CN101261900B - 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
- CN101261900B CN101261900B CN2008100923529A CN200810092352A CN101261900B CN 101261900 B CN101261900 B CN 101261900B CN 2008100923529 A CN2008100923529 A CN 2008100923529A CN 200810092352 A CN200810092352 A CN 200810092352A CN 101261900 B CN101261900 B CN 101261900B
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- China
- Prior art keywords
- electrolyte
- methylimidazole
- salt
- electrolytic capacitor
- solvent
- 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.)
- Expired - Fee Related
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- 239000003990 capacitor Substances 0.000 title claims abstract description 145
- 239000003792 electrolyte Substances 0.000 title claims abstract description 69
- 239000002904 solvent Substances 0.000 claims abstract description 129
- 150000003839 salts Chemical class 0.000 claims abstract description 54
- -1 aluminic acid ion Chemical class 0.000 claims description 84
- 238000009835 boiling Methods 0.000 claims description 36
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 claims description 28
- MCTWTZJPVLRJOU-UHFFFAOYSA-N 1-methyl-1H-imidazole Chemical compound CN1C=CN=C1 MCTWTZJPVLRJOU-UHFFFAOYSA-N 0.000 claims description 27
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 27
- 150000002500 ions Chemical class 0.000 claims description 25
- 229910052799 carbon Inorganic materials 0.000 claims description 20
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 17
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical group O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 claims description 12
- 239000000654 additive Substances 0.000 claims description 10
- 150000003863 ammonium salts Chemical class 0.000 claims description 10
- KYRYHBRYSSBWLU-UHFFFAOYSA-N 1,2,3,4-tetramethylimidazolidine Chemical compound CC1CN(C)C(C)N1C KYRYHBRYSSBWLU-UHFFFAOYSA-N 0.000 claims description 9
- 150000003457 sulfones Chemical class 0.000 claims description 9
- 229910052783 alkali metal Inorganic materials 0.000 claims description 8
- 150000001408 amides Chemical class 0.000 claims description 8
- 150000002825 nitriles Chemical class 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
- 150000007942 carboxylates Chemical class 0.000 claims description 7
- ZJHQDSMOYNLVLX-UHFFFAOYSA-N diethyl(dimethyl)azanium Chemical compound CC[N+](C)(C)CC ZJHQDSMOYNLVLX-UHFFFAOYSA-N 0.000 claims description 5
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 5
- BEUKLVYOGCCEPF-UHFFFAOYSA-N 1,3-diethylimidazolidine Chemical compound CCN1CCN(CC)C1 BEUKLVYOGCCEPF-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
- SHTANHZPDWEAAR-UHFFFAOYSA-N 2-heptyl-1,3-dimethylimidazolidine Chemical compound CCCCCCCC1N(C)CCN1C SHTANHZPDWEAAR-UHFFFAOYSA-N 0.000 claims description 4
- 230000015572 biosynthetic process Effects 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
- 229910019142 PO4 Inorganic materials 0.000 claims description 3
- 150000001639 boron compounds Chemical class 0.000 claims description 3
- 150000002148 esters 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
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims 24
- 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 3
- FAHBNUUHRFUEAI-UHFFFAOYSA-M hydroxidooxidoaluminium Chemical compound O[Al]=O FAHBNUUHRFUEAI-UHFFFAOYSA-M 0.000 claims 3
- WWGQFLPUAVUZSE-UHFFFAOYSA-N 1,2,3,4-tetramethyl-2h-imidazole Chemical class CC1N(C)C=C(C)N1C WWGQFLPUAVUZSE-UHFFFAOYSA-N 0.000 claims 2
- RYNROCNODWBDCM-UHFFFAOYSA-N 1,3-diethyl-2h-imidazole Chemical class CCN1CN(CC)C=C1 RYNROCNODWBDCM-UHFFFAOYSA-N 0.000 claims 2
- NWYSZNAYMPDEAA-UHFFFAOYSA-N 1,3-dimethyl-2-pentyl-2h-imidazole Chemical class CCCCCC1N(C)C=CN1C NWYSZNAYMPDEAA-UHFFFAOYSA-N 0.000 claims 2
- MNYOKDIIUJDYBM-UHFFFAOYSA-N 1-benzyl-3-methyl-2h-imidazole Chemical compound C1=CN(C)CN1CC1=CC=CC=C1 MNYOKDIIUJDYBM-UHFFFAOYSA-N 0.000 claims 2
- IBZJNLWLRUHZIX-UHFFFAOYSA-N 1-ethyl-3-methyl-2h-imidazole Chemical compound CCN1CN(C)C=C1 IBZJNLWLRUHZIX-UHFFFAOYSA-N 0.000 claims 2
- KRDZGTPEAREWNG-UHFFFAOYSA-N 1-methyl-3-phenyl-2h-imidazole Chemical compound C1=CN(C)CN1C1=CC=CC=C1 KRDZGTPEAREWNG-UHFFFAOYSA-N 0.000 claims 2
- YQBAQZJAJHZGIG-UHFFFAOYSA-N 2-heptyl-1,3-dimethyl-2h-imidazole Chemical class CCCCCCCC1N(C)C=CN1C YQBAQZJAJHZGIG-UHFFFAOYSA-N 0.000 claims 2
- 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 2
- 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 2
- 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 2
- 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 2
- 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 2
- 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 2
- 150000002460 imidazoles Chemical class 0.000 claims 2
- 229910052698 phosphorus Inorganic materials 0.000 claims 2
- 239000011574 phosphorus Substances 0.000 claims 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- 239000010452 phosphate Substances 0.000 claims 1
- 239000008151 electrolyte solution Substances 0.000 description 101
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 27
- 229910052782 aluminium Inorganic materials 0.000 description 26
- 230000000052 comparative effect Effects 0.000 description 22
- 239000011888 foil Substances 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 238000002844 melting Methods 0.000 description 12
- 230000008018 melting Effects 0.000 description 12
- 229940021013 electrolyte solution Drugs 0.000 description 10
- 150000001450 anions Chemical class 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 9
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 8
- 239000003125 aqueous solvent Substances 0.000 description 8
- 150000001298 alcohols Chemical class 0.000 description 7
- JIFXKZJGKSXAGZ-UHFFFAOYSA-N 1-ethyl-2,3-dimethylimidazolidine Chemical compound CCN1CCN(C)C1C JIFXKZJGKSXAGZ-UHFFFAOYSA-N 0.000 description 6
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 6
- PCXWYMXJVNPICR-UHFFFAOYSA-K aluminum;1-ethyl-2,3-dimethylimidazolidin-1-ium;tetrafluoride Chemical compound [F-].[F-].[F-].[F-].[Al+3].CC[NH+]1CCN(C)C1C PCXWYMXJVNPICR-UHFFFAOYSA-K 0.000 description 6
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 125000000909 amidinium group Chemical group 0.000 description 5
- 239000004327 boric acid Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- VSKIZLPBNBFXMZ-UHFFFAOYSA-N 2-carboxybenzoate;1-ethyl-2,3-dimethylimidazolidin-1-ium Chemical compound CC[NH+]1CCN(C)C1C.OC(=O)C1=CC=CC=C1C([O-])=O VSKIZLPBNBFXMZ-UHFFFAOYSA-N 0.000 description 4
- FWWOWPGPERBCNJ-UHFFFAOYSA-N 2-hydroxy-4-(2-hydroxyethoxy)-4-oxobutanoic acid Chemical compound OCCOC(=O)CC(O)C(O)=O FWWOWPGPERBCNJ-UHFFFAOYSA-N 0.000 description 4
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 4
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 4
- 229920005549 butyl rubber Polymers 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- XNGIFLGASWRNHJ-UHFFFAOYSA-M phthalate(1-) Chemical compound OC(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-M 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
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- 229910000077 silane Inorganic materials 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- UJBYZFKDBNQRBW-UHFFFAOYSA-N 2-benzyl-1,3-dimethylimidazol-1-ium Chemical compound CN1C=C[N+](C)=C1CC1=CC=CC=C1 UJBYZFKDBNQRBW-UHFFFAOYSA-N 0.000 description 3
- OTLNPYWUJOZPPA-UHFFFAOYSA-N 4-nitrobenzoic acid Chemical compound OC(=O)C1=CC=C([N+]([O-])=O)C=C1 OTLNPYWUJOZPPA-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Natural products OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-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
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- 125000003118 aryl group Chemical group 0.000 description 3
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- GARJMFRQLMUUDD-UHFFFAOYSA-N 1,1-dimethylpyrrolidin-1-ium Chemical compound C[N+]1(C)CCCC1 GARJMFRQLMUUDD-UHFFFAOYSA-N 0.000 description 2
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- IFGGXMRDYJZDJE-UHFFFAOYSA-N 1,2-dimethyl-3-phenylimidazol-1-ium Chemical compound CN1C=C[N+](C=2C=CC=CC=2)=C1C IFGGXMRDYJZDJE-UHFFFAOYSA-N 0.000 description 2
- UHIFZEQUAVFJKZ-UHFFFAOYSA-N 1,2-dimethyl-3-phenylimidazolidine Chemical compound CC1N(C)CCN1C1=CC=CC=C1 UHIFZEQUAVFJKZ-UHFFFAOYSA-N 0.000 description 2
- CDIWYWUGTVLWJM-UHFFFAOYSA-N 1,3,4-trimethylimidazol-1-ium Chemical compound CC1=C[N+](C)=CN1C CDIWYWUGTVLWJM-UHFFFAOYSA-N 0.000 description 2
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- NVHSSCNZSOYDCO-UHFFFAOYSA-N 1,3-dimethyl-2-pentylimidazol-1-ium Chemical compound CCCCCC=1N(C)C=C[N+]=1C NVHSSCNZSOYDCO-UHFFFAOYSA-N 0.000 description 2
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- CXSBCXDVNBHHOP-UHFFFAOYSA-N 1,3-dimethyl-2-propylimidazolidine Chemical compound CCCC1N(C)CCN1C CXSBCXDVNBHHOP-UHFFFAOYSA-N 0.000 description 2
- DZEHNHDJHLMTNH-UHFFFAOYSA-N 1,3-dimethyl-2-undecylimidazol-1-ium Chemical compound CCCCCCCCCCCC=1N(C)C=C[N+]=1C DZEHNHDJHLMTNH-UHFFFAOYSA-N 0.000 description 2
- DSPUBTKMQXMJCI-UHFFFAOYSA-N 1,3-dimethylbenzimidazol-3-ium Chemical compound C1=CC=C2N(C)C=[N+](C)C2=C1 DSPUBTKMQXMJCI-UHFFFAOYSA-N 0.000 description 2
- SMWUDAKKCDQTPV-UHFFFAOYSA-N 1,3-dimethylimidazolidine Chemical compound CN1CCN(C)C1 SMWUDAKKCDQTPV-UHFFFAOYSA-N 0.000 description 2
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- XMPRLBUMOCTEHU-UHFFFAOYSA-N tert-butyl-ethyl-dimethylazanium Chemical compound CC[N+](C)(C)C(C)(C)C XMPRLBUMOCTEHU-UHFFFAOYSA-N 0.000 description 1
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- QNUAQGIIURYMJX-UHFFFAOYSA-N tri(propan-2-yl)-propylazanium Chemical compound CCC[N+](C(C)C)(C(C)C)C(C)C QNUAQGIIURYMJX-UHFFFAOYSA-N 0.000 description 1
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- TZWFFXFQARPFJN-UHFFFAOYSA-N triethyl(methyl)phosphanium Chemical compound CC[P+](C)(CC)CC TZWFFXFQARPFJN-UHFFFAOYSA-N 0.000 description 1
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- WVLBCYQITXONBZ-UHFFFAOYSA-N trimethyl phosphate Chemical compound COP(=O)(OC)OC WVLBCYQITXONBZ-UHFFFAOYSA-N 0.000 description 1
- COOSQAXLLKTSQO-UHFFFAOYSA-N trimethyl(2-methylpropyl)azanium Chemical compound CC(C)C[N+](C)(C)C COOSQAXLLKTSQO-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
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- ZNEOHLHCKGUAEB-UHFFFAOYSA-N trimethylphenylammonium Chemical group C[N+](C)(C)C1=CC=CC=C1 ZNEOHLHCKGUAEB-UHFFFAOYSA-N 0.000 description 1
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- 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
Landscapes
- 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 (24)
Applications Claiming Priority (4)
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JP141405/2001 | 2001-05-11 | ||
JP2001141405 | 2001-05-11 | ||
JP2001252628 | 2001-08-23 | ||
JP252628/2001 | 2001-08-23 |
Related Parent Applications (1)
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CNB028097165A Division 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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CN101261900A CN101261900A (zh) | 2008-09-10 |
CN101261900B true CN101261900B (zh) | 2011-02-02 |
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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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Also Published As
Publication number | Publication date |
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JP4924658B2 (ja) | 2012-04-25 |
US20040095708A1 (en) | 2004-05-20 |
JP2011181956A (ja) | 2011-09-15 |
CN100394522C (zh) | 2008-06-11 |
JP2009161537A (ja) | 2009-07-23 |
CN1511327A (zh) | 2004-07-07 |
US7460357B2 (en) | 2008-12-02 |
WO2002101773A1 (en) | 2002-12-19 |
JP4631975B2 (ja) | 2011-02-16 |
EP1394824A4 (en) | 2008-01-23 |
JP2009239291A (ja) | 2009-10-15 |
US20060092597A1 (en) | 2006-05-04 |
EP1394824A1 (en) | 2004-03-03 |
CN101261900A (zh) | 2008-09-10 |
US7072173B2 (en) | 2006-07-04 |
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