JP2021521297A - 官能性フルオロポリマー - Google Patents
官能性フルオロポリマー Download PDFInfo
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- JP2021521297A JP2021521297A JP2020555471A JP2020555471A JP2021521297A JP 2021521297 A JP2021521297 A JP 2021521297A JP 2020555471 A JP2020555471 A JP 2020555471A JP 2020555471 A JP2020555471 A JP 2020555471A JP 2021521297 A JP2021521297 A JP 2021521297A
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- Prior art keywords
- fluorinated
- acid
- sulfonic acid
- copolymer according
- salt
- Prior art date
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- 229920002313 fluoropolymer Polymers 0.000 title abstract description 21
- 239000004811 fluoropolymer Substances 0.000 title abstract description 19
- 239000000178 monomer Substances 0.000 claims abstract description 92
- 229920002554 vinyl polymer Polymers 0.000 claims abstract description 19
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims abstract description 18
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims abstract description 7
- 125000005670 ethenylalkyl group Chemical group 0.000 claims abstract description 7
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 claims description 46
- 229920001577 copolymer Polymers 0.000 claims description 45
- -1 alkoxy compound Chemical class 0.000 claims description 42
- 238000000034 method Methods 0.000 claims description 31
- 238000006116 polymerization reaction Methods 0.000 claims description 31
- 239000003999 initiator Substances 0.000 claims description 30
- 125000006165 cyclic alkyl group Chemical group 0.000 claims description 28
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 26
- 125000003118 aryl group Chemical group 0.000 claims description 24
- 239000004816 latex Substances 0.000 claims description 21
- 229920000126 latex Polymers 0.000 claims description 21
- 238000003756 stirring Methods 0.000 claims description 20
- 239000000203 mixture Substances 0.000 claims description 19
- 229910052783 alkali metal Inorganic materials 0.000 claims description 17
- 125000000217 alkyl group Chemical group 0.000 claims description 17
- 229910052739 hydrogen Inorganic materials 0.000 claims description 17
- 239000001257 hydrogen Substances 0.000 claims description 17
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 15
- 229910052731 fluorine Inorganic materials 0.000 claims description 15
- 229910052736 halogen Inorganic materials 0.000 claims description 15
- 150000002367 halogens Chemical class 0.000 claims description 15
- 150000003839 salts Chemical class 0.000 claims description 15
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 13
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 12
- 229910052794 bromium Inorganic materials 0.000 claims description 12
- 229910052801 chlorine Inorganic materials 0.000 claims description 12
- 238000007334 copolymerization reaction Methods 0.000 claims description 12
- 229910052740 iodine Inorganic materials 0.000 claims description 12
- 239000002904 solvent Substances 0.000 claims description 12
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 11
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 11
- LOUICXNAWQPGSU-UHFFFAOYSA-N 2,2,3,3-tetrafluorooxirane Chemical compound FC1(F)OC1(F)F LOUICXNAWQPGSU-UHFFFAOYSA-N 0.000 claims description 10
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims description 10
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 10
- 238000009472 formulation Methods 0.000 claims description 10
- PGFXOWRDDHCDTE-UHFFFAOYSA-N hexafluoropropylene oxide Chemical compound FC(F)(F)C1(F)OC1(F)F PGFXOWRDDHCDTE-UHFFFAOYSA-N 0.000 claims description 10
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical group CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 9
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 8
- 150000001408 amides Chemical class 0.000 claims description 8
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 8
- 239000000839 emulsion Substances 0.000 claims description 8
- 229910052751 metal Inorganic materials 0.000 claims description 8
- 239000002184 metal Substances 0.000 claims description 8
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 7
- 239000000872 buffer Substances 0.000 claims description 7
- 150000002576 ketones Chemical class 0.000 claims description 7
- 239000000758 substrate Substances 0.000 claims description 7
- POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 claims description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 6
- 239000003513 alkali Substances 0.000 claims description 6
- 239000012431 aqueous reaction media Substances 0.000 claims description 5
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 claims description 5
- 239000003381 stabilizer Substances 0.000 claims description 5
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 claims description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 4
- OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 claims description 4
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 4
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 claims description 4
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 claims description 4
- YXHXDEBLSQQHQE-UHFFFAOYSA-N N.N.OP(O)=O Chemical group N.N.OP(O)=O YXHXDEBLSQQHQE-UHFFFAOYSA-N 0.000 claims description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 4
- 150000001340 alkali metals Chemical class 0.000 claims description 4
- JBTWLSYIZRCDFO-UHFFFAOYSA-N ethyl methyl carbonate Chemical compound CCOC(=O)OC JBTWLSYIZRCDFO-UHFFFAOYSA-N 0.000 claims description 4
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 claims description 4
- 150000002431 hydrogen Chemical class 0.000 claims description 4
- 229910002102 lithium manganese oxide Inorganic materials 0.000 claims description 4
- VLXXBCXTUVRROQ-UHFFFAOYSA-N lithium;oxido-oxo-(oxomanganiooxy)manganese Chemical compound [Li+].[O-][Mn](=O)O[Mn]=O VLXXBCXTUVRROQ-UHFFFAOYSA-N 0.000 claims description 4
- 239000012528 membrane Substances 0.000 claims description 4
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims description 4
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 4
- BDZBKCUKTQZUTL-UHFFFAOYSA-N triethyl phosphite Chemical compound CCOP(OCC)OCC BDZBKCUKTQZUTL-UHFFFAOYSA-N 0.000 claims description 4
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 claims description 3
- 229910001416 lithium ion Inorganic materials 0.000 claims description 3
- GELKBWJHTRAYNV-UHFFFAOYSA-K lithium iron phosphate Chemical compound [Li+].[Fe+2].[O-]P([O-])([O-])=O GELKBWJHTRAYNV-UHFFFAOYSA-K 0.000 claims description 3
- VGYDTVNNDKLMHX-UHFFFAOYSA-N lithium;manganese;nickel;oxocobalt Chemical compound [Li].[Mn].[Ni].[Co]=O VGYDTVNNDKLMHX-UHFFFAOYSA-N 0.000 claims description 3
- 239000002923 metal particle Substances 0.000 claims description 3
- 229910001317 nickel manganese cobalt oxide (NMC) Inorganic materials 0.000 claims description 3
- XVOUMQNXTGKGMA-OWOJBTEDSA-N (E)-glutaconic acid Chemical compound OC(=O)C\C=C\C(O)=O XVOUMQNXTGKGMA-OWOJBTEDSA-N 0.000 claims description 2
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 claims description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 2
- VIEVWNYBKMKQIH-UHFFFAOYSA-N [Co]=O.[Mn].[Li] Chemical compound [Co]=O.[Mn].[Li] VIEVWNYBKMKQIH-UHFFFAOYSA-N 0.000 claims description 2
- ZYXUQEDFWHDILZ-UHFFFAOYSA-N [Ni].[Mn].[Li] Chemical compound [Ni].[Mn].[Li] ZYXUQEDFWHDILZ-UHFFFAOYSA-N 0.000 claims description 2
- 150000008065 acid anhydrides Chemical class 0.000 claims description 2
- 229910001413 alkali metal ion Inorganic materials 0.000 claims description 2
- 125000005210 alkyl ammonium group Chemical group 0.000 claims description 2
- 150000003863 ammonium salts Chemical class 0.000 claims description 2
- 125000005587 carbonate group Chemical group 0.000 claims description 2
- 239000011248 coating agent Substances 0.000 claims description 2
- 238000000576 coating method Methods 0.000 claims description 2
- 125000004122 cyclic group Chemical group 0.000 claims description 2
- 239000011737 fluorine Substances 0.000 claims description 2
- 239000001530 fumaric acid Substances 0.000 claims description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 2
- 239000011976 maleic acid Substances 0.000 claims description 2
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims description 2
- 150000001451 organic peroxides Chemical class 0.000 claims description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 2
- 125000005208 trialkylammonium group Chemical group 0.000 claims description 2
- ZTWTYVWXUKTLCP-UHFFFAOYSA-L ethenyl-dioxido-oxo-$l^{5}-phosphane Chemical compound [O-]P([O-])(=O)C=C ZTWTYVWXUKTLCP-UHFFFAOYSA-L 0.000 claims 3
- 229940043265 methyl isobutyl ketone Drugs 0.000 claims 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- 239000012736 aqueous medium Substances 0.000 claims 1
- LTXHKPDRHPMBKA-UHFFFAOYSA-N dialuminum;cobalt(2+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[Al+3].[Al+3].[Co+2] LTXHKPDRHPMBKA-UHFFFAOYSA-N 0.000 claims 1
- RSNHXDVSISOZOB-UHFFFAOYSA-N lithium nickel Chemical compound [Li].[Ni] RSNHXDVSISOZOB-UHFFFAOYSA-N 0.000 claims 1
- 150000005621 tetraalkylammonium salts Chemical class 0.000 claims 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 abstract description 3
- ZTWTYVWXUKTLCP-UHFFFAOYSA-N vinylphosphonic acid Chemical class OP(O)(=O)C=C ZTWTYVWXUKTLCP-UHFFFAOYSA-N 0.000 abstract description 3
- 150000003926 acrylamides Chemical class 0.000 abstract description 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 23
- 239000008367 deionised water Substances 0.000 description 17
- 229910021641 deionized water Inorganic materials 0.000 description 17
- 229920000642 polymer Polymers 0.000 description 16
- 239000004094 surface-active agent Substances 0.000 description 16
- FCBZNZYQLJTCKR-UHFFFAOYSA-N 1-prop-2-enoxyethanol Chemical compound CC(O)OCC=C FCBZNZYQLJTCKR-UHFFFAOYSA-N 0.000 description 15
- 150000003254 radicals Chemical class 0.000 description 15
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 14
- 238000006243 chemical reaction Methods 0.000 description 14
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 11
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 10
- 229920002125 Sokalan® Polymers 0.000 description 9
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 9
- 239000011230 binding agent Substances 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 8
- 238000012546 transfer Methods 0.000 description 8
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 7
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- 239000011541 reaction mixture Substances 0.000 description 7
- VAYTZRYEBVHVLE-UHFFFAOYSA-N 1,3-dioxol-2-one Chemical compound O=C1OC=CO1 VAYTZRYEBVHVLE-UHFFFAOYSA-N 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 239000002519 antifouling agent Substances 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- XUKWFDWKURBTFK-UHFFFAOYSA-N 3-ethenoxypropanoic acid Chemical compound OC(=O)CCOC=C XUKWFDWKURBTFK-UHFFFAOYSA-N 0.000 description 4
- 239000012986 chain transfer agent Substances 0.000 description 4
- 239000003638 chemical reducing agent Substances 0.000 description 4
- 125000000524 functional group Chemical group 0.000 description 4
- 239000007800 oxidant agent Substances 0.000 description 4
- FRPZMMHWLSIFAZ-UHFFFAOYSA-N 10-undecenoic acid Chemical compound OC(=O)CCCCCCCCC=C FRPZMMHWLSIFAZ-UHFFFAOYSA-N 0.000 description 3
- QMIWYOZFFSLIAK-UHFFFAOYSA-N 3,3,3-trifluoro-2-(trifluoromethyl)prop-1-ene Chemical group FC(F)(F)C(=C)C(F)(F)F QMIWYOZFFSLIAK-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 238000005481 NMR spectroscopy Methods 0.000 description 3
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical group [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 3
- KHAVLLBUVKBTBG-UHFFFAOYSA-N caproleic acid Natural products OC(=O)CCCCCCCC=C KHAVLLBUVKBTBG-UHFFFAOYSA-N 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 238000011068 loading method Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 150000002978 peroxides Chemical class 0.000 description 3
- 239000001632 sodium acetate Substances 0.000 description 3
- 235000017281 sodium acetate Nutrition 0.000 description 3
- 229960002703 undecylenic acid Drugs 0.000 description 3
- MIZLGWKEZAPEFJ-UHFFFAOYSA-N 1,1,2-trifluoroethene Chemical group FC=C(F)F MIZLGWKEZAPEFJ-UHFFFAOYSA-N 0.000 description 2
- WUMVZXWBOFOYAW-UHFFFAOYSA-N 1,2,3,3,4,4,4-heptafluoro-1-(1,2,3,3,4,4,4-heptafluorobut-1-enoxy)but-1-ene Chemical compound FC(F)(F)C(F)(F)C(F)=C(F)OC(F)=C(F)C(F)(F)C(F)(F)F WUMVZXWBOFOYAW-UHFFFAOYSA-N 0.000 description 2
- GVEUEBXMTMZVSD-UHFFFAOYSA-N 3,3,4,4,5,5,6,6,6-nonafluorohex-1-ene Chemical group FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C=C GVEUEBXMTMZVSD-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000008351 acetate buffer Substances 0.000 description 2
- 239000011149 active material Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000006172 buffering agent Substances 0.000 description 2
- 239000006257 cathode slurry Substances 0.000 description 2
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical group CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 2
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 2
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 125000001475 halogen functional group Chemical group 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000012510 hollow fiber Substances 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 229910000625 lithium cobalt oxide Inorganic materials 0.000 description 2
- 229910003002 lithium salt Inorganic materials 0.000 description 2
- 159000000002 lithium salts Chemical class 0.000 description 2
- BFZPBUKRYWOWDV-UHFFFAOYSA-N lithium;oxido(oxo)cobalt Chemical compound [Li+].[O-][Co]=O BFZPBUKRYWOWDV-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 150000007524 organic acids Chemical group 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 125000005634 peroxydicarbonate group Chemical group 0.000 description 2
- 239000008363 phosphate buffer Substances 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 239000012265 solid product Substances 0.000 description 2
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- KHXKESCWFMPTFT-UHFFFAOYSA-N 1,1,1,2,2,3,3-heptafluoro-3-(1,2,2-trifluoroethenoxy)propane Chemical compound FC(F)=C(F)OC(F)(F)C(F)(F)C(F)(F)F KHXKESCWFMPTFT-UHFFFAOYSA-N 0.000 description 1
- NDMMKOCNFSTXRU-UHFFFAOYSA-N 1,1,2,3,3-pentafluoroprop-1-ene Chemical compound FC(F)C(F)=C(F)F NDMMKOCNFSTXRU-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
- XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 description 1
- ABADUMLIAZCWJD-UHFFFAOYSA-N 1,3-dioxole Chemical class C1OC=CO1 ABADUMLIAZCWJD-UHFFFAOYSA-N 0.000 description 1
- FXPHNQAHHHWMAV-UHFFFAOYSA-N 1-ethenoxy-1,1,2,2,3,3,4,4,4-nonafluorobutane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)OC=C FXPHNQAHHHWMAV-UHFFFAOYSA-N 0.000 description 1
- FXRLMCRCYDHQFW-UHFFFAOYSA-N 2,3,3,3-tetrafluoropropene Chemical compound FC(=C)C(F)(F)F FXRLMCRCYDHQFW-UHFFFAOYSA-N 0.000 description 1
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- CGQZIFGCHVCAHE-UHFFFAOYSA-L disodium;ethenyl-dioxido-oxo-$l^{5}-phosphane Chemical compound [Na+].[Na+].[O-]P([O-])(=O)C=C CGQZIFGCHVCAHE-UHFFFAOYSA-L 0.000 description 1
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- RUTXIHLAWFEWGM-UHFFFAOYSA-H iron(3+) sulfate Chemical compound [Fe+3].[Fe+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O RUTXIHLAWFEWGM-UHFFFAOYSA-H 0.000 description 1
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- BHZRJJOHZFYXTO-UHFFFAOYSA-L potassium sulfite Chemical compound [K+].[K+].[O-]S([O-])=O BHZRJJOHZFYXTO-UHFFFAOYSA-L 0.000 description 1
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- 238000002360 preparation method Methods 0.000 description 1
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- 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 1
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- YPVDWEHVCUBACK-UHFFFAOYSA-N propoxycarbonyloxy propyl carbonate Chemical compound CCCOC(=O)OOC(=O)OCCC YPVDWEHVCUBACK-UHFFFAOYSA-N 0.000 description 1
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- HRQDCDQDOPSGBR-UHFFFAOYSA-M sodium;octane-1-sulfonate Chemical compound [Na+].CCCCCCCCS([O-])(=O)=O HRQDCDQDOPSGBR-UHFFFAOYSA-M 0.000 description 1
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- 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
- 125000005207 tetraalkylammonium group Chemical group 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- WZEOZJQLTRFNCU-UHFFFAOYSA-N trifluoro(trifluoromethoxy)methane Chemical compound FC(F)(F)OC(F)(F)F WZEOZJQLTRFNCU-UHFFFAOYSA-N 0.000 description 1
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Abstract
Description
a)少なくとも1種の開始剤、安定剤、少なくとも1種のフルオロモノマー及び親水性モノマーを含む水性エマルションを形成させ;
b)前記少なくとも1種のフルオロモノマーと前記親水性モノマーとの共重合を撹拌しながら熱及び加圧下で開始させる:
ことを含む前記方法をも意図する。
a)少なくとも1種の開始剤、安定剤、少なくとも1種のフッ素化ビニル系モノマー及び前記の親水性モノマーを含む水性エマルションを形成させ、
b)前記少なくとも1種のフッ素化ビニル系モノマーと前記親水性モノマーとの共重合を撹拌しながら熱及び加圧下で開始させる
ことを含む。
1種以上のフルオロモノマーと組み合わせて用いられる前記親水性コモノマーには、限定されるわけではないが、以下のものの内の1種以上が含まれ、特定の類における1種より多くのモノマーの混合物、並びに下記の様々な類からの2種以上のモノマーの混合物がターポリマーを生成するために一緒にブレンドされる:
R1、R2及びR3は水素又はハロゲン(F、Cl、Br、I)であり、
R4はC1〜C16直鎖状、分岐鎖状、アリール若しくは環状アルキル基、C1〜C16フッ素化直鎖状、分岐鎖状、アリール若しくは環状アルキル基、ヘキサフルオロプロピレンオキシドのオリゴマー又はテトラフルオロエチレンオキシドのオリゴマーであり、
R5はカルボン酸(C(O)OH)、カルボン酸アルカリ金属塩(COO-M+)、カルボン酸アンモニウム塩(COO-NH4 +)、カルボン酸アルキルアンモニウム塩(COO-N(Alk)4 +)、アルコール(OH)、アミド(C(O)NH2)、ジアルキルアミド(C(O)NAlk2)、スルホン酸(S(O)(O)OH)、スルホン酸アルカリ金属塩(S(O)(O)O-M+)、スルホン酸アンモニウム塩(S(O)(O)O-NH4 +)、スルホン酸アルキルアンモニウム塩(S(O)(O)O-N(Alk)4 +)である。
R1、R2及びR3は水素又はハロゲン(F、Cl、Br、I)であり、
R4及びR5は別々に、水素、C1〜C16直鎖状アルキル、分岐鎖状アルキル、アリール若しくは環状アルキル基、C1〜C16フッ素化直鎖状アルキル、分岐鎖状アルキル、アリール若しくは環状アルキル基、ヘキサフルオロプロピレンオキシドのオリゴマー若しくはテトラフルオロエチレンオキシドのオリゴマー、アルカリ金属イオン(Li+、Na+、K+、Rb+、Cs+)、アンモニウムイオン(NH4 +)又はアルキルアンモニウム(NAlk4 +)である。
R1、R2及びR3は水素又はハロゲン(F、Cl、Br、I)であり、
R4及びR6は別々に、水素、C1〜C16直鎖状、分岐鎖状、アリール若しくは環状アルキル基、C1〜C16フッ素化直鎖状、分岐鎖状、アリール若しくは環状アルキル基、ヘキサフルオロプロピレンオキシドのオリゴマー又はテトラフルオロエチレンオキシドのオリゴマーであり、
R5及びR7は別々に、カルボン酸(C(O)OH)、カルボン酸アルカリ金属塩(COO-M+)、カルボン酸アンモニウム塩(COO-NH4 +)、カルボン酸アルキルアンモニウム塩(COO-N(Alk)4 +)、アルコール(OH)、アミド(C(O)NH2)、ジアルキルアミド(C(O)NAlk2)、スルホン酸(S(O)(O)OH)、スルホン酸アルカリ金属塩(S(O)(O)O-M+)、スルホン酸アンモニウム塩(S(O)(O)O-NH4 +)、スルホン酸アルキルアンモニウム塩(S(O)(O)O-N(Alk)4 +)、ケトン(C(O))若しくはアセチルアセトネート(C(O)−CH2−C(O))、又はホスホネート(P(O)(OH)2)、アルカリ金属若しくはアンモニウムホスホネートである。
R1、R2及びR3は水素又はハロゲン(F、Cl、Br、I)であり、
R4は結合、C1〜C16直鎖状アルキル、分岐鎖状アルキル、アリール若しくは環状アルキル基、C1〜C16フッ素化直鎖状アルキル、分岐鎖状アルキル、又はアリール若しくは環状アルキル基であり、
R5は環状構造の一部としてカーボネート基を含有するC1〜C16環状アルキル基又はC1〜C16フッ素化環状アルキル基である。
R1、R2及びR3は水素又はハロゲン(F、Cl、Br、I)であり、
R4はC1〜C16直鎖状、分岐鎖状、アリール若しくは環状アルキル基、C1〜C16フッ素化直鎖状、分岐鎖状、アリール若しくは環状アルキル基、ヘキサフルオロプロピレンオキシドのオリゴマー又はテトラフルオロエチレンオキシドのオリゴマーであり、
R5はカルボン酸(C(O)OH)、カルボン酸アルカリ金属塩(COO-M+)、カルボン酸アンモニウム塩(COO-NH4 +)、カルボン酸アルキルアンモニウム塩(COO-N(Alk)4 +)、アルコール(OH)、アミド(C(O)NH2)、ジアルキルアミド(C(O)NAlk2)、スルホン酸(S(O)(O)OH)、スルホン酸アルカリ金属塩(S(O)(O)O-M+)、スルホン酸アンモニウム塩(S(O)(O)O-NH4 +)、スルホン酸アルキルアンモニウム塩(S(O)(O)O-N(Alk)4 +)、ケトン(C(O))又はアセチルアセトネート(C(O)−CH2−C(O))である。
R1、R2及びR3は水素又はハロゲン(F、Cl、Br、I)であり、
R4はCH2又はCF2であり、
R5はC1〜C16直鎖状、分岐鎖状、アリール若しくは環状アルキル基、C1〜C16フッ素化直鎖状、分岐鎖状、アリール若しくは環状アルキル基、ヘキサフルオロプロピレンオキシドのオリゴマー又はテトラフルオロエチレンオキシドのオリゴマーであり、
R6はカルボン酸(C(O)OH)、カルボン酸アルカリ金属塩(COO-M+)、カルボン酸アンモニウム塩(COO-NH4 +)、カルボン酸アルキルアンモニウム塩(COO-N(Alk)4 +)、アルコール(OH)、アミド(C(O)NH2)、ジアルキルアミド(C(O)NAlk2)、スルホン酸(S(O)(O)OH)、スルホン酸アルカリ金属塩(S(O)(O)O-M+)、スルホン酸アンモニウム塩(S(O)(O)O-NH4 +)、スルホン酸アルキルアンモニウム塩(S(O)(O)O-N(Alk)4 +)、ケトン(C(O))若しくはアセチルアセトネート(C(O)−CH2−C(O))、又はホスホネート(P(O)(OH)2)、アルカリ金属若しくはアンモニウムホスホネートである。
重合に用いる界面活性剤は、PVDF乳化重合において有用であることが当技術分野において周知の任意の界面活性剤であることができ、ペルフッ素化界面活性剤、部分フッ素化界面活性剤及び非フッ素化界面活性剤が含まれる。好ましい実施形態において、本開示のPVDFエマルションは、フルオロ界面活性剤を含まないものであることができ、重合のいずれの部分においてもフルオロ界面活性剤は何ら用いられない。PVDF重合において有用な非フッ素化界面活性剤は、イオン性及び非イオン性の両方であることができ、限定されるわけではないが、3−アリルオキシ−2−ヒドロキシー1−プロパンスルホン酸塩、ポリビニルホスホン酸、ポリアクリル酸、ポリビニルスルホン酸及びそれらの塩、ポリエチレングリコール及び/又はポリプロピレングリコール並びにそれらのブロックコポリマー、アルキルホスホネート並びにシロキサン系界面活性剤が含まれる。
用語「開始剤」並びに「ラジカル開始剤」及び「フリーラジカル開始剤」という表現は、自発的に又は熱若しくは光への曝露によって誘導されるフリーラジカル源を提供することができる化学物質を指す。好適な開始剤の例には、ペルオキシド、ペルオキシジカーボネート及びアゾ化合物がある。「開始剤」にはまた、フリーラジカル源を提供するのに有用なレドックス系も含まれる。用語「ラジカル」及び「フリーラジカル」という表現は、不対電子を少なくとも1個含有する化学種を指す。
連鎖移動剤は、生成物の分子量を調節するために重合に加えられる。これらは、反応の初めに単一の場所で重合に加えることもでき、反応全体を通じて漸進的に又は連続的に重合に加えてもよい。連鎖移動剤の添加量及び添加方法は、用いる連鎖移動剤の活性及びポリマー生成物に望まれる分子量に依存する。重合反応に加えられる連鎖移動剤の量は、反応混合物に加えられるモノマーの総重量を基準として、好ましくは約0.05〜約5重量%、より一層好ましくは約0.1〜約2重量%である。
重合反応混合物には、重合反応の間を通じて調節されたpHを維持するために、緩衝剤を随意に含有させることができる。生成物中における望ましくない発色を最小限に抑えるためには、pHを好ましくは約4〜約8の範囲内に調節する。
パラフィンワックス又は炭化水素オイルは、反応に加えられると、防汚剤としての働きをして、反応器の部品にポリマーが付着するのを最小限に抑え又は防止する。任意の長鎖飽和炭化水素ワックス又はオイルがこの働きをすることができる。反応器に加えられるオイル又はワックスの量は、反応器の部品上にポリマー付着物が形成するのを最小限に抑える働きをする量である。この量は一般的に反応器の内部表面積に比例し、反応器内部表面積1cm2当たり約1〜約40mgで変えることができる。パラフィンワックス又は炭化水素オイルの量は、反応器表面積1cm2当たり約5mgであるのが好ましい。
重合のために採用される温度は、選択した開始剤系に依存して、例えば20〜130℃で変えることができる。この重合温度は、好ましくは35〜130℃、特に好ましくは70〜125℃である。
共重合の生成物はラテックスであり、これは、通常は重合プロセスからの固体状副生成物を濾過した後に、その形で用いることができ、又は凝固させて固形分を単離させ、これを次いで洗浄して乾燥させることもできる。ラテックスの形での使用のためには、界面活性剤を加えることによってラテックスを安定化させることができ、この界面活性剤は、(用いた場合の)重合の際に存在させる界面活性剤と同一であっても異なっていてもよい。この後から加えられる界面活性剤は、例えばイオン性又は非イオン性界面活性剤であることができる。本発明の1つの実施形態において、ラテックス中にフルオロ界面活性剤は何ら加えられない。固体状生成物については、ラテックスを機械的に又は塩若しくは酸を加えることによって凝固させ、次いで濾過等のよく知られた手段によって単離することができる。ひとたび単離したら、固体状生成物を洗浄又は他の技術によって精製することができ、粉体として用いるために乾燥させることができ、これをさらに加工して顆粒やペレットにすることもできる。
Claims (24)
- フッ素化ビニル系モノマーと1種以上の親水性モノマーとを含むフッ素化コポリマーであって、前記親水性モノマーが、ビニルアルキル酸、ビニルホスホネート、官能性アクリルアミド、カーボネート、ビニルエーテル、アルコキシ化合物及び二重親水性基モノマーより成る群から選択される、前記フッ素化コポリマー。
- 前記親水性モノマーを10.0重量%まで含む、請求項1に記載のコポリマー。
- 前記フッ素化ビニル系モノマーがフッ化ビニリデンを含む、請求項1に記載のコポリマー。
- 前記親水性モノマーの少なくとも1種がビニルの炭素上に少なくとも1個のハロゲンを含む、請求項1に記載のコポリマー。
- 前記少なくとも1個のハロゲンがフッ素を含む、請求項4に記載のコポリマー。
- 前記ビニルアルキル酸コモノマーが式(M1)を有する、請求項1に記載のコポリマー。
R1、R2及びR3は水素又はハロゲン(F、Cl、Br、I)であり;
R4はC1〜C16直鎖状、分岐鎖状、アリール若しくは環状アルキル基、C1〜C16フッ素化直鎖状、分岐鎖状、アリール若しくは環状アルキル基、ヘキサフルオロプロピレンオキシドのオリゴマー又はテトラフルオロエチレンオキシドのオリゴマーであり;
R5はカルボン酸(C(O)OH)、カルボン酸アルカリ金属塩(COO-M+)、カルボン酸アンモニウム塩(COO-NH4 +)、カルボン酸アルキルアンモニウム塩(COO-N(Alk)4 +)、アルコール(OH)、アミド(C(O)NH2)、ジアルキルアミド(C(O)NAlk2)、スルホン酸(S(O)(O)OH)、スルホン酸アルカリ金属塩(S(O)(O)O-M+)、スルホン酸アンモニウム塩(S(O)(O)O-NH4 +)、スルホン酸アルキルアンモニウム塩(S(O)(O)O-N(Alk)4 +)である。) - 前記官能性アクリルアミドコモノマーが式(M3)を有する、請求項1に記載のコポリマー。
R4及びR6は別々に、水素、C1〜C16直鎖状、分岐鎖状、アリール若しくは環状アルキル基、C1〜C16フッ素化直鎖状、分岐鎖状、アリール若しくは環状アルキル基、ヘキサフルオロプロピレンオキシドのオリゴマー又はテトラフルオロエチレンオキシドのオリゴマーであり;
R5及びR7は別々に、カルボン酸(C(O)OH)、カルボン酸アルカリ金属塩(COO-M+)、カルボン酸アンモニウム塩(COO-NH4 +)、カルボン酸アルキルアンモニウム塩(COO-N(Alk)4 +)、アルコール(OH)、アミド(C(O)NH2)、ジアルキルアミド(C(O)NAlk2)、スルホン酸(S(O)(O)OH)、スルホン酸アルカリ金属塩(S(O)(O)O-M+)、スルホン酸アンモニウム塩(S(O)(O)O-NH4 +)、スルホン酸アルキルアンモニウム塩(S(O)(O)O-N(Alk)4 +)、ケトン(C(O))若しくはアセチルアセトネート(C(O)−CH2−C(O))、又はホスホネート(P(O)(OH)2)、アルカリ金属若しくはアンモニウムホスホネートである。) - 前記ビニルエーテルコモノマーが式(M5)を有する、請求項1に記載のコポリマー。
R1、R2及びR3は水素又はハロゲン(F、Cl、Br、I)であり;
R4はC1〜C16直鎖状、分岐鎖状、アリール若しくは環状アルキル基、C1〜C16フッ素化直鎖状、分岐鎖状、アリール若しくは環状アルキル基、ヘキサフルオロプロピレンオキシドのオリゴマー又はテトラフルオロエチレンオキシドのオリゴマーであり;
R5はカルボン酸(C(O)OH)、カルボン酸アルカリ金属塩(COO-M+)、カルボン酸アンモニウム塩(COO-NH4 +)、カルボン酸アルキルアンモニウム塩(COO-N(Alk)4 +)、アルコール(OH)、アミド(C(O)NH2)、ジアルキルアミド(C(O)NAlk2)、スルホン酸(S(O)(O)OH)、スルホン酸アルカリ金属塩(S(O)(O)O-M+)、スルホン酸アンモニウム塩(S(O)(O)O-NH4 +)、スルホン酸アルキルアンモニウム塩(S(O)(O)O-N(Alk)4 +)、ケトン(C(O))又はアセチルアセトネート(C(O)−CH2−C(O))である。) - 前記アリルオキシコモノマーが式(M6)を有する、請求項1に記載のコポリマー。
R1、R2及びR3は水素又はハロゲン(F、Cl、Br、I)であり;
R4はCH2又はCF2であり;
R5はC1〜C16直鎖状、分岐鎖状、アリール若しくは環状アルキル基、C1〜C16フッ素化直鎖状、分岐鎖状、アリール若しくは環状アルキル基、ヘキサフルオロプロピレンオキシドのオリゴマー又はテトラフルオロエチレンオキシドのオリゴマーであり;
R6はカルボン酸(C(O)OH)、カルボン酸アルカリ金属塩(COO-M+)、カルボン酸アンモニウム塩(COO-NH4 +)、カルボン酸アルキルアンモニウム塩(COO-N(Alk)4 +)、アルコール(OH)、アミド(C(O)NH2)、ジアルキルアミド(C(O)NAlk2)、スルホン酸(S(O)(O)OH)、スルホン酸アルカリ金属塩(S(O)(O)O-M+)、スルホン酸アンモニウム塩(S(O)(O)O-NH4 +)、スルホン酸アルキルアンモニウム塩(S(O)(O)O-N(Alk)4 +)、ケトン(C(O))若しくはアセチルアセトネート(C(O)−CH2−C(O))、又はホスホネート(P(O)(OH)2)、アルカリ金属若しくはアンモニウムホスホネートである。) - 前記複数親水性官能性コモノマーがイタコン酸、マレイン酸、グルタコン酸及びフマル酸並びにそれらの酸無水物、アルカリ金属塩、アンモニウム塩及びモノ−、ジ−、トリ−及びテトラアルキルアンモニウム塩より成る群から選択される、請求項1に記載のコポリマー。
- 請求項1〜12のいずれかに記載のフッ素化コポリマーを溶剤中に含む配合物。
- 前記溶剤がN−メチルピロリドン(NMP)、ジメチルスルホキシド(DMSO)、N,N−ジメチルホルムアミド(DMF)、トリエチルホスファイト(TEP)、アセトン、テトラヒドロフラン、メチルエチルケトン(MEK)、メチルイソブチルケトン(MiBK)、酢酸エチル(EA)、酢酸ブチル(BA)、ジメチルカーボネート(DMC)、ジエチルカーボネート(DEC)及びメチルエチルカーボネート(MEC)より成る群から選択される、請求項13に記載の配合物。
- 活性炭及び金属粒子を前記溶剤中に懸濁状でさらに含み、前記金属粒子がリン酸鉄リチウム(LFP)、リチウムニッケルマンガンコバルト酸化物(NMC)、リチウム−マンガン−コバルトー酸化物、リチウム−ニッケル−コバルト−アルミニウム酸化物、リチウム−マンガン酸化物及びリチウム−ニッケル−マンガン(LMNO)より成る群から選択される、請求項13に記載の配合物。
- 水性反応媒体中で請求項1に記載のフッ素化コポリマーを製造するための方法であって、
a)少なくとも1種の開始剤、安定剤、少なくとも1種のフッ素化ビニル系モノマー、並びにビニルアルキル酸、ビニルホスホネート、官能性アクリルアミド、カーボネート、ビニルエーテル、アルコキシ化合物及び二重親水性基モノマーより成る群から選択される少なくとも1種の親水性モノマーを含む水性エマルションを形成させ;
b)前記少なくとも1種のフッ素化ビニル系モノマーと前記親水性モノマーとの共重合を撹拌しながら熱及び超大気圧下で開始させる:
ことを含む、前記方法。 - 前記水性媒体が追加的に少なくとも1種の緩衝剤を含む、請求項16に記載の方法。
- 重合を約70〜約125℃の温度で実施する、請求項16又は17に記載の方法。
- 重合を約2750〜約6900kPaの重合圧力において実施する、請求項16〜18のいずれかに記載の方法。
- 前記開始剤が過硫酸塩又は有機ペルオキシドである、請求項16〜19のいずれかに記載の方法。
- 請求項11〜13のいずれかに記載の配合物を含む物品であって、バッテリー電極フィルム、特にリチウムイオンバッテリー用の正極である、前記物品。
- 請求項1〜12のいずれかに記載のフッ素化コポリマーを含むバッテリー。
- 請求項1〜12のいずれかに記載のコポリマーを水中のラテックスとして又は溶剤溶液として適用された被覆基材。
- 水中のラテックスとして又は溶剤溶液として適用された請求項1〜12のいずれかに記載のコポリマーを含む多孔質膜。
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Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5770144A (en) * | 1980-10-17 | 1982-04-30 | Asahi Glass Co Ltd | Organic solution of fluorinated copolymer containing carboxyl group |
JPH02604A (ja) * | 1988-12-28 | 1990-01-05 | Daikin Ind Ltd | 含フッ素共重合体 |
JPH02302411A (ja) * | 1989-05-17 | 1990-12-14 | Daikin Ind Ltd | 新規含フッ素共重合体 |
JPH06172452A (ja) * | 1992-12-02 | 1994-06-21 | Kureha Chem Ind Co Ltd | フッ化ビニリデン系共重合体 |
JPH0912817A (ja) * | 1995-06-23 | 1997-01-14 | Elf Atochem Sa | 自己架橋性ワニス及び塗料用結合剤 |
JPH10272744A (ja) * | 1997-03-31 | 1998-10-13 | Daikin Ind Ltd | 耐候性複合材 |
WO2016133206A1 (ja) * | 2015-02-20 | 2016-08-25 | ダイキン工業株式会社 | 親水化剤、親水化剤を含む組成物及び高分子多孔質膜 |
JP6269890B1 (ja) * | 2016-10-07 | 2018-01-31 | ダイキン工業株式会社 | 二次電池用結着剤及び二次電池用電極合剤 |
JP2018154802A (ja) * | 2017-03-21 | 2018-10-04 | 株式会社クレハ | 樹脂組成物、二次電池のセパレータ、および二次電池 |
Family Cites Families (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3057812A (en) * | 1958-07-15 | 1962-10-09 | Union Carbide Corp | Coating compositions comprising a resinous copolymer having a reduced viscosity of 0.2 to 0.8 and a second order transition temperature of 45 deg. c. to 125 deg. c. |
GB1550874A (en) * | 1976-10-28 | 1979-08-22 | Asahi Glass Co Ltd | Process for producing fluorinated copolymer having ion-exchange groups |
JPS5645911A (en) * | 1979-09-25 | 1981-04-25 | Asahi Glass Co Ltd | Production of ion-exchangeable fluorinated polymer |
FR2646429B1 (fr) | 1989-04-28 | 1991-07-26 | Atochem | Copolymere durcissable fluore, son procede de fabrication et son application dans les vernis et peintures |
US5166284A (en) | 1989-11-16 | 1992-11-24 | Atochem | Cross-linkable fluorinated copolymer, process for its manufacture and its application in protective coatings |
US5200479A (en) | 1990-10-19 | 1993-04-06 | Atochem | Hardenable fluorinated copolymer, the process for making the same, and its application in paints and varnishes |
JPH07201316A (ja) * | 1993-12-29 | 1995-08-04 | Sony Corp | 非水電解液二次電池 |
FR2720750B1 (fr) | 1994-06-01 | 1996-07-19 | Atochem Elf Sa | Dispersion stable aqueuse de copolymères fluorés hydroxyles et de copolymères acryliques, son procédé de préparation et son utilisation comme peinture en phase aqueuse. |
DE69611103T2 (de) * | 1995-09-27 | 2001-04-05 | Honeywell Int Inc | Bei raumtemperatur koalizierende wässrige fluorpolymer dispersionen und verfahren zu deren herstellung |
JP3703582B2 (ja) * | 1996-02-22 | 2005-10-05 | 呉羽化学工業株式会社 | 電極バインダー、電極バインダー溶液、電極合剤、電極構造体および電池 |
CN1529917A (zh) | 2001-04-10 | 2004-09-15 | 三菱麻铁里亚尔株式会社 | 锂离子聚合物二次电池、该电池用电极及用于该电池的粘合层的粘结剂中的高分子化合物的合成方法 |
EP1551036A1 (en) * | 2002-10-03 | 2005-07-06 | Daikin Industries, Ltd. | Fluorine-containing polymer solid electrolyte having fluorine-containing ether chain |
WO2004092257A1 (ja) * | 2003-04-16 | 2004-10-28 | Kureha Corporation | フッ化ビニリデン系樹脂多孔膜及びその製造方法 |
US6869997B2 (en) | 2003-05-06 | 2005-03-22 | Arkema, Inc. | Polymerization of fluoromonomers using a 3-allyloxy-2-hydroxy-1-propanesulfonic acid salt as surfactant |
US7241817B2 (en) | 2003-06-06 | 2007-07-10 | Arkema France | Process for grafting a fluoropolymer and multilayer structures comprising this grafted polymer |
US7244443B2 (en) * | 2004-08-31 | 2007-07-17 | Advanced Cardiovascular Systems, Inc. | Polymers of fluorinated monomers and hydrophilic monomers |
TWI437009B (zh) | 2007-04-24 | 2014-05-11 | Solvay Solexis Spa | 1,1-二氟乙烯共聚物類 |
KR101612699B1 (ko) * | 2007-05-02 | 2016-04-15 | 롤리크 아게 | 열안정성 정렬 물질 |
CN101687763B (zh) * | 2007-05-25 | 2014-02-19 | 罗利克有限公司 | 包含脂环基的光可交联材料 |
US9434837B2 (en) * | 2010-09-01 | 2016-09-06 | Arkema Inc. | Method of producing fluoropolymers using acid-functionalized monomers |
JP5742384B2 (ja) * | 2010-09-30 | 2015-07-01 | ダイキン工業株式会社 | 含フッ素重合体の製造方法 |
WO2013005796A1 (ja) * | 2011-07-06 | 2013-01-10 | 日本ゼオン株式会社 | 二次電池用多孔膜、二次電池用セパレーター及び二次電池 |
KR101599658B1 (ko) * | 2012-01-24 | 2016-03-03 | 다이킨 고교 가부시키가이샤 | 결착제, 정극합제 및 부극합제 |
WO2013110740A1 (en) | 2012-01-25 | 2013-08-01 | Solvay Sa | Fluoropolymers as binder for the electrodes in supercapacitors |
CN103588922A (zh) * | 2012-08-14 | 2014-02-19 | 中化蓝天集团有限公司 | 一种偏氟乙烯共聚物、其制备方法及应用 |
PL3070764T3 (pl) * | 2013-12-06 | 2019-07-31 | Daikin Industries, Ltd. | Separator do baterii akumulatorowej i bateria akumulatorowa |
JP6941604B2 (ja) * | 2015-09-23 | 2021-09-29 | スリーエム イノベイティブ プロパティズ カンパニー | スルホニルペンダント基を有するテトラフルオロエチレンのコポリマーを作製する方法 |
FR3047008B1 (fr) | 2016-01-25 | 2019-10-25 | Arkema France | Utilisation d'un copolymere de fluorure de vinylidene pour conferer a un film des proprietes d'adhesion |
JP6642096B2 (ja) * | 2016-02-23 | 2020-02-05 | 凸版印刷株式会社 | 不燃シート及びその製造方法 |
KR102261507B1 (ko) * | 2017-05-26 | 2021-06-07 | 다이킨 고교 가부시키가이샤 | 이차 전지용 세퍼레이터 및 이차 전지 |
KR102369813B1 (ko) * | 2017-10-30 | 2022-03-03 | 다이킨 고교 가부시키가이샤 | 이차 전지용 결착제, 이차 전지용 전극 합제, 이차 전지용 전극 및 이차 전지 |
-
2018
- 2018-05-02 FR FR1853772A patent/FR3079834B1/fr active Active
-
2019
- 2019-04-09 WO PCT/US2019/026492 patent/WO2019199753A1/en unknown
- 2019-04-09 CN CN201980024555.0A patent/CN111954658A/zh active Pending
- 2019-04-09 EP EP19784254.5A patent/EP3774713A4/en active Pending
- 2019-04-09 JP JP2020555471A patent/JP2021521297A/ja active Pending
- 2019-04-09 KR KR1020207032365A patent/KR20200143717A/ko not_active Application Discontinuation
- 2019-04-09 US US17/045,274 patent/US20210163647A1/en active Pending
Patent Citations (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5770144A (en) * | 1980-10-17 | 1982-04-30 | Asahi Glass Co Ltd | Organic solution of fluorinated copolymer containing carboxyl group |
JPH02604A (ja) * | 1988-12-28 | 1990-01-05 | Daikin Ind Ltd | 含フッ素共重合体 |
JPH02302411A (ja) * | 1989-05-17 | 1990-12-14 | Daikin Ind Ltd | 新規含フッ素共重合体 |
US5053469A (en) * | 1989-05-17 | 1991-10-01 | Daikin Industries Ltd. | Novel fluorine-containing copolymer |
JPH06172452A (ja) * | 1992-12-02 | 1994-06-21 | Kureha Chem Ind Co Ltd | フッ化ビニリデン系共重合体 |
US5415958A (en) * | 1992-12-02 | 1995-05-16 | Kureha Kagaku Kogyo Kabushiki Kaisha | Vinylidene fluoride copolymer, and binder composition containing the copolymer for non-aqueous solvent-type secondary battery |
JPH0912817A (ja) * | 1995-06-23 | 1997-01-14 | Elf Atochem Sa | 自己架橋性ワニス及び塗料用結合剤 |
JPH10272744A (ja) * | 1997-03-31 | 1998-10-13 | Daikin Ind Ltd | 耐候性複合材 |
WO2016133206A1 (ja) * | 2015-02-20 | 2016-08-25 | ダイキン工業株式会社 | 親水化剤、親水化剤を含む組成物及び高分子多孔質膜 |
JP6269890B1 (ja) * | 2016-10-07 | 2018-01-31 | ダイキン工業株式会社 | 二次電池用結着剤及び二次電池用電極合剤 |
JP2018154802A (ja) * | 2017-03-21 | 2018-10-04 | 株式会社クレハ | 樹脂組成物、二次電池のセパレータ、および二次電池 |
US20200020909A1 (en) * | 2017-03-21 | 2020-01-16 | Kureha Corporation | Resin composition, separator of secondary battery, and secondary battery |
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