JP4405905B2 - アルミニウム電解コンデンサの駆動用電解液 - Google Patents
アルミニウム電解コンデンサの駆動用電解液 Download PDFInfo
- Publication number
- JP4405905B2 JP4405905B2 JP2004380069A JP2004380069A JP4405905B2 JP 4405905 B2 JP4405905 B2 JP 4405905B2 JP 2004380069 A JP2004380069 A JP 2004380069A JP 2004380069 A JP2004380069 A JP 2004380069A JP 4405905 B2 JP4405905 B2 JP 4405905B2
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- Prior art keywords
- electrolytic solution
- electrolytic
- driving
- alanylproline
- specific resistance
- 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.)
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- 239000008151 electrolyte solution Substances 0.000 title claims description 27
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims description 8
- 229910052782 aluminium Inorganic materials 0.000 title claims description 8
- 239000003990 capacitor Substances 0.000 title claims description 8
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 claims description 14
- WPWUFUBLGADILS-WDSKDSINSA-N Ala-Pro Chemical compound C[C@H](N)C(=O)N1CCC[C@H]1C(O)=O WPWUFUBLGADILS-WDSKDSINSA-N 0.000 claims description 14
- 108010087924 alanylproline Proteins 0.000 claims description 14
- 239000002904 solvent Substances 0.000 claims description 9
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 5
- 238000002156 mixing Methods 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- 150000005846 sugar alcohols Polymers 0.000 description 5
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 4
- 229930195725 Mannitol Natural products 0.000 description 4
- 239000000594 mannitol Substances 0.000 description 4
- 235000010355 mannitol Nutrition 0.000 description 4
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 3
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000003792 electrolyte Substances 0.000 description 3
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000000600 sorbitol Substances 0.000 description 3
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-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
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
- ATHHXGZTWNVVOU-UHFFFAOYSA-N N-methylformamide Chemical compound CNC=O ATHHXGZTWNVVOU-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- DNSADNILRQYBAB-UHFFFAOYSA-N 1,2,3,4-tetramethylimidazol-1-ium Chemical compound CC1=C[N+](C)=C(C)N1C DNSADNILRQYBAB-UHFFFAOYSA-N 0.000 description 1
- KYRYHBRYSSBWLU-UHFFFAOYSA-N 1,2,3,4-tetramethylimidazolidine Chemical compound CC1CN(C)C(C)N1C KYRYHBRYSSBWLU-UHFFFAOYSA-N 0.000 description 1
- HJSYENHCQNNLAS-UHFFFAOYSA-N 1,2,4-trimethyl-4,5-dihydroimidazole Chemical compound CC1CN(C)C(C)=N1 HJSYENHCQNNLAS-UHFFFAOYSA-N 0.000 description 1
- ZZXUZKXVROWEIF-UHFFFAOYSA-N 1,2-butylene carbonate Chemical compound CCC1COC(=O)O1 ZZXUZKXVROWEIF-UHFFFAOYSA-N 0.000 description 1
- QEIHVTKMBYEXPZ-UHFFFAOYSA-N 1,2-dimethyl-4,5-dihydroimidazole Chemical compound CN1CCN=C1C QEIHVTKMBYEXPZ-UHFFFAOYSA-N 0.000 description 1
- CDIWYWUGTVLWJM-UHFFFAOYSA-N 1,3,4-trimethylimidazol-1-ium Chemical compound CC1=C[N+](C)=CN1C CDIWYWUGTVLWJM-UHFFFAOYSA-N 0.000 description 1
- JJNFHWKVZWAKEB-UHFFFAOYSA-N 1,3,4-trimethylimidazolidin-2-one Chemical compound CC1CN(C)C(=O)N1C JJNFHWKVZWAKEB-UHFFFAOYSA-N 0.000 description 1
- HVVRUQBMAZRKPJ-UHFFFAOYSA-N 1,3-dimethylimidazolium Chemical compound CN1C=C[N+](C)=C1 HVVRUQBMAZRKPJ-UHFFFAOYSA-N 0.000 description 1
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 1
- NFJSYLMJBNUDNG-UHFFFAOYSA-N 1,3-dipropylimidazolidin-2-one Chemical compound CCCN1CCN(CCC)C1=O NFJSYLMJBNUDNG-UHFFFAOYSA-N 0.000 description 1
- VHQUSQAWNQDYNA-UHFFFAOYSA-N 1-benzyl-2-methyl-4,5-dihydroimidazole Chemical compound CC1=NCCN1CC1=CC=CC=C1 VHQUSQAWNQDYNA-UHFFFAOYSA-N 0.000 description 1
- BIYYPNHUTXIIMS-UHFFFAOYSA-N 1-butyl-2-methyl-4,5-dihydroimidazole Chemical compound CCCCN1CCN=C1C BIYYPNHUTXIIMS-UHFFFAOYSA-N 0.000 description 1
- JIFXKZJGKSXAGZ-UHFFFAOYSA-N 1-ethyl-2,3-dimethylimidazolidine Chemical compound CCN1CCN(C)C1C JIFXKZJGKSXAGZ-UHFFFAOYSA-N 0.000 description 1
- VMZNMSUASLBPDS-UHFFFAOYSA-N 1-ethyl-2-methyl-4,5-dihydroimidazole Chemical compound CCN1CCN=C1C VMZNMSUASLBPDS-UHFFFAOYSA-N 0.000 description 1
- RPAPZZDFBPUORQ-UHFFFAOYSA-N 1-methyl-2-pentyl-4,5-dihydroimidazole Chemical compound CCCCCC1=NCCN1C RPAPZZDFBPUORQ-UHFFFAOYSA-N 0.000 description 1
- VWUDGSYCJGEGOI-UHFFFAOYSA-N 1-methyl-2-phenyl-4,5-dihydroimidazole Chemical compound CN1CCN=C1C1=CC=CC=C1 VWUDGSYCJGEGOI-UHFFFAOYSA-N 0.000 description 1
- IJXUZJPYXXEMNG-UHFFFAOYSA-N 1-methyl-2-propyl-4,5-dihydroimidazole Chemical compound CCCC1=NCCN1C IJXUZJPYXXEMNG-UHFFFAOYSA-N 0.000 description 1
- ANFXTILBDGTSEG-UHFFFAOYSA-N 1-methyl-4,5-dihydroimidazole Chemical compound CN1CCN=C1 ANFXTILBDGTSEG-UHFFFAOYSA-N 0.000 description 1
- MCTWTZJPVLRJOU-UHFFFAOYSA-O 1-methylimidazole Chemical compound CN1C=C[NH+]=C1 MCTWTZJPVLRJOU-UHFFFAOYSA-O 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- FGIHSZXDNYRAKQ-UHFFFAOYSA-N 2-benzyl-1-methyl-4,5-dihydroimidazole Chemical compound CN1CCN=C1CC1=CC=CC=C1 FGIHSZXDNYRAKQ-UHFFFAOYSA-N 0.000 description 1
- 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 1
- LLTLVSUMJNRKPD-UHFFFAOYSA-N 2-ethyl-1,3,4-trimethylimidazolidine Chemical compound CCC1N(C)CC(C)N1C LLTLVSUMJNRKPD-UHFFFAOYSA-N 0.000 description 1
- XMWVQAXQVZXGGP-UHFFFAOYSA-N 2-ethyl-1-methyl-4,5-dihydroimidazole Chemical compound CCC1=NCCN1C XMWVQAXQVZXGGP-UHFFFAOYSA-N 0.000 description 1
- SHTANHZPDWEAAR-UHFFFAOYSA-N 2-heptyl-1,3-dimethylimidazolidine Chemical compound CCCCCCCC1N(C)CCN1C SHTANHZPDWEAAR-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- AHMRPFXKAHLQRX-UHFFFAOYSA-N C(C)N1C(N(C(C1)CC)CC)=O Chemical compound C(C)N1C(N(C(C1)CC)CC)=O AHMRPFXKAHLQRX-UHFFFAOYSA-N 0.000 description 1
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 150000001734 carboxylic acid salts Chemical class 0.000 description 1
- 230000009918 complex formation Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- KTHXBEHDVMTNOH-UHFFFAOYSA-N cyclobutanol Chemical compound OC1CCC1 KTHXBEHDVMTNOH-UHFFFAOYSA-N 0.000 description 1
- QCRFMSUKWRQZEM-UHFFFAOYSA-N cycloheptanol Chemical compound OC1CCCCCC1 QCRFMSUKWRQZEM-UHFFFAOYSA-N 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- XCIXKGXIYUWCLL-UHFFFAOYSA-N cyclopentanol Chemical compound OC1CCCC1 XCIXKGXIYUWCLL-UHFFFAOYSA-N 0.000 description 1
- GAEKPEKOJKCEMS-UHFFFAOYSA-N gamma-valerolactone Chemical compound CC1CCC(=O)O1 GAEKPEKOJKCEMS-UHFFFAOYSA-N 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- LHGVFZTZFXWLCP-UHFFFAOYSA-N guaiacol Chemical compound COC1=CC=CC=C1O LHGVFZTZFXWLCP-UHFFFAOYSA-N 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- AJFDBNQQDYLMJN-UHFFFAOYSA-N n,n-diethylacetamide Chemical compound CCN(CC)C(C)=O AJFDBNQQDYLMJN-UHFFFAOYSA-N 0.000 description 1
- KERBAAIBDHEFDD-UHFFFAOYSA-N n-ethylformamide Chemical compound CCNC=O KERBAAIBDHEFDD-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
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Description
すなわち、本発明では、γ-ブチロラクトンを主溶媒とし、少なくとも、カルボン酸またはその塩を配合したアルミニウム電解コンデンサの駆動用電解液において、以下の化学式で示されるアラニルプロリンを配合したことを特徴とする。
〜4に係る電解液と比較して、比抵抗を大きく上昇させずに、少量で火花発生電圧を向上させている。
Claims (2)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004380069A JP4405905B2 (ja) | 2004-12-28 | 2004-12-28 | アルミニウム電解コンデンサの駆動用電解液 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004380069A JP4405905B2 (ja) | 2004-12-28 | 2004-12-28 | アルミニウム電解コンデンサの駆動用電解液 |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2006186212A JP2006186212A (ja) | 2006-07-13 |
JP4405905B2 true JP4405905B2 (ja) | 2010-01-27 |
Family
ID=36739091
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2004380069A Expired - Fee Related JP4405905B2 (ja) | 2004-12-28 | 2004-12-28 | アルミニウム電解コンデンサの駆動用電解液 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP4405905B2 (ja) |
-
2004
- 2004-12-28 JP JP2004380069A patent/JP4405905B2/ja not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JP2006186212A (ja) | 2006-07-13 |
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