JPH04350920A - Electrolyte for electrolytic capacitor - Google Patents
Electrolyte for electrolytic capacitorInfo
- Publication number
- JPH04350920A JPH04350920A JP12388191A JP12388191A JPH04350920A JP H04350920 A JPH04350920 A JP H04350920A JP 12388191 A JP12388191 A JP 12388191A JP 12388191 A JP12388191 A JP 12388191A JP H04350920 A JPH04350920 A JP H04350920A
- Authority
- JP
- Japan
- Prior art keywords
- acid
- electrolyte
- electrolytic
- electrolytic capacitor
- polyvinyl alcohol
- 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.)
- Pending
Links
- 239000003990 capacitor Substances 0.000 title claims abstract description 39
- 239000003792 electrolyte Substances 0.000 title claims abstract description 21
- 229920002451 polyvinyl alcohol Polymers 0.000 claims abstract description 19
- 239000004372 Polyvinyl alcohol Substances 0.000 claims abstract description 18
- 239000002904 solvent Substances 0.000 claims abstract description 15
- 239000002798 polar solvent Substances 0.000 claims abstract description 9
- 150000007522 mineralic acids Chemical class 0.000 claims abstract description 6
- 150000007524 organic acids Chemical class 0.000 claims abstract description 6
- 150000003839 salts Chemical class 0.000 claims abstract description 6
- 239000008151 electrolyte solution Substances 0.000 claims description 24
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims description 10
- 239000007788 liquid Substances 0.000 claims 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 15
- -1 alkyl phosphoric acid Chemical compound 0.000 description 15
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 15
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 9
- 239000000654 additive Substances 0.000 description 8
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 6
- 230000000996 additive effect Effects 0.000 description 6
- 239000004327 boric acid Substances 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 125000003545 alkoxy group Chemical group 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 4
- TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-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
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 239000010416 ion conductor Substances 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 3
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 2
- 239000005711 Benzoic acid Substances 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
- PMDCZENCAXMSOU-UHFFFAOYSA-N N-ethylacetamide Chemical compound CCNC(C)=O PMDCZENCAXMSOU-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
- 239000003513 alkali Substances 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 235000010233 benzoic acid Nutrition 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 238000003487 electrochemical reaction Methods 0.000 description 2
- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- WEVYAHXRMPXWCK-UHFFFAOYSA-N methyl cyanide Natural products CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 230000003647 oxidation Effects 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
- WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 2
- 239000003586 protic polar solvent Substances 0.000 description 2
- CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical compound OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 description 2
- 238000006722 reduction reaction Methods 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 230000000087 stabilizing effect Effects 0.000 description 2
- IMFACGCPASFAPR-UHFFFAOYSA-O tributylazanium Chemical compound CCCC[NH+](CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-O 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- XLSXKCPCBOMHON-UHFFFAOYSA-N 1,1-dimethoxypropan-1-ol Chemical compound CCC(O)(OC)OC XLSXKCPCBOMHON-UHFFFAOYSA-N 0.000 description 1
- GARJMFRQLMUUDD-UHFFFAOYSA-N 1,1-dimethylpyrrolidin-1-ium Chemical compound C[N+]1(C)CCCC1 GARJMFRQLMUUDD-UHFFFAOYSA-N 0.000 description 1
- OEYNWAWWSZUGDU-UHFFFAOYSA-N 1-methoxypropane-1,2-diol Chemical compound COC(O)C(C)O OEYNWAWWSZUGDU-UHFFFAOYSA-N 0.000 description 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- KWIPUXXIFQQMKN-UHFFFAOYSA-N 2-azaniumyl-3-(4-cyanophenyl)propanoate Chemical compound OC(=O)C(N)CC1=CC=C(C#N)C=C1 KWIPUXXIFQQMKN-UHFFFAOYSA-N 0.000 description 1
- KQTFRASJMFIJPC-UHFFFAOYSA-M 2-carboxybenzoate;tetramethylazanium Chemical compound C[N+](C)(C)C.OC(=O)C1=CC=CC=C1C([O-])=O KQTFRASJMFIJPC-UHFFFAOYSA-M 0.000 description 1
- SZIFAVKTNFCBPC-UHFFFAOYSA-N 2-chloroethanol Chemical compound OCCCl SZIFAVKTNFCBPC-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 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 1
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 229910004039 HBF4 Inorganic materials 0.000 description 1
- 229910004713 HPF6 Inorganic materials 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- BAVYZALUXZFZLV-UHFFFAOYSA-O Methylammonium ion Chemical compound [NH3+]C BAVYZALUXZFZLV-UHFFFAOYSA-O 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- SUAKHGWARZSWIH-UHFFFAOYSA-N N,N‐diethylformamide Chemical compound CCN(CC)C=O SUAKHGWARZSWIH-UHFFFAOYSA-N 0.000 description 1
- OHLUUHNLEMFGTQ-UHFFFAOYSA-N N-methylacetamide Chemical compound CNC(C)=O OHLUUHNLEMFGTQ-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical group CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- XKMRRTOUMJRJIA-UHFFFAOYSA-N ammonia nh3 Chemical compound N.N XKMRRTOUMJRJIA-UHFFFAOYSA-N 0.000 description 1
- 229940090948 ammonium benzoate Drugs 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- IKFMRFYLIRAXAJ-UHFFFAOYSA-N azane;nonanedioic acid Chemical compound N.OC(=O)CCCCCCCC(O)=O IKFMRFYLIRAXAJ-UHFFFAOYSA-N 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
- 229940018557 citraconic acid Drugs 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 150000003950 cyclic amides Chemical class 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
- 125000005131 dialkylammonium group Chemical group 0.000 description 1
- JQVDAXLFBXTEQA-UHFFFAOYSA-O dibutylazanium Chemical compound CCCC[NH2+]CCCC JQVDAXLFBXTEQA-UHFFFAOYSA-O 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-O diethylammonium Chemical compound CC[NH2+]CC HPNMFZURTQLUMO-UHFFFAOYSA-O 0.000 description 1
- ZJIPHXXDPROMEF-UHFFFAOYSA-N dihydroxyphosphanyl dihydrogen phosphite Chemical compound OP(O)OP(O)O ZJIPHXXDPROMEF-UHFFFAOYSA-N 0.000 description 1
- TVACALAUIQMRDF-UHFFFAOYSA-N dodecyl dihydrogen phosphate Chemical compound CCCCCCCCCCCCOP(O)(O)=O TVACALAUIQMRDF-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000003411 electrode reaction Methods 0.000 description 1
- 229940021013 electrolyte solution Drugs 0.000 description 1
- 125000005670 ethenylalkyl group Chemical group 0.000 description 1
- QUSNBJAOOMFDIB-UHFFFAOYSA-O ethylaminium Chemical compound CC[NH3+] QUSNBJAOOMFDIB-UHFFFAOYSA-O 0.000 description 1
- LIWAQLJGPBVORC-UHFFFAOYSA-N ethylmethylamine Chemical compound CCNC LIWAQLJGPBVORC-UHFFFAOYSA-N 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 230000037427 ion transport Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 150000002596 lactones Chemical class 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
- 235000010355 mannitol Nutrition 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- YHLVIDQQTOMBGN-UHFFFAOYSA-N methyl prop-2-enyl carbonate Chemical compound COC(=O)OCC=C YHLVIDQQTOMBGN-UHFFFAOYSA-N 0.000 description 1
- ZIYVHBGGAOATLY-UHFFFAOYSA-N methylmalonic acid Chemical compound OC(=O)C(C)C(O)=O ZIYVHBGGAOATLY-UHFFFAOYSA-N 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 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
- ZWLPBLYKEWSWPD-UHFFFAOYSA-N o-toluic acid Chemical compound CC1=CC=CC=C1C(O)=O ZWLPBLYKEWSWPD-UHFFFAOYSA-N 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 125000005496 phosphonium group Chemical group 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- WGYKZJWCGVVSQN-UHFFFAOYSA-O propan-1-aminium Chemical compound CCC[NH3+] WGYKZJWCGVVSQN-UHFFFAOYSA-O 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 230000002123 temporal effect Effects 0.000 description 1
- CBXCPBUEXACCNR-UHFFFAOYSA-N tetraethylammonium Chemical compound CC[N+](CC)(CC)CC CBXCPBUEXACCNR-UHFFFAOYSA-N 0.000 description 1
- CIFIGXMZHITUAZ-UHFFFAOYSA-M tetraethylazanium;benzoate Chemical compound CC[N+](CC)(CC)CC.[O-]C(=O)C1=CC=CC=C1 CIFIGXMZHITUAZ-UHFFFAOYSA-M 0.000 description 1
- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-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
- 125000005208 trialkylammonium group Chemical group 0.000 description 1
- SEACXNRNJAXIBM-UHFFFAOYSA-N triethyl(methyl)azanium Chemical compound CC[N+](C)(CC)CC SEACXNRNJAXIBM-UHFFFAOYSA-N 0.000 description 1
- ZMANZCXQSJIPKH-UHFFFAOYSA-O triethylammonium ion Chemical compound CC[NH+](CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-O 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、電解コンデンサ用電解
液の改良に関し、更に詳しくは、特定の添加物を添加す
ることにより、電導度を維持しつつ耐電圧特性を向上さ
せることができる電解コンデンサ用電解液の改良に関す
る。[Industrial Application Field] The present invention relates to the improvement of electrolytic solutions for electrolytic capacitors, and more specifically, the present invention relates to the improvement of electrolytic solutions for electrolytic capacitors. Concerning improvements in electrolytes for capacitors.
【0002】0002
【従来の技術】電解コンデンサは、小形、大容量、安価
で整流出力の平滑化等に優れた特性を示し、各種電気・
電子機器の重要な構成要素の1つであり、一般に、表面
を電解酸化によって酸化皮膜に変えたアルミニウムフィ
ルムを陽極とし、この酸化皮膜を誘電体として集電陰極
との間に電解液を介在させて作製される。使用中は常に
酸化皮膜を再生しているため安定であるが、例えば長期
間使用しないと再生が不十分となり劣化する。[Prior Art] Electrolytic capacitors are small, large capacity, inexpensive, and have excellent characteristics such as smoothing rectified output.
It is one of the important components of electronic equipment, and generally an aluminum film whose surface has been changed into an oxide film by electrolytic oxidation is used as an anode, and an electrolyte is interposed between it and the current collector cathode, using this oxide film as a dielectric. It is made by During use, the oxide film is constantly regenerated, so it is stable, but if it is not used for a long time, for example, regeneration becomes insufficient and it deteriorates.
【0003】電解コンデンサの使用中に進行する化学反
応において、電解液はイオン移動の媒体たるイオン伝導
体を形成する。電解液と電極との界面では電極反応の進
行によって電荷が移動し、陽極面では酸化反応が、陰極
面では還元反応が進行し、それと共にイオン伝導体たる
電解液の中をイオンが移動して電流が流れる。したがっ
て、電解液の電気電導度は、電解コンデンサの使用中に
進行する化学反応におけるイオン伝導体たる電解液の特
性を反映し、コンデンサの総合性能を評価する重要な指
標の1つである。In the chemical reactions that occur during use of electrolytic capacitors, the electrolyte forms an ionic conductor that is a medium for ion transport. Charges move at the interface between the electrolyte and the electrode as the electrode reaction progresses, an oxidation reaction progresses at the anode surface, a reduction reaction progresses at the cathode surface, and at the same time, ions move through the electrolyte, which is an ionic conductor. Current flows. Therefore, the electrical conductivity of the electrolytic solution reflects the characteristics of the electrolytic solution as an ionic conductor in the chemical reactions that occur during use of the electrolytic capacitor, and is one of the important indicators for evaluating the overall performance of the capacitor.
【0004】電解コンデンサは化学反応を行わせながら
使用するため、その特性は電解液の性質に大きく依存す
る。表面を酸化皮膜としたアルミニウム電極と電解液と
の間で起る化学反応の定常状態を維持し、誘電体とする
アルミニウム酸化皮膜を良好に保持することが性能の安
定化に重要であり、使用法を誤って例えば過剰の高電圧
負荷等により化学的定常状態が乱れると、アルミニウム
酸化皮膜が破壊されやがては絶縁が破れるに至る。[0004] Since electrolytic capacitors are used while undergoing chemical reactions, their characteristics greatly depend on the properties of the electrolyte. Maintaining a steady state of the chemical reaction that occurs between the aluminum electrode, which has an oxide film on its surface, and the electrolyte, and maintaining the aluminum oxide film, which serves as a dielectric, in good condition is important for stabilizing performance. If the chemical steady state is disturbed due to an incorrect method, for example, due to an excessively high voltage load, the aluminum oxide film will be destroyed and eventually the insulation will be broken.
【0005】コンデンサの負荷電圧が上昇し高電圧負荷
による誘電体の物性変化が進行し、時間的な誘電率の変
化が生じる結果電気化学的状態が動揺する現象をシンチ
レーションというが、このような現象が認められる電圧
をシンチレーション電圧(火花電圧)としてコンデンサ
の耐電圧性の尺度とすることができ、シンチレーション
電圧(火花電圧)が高い程コンデンサの耐電圧性が大き
いことを示す。これは簡便には、最終コンデンサ製品ま
で組み上げることなく、適当な大きさの未化成アルミニ
ウム箔を測定しようとする電解液に浸した状態でも測定
することができる。[0005] Scintillation is a phenomenon in which the load voltage of a capacitor increases and the physical properties of the dielectric material change due to the high voltage load, and the electrochemical state fluctuates as a result of temporal changes in dielectric constant. The voltage at which this is observed can be used as a scintillation voltage (spark voltage) as a measure of the voltage resistance of the capacitor, and the higher the scintillation voltage (spark voltage), the greater the voltage resistance of the capacitor. This can be easily measured by immersing an unformed aluminum foil of an appropriate size in the electrolytic solution to be measured, without assembling the final capacitor product.
【0006】従来の一般的な電解コンデンサ用電解液に
おいては、高耐電圧性を得るために電解液にホウ酸等の
酸またはこれらの塩が主溶質として添加された。また、
これら以外にも種々の添加物を添加することにより電解
コンデンサ用電解液を改良して高耐電圧性を得る試みが
なされている。[0006] In conventional electrolytic solutions for general electrolytic capacitors, an acid such as boric acid or a salt thereof is added as a main solute in order to obtain high voltage resistance. Also,
In addition to these, attempts have been made to improve the electrolytic solution for electrolytic capacitors and obtain high voltage resistance by adding various additives.
【0007】高耐電圧性を得るための添加剤としては、
例えば、スルファミン酸の添加(特公昭49−8296
3 号)、スベリン酸の添加(特開昭49−13386
0号)、リン酸ドデシルの添加(特開昭49−7365
9 号)、アルキルリン酸の添加(特開昭52−153
154号)、ジ亜リン酸の添加(特開昭57−1419
13号)、ホウ酸−マンニット系の使用(特開昭57−
60829 号)、ホウ酸−マンニット−ポリビニルア
ルコール系の使用(特開昭59−177915号)、変
性シリコーンオイルの添加(特開平1−175722号
)等が提案されているが、高電導度を維持した耐電圧の
向上は必ずしも十分には望めなかった。[0007] Additives for obtaining high voltage resistance include:
For example, addition of sulfamic acid (Japanese Patent Publication No. 49-8296
No. 3), addition of suberic acid (JP-A-49-13386)
No. 0), addition of dodecyl phosphate (JP-A-49-7365)
No. 9), addition of alkyl phosphoric acid (JP-A-52-153)
No. 154), addition of diphosphorous acid (JP-A-57-1419)
No. 13), use of boric acid-mannite system (JP-A-57-
60829), the use of boric acid-mannitol-polyvinyl alcohol system (Japanese Patent Application Laid-open No. 177915-1982), and the addition of modified silicone oil (Japanese Patent Application Laid-open No. 175722-1999), etc. The maintained voltage resistance could not necessarily be sufficiently improved.
【0008】[0008]
【発明が解決しようとする課題】従来より、ある種の電
解液にポリビニルアルコールを添加し、その特性を向上
させる試みが幾つか行われている。ポリビニルアルコー
ルを用いた先行技術として、例えば、特公昭37−15
073号、特開昭49−121162 号、特開昭52
−129963 号並びに特開昭60−91618号を
例示することができる。[Problems to be Solved by the Invention] Several attempts have been made to improve the properties of certain electrolytic solutions by adding polyvinyl alcohol to them. As a prior art using polyvinyl alcohol, for example, Japanese Patent Publication No. 37-15
No. 073, JP-A-49-121162, JP-A-52
-129963 and JP-A-60-91618 can be exemplified.
【0009】この度、このポリビニルアルコールの特性
に着目し、その種々の誘導体を電解コンデンサ用電解液
に添加した場合の効果について鋭意検討を続けた結果、
ある種の特定の誘導体が、電導度を維持しつつ耐電圧特
性を顕著に向上させることを突き止めた。[0009] As a result of paying attention to the properties of this polyvinyl alcohol and continuing to study the effects of adding various derivatives thereof to electrolyte solutions for electrolytic capacitors, we found that:
We have discovered that certain specific derivatives can significantly improve withstand voltage characteristics while maintaining electrical conductivity.
【0010】よって本発明は、ポリビニルアルコールの
所定の誘導体を添加することにより、電導度を維持しつ
つ耐電圧特性を顕著に向上させた電解コンデンサ用電解
液を提供することを目的とする。[0010] Accordingly, an object of the present invention is to provide an electrolytic solution for electrolytic capacitors which has significantly improved dielectric strength characteristics while maintaining electrical conductivity by adding a predetermined derivative of polyvinyl alcohol.
【0011】[0011]
【課題を解決するための手段】本発明によれば、有機極
性溶媒を主溶媒とし、有機酸もしくは無機酸またはその
塩を溶質とした電解コンデンサ用電解液に、ヒドロキシ
エチルアルキル化ポリビニルアルコールを添加したこと
を特徴とする電解コンデンサ用電解液が提供される。[Means for Solving the Problems] According to the present invention, hydroxyethyl alkylated polyvinyl alcohol is added to an electrolytic solution for an electrolytic capacitor using an organic polar solvent as a main solvent and an organic acid or an inorganic acid or a salt thereof as a solute. An electrolytic solution for an electrolytic capacitor is provided.
【0012】ヒドロキシエチルアルキル化ポリビニルア
ルコールは、例えばその合成法の1つとして、次のよう
にして得ることができる。[0012] Hydroxyethyl alkylated polyvinyl alcohol can be obtained, for example, as one of its synthetic methods as follows.
【0013】ビニルアルキルエーテルと酢酸ビニルモノ
マーとを過酸化ベンゾイル存在下に反応させ、酢酸ビニ
ルビニルアルキルエーテル共重合体を得る。得られた共
重合体をアルカリによりケン化し、ビニルアルコールビ
ニルアルキルエーテル共重合体とする。更にこの共重合
体に対し、アルカリ触媒存在下に、酸化エチレン(また
はエチレンクロルヒドリン)を作用させることにより、
ヒドロキシエチルアルキル化ポリビニルアルコールが得
られる。Vinyl alkyl ether and vinyl acetate monomer are reacted in the presence of benzoyl peroxide to obtain a vinyl acetate vinyl alkyl ether copolymer. The obtained copolymer is saponified with an alkali to obtain a vinyl alcohol vinyl alkyl ether copolymer. Furthermore, by allowing ethylene oxide (or ethylene chlorohydrin) to act on this copolymer in the presence of an alkali catalyst,
Hydroxyethyl alkylated polyvinyl alcohol is obtained.
【0014】電解液の有機極性溶媒に単独または組合せ
て使用し得る溶媒の具体例として次のような溶媒を例示
することができる:
プロトン性極性溶媒
エタノール、プロパノール、ブタノール、ペンタノール
、ヘキサノール、シクロブタノール、シクロペンタノー
ル、シクロヘキサノール、並びにベンジルアルコール等
の1価アルコール類、エチレングリコール、プロピレン
グリコール、グリセリン、メトキシエタノール、エトキ
シエタノール、メトキシプロピレングリコール、ジメト
キシプロパノール、メチルセロソルブ並びにエチルセロ
ソルブ等の多価アルコールおよびアルコールエーテル類
、
非プロトン性極性溶媒
N−メチルホルムアミド、N,N−ジメチルホルムアミ
ド、N−エチルホルムアミド、N,N−ジエチルホルム
アミド、N−メチルアセトアミド、N,N−ジメチルア
セトアミド、N−エチルアセトアミド、N,N−ジエチ
ルアセトアミド、並びにヘキサメチルホスホリックアミ
ド等のアミド系溶媒、γ−ブチロラクトン、N−メチル
−2− ピロリドン、エチレンカーボネイト、プロピレ
ンカーボネイト、イソブチレンカーボネイト等のラクト
ン、環状アミド系溶媒、アセトニトリル等のニトリル系
溶媒、ジメチルスルホキシド等のオキシド系溶媒。Specific examples of solvents that can be used alone or in combination as the organic polar solvent of the electrolytic solution include the following: Protic polar solvents ethanol, propanol, butanol, pentanol, hexanol, cycloprotic polar solvents Monohydric alcohols such as butanol, cyclopentanol, cyclohexanol, and benzyl alcohol; polyhydric alcohols such as ethylene glycol, propylene glycol, glycerin, methoxyethanol, ethoxyethanol, methoxypropylene glycol, dimethoxypropanol, methyl cellosolve, and ethyl cellosolve. and alcohol ethers, aprotic polar solvents N-methylformamide, N,N-dimethylformamide, N-ethylformamide, N,N-diethylformamide, N-methylacetamide, N,N-dimethylacetamide, N-ethylacetamide , N,N-diethylacetamide, amide solvents such as hexamethylphosphoric amide, lactones such as γ-butyrolactone, N-methyl-2-pyrrolidone, ethylene carbonate, propylene carbonate, isobutylene carbonate, cyclic amide solvents, acetonitrile Nitrile solvents such as, oxide solvents such as dimethyl sulfoxide.
【0015】有機酸もしくは無機酸またはその塩たる電
解液の電解質に単独または組合せて使用し得る電解質の
具体例として次のような電解質を例示することができる
:
有機酸
ギ酸、酢酸、プロピオン酸、エナント酸等の脂肪族モノ
カルボン酸、マロン酸、コハク酸、グルタル酸、アジピ
ン酸、メチルマロン酸、ピメリン酸、スベリン酸、アゼ
ライン酸、セバシン酸、デカンジカルボン酸、マレイン
酸、シトラコン酸、並びにイタコン酸等の脂肪族ジカル
ボン酸、安息香酸、フタル酸、サリチル酸、トルイル酸
、並びにピロメリト酸等の芳香族カルボン酸、無機酸
ホウ酸、リン酸、ケイ酸、HBF4、
HPF6等の無機酸、
アンモニウム
アンモニウム(NH4+)、メチルアンモニウム、エチ
ルアンモニウム、並びにプロピルアンモニウム等のモノ
アルキルアンモニウム、ジメチルアンモニウム、ジエチ
ルアンモニウム、エチルメチルアンモニウム、並びにジ
ブチルアンモニウム等のジアルキルアンモニウム、トリ
メチルアンモニウム、トリエチルアンモニウム、並びに
トリブチルアンモニウム等のトリアルキルアンモニウム
、テトラメチルアンモニウム、トリエチルメチルアンモ
ニウム、トリブチルアンモニウム、テトラエチルアンモ
ニウム、並びにN,N−ジメチルピロリジニウム等の第
4級アンモニウム、
その他
ホスホニウムおよびアルソニウムも使用することができ
る。[0015] Specific examples of electrolytes that can be used alone or in combination in the electrolyte of organic acids, inorganic acids, or salts thereof include the following: organic acids formic acid, acetic acid, propionic acid, Aliphatic monocarboxylic acids such as enanthic acid, malonic acid, succinic acid, glutaric acid, adipic acid, methylmalonic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, decanedicarboxylic acid, maleic acid, citraconic acid, and itacone Aliphatic dicarboxylic acids such as benzoic acid, phthalic acid, salicylic acid, toluic acid, aromatic carboxylic acids such as pyromellitic acid, inorganic acids such as boric acid, phosphoric acid, silicic acid, HBF4, HPF6, ammonium ammonium (NH4+), monoalkylammoniums such as methylammonium, ethylammonium, and propylammonium; dialkylammoniums such as dimethylammonium, diethylammonium, ethylmethylammonium, and dibutylammonium; trialkylammoniums such as trimethylammonium, triethylammonium, and tributylammonium; Quaternary ammoniums such as ammonium, tetramethylammonium, triethylmethylammonium, tributylammonium, tetraethylammonium, and N,N-dimethylpyrrolidinium, as well as other phosphoniums and arsoniums can also be used.
【0016】本発明による電解コンデンサ用電解液の有
機極性溶媒は、前記したプロトン性極性溶媒もしくは非
プロトン性極性溶媒単独または任意の混合溶媒とするこ
とができ、これらの溶媒100 重量部に対して、必要
に応じて0.1〜10重量部程度の水を混合することに
より、電導度の低下および化成性(酸化皮膜形成性)の
更なる向上を図ることができる。このような溶媒系に対
し、溶質とする有機酸もしくは無機酸あるいはその塩を
1.0〜40重量部溶解すれば好適である。The organic polar solvent of the electrolytic solution for an electrolytic capacitor according to the present invention can be the above-mentioned protic polar solvent or aprotic polar solvent alone or any mixed solvent, and the amount of the organic polar solvent in the electrolytic solution for an electrolytic capacitor according to the present invention is By mixing water in an amount of about 0.1 to 10 parts by weight, if necessary, it is possible to further improve the reduction in electrical conductivity and the chemical formation property (oxidation film forming property). It is preferable that 1.0 to 40 parts by weight of an organic or inorganic acid or a salt thereof to be used as a solute be dissolved in such a solvent system.
【0017】このような溶質−溶媒系からなる電解液に
対し、好ましくは前記したヒドロキシエチルアルキル化
ポリビニルアルコールを1.0〜10重量部、更に好ま
しくは1.0〜5.0重量部添加することにより、電導
度を維持しつつ耐電圧特性を向上させることのできる電
解コンデンサ用電解液が得られる。Preferably, 1.0 to 10 parts by weight, more preferably 1.0 to 5.0 parts by weight of the above-mentioned hydroxyethyl alkylated polyvinyl alcohol is added to the electrolytic solution consisting of such a solute-solvent system. As a result, an electrolytic solution for an electrolytic capacitor can be obtained that can improve the withstand voltage characteristics while maintaining the electrical conductivity.
【0018】[0018]
【作用】本発明が開示した電解コンデンサ用電解液に添
加する独特の添加物であるヒドロキシエチルアルキル化
ポリビニルアルコールが、電解コンデンサ用電解液中で
どのような作用をするのか、その作用機構自体は明らか
ではない。しかしながら、本発明による電解コンデンサ
用電解液は、電解コンデンサの陽極、陰極、アルミニウ
ム酸化皮膜誘電体並びに電解液から構成される電気化学
的反応系の化学的定常状態の安定化に何らかの寄与をし
ているものと推定される。[Operation] How does hydroxyethyl alkylated polyvinyl alcohol, which is a unique additive added to the electrolytic solution for electrolytic capacitors disclosed in the present invention, act in the electrolytic solution for electrolytic capacitors?The mechanism of its action itself is unclear. It's not clear. However, the electrolytic solution for an electrolytic capacitor according to the present invention does not contribute in some way to stabilizing the chemical steady state of the electrochemical reaction system consisting of the anode, cathode, aluminum oxide film dielectric, and electrolyte of the electrolytic capacitor. It is estimated that there are.
【0019】前記したように、電解コンデンサは化学反
応を行わせながら使用するため、その特性は電解液の性
質に大きく依存する。表面を酸化皮膜としたアルミニウ
ム電極と電解液との間で起る化学反応の定常状態を維持
し、誘電体とするアルミニウム酸化皮膜を良好に保持す
ることが性能の安定化に重要である。As described above, since an electrolytic capacitor is used while undergoing a chemical reaction, its characteristics largely depend on the properties of the electrolyte. It is important to maintain a steady state of the chemical reaction that occurs between the aluminum electrode, which has an oxide film on its surface, and the electrolyte, and to maintain the aluminum oxide film, which serves as a dielectric, in a good condition to stabilize performance.
【0020】本発明は、独特の添加物であるヒドロキシ
エチルアルキル化ポリビニルアルコールを添加すること
により、電気化学的反応系である電解コンデンサ全体が
安定化され、良好なコンデンサ特性を与えるものと推定
される。In the present invention, it is presumed that by adding hydroxyethyl alkylated polyvinyl alcohol, which is a unique additive, the entire electrolytic capacitor, which is an electrochemical reaction system, is stabilized and provides good capacitor characteristics. Ru.
【0021】[0021]
【発明の効果】本発明によれば、ポリビニルアルコール
の所定の誘導体を添加することにより、電導度を維持し
つつ耐電圧特性を顕著に向上させた電解コンデンサ用電
解液が提供される。According to the present invention, there is provided an electrolytic solution for electrolytic capacitors which has significantly improved dielectric strength characteristics while maintaining electrical conductivity by adding a specified derivative of polyvinyl alcohol.
【0022】[0022]
【実施例】以下に実施例により本発明を更に詳細に説明
するが、本発明は以下の実施例にのみ限定されるもので
はない。[Examples] The present invention will be explained in more detail with reference to Examples below, but the present invention is not limited to the following Examples.
【0023】以下の実施例では、本発明に使用するヒド
ロキシエチルアルキル化ポリビニルアルコールとして、
アルコキシル基、メトキシル基、エトキシル基およびヒ
ドロキシプロポキシル基の含有量が異なる次の記号で示
すものを用いた:
A:アルコキシル基、メトキシル基含有量5〜10%ヒ
ドロキシプロポキシル基含有量60〜65%粘度(20
°CにおけるCPS)15.5B:アルコキシル基、エ
トキシル基含有量15〜20%ヒドロキシプロポキシル
基含有量75〜80%粘度(20°CにおけるCPS)
7.5C:アルコキシル基、メトキシル基含有量20〜
25%ヒドロキシプロポキシル基含有量60〜65%粘
度(20°CにおけるCPS)25.0なお、粘度は2
%水溶液での測定値である。所定の溶媒および溶質に対
して、これらのヒドロキシエチルアルキル化ポリビニル
アルコールを所定量添加して電解コンデンサ用電解液を
作製した。電解コンデンサは常法によって作製した。In the following examples, hydroxyethyl alkylated polyvinyl alcohol used in the present invention includes:
Those shown by the following symbols having different contents of alkoxyl group, methoxyl group, ethoxyl group and hydroxypropoxyl group were used: A: Alkoxyl group, methoxyl group content 5-10% Hydroxypropoxyl group content 60-65 % viscosity (20
CPS at °C) 15.5B: Alkoxyl group, ethoxyl group content 15-20% Hydroxypropoxyl group content 75-80% Viscosity (CPS at 20 °C)
7.5C: Alkoxyl group, methoxyl group content 20~
25% Hydroxypropoxyl group content 60-65% Viscosity (CPS at 20°C) 25.0 Note that the viscosity is 2
% aqueous solution. A predetermined amount of these hydroxyethyl alkylated polyvinyl alcohols was added to a predetermined solvent and solute to prepare an electrolytic solution for an electrolytic capacitor. The electrolytic capacitor was manufactured by a conventional method.
【0024】以下に本発明によるヒドロキシエチルアル
キル化ポリビニルアルコール添加後における電導度およ
び耐電圧(実施例1〜4)、並びに添加前における電導
度および耐電圧(比較例1〜4)を示す。なお、耐電圧
は、315V、22μFコンデンサ素子に含浸し、10
mAにて測定した。The electrical conductivity and withstand voltage after addition of the hydroxyethyl alkylated polyvinyl alcohol according to the present invention (Examples 1 to 4) and the electrical conductivity and withstand voltage before addition (Comparative Examples 1 to 4) are shown below. The withstand voltage is 315V, 22μF capacitor element is impregnated,
Measured at mA.
【0025】実施例1および比較例1
電解液組成( )内は重量部
溶媒: エチレングリコール(100)溶質: 安
息香酸アンモニウム(15)、安息香酸(3)、ホウ酸
(2)
添加剤:A(1.5)
電導度および耐電圧の測定結果は次の通りであった。
実施例1の耐電圧性は、比較例1に対して20%増加し
た。Example 1 and Comparative Example 1 Electrolyte composition (Figures in parentheses are parts by weight. Solvent: Ethylene glycol (100) Solute: Ammonium benzoate (15), Benzoic acid (3), Boric acid (2) Additive: A (1.5) The measurement results of conductivity and withstand voltage were as follows. The voltage resistance of Example 1 was increased by 20% compared to Comparative Example 1.
【0026】実施例2および比較例2
電解液組成( )内は重量部
溶媒: エチレングリコール(100)、水(3)溶
質: アゼライン酸モノアンモニウム(10)、ホウ
酸(2)
添加剤:B(2)
電導度および耐電圧の測定結果は次の通りであった。
実施例2の耐電圧性は、比較例2に対して27%増加し
た。Example 2 and Comparative Example 2 Electrolyte composition (Figures in parentheses are parts by weight. Solvent: Ethylene glycol (100), water (3) Solute: Monoammonium azelaate (10), boric acid (2) Additive: B (2) The measurement results of electrical conductivity and withstand voltage were as follows. The voltage resistance of Example 2 increased by 27% compared to Comparative Example 2.
【0027】実施例3および比較例3
電解液組成( )内は重量部
溶媒: γ−ブチロラクトン(60)、メチルセルソ
ルブ(15)、エチレングリコール(10)溶質:
フタル酸モノテトラメチルアンモニウム(15)、ホウ
酸(2)
添加剤:B(2)
電導度および耐電圧の測定結果は次の通りであった。
実施例3の耐電圧性は、比較例3に対して13%増加し
た。Example 3 and Comparative Example 3 Electrolyte composition () Parts by weight Solvent: γ-Butyrolactone (60), Methyl Cellosolve (15), Ethylene Glycol (10) Solute:
Monotetramethylammonium phthalate (15), boric acid (2) Additive: B (2) The measurement results of electrical conductivity and withstand voltage were as follows. The voltage resistance of Example 3 increased by 13% compared to Comparative Example 3.
【0028】実施例4および比較例4
電解液組成( )内は重量部
溶媒: γ−ブチロラクトン(60)、メチルセルソ
ルブ(10)、エチレングリコール(15)溶質:
安息香酸テトラエチルアンモニウム(15)、ホウ酸(
2)マンニット(2)
添加剤:C(1.5)
電導度および耐電圧の測定結果は次の通りであった。
実施例4の耐電圧性は、比較例4に対して42%増加し
た。Example 4 and Comparative Example 4 Electrolyte composition (Figures in parentheses indicate parts by weight of solvent: γ-butyrolactone (60), methylcellosolve (10), ethylene glycol (15) Solute:
Tetraethylammonium benzoate (15), boric acid (
2) Mannitol (2) Additive: C (1.5) The measurement results of electrical conductivity and withstand voltage were as follows. The voltage resistance of Example 4 increased by 42% compared to Comparative Example 4.
【0029】以上の結果から、本発明によれば、ポリビ
ニルアルコールの所定の誘導体を添加することにより、
電導度を維持しつつ耐電圧特性を顕著に向上させた電解
コンデンサ用電解液が得られることが分る。From the above results, according to the present invention, by adding a specified derivative of polyvinyl alcohol,
It can be seen that an electrolytic solution for electrolytic capacitors can be obtained which has significantly improved voltage resistance characteristics while maintaining electrical conductivity.
Claims (1)
しくは無機酸またはその塩を溶質とした電解コンデンサ
用電解液に、ヒドロキシエチルアルキル化ポリビニルア
ルコールを添加したことを特徴とする電解コンデンサ用
電解液。1. An electrolyte for electrolytic capacitors, characterized in that hydroxyethyl alkylated polyvinyl alcohol is added to an electrolytic solution for electrolytic capacitors, the main solvent being an organic polar solvent and the solute being an organic acid or an inorganic acid or a salt thereof. liquid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12388191A JPH04350920A (en) | 1991-05-28 | 1991-05-28 | Electrolyte for electrolytic capacitor |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12388191A JPH04350920A (en) | 1991-05-28 | 1991-05-28 | Electrolyte for electrolytic capacitor |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04350920A true JPH04350920A (en) | 1992-12-04 |
Family
ID=14871679
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP12388191A Pending JPH04350920A (en) | 1991-05-28 | 1991-05-28 | Electrolyte for electrolytic capacitor |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04350920A (en) |
-
1991
- 1991-05-28 JP JP12388191A patent/JPH04350920A/en active Pending
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