |
CN (1) | CN1088717C (ja) |
DE (1) | DE69610099T2 (ja) |
WO (1) | WO1997002300A1 (ja) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2005534751A (ja) * | 2002-07-29 | 2005-11-17 | スリーエム イノベイティブ プロパティズ カンパニー | 電子部品製造に用いるのに適する超クリーンフルオロエラストマー |
JP2013545880A (ja) * | 2010-12-17 | 2013-12-26 | スリーエム イノベイティブ プロパティズ カンパニー | スルフィネート含有分子を含むフッ素含有ポリマー |
JP2013545877A (ja) * | 2010-12-17 | 2013-12-26 | スリーエム イノベイティブ プロパティズ カンパニー | マイクロエマルジョン及びマイクロエマルジョンを用いて作製されたフルオロポリマー |
JP2014507386A (ja) * | 2010-12-17 | 2014-03-27 | スリーエム イノベイティブ プロパティズ カンパニー | 部分的にフッ素化されたスルフィン酸モノマー及びその塩 |
Families Citing this family (11)
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US6462228B1 (en) | 1997-12-22 | 2002-10-08 | 3M Innovative Properties Company | Process for preparation of fluorinated sulfinates |
AU5805598A (en) * | 1997-12-22 | 1999-07-12 | Minnesota Mining And Manufacturing Company | Process for preparation of fluorinated sulfinates |
JP2002507640A (ja) * | 1998-03-23 | 2002-03-12 | ダイネオン エルエルシー | ペルフルオロエラストマ組成物 |
FR2805258A1 (fr) * | 2000-02-22 | 2001-08-24 | Central Glass Co Ltd | Procede pour fabriquer du perfluoroalcanesulfinate |
IT1318488B1 (it) | 2000-04-21 | 2003-08-25 | Ausimont Spa | Fluorovinileteri e polimeri da essi ottenibili. |
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 |
CN102006419B (zh) * | 2010-09-17 | 2013-01-02 | 惠州Tcl移动通信有限公司 | 一种具有自动对焦驱动电路的移动终端及其驱动电路 |
CN103354814B (zh) * | 2010-12-17 | 2017-04-26 | 3M创新有限公司 | 部分氟化的聚亚磺酸和它们的盐 |
JP5902712B2 (ja) * | 2010-12-17 | 2016-04-13 | スリーエム イノベイティブ プロパティズ カンパニー | ペルフルオロビニルエーテルスルフィン酸及びその塩類の調製 |
FR3110168B1 (fr) * | 2020-05-15 | 2022-08-26 | Arkema France | Procédé pour produire des polymères à base de fluorure de vinylidène thermiquement stables et hautement cristallins |
US20240132643A1 (en) * | 2021-02-26 | 2024-04-25 | 3M Innovative Properties Company | Process for Making a Fluoropolymer and Fluoropolymer Made Therefrom |
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FR1155143A (fr) * | 1956-06-12 | 1958-04-23 | Electro Chimie Soc D | Procédé de polymérisation des oléfines fluorées |
DE2050723C3 (de) * | 1970-10-15 | 1980-11-06 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von Vinylchloridpolymerisaten |
DE2128012A1 (de) * | 1971-06-05 | 1972-12-14 | Cassella Farbwerke Mainkur Ag | Verfahren zur Herstellung von Polymerisaten |
EP0048308B1 (en) * | 1980-09-19 | 1984-12-19 | Asahi Glass Company Ltd. | Process for producing propylene-tetrafluoroethylene copolymer |
DE3834734A1 (de) * | 1988-10-12 | 1990-04-19 | Basf Ag | Verfahren zur herstellung von polymerisaten aus olefinisch ungesaettigten monomeren |
US5285002A (en) * | 1993-03-23 | 1994-02-08 | Minnesota Mining And Manufacturing Company | Fluorine-containing polymers and preparation and use thereof |
-
1996
- 1996-06-13 CN CN 96195117 patent/CN1088717C/zh not_active Expired - Fee Related
- 1996-06-13 JP JP50514997A patent/JP3806941B2/ja not_active Expired - Fee Related
- 1996-06-13 EP EP96923300A patent/EP0835270B1/en not_active Expired - Lifetime
- 1996-06-13 WO PCT/US1996/010265 patent/WO1997002300A1/en active IP Right Grant
- 1996-06-13 DE DE69610099T patent/DE69610099T2/de not_active Expired - Fee Related
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005534751A (ja) * | 2002-07-29 | 2005-11-17 | スリーエム イノベイティブ プロパティズ カンパニー | 電子部品製造に用いるのに適する超クリーンフルオロエラストマー |
JP2012072417A (ja) * | 2002-07-29 | 2012-04-12 | Three M Innovative Properties Co | 電子部品製造に用いるのに適する超クリーンフルオロエラストマー |
JP2013545880A (ja) * | 2010-12-17 | 2013-12-26 | スリーエム イノベイティブ プロパティズ カンパニー | スルフィネート含有分子を含むフッ素含有ポリマー |
JP2013545877A (ja) * | 2010-12-17 | 2013-12-26 | スリーエム イノベイティブ プロパティズ カンパニー | マイクロエマルジョン及びマイクロエマルジョンを用いて作製されたフルオロポリマー |
JP2014507386A (ja) * | 2010-12-17 | 2014-03-27 | スリーエム イノベイティブ プロパティズ カンパニー | 部分的にフッ素化されたスルフィン酸モノマー及びその塩 |
Also Published As
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JP3806941B2 (ja) | 2006-08-09 |
CN1189169A (zh) | 1998-07-29 |
EP0835270A1 (en) | 1998-04-15 |
DE69610099T2 (de) | 2001-05-10 |
EP0835270B1 (en) | 2000-08-30 |
CN1088717C (zh) | 2002-08-07 |
WO1997002300A1 (en) | 1997-01-23 |
DE69610099D1 (de) | 2000-10-05 |
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