JP2003514036A - 低結晶度の弗化ビニリデンヘキサフルオルプロピレン共重合体 - Google Patents
低結晶度の弗化ビニリデンヘキサフルオルプロピレン共重合体Info
- Publication number
- JP2003514036A JP2003514036A JP2001535424A JP2001535424A JP2003514036A JP 2003514036 A JP2003514036 A JP 2003514036A JP 2001535424 A JP2001535424 A JP 2001535424A JP 2001535424 A JP2001535424 A JP 2001535424A JP 2003514036 A JP2003514036 A JP 2003514036A
- Authority
- JP
- Japan
- Prior art keywords
- hfp
- weight
- vinylidene fluoride
- hexafluoropropylene
- content
- 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.)
- Pending
Links
- 229920001577 copolymer Polymers 0.000 title claims abstract description 77
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 claims abstract description 41
- 238000000034 method Methods 0.000 claims abstract description 29
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 claims abstract description 24
- 238000006243 chemical reaction Methods 0.000 claims description 23
- 238000002844 melting Methods 0.000 claims description 19
- 230000008018 melting Effects 0.000 claims description 19
- 238000006116 polymerization reaction Methods 0.000 claims description 17
- 239000003999 initiator Substances 0.000 claims description 15
- 239000004094 surface-active agent Substances 0.000 claims description 9
- 239000007787 solid Substances 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- 230000001804 emulsifying effect Effects 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 abstract description 5
- 229920000642 polymer Polymers 0.000 description 34
- 239000000203 mixture Substances 0.000 description 29
- 239000000178 monomer Substances 0.000 description 24
- 239000000523 sample Substances 0.000 description 17
- 239000011347 resin Substances 0.000 description 12
- 229920005989 resin Polymers 0.000 description 12
- 229920001169 thermoplastic Polymers 0.000 description 10
- -1 alkali metal salt Chemical class 0.000 description 8
- 239000004416 thermosoftening plastic Substances 0.000 description 8
- 239000012986 chain transfer agent Substances 0.000 description 7
- 238000000576 coating method Methods 0.000 description 7
- 239000004816 latex Substances 0.000 description 6
- 229920000126 latex Polymers 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 5
- 239000013078 crystal Substances 0.000 description 5
- 229910052731 fluorine Inorganic materials 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 4
- 229920006370 Kynar Polymers 0.000 description 4
- 238000005481 NMR spectroscopy Methods 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 229920002313 fluoropolymer Polymers 0.000 description 4
- 239000004811 fluoropolymer Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 150000002978 peroxides Chemical class 0.000 description 4
- 230000009467 reduction Effects 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000015271 coagulation Effects 0.000 description 3
- 238000005345 coagulation Methods 0.000 description 3
- 238000007334 copolymerization reaction Methods 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000007720 emulsion polymerization reaction Methods 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- 230000033001 locomotion Effects 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 229920000058 polyacrylate Polymers 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- 238000010189 synthetic method Methods 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-WFGJKAKNSA-N acetone d6 Chemical compound [2H]C([2H])([2H])C(=O)C([2H])([2H])[2H] CSCPPACGZOOCGX-WFGJKAKNSA-N 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 125000001153 fluoro group Chemical group F* 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 150000001451 organic peroxides Chemical class 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 125000005634 peroxydicarbonate group Chemical group 0.000 description 2
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical class [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- BWJUFXUULUEGMA-UHFFFAOYSA-N propan-2-yl propan-2-yloxycarbonyloxy carbonate Chemical compound CC(C)OC(=O)OOC(=O)OC(C)C BWJUFXUULUEGMA-UHFFFAOYSA-N 0.000 description 2
- 125000001453 quaternary ammonium group Chemical group 0.000 description 2
- 230000002441 reversible effect Effects 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 238000010561 standard procedure Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 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
- OHMHBGPWCHTMQE-UHFFFAOYSA-N 2,2-dichloro-1,1,1-trifluoroethane Chemical compound FC(F)(F)C(Cl)Cl OHMHBGPWCHTMQE-UHFFFAOYSA-N 0.000 description 1
- ZACVGCNKGYYQHA-UHFFFAOYSA-N 2-ethylhexoxycarbonyloxy 2-ethylhexyl carbonate Chemical compound CCCCC(CC)COC(=O)OOC(=O)OCC(CC)CCCC ZACVGCNKGYYQHA-UHFFFAOYSA-N 0.000 description 1
- AQKYLAIZOGOPAW-UHFFFAOYSA-N 2-methylbutan-2-yl 2,2-dimethylpropaneperoxoate Chemical compound CCC(C)(C)OOC(=O)C(C)(C)C AQKYLAIZOGOPAW-UHFFFAOYSA-N 0.000 description 1
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Natural products OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical class [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004721 Polyphenylene oxide Chemical class 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 150000001346 alkyl aryl ethers Chemical class 0.000 description 1
- 125000005599 alkyl carboxylate group Chemical group 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 239000002519 antifouling agent Substances 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- NSGQRLUGQNBHLD-UHFFFAOYSA-N butan-2-yl butan-2-yloxycarbonyloxy carbonate Chemical compound CCC(C)OC(=O)OOC(=O)OC(C)CC NSGQRLUGQNBHLD-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000001934 delay Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 238000000113 differential scanning calorimetry Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 239000008393 encapsulating agent Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 229920001973 fluoroelastomer Polymers 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- TYQCGQRIZGCHNB-JLAZNSOCSA-N l-ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(O)=C(O)C1=O TYQCGQRIZGCHNB-JLAZNSOCSA-N 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 238000011020 pilot scale process Methods 0.000 description 1
- 229920001490 poly(butyl methacrylate) polymer Polymers 0.000 description 1
- 229920001483 poly(ethyl methacrylate) polymer Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920000570 polyether Chemical class 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- YPVDWEHVCUBACK-UHFFFAOYSA-N propoxycarbonyloxy propyl carbonate Chemical compound CCCOC(=O)OOC(=O)OCCC YPVDWEHVCUBACK-UHFFFAOYSA-N 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- XWGJFPHUCFXLBL-UHFFFAOYSA-M rongalite Chemical compound [Na+].OCS([O-])=O XWGJFPHUCFXLBL-UHFFFAOYSA-M 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 229920006126 semicrystalline polymer Polymers 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 238000007614 solvation Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- OPQYOFWUFGEMRZ-UHFFFAOYSA-N tert-butyl 2,2-dimethylpropaneperoxoate Chemical compound CC(C)(C)OOC(=O)C(C)(C)C OPQYOFWUFGEMRZ-UHFFFAOYSA-N 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 1
- 229940029284 trichlorofluoromethane Drugs 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920005609 vinylidenefluoride/hexafluoropropylene copolymer Polymers 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000002023 wood Substances 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
- C08F214/28—Hexyfluoropropene
-
- 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
- C08F214/22—Vinylidene fluoride
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 (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16322999P | 1999-11-03 | 1999-11-03 | |
| US60/163,229 | 1999-11-03 | ||
| PCT/US2000/030449 WO2001032726A1 (en) | 1999-11-03 | 2000-11-03 | Low crystallinity vinylidene fluoride hexafluoropropylene copolymers |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012005401A Division JP2012067324A (ja) | 1999-11-03 | 2012-01-13 | 低結晶度の弗化ビニリデンヘキサフルオルプロピレン共重合体 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2003514036A true JP2003514036A (ja) | 2003-04-15 |
| JP2003514036A5 JP2003514036A5 (enExample) | 2007-12-20 |
Family
ID=22589039
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001535424A Pending JP2003514036A (ja) | 1999-11-03 | 2000-11-03 | 低結晶度の弗化ビニリデンヘキサフルオルプロピレン共重合体 |
| JP2012005401A Pending JP2012067324A (ja) | 1999-11-03 | 2012-01-13 | 低結晶度の弗化ビニリデンヘキサフルオルプロピレン共重合体 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012005401A Pending JP2012067324A (ja) | 1999-11-03 | 2012-01-13 | 低結晶度の弗化ビニリデンヘキサフルオルプロピレン共重合体 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US6586547B1 (enExample) |
| EP (1) | EP1144469B1 (enExample) |
| JP (2) | JP2003514036A (enExample) |
| CN (1) | CN1189489C (enExample) |
| DE (1) | DE60045408D1 (enExample) |
| MX (1) | MXPA01006827A (enExample) |
| RU (1) | RU2256669C2 (enExample) |
| WO (1) | WO2001032726A1 (enExample) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005314699A (ja) * | 2004-04-27 | 2005-11-10 | Arkema Inc | アルキルスルホン酸塩界面活性剤を使用したフルオロポリマーの製造方法 |
| JP2014508209A (ja) * | 2011-03-16 | 2014-04-03 | アーケマ・インコーポレイテッド | 高融点フルオロポリマー |
| JP2014517128A (ja) * | 2011-06-21 | 2014-07-17 | ソルベイ スペシャルティ ポリマーズ イタリー エス．ピー．エー． | フッ化ビニリデンを重合させる方法 |
| WO2019230075A1 (ja) | 2018-05-31 | 2019-12-05 | 株式会社クレハ | 非水電解質二次電池用樹脂組成物、ならびにこれを用いた非水電解質二次電池用セパレータ、電極合剤層用樹脂組成物、非水電解質二次電池用電極、および非水電解質二次電池 |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040211943A1 (en) * | 2001-11-21 | 2004-10-28 | Masahiro Okahara | Coating material for fuel cell separator |
| EP1479702A1 (fr) * | 2003-05-19 | 2004-11-24 | Atofina | Polymères à base de chlorotrifluoroéthylène/carbonate de vinylène/hexafluoropropène ou tétrafluoroéthylène/carbonate de vinylène/hexafluoropropène |
| US7722819B2 (en) | 2005-10-11 | 2010-05-25 | Meadwestvaco Calmar, Inc. | Fragrance product, dispenser, and dispenser assembly |
| JP2009511580A (ja) * | 2005-10-11 | 2009-03-19 | ジュリア， ディコーレト ギブソン， | フレグランス製品、ディスペンサ及びディスペンサアセンブリ |
| US20070100099A1 (en) * | 2005-10-28 | 2007-05-03 | Ming-Hong Hung | Copolymers of vinylidene fluoride and vinyl esters |
| JP5693845B2 (ja) | 2006-07-06 | 2015-04-01 | アーケマ・インコーポレイテッド | 超高分子量ポリ（弗化ビニリデン） |
| FR2904828B1 (fr) * | 2006-08-08 | 2008-09-19 | Arkema France | Copolymere de fluorure de vinylidene fonctionnalise par greffage par irradiation par un monomere polaire insature |
| FR2918067B1 (fr) * | 2007-06-27 | 2011-07-01 | Arkema France | Materiau composite comprenant des nanotubes disperses dans une matrice polymerique fluroree. |
| US20100317815A1 (en) * | 2007-11-28 | 2010-12-16 | Unimatec Co., Ltd. | Process for manufacturing fluoroelastomer |
| CN101851314B (zh) * | 2009-04-02 | 2014-01-29 | 中化蓝天集团有限公司 | 一种用作锂离子电池隔膜的vdf-hfp共聚物的制备方法 |
| US8809471B2 (en) | 2011-03-16 | 2014-08-19 | Arkema Inc. | Synthesis of making 2,3,3,3-tetrafluoropropene containing fluoropolymers |
| US20150303338A1 (en) * | 2012-12-06 | 2015-10-22 | Lg Chem, Ltd. | Backsheet |
| EP2970536B1 (en) * | 2013-03-15 | 2017-05-24 | Arkema, Inc. | Fluoropolymers |
| FR3010089B1 (fr) | 2013-09-02 | 2015-08-14 | Arkema France | Composition de polymeres fluores thermoplastiques pour les tubes off-shore |
| FR3010082A1 (fr) | 2013-09-02 | 2015-03-06 | Arkema France | Procede de preparation d'une composition de polymeres fluores reticules |
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| KR20250039406A (ko) * | 2023-01-13 | 2025-03-20 | 컨템포러리 엠퍼렉스 테크놀로지 (홍콩) 리미티드 | 폴리머, 전극 시트 및 이와 관련된 전지 셀, 전지 및 전기 장치 |
| EP4458869A1 (en) * | 2023-05-03 | 2024-11-06 | Arkema, Inc. | Process for the production of polyvinylidene fluoride copolymers |
| FR3157869A1 (fr) | 2023-12-31 | 2025-07-04 | Arkema France | Composition de polymère(s) fluoré(s) à adhérence améliorée |
| FR3157871A1 (fr) | 2023-12-31 | 2025-07-04 | Arkema France | Utilisation d’une composition réactive comme précurseur de primaire d’adhérence entre un polymère fluoré et un substrat, procédés de fabrication de revêtements, substrats revêtus et dispositifs les comprenant |
| FR3157870A1 (fr) | 2023-12-31 | 2025-07-04 | Arkema France | Utilisation d’un polymère comme primaire d’adhérence entre un polymère fluoré et un substrat, procédés de fabrication de revêtements, substrats revêtus et dispositifs les comprenant |
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- 2000-11-03 WO PCT/US2000/030449 patent/WO2001032726A1/en not_active Ceased
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- 2000-11-03 JP JP2001535424A patent/JP2003514036A/ja active Pending
- 2000-11-03 EP EP00976943A patent/EP1144469B1/en not_active Expired - Lifetime
- 2000-11-03 RU RU2001121682/04A patent/RU2256669C2/ru not_active IP Right Cessation
- 2000-11-03 DE DE60045408T patent/DE60045408D1/de not_active Expired - Lifetime
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| JPH0718002A (ja) * | 1993-07-02 | 1995-01-20 | Asahi Glass Co Ltd | 含フッ素共重合体の製造方法 |
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| JP2005314699A (ja) * | 2004-04-27 | 2005-11-10 | Arkema Inc | アルキルスルホン酸塩界面活性剤を使用したフルオロポリマーの製造方法 |
| JP2014508209A (ja) * | 2011-03-16 | 2014-04-03 | アーケマ・インコーポレイテッド | 高融点フルオロポリマー |
| JP2014517128A (ja) * | 2011-06-21 | 2014-07-17 | ソルベイ スペシャルティ ポリマーズ イタリー エス．ピー．エー． | フッ化ビニリデンを重合させる方法 |
| WO2019230075A1 (ja) | 2018-05-31 | 2019-12-05 | 株式会社クレハ | 非水電解質二次電池用樹脂組成物、ならびにこれを用いた非水電解質二次電池用セパレータ、電極合剤層用樹脂組成物、非水電解質二次電池用電極、および非水電解質二次電池 |
| KR20200142097A (ko) | 2018-05-31 | 2020-12-21 | 가부시끼가이샤 구레하 | 비수 전해질 이차전지용 수지 조성물 및 이를 이용한 비수 전해질 이차전지용 세퍼레이터, 전극 합제층용 수지 조성물, 비수 전해질 이차전지용 전극, 및 비수 전해질 이차전지 |
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Also Published As
| Publication number | Publication date |
|---|---|
| DE60045408D1 (de) | 2011-02-03 |
| US6586547B1 (en) | 2003-07-01 |
| RU2256669C2 (ru) | 2005-07-20 |
| CN1327455A (zh) | 2001-12-19 |
| CN1189489C (zh) | 2005-02-16 |
| EP1144469B1 (en) | 2010-12-22 |
| WO2001032726A1 (en) | 2001-05-10 |
| JP2012067324A (ja) | 2012-04-05 |
| MXPA01006827A (es) | 2004-08-19 |
| EP1144469A1 (en) | 2001-10-17 |
| EP1144469A4 (en) | 2005-02-09 |
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