JP2011108675A - 電解コンデンサ用電解液及び電解コンデンサ - Google Patents
電解コンデンサ用電解液及び電解コンデンサ Download PDFInfo
- Publication number
- JP2011108675A JP2011108675A JP2009258773A JP2009258773A JP2011108675A JP 2011108675 A JP2011108675 A JP 2011108675A JP 2009258773 A JP2009258773 A JP 2009258773A JP 2009258773 A JP2009258773 A JP 2009258773A JP 2011108675 A JP2011108675 A JP 2011108675A
- Authority
- JP
- Japan
- Prior art keywords
- acid
- electrolytic
- electrolytic solution
- electrolyte
- electrolytic capacitor
- 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 80
- 239000003792 electrolyte Substances 0.000 title claims abstract description 25
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims abstract description 28
- CBXCPBUEXACCNR-UHFFFAOYSA-N tetraethylammonium Chemical compound CC[N+](CC)(CC)CC CBXCPBUEXACCNR-UHFFFAOYSA-N 0.000 claims abstract description 13
- ONQBOTKLCMXPOF-UHFFFAOYSA-N 1-ethylpyrrolidine Chemical compound CCN1CCCC1 ONQBOTKLCMXPOF-UHFFFAOYSA-N 0.000 claims abstract description 7
- AVFZOVWCLRSYKC-UHFFFAOYSA-N 1-methylpyrrolidine Chemical compound CN1CCCC1 AVFZOVWCLRSYKC-UHFFFAOYSA-N 0.000 claims abstract description 7
- AHVYPIQETPWLSZ-UHFFFAOYSA-N N-methyl-pyrrolidine Natural products CN1CC=CC1 AHVYPIQETPWLSZ-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000008151 electrolyte solution Substances 0.000 claims description 67
- 239000002253 acid Substances 0.000 claims description 17
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 15
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 claims description 14
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 14
- 239000008119 colloidal silica Substances 0.000 claims description 13
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 12
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 11
- 239000011976 maleic acid Substances 0.000 claims description 11
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 10
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 9
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims description 6
- 239000002245 particle Substances 0.000 claims description 5
- 239000005711 Benzoic acid Substances 0.000 claims description 4
- 235000010233 benzoic acid Nutrition 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims description 3
- 229960004889 salicylic acid Drugs 0.000 claims description 3
- 238000005868 electrolysis reaction Methods 0.000 claims description 2
- 230000007774 longterm Effects 0.000 abstract description 7
- ZMKHDVWIHTXNTM-UHFFFAOYSA-N 1,2,3,5-tetramethylpyrazol-1-ium Chemical compound CC1=CC(C)=[N+](C)N1C ZMKHDVWIHTXNTM-UHFFFAOYSA-N 0.000 abstract description 4
- DADKKHHMGSWSPH-UHFFFAOYSA-N 1-butyl-3-methylpyridin-1-ium Chemical compound CCCC[N+]1=CC=CC(C)=C1 DADKKHHMGSWSPH-UHFFFAOYSA-N 0.000 abstract description 4
- NJMWOUFKYKNWDW-UHFFFAOYSA-N 1-ethyl-3-methylimidazolium Chemical compound CCN1C=C[N+](C)=C1 NJMWOUFKYKNWDW-UHFFFAOYSA-N 0.000 abstract description 4
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 abstract description 4
- 239000000470 constituent Substances 0.000 abstract 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 12
- 239000002904 solvent Substances 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 5
- -1 aliphatic carboxylic acid Acids Chemical class 0.000 description 5
- WXUAQHNMJWJLTG-UHFFFAOYSA-N 2-methylbutanedioic acid Chemical compound OC(=O)C(C)CC(O)=O WXUAQHNMJWJLTG-UHFFFAOYSA-N 0.000 description 4
- XJMMNTGIMDZPMU-UHFFFAOYSA-N 3-methylglutaric acid Chemical compound OC(=O)CC(C)CC(O)=O XJMMNTGIMDZPMU-UHFFFAOYSA-N 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 230000007547 defect Effects 0.000 description 4
- 239000011888 foil Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-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
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 3
- 239000004327 boric acid Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 3
- WVUYYXUATWMVIT-UHFFFAOYSA-N 1-bromo-4-ethoxybenzene Chemical compound CCOC1=CC=C(Br)C=C1 WVUYYXUATWMVIT-UHFFFAOYSA-N 0.000 description 2
- PAMIQIKDUOTOBW-UHFFFAOYSA-N 1-methylpiperidine Chemical compound CN1CCCCC1 PAMIQIKDUOTOBW-UHFFFAOYSA-N 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- JYFHYPJRHGVZDY-UHFFFAOYSA-N Dibutyl phosphate Chemical compound CCCCOP(O)(=O)OCCCC JYFHYPJRHGVZDY-UHFFFAOYSA-N 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
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-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
- QCOGKXLOEWLIDC-UHFFFAOYSA-N N-methylbutylamine Chemical compound CCCCNC QCOGKXLOEWLIDC-UHFFFAOYSA-N 0.000 description 2
- ATHHXGZTWNVVOU-UHFFFAOYSA-N N-methylformamide Chemical compound CNC=O ATHHXGZTWNVVOU-UHFFFAOYSA-N 0.000 description 2
- BTZVDPWKGXMQFW-UHFFFAOYSA-N Pentadecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCCC(O)=O BTZVDPWKGXMQFW-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 230000004075 alteration Effects 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- 239000000010 aprotic solvent Substances 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- LIWAQLJGPBVORC-UHFFFAOYSA-N ethylmethylamine Chemical compound CCNC LIWAQLJGPBVORC-UHFFFAOYSA-N 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 2
- QQHJDPROMQRDLA-UHFFFAOYSA-N hexadecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCCCC(O)=O QQHJDPROMQRDLA-UHFFFAOYSA-N 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical compound [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- GVWISOJSERXQBM-UHFFFAOYSA-N n-methylpropan-1-amine Chemical compound CCCNC GVWISOJSERXQBM-UHFFFAOYSA-N 0.000 description 2
- XHFGWHUWQXTGAT-UHFFFAOYSA-N n-methylpropan-2-amine Chemical compound CNC(C)C XHFGWHUWQXTGAT-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
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- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
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- 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
- 238000007789 sealing Methods 0.000 description 2
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- 239000000243 solution Substances 0.000 description 2
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- 150000005846 sugar alcohols Polymers 0.000 description 2
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- HQHCYKULIHKCEB-UHFFFAOYSA-N tetradecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCC(O)=O HQHCYKULIHKCEB-UHFFFAOYSA-N 0.000 description 2
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- NNLHWTTWXYBJBQ-UHFFFAOYSA-N 1-butyl-4-methylpyridin-1-ium Chemical compound CCCC[N+]1=CC=C(C)C=C1 NNLHWTTWXYBJBQ-UHFFFAOYSA-N 0.000 description 1
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- XAMMKFSEEQGBIC-UHFFFAOYSA-N tetra(propan-2-yl)azanium Chemical compound CC(C)[N+](C(C)C)(C(C)C)C(C)C XAMMKFSEEQGBIC-UHFFFAOYSA-N 0.000 description 1
- 125000005207 tetraalkylammonium group Chemical group 0.000 description 1
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical compound CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 229940073455 tetraethylammonium hydroxide Drugs 0.000 description 1
- LRGJRHZIDJQFCL-UHFFFAOYSA-M tetraethylazanium;hydroxide Chemical compound [OH-].CC[N+](CC)(CC)CC LRGJRHZIDJQFCL-UHFFFAOYSA-M 0.000 description 1
- OSBSFAARYOCBHB-UHFFFAOYSA-N tetrapropylammonium Chemical compound CCC[N+](CCC)(CCC)CCC OSBSFAARYOCBHB-UHFFFAOYSA-N 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- DXNCZXXFRKPEPY-UHFFFAOYSA-N tridecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCC(O)=O DXNCZXXFRKPEPY-UHFFFAOYSA-N 0.000 description 1
- SEACXNRNJAXIBM-UHFFFAOYSA-N triethyl(methyl)azanium Chemical compound CC[N+](C)(CC)CC SEACXNRNJAXIBM-UHFFFAOYSA-N 0.000 description 1
- WGYXSYLSCVXFDU-UHFFFAOYSA-N triethyl(propyl)azanium Chemical compound CCC[N+](CC)(CC)CC WGYXSYLSCVXFDU-UHFFFAOYSA-N 0.000 description 1
- RKBCYCFRFCNLTO-UHFFFAOYSA-N triisopropylamine Chemical compound CC(C)N(C(C)C)C(C)C RKBCYCFRFCNLTO-UHFFFAOYSA-N 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- 229940005605 valeric acid Drugs 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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- Electric Double-Layer Capacitors Or The Like (AREA)
Abstract
【解決手段】カルボン酸成分(A)とテトラエチルアンモニウム,スピロ−(1,1’)−ビピロリジニウム等からなる群(1),N−メチルピロリジン,N−エチルピロリジン等からなる群(2),ジエチルアミン等からなる群(3),1−エチル−3−メチルイミダゾリウム等からなる群(4),1,2,3,5−テトラメチルピラゾリウム等からなる群(5),N−ブチル−3−メチルピリジニウム等からなる群(6)のいずれかの群から選択した塩基成分(B)からなる電解質において、カルボン酸成分(A)と塩基成分(B)のモル比が、カルボン酸成分(A)を過剰にした電解コンデンサ用電解液とそれを用いた電解コンデンサ。電解コンデンサ用電解液とそれを用いた電解コンデンサは、高い電導度と火花電圧を有し、長期安定性に優れる。
【選択図】なし
Description
電解コンデンサ用電解液に含有されるカルボン酸成分(A)と塩基成分(B)とのモル比が、カルボン酸成分(A)が過剰であることを特徴とする電解コンデンサ用電解液である。
これらの中でも、電導度が高く熱的にも安定な点から、フタル酸、マレイン酸、サリチル酸、安息香酸、ボロジグリコール酸、ボロジシュウ酸、ボロジサリチル酸が好ましく、マレイン酸が特に好ましく挙げられる。
これらの中でも、高い電導度を有し、さらに火花電圧が向上する点より、テトラエチルアンモニウム、スピロ−(1,1’)−ビピロリジニウムが特に好ましく挙げられる。
これらの中でも、高い電導度を有し、さらに火花電圧が向上する点より、N−メチルピロリジン、N−エチルピロリジンが特に好ましく挙げられる。
電解コンデンサ用電解液に含有されるカルボン酸成分(A)と一般式(1)〜(6)のいずれかより表される塩基成分(B)とのモル比において、カルボン酸成分(A)が過剰であることを特徴とする電解コンデンサ用電解液である。
1.0質量%未満の場合、十分な火花電圧が得られない欠点があり、60質量%超の場合、比抵抗が上昇する欠点がある。
電解液の火花電圧を向上させる点からジブチルリン酸又は亜リン酸のリン酸化合物が特に好ましく挙げられる。
0.1質量%未満の場合、十分な火花電圧が得られない欠点があり、30質量%超の場合、電導度が低下する欠点がある。
これらの中でも、副成分としては、エチレングリコール又はスルホランが好ましく挙げられる。
0.001質量%未満の場合及び30質量%超の場合は、十分な電導度と火花電圧が得られない欠点がある。
マレイン酸116.2部(1.001mol)を含む20%マレイン酸水溶液と、35%テトラエチルアンモニウムヒドロキシド水溶液420.8部(1.00mol)を混合して、テトラエチルアンモニウムマレイン酸水溶液を得た後、日産化学株式会社製20%コロイダルシリカ(スノーテックスN、シリカ粒径10〜20nm)水溶液283.0部と、γ−ブチロラクトン1585部を混合、80℃で濃縮して、電解液を得た。
マレイン酸を、表1に示したモル数になるように使用して、実施例1と同様の方法にて、電解液を得た。
実施例1のテトラエチルアンモニウムをスピロ−(1,1‘)−ビピロリジニウムに代え、表1に示したモル数になるようにした以外は、実施例1と同様の方法で電解コンデンサ用電解液を得た。
実施例1のテトラエチルアンモニウムをN−メチルピロリジンに代え、表1に示したモル数になるようにした以外は、実施例1と同様の方法で電解コンデンサ用電解液を得た。
実施例1のテトラエチルアンモニウムをN−エチルピロリジンに代え、表1に示したモル数になるようにした以外は、実施例1と同様の方法で電解コンデンサ用電解液を得た。
実施例1のテトラエチルアンモニウムをジエチルアンモニウムに代え、表1に示したモル数になるようにした以外は、実施例1と同様の方法で電解コンデンサ用電解液を得た。
実施例1のテトラエチルアンモニウムを1−エチル−3−メチルイミダゾリウムに代え、表1に示したモル数になるようにした以外は、実施例1と同様の方法で電解コンデンサ用電解液を得た。
実施例1のテトラエチルアンモニウムを1,2,3,5−テトラメチルピラゾリウムに代え、表1に示したモル数になるようにした以外は、実施例1と同様の方法で電解コンデンサ用電解液を得た。
実施例1のテトラエチルアンモニウムをN−ブチル−3−メチルピリジニウムに代え、表1に示したモル数になるようにした以外は、実施例1と同様の方法で電解コンデンサ用電解液を得た。
マレイン酸を、表1に示したモル数になるように使用して、実施例1と同様の方法にて、電解液を得た。
300Vで化成した陽極箔を、セパレータ、陰極箔と共に巻回し、巻回端面からリード線を導出させたコンデンサ素子に、得られた電解液を減圧下、80℃で含浸し、この素子を金属ケースに収納し、開口部を封口ゴムで閉じ、外装ケースの端部を巻き締めて電解コンデンサとした。この電解コンデンサは、定格電圧160WV、静電容量22μF、外形寸法は10φ×200である。
(電導度の評価方法)
電導度の評価方法は、電解コンデンサ用電解液の30℃における電導度(mS/cm)を、横河電機株式会社製SCメーターSC72を用いて測定した。
(火花電圧の評価方法)
火花電圧の評価方法は、各電解液を用いた電解コンデンサを作製し、25℃で、5mAの定電流を印加し、電圧−時間カーブを調べることで行い、電圧の上昇カーブで始めにスパーク又はシンチレーションが観測された電圧(V)を火花電圧とした。
耐熱性は、温度105℃の条件下で、2000時間後の電導度、火花電圧を測定した。
TEA:テトラエチルアンモニウム
SBP:スピロ−(1,1’)−ビピロリジニウム
MP:N−メチルピロリジン
EP:N−エチルピロリジン
DEA:ジエチルアミン
EMI:1−エチル−3−メチルイミダゾリウム
TM−PZL:1,2,3,5−テトラメチルピラゾリウム
BMP:N−ブチル−3−メチルピリジニウム
MA:マレイン酸
特に実施例7〜13が優れた電導度、火花電圧、耐熱性であった。
Claims (7)
- カルボン酸成分(A)と下記一般式(1)〜(6)より表される塩基成分(B)からなる電解質塩をγ−ブチロラクトンを主成分とする有機溶媒に溶解させ、コロイダルシリカを含有させた電解液からなる電解コンデンサ用電解液において、
電解コンデンサ用電解液に含有されるカルボン酸成分(A)と塩基成分(B)とのモル比が、カルボン酸成分(A)が過剰であることを特徴とする電解コンデンサ用電解液。
- カルボン酸成分(A)がフタル酸、マレイン酸、サリチル酸、安息香酸、ボロジグリコール酸、ボロジシュウ酸、ボロジサリチル酸からなる群より選ばれる一種であることを特徴とする請求項1に記載の電解コンデンサ用電解液。
- 塩基成分(B)が、テトラエチルアンモニウム、スピロ−(1,1’)−ビピロリジニウム、N−メチルピロリジン、N−エチルピロリジンの群より選ばれる1種以上である請求項1又は2に記載の電解コンデンサ用電解液。
- コロイダルシリカの添加量が、0.1〜20質量%であることを特徴とする請求項1から3のいずれかに記載の電解コンデンサ用電解液。
- コロイダルシリカの粒径が、4〜50nmであることを特徴とする請求項1から4のいずれかに記載の電解コンデンサ用電解液。
- 電解コンデンサ用電解液に含有されるカルボン酸成分(A)と塩基成分(B)のモル比が、(A):(B)=1.005〜1.50:1であることを特徴とする請求項1から5のいずれかに記載の電解コンデンサ用電解液。
- 請求項1から6のいずれかに記載の電解コンデンサ用電解液を用いてなることを特徴とする電解コンデンサ。
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WO2014103002A1 (ja) * | 2012-12-28 | 2014-07-03 | カーリットホールディングス株式会社 | 電解コンデンサ用電解液及び電解コンデンサ |
JP2015090934A (ja) * | 2013-11-06 | 2015-05-11 | カーリットホールディングス株式会社 | 電解コンデンサ用電解液及び電解コンデンサ |
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JPWO2014103002A1 (ja) * | 2012-12-28 | 2017-01-12 | カーリットホールディングス株式会社 | 電解コンデンサ用電解液及び電解コンデンサ |
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JP2015090934A (ja) * | 2013-11-06 | 2015-05-11 | カーリットホールディングス株式会社 | 電解コンデンサ用電解液及び電解コンデンサ |
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