GB2448441A - Copolymer,polymer electrolyte and use thereof - Google Patents
Copolymer,polymer electrolyte and use thereof Download PDFInfo
- Publication number
- GB2448441A GB2448441A GB0812688A GB0812688A GB2448441A GB 2448441 A GB2448441 A GB 2448441A GB 0812688 A GB0812688 A GB 0812688A GB 0812688 A GB0812688 A GB 0812688A GB 2448441 A GB2448441 A GB 2448441A
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- United Kingdom
- Prior art keywords
- group
- groups
- substituent
- carbon atoms
- polymer electrolyte
- Prior art date
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- 229920001577 copolymer Polymers 0.000 title claims abstract description 96
- 239000005518 polymer electrolyte Substances 0.000 title claims description 81
- 239000002253 acid Substances 0.000 claims abstract description 88
- 239000000178 monomer Substances 0.000 claims abstract description 46
- 239000000203 mixture Substances 0.000 claims abstract description 44
- 230000000269 nucleophilic effect Effects 0.000 claims abstract description 27
- 239000012528 membrane Substances 0.000 claims description 103
- 125000001424 substituent group Chemical group 0.000 claims description 56
- 125000004432 carbon atom Chemical group C* 0.000 claims description 54
- 125000003118 aryl group Chemical group 0.000 claims description 51
- 239000003054 catalyst Substances 0.000 claims description 50
- 229920000642 polymer Polymers 0.000 claims description 48
- 239000000446 fuel Substances 0.000 claims description 37
- 238000000034 method Methods 0.000 claims description 36
- 238000005342 ion exchange Methods 0.000 claims description 23
- 125000000217 alkyl group Chemical group 0.000 claims description 17
- 125000003545 alkoxy group Chemical group 0.000 claims description 16
- 125000004104 aryloxy group Chemical group 0.000 claims description 15
- 239000002131 composite material Substances 0.000 claims description 15
- 239000000758 substrate Substances 0.000 claims description 13
- 125000001153 fluoro group Chemical group F* 0.000 claims description 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 10
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 10
- 125000003277 amino group Chemical group 0.000 claims description 8
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 6
- 238000009833 condensation Methods 0.000 claims description 5
- 230000005494 condensation Effects 0.000 claims description 5
- 239000003930 superacid Substances 0.000 claims description 5
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 3
- 239000003792 electrolyte Substances 0.000 claims description 3
- 125000005951 trifluoromethanesulfonyloxy group Chemical group 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims 1
- 238000006482 condensation reaction Methods 0.000 abstract description 11
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 51
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 45
- 150000001875 compounds Chemical class 0.000 description 44
- -1 pyridinediyl group Chemical group 0.000 description 39
- 239000000243 solution Substances 0.000 description 39
- 238000006243 chemical reaction Methods 0.000 description 35
- 239000002904 solvent Substances 0.000 description 31
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 30
- 238000004519 manufacturing process Methods 0.000 description 25
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 24
- 239000007789 gas Substances 0.000 description 23
- 238000002156 mixing Methods 0.000 description 21
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 20
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 20
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 20
- 229910052799 carbon Inorganic materials 0.000 description 17
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 14
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 14
- 229910006069 SO3H Inorganic materials 0.000 description 12
- 150000007514 bases Chemical class 0.000 description 12
- 238000010521 absorption reaction Methods 0.000 description 11
- 238000005259 measurement Methods 0.000 description 11
- 238000005227 gel permeation chromatography Methods 0.000 description 10
- 239000000463 material Substances 0.000 description 10
- 229910000027 potassium carbonate Inorganic materials 0.000 description 10
- 235000011181 potassium carbonates Nutrition 0.000 description 10
- 229920001400 block copolymer Polymers 0.000 description 9
- 239000004744 fabric Substances 0.000 description 9
- 238000010438 heat treatment Methods 0.000 description 9
- 239000007787 solid Substances 0.000 description 9
- 125000000542 sulfonic acid group Chemical group 0.000 description 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 8
- 239000012300 argon atmosphere Substances 0.000 description 8
- 230000018044 dehydration Effects 0.000 description 8
- 238000006297 dehydration reaction Methods 0.000 description 8
- 238000005507 spraying Methods 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 7
- 239000007810 chemical reaction solvent Substances 0.000 description 7
- 238000009792 diffusion process Methods 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 7
- 239000001257 hydrogen Substances 0.000 description 7
- 229910052739 hydrogen Inorganic materials 0.000 description 7
- 125000004957 naphthylene group Chemical group 0.000 description 7
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 7
- 229910052697 platinum Inorganic materials 0.000 description 7
- 238000006116 polymerization reaction Methods 0.000 description 7
- 229920005604 random copolymer Polymers 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000007795 chemical reaction product Substances 0.000 description 6
- VKDSBABHIXQFKH-UHFFFAOYSA-M potassium;4-hydroxy-3-sulfophenolate Chemical compound [K+].OC1=CC=C(O)C(S([O-])(=O)=O)=C1 VKDSBABHIXQFKH-UHFFFAOYSA-M 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 5
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 5
- 239000000706 filtrate Substances 0.000 description 5
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 5
- 125000001624 naphthyl group Chemical group 0.000 description 5
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
- 230000003014 reinforcing effect Effects 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- 125000001989 1,3-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([H])C([*:2])=C1[H] 0.000 description 4
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 4
- PLVUIVUKKJTSDM-UHFFFAOYSA-N 1-fluoro-4-(4-fluorophenyl)sulfonylbenzene Chemical compound C1=CC(F)=CC=C1S(=O)(=O)C1=CC=C(F)C=C1 PLVUIVUKKJTSDM-UHFFFAOYSA-N 0.000 description 4
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 4
- KZTYYGOKRVBIMI-UHFFFAOYSA-N diphenyl sulfone Chemical compound C=1C=CC=CC=1S(=O)(=O)C1=CC=CC=C1 KZTYYGOKRVBIMI-UHFFFAOYSA-N 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- 125000005843 halogen group Chemical group 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 125000005186 naphthyloxy group Chemical group C1(=CC=CC2=CC=CC=C12)O* 0.000 description 4
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-dimethylformamide Substances CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- VCCBEIPGXKNHFW-UHFFFAOYSA-N biphenyl-4,4'-diol Chemical group C1=CC(O)=CC=C1C1=CC=C(O)C=C1 VCCBEIPGXKNHFW-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 239000010419 fine particle Substances 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- QESVBYKECHLZTB-UHFFFAOYSA-M potassium 2-fluorobenzenesulfonate Chemical compound FC1=CC=CC=C1S(=O)(=O)[O-].[K+] QESVBYKECHLZTB-UHFFFAOYSA-M 0.000 description 3
- 238000010248 power generation Methods 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 2
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 2
- JOLQKTGDSGKSKJ-UHFFFAOYSA-N 1-ethoxypropan-2-ol Chemical compound CCOCC(C)O JOLQKTGDSGKSKJ-UHFFFAOYSA-N 0.000 description 2
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 2
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 2
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- ATHHXGZTWNVVOU-UHFFFAOYSA-N N-methylformamide Chemical compound CNC=O ATHHXGZTWNVVOU-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- DFPOZTRSOAQFIK-UHFFFAOYSA-N S,S-dimethyl-beta-propiothetin Chemical compound C[S+](C)CCC([O-])=O DFPOZTRSOAQFIK-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 239000005456 alcohol based solvent Substances 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 238000010533 azeotropic distillation Methods 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 230000005587 bubbling Effects 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- 229940117389 dichlorobenzene Drugs 0.000 description 2
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 239000004210 ether based solvent Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- AMXOYNBUYSYVKV-UHFFFAOYSA-M lithium bromide Chemical compound [Li+].[Br-] AMXOYNBUYSYVKV-UHFFFAOYSA-M 0.000 description 2
- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 description 2
- 239000011259 mixed solution Substances 0.000 description 2
- 239000004745 nonwoven fabric Substances 0.000 description 2
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- ABLZXFCXXLZCGV-UHFFFAOYSA-N phosphonic acid group Chemical group P(O)(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 239000011877 solvent mixture Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 238000009210 therapy by ultrasound Methods 0.000 description 2
- 239000002759 woven fabric Substances 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- JIFAWAXKXDTUHW-UHFFFAOYSA-N 2-fluorobenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1F JIFAWAXKXDTUHW-UHFFFAOYSA-N 0.000 description 1
- 125000005916 2-methylpentyl group Chemical group 0.000 description 1
- 125000005924 2-methylpentyloxy group Chemical group 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- OHLUUHNLEMFGTQ-UHFFFAOYSA-N N-methylacetamide Chemical compound CNC(C)=O OHLUUHNLEMFGTQ-UHFFFAOYSA-N 0.000 description 1
- 229920000557 Nafion® Polymers 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical group OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910001413 alkali metal ion Inorganic materials 0.000 description 1
- 229910001420 alkaline earth metal ion Inorganic materials 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 238000012661 block copolymerization Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- KVNRLNFWIYMESJ-UHFFFAOYSA-N butyronitrile Chemical compound CCCC#N KVNRLNFWIYMESJ-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229920000891 common polymer Polymers 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 230000001268 conjugating effect Effects 0.000 description 1
- 230000008094 contradictory effect Effects 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000002933 cyclohexyloxy group Chemical group C1(CCCCC1)O* 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001887 cyclopentyloxy group Chemical group C1(CCCC1)O* 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 125000004989 dicarbonyl group Chemical group 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 125000002510 isobutoxy group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])O* 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000005453 ketone based solvent Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 150000002641 lithium Chemical group 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001298 n-hexoxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000003935 n-pentoxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- MNZMMCVIXORAQL-UHFFFAOYSA-N naphthalene-2,6-diol Chemical compound C1=C(O)C=CC2=CC(O)=CC=C21 MNZMMCVIXORAQL-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- DDBREPKUVSBGFI-UHFFFAOYSA-N phenobarbital Chemical compound C=1C=CC=CC=1C1(CC)C(=O)NC(=O)NC1=O DDBREPKUVSBGFI-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 229940086066 potassium hydrogencarbonate Drugs 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000006479 redox reaction Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 125000004436 sodium atom Chemical group 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 230000003685 thermal hair damage Effects 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 238000001132 ultrasonic dispersion Methods 0.000 description 1
Classifications
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- B01D—SEPARATION
- B01D69/00—Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor
- B01D69/12—Composite membranes; Ultra-thin membranes
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- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/06—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
- H01B1/12—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances organic substances
- H01B1/122—Ionic conductors
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
- C08G65/38—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols
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- C08G65/38—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols
- C08G65/40—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols from phenols (I) and other compounds (II), e.g. OH-Ar-OH + X-Ar-X, where X is halogen atom, i.e. leaving group
- C08G65/4012—Other compound (II) containing a ketone group, e.g. X-Ar-C(=O)-Ar-X for polyetherketones
- C08G65/4056—(I) or (II) containing sulfur
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- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
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- C08J5/2206—Films, membranes or diaphragms based on organic and/or inorganic macromolecular compounds
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- C08J5/2256—Synthetic macromolecular compounds based on macromolecular compounds obtained by reactions other than those involving carbon-to-carbon bonds, e.g. obtained by polycondensation
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- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/06—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
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- H01M8/10—Fuel cells with solid electrolytes
- H01M8/1016—Fuel cells with solid electrolytes characterised by the electrolyte material
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- H01M8/102—Polymeric electrolyte materials characterised by the chemical structure of the main chain of the ion-conducting polymer
- H01M8/1027—Polymeric electrolyte materials characterised by the chemical structure of the main chain of the ion-conducting polymer having carbon, oxygen and other atoms, e.g. sulfonated polyethersulfones [S-PES]
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- H01M8/1016—Fuel cells with solid electrolytes characterised by the electrolyte material
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- H01M8/1032—Polymeric electrolyte materials characterised by the chemical structure of the main chain of the ion-conducting polymer having sulfur, e.g. sulfonated-polyethersulfones [S-PES]
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- C08G2650/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G2650/28—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type
- C08G2650/38—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type containing oxygen in addition to the ether group
- C08G2650/40—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type containing oxygen in addition to the ether group containing ketone groups, e.g. polyarylethylketones, PEEK or PEK
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- C08J2371/00—Characterised by the use of polyethers obtained by reactions forming an ether link in the main chain; Derivatives of such polymers
- C08J2371/08—Polyethers derived from hydroxy compounds or from their metallic derivatives
- C08J2371/10—Polyethers derived from hydroxy compounds or from their metallic derivatives from phenols
- C08J2371/12—Polyphenylene oxides
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- C08J2381/00—Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur with or without nitrogen, oxygen, or carbon only; Polysulfones; Derivatives of such polymers
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Abstract
Disclosed is a copolymer obtained by a condensation reaction between a leaving group and a nucleophilic group. Specifically disclosed is a copolymer obtained by condensing a mixture of (A) and (C) shown below and a mixture of (B) and (D) shown below, or a mixture of (A), (B), (C) and (D) shown below. (A) a monomer having two leaving groups and at least one acid radical in a molecule (B) a monomer having two nucleophilic groups and at least one acid radical in a molecule (C) a monomer having two leaving groups and substantially no acid radical in a molecule (D) a monomer having two nucleophilic groups and substantially no acid radical in a molecule.
Description
S14588
DESCRIPTION
COPOLYMER, POLYMER ELECTROLYTE, AND USE THEREOF
TECHNICAL FIELD
The invention relates to a copolyrner preferably used for materials of separating membrane for batteries, particularly fuel cells, to a polymer electrolyte and use thereof.
BACKGROUND ART
As separating membranes for electrochemical devices such as primary batteries, secondary batteries, or solid polymer fuel cells, polymer electrolytes having proton conductivity are employed. For example, when polymer electrolytes containing perfluoroalkane based polymers having perfluoroalkylsulfonic acid groups as a superacid in the side chains, e.g., Naf ion (registered trade name; from Du Pont (E.I) de Nemours & Co.), as an effective component are used as materials of separating membrane for fuel cells, such polymer electrolytes are excellent in properties of power generation and therefore are mainly used at the present. However, such problems have been pointed out that they are very expensive and inferior in heat resistance and that those membranes has low strength for using practically unless being somehow reinforced.
At the present situation, developments of polymer electrolytes economical and excellent in properties and usable S14588 in place of the above-mentioned polymer electrolytes have been made actively in recent years.
For example, block copolymers having a segment into which substantially no sulfonic acid group is introduced and a segment into which a sulfonic acid group is introduced, wherein the former segment comprises a polyether suif one and the latter segment is a condensate of a diphenylsulfone and a biphenol having sulfonic acid group are proposed (Japanese Unexamined Patent Publication No. 2003-031232).
On the other hand, in place of the above-mentioned block copolyiners, so-called random copolymers having an acid group distributed randomly along polymer chains has been also investigated and random copolymers of one kind monomer into which a sulfonic acid group is introduced and a monomer into which no sulfonic acid group is introduced have been proposed (see e.g., Japanese Unexamined Patent Publication Nos. 2004-509224 and 2006-523258, U.S. Patent Publication No. 2002/0091225, and Japanese Unexamined Patent Publication No. 2004-149779), or random copolymers obtained by sulfonatlon of polyether suif one copolymers (see e.g., Japanese Unexamined Patent Publication No. 10-021943) have been proposed.
DISCLOSURE OF THE INVENTION
With respect to the block copolymers disclosed in Japanese Unexamined Patent Publication No. 2003-031232, it was ...d S14588 required to previously synthesize either one of the segment into which substantially no sulfonic acid group is introduced or the segment into which a sulfonic acid group is introduced and thereafter carry out copolymerization with a monomer capable of forming the other segment, or separately synthesize polymers capable of forming the above-mentioned segments and thereafter further carry out coupling both polymers.
On the other hand, with respect to the random copolymers disclosed in Japanese Unexamined Patent Publication Nos. 2004-509224 and 2006-523258, U.S. Patent Publication No. 2002/0091225, Japanese Unexamined Patent Publication No. 2004-149779, and Japanese Unexamined Patent Publication No. 10-021943, as compared with the above-mentioned block copolymers, their synthesis itself is relatively easy, however, when it is tried to obtain practically useful proton conductivity for materials of separating membrane for batteries, the water absorbability of the random copolymers is increased and separating membranes to be obtained have problems that their sizes are significantly changed due to the water produced at the time of operating fuel cell and consequently mechanical strength is decreased. Particularly, according to the results of the investigations the inventors of the present invention have carried out, polymer electrolytes containing the random copolymers which have been disclosed previously have considerably high water absorbability of hot water at about s..) S14588 100 C and therefore, when they are used for separating membranes (polymer electrolyte membranes) of fuel cells, the polymer electrolyte membranes themselves tend to be deformed by water absorption due to heat generated by power generation.
The inventors of the present Invention have investigated repeatedly to solve the above-mentioned problems and consequently, they have now completed the present invention.
That is, the Invention provides a copolymer obtained by nucleophilic condensation of a mixture of (A) and (C) with a mixture of (B) and (D), or of a mixture of (A), (B), (C) and (D) as follows: (A) a monomer having two leaving groups and further at least one acid group in a molecule; (B) a monomer having two nucleophilic groups and further at least one acid group in a molecule; (C) a monomer having two leaving groups and substantially no acid group in a molecule; and (D) a monomer having two nucleophilic groups and substantially no acid group in a molecule.
Herein, the nucleophilic groups means groups having nucleophilicity, causing nucleophilic attack to atoms to which the leaving groups are bonded and being thus capable of forming new covalent bonds by condensation reaction which is accompanied with elimination of the leaving groups. The nucleophilic groups in the present invention differ from acid J S14588 groups described below and have higher nucleophilicity than that of the acid groups.
Since monomers having the nucleophilic groups and leaving groups are different, the monomers having the nucleophilic groups cause condensation reaction only with the monomers having the leaving groups and form covalent bonds. In the copolymers of the present invention, a structural unit (A') derived from the above-mentioned (A) is adjacent to a structural unit (B') derived from the above-mentioned (B) or a structural unit (D') derived from the above-mentioned (D): similarly the structural unit (B') is adjacent to the structural unit (A') or a structural unit) derived from the above-mentioned (C): also the structural unit (C') is adjacent to the structural unit (B') or the structural unit (D'): and the structural unit (D') is adjacent to the structural unit (A') or the structural unit (C').
Further, the present invention provides a copolymer represented by the following [2] to [8].
[2] The copolymer according to the above-mentioned [1], in which the above-mentioned (A) is represented by the following formula (1): (1) S14 588 wherein, k denotes 0, 1, or 2; Ar' and Ar2 each independently denote a divalent aromatic group; when k is 2, two Ar2 groups may be the same or different with each other and these divalent aromatic groups may be substituted with an alkyl group having 1 to 10 carbon atoms which may have a substituent, an alkoxy group having 1 to 10 carbon atoms which may have a substituent, an aryl group having 6 to 10 carbon atoms which may have a substituent, an aryloxy group having 6 to 10 carbon atoms which may have a substituent, a fluoro group, a nitro group, or a benzoyl group; when k is 0, Ar' has at least one acid group, and when k is 1 or more, at least one of Ar' and Ar2 has at least one acid group; X' denotes one of a fluoro group, a chioro group, a nitro group, or a trifluoromethanesulfony].oxy group; two X' groups may be the same or different with each other; Z' denotes a group selected from the following groups; and when k is 2, two Z' groups may be the same or different with each other: o o 00 -----&---3] The copolymer according to the above-mentioned [1] or [2], wherein the above-mentioned (B) is represented by the following formula (2): uS S14588 Y1Ar3Q1_Ar4).Y1 (2) wherein, j denotes 0, 1, or 2; Ar3 and Ar4 each independently denote a divalent aromatic group; when j is 2, two Ar4 groups may be the same or different with each other and these divalent aromatic groups may be substituted with an alkyl group having 1 to 10 carbon atoms which may have a substituent, an alkoxy group having 1 to 10 carbon atoms which may have a substituent, an aryl group having 6 to 10 carbon atoms which may have a substituent, or an aryloxy group having 6 to 10 carbon atoms which may have a substituent; when j is 0, Ar3 has at least one acid group, and when j is 1 or more, at least one of Ar3 and Ar4 has at least one acid group; Y1 denotes a hydroxyl group, a thiol group, or an amino group; two Y' groups may be the same or different with each other; Q' denotes a direct bond or a group selected from the following groups; and when j is 2, two Q1 groups may be the same or different with each other: H2 9H3 CF3 Q -0---C --y---cS--c--s----CH3 F3 ---; 9 ..d S14588 [4] The copolymer according to the above-mentioned [1] to [3], wherein the above-mentioned (C) is represented by the following formula (3): (3) wherein, m denotes 0, 1, or 2; Ar5 and Ar6 each independently denote a divalent aromatic group; when m is 2, two Ar6 groups may be the same or different with each other and these divalent aromatic groups may be substituted with an alkyl group having 1 to 10 carbon atoms which may have a substituent, an alkoxy group having 1 to 10 carbon atoms which may have a substituent, an aryl group having 6 to 10 carbon atoms which may have a substituent, an aryloxy group having 6 to 10 carbon atoms which may have a substituent, a fluoro group, a nitro group, or a benzoyl group; X2 denotes a fluoro group, a chioro group, a nitro group, or a trifluoromethanesulfonyloxy group; two X2 groups may be the same or different with each other; Z2 denotes a group selected from the following groups; and when mis 2, two Z2 groups may be the same or different with each other: -S14588 o 0 00 ---&--__&_a____ (5] The copolymer according to the above-mentioned [1] to [4], wherein the above-mentioned (D) is represented by the following formula (4): Y2-Ar7-( 02A r8)Y2 (4) wherein, n denotes 0, 1, or 2; Ar7 and Ar8 each independently denote a divalent aromatic group; when n is 2, two Ar8 groups may be the same or different with each other and these divalent aromatic groups may be substituted with an alkyl group having 1 to 10 carbon atoms which may have a substituent, an alkoxy group having 1 to 10 carbon atoms which may have a substituent, an aryl group having 6 to 10 carbon atoms which may have a substituent, or an aryloxy group having 6 to 10 carbon atoms which may have a substituent; Y2 denotes a hydroxyl group, a thiol group, or an amino group; two Y2 groups may be the same or different with each other; Q2 denotes a direct bond or a group selected from the following groups; and when n is 2, two Q2 groups may be the same or different with each other: _) S].4588 H2 OH3 CF3 0 -0--c --------s---OH3 CF3 ---; 0-0 [6] The copolymer according to the above-mentioned [1] to (5], wherein the acid group is a strong acid group or a superacid group.
[7] The copolymer according to the above-mentioned [1] to [61 having an ion exchange capacity of 0.1 meq/g to 4.0 meq/g.
[8] The copolymer according to the above-mentioned [1] to (7], wherein the weight composition ratio of the structural unit into which the acid group is introduced and the structural unit into which substantially no acid group is introduced, [structural unit into which the acid group is introduced] [structural unit into which substantially no acid group is introduced], is 3 97 to 70: 30.
In addition, the invention also provides the following.
[9] A polymer electrolyte containing the copolymer according to any one of the [1] to (8].
i." S14588 [10] A polymer electrolyte membrane containing the polymer electrolyte according to the [9].
[11] A polymer electrolyte composite membrane comprising the polymer electrolyte according to the [9] and a porous substrate.
[12] A polymer electrolyte composite membrane obtained by impregnating a porous substrate with the polymer electrolyte according to the [9], and compositing those.
[13] A catalyst composition comprising the polymer electrolyte according to the [9] and a catalyt material.
[14] A fuel cell using the polymer electrolyte membrane according to the [10].
[15) A fuel cell using the polymer electrolyte composite membrane according to the (11] or [12].
[16] A fuel cell having a catalyst layer comprising the catalyst composition according to the [13].
Further, the present invention provides [17] A method of producing a copolymer, wherein a mixture of (A) and (C) with a mixture of (B) and (D) is condensed, or a .d S14588 mixture of (A), (B), (C) and (D) is condensed as follows: (A) a monomer having two leaving groups and further at least one acid group in a molecule; (B) a monomer having two nucleophilic groups and further at least one acid group in a molecule; (C) a monomer having two leaving groups and substantially no acid group in a molecule; and (D) a monomer having two nucleophilic groups and substantially no acid group in a molecule.
BEST MODES FOR CARRYING OUT THE INVENTION
Hereinafter, preferable embodiments of the present invention will be described.
A copolymer of the present invention can be obtained by mixing and condensing, as indispensable monomers, a mixture of two kind specified monomers having acid groups (the above-mentioned (A) and (B)) with a mixture of two kind specified monomers substantially having no acid group (the above-mentioned (C) and (D)). One or more kinds of monomers (A), (B), (C), and (D) may be used respectively.
The above-mentioned (A) is preferably a compound represented by the above-mentioned formula (1). Herein, the acid groups are characterized in that when k is 0, Ar' has the acid groups, and when k is 1 or more, at least one of Ar' and Ar2 has the acid groups. Ar' and Ar2 denote a divalent aromatic 1..d S14588 group and examples of the divalent aromatic group may be hydrocarbon based aromatic groups such as a phenylene group, a naphthylene group, a biphenylylene group, and a fluorenediyl group and heterocyclic groups such as a pyridinediyl group, a quinoxalinedlyl group and a thiophenediyl group and among them, divalent hydrocarbon based aromatic groups are preferable and a phenylene group and a naphthylene group are particularly preferable. When k is 1, Ar' and Ar2 may be the same or different and when k is 2, Ar' and two Ar2 groups may be the same or different.
Herein, the above-mentioned divalent aromatic groups may be substituted with an alkyl group having 1 to 10 carbon atoms which may have a substituent, an alkoxy group having 1 to 10 carbon atoms which may have a substituent, an aryl group having 6 to 10 carbon atoms which may have a substituent, an aryloxy group having 6 to 10 carbon atoms which may have a substituent, a nitro group and a benzoyl group and examples of the alkyl group having 1 to 10 carbon atoms may include such as a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an allyl group, an n-butyl group, a sec-butyl group, a tert-butyl group, an isobutyl group, an n-pentyl group, 2, 2-dimethyipropyl group.
a cyclopentyl group, an n-hexyl group, a cyclohexyl group, 2-methylpentyl group and 2-ethyihexyl group and these groups may have halogen atoms such as fluorine atom, chlorine atom, bromine atom or iodine atom, a hydroxyl group, an amino group, L-S14588 a methoxy group, an ethoxy group, an isopropyloxy group, a phenyl group, a naphthyl group, a phenoxy group, and a Examples of the alkoxy group having 1 to 10 carbon atoms may include a methoxy group, an ethoxy group, an n-propyloxy group, an isopropyloxy group, an n-butyloxy group, a sec-butyloxy group, a tert-butyloxy group, an isobutyloxy group, an n-pentyloxy group, 2,2-dimethylpropyloxy group, a cyclopentyloxy group, an n-hexyloxy group, a cyclohexyloxy group, 2-methylpentyloxy group and 2-ethyihexyloxy group and these groups may have substituents selected from a halogen atom, a hydroxyl group, an amino group, a methoxy group, an ethoxy group, an isopropyloxy group, a phenyl group, a naphthyl group, a phenoxy group, and a naphthyloxy group as a substituent.
Examples of the aryl group having 6 to 10 carbon atoms may include a phenyl group and a naphthyl group and these groups may have substituents selected from halogen atoms, a hydroxyl group, an amino group, a methoxy group, an ethoxy group, an isopropyloxy group, a phenyl group, a naphthyl group, a phenoxy group, and a naphthyloxy group as a substituent.
Examples of the aryloxy group having 6 to 10 carbon atoms may include a phenoxy group and a naphthyl oxy group and these groups may have substituents selected from halogen atoms such as fluorine atom, chlorine atom, bromine atom or iodine atom, a hydroxyl group, an amino group, a methoxy group, an ethoxy ...,1 S14588 group, an isopropyloxy group, a phenyl group, a naphthyl group, a phenoxy group, and a naphthyloxy group as a substituent.
Ar' and Ar2 in the formula (1) respectively denote a divalent aromatic group which may have a substituent as described above, and as Ar' and Ar2, particularly an unsubstituted phenylene group or an unsubstituted naphthylene group is preferable and 1,3-phenylene group, 1,4-phenylene group, 1,3-naphthalenediyl group, 1,4-naphthalenediyl group, 1.5 -naphthalenediyl group, 1,6 -naphthalenedlyl group, 1, 7-naphthalenediyl group, 2, 6-naphthalenediyl group, 2,7 -naphthalenediyl group, 3,3' -biphenylylene group, 3,4'-biphenylylene group, and 4,4'-biphenylylene group are preferable.
Further, k in the formula (1) denotes 0, 1, or 2 and Z' denotes CO (carbonyl group), or SO2 (sulfonyl group), or COCO (dicarbonyl group). When k is 2, two Z' groups may be the same or different with each other and it is particularly preferable that Z' groups are the same.
The present invention is characterized in that, among Ar' and Ar2 groups as described above, at least one of Ar' and Ar2 has an acid group and when k is 1 or more, all of the groups represented by Ar' and Ar2 are preferable to have acid groups.
Herein, examples of the acid groups are weak acid groups such as a carboxyl group (-COOH), a phosphonic acid group (-P03H2) and a phosphoric acid group (-0P03H2); strong acid S14 588 groups such as a sulfonic acid group (-SO3H)and a sulfonylimido group (-SO2NHSO2-R, wherein R denotes an alkyl group having 1 to 6 carbon atoms or an aryl group having 6 to 10 carbon atoms); and a superacid group such as a perfluoroalkylenesulfonic acid group, a perfluorophenylenesulfonic acid group, and a perfluoroalkylenesulfonylimido group. Among them, a strong acid group or a superacid group whose acid dissociation constant represented by a pKa value is 2 or lower is preferable, for example, a sulfonic acid group, a perfluoroalkylenesulfonic acid group, or a perfluorophenylenesulfonic acid group is preferable. When these acid groups are protonic acids, they may form salts with such as alkali metal ions, alkaline earth metal ions, or ammonium ion and the acid groups forming the salts can easily be turned back to free acid forms by ion exchange with acid treatment after formation of the copolymerization of the present invention.
Preferable examples of the compound represented by the formula (1) are, for example, the following (1)-i to (1)-4: F_QlQ__F (1)-i ci__ _fQ__ci (1)-3 (SO3M)1 0 (SO3M) (SO3M)r 0 (S03M) F__-4Q_F (1)-2 cF-Q-i-Q--cI (1)-4 (SO3M)r (SO3M) (SO3M)r (SO3M) .s' S14588 wherein, r and s each independently denote 0 or 1 and r + s is 1 or 2; M denotes hydrogen atom, potassium atom, sodium atom, or lithium atom; and when there are a plurality of M, they may be same or different.
It is preferable that the above-mentioned (B) should contain a compound represented by the formula (2).
Herein, the acid groups are characterized in that when j is 0, Ar3 has the acid groups, and when j is 1 or higher, at least one of Ar3 and Ar4 have the acid groups. Ar3 and Ar4 denote a divalent aromatic group and examples of the divalent aromatic group may be groups same as the above-mentioned groups for Ar1 and Ar2 and when j is 2, Ar3 and two Ar4 groups may be the same or different with each other. In addition, a phenolic hydroxyl group among the nucleophilic groups represented by Y' is a group which can be converted into a phenolate group with a proper base in the condensation reaction process and reacts as a nucleophilic group and also a group existing in form of an ether bond in the copolymer of the present invention and is thus not regarded as an acid group.
These divalent aromatic groups may be substituted with an alkyl group having 1 to 10 carbon atoms which may have a substituent, an alkoxy group having 1 to 10 carbon atoms which may have a substituent, an aryl group having 6 to 10 carbon atoms which may have a substituent, an aryloxy group having 6 to 10 carbon atoms which may have a substituent, and specific examples S14588 of the alkyl group, the alkoxy group, the aryl group, or the aryloxy group are those same as the exemplified above.
Ar3 and Ar4 in the formula (2) denote a divalent aromatic group which may have the above-mentioned substituent group and as Ar3 and Ar4, particularly an unsubstituted phenylene group, an unsubstituted biphenylylene group, or an unsubstituted naphthylene group is preferable and 1,3-phenylene group, 1,4 -phenylene group, 1,3 -naphthalenediyl group, 1,4 -naphtha].enediyl group, 1,5 -naphthalenediyl group, 1,6 -naphthalenediyl group, 1,7 -naphthalenediyl group, 2,6 -naphthalenediyl group, 2,7 -naphthalenediyl group, 3,3' -blphenylylene group, 3,4' -biphenylylene group, or 44'-biphenylylene group is preferable.
In addition, j in the formula (2) denotes 0, 1 or 2; Q1 denotes a direct bond or a group selected from the following groups. When j is 2, two Q' groups may be the same or different with each other, and two Q' groups are preferably the same as each other.
S 14 5 88 9H3 0
U
-0--0--C--C----C--S-H2 H3 c5F3
II o fl
-s---c-
II I o Ph
Preferable examples of the compound represented by the formula (2) include the following (2)-i to (2)-12.
ii,J.ru -HO-C'--COH (2'-4 MO3S,-<SOsM * (2)-.L * SO3M,(MO3S) (SO3M) HO-(J--1-%.j-oPi (2)-S CF9 HO--0-CJP-OH (2)-5 MO3S Me 803M HOyOH (2)-2,(MO3S) (SO3M)5 HO-fl--I--j,-OH (2)-9 SO3M HO.,OH HOE-OH (2)-3 MO3S'''SO3M (2)-6 Me MO3S OH MO3S SO3M SO3M HOSOSM (2)-7 Ho-tj--C-Cj-oH (2)-b HO-l-OH MO3S SO3M MO3Stk,so3M (2)42 HO--S--OH (2)-Il MO3S-(J?-(JJ-SO3M Next, monomers having substantially no acid group will be described. Herein, "having substantially no acid group" means, similar to the above-mentioned hydroxyl group, a kind of acid groups which exists in a monomer as a nucleophilic group and disappears in the process of forming a copolymer is not regarded as an acid group in the present invention and therefore, S14 588 even such a monomer having an acid group is regarded as monomers having substantially no acid group in the present invention.
The above-mentioned (C) is preferably a compound represented by the formula (3).
Ar5 and Ar6 in the formula (3) denote, as a divalent aromatic, a hydrocarbon based aromatic group such as a phenylene group, a naphthylene group, a biphenylylene group and a fluorenediyl group and a heterocyclic group such as a pyridinediyl group, a qulnoxalinedlyl group, and a thiophenediyl and preferably a divalent hydrocarbon based aromatic group. When m is 1, Ar5 and Ar6 may be the same or different, and when m is 2, Ar5 and two Ar6 groups may be the same or different.
These divalent aromatic groups may be substituted with an alkyl group having 1 to 10 carbon atoms which may have a substituent, an alkoxy group having 1 to 10 carbon atoms which may have a substituent, an aryl group having 6 to 10 carbon atoms which may have a substituent, an ary].oxy group having 6 to 10 carbon atoms which may have a substituent, a nitro group, and a benzoyl group and specific examples of the alkyl group, the alkoxy group, the aryl group, or the aryloxy group are those same as exemplified above.
As Ar5 and Ar6, particularly an unsubstituted phenylene group, or an unsubstituted naphthylene group is preferable and 1, 3-phenylene group, 1, 4-phenylene group, 1, 3-naphthalenediyl S14588 group, 1,4-naphthalenediyl group, 1,5-naphthalenediyl group, 1, 6- naphthalenediyl group, 1, 7-naphthalenediyl group, 2, 6-naphthalenediyl group, 2, 7-naphthalenediyl group, 3,3' -biphenylylene group, 3,4' -biphenylylene group, or 4,4'-biphenylylene group is preferable.
In addition, m in the formula (3) denotes 0, 1, or 2 and Z2 denotes CO. SO2, or COCO. When m is 2, two Z2 groups may be the same or different and it is preferable that two Z2 groups are the same each other.
Preferable examples of the compound represented by the formula (3) include the following (3)-i to (3)-9.
(3)-i cl-i4D-cI (3)-6 (3)-2 (3)-7 (3)-3 FQ'F (3)-S NO2 (3)-4 F--F (3)-9
F FF F F F F**F
F FF F
It is preferable that the above-mentioned (D) preferably contains a compound represented by the formula (4) Ar7 and Ar8 in the formula (4) denote a divalent aromatic group and examples of the divalent aromatic group may be groups same as the above-mentioned groups for Ar5 and Ar6 and these S14 588 divalent aromatic groups may be substituted with an alkyl group having 1 to 10 carbon atoms which may have a substituent, an alkoxy group having 1 to 10 carbon atoms which may have a substituent, an aryl group having 6 to 10 carbon atoms which may have a substituent, an aryloxy group having 6 to 10 carbon atoms which may have a substituent, and specific examples of the alkyl group, the alkoxy group, the aryl group, or the aryloxy group are those same as the exemplified above.
As Ar7 and Ar8, particularly an unsubstituted phenylene group, an unsubstituted biphenylylene group, or an unsubstituted naphthylene group is preferable and 1, 3-phenylene group, 1,4 -phenylene group, 1,3 -naphthalenediyl group, 1.4-naphtha].enediyl group, 1,5-naphthalenediyl group, 1,6 -naphthalenediyl group, 1,7 -naphthalenediyl group, 2,6 -naphthalenediyl group, 2,7 -naphthalenediyl group, 3,3'-biphenylylene group, 3,4'-biphenylylene group, or 4,4'-biphenylylene group is preferable.
In addition, n in the formula (4) denotes 0, 1 or 2; Q2 denotes a direct bond or a group selected from the following groups. When n is 2, two Q2 groups may be the same as or different each other, and two Q2 groups are preferably the same each other.
S14 588 H2 9H3 9F3 0
II
-0----C --C--C--C--S-CH3 CF3 o Ph
II I
---0-Q;0
II I, I o Ph
Preferable examples of the compound represented by the formula (4) include the following (4)-i to (4)-26.
HO-O-O-O-OH (4)-i -QQ--OH (4)-b
HO
(4 \J) , I. t...r/ ..h' -HO-O-C-O-OH (4)3 (4)-li
HO OH Me
(4)4 HO-O--c,OH (4)42 Me Ho-D.lO-OH H/\/OH 4)-13 o 0 HO-D-LD_oH (4)-6 HO-Q-cLQ--OH (4)-14 CF3 (4)-7 Me Me CF3 HO_(D-c-(D-c!..-OH (4)-is
HO
(4)-8 Me Me (>9 S].4588 HO-G-oH (4)-16 -OH (4)-23 -jkJ (4)-20 HO''' HO-Q-.OH (4)-17 OH (4)-24 HO-f %-OH OO HO OH (4)-1 HO (4)-18 HO OH HO.1yOH (4)-25 HO-8-OH (4)-19 ( )-22 (4)-26 A copolymer of the present invention can be produced by either mixing a mixture of the above-mentioned (A), (B), (C).
and (D), or mixing monomers having nucleophilic groups, for example, (B) and (D) and separately mixing monomers having leaving groups, for example, (A) and (C) and furthermixing the respective mixtures, and successively subjecting to nucleophilic condensation reaction of the monomers having nucleophilic groups and the monomers having leaving groups.
A preferable copolymer of the present invention can be obtained using the compounds represented by the above-mentioned formulas (1) to (4) as monomers and mixing and condensing them.
An example includes a method of carrying out nucleophilic condensation of the compounds represented by the formulas (1) to (4) in the presence of a base.
Specifically, the compounds represented by the formulas (1) to (4) and a basic compound are charged into a reaction solvent and mixed. The order of mixing is not particularly limited, however, preferable mixing method is previously S14588 charging the compound represented by the formula (2), the compound represented by the formula (4), the basic compound and thesolvent, and then mixing the above-mentioned (1) and (3); or mixing the compounds represented by the formulas (1) to (4) and the solvent, and then charging and mixing the basic compound; or charging and mixing the compounds represented by the formulas (1) to (4), the basic compound and the solvent.
In the condensation, the reaction temperature is preferably 20 to 300 C and further preferably 50 to 250 C and the reaction time can be carried out preferably 0.5 to 500 hours and more preferably 1 to 100 hours. In addition, with respect to the pressure at the time of the reaction, the pressure may be pressurized or reduced, and normal pressure (about atmospheric pressure) is preferable since it is convenient in terms of facilities. As a reaction solvent, alcohol based solvents such as methanol, ethanol, isopropanol, and butanol; ether based solvents such as diethyl ether, dibutyl ether, diphenyl ether, tetrahydrofuran, dioxane, dioxolane, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, propylene glycol monomethyl ether, and propylene glycol monoethyl ether; ketone based solvents such as acetone, methyl isobutyl ketone, methyl ethyl ketone, and benzophenone; halogen based solvents such as chloroform, dichioromethane, 1,2-dichloroethane, 1,1,2, 2-tetrachloroethane, chlorobenzene, and dichlorobenzene; amide based solvents such as S14 588 N,N-dimethylacetainide (hereinafter, sometimes abbreviated as DMAc), N-methylacetamide, N,N-dimethylformamjde (hereinafter, sometimes abbreviated as DMF), N-methylformamide, formamide, and N-methyl-2-pyrroljdone (hereinafter, sometimes abbreviated as NM?); esters such as methyl formate, methyl acetate, and 7-butyrolactone; nitriles such as acetonitrile and butyronitrile; sulfoxydimethyl suif oxide (hereinafter, sometimes abbreviated as DMSO), diphenylsulfone, sulfolane, and the like can be used. The reaction solvents may be used alone, or two or more kinds of the reaction solution may be used in rmhintjon The used amount of the reaction solvents is 1.0 to 200.0 times by weight, preferably 2.0 to 100.0 times by weight, based on the total weight of the used monomers. Here, it is preferable to remove water of by-product in the initial period of condensation reaction or during the condensation reaction. The method of removing the water to be employed may be the method of removing water in form of an azeotropy by making toluerie and xylene coexist in the reaction system and the method of dehydrating by making water absorbent such as a molecular sieve coexist in the reaction system. As the above-mentioned basic compound, sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, sodium hydrogen carbonate, or potassium hydrogen carbonate may be used, and the mixture of two or more basic compounds may be used and especially potassium carbonate, sodium carbonate, or sodium hydroxide is preferable.
S14588 Here, the used amount of the basic compound may be 0.90 to 10.00 times by mole equivalent, preferably 1.00 to 3.00 times by mole equivalent based on the total mole equivalent to the nucleophilic groups in the used monomers in the condensation reaction.
Another embodiment in a preferable production method of the copolymer of the present invention may be a method of previously reacting the compound represented by the formula (2) and the compound represented by the formula (4) with the basic compound, and then charging the compounds represented the formula (1) and the compound represented by the formula (3) and mixing the compounds, and successively carrying out condensation. That is, after compound represented by the formula (2), the compound represented by the formula (4), and the basic compound are mixed in the reaction solvent and, if necessary, heating treatment is carried out to react the basic compound with the compound represented by the formula (2) and the compound represented by the formula (4), the compounds represented by the formula (1) and the compound represented by the formula (3) are added to the mixture and then the condensation reaction is carried out. The reaction solvent to be used and used amount thereof and the basic compound to be used and used amount thereof are the same as described above and the reaction temperature and the reaction time relevant to the condensation reaction are in the same ranges as described S14588 above. Removal of the water of by-product may be carried out in the same manner as described above or it may be a method of sufficiently removing water in form of azeotropy by making toluene and xylene coexist in the reaction system upon mixing the compound represented by the formula (2), the compound represented by the formula (4), and the basic compound with the reaction solvent, and successively adding the compound represented by the formula (1) and the compound represented by the formula (3) to the mixture and carrying out condensation reaction.
Consequently, the copolymer of the present invention is obtained. With respect to the copolymer, the weight composition ratio of the structural unit into which the acid group is introduced and the structural unit into which substantially no acid group is introduced is not particularly limited, however, in general, the ratio of [structural unit into which the acid group is introducedi: (structural unit into which substantially no acid group is Introduced] is 3: 97 to 70: 30, preferably 5 95 to 45: 55, more preferably 10: 90 to 40: 60, and even more preferably 20 80 to 35 65. The copolymer having the ratio of the structural unit into which the acid group is introduced within the above-mentioned range, becomes a polymer electrolyte membrane having both of proton conductivity and water-proofness at a high level, when the copolymer is used for a polymer electrolyte membrane of a S14588 separating membrane of a fuel cell.
Here, the weight composition ratio of the structural unit into which the acid group is introduced and the structural unit into which substantially no acid group is introduced can be controlled by the used amount of the monomers and, for example, the weight composition ratio can be properly controlled by changing the charging (mixing) mole ratio in the initial reaction stage of the total mole amount of the monomers having acid groups, containing the compound represented by the formula (1) and the compound represented by the formula (2) and the total mole amount of the monomers having substantially no acid group, containing the compound represented by the formula (3) and the compound represented by the formula (4).
On the basis of equivalent amount of the acid group per 1 g of the copolymer, that is, the ion exchange capacity, the introduction amount of the acid group in the entire copolymer is preferably 0.1 meq/g to 4.0 meq/g, more preferably 0.5 meq/g to 2.5 meq/g. and even more preferably 1.3 meq/g to 2.3 meq/g.
The reason for that the ion exchange capacity is preferably in the above-mentioned range is the same reason for the ratio of the content weight the structural unit into which the acid group is introduced in the copolymer and the ion exchange capacity can also be controlled arbitrarily in the same manner of changing the charging (mixing) mole ratio of the respective monomers in the initial reaction stage.
S14588 The average molecular weight of the copolymer of the present invention is preferably 5000 to 1000000 and especially further preferably 15000 to 200000 on the basis of the number average molecular weight converted Into polystyrene.
The above-mentioned average molecular weight can be controlled in accordance with such the ratio of total mole equivalent amount of the nucleophilic groups of the monomers to be used and the total mole equivalent of the leaving groups and the reaction time.
Next, the case of using the copolymer of the present invention for a separating membrane (polymer electrolyte membrane) of an electrochemical device such as a fuel cell will be described.
In this case, the copolymer of the present invention may be used, in general, In form of a membrane. A method for converting the copolymer into a membrane is not particularly limited; however a method of forming a membrane from a solution (a solution cast method) is preferably employed.
Specifically, the copolymer Is dissolved in a suitable solvent and the obtained solution is applied to a glass plate and the solvent is removed to form a membrane. The solvent to be used for membrane formation is not particularly limited if it is capable of dissolving the copolymer and removing thereafter and water and non-protonic polar solvents such as N,N-dimethy].formamlde, N, N-dimethylacetamide, ) S14588 N-methyl-2-pyrrolidone, and dimethyl suif oxide; chlorinated solvents such as dichioromethane, chloroform, 1, 2-dichioroethane, chlorobenzene, and dichlorobenzene; alcohols such as methanol, ethanol, and propariol; and alkylene glycol monoalkyl ethers such as ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, propylene glycol monomethyl ether, and propylene glycol monoethyl ether are preferably used. They may be used alone and if necessary two or more kinds of solvents may be used in form of a mixture.
Especially, DMSO, DMF, DMAc, andNNP are preferable, having high solubility of polymers.
The thickness of the membrane is not particularly limited and preferably 10 to 300 pm and particularly preferably 20 to pm. If a film is thinner than 10 pm, the practical strength is sometimes insufficient and if a film is thicker than 300 pm, the membrane resistance becomes high and the properties of the electrochemical device tend to deteriorate. The thickness of the membrane can be controlled by the concentration of the solution and the application thickness of the solution to the substrate.
As a purpose of improving the various kinds of physical properties of the polymer electrolyte membrane, such as a plasticizer, a stabilizer, and a release agent to be used for common polymers may be added to the copolymer of the present invention. In addition, it is also possible that another S14588 polymer is composite alloyed with the copolymer of the present invention by a method for mixing and cocasting the polymer in the same solvent.
To make water control easy in application to a fuel cell, it is also known that inorganic or organic fine particles are added as a water retention agent. Any of these conventionally known methods can be employed unless it is contradictory for the purpose of the present invention. Further, in order to improve the mechanical strength of the polymer electrolyte membrane comprising the polymer electrolyte containing the copolymer of the present invention, electron beam and radiation beam may be radiated to cross-link the polymer electrolyte composing the polymer electrolyte membrane.
In addition, in order to further improve strength, flexibility, and durability of the polymer electrolyte membrane, it is allowed to impregnate a porous substrate with the copolymer of the present invention to produce a polymer electrolyte composite membrane. A conventionally known method can be employed for a compositing method. The porous substrate is not particularly limited if it can satisfy the above-mentioned purpose of the use and examples may include, such as a porous membrane, a woven fabric, a non-woven fabric, and fibril and they may be used regardless of the shape and quality of material thereof.
When the polymer electrolyte composite membrane using the S14 588 copolymer of the present invention is used as a separating membrane for fuel cells, the thickness of the porous substrate is 1 to 100 pm, preferably 3 to 30 pm, and more preferably 5 to 20 pm; the pore diameter is 0.01 to 100 pm and preferably 0.02 to 10 pm; and the porosity is 20 to 98% and preferably 40 to 95%. If the thickness of the porous substrate is too thin, the effect of reinforcing the strength after compositing or the reinforcing effect of imparting flexibility and durability becomes insufficient and thus gas leakage (cross leakage) is caused easily. In addition, if the thickness of the membrane is too thick, the electric resistance becomes high and the obtained composite membrane becomes improper as the separating membrane of a solid polymer fuel cell. If the pore diameter is too small, it becomes difficult to fill the copolymer of the present invention and if it is too high, the reinforcing effect on the solid polymer electrolyte becomes weak. If the porosity is too low, the resistance of the composite membrane becomes high and if it is too high, the strength of the porous substrate itself generally becomes weak and the reinforcing effect is reduced.
From the viewpoint of the heat resistance and the reinforcing effect of the physical strength, the above-mentioned porous substrate is preferably a substrate comprising an aliphatic based polymer, an aromatic based polymer, or a fluorine-containing polymer.
S14 588 Next, a fuel cell of the present invention will be described. As the fuel cell using the polymer electrolyte membrane, while there are, for example a solid polymer fuel cell using hydrogen gas as fuel and a direct methanol solid polymer fuel cell to which methanol as fuel is directly supplied, the copolymer of the present invention may be used preferably for both.
Examples of the fuel cell obtained according to the present invention may be those using the copolymer of the present invention for a polymer electrolyte membrane and/or a polymer electrolyte composite membrane and those using the polymer electrolyte of the present invention for a polymer electrolyte in a catalyst layer.
The fuel cell using the copolymer of the present invention for a polymer electrolyte membrane or a polymer electrolyte composite membrane can be produced by conjugating a catalyst and a gas diffusion layer on both sides of the polymer electrolyte membrane or the polymer electrolyte composite membrane. Conventionally known materials can be used for the gas diffusion layer and a porous carbon woven fabric, carbon non-woven fabric, or carbon paper is preferable for efficiently transporting a raw material gas to the catalyst.
Herein, the catalyst is not particularly limited as far as it can activate redox reaction of hydrogen or oxygen and conventionally known ones may be used, however, fine particles S14 588 of platinum are preferably used. Fine particles of platinum are often preferably used with being supported on particulate or fibrous carbon such as activated carbon and graphite. In addition, a paste obtained by mixing platinum supported on carbon with an alcohol solution of a perfluoroalkylsulfonic acid resin as a polymer electrolyte is applied to a gas diffusion layer, a polymer electrolyte membrane, or a polymer electrolyte composite membrane and dried to obtain the catalyst layer.
Specific methods may be conventionally known method such as those described in, for example, J. Electrochem. Soc.: Electrochemj.cal Science and Technology, 1988, 135(9), 2209.
Examples of the fuel cell using the copolymer of the present invention as the polymer electrolyte in the catalyst layer may include those using the copolymer of the present invention in place of a perfluoroalkylsulfonic acid resin composing the above-mentioned catalyst layer. When the catalyst layer containing the copolymer of the present invention is used, the polymer electrolyte membrane is not limited to the membrane using the copolymer of the present invention and conventionally known polymer electrolyte membranes may be used.
When the catalyst layer using the copolymer of the present invention is obtained, a solvent to be used for preparing a catalyst paste is arbitrary and not particularly limited; however it is desired that the solvent be capable of dissolving S14588 components besides the solvents composing the catalyst paste, or dispersing the components evenly in molecular level, or forming agglomerates in nano-to micro-level and dispersing the agglomerates. The solvent may be a single solvent or a mixture of a plurality of solvents and those exemplified as the solvents usable when a membrane of the copolymer of the present invention is formed, may be used.
Other components composing the catalyst paste are arbitrary and not particularly limited; however the components may sometimes contain a water-repelling material such as PTFE to improve the water-repellency of the catalyst layer, a pore forming material such as calcium carbonate to improve the gas diffusion property of the catalyst layer, a stabilizer such as a metal oxide and a polymer having phosphonic acid group to improve the durability.
The catalyst paste is obtained by mixing the above-mentioned polymer electrolyte, a catalytic material and/or a conductive material supporting a catalytic material on a surface, a solvent, and other components by a conventionally known method. The mixing method may include an ultrasonic dispersion apparatus, a homogenizer, a ball mill, a planetary ball mill, and a sand mill.
A method of directly applying the catalyst paste is not particularly limited and an already known method such as a die coater, a screen printing, a spraying method, and an ink jet S14 588 method can be employed; however a spraying method is preferable since its operation is industrially convenient.
As the spraying method of the catalyst paste, the apparatus and method disclosed in, for example, Japanese Unexamined Patent Publication No. 2004-89976 can be specifically illustrated and the method can be carried out using them. That is, a polymer electrolyte is set on a stage and a catalyst ink is directly applied to the polymer electrolyte.
In a spraying method, the catalyst ink is sprayed in particle state out of a jetting outlet and is adhered on the polymer electrolyte. It is desired that the stage should be heated to remove the solvent quickly after application and the temperature is preferably 50 C to 150 C. If the temperature is within the above-mentioned range, the solvent of the catalyst ink is easy to be removed quickly and the tendency of thermal damages on the polymer electrolyte membrane is small and therefore, it is preferable. As described, the solvent is removed by heating the stage successively to the application by the spraying method to produce the catalyst layer on the polymer electrolyte membrane. For the purpose of removing the solvent completely, the membrane on which the catalyst layer is formed may be put in such as a heated oven and dried or, if necessary, drying in a vacuum can be carried out. To remove the solvent more quickly, a preferable solvent composing the catalyst paste is a solvent having a boiling point of 150 C or ) lower and water, alcohol based solvents such as methanol and ethanol, ether based solvents such as diethyl ether and tetrahydrofuran, and solvent mixture thereof may be used and the copolymer of the present invention is also excellent in that it is easy to dissolve in these solvents. The catalyst paste may be sprayed a plurality of times and respective layers obtained by spraying may be coated over on the polymer electrolyte membrane to form a multi-layer coating.
Hereinafter, the invention will be described with reference to Examples, however it is not intended at all that the invention be limited to the illustrated Examples.
Measurement of molecular weight: The number average molecular weight (Mn) based on polystyrene standard calibration, was measured by gel permeation chromatography (GPC) in the following conditions.
GPC measurement apparatus: HLC-8220 GPC, manufactured by TOSOH Co., Ltd. Column: TSKge1 GHMHR-M, manufactured by Showa Denko K.K.
Column temperature: 40 C mobile phase solvent: DMAc (adding LiBr in a concentration of 10 mmol/dzn3) solvent flow rate: 0.5 mL/min Measurement of proton conductivity: Measured by an AC method at a temperature of 80 C and relative humidity of 90%.
S14 588 Measurement of ion exchange capacity: Measured by a titration method.
Measurement of water absorption ratio: After a dried polymer electrolyte membrane was weighed and immersed in deionized water at 100 C for 2 hours, the water absorption ratio was calculated from the increase of the membrane weight amount and the ratio to the above-mentioned dried membrane was calculated.
Example 1
Production of copolymer A Polymerization was carried out by charging a 200 mL separable flask equipped with a Dean-Stark apparatus with 3.50 g (15.33 mmol) of potassium hydroquinonesulfonate, 6.29 g (33.76minol)of4,4'-dihydroxybiphenyl, and7.36g(53.24mmol) of potassium carbonate and carrying out azeotropic dehydration in 121 mL of dimethyl sulfoxide and 70 mL of toluene under argon atmosphere at bath temperature of 150 C (inner temperature of 5 C) for 1.5 hours. After 1.5 hours, toluene was removed to the outside of the system and the reaction product was spontaneously cooled to room temperature. Thereafter, 9.03 g (18.40 mmol) of 3,3'-sulfonylbis(potassium 6-fluorobenzenesulfonate) and 7.80 g (30.69 mmol) of 44'-difluorodiphenylsulf one were added to the reaction product and further reaction was carried out at an inner ) temperature of 150 C for 11 hours. The reaction was traced by GPC measurement. On completion of the reaction, the reaction solution was spontaneously cooled to 80 C and dropwise added to 3 L of an aqueous 2 M hydrochloric acid solution. The precipitated white polymer was filtered and washed until pH of the washing filtrate became about 7 and thereafter, a step of treatment with water at 80 C for 2 hours was repeated twice.
The resulting polymer was dried by an oven (80 C) to obtain 20.86 g (yield 92%) of the following copolymer A. Thereafter, the following dried polymer was dissolved in N-methylpyrrolidone and then filtered to obtain a solvent solution in a concentration of 18% by weight. Then, the solution was applied to a glass substrate and N-methylpyrrolidone was removed at 80 C in a fully evacuated oven for about 5 hours. Thereafter, a step of treatment with 2N hydrochloric acid for 1 hour was repeated twice and washed with flowing water (deionized water) for 8 hours to obtain a polymer electrolyte membrane. A thickness of the membrane was 33 pm.
Copolymer A The copolymer A was a polymer having the following structural units.
S14 588 (A-a) (A-b) (A-c) HO3S SO3H _(f-O.). (A-d) SO3H The molar ratio of the respective structural units (A-a) (A-b), (A-c), and (A-d) calculated from the charged amounts to the total of the above-mentioned structural units: (A-a) : (A-b) (A-c) : (A-d) = 2.00: 2.20: 1.20: 1.00 The ion exchange capacity calculated from the molar ratio of the above-mentioned structural units: 2.30 meqfg Mn 8.1Ox10 Actually measured value of ion exchange capacity: 2.10 meq/g Membrane production: NMP solution cast method: membrane thickness 33 pm Proton conductivity: 1.56x101 S/cm Water absorption ratio: 169%
Example 2
Production of copolymer B Polymerization was carried out by charging a 200 mL ) separable flask equipped with a Dean-Stark apparatus with 3.50 g (15.33 nunol) of potassium hydroquinonesulfonate, 7.87 g (42.25 mxnol) of 4,4' -dihydroxybiphenyl, and 8.65 g (62.57 mmol) of potassium carbonate and carrying out azeotropic dehydration in 138 mL of dimethyl suif oxide and 70 mL of toluene under argon atmosphere at bath temperature of 150 C (inner temperature of 5 C) for 1.5 hours. After 1. 5 hours, toluene was removed to the outside of the system and the reaction product was spontaneously cooled to room temperature. Thereafter, 9.03 g (18.40 nimol) of 3,3'-sulfonylbis(potassiuin 6-fluorobenzenesulfonate) and 9.96 g (39.18 mmol) of 4,4'-difluorodiphenylsulf one were added to the reaction product and further reaction was carried out at an inner temperature of 150 C for 5 hours. The reaction was traced by GPC measurement. On completion of the reaction, the reaction solution was spontaneously cooled to 80 C and dropwise added to 3 L of an aqueous 2 M hydrochloric acid solution. The precipitated white polymer was filtered and washed until pH of the washing filtrate became about 7 and thereafter, a step of treatment with water at 80 C for 2 hours was repeated twice.
The resulting polymer was dried by an oven (80 C) to obtain 23.62 g (yield 91%) of the following copolyrner B. The membrane production was carried out according to Example 1.
Copolymer B ) The copolymer B was a polymer having the following structural units.
-(-OtO-)-(B-a) _((j.-)-.o.)_ (B-b) (B-c) HO3S SO3H (B-d) SO3H The molar ratio of the respective structural units (B-a). (B-b), (B-c), and (B-d) calculated from the charged amounts to the total of the above-mentioned structural units: (B-a) : (B-b) (B-c) : (B-d) = 2.56: 2.76: 1.20 1.00 The ion exchange capacity calculated from the molar ratio of the above-mentioned structural units: 2.00 meq/g Mn 8.20x10 Actually measured value of ion exchange capacity: 1.80 meq/g Membrane production: NMP solution cast method: membrane thickness 26 pm Proton conductivity: 8.84x102 S/cm Water absorption ratio: 94% Comparative Example 1 S14 588 Production of copolymer C Polymerization was carried out by charging a 200 mL separable flask equipped with a Dean-Stark apparatus with 6. 18 g (27.09 mmol) of potassium hydroquinonesulfonate, 10.00 g (39.33 mmol) of 4,4'-difluorodiphenylsulfone, 2.28 g (12.25 mmol) of 4,4'-dihydroxybiphenyl, and 5.98 g (43.26 mmol) of potassium carbonate and carrying out azeotropic dehydration in 74 mL of dimethyl sulfoxide and 40 mL of toluene under argon atmosphere at bath temperature of 150 C (inner temperature of 5 C) for 3 hours. After 3 hours, toluene was removed to the outside of the system and reaction was carried out at an inner temperature of 150 C for 12 hours. The reaction was traced by GPC measurement. On completion of the reaction, the reaction solution was spontaneously cooled to 80 C and dropwise added to 3 L of an aqueous 2 M hydrochloric acid solution. The precipitated white polymer was filtered and washed until pH of the washing filtrate became about 7 and thereafter, a step of treatment with water at 80 C for 2 hours was repeated twice.
The resulting polymer was dried by an oven (80 C) to obtain 14.67 g (yield 92%) of the following copolymer C. The membrane production was carried out according to Example 1.
Copolymer C The copolymer C was a polymer having the following structural units.
S14 588 -(j-$-(j-o)-(C-a) -(-(J-t_o-)-(C-b) -(-c-} SO3H The molar ratio of the respective structural units (C-a), (C-b), and (C-c) calculated from the charged amounts to the total of the above-mentioned structural units: (C-a) : (C-b) : (C-c) 1.45: 0.45: 1.00 The ion exchange capacity calculated from the molar ratio of the above-mentioned structural units: 1.71 meq/g Mn 4.06x10 Actually measured value of ion exchange capacity: 1.56 meq/g Membrane production: NMP solution cast method: membrane thickness 54 pm Proton conductivity: 4.60x102 S/cm Water absorption ratio: 302% Comparative Example 2 Production of copolymer D Polymerization was carried out by charging a 500 mL separable flask equipped with a Dean-Stark apparatus with 12.74 g(50.lOmrnol) of 4,4'-difluorodiphenylsulfone, 18.62g (100.00 S14 588 mmol) of 4,4'-dihydroxybiphenyl, and 25.08 g (50.00 mmol) of 3,3' -sulfonyl bis(potassium 6-fluorobenzenesulfonate), 15.20 g (110.00 inmol) of potassium carbonate and carrying out azeotropic dehydration in 160 mL of N-methyl-2-pyrrolidone and mL of toluene under argon atmosphere at inner temperature of 140 C for 5 hours. After 3 hours, toluene was removed to the outside of the system and reaction was carried out at an inner temperature of 170 C for 8 hours. The reaction was traced by GPC measurement. On completion of the reaction, the reaction solution was spontaneously cooled to room temperature and dropwise added to 500 mL of an aqueous 2 H hydrochloric acid solution. After the precipitated white polymer was washed with water, the polymer was pulverized to powder and then was washed again with water until pH of the washing water became about 7.
Thereafter, a step of treatment with water at 95 C for 2 hours was repeated twice. The resulting polymer was dried in reduced pressure by an oven (60 C) to obtain 45.31 g (yield 93%) of the following polymer. Themembrane production was carried out according to Example 1.
Copolymer D The copolymer D was a polymer having the following structural units.
S14 588 ffQ_o3. (D-a) HO3S SO3H (0-b) The molar ratio of the respective structural units (D-a), (D-b), and (D-c) calculated from the charged amounts to the total of the above-mentioned structural units: (D-a) : (D-b) : (D-c) 1.00: 2.00: 1.02 The ion exchange capacity calculated from the molar ratio of the above-mentioned structural units: 2.08 meq/g Mn 7.70x10 Actually measured value of ion exchange capacity: 1.97 meq/g Membrane production: NMP solution cast method: membrane thickness 26 pin Proton conductivity: 0.97x101 S/cm Water absorption ratio: 460%
Example 3
Production of copolymer E Polymerization was carried out by charging a 200 mL separable flask equipped with a Dean-Stark tube with 3.00 g (13.14 mmol) of potassium hydroquinonesulfonate, 8.31 g (24.57 S14588 mol) of 4,4'-dihyd.roxy-3,3'-diphenylbiphenyl, and 5.42 g (39.21 mmol) of potassium carbonate and carrying out azeotropic dehydration in 105 mL of dimethyl sulfoxide and 60 mL of toluene under argon atmosphere at bath temperature of 150 C (inner temperature of 130 5 C) for 2 hours. After 2 hours, toluene was removed to the outside of the system and the reaction product was spontaneously cooled to room temperature. Thereafter, 7.17 g (15.77 mmol) of 4,4' -difluorobenzophenone-3, 3' -dipotassium disulfonate and 5.57 g (21.90 mmol) of 4,4' -difluorodiphenylsuif one were added to the reaction product and further reaction was carried out at an inner temperature of 150 C for 25 hours. The reaction was traced by GPC measurement. On completion of the reaction, the reaction solution was spontaneously cooled to 80 C and dropwise added to 3 L of an aqueous 2 M hydrochloric acid solution.
The precipitated white polymer was filtered and washed until pH of the washing filtrate became about 7 and thereafter, a step of treatment with water at 60 C for 2 hours was repeated twice.
The resulting polymer was dried by an oven (80 C) to obtain 18.96 g (yield 91%) of the following copolymer E. Thereafter, the membrane production was carried out according to Example 1.
Copolyrner E The copolymer E was a polymer having the following structural units.
S14588 -*Y& (E-b) (c) HO3S SO3H (E-d) SO3H The molar ratio of the respective structural units (E-a), (E-b), (E-c), and (E-d) calculated from the charged amounts to the above-mentioned structural units: (E-a) : (E-b) : (E-c) : (E-d) = 1.67: 1.87: 1.20: 1.00 The ion exchange capacity calculated from the molar ratio of the above-mentioned structural units: 2.00 meq/g Mn 6.2x10 Actually measured value of ion exchange capacity: 1.90 meq/g Membrane production: NNP solution cast method: membrane thickness 33 pm Proton conductivity: 0.95x10' S/cm Water absorption ratio: 88%
Example 4
Production of copolymer F S14588 Polymerization was carried out by charging a 200 mL separable flask equipped with a Dean-Stark apparatus with 3.00 g (13.14 mmol) of potassium hydroquinonesulfonate, 5.79 g (17. 11 mmol) of 4,4' -dihydroxy-3.3, -diphenylbiphenyl, 3.91 g (17.11 rnmol) of 2,2'-bis(4-hydroxyphenyl)propane, 7.74 g (15.77 rnmol) of 3,3'-sulfonyl bis(potassium 6-fluorobenzenesulfonate), 8.04 g (31.60 mmol) of 44'-d fluorodiphenylsulfone, and 6.87 g (49.74 mmol) of potassium carbonate and carrying out azeotropic dehydration in 114 mL of dimethyl suif oxide and 40 mL of toluene under argon atmosphere at bath temperature of 150 C (inner temperature of 5 C) for 2 hours. After 2 hours, toluene was removed to the outside of the system and the reaction was further carried out at 150 C for 3 hours. The reaction was traced by GPC measurement. On completion of the reaction, the reaction solution was spontaneously cooled to 80 C and dropwise added to 1 L of an aqueous 2 M hydrochloric acid solution. The precipitated polymer was filtered and washed until pH of the washing filtrate became about 7 and thereafter, a step of treatment with water at 80 C for 2 hours was repeated twice.
The resulting polymer was dried by an oven (80 C) to obtain 23.31 g (yield 87%) of the following copolymer F. The membrane production was carried out according to Example 1.
Copolymer F \i S14588 The copolymer F was a polymer having the following structural units. (F-a)
-({j4--CJ-o (F-b) (F-c) (F-d) HO3S SO3H f/\ \ -.( ..,i t. SO3H
The molar ratio of the respective structural units (F-a), (F-b), (F-c), (F-d),and (F-e) calculated from the charged amounts to the total of the above-mentioned structural units: (F-a) (F-b) : (F-c) : (F-d) : (F-e) = 2.40: 1.30: 1.30: 1.20: 1.00 The ion exchange capacity calculated from the molar ratio of the above-mentioned structural units: 1.80 meq/g Mn 3.3x1O Actually measured value of ion exchange capacity: 1.62 meq/g Membrane production: NMP solution cast method: membrane thickness 60 pm Proton Conductivity: 0.62x101 S/cm Water absorption ratio: 104% S14 588
Example 5
[Production of catalyst paste] A uniform copolymer A solution (concentration of copolymer A: 5% by weight) was produced by mixing 95 g of a solvent mixture of water: ethanol = 1: 9 (ratio by weight) and 5 g of the copolymer A obtained in Example 1. Separately, 0.64 g of platinum-supporting carbon (SA 50 BK, manufactured by N.E. CHEMCAT CORPORATION; platinum support amount 50% by weight) was charged to 11 mL of ethanol and further 1.05 g of the previously prepared copolymer A solution was added to the mixture. After the obtained mixture was treated for 1 hour by ultrasonic treatment, it was stirred by a stirrer for 6 hours to obtain a catalyst ink A. [Production of polymer electrolyte membrane] Referring to Japanese Unexamined Patent Publication No. 2005-139432, a polymer electrolyte membrane comprising the block copolymer type polymer electrolyte represented by the following formula was obtained. Specifically, a first polymer compound having ion exchange groups and a second polymer compound having substantially no ion exchange group were respectively synthesized as described below and they were further subjected to coupling to synthesize the block copolymer type polymer electrolyte. C.
(Synthesis of first polymer compound) To a flask provided with an azeotropic distillation apparatus was added 283.68 g of 4,4' -dif1uorodiphenylsulfone-3, 3' -dipotassium disulfonate, 120.00 g of Potassium 2, 5-dihydroxybenzenesulfonate, 1778 g of DMSO, and 279 g of toluene under argon atmosphere and while they were being stirred at room temperature, bubbling of argon gas was carried out for 1 hour.
Thereafter, 76.29 g of potassium carbonate was added to the obtained mixture and the mixture was heated and stirred at 140 C for azeotropic dehydration. Thereafter, while toluene was removed by distillation, heating was continued to obtain a DM50 solution of the first polymer compound. The total heating time was 16 hours. The obtained solution was spontaneously cooled at room temperature.
The first polymer compound had Mn of 3.0x10.
(Synthesis of second polymer compound) To a flask provided with an azeotropic distillation apparatus was added 247.55 g of 4,4'-difluorodiphenylsulfone, 164.44 g of 2,6-dihydroxynaphthalene, 902 g of DMSO, 902 g of NMP, and 310 g of toluene under argon atmosphere and while they were being stirred at room temperature, bubbling of argon gas was carried out for 1 hour.
C
Thereafter, 156.09 g of potassium carbonate was added to the obtained mixture and the mixture was heated and stirred at 100 C for vacuum azeotropic dehydration. Thereafter, toluene was removed by distillation after 17 hours and thereafter, heating was further continued at 100 C. The total heating time was 19 hours. The obtained solution was spontaneously cooled at room temperature to obtain a NMP/DMSP mixed solution of the second polymer compound.
The second polymer compound had Mn of 2.7x10.
(Synthesis of block copolymer) While the obtained NMP/DMSP mixed solution of the second polymer compound was being stirred, all of the above-mentioned DMSO solution of the first polymer compound, 610 g of DMSO, and 1790 g of NMP were added to the mixture solution and block copolymerization reaction was carried out at 150 C for 39 hours.
The obtained reaction solution was dropwise added to a large quantity of 2N hydrochloric acid and immersed for 1 hour.
Thereafter, the precipitate produced was separated by filtration and again immersed in 2N hydrochloric acid for 1 hour.
The obtained precipitate was separated by filtration and washed with water and then immersed in a large quantity of hot water at 95 C for 1 hour. After a solid was separated by filtration, the solid was again immersed in a large quantity of hot water at 95 C for 1 hour. After the solid was separated by filtration, S14588 the solid was dried overnight at 80 C to obtain a block copolyrner.
Membrane production was carried out in the same manner
as Example 1.
[Obtained block copolytner type polymer electrolyte] HO3 SO3H 8031-I m In the formula, ni and ml denote the average polymerization degree of the respective blocks of the block copolymer type polymer electrolyte.
Mn 7.9x1O.
Actually measured value of ion exchange capacity: 1.94 meq/g Membrane production: NMP solution cast method: membrane thickness: 27 pm Proton conductivity: 2.37x10' S/cm Water absorption ratio: 115% Being calculated from charging, ni = 36.2 and ml =10.5. [MEAl
The polymer electrolyte membrane comprising the block copolymer type polymer electrolyte obtained in the above-mentioned manner was cut out in a square shape and set ( on a heating stage and the catalyst ink A was applied to a region of 5.2 cm square in the center part of the main face of the membrane by a spraying method. The distance from the outlet to the membrane was 5 cm and the stage temperature was set at 76 C. After the application, the membrane was left for 3 minutes on the stage to remove the solvent and form a catalyst layer. The polymer electrolyte membrane provided with the catalyst layer on one face in the above-mentioned manner was turned upside down and set on the heating stage and again a catalyst layer was formed using the catalyst ink A also on the other face in the same manner as the former catalyst layer to obtain a membrane-electrode assembly. The platinum amount in the catalyst layers calculated from the weight composition of the catalyst layers and the catalyst layer weight was 0.6 mg/cm2 for each face.
[Cell assembly for fuel cell evaluation) A fuel cell was produced using a commercially available JARI standard cell. That is, a carbon cloth as a gas diffusion layer and a separator made of carbon having a groove formed by cutting processing for a gas channel were arranged in both catalyst layers of the membrane-electrode assembly obtained in the above-mentioned manner and current collectors and end plates were successively arranged further outside thereof and the arranged parts were fastened by bolts to assemble a fuel ( cell with an effective membrane surface area of 25 cm2.
[Fuel cell evaluation] While the obtained fuel cells was kept at 80 C, humidified hydrogen and humidified air were supplied to an anode and a cathode, respectively. At that time, the back-pressure at the gas outlet of the cell was adjusted to be 0.1 MPaG. The humidification of the respective raw material gases was carried out by leading the gases to bubblers and the water temperature of the bubbler for hydrogen was set to be 45 C and the water temperature of the bubbler for air was set to be 55 C.
Herein, the gas flow rate of hydrogen was set to be 529 mL/min and the gas flow rate of air was set to be 1665 mL/min.
The current density at 0.2 V of the cell potential was 1.5 A/cm.
The cell potential at 0.5 A/cm of the current density was 0.59 V. Comparative Example 3 (Synthesis of copolymer G) A polymer electrolyte membrane comprising a copolymer G represented by the following formula was obtained in the same manner as Example 3 of Japanese Unexamined Patent Publication No. 10-021943.
Herein, nl and ml denote the molar ratio of the respective structural units of the random copolymer type polymer ( electrolyte.
[Copolymer G] +14_D_0) random()__()_O)- 0 n2 SOH SO.H m2 Mn 4.5xlO.
Actually measured value of ion exchange capacity: 1.11 meq/g Membrane production: DMAc solution cast method: membrane thickness: 20 pin Proton conductivity: 7.81x10 S/cm Water absorption ratio: 41% m2/(n2 + m2) = 0.14 [Production of catalyst paste] A uniform copolymer B solution (concentration of copolymer B: 5% by weight) was produced by mixing 9.5 g of NMP and 0.5 g of the copolymer G. Separately, 0.64 g of platinum-supporting carbon (SA 50 BK, manufactured by N.E.
CHEMCAT CORPORATION; platinum support amount 50% by weight) was charged to 11 mL of ethanol and further 1.05 g of the previously prepared copolymer A solution was added to the mixture. After the obtained mixture was treated for 1 hour by ultrasonic treatment, it was stirred by a stirrer for 6 hours to obtain a catalyst ink B.
C
[Production of polymer electrolyte membrane] The polymer electrolyte membrane comprising the block copolymer type polymer electrolyte used in Example 5 was used. [MEA]
A carbon cloth to be a gas diffusion layer was cut out in a square shape and set on a heating stage and the catalyst ink B was applied to a region of 5.2 cm square in the center part of the main face of the carbon cloth by a spraying method.
The distance from the outlet to the carbon cloth was 5 cm and the stage temperature was set at 76 C. After the application, the cloth was left for 3 minutes on the stage to remove the solvent and form a catalyst layer. Two sheets of a carbon cloth on which the catalyst layer was formed in the above-mentioned manner were produced. The platinum amount in the catalyst layers calculated from the weight composition of the catalyst layers and the catalyst layer weight was 0.6 mg/cm2 for each face. Thereafter, to remove NNP remaining in the carbon cloth, the resulting carbon cloth sheets were immersed in 1 N hydrochloric acid and successively washed with water for 1 hour.
An electrolyte membrane was sandwiched with these two carbon cloth sheets from which NMP was removed and the product was pressed at 120 C and 10 kgf/cm2 for 15 minutes to complete a membrane-electrode assembly. (
[Cell assembly for fuel cell evaluation] A fuel cell was produced using a commercially available JARI standard cell. That is, a separator made of carbon having a groove formed by cutting processing for a gas channel was arranged in both gas diffusion layers of the membrane-electrode assembly obtained in the above-mentioned manner and current collectors and end plates were successively arranged further outside thereof and the arranged parts were fastened by bolts to assemble a fuel cell with an effective membrane surface area of 25 cm2.
[Fuel cell evaluation] While the obtained fuel cells was kept at 80 C, humidified hydrogen and humidified air were supplied to an anode and a cathode, respectively. At that time, the back-pressure at the gas outlet of the cell was adjusted to be 0.1 MPaG. The humidification of the respective raw material gases was carried out by leading the gases to bubblers and the water temperature of the bubbler for hydrogen was set to be 45 C and the water temperature of the bubbler for air was set to be 55 C.
Herein, the gas flow rate of hydrogen was set to be 529 mL/min and the gas flow rate of air was set to be 1665 mL/min.
The current density at 0.2 V of the cell potential was 1. 1 A/cm.
The cell potential at 0.5 A/cm of the current density was 0.44 S14588 V. The copolymer of the present invention shows excellent capabilities for properties such as water-proofness, membrane formability, and proton conductivity as a polymer electrolyte, particularly a proton conductive membrane of a fuel cell. It is particularly excellent in water-proofness.
Further, when the copolymer is used as a proton conductive membrane for a fuel cell, since it shows high power generation characteristics, the copolyiner of the present invention is industrially advantageous as a polymer electrolyte. (
Claims (17)
1. A copolymer obtained by nucleophilic condensation of a mixture of the following (A) and (C) with a mixture of (B) and (D), or of a mixture of (A), (B), (C) and (D): (A) a monomer having two leaving groups and further at least one acid group in a molecule; (B) a monomer having two nucleophilic groups and further at least one acid group in a molecule; (C) a monomer having two leaving groups and substantially no acid group in a molecule; and (D) a monomer having two nucleophilic groups and substantially no acid group in a molecule.
2. The copolymer according to claim 1, wherein said (A) is represented by the following formula (1): (1) wherein, k denotes 0, 1, or 2; Ar1 and Ar2 each independently denote a divalent aromatic group; when k is 2, two Ar2 groups may be the same or different with each other and these divalent aromatic groups may be substituted with an alkyl group having 1 to 10 carbon atoms which may have a substituent, an alkoxy ( group having 1 to 10 carbon atoms which may have a substituent, an aryl group having 6 to 10 carbon atoms which may have a substituent, an aryloxy group having 6 to 10 carbon atoms which may have a substituent, a fluoro group, a nitro group, or a benzoyl group; when k is 0, Ar' has at least one acid group, and when k is 1 or more, at least one of Ar1 and Ar2 has at least one acid group; X1 denotes one of a fluoro group, a chioro group, a nitro group, or a trifluoromethanesulfonyloxy group; two X' groups may be the same or different with each other; Z' denotes a group selected from the following groups; arid when k is 2, two Z' groups may be the same or different with each other: o 0 00 ---a--_&o_
3. The copolymer according to claim 1, wherein said (B) is represented by the following formula (2): y1Ar3Q1Ar4y1 (2) j wherein, j denotes 0, 1, or 2; Ar3 and Ar4 each independently denote a divalent aromatic group; when j is 2, two Ar4 groups may be the same or different with each other and these divalent ( aromatic groups may be substituted with an alkyl group having 1 to 10 carbon atoms which may have a substituent, an alkoxy group having 1 to 10 carbon atoms which may have a substituent, an aryl group having 6 to 10 carbon atoms which may have a substituent, or an aryloxy group having 6 to 10 carbon atoms which may have a substituent; when j is 0, Ar3 has at least one acid group, and when j is 1 or more, at least one of Ar3 and Ar4 has at least one acid group; Y1 denotes a hydroxyl group, a thiol group, or an amino group; two Y' groups may be the same or different with each other; Q1 denotes a direct bond or a group selected from the following groups; and when j is 2, two Q' groups may be the same or different with each other: H2 9H3 9F3 9 -0--c --c--C--C--S-OH3 F3 ---Q Q 9
4. The copolymer according to claim 1, wherein said (C) is represented by the following formula (3): (3) ( wherein, m denotes 0, 1, or 2; Ar5 and Ar6 each independently denote a divalent aromatic group; when m is 2, two Ar' groups may be the same or different with each other and these divalent aromatic groups may be substituted with an alkyl group having 1 to 10 carbon atoms which may have a substituent, an alkoxy group having 1 to 10 carbon atoms which may have a substituent, an aryl group having 6 to 10 carbon atoms which may have a substituent, an aryloxy group having 6 to 10 carbon atoms which may have a substituent, a fluoro group, a nitro group, or a benzoyl group; X2 denotes a fluoro group, a chloro group, a nitro group, or a trifluoromethanesulfonyloxy group; two X2 groups may be the same or different with each other; Z2 denotes a group selected from the following groups; and when m is 2, two Z2 groups may be the same or different with each other: 9 99 -r--C--C-C---
5. The copolymer according to claim 1, wherein said (D) is represented by the following formula (4): Y2-A r7o2_Ar8.3Y2 (4) ( wherein, n denotes 0, 1, or 2; Ar7 and Ar8 each independently denote a divalent aromatic group; when n is 2, two Ar8 groups may be the same or different with each other and these divalent aromatic groups may be substituted with an alkyl group having 1 to 10 carbon atoms which may have a substituent, an alkoxy group having 1 to 10 carbon atoms which may have a substituent, an aryl group having
6 to 10 carbon atoms which may have a substituent, or an aryloxy group having 6 to 10 carbon atoms which may have a substituent; Y2 denotes a hydroxyl group, a thiol group, or an amino group; two Y2 groups may be the same or different with each other; Q2 denotes a direct bond or a group selected from the following groups; and when n is 2, two Q2 groups may be the same or different with each other: H2 9H3 CF3 -0----C --9---ó----C S CH3 F3 ---; 9 6. The copolymer according to claim 1, wherein the acid group is a strong acid group or a superacid group. (
7. The copolymer according to claim 1 having an ion exchange capacity of 0.1 meq/g to 4.0 meq/g.
8. The copolymer according to claim 1, wherein the weight composition ratio of the structural unit having the acid group and the structural unit having substantially no acid group, [structural unit into which the acid group is introduced] [structural unit into which substantially no acid group is introduced], Is 3: 97 to 70: 30.
9. A polymer electrolyte containing the copolymer according to any one of claims 1 to 8.
10. A polymer electrolyte membrane containing the polymer electrolyte according to claim 9.
11. A polymer electrolyte composite membrane comprising the polymer electrolyte according to claim 9 and a porous substrate.
12. A polymer electrolyte composite membrane obtained by impregnating a porous substrate with the polymer electrolyte according to claim 9, and compositing those.
13. A catalyst composition comprising the polymer S14588 electrolyte according to claim 9 and a catalyt substance.
14. A fuel cell using the polymer electrolyte membrane according to claim 10.
15. A fuel cell using the polymer electrolyte composite membrane according to claim 11 or 12.
16. A fuel cell having a catalyst layer comprising the catalyst composition according to claim 13.
17. A method of producing a copolymer, wherein a mixture of the following (A) and (C) with a mixture of (B) and (D) is condensed, or a mixture of (A), (B), (C) and (D) is condensed: (A) a monomer having two leaving groups and further at least one acid group in a molecule; (B) a monomer having two nucleophilic groups and further at least one acid group in a molecule; (C) a monomer having two leaving groups and substantially no acid group in a molecule; and (D) a monomer having two nucleophilic groups and substantially no acid group in a molecule.
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PCT/JP2006/325700 WO2007072978A1 (en) | 2005-12-20 | 2006-12-19 | Copolymer, polymer electrolyte and use thereof |
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2005013399A1 (en) * | 2003-07-31 | 2005-02-10 | Toyo Boseki Kabushiki Kaisha | Electrolyte membrane-electrode assembly, fuel cell using same, and method for producing electrolyte membrane-electrode assembly |
WO2005037892A1 (en) * | 2003-10-17 | 2005-04-28 | Sumitomo Chemical Company, Limited | Block copolymer and use thereof |
WO2005063854A1 (en) * | 2003-12-25 | 2005-07-14 | Sumitomo Chemical Company, Limited | Polymer electrolyte and use thereof |
JP2005232439A (en) * | 2004-01-16 | 2005-09-02 | Idemitsu Kosan Co Ltd | Polyaryl ether copolymer, method for producing the same, and polymer electrolyte film prepared by using the same |
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2008
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Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2005013399A1 (en) * | 2003-07-31 | 2005-02-10 | Toyo Boseki Kabushiki Kaisha | Electrolyte membrane-electrode assembly, fuel cell using same, and method for producing electrolyte membrane-electrode assembly |
WO2005037892A1 (en) * | 2003-10-17 | 2005-04-28 | Sumitomo Chemical Company, Limited | Block copolymer and use thereof |
WO2005063854A1 (en) * | 2003-12-25 | 2005-07-14 | Sumitomo Chemical Company, Limited | Polymer electrolyte and use thereof |
JP2005232439A (en) * | 2004-01-16 | 2005-09-02 | Idemitsu Kosan Co Ltd | Polyaryl ether copolymer, method for producing the same, and polymer electrolyte film prepared by using the same |
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