CN1511327A - 电解电容器用电解液及使用该电解液的电解电容器 - Google Patents
电解电容器用电解液及使用该电解液的电解电容器 Download PDFInfo
- Publication number
- CN1511327A CN1511327A CNA028097165A CN02809716A CN1511327A CN 1511327 A CN1511327 A CN 1511327A CN A028097165 A CNA028097165 A CN A028097165A CN 02809716 A CN02809716 A CN 02809716A CN 1511327 A CN1511327 A CN 1511327A
- Authority
- CN
- China
- Prior art keywords
- electrolyte
- electrolytic capacitor
- solvent
- methylimidazole
- salt
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000003990 capacitor Substances 0.000 title claims abstract description 156
- 239000008151 electrolyte solution Substances 0.000 title 1
- 239000003792 electrolyte Substances 0.000 claims abstract description 181
- 239000002904 solvent Substances 0.000 claims abstract description 145
- 150000003839 salts Chemical class 0.000 claims abstract description 52
- -1 aluminic acid ion Chemical class 0.000 claims description 134
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims description 62
- MCTWTZJPVLRJOU-UHFFFAOYSA-N 1-methyl-1H-imidazole Chemical compound CN1C=CN=C1 MCTWTZJPVLRJOU-UHFFFAOYSA-N 0.000 claims description 61
- 238000009835 boiling Methods 0.000 claims description 41
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 27
- FAHBNUUHRFUEAI-UHFFFAOYSA-M hydroxidooxidoaluminium Chemical compound O[Al]=O FAHBNUUHRFUEAI-UHFFFAOYSA-M 0.000 claims description 20
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical group O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 claims description 17
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 17
- 229910052799 carbon Inorganic materials 0.000 claims description 17
- 150000002500 ions Chemical class 0.000 claims description 15
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical group O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 claims description 13
- 150000002148 esters Chemical class 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 11
- 150000003457 sulfones Chemical class 0.000 claims description 11
- ATVGJKFOXVMUES-UHFFFAOYSA-N N1=CC=CC2=CC=CC=C12.CN1C=NC=C1 Chemical compound N1=CC=CC2=CC=CC=C12.CN1C=NC=C1 ATVGJKFOXVMUES-UHFFFAOYSA-N 0.000 claims description 10
- 229910019142 PO4 Inorganic materials 0.000 claims description 10
- 239000000654 additive Substances 0.000 claims description 10
- 150000001408 amides Chemical class 0.000 claims description 10
- 150000002825 nitriles Chemical class 0.000 claims description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 9
- 150000007942 carboxylates Chemical class 0.000 claims description 9
- 150000002460 imidazoles Chemical class 0.000 claims description 9
- 239000010452 phosphate Substances 0.000 claims description 9
- 229910052783 alkali metal Inorganic materials 0.000 claims description 8
- CMJLMPKFQPJDKP-UHFFFAOYSA-N 3-methylthiolane 1,1-dioxide Chemical compound CC1CCS(=O)(=O)C1 CMJLMPKFQPJDKP-UHFFFAOYSA-N 0.000 claims description 7
- 150000003863 ammonium salts Chemical class 0.000 claims description 7
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 5
- WWGQFLPUAVUZSE-UHFFFAOYSA-N 1,2,3,4-tetramethyl-2h-imidazole Chemical class CC1N(C)C=C(C)N1C WWGQFLPUAVUZSE-UHFFFAOYSA-N 0.000 claims description 4
- KYRYHBRYSSBWLU-UHFFFAOYSA-N 1,2,3,4-tetramethylimidazolidine Chemical compound CC1CN(C)C(C)N1C KYRYHBRYSSBWLU-UHFFFAOYSA-N 0.000 claims description 4
- RYNROCNODWBDCM-UHFFFAOYSA-N 1,3-diethyl-2h-imidazole Chemical class CCN1CN(CC)C=C1 RYNROCNODWBDCM-UHFFFAOYSA-N 0.000 claims description 4
- BEUKLVYOGCCEPF-UHFFFAOYSA-N 1,3-diethylimidazolidine Chemical compound CCN1CCN(CC)C1 BEUKLVYOGCCEPF-UHFFFAOYSA-N 0.000 claims description 4
- NWYSZNAYMPDEAA-UHFFFAOYSA-N 1,3-dimethyl-2-pentyl-2h-imidazole Chemical class CCCCCC1N(C)C=CN1C NWYSZNAYMPDEAA-UHFFFAOYSA-N 0.000 claims description 4
- CWLPKGGXFGIRRR-UHFFFAOYSA-N 1,3-dimethyl-2-pentylimidazolidine Chemical compound CCCCCC1N(C)CCN1C CWLPKGGXFGIRRR-UHFFFAOYSA-N 0.000 claims description 4
- MNYOKDIIUJDYBM-UHFFFAOYSA-N 1-benzyl-3-methyl-2h-imidazole Chemical compound C1=CN(C)CN1CC1=CC=CC=C1 MNYOKDIIUJDYBM-UHFFFAOYSA-N 0.000 claims description 4
- IBZJNLWLRUHZIX-UHFFFAOYSA-N 1-ethyl-3-methyl-2h-imidazole Chemical compound CCN1CN(C)C=C1 IBZJNLWLRUHZIX-UHFFFAOYSA-N 0.000 claims description 4
- KRDZGTPEAREWNG-UHFFFAOYSA-N 1-methyl-3-phenyl-2h-imidazole Chemical compound C1=CN(C)CN1C1=CC=CC=C1 KRDZGTPEAREWNG-UHFFFAOYSA-N 0.000 claims description 4
- YQBAQZJAJHZGIG-UHFFFAOYSA-N 2-heptyl-1,3-dimethyl-2h-imidazole Chemical class CCCCCCCC1N(C)C=CN1C YQBAQZJAJHZGIG-UHFFFAOYSA-N 0.000 claims description 4
- SHTANHZPDWEAAR-UHFFFAOYSA-N 2-heptyl-1,3-dimethylimidazolidine Chemical compound CCCCCCCC1N(C)CCN1C SHTANHZPDWEAAR-UHFFFAOYSA-N 0.000 claims description 4
- DMEOUDQMSMNVQH-UHFFFAOYSA-N N1=CC=CC2=CC=CC=C12.C(C)C1=[N+](C=C(N1C)C)C Chemical compound N1=CC=CC2=CC=CC=C12.C(C)C1=[N+](C=C(N1C)C)C DMEOUDQMSMNVQH-UHFFFAOYSA-N 0.000 claims description 4
- NPGXALYHLQTILN-UHFFFAOYSA-N N1=CC=CC2=CC=CC=C12.C(C)N1CN(C=C1)C Chemical compound N1=CC=CC2=CC=CC=C12.C(C)N1CN(C=C1)C NPGXALYHLQTILN-UHFFFAOYSA-N 0.000 claims description 4
- GPUFFASNPGNLCB-UHFFFAOYSA-N N1=CC=CC2=CC=CC=C12.C(C1=CC=CC=C1)N1CN(C=C1)C Chemical compound N1=CC=CC2=CC=CC=C12.C(C1=CC=CC=C1)N1CN(C=C1)C GPUFFASNPGNLCB-UHFFFAOYSA-N 0.000 claims description 4
- JNIPOSRYRFTRKJ-UHFFFAOYSA-N N1=CC=CC2=CC=CC=C12.C1(=CC=CC=C1)N1CN(C=C1)C Chemical compound N1=CC=CC2=CC=CC=C12.C1(=CC=CC=C1)N1CN(C=C1)C JNIPOSRYRFTRKJ-UHFFFAOYSA-N 0.000 claims description 4
- AHJXFCRLVZEMBQ-UHFFFAOYSA-N N1=CC=CC2=CC=CC=C12.C[N+]1=C(N(C=C1)C)C Chemical compound N1=CC=CC2=CC=CC=C12.C[N+]1=C(N(C=C1)C)C AHJXFCRLVZEMBQ-UHFFFAOYSA-N 0.000 claims description 4
- AXJDUAZIGJCUSH-UHFFFAOYSA-N N1=CC=CC2=CC=CC=C12.C[N+]1=CN(C(=C1)C)C Chemical compound N1=CC=CC2=CC=CC=C12.C[N+]1=CN(C(=C1)C)C AXJDUAZIGJCUSH-UHFFFAOYSA-N 0.000 claims description 4
- 230000015572 biosynthetic process Effects 0.000 claims description 4
- ZJHQDSMOYNLVLX-UHFFFAOYSA-N diethyl(dimethyl)azanium Chemical compound CC[N+](C)(C)CC ZJHQDSMOYNLVLX-UHFFFAOYSA-N 0.000 claims description 4
- YOMFVLRTMZWACQ-UHFFFAOYSA-N ethyltrimethylammonium Chemical compound CC[N+](C)(C)C YOMFVLRTMZWACQ-UHFFFAOYSA-N 0.000 claims description 4
- CBXCPBUEXACCNR-UHFFFAOYSA-N tetraethylammonium Chemical compound CC[N+](CC)(CC)CC CBXCPBUEXACCNR-UHFFFAOYSA-N 0.000 claims description 4
- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 claims description 4
- 150000001639 boron compounds Chemical class 0.000 claims description 3
- 229910044991 metal oxide Inorganic materials 0.000 claims description 3
- 150000004706 metal oxides Chemical class 0.000 claims description 3
- 239000011859 microparticle Substances 0.000 claims description 3
- 150000002828 nitro derivatives Chemical group 0.000 claims description 3
- 229920001296 polysiloxane Polymers 0.000 claims description 3
- 239000004020 conductor Substances 0.000 claims description 2
- 229910052698 phosphorus Inorganic materials 0.000 claims 2
- 239000011574 phosphorus Substances 0.000 claims 2
- 230000000052 comparative effect Effects 0.000 description 25
- 229910052782 aluminium Inorganic materials 0.000 description 22
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 22
- 239000004411 aluminium Substances 0.000 description 21
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 20
- 150000004645 aluminates Chemical class 0.000 description 14
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 12
- 239000011888 foil Substances 0.000 description 11
- 150000001450 anions Chemical class 0.000 description 9
- 230000003068 static effect Effects 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 8
- 239000007789 gas Substances 0.000 description 8
- 239000001257 hydrogen Substances 0.000 description 8
- 229910052739 hydrogen Inorganic materials 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 239000002585 base Substances 0.000 description 7
- 235000021317 phosphate Nutrition 0.000 description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 230000000996 additive effect Effects 0.000 description 5
- 239000005030 aluminium foil Substances 0.000 description 5
- 239000000470 constituent Substances 0.000 description 5
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 229920001971 elastomer Polymers 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- XLSZMDLNRCVEIJ-UHFFFAOYSA-N 4-methylimidazole Chemical compound CC1=CNC=N1 XLSZMDLNRCVEIJ-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 4
- 150000001409 amidines Chemical class 0.000 description 4
- 229920005549 butyl rubber Polymers 0.000 description 4
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229910000077 silane Inorganic materials 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Natural products OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Natural products C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 125000002723 alicyclic group Chemical group 0.000 description 3
- 229910052786 argon Inorganic materials 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 238000003556 assay Methods 0.000 description 3
- 239000004327 boric acid Substances 0.000 description 3
- 150000001768 cations Chemical class 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- JJWLVOIRVHMVIS-UHFFFAOYSA-O isopropylaminium Chemical compound CC(C)[NH3+] JJWLVOIRVHMVIS-UHFFFAOYSA-O 0.000 description 3
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- 238000012545 processing Methods 0.000 description 3
- 238000007789 sealing Methods 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 2
- KDSNLYIMUZNERS-UHFFFAOYSA-N 2-methylpropanamine Chemical compound CC(C)CN KDSNLYIMUZNERS-UHFFFAOYSA-N 0.000 description 2
- SLAMLWHELXOEJZ-UHFFFAOYSA-N 2-nitrobenzoic acid Chemical compound OC(=O)C1=CC=CC=C1[N+]([O-])=O SLAMLWHELXOEJZ-UHFFFAOYSA-N 0.000 description 2
- QGHDLJAZIIFENW-UHFFFAOYSA-N 4-[1,1,1,3,3,3-hexafluoro-2-(4-hydroxy-3-prop-2-enylphenyl)propan-2-yl]-2-prop-2-enylphenol Chemical group C1=C(CC=C)C(O)=CC=C1C(C(F)(F)F)(C(F)(F)F)C1=CC=C(O)C(CC=C)=C1 QGHDLJAZIIFENW-UHFFFAOYSA-N 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- ATHHXGZTWNVVOU-UHFFFAOYSA-N N-methylformamide Chemical compound CNC=O ATHHXGZTWNVVOU-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
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- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 125000005210 alkyl ammonium group Chemical group 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 230000001174 ascending effect Effects 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 229940063013 borate ion Drugs 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
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- 238000010612 desalination reaction Methods 0.000 description 2
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 238000005530 etching Methods 0.000 description 2
- MTZQAGJQAFMTAQ-UHFFFAOYSA-N ethyl benzoate Chemical compound CCOC(=O)C1=CC=CC=C1 MTZQAGJQAFMTAQ-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-O ethylaminium Chemical compound CC[NH3+] QUSNBJAOOMFDIB-UHFFFAOYSA-O 0.000 description 2
- GAEKPEKOJKCEMS-UHFFFAOYSA-N gamma-valerolactone Chemical compound CC1CCC(=O)O1 GAEKPEKOJKCEMS-UHFFFAOYSA-N 0.000 description 2
- 238000001879 gelation Methods 0.000 description 2
- 229940015043 glyoxal Drugs 0.000 description 2
- XTPRURKTXNFVQT-UHFFFAOYSA-N hexyl(trimethyl)azanium Chemical compound CCCCCC[N+](C)(C)C XTPRURKTXNFVQT-UHFFFAOYSA-N 0.000 description 2
- 230000036571 hydration Effects 0.000 description 2
- 238000006703 hydration reaction Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 2
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- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 description 2
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- 239000012046 mixed solvent Substances 0.000 description 2
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- 229910052715 tantalum Inorganic materials 0.000 description 2
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
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- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
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- YQMUORJJDBQCOV-UHFFFAOYSA-N $l^{1}-phosphanylmethane Chemical compound [P]C YQMUORJJDBQCOV-UHFFFAOYSA-N 0.000 description 1
- OLDRGPVQKBDGRF-UHFFFAOYSA-N 1,2,3,4,5-pentamethyl-2h-imidazole Chemical class CC1N(C)C(C)=C(C)N1C OLDRGPVQKBDGRF-UHFFFAOYSA-N 0.000 description 1
- OTPDWCMLUKMQNO-UHFFFAOYSA-N 1,2,3,4-tetrahydropyrimidine Chemical compound C1NCC=CN1 OTPDWCMLUKMQNO-UHFFFAOYSA-N 0.000 description 1
- GRHNKLNJAYKFIG-UHFFFAOYSA-N 1,2,3-trimethyl-1,3-diazinane Chemical compound CC1N(C)CCCN1C GRHNKLNJAYKFIG-UHFFFAOYSA-N 0.000 description 1
- LZDKZFUFMNSQCJ-UHFFFAOYSA-N 1,2-diethoxyethane Chemical compound CCOCCOCC LZDKZFUFMNSQCJ-UHFFFAOYSA-N 0.000 description 1
- OTZZHNIHWYIJRR-UHFFFAOYSA-N 1,2-diethyl-3-methyl-1,3-diazinane Chemical compound CCC1N(C)CCCN1CC OTZZHNIHWYIJRR-UHFFFAOYSA-N 0.000 description 1
- QYFYUEJHZUTRKT-UHFFFAOYSA-N 1,2-diethyl-3-methyl-2h-imidazole Chemical compound CCC1N(C)C=CN1CC QYFYUEJHZUTRKT-UHFFFAOYSA-N 0.000 description 1
- GLZQDVBWYHDUPP-UHFFFAOYSA-N 1,3-diethyl-1,3-diazinane Chemical compound CCN1CCCN(CC)C1 GLZQDVBWYHDUPP-UHFFFAOYSA-N 0.000 description 1
- VLUQSQIDSZAISP-UHFFFAOYSA-N 1,3-diethyl-2-methyl-1,3-diazinane Chemical compound CCN1CCCN(CC)C1C VLUQSQIDSZAISP-UHFFFAOYSA-N 0.000 description 1
- DCPLDPXQOOHYSU-UHFFFAOYSA-N 1,3-dimethyl-1,3-diazinane Chemical compound CN1CCCN(C)C1 DCPLDPXQOOHYSU-UHFFFAOYSA-N 0.000 description 1
- CFQPVBJOKYSPKG-UHFFFAOYSA-N 1,3-dimethylimidazol-2-one Chemical compound CN1C=CN(C)C1=O CFQPVBJOKYSPKG-UHFFFAOYSA-N 0.000 description 1
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- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- WGYKZJWCGVVSQN-UHFFFAOYSA-O propan-1-aminium Chemical compound CCC[NH3+] WGYKZJWCGVVSQN-UHFFFAOYSA-O 0.000 description 1
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
- 229940090181 propyl acetate Drugs 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
- 150000005326 tetrahydropyrimidines Chemical class 0.000 description 1
- CZMILNXHOAKSBR-UHFFFAOYSA-N tetraphenylazanium Chemical compound C1=CC=CC=C1[N+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 CZMILNXHOAKSBR-UHFFFAOYSA-N 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- WVLBCYQITXONBZ-UHFFFAOYSA-N trimethyl phosphate Chemical compound COP(=O)(OC)OC WVLBCYQITXONBZ-UHFFFAOYSA-N 0.000 description 1
- ZVFDPYZBJGKPII-UHFFFAOYSA-N trimethyl(nonyl)azanium Chemical compound CCCCCCCCC[N+](C)(C)C ZVFDPYZBJGKPII-UHFFFAOYSA-N 0.000 description 1
- ACZOGADOAZWANS-UHFFFAOYSA-N trimethyl(pentyl)azanium Chemical compound CCCCC[N+](C)(C)C ACZOGADOAZWANS-UHFFFAOYSA-N 0.000 description 1
- BMTHNVMASXVELE-UHFFFAOYSA-N trimethyl(propan-2-yl)azanium Chemical compound CC(C)[N+](C)(C)C BMTHNVMASXVELE-UHFFFAOYSA-N 0.000 description 1
- ZNEOHLHCKGUAEB-UHFFFAOYSA-N trimethylphenylammonium Chemical compound C[N+](C)(C)C1=CC=CC=C1 ZNEOHLHCKGUAEB-UHFFFAOYSA-N 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/004—Details
- H01G9/022—Electrolytes; Absorbents
- H01G9/035—Liquid electrolytes, e.g. impregnating materials
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/004—Details
- H01G9/08—Housing; Encapsulation
- H01G9/10—Sealing, e.g. of lead-in wires
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/145—Liquid electrolytic capacitors
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- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Electric Double-Layer Capacitors Or The Like (AREA)
- Secondary Cells (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
实施例 | 盐 | 浓度 | 电导率/mS cm-1 | 电压强度 | |
wt% | 初始 | 加热后 | V | ||
实施例1 | Et3MeN+AlF4 - | 25 | 21.00 | 21.00 | 165 |
对比例1 | Et3MeN+PH- | 25 | 10.86 | 10.77 | 60 |
对比例2 | EDMI+PH- | 25 | 11.89 | 10.84 | 55 |
实施例 | 盐 | 浓度 | 电导率/mS cm-1 | 电压强度 | |
wt% | 初始 | 加热后 | V | ||
实施例2 | Et3MeN+AlF4 - | 10 | 11.08 | 11.08 | 195 |
对比例3 | Et3MeN+PH- | 14 | 8.17 | 7.98 | 75 |
对比例4 | EDMI+PH- | 10 | 7.13 | 6.60 | 80 |
实施例3 | 实施例4 | 实施例5 | 实施例6 | 实施例7 | 实施例8 | |
四氟铝酸1-乙基-2,3-二甲基咪唑啉鎓盐 | 25 | 25 | 25 | 25 | 20 | 20 |
四氟铝酸1,2,3,4-四甲基咪唑啉鎓盐 | ||||||
苯二甲酸氢1-乙基-2,3-二甲基咪唑啉鎓盐 | ||||||
γ-丁内酯 | 75 | 35.5 | 72 | 72 | ||
环丁砜 | 75 | 35.5 | 35.5 | |||
3-甲基环丁砜 | 35.5 | |||||
乙二醇 | 8 | 8 | ||||
硅烷 | 6 | |||||
磷酸 | ||||||
硼酸 | ||||||
对硝基安息香酸 | ||||||
聚乙二醇(平均分子量300) | ||||||
电导率/mS cm-1在25℃ | 24.10 | 6.56 | 14.41 | 5.94 | 20.50 | 19.38 |
耐电压/V在125℃ | 160 | 160 | 165 | 170 | 170 | 185 |
对比例5 | 对比例6 | 对比例7 | 对比例8 | 对比例9 | 对比例10 | |
四氟铝酸1-乙基-2,3-二甲基咪唑啉鎓盐 | ||||||
四氟铝酸1,2,3,4-四甲基咪唑啉鎓盐 | ||||||
苯二甲酸氢1-乙基-2,3-二甲基咪唑啉鎓盐 | 25 | 25 | 25 | 25 | 20 | 20 |
γ-丁内酯 | 75 | 35.5 | 72 | 72 | ||
环丁砜 | 75 | 35.5 | 35.5 | |||
3-甲基环丁砜 | 35.5 | |||||
乙二醇 | 8 | 8 | ||||
硅烷 | 6 | |||||
电导率/mS cm-1在25℃ | 11.70 | 3.24 | 7.34 | 2.94 | 9.86 | 9.31 |
耐电压/V在125℃ | 60 | 55 | 60 | 60 | 70 | 80 |
实施例9 | 实施例10 | 实施例11 | 实施例12 | 实施例13 | 实施例14 | |
四氟铝酸1-乙基-2,3-二甲基咪唑啉鎓盐 | 25 | 25 | 25 | 25 | 12.5 | |
四氟铝酸1,2,3,4-四甲基咪唑啉鎓盐 | 25 | |||||
苯二甲酸氢1-乙基-2,3-二甲基咪唑啉鎓盐 | 12.5 | |||||
γ-丁内酯 | 75 | 75 | 75 | 75 | 75 | 75 |
环丁砜 | ||||||
3-甲基环丁砜 | ||||||
乙二醇 | ||||||
硅烷 | ||||||
磷酸 | 1 | |||||
硼酸 | 1 | |||||
对硝基安息香酸 | 1 | |||||
聚乙二醇(平均分子量300) | 1 | |||||
电导率/mS cm-1在25℃ | 23.85 | 23.81 | 23.85 | 23.05 | 24.00 | 17.82 |
耐电压/V在125℃ | 165 | 165 | 165 | 170 | 160 | 110 |
实施例1 | 实施例3 | 实施例4 | 实施例15 | |
静电容量/μF | 54.8 | 54.8 | 54.8 | 54.5 |
静电容量(无负荷试验后)/μF | 55.9 | 53.7 | 55.2 | 38.4 |
等价串联电阻/Ω | 0.0066 | 0.0063 | 0.0105 | 0.0073 |
等价串联电阻(无负荷试验后)/Ω | 0.0067 | 0.0063 | 0.0107 | 0.0545 |
外观(无负荷试验后) | 封口部膨胀 | 无变化 | 无变化 | 封口部膨胀 |
Claims (34)
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JP141405/2001 | 2001-05-11 | ||
JP2001141405 | 2001-05-11 | ||
JP252628/2001 | 2001-08-23 | ||
JP2001252628 | 2001-08-23 | ||
PCT/JP2002/004571 WO2002101773A1 (en) | 2001-05-11 | 2002-05-10 | Electrolytic solution for electrolytic capacitor and electrolytic capacitor using it |
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CN2008100923529A Division CN101261900B (zh) | 2001-05-11 | 2002-05-10 | 电解电容器用电解液及使用该电解液的电解电容器 |
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CNB028097165A Expired - Fee Related CN100394522C (zh) | 2001-05-11 | 2002-05-10 | 电解电容器用电解液及使用该电解液的电解电容器 |
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US (2) | US7072173B2 (zh) |
EP (1) | EP1394824A4 (zh) |
JP (3) | JP4631975B2 (zh) |
CN (2) | CN101261900B (zh) |
WO (1) | WO2002101773A1 (zh) |
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Family Cites Families (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3415687A (en) * | 1966-03-29 | 1968-12-10 | Honeywell Inc | Electric current producing cell |
JPS62288815A (ja) * | 1986-02-21 | 1987-12-15 | Sanyo Chem Ind Ltd | 電解液 |
JPS63122112A (ja) | 1986-11-11 | 1988-05-26 | 旭硝子株式会社 | 新規な電解コンデンサ |
JPH01124210A (ja) * | 1987-11-09 | 1989-05-17 | Matsushita Electric Ind Co Ltd | 電解コンデンサ駆動用電解液 |
JPH01246386A (ja) * | 1987-11-25 | 1989-10-02 | Asahi Glass Co Ltd | オニウム塩の製造方法 |
GB8804860D0 (en) * | 1988-03-01 | 1988-03-30 | Ici Plc | Solid electrolyte devices |
JP2739217B2 (ja) * | 1988-10-15 | 1998-04-15 | 松下電器産業株式会社 | 電解コンデンサ駆動用電解液およびその製造方法 |
US5714279A (en) * | 1989-10-24 | 1998-02-03 | The United States Of America As Represented By The Secretary Of The Navy | Non-aqueous lithium cells |
JP2958576B2 (ja) * | 1991-01-24 | 1999-10-06 | 富士写真フイルム株式会社 | 電池用正極材料 |
JPH0513273A (ja) | 1991-07-04 | 1993-01-22 | Matsushita Electric Ind Co Ltd | 電解コンデンサ駆動用電解液 |
JPH06196366A (ja) | 1992-11-09 | 1994-07-15 | Mitsubishi Petrochem Co Ltd | 電解コンデンサ用電解液 |
JPH06196367A (ja) * | 1992-12-24 | 1994-07-15 | Mitsubishi Petrochem Co Ltd | 電解コンデンサ用電解液 |
JP3387144B2 (ja) | 1993-03-30 | 2003-03-17 | 三菱化学株式会社 | 電解コンデンサ用電解液 |
JP3078948B2 (ja) * | 1993-03-31 | 2000-08-21 | 日石三菱株式会社 | 有機溶媒及び電解液 |
US5870275A (en) * | 1993-12-03 | 1999-02-09 | Sanyo Chemical Industries, Ltd. | Electrolyte and electronic component using same |
JP3245604B2 (ja) * | 1993-12-03 | 2002-01-15 | 三洋化成工業株式会社 | 電解液及びそれを用いた電気化学素子 |
JP3504349B2 (ja) * | 1994-08-29 | 2004-03-08 | 三洋化成工業株式会社 | イミダゾリニウム有機酸塩の製造方法 |
KR100366551B1 (ko) * | 1994-09-29 | 2003-03-12 | 닛뽄 케미콘 가부시끼가이샤 | 전해콘덴서 |
JPH10116629A (ja) * | 1996-10-15 | 1998-05-06 | Mitsui Chem Inc | 非水電解液 |
JP3349399B2 (ja) | 1996-11-01 | 2002-11-25 | 三洋電機株式会社 | リチウム二次電池 |
JPH10233343A (ja) | 1997-02-19 | 1998-09-02 | Elna Co Ltd | アルミニウム電解コンデンサおよびアルミニウム電解コンデンサ駆動用電解液 |
JP3669804B2 (ja) * | 1997-03-03 | 2005-07-13 | 日本ケミコン株式会社 | 電解コンデンサ用電解液 |
DE69801466T2 (de) * | 1997-06-19 | 2002-05-02 | Sanyo Electric Co | Lithiumakkumulator |
JP4780812B2 (ja) | 1997-08-01 | 2011-09-28 | 日本ケミコン株式会社 | アルミニウム電解コンデンサ |
BR9815323A (pt) * | 1997-11-24 | 2001-10-09 | Procter & Gamble | Composições aquosas claras ou translúcidas de amaciante para tecidos, as quais contêm alto teor de eletrólito e estabilizador de fase opcional |
US6166899A (en) * | 1997-12-18 | 2000-12-26 | Nippon Chemi-Con Corporation | Electrolyte for electrolytic capacitor and electrolytic capacitor having the same |
JPH11283880A (ja) | 1998-03-31 | 1999-10-15 | Mitsubishi Chemical Corp | 電解コンデンサ用電解液及びそれを用いた電解コンデンサ |
JP3702645B2 (ja) | 1998-05-12 | 2005-10-05 | 三菱化学株式会社 | 有機オニウム塩の製造方法 |
JP3702644B2 (ja) | 1998-05-12 | 2005-10-05 | 三菱化学株式会社 | 有機オニウム塩の製造方法 |
JP2964244B1 (ja) * | 1998-05-14 | 1999-10-18 | 三洋化成工業株式会社 | 4級環状アミジン有機酸塩の製造法 |
JP2000016995A (ja) * | 1998-06-30 | 2000-01-18 | Mitsubishi Chemicals Corp | 4級アンモニウムテトラフルオロボレートの製造方法 |
JP2001085281A (ja) * | 1999-09-09 | 2001-03-30 | Honda Motor Co Ltd | 電気二重層コンデンサの配線構造 |
JP3574067B2 (ja) * | 1999-11-29 | 2004-10-06 | 三洋化成工業株式会社 | 2置換ジアミンモノアミド化合物の製造法 |
JP3967551B2 (ja) * | 2001-02-08 | 2007-08-29 | 本田技研工業株式会社 | 電気二重層キャパシタ容器の蓋体 |
EP1394824A4 (en) * | 2001-05-11 | 2008-01-23 | Mitsubishi Chem Corp | ELECTROLYTIC SOLUTION FOR AN ELECTROLYTE CONDENSER AND ELECTROLYTE CONDENSER THEREWITH |
-
2002
- 2002-05-10 EP EP02778902A patent/EP1394824A4/en not_active Withdrawn
- 2002-05-10 CN CN2008100923529A patent/CN101261900B/zh not_active Expired - Fee Related
- 2002-05-10 CN CNB028097165A patent/CN100394522C/zh not_active Expired - Fee Related
- 2002-05-10 WO PCT/JP2002/004571 patent/WO2002101773A1/ja active Application Filing
-
2003
- 2003-11-12 US US10/704,803 patent/US7072173B2/en not_active Expired - Lifetime
-
2005
- 2005-12-16 US US11/304,600 patent/US7460357B2/en not_active Expired - Lifetime
-
2009
- 2009-01-23 JP JP2009013110A patent/JP4631975B2/ja not_active Expired - Fee Related
- 2009-05-20 JP JP2009121558A patent/JP4924658B2/ja not_active Expired - Fee Related
-
2011
- 2011-05-20 JP JP2011113784A patent/JP2011181956A/ja not_active Withdrawn
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
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US7430108B2 (en) | 2002-11-08 | 2008-09-30 | Nippon Chemi-Con Corporation | Electrolyte for electrolytic capacitor and electrolytic capacitor containing the same |
CN1692459B (zh) * | 2002-11-08 | 2010-05-12 | 日本贵弥功株式会社 | 电解电容器用电解液以及采用了它的电解电容器 |
US7724501B2 (en) | 2002-11-08 | 2010-05-25 | Nippon Chemi-Con Corporation | Electrolytic capacitor |
CN101278364B (zh) * | 2005-09-30 | 2012-09-05 | 三菱化学株式会社 | 电解电容器用电解液以及电解电容器 |
TWI399771B (zh) * | 2005-12-08 | 2013-06-21 | Nichicon Corp | 電解電容器 |
CN101512825B (zh) * | 2006-09-14 | 2011-10-05 | 国立大学法人静冈大学 | 电化学设备用电解液 |
CN101935285A (zh) * | 2009-07-02 | 2011-01-05 | 中国科学院过程工程研究所 | 有机鎓的六氟铝酸盐及其制备方法和用途 |
CN104067361A (zh) * | 2012-03-29 | 2014-09-24 | 住友精化株式会社 | 电化学器件用电解液、铝电解电容器和双电层电容器 |
US9583272B2 (en) | 2012-03-29 | 2017-02-28 | Sumitomo Seika Chemicals Co., Ltd. | Electrolyte solution for electrochemical devices, aluminum electrolytic capacitor, and electric double layer capacitor |
CN107112145A (zh) * | 2014-12-11 | 2017-08-29 | 大塚化学株式会社 | 双电层电容器用非水电解液 |
CN107112145B (zh) * | 2014-12-11 | 2020-07-07 | 大塚化学株式会社 | 双电层电容器用非水电解液 |
CN104979102A (zh) * | 2015-07-08 | 2015-10-14 | 深圳新宙邦科技股份有限公司 | 一种电解液溶质、电解液及超级电容器 |
Also Published As
Publication number | Publication date |
---|---|
US20060092597A1 (en) | 2006-05-04 |
EP1394824A1 (en) | 2004-03-03 |
CN101261900B (zh) | 2011-02-02 |
JP4631975B2 (ja) | 2011-02-16 |
US7460357B2 (en) | 2008-12-02 |
EP1394824A4 (en) | 2008-01-23 |
CN101261900A (zh) | 2008-09-10 |
US20040095708A1 (en) | 2004-05-20 |
JP2009161537A (ja) | 2009-07-23 |
WO2002101773A1 (en) | 2002-12-19 |
JP4924658B2 (ja) | 2012-04-25 |
JP2011181956A (ja) | 2011-09-15 |
JP2009239291A (ja) | 2009-10-15 |
CN100394522C (zh) | 2008-06-11 |
US7072173B2 (en) | 2006-07-04 |
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