JPS631018A - Electrolyte for capacitor - Google Patents
Electrolyte for capacitorInfo
- Publication number
- JPS631018A JPS631018A JP14458586A JP14458586A JPS631018A JP S631018 A JPS631018 A JP S631018A JP 14458586 A JP14458586 A JP 14458586A JP 14458586 A JP14458586 A JP 14458586A JP S631018 A JPS631018 A JP S631018A
- Authority
- JP
- Japan
- Prior art keywords
- electrolytic solution
- capacitor
- electrolyte
- quaternary phosphonium
- carbonate
- 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 description 10
- 239000003792 electrolyte Substances 0.000 title description 6
- 239000008151 electrolyte solution Substances 0.000 claims description 13
- 150000004714 phosphonium salts Chemical group 0.000 claims description 9
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims description 8
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 15
- 239000002904 solvent Substances 0.000 description 14
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 11
- PCYIUVKHYVQEPD-UHFFFAOYSA-N CC[PH3]CC Chemical compound CC[PH3]CC PCYIUVKHYVQEPD-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 239000000428 dust Substances 0.000 description 3
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- OZJPLYNZGCXSJM-UHFFFAOYSA-N 5-valerolactone Chemical compound O=C1CCCCO1 OZJPLYNZGCXSJM-UHFFFAOYSA-N 0.000 description 2
- ZXULZCCIIYDGCE-UHFFFAOYSA-N CC[PH3]C Chemical compound CC[PH3]C ZXULZCCIIYDGCE-UHFFFAOYSA-N 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-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
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical class CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 2
- XCPGSFBEQZMSTL-UHFFFAOYSA-N butyl(triethyl)phosphanium Chemical compound CCCC[P+](CC)(CC)CC XCPGSFBEQZMSTL-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- LKMVFSZYGHUDKW-UHFFFAOYSA-N dibutyl(diethyl)phosphanium Chemical compound CCCC[P+](CC)(CC)CCCC LKMVFSZYGHUDKW-UHFFFAOYSA-N 0.000 description 2
- UUWXBQMAEMOZSL-UHFFFAOYSA-N dimethyl(dipropyl)phosphanium Chemical compound CCC[P+](C)(C)CCC UUWXBQMAEMOZSL-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- GAEKPEKOJKCEMS-UHFFFAOYSA-N gamma-valerolactone Chemical compound CC1CCC(=O)O1 GAEKPEKOJKCEMS-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- PSURFDQPSMCWMT-UHFFFAOYSA-L tetraethylphosphanium;carbonate Chemical compound [O-]C([O-])=O.CC[P+](CC)(CC)CC.CC[P+](CC)(CC)CC PSURFDQPSMCWMT-UHFFFAOYSA-L 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- ZZXUZKXVROWEIF-UHFFFAOYSA-N 1,2-butylene carbonate Chemical compound CCC1COC(=O)O1 ZZXUZKXVROWEIF-UHFFFAOYSA-N 0.000 description 1
- OOWFYDWAMOKVSF-UHFFFAOYSA-N 3-methoxypropanenitrile Chemical compound COCCC#N OOWFYDWAMOKVSF-UHFFFAOYSA-N 0.000 description 1
- BYHZPCZRCSCPHG-UHFFFAOYSA-N C[PH3]C Chemical compound C[PH3]C BYHZPCZRCSCPHG-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 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
- 150000008043 acidic salts Chemical class 0.000 description 1
- 239000005456 alcohol based solvent Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- YQPAAVMEUPILEE-UHFFFAOYSA-N butyl(trimethyl)phosphanium Chemical compound CCCC[P+](C)(C)C YQPAAVMEUPILEE-UHFFFAOYSA-N 0.000 description 1
- ARTHGSQAXVXICL-UHFFFAOYSA-N butyl(tripropyl)phosphanium Chemical compound CCCC[P+](CCC)(CCC)CCC ARTHGSQAXVXICL-UHFFFAOYSA-N 0.000 description 1
- 229930188620 butyrolactone Natural products 0.000 description 1
- 150000005323 carbonate salts Chemical class 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- BBWVMXYKVQQWCK-UHFFFAOYSA-N dibutyl(dimethyl)phosphanium Chemical compound CCCC[P+](C)(C)CCCC BBWVMXYKVQQWCK-UHFFFAOYSA-N 0.000 description 1
- RBECNRCKEQGFRU-UHFFFAOYSA-N diethyl(dimethyl)phosphanium Chemical compound CC[P+](C)(C)CC RBECNRCKEQGFRU-UHFFFAOYSA-N 0.000 description 1
- 239000003759 ester based solvent Substances 0.000 description 1
- IQLVJVXTKNBZRC-UHFFFAOYSA-N ethyl(trimethyl)phosphanium Chemical compound CC[P+](C)(C)C IQLVJVXTKNBZRC-UHFFFAOYSA-N 0.000 description 1
- JLHMVTORNNQCRM-UHFFFAOYSA-O ethylphosphanium Chemical compound CC[PH3+] JLHMVTORNNQCRM-UHFFFAOYSA-O 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 231100000053 low toxicity Toxicity 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
- 230000007935 neutral effect Effects 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 125000005496 phosphonium group Chemical group 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- UNQNIRQQBJCMQR-UHFFFAOYSA-N phosphorine Chemical compound C1=CC=PC=C1 UNQNIRQQBJCMQR-UHFFFAOYSA-N 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- BJQWBACJIAKDTJ-UHFFFAOYSA-N tetrabutylphosphanium Chemical compound CCCC[P+](CCCC)(CCCC)CCCC BJQWBACJIAKDTJ-UHFFFAOYSA-N 0.000 description 1
- FQQANIIWRNLXFA-UHFFFAOYSA-L tetrabutylphosphanium;carbonate Chemical compound [O-]C([O-])=O.CCCC[P+](CCCC)(CCCC)CCCC.CCCC[P+](CCCC)(CCCC)CCCC FQQANIIWRNLXFA-UHFFFAOYSA-L 0.000 description 1
- BXYHVFRRNNWPMB-UHFFFAOYSA-N tetramethylphosphanium Chemical compound C[P+](C)(C)C BXYHVFRRNNWPMB-UHFFFAOYSA-N 0.000 description 1
- XOGCTUKDUDAZKA-UHFFFAOYSA-N tetrapropylphosphanium Chemical compound CCC[P+](CCC)(CCC)CCC XOGCTUKDUDAZKA-UHFFFAOYSA-N 0.000 description 1
- HOMONHWYLOPSLL-UHFFFAOYSA-N tributyl(ethyl)phosphanium Chemical compound CCCC[P+](CC)(CCCC)CCCC HOMONHWYLOPSLL-UHFFFAOYSA-N 0.000 description 1
- XKFPGUWSSPXXMF-UHFFFAOYSA-N tributyl(methyl)phosphanium Chemical compound CCCC[P+](C)(CCCC)CCCC XKFPGUWSSPXXMF-UHFFFAOYSA-N 0.000 description 1
- WJLSOXBTGDOFOQ-UHFFFAOYSA-N tributyl(propyl)phosphanium Chemical compound CCCC[P+](CCC)(CCCC)CCCC WJLSOXBTGDOFOQ-UHFFFAOYSA-N 0.000 description 1
- WVLBCYQITXONBZ-UHFFFAOYSA-N trimethyl phosphate Chemical compound COP(=O)(OC)OC WVLBCYQITXONBZ-UHFFFAOYSA-N 0.000 description 1
- YGDBTMJEJNVHPZ-UHFFFAOYSA-N trimethyl(propyl)phosphanium Chemical compound CCC[P+](C)(C)C YGDBTMJEJNVHPZ-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Networks Using Active Elements (AREA)
- Electric Double-Layer Capacitors Or The Like (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
産業上の利用分野
本発明によれば、電導塵の高い優れたコンデンサ用電解
液(以下単に電解液と称することがある)が得られる。DETAILED DESCRIPTION OF THE INVENTION Industrial Field of Application According to the present invention, an excellent electrolytic solution for capacitors (hereinafter sometimes simply referred to as electrolytic solution) with high conductive dust can be obtained.
従来の技術
]ンデンサの特性は種々の要因によって決定されている
が、特にコンデンサ素子とともに外装ケースに収納され
る電解液の特性は、インピーダンスあるいは等価直列抵
抗(E S R)に大きな影響を文ぼすことが判明して
いる。[Prior art] The characteristics of a capacitor are determined by various factors, but in particular the characteristics of the electrolyte that is housed in the outer case together with the capacitor element have a large effect on impedance or equivalent series resistance (ESR). It has been found that
たとえば、低圧用電解コンデンサには、γ−ブチロラク
トン溶媒に、マレイン酸のトリエチルアミン塩等を溶解
した電解液が使用されている。For example, low-voltage electrolytic capacitors use an electrolytic solution in which a triethylamine salt of maleic acid or the like is dissolved in a γ-butyrolactone solvent.
発明が解決しようとする問題点
しかし、近年のスイッチングレギュレーターの高周波化
に伴ない、更に低インピーダンスあるいは低等価直列抵
抗のコンデンサが必要となり、高電導度の電解液の開発
が望まれている。Problems to be Solved by the Invention However, as the frequency of switching regulators has increased in recent years, capacitors with lower impedance or lower equivalent series resistance are required, and the development of electrolytes with high conductivity is desired.
問題点を解決するだめの手段
本発明者らは、電導塵の高い電解液を見い出すべく鋭意
検討を行ない、炭酸の四級ホスホニウム塩が高い電導塵
を示すことを見い出し本発明を完成した。Means to Solve the Problems The present inventors conducted intensive studies to find an electrolytic solution with high conductive dust, and found that a quaternary phosphonium salt of carbonic acid exhibits high conductive dust, and completed the present invention.
即ち、本発明は炭酸の四級ホスホニウム塩を溶質として
使用することを特徴とするコンデンサ用電解液を提供す
るものである。That is, the present invention provides an electrolytic solution for a capacitor characterized by using a quaternary phosphonium salt of carbonic acid as a solute.
発明の詳細な説明
本発明において溶質として用いられる炭酸の四級ホスホ
ニウム塩に訃ける四級ホスホニウム塩トしては、テトラ
メチルホスホニウム、テトラエテルホスホニウム、テト
ラプロピルホスホニウム、テトラブチルホスホニウム、
メチル) IJエチルホスホニウム、メチルトリグロビ
ルホスホニウム、メチルトリブチルホスホニウム、ジメ
チルジエチルホスホニウム、ジメチルジプロピルホスホ
ニウム、ジメチルジブチルホスホニウム、トリメチルエ
チルホスホニウム、トリメチルプロピルホスホニウム、
トリメチルブチルホスホニウム、エチルトリフロビルホ
スホニウム、エテルトリブチルホスホニウム、ジメチル
ジプロピルホスホニウム、ジエチルジブチルホスホニウ
ム、トリエチルブチルホスホニウム、トリエチルブチル
ホスホニウム、プロピルトリブチルホスホニウム、ジエ
チルジブチルホスホニウム、トリプロピルブチルホスホ
ニウム等の脂肪族四級ホスホニウム塩および1.1−ジ
メチルホスホラニウム、1−メチル−1−エチルホスホ
ラニウム、1,1−ジエチルホスホラニウム、1,1−
ジエチルホスホラニウム、1−メチル−1−エチルホス
ホラニウム、1.1−ジエチルホスホラニウム、1,1
−ベンタメチレンホスホリナニウム等の脂環式四級ホス
ホニウム塩を例示することができる。Detailed Description of the Invention In the present invention, the quaternary phosphonium salts of carbonic acid used as solutes include tetramethylphosphonium, tetraetherphosphonium, tetrapropylphosphonium, tetrabutylphosphonium,
methyl) IJ ethylphosphonium, methyltriglobylphosphonium, methyltributylphosphonium, dimethyldiethylphosphonium, dimethyldipropylphosphonium, dimethyldibutylphosphonium, trimethylethylphosphonium, trimethylpropylphosphonium,
Aliphatic quaternary phosphoniums such as trimethylbutylphosphonium, ethyltriflobylphosphonium, ethyltributylphosphonium, dimethyldipropylphosphonium, diethyldibutylphosphonium, triethylbutylphosphonium, triethylbutylphosphonium, propyltributylphosphonium, diethyldibutylphosphonium, tripropylbutylphosphonium, etc. salts and 1,1-dimethylphosphoranium, 1-methyl-1-ethylphosphoranium, 1,1-diethylphosphoranium, 1,1-
Diethylphosphoranium, 1-methyl-1-ethylphosphoranium, 1,1-diethylphosphoranium, 1,1
-Alicyclic quaternary phosphonium salts such as bentamethylene phosphorinium can be exemplified.
本発明の炭酸の四級ホスホニウム塩を溶解させるτ媒と
しては、N−メチルホルムアミド、N−エチルホルムア
ミド、N、N−ジメチルホルムアミド、N、N−ジエチ
ルホルムアミド、N−メチルアセトアミド、N−エチル
アセトアミド、N、N−ジメチルアセトアミド、N、N
−ジエチルアセトアミド、N−メチルピロリジノン等の
アミド溶媒、γ−ブチロラクトン、γ−バレロラクトン
、δ−バレロラクトン等のラクトン溶媒、エチレンカー
ボネート、プロピレンカーボネート、ブチレンカーボネ
ート等のカーボネート溶媒、エチレングリコール、クリ
セリン、メチルセロノルブ等のアルコール溶媒、3−メ
トキシプロピオニトリル等のニトリル溶媒、およびトリ
メチルホスフェート等の燐酸エステル溶媒の単独あるい
は混合溶媒を例示することができる。これらの中でもγ
−ブチロラクトンを主体とする溶媒が毒性が低く、コン
デンサの封孔剤のアタックやハロゲンの混入が少ない等
のことから特に好ましい。Examples of the τ medium for dissolving the quaternary phosphonium salt of carbonic acid of the present invention include N-methylformamide, N-ethylformamide, N,N-dimethylformamide, N,N-diethylformamide, N-methylacetamide, and N-ethylacetamide. , N, N-dimethylacetamide, N, N
- Amide solvents such as diethylacetamide and N-methylpyrrolidinone, lactone solvents such as γ-butyrolactone, γ-valerolactone, and δ-valerolactone, carbonate solvents such as ethylene carbonate, propylene carbonate, butylene carbonate, ethylene glycol, chrycerin, methyl Examples include alcohol solvents such as celonorb, nitrile solvents such as 3-methoxypropionitrile, and phosphoric acid ester solvents such as trimethyl phosphate, alone or in combination. Among these, γ
- A solvent mainly composed of butyrolactone is particularly preferable because it has low toxicity and is less likely to attack capacitor sealants or contain halogens.
上記溶媒に対する炭酸の四級ホスホニウム塩の溶解量は
飽和濃度以下、好ましくは5〜40重量聾である。The amount of the quaternary phosphonium salt of carbonic acid dissolved in the above solvent is below the saturation concentration, preferably 5 to 40% by weight.
まだ、上記電解液中の溶解塩は中性塩でも酸性塩でも良
い。However, the dissolved salt in the electrolytic solution may be a neutral salt or an acidic salt.
本発明の電解液は、本質的には、炭酸の四級ホスホニウ
ム塩と溶媒よりなるが、電蝕防止、漏れ電流の低減等、
種々の目的で少量の助溶質を添加しても差し支えない。The electrolytic solution of the present invention essentially consists of a quaternary phosphonium salt of carbonic acid and a solvent, but has the following properties: prevention of galvanic corrosion, reduction of leakage current, etc.
Small amounts of co-solutes may be added for various purposes.
発明の効果
本発明で溶質として使用する炭酸の四級ホスホニウム塩
は溶媒に対する溶解性が良く、その電解液は高い電導度
を示し、凝固点〜沸点範囲の広い溶媒と伴に用いること
により、使用温度範囲の広いコンデンサ用屯解液となる
。Effects of the Invention The quaternary phosphonium salt of carbonic acid used as a solute in the present invention has good solubility in solvents, and its electrolyte exhibits high conductivity. This is a wide range of capacitor solution.
実験例
以下に実施例、比較例を挙げて本発明を更に具体的に説
明する。EXPERIMENTAL EXAMPLES The present invention will be explained in more detail below with reference to Examples and Comparative Examples.
実施例1
γ−ブチロラクトン溶媒に20重量%の炭酸のテトラエ
チルホスホニウム塩を溶解させて電解液を得た。この電
解液の25℃におけるiπ導度は8 、3 mS/cl
nであり、+、−一1組のアルミニウム平滑箔に4 m
A、z智の定電流印加時の火花発生電圧は208vであ
った。Example 1 An electrolytic solution was obtained by dissolving 20% by weight of tetraethylphosphonium carbonate in a γ-butyrolactone solvent. The iπ conductivity of this electrolyte at 25°C is 8.3 mS/cl.
n, and 4 m on 1 set of + and -1 aluminum smooth foils.
The spark generation voltage when constant current was applied to A and Z was 208V.
実施例2
実施例1において、γ−ブチロラクトン溶媒の代わりに
N、N−ジメチルホルムアミド溶媒を洟用した電解液を
作成した。Example 2 In Example 1, an electrolytic solution was prepared using N,N-dimethylformamide solvent instead of the γ-butyrolactone solvent.
実施例3
実施例1において、炭酸のテトラエチルホスホニウム塩
の代わしに、炭酸のテトラブチルホスホニウム塩を使用
した電解液を作成した。Example 3 In Example 1, an electrolytic solution was prepared using tetrabutylphosphonium carbonate instead of tetraethylphosphonium carbonate.
実施例4
実施例3(ておいて、γ−ブチロラクトン溶媒の代わり
に、プロピレンカーボネート溶媒を使用した電解液を作
成した。Example 4 Similar to Example 3, an electrolytic solution was prepared using a propylene carbonate solvent instead of the γ-butyrolactone solvent.
比較例
実施例1において、炭酸のテトラエテルホスホニウム塩
の代わりに、マレイン酸のトリエチルアミン塩を使用し
た電解液を作成した。Comparative Example In Example 1, an electrolytic solution was prepared using triethylamine salt of maleic acid instead of tetraetherphosphonium carbonate salt.
これらの電解液の電導度および火花発生1ヱ圧を第1表
に示した。なお、第1表では次の略号を使用した。The electrical conductivity and spark generation pressure of these electrolytes are shown in Table 1. In Table 1, the following abbreviations were used.
GBL:γ−ブチロラクトン
DMF:N、N−ジメチルホルムアミドPC:プロピレ
ンカーボネート
第1表GBL: γ-butyrolactone DMF: N,N-dimethylformamide PC: Propylene carbonate Table 1
Claims (1)
を特徴とするコンデンサ用電解液。An electrolytic solution for capacitors characterized by using a quaternary phosphonium salt of carbonic acid as a solute.
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14458586A JPS631018A (en) | 1986-06-20 | 1986-06-20 | Electrolyte for capacitor |
EP87304335A EP0246825B1 (en) | 1986-05-20 | 1987-05-15 | Quaternary salt solution electrolyte for electrolytic capacitors |
DE8787304335T DE3768141D1 (en) | 1986-05-20 | 1987-05-15 | ELECTROLYTIC SOLUTION OF QUATERNAIAL SALTS FOR ELECTROLYTIC CAPACITOR. |
US07/050,574 US4774011A (en) | 1986-05-20 | 1987-05-18 | Electrolyte for aluminum electrolytic capacitor |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14458586A JPS631018A (en) | 1986-06-20 | 1986-06-20 | Electrolyte for capacitor |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS631018A true JPS631018A (en) | 1988-01-06 |
Family
ID=15365529
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP14458586A Pending JPS631018A (en) | 1986-05-20 | 1986-06-20 | Electrolyte for capacitor |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS631018A (en) |
-
1986
- 1986-06-20 JP JP14458586A patent/JPS631018A/en active Pending
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