JPH08293437A - Electrolyte for driving electrolytic capacitor - Google Patents

Electrolyte for driving electrolytic capacitor

Info

Publication number
JPH08293437A
JPH08293437A JP9821795A JP9821795A JPH08293437A JP H08293437 A JPH08293437 A JP H08293437A JP 9821795 A JP9821795 A JP 9821795A JP 9821795 A JP9821795 A JP 9821795A JP H08293437 A JPH08293437 A JP H08293437A
Authority
JP
Japan
Prior art keywords
electrolytic
electrolyte
electrolytic capacitor
amine derivatives
organic 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.)
Pending
Application number
JP9821795A
Other languages
Japanese (ja)
Inventor
Yuichiro Tsubaki
雄一郎 椿
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP9821795A priority Critical patent/JPH08293437A/en
Publication of JPH08293437A publication Critical patent/JPH08293437A/en
Pending legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

PURPOSE: To improve for a long time variations in the capacitance and tanδ of an electrolytic capacitor at high temperature by adding to a solution with an organic solvent and electrolytic salt bases one or more compounds selected from among amine derivatives expressed by a specific formula. CONSTITUTION: An electrolyte for driving electrolytic capacitors is prepared by adding one or more compounds, selected from among amine derivatives expressed by the formula (however, R1 , R2 =H, CH3 , C2 H5 , C3 H7 , C4 H9 , Ph) to solution composed of an organic solvent and electrolytic salt. Since these amine derivatives are easily absorbed to metal, they will bee absorbed to electrode foil and protect it. This suppresses hydration and the like of such an electrode foil. Since the amine derivatives are unreactive to the compositions of electrolyte, such as ethylene glycol, it is possible to improve for a long time variations in the capacitance and tanδ of an electrolyte capacitor at high temperature.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は電解コンデンサ駆動用電
解液に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an electrolytic solution for driving an electrolytic capacitor.

【0002】[0002]

【従来の技術】近年、電子機器の小形化・高信頼化に伴
い、その中で使用されている電解コンデンサについて
も、その小形化・高信頼化が求められている。
2. Description of the Related Art In recent years, with downsizing and high reliability of electronic equipment, there is a demand for downsizing and high reliability of electrolytic capacitors used therein.

【0003】電解コンデンサを小形化する場合、通常は
電極箔の静電容量を向上させることにより行われている
が、電極箔の静電容量向上により有効電極面積は減少
し、その結果、等価直列抵抗は増加するもので、この増
加した等価直列抵抗を下げるためには電解液の高電導度
化が必要となる。
The miniaturization of the electrolytic capacitor is usually carried out by improving the electrostatic capacity of the electrode foil, but the effective electrode area is reduced by improving the electrostatic capacity of the electrode foil, and as a result, the equivalent series. The resistance increases, and it is necessary to increase the conductivity of the electrolytic solution in order to reduce the increased equivalent series resistance.

【0004】このような必要性に対し、従来のエチレン
グリコールを主体とする電解液においては、水を加えて
電解質塩の解離度を向上させることにより電導度向上を
はかってきた。
In response to such a need, in the conventional electrolytic solution mainly composed of ethylene glycol, it has been attempted to improve the electric conductivity by adding water to improve the dissociation degree of the electrolyte salt.

【0005】[0005]

【発明が解決しようとする課題】しかしながら電解液に
水を加える場合、その添加量が多ければ多いほど電極と
なるアルミニウムとの水和反応が促進されるため、経時
的に電解コンデンサの静電容量の減少や損失角の正接
(tanδ)の増大といった課題を引き起こしていた。
However, when water is added to the electrolytic solution, the larger the amount of water added, the more the hydration reaction with aluminum serving as the electrode is promoted. And the loss tangent (tan δ) increase.

【0006】この静電容量の減少を防止するために、例
えば、特開昭63−7613号にはグリシン、L−アス
パラギン酸、アラニン、グルタミン酸を含有する電解液
が、特開昭64−37823号にはグリシン、アラニ
ン、バリンを含有する電解液が、特開平3−91225
号にはグリシン、アラニンを含有する電解液が、特開平
3−257811号にはシランカップリング剤を含有す
る電解液がそれぞれ開示されている。
In order to prevent this decrease in electrostatic capacity, for example, JP-A-63-7613 discloses an electrolytic solution containing glycine, L-aspartic acid, alanine and glutamic acid, which is disclosed in JP-A-64-37823. An electrolytic solution containing glycine, alanine, and valine is disclosed in JP-A-3-91225.
JP-A-3-257811 discloses an electrolytic solution containing glycine and alanine, and JP-A-3-257811 discloses an electrolytic solution containing a silane coupling agent.

【0007】しかしながらこれらの添加剤は、水やエチ
レングリコール等の電解液組成物と反応し易いため、短
期的な効果がある反面、長期的な効果はないといった問
題点を有していた。
However, since these additives easily react with the electrolyte composition such as water and ethylene glycol, they have a short-term effect but no long-term effect.

【0008】本発明は上記従来の問題点を解決するもの
で、高温中における電解コンデンサの静電容量変化およ
びtanδ変化を長期間改善することができる電解コン
デンサ駆動用電解液を提供することを目的とするもので
ある。
The present invention solves the above-mentioned conventional problems, and an object of the present invention is to provide an electrolytic solution for driving an electrolytic capacitor, which can improve the capacitance change and tan δ change of the electrolytic capacitor at high temperature for a long period of time. It is what

【0009】[0009]

【課題を解決するための手段】上記目的を達成するため
に本発明の電解コンデンサ駆動用電解液は、有機溶媒と
電解質塩を主体としてなる溶液に(化2)で示されるア
ミン誘導体より選ばれる少なくとも1種以上の化合物を
添加したものである。
In order to achieve the above object, the electrolytic capacitor driving electrolytic solution of the present invention is selected from the amine derivatives represented by the chemical formula 2 in a solution mainly composed of an organic solvent and an electrolyte salt. At least one compound is added.

【0010】[0010]

【化2】 Embedded image

【0011】[0011]

【作用】上記構成の電解コンデンサ駆動用電解液は、有
機溶媒と電解質塩からなる溶液に(化3)で示されるア
ミン誘導体より選ばれる少なくとも1種以上の化合物を
添加しているもので、このアミン誘導体は金属に吸着し
やすいため、電極箔に吸着して電極箔を保護することに
なり、これにより電極箔の水和反応等が起こりにくくな
る。
The electrolytic solution for driving the electrolytic capacitor having the above-mentioned structure is obtained by adding at least one compound selected from the amine derivative shown in Chemical formula 3 to a solution consisting of an organic solvent and an electrolyte salt. Since the amine derivative is easily adsorbed on the metal, it is adsorbed on the electrode foil to protect the electrode foil, which makes it difficult for the hydration reaction of the electrode foil to occur.

【0012】また、水やエチレングリコール等の電解液
組成物との反応性が低いため、長期にわたり高温中にお
ける電解コンデンサの静電容量変化およびtanδ変化
を改善することができるものである。
Further, since the reactivity with the electrolytic solution composition such as water or ethylene glycol is low, it is possible to improve the capacitance change and tan δ change of the electrolytic capacitor at high temperature for a long period of time.

【0013】[0013]

【化3】 Embedded image

【0014】[0014]

【実施例】以下、本発明の一実施例について説明する。EXAMPLES An example of the present invention will be described below.

【0015】本発明の基本は、有機溶媒と電解質塩を主
体としてなる溶液に(化4)で示されるアミン誘導体よ
り選ばれる少なくとも1種以上の化合物を添加したもの
である。
The basis of the present invention is to add at least one compound selected from the amine derivatives represented by the chemical formula 4 to a solution mainly composed of an organic solvent and an electrolyte salt.

【0016】[0016]

【化4】 [Chemical 4]

【0017】本発明で使用できる有機溶媒としては、例
えばアミド類、ラクトン類、グリコール類、硫黄化合物
類または炭素塩類が好ましく、その具体的な例として
は、N−メチルホルムアミド、γ−ブチロラクトン、β
−ブチロラクトン、γ−バレロラクトン、N−メチルピ
ロリドン、エチレングリコール、エチレングリコール・
モノアルキルエーテル、エチレングリコール・ジアルキ
ルエーテル、ジメチルスルホキシド、炭酸プロピレン、
エチレンシアノヒドリン等が挙げられ、これらの溶媒は
単独、あるいは複数の組み合わせで使用できる。
As the organic solvent usable in the present invention, for example, amides, lactones, glycols, sulfur compounds or carbon salts are preferable. Specific examples thereof include N-methylformamide, γ-butyrolactone and β.
-Butyrolactone, γ-valerolactone, N-methylpyrrolidone, ethylene glycol, ethylene glycol
Monoalkyl ether, ethylene glycol dialkyl ether, dimethyl sulfoxide, propylene carbonate,
Examples thereof include ethylene cyanohydrin, and these solvents can be used alone or in combination of two or more.

【0018】またこのような有機溶媒に溶解する電解質
塩としては、アンモニウム塩、アミン塩、四級アンモニ
ウム塩等が使用できるが、アミン塩としては、メチルア
ミン、エチルアミン、ジメチルアミン、ジエチルアミ
ン、トリメチルアミン、トリエチルアミン、ジメチルエ
チルアミンが好ましく、四級アンモニウム塩としては、
テトラメチルアンモニウム、テトラエチルアンモニウ
ム、メチルトリエチルアンモニウム、エチルトリメチル
アンモニウム、ジメチルジエチルアンモニウムが好まし
い。
Ammonium salts, amine salts, quaternary ammonium salts, and the like can be used as the electrolyte salt dissolved in such an organic solvent, and as the amine salt, methylamine, ethylamine, dimethylamine, diethylamine, trimethylamine, Triethylamine and dimethylethylamine are preferable, and as the quaternary ammonium salt,
Tetramethylammonium, tetraethylammonium, methyltriethylammonium, ethyltrimethylammonium and dimethyldiethylammonium are preferred.

【0019】(表1)は本発明の実施例および従来例の
電解液の組成を示したものである。
Table 1 shows the compositions of the electrolytic solutions of the examples of the present invention and the conventional examples.

【0020】[0020]

【表1】 [Table 1]

【0021】(表2)は(表1)に示すそれぞれの組成
の電解コンデンサ駆動用電解液を調製し、これらの電解
液を使用して定各電圧10V、公称静電容量100μF
のアルミ電解コンデンサを作成し、そしてこの作成した
アルミ電解コンデンサの初期における静電容量値(12
0Hz)、tanδ(120Hz)および漏れ電流値と、9
5℃中で2000時間、高温負荷試験を行ったときの静
電容量変化率、tanδおよび漏れ電流値を示したもの
である。
(Table 2) prepares electrolytic solutions for driving electrolytic capacitors having the respective compositions shown in (Table 1), and using these electrolytic solutions, a constant voltage of 10 V and a nominal capacitance of 100 μF.
Of the aluminum electrolytic capacitor, and the initial capacitance value (12
0Hz), tan δ (120Hz) and leakage current value, 9
3 shows the rate of change in capacitance, tan δ, and leakage current value when a high temperature load test was performed at 5 ° C. for 2000 hours.

【0022】[0022]

【表2】 [Table 2]

【0023】この(表2)から明らかなように、従来例
2,3は従来例1に比べ、静電容量変化が小さく効果が
見られるものの、本発明の実施例1,2,3と比べると
静電容量変化は大きいものである。また従来例2,3で
は初期特性に対する高温負荷試験後のtanδ変化が大
きいもので、このtanδ変化に対する添加剤の効果は
見られないが、本発明の実施例1,2,3では、tan
δ変化が従来例1,2,3,4に比べてかなり小さいも
ので、添加剤の効果がみられた。
As is clear from (Table 2), the conventional examples 2 and 3 are smaller in capacitance change than the conventional example 1 and are effective, but are compared with the first, second and third examples of the present invention. And the change in capacitance is large. Further, in the conventional examples 2 and 3, the tan δ change after the high temperature load test with respect to the initial characteristics is large, and the effect of the additive on this tan δ change is not seen, but in Examples 1, 2 and 3 of the present invention, tan
The change in δ was much smaller than in Conventional Examples 1, 2, 3, and 4, and the effect of the additive was observed.

【0024】したがって、本発明の各実施例は各従来例
と比較して、高温中における電解コンデンサの特性変化
を改善することができるもので、特に静電容量変化およ
びtanδ変化の双方の改善効果は大きく、信頼性の高
い電解コンデンサを得ることができるものである。
Therefore, each of the embodiments of the present invention can improve the characteristic change of the electrolytic capacitor at high temperature as compared with each of the conventional examples, and particularly the effect of improving both the capacitance change and the tan δ change. Is a large and highly reliable electrolytic capacitor.

【0025】なお、上記本発明の実施例1,2,3にお
いては、(表1)からも明らかなように、アミン誘導体
として、p−アミノ安息香酸−n−ブチル、ベンジルエ
タノールアミンを用いたが、N,N−ジブチル−m−ア
ミノフェノール、N−フェニル−β−ナフチルアミン、
p−n−アミノフェノールについても実施例と同様の効
果が得られるものである。また添加するアミン誘導体の
添加量は、電解液重量に対して、0.01〜2.0重量
%の範囲が好ましいものである。すなわち、0.01重
量%以下の場合は効果が少なく、一方、2.0重量%を
越えると溶解しにくいもので、したがって、アミン誘導
体の添加量は、電解液重量に対して0.01〜2.0重
量%の範囲が好ましいものである。
In Examples 1, 2 and 3 of the present invention, as is apparent from (Table 1), p-aminobenzoic acid-n-butyl and benzylethanolamine were used as amine derivatives. Is N, N-dibutyl-m-aminophenol, N-phenyl-β-naphthylamine,
With pn-aminophenol, the same effect as in the example can be obtained. Further, the addition amount of the amine derivative to be added is preferably in the range of 0.01 to 2.0% by weight based on the weight of the electrolytic solution. That is, if it is less than 0.01% by weight, the effect is small, while if it exceeds 2.0% by weight, it is difficult to dissolve it. A range of 2.0% by weight is preferred.

【0026】[0026]

【発明の効果】以上のように本発明の電解コンデンサ駆
動用電解液は、有機溶媒と電解質塩からなる溶液に(化
5)で示されるアミン誘導体を添加したもので、このア
ミン誘導体は、金属に吸着しやすいため、電極箔に吸着
して電極箔を保護することになり、これにより電極箔の
水和反応等が起こりにくくなるため、高温中における電
解コンデンサの静電容量変化およびtanδ変化を改善
することができるものである。
INDUSTRIAL APPLICABILITY As described above, the electrolytic capacitor driving electrolytic solution of the present invention is a solution comprising an organic solvent and an electrolyte salt to which the amine derivative represented by Chemical formula 5 is added. Since it is easily adsorbed on the electrode foil, it is adsorbed on the electrode foil to protect the electrode foil, and this makes it difficult for the hydration reaction of the electrode foil to occur. It can be improved.

【0027】[0027]

【化5】 Embedded image

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 有機溶媒と電解質塩を主体としてなる溶
液に(化1)で示されるアミン誘導体より選ばれる少な
くとも1種以上の化合物を添加した電解コンデンサ駆動
用電解液。 【化1】
1. An electrolytic solution for driving an electrolytic capacitor, which is obtained by adding at least one compound selected from the amine derivative represented by the chemical formula 1 to a solution mainly composed of an organic solvent and an electrolyte salt. Embedded image
【請求項2】 アミン誘導体が、N−フェニル−β−ナ
フチルアミン、p−アミノ安息香酸−n−ブチル、p−
n−アミノフェノール、ベンジルエタノールアミン、
N,N−ジブチル−m−アミノフェノールのいずれかで
あり、かつその添加量が電解液重量に対して0.01〜
2.0重量%である請求項1記載の電解コンデンサ駆動
用電解液。
2. The amine derivative is N-phenyl-β-naphthylamine, n-butyl p-aminobenzoate, p-
n-aminophenol, benzylethanolamine,
It is any one of N, N-dibutyl-m-aminophenol, and the addition amount thereof is 0.01 to the weight of the electrolytic solution.
The electrolytic solution for driving an electrolytic capacitor according to claim 1, which is 2.0% by weight.
JP9821795A 1995-04-24 1995-04-24 Electrolyte for driving electrolytic capacitor Pending JPH08293437A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9821795A JPH08293437A (en) 1995-04-24 1995-04-24 Electrolyte for driving electrolytic capacitor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9821795A JPH08293437A (en) 1995-04-24 1995-04-24 Electrolyte for driving electrolytic capacitor

Publications (1)

Publication Number Publication Date
JPH08293437A true JPH08293437A (en) 1996-11-05

Family

ID=14213811

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9821795A Pending JPH08293437A (en) 1995-04-24 1995-04-24 Electrolyte for driving electrolytic capacitor

Country Status (1)

Country Link
JP (1) JPH08293437A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001202994A (en) * 2000-01-20 2001-07-27 Sony Corp Secondary battery
WO2007037396A1 (en) * 2005-09-30 2007-04-05 Mitsubishi Chemical Corporation Electrolysis solution for electrolytic capacitor, and electrolytic capacitor
JP2007103498A (en) * 2005-09-30 2007-04-19 Mitsubishi Chemicals Corp Electrolyte for electrolytic capacitor, and electrolytic capacitor

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001202994A (en) * 2000-01-20 2001-07-27 Sony Corp Secondary battery
WO2007037396A1 (en) * 2005-09-30 2007-04-05 Mitsubishi Chemical Corporation Electrolysis solution for electrolytic capacitor, and electrolytic capacitor
JP2007103498A (en) * 2005-09-30 2007-04-19 Mitsubishi Chemicals Corp Electrolyte for electrolytic capacitor, and electrolytic capacitor
US7998360B2 (en) 2005-09-30 2011-08-16 Mitsubishi Chemical Corporation Electrolysis solution for electrolytic capacitor, and electrolytic capacitor

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