JP3078171B2 - Electrolyte for driving electrolytic capacitors - Google Patents

Electrolyte for driving electrolytic capacitors

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Publication number
JP3078171B2
JP3078171B2 JP06042420A JP4242094A JP3078171B2 JP 3078171 B2 JP3078171 B2 JP 3078171B2 JP 06042420 A JP06042420 A JP 06042420A JP 4242094 A JP4242094 A JP 4242094A JP 3078171 B2 JP3078171 B2 JP 3078171B2
Authority
JP
Japan
Prior art keywords
electrolyte
present
electrolytic
electrolytic solution
electrolytic capacitors
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.)
Expired - Fee Related
Application number
JP06042420A
Other languages
Japanese (ja)
Other versions
JPH07249546A (en
Inventor
隆聡 佐野
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.)
Nichicon Capacitor Ltd
Original Assignee
Nichicon Capacitor 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 Nichicon Capacitor Ltd filed Critical Nichicon Capacitor Ltd
Priority to JP06042420A priority Critical patent/JP3078171B2/en
Publication of JPH07249546A publication Critical patent/JPH07249546A/en
Application granted granted Critical
Publication of JP3078171B2 publication Critical patent/JP3078171B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Electric Double-Layer Capacitors Or The Like (AREA)

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、電解コンデンサの駆動
用電解液(以下電解液という)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 (hereinafter referred to as an electrolytic solution).

【0002】[0002]

【従来の技術】従来より電解コンデンサの電解液には、
エチレングリコ−ルを主体とした溶媒に、ほう酸あるい
はほう酸アンモニウムを溶解した電解液が多用されてい
る。しかしこの種の電解液は、100℃を超える高温雰
囲気中での特性が極端に劣る。そこで、高温での特性を
向上させるため、エチレングリコ−ルを主体とした溶媒
に、7−ビニル−9−ヘキサデセン−1,16−ジカル
ボン酸、1,6−デカンジカルボン酸、アゼライン酸、
アジピン酸等の有機カルボン酸およびその塩を使用した
有機酸系電解液が知られている。
2. Description of the Related Art Conventionally, electrolytic solutions for electrolytic capacitors include:
An electrolytic solution in which boric acid or ammonium borate is dissolved in a solvent mainly composed of ethylene glycol has been widely used. However, this type of electrolyte has extremely poor properties in a high-temperature atmosphere exceeding 100 ° C. Therefore, in order to improve the properties at high temperatures, 7-vinyl-9-hexadecene-1,16-dicarboxylic acid, 1,6-decanedicarboxylic acid, azelaic acid,
Organic acid-based electrolytes using organic carboxylic acids such as adipic acid and salts thereof are known.

【0003】[0003]

【発明が解決しようとする課題】しかしながら上述の有
機酸系電解液は、高温における火花電圧が十分でなく改
善が望まれていた。本発明は、この問題を解決するもの
である。即ち、高温における火花電圧を高め、耐熱性に
優れた、高温雰囲気中での信頼性の高い中高圧コンデン
サ用電解液を提供するものである。
However, the above-mentioned organic acid-based electrolyte does not have a sufficient spark voltage at a high temperature, and it has been desired to improve the spark voltage. The present invention solves this problem. That is, an object of the present invention is to provide an electrolyte solution for a medium-to-high voltage capacitor which has a high spark voltage at a high temperature and has excellent heat resistance and high reliability in a high temperature atmosphere.

【0004】[0004]

【課題を解決するための手段】これらの問題を解決する
為に、有機酸あるいはその塩を溶質とし、エチレングリ
コ−ルを主溶媒とした電解コンデンサの電解液におい
て、3−メチル−1,5−ペンタンジオ−ルを副溶媒と
することを特徴とする電解コンデンサの電解液である。
またその副溶媒の添加量は、溶液全体に占める比率が
2.0〜20.0重量%存在する事を特徴とするもので
ある。
In order to solve these problems, an electrolytic solution of an electrolytic capacitor using an organic acid or a salt thereof as a solute and ethylene glycol as a main solvent is used as a solvent. -An electrolytic solution for an electrolytic capacitor, characterized in that pentanediol is used as a secondary solvent.
The amount of the co-solvent added is characterized in that the ratio of the co-solvent to the whole solution is 2.0 to 20.0% by weight.

【0005】[0005]

【作用】本発明の電解液に使用した3−メチル−1,5
−ペンタンジオ−ルは、沸点がエチレングリコ−ルの1
98℃に対し250℃と高く、高沸点かつ低蒸気圧であ
るため、電解液の気化による外観異常が発生せず、ま
た、側鎖が存在することによる立体障害のためにエステ
ル化反応が抑制される。さらにエチレングリコ−ルより
も分子量が大きいため、電極箔の表面に付着することに
より、絶縁破壊を抑制し火花電圧が上昇するものと考え
られる。
The 3-methyl-1,5 used in the electrolyte of the present invention.
-Pentanediol has a boiling point of 1 of ethylene glycol.
High boiling point and low vapor pressure at 250 ° C compared to 98 ° C, no abnormal appearance due to vaporization of electrolyte, and suppression of esterification reaction due to steric hindrance due to the presence of side chains Is done. Furthermore, since the molecular weight is larger than that of ethylene glycol, it is considered that, by adhering to the surface of the electrode foil, dielectric breakdown is suppressed and the spark voltage is increased.

【0006】[0006]

【実施例】以下、本発明の具体的実施例について説明す
る。表1,2は、従来の電解液と本発明の電解液の組
成、比抵抗、および火花発生電圧について比較例を示
す。表3は、表1,2に示した電解液を用いて試作した
定格450V,10μFのアルミニウム電解コンデンサ
による、125℃における1000時間高温負荷試験を
行った結果を示す。なお、表中電解液試料記号A,B,
Cは従来例、記号D,E,F,G,Hは本発明例であ
り、また記号EGはエチレングリコ−ル、記号MPDは
3−メチル−1,5−ペンタンジオ−ルを示す。
DESCRIPTION OF THE PREFERRED EMBODIMENTS Hereinafter, specific embodiments of the present invention will be described. Tables 1 and 2 show comparative examples of the composition, specific resistance, and spark generation voltage of the conventional electrolytic solution and the electrolytic solution of the present invention. Table 3 shows the results of a 1000-hour high-temperature load test at 125 ° C. using a 450-V rated, 10 μF aluminum electrolytic capacitor that was prototyped using the electrolytes shown in Tables 1 and 2. The electrolyte sample symbols A, B, and
C is a conventional example, symbols D, E, F, G, and H are examples of the present invention. Symbol EG is ethylene glycol, and symbol MPD is 3-methyl-1,5-pentaneddiol.

【0007】[0007]

【表1】 [Table 1]

【0008】[0008]

【表2】 [Table 2]

【0009】[0009]

【表3】 [Table 3]

【0010】表1,2から明らかなように、本発明例の
試料記号D,E,F,G,Hの電解液は従来の電解液に
比べて火花発生電圧が高く、特に高温になるほどその効
果は大きい。また、表3から明かなように、本発明例の
試料記号D,E,F,G,Hの電解液は従来の電解液に
比べ、高温雰囲気中での電解液の気化による外観膨張が
見られず、また、信頼性の低下も見られない。なお、3
−メチル−1,5−ペンタンジオ−ルの溶液全体に占め
る割合が2.0重量%未満の場合には、主溶媒であるエ
チレングリコ−ルの性質が強く改善効果が少なく、ま
た、20.0重量%を超えると比抵抗の上昇が著しい為
好ましくない。また、本発明は、例として7−ビニル−
9−ヘキサデセン−1,16−ジカルボン酸、1,6−
デカンジカルボン酸、アゼライン酸を示したが、これら
の有機酸に限定されるものではなく、他の有機酸および
その塩の場合でも上述の効果が得られる。
As is clear from Tables 1 and 2, the electrolytes of the sample symbols D, E, F, G and H of the present invention have a higher spark generation voltage than the conventional electrolytes. The effect is great. Further, as is apparent from Table 3, the electrolytes of the sample symbols D, E, F, G, and H of the present invention exhibited a larger external expansion due to the vaporization of the electrolyte in a high-temperature atmosphere than the conventional electrolyte. No decrease in reliability was observed. In addition, 3
When the proportion of -methyl-1,5-pentaneddiol in the whole solution is less than 2.0% by weight, the properties of ethylene glycol which is a main solvent are strong and the improvement effect is small, and 20.0% by weight. Exceeding the percentage by weight is not preferred because the specific resistance increases significantly. The present invention also provides, for example, 7-vinyl-
9-hexadecene-1,16-dicarboxylic acid, 1,6-
Although decanedicarboxylic acid and azelaic acid are shown, the present invention is not limited to these organic acids, and the above-mentioned effects can be obtained with other organic acids and salts thereof.

【0011】[0011]

【発明の効果】以上のように、本発明の電解液は、高温
での火花発生電圧が上昇し、この電解液を用いた電解コ
ンデンサは、高温度において長時間安定した特性を有
し、工業的ならびに実用的価値の大なるものである。
As described above, the electrolytic solution of the present invention has a high spark generation voltage at a high temperature, and an electrolytic capacitor using this electrolytic solution has stable characteristics at a high temperature for a long time. It is of great target and practical value.

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 有機酸あるいはその塩を溶質とし、エチ
レングリコ−ルを主溶媒とした電解コンデンサの駆動用
電解液において、3−メチル−1,5−ペンタンジオ−
ルを副溶媒とすることを特徴とする電解コンデンサの駆
動用電解液。
1. An electrolyte for driving an electrolytic capacitor comprising an organic acid or a salt thereof as a solute and ethylene glycol as a main solvent, comprising 3-methyl-1,5-pentanedio-
An electrolytic solution for driving an electrolytic capacitor, wherein the electrolytic solution is a solvent.
【請求項2】 上記3−メチル−1,5−ペンタンジオ
−ルは、溶液全体に占める比率が、2.0〜20.0重
量%存在することを特徴とする請求項1の電解コンデン
サの駆動用電解液。
2. A driving method for an electrolytic capacitor according to claim 1, wherein said 3-methyl-1,5-pentaneddiol has a ratio of 2.0 to 20.0% by weight in the whole solution. Electrolyte.
JP06042420A 1994-03-14 1994-03-14 Electrolyte for driving electrolytic capacitors Expired - Fee Related JP3078171B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP06042420A JP3078171B2 (en) 1994-03-14 1994-03-14 Electrolyte for driving electrolytic capacitors

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP06042420A JP3078171B2 (en) 1994-03-14 1994-03-14 Electrolyte for driving electrolytic capacitors

Publications (2)

Publication Number Publication Date
JPH07249546A JPH07249546A (en) 1995-09-26
JP3078171B2 true JP3078171B2 (en) 2000-08-21

Family

ID=12635579

Family Applications (1)

Application Number Title Priority Date Filing Date
JP06042420A Expired - Fee Related JP3078171B2 (en) 1994-03-14 1994-03-14 Electrolyte for driving electrolytic capacitors

Country Status (1)

Country Link
JP (1) JP3078171B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3705864B2 (en) * 1996-05-09 2005-10-12 ニチコン株式会社 Electrolytic solution for electrolytic capacitor drive
JP2017228738A (en) * 2016-06-24 2017-12-28 ニチコン株式会社 Electrolytic solution and electrolytic capacitor

Also Published As

Publication number Publication date
JPH07249546A (en) 1995-09-26

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