JPH08264388A - Electrolyte for driving electrolytic capacitor - Google Patents

Electrolyte for driving electrolytic capacitor

Info

Publication number
JPH08264388A
JPH08264388A JP6452695A JP6452695A JPH08264388A JP H08264388 A JPH08264388 A JP H08264388A JP 6452695 A JP6452695 A JP 6452695A JP 6452695 A JP6452695 A JP 6452695A JP H08264388 A JPH08264388 A JP H08264388A
Authority
JP
Japan
Prior art keywords
electrolyte
salt
acid
solvent
electrolytic solution
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
Application number
JP6452695A
Other languages
Japanese (ja)
Other versions
JP3499639B2 (en
Inventor
Shuzo Hongo
修三 本合
Hidetoshi Hara
英俊 原
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 Corp
Original Assignee
Nichicon Corp
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 Corp filed Critical Nichicon Corp
Priority to JP06452695A priority Critical patent/JP3499639B2/en
Publication of JPH08264388A publication Critical patent/JPH08264388A/en
Application granted granted Critical
Publication of JP3499639B2 publication Critical patent/JP3499639B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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

Abstract

PURPOSE: To increase the voltage withholding strength of an electrolyte by making the number of carbons on the side chain including a carboxyl group which is attached to a benzene ring larger than that of a benzoic acid. CONSTITUTION: This is an electrolyte for driving an electrolytic capacitor wherein polyhydric alcohol is used as a main solvent and monocarboxylic acid which has a benzyl group as shown by the formula I or a salt of it is dissolved in the solvent. In more specific, a solvent, chief of which are ethylene glycol and 1,3-propanediol, is used and at least one kind of the acid shown by the formula I or the salt of it (an ammonium salt is generally used as a salt) is dissolved as a salute in this electrolyte. With this electrolyte, a capacitor for medium and high voltages can be obtained wherein an initial value of tanδ can be held low and the change in the capacity and the increase in the value of tanδ can be held small over a long period of time at high temperatures and a voltage withholding strength is increased.

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、特に中高圧用アルミ電解コンデンサの駆動用
電解液に関し、耐電圧の向上および高温での寿命特性の
長期安定化を実現した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, in particular, an electrolytic solution for an aluminum electrolytic capacitor for medium and high voltage, which has improved withstand voltage and long-term stability of life characteristics at high temperature. 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、特に中高圧用のアルミニウム電解
コンデンサの電解液としては、エチレングリコールにホ
ウ酸あるいはホウ酸アンモニウムを溶解した、いわゆる
エチレングリコールホウ酸系の電解液が85℃用電解コ
ンデンサに多用されている。この種の電解液は、難燃性
という優れた特性を有する反面、ホウ酸とエチレングリ
コールとのエステル化反応によるエステル化水の発生お
よびこれに起因した水素ガスの発生により、105℃用
電解コンデンサへの対応が困難な状況にあった。一方、
高温下での耐電圧性を向上させる目的で炭素数が8から
22である二塩基酸のアンモニウム塩を使用した電解液
も知られている。後者においては、モノカルボン酸であ
るにもかかわらず、化成性に優れ、かつベンゼン環を持
っていることで高温下で安定な安息香酸またはその塩と
組み合わせて用いられている。このような二塩基酸のア
ンモニウム塩に安息香酸またはその塩を組み合わせてエ
チレングリコールに溶解された電解液においては、耐熱
性の面で大幅な改善効果が認められるものの、高温下で
はエステル化を経てアミド化した析出物が電極表面を覆
うことによる容量減少及びtanδの増大を避けることが
出来なかった。また、安息香酸の熱的安定性は非常に優
れているものの、耐電圧的に限界があった。
2. Description of the Related Art Conventionally, a so-called ethylene glycol boric acid-based electrolytic solution prepared by dissolving boric acid or ammonium borate in ethylene glycol has been used as an electrolytic solution for an aluminum electrolytic capacitor for medium- and high-voltages. It is used a lot. This type of electrolytic solution has an excellent property of being flame retardant, but on the other hand, due to the generation of esterified water due to the esterification reaction of boric acid and ethylene glycol and the resulting generation of hydrogen gas, an electrolytic capacitor for 105 ° C. Was difficult to deal with. on the other hand,
Also known is an electrolytic solution using an ammonium salt of a dibasic acid having 8 to 22 carbon atoms for the purpose of improving the withstand voltage property at high temperature. In the latter, it is used in combination with benzoic acid or a salt thereof, which is a monocarboxylic acid but has excellent chemical conversion properties and has a benzene ring and is stable at high temperatures. In the electrolytic solution in which benzoic acid or its salt is combined with the ammonium salt of dibasic acid and dissolved in ethylene glycol, although a significant improvement effect in terms of heat resistance is observed, it undergoes esterification at high temperature. It was unavoidable to reduce the capacity and increase tan δ due to the amidated precipitate covering the electrode surface. Although benzoic acid has excellent thermal stability, it has a limited withstand voltage.

【0003】[0003]

【発明が解決しようとする課題】本発明は上記の問題点
を解決するため、電解液を改良することにより、初期の
tanδ値を低く抑えるとともに、高温下での容量変化及び
tanδ増加を長期にわたって小さく抑えることができ、か
つ耐電圧性をも改善した中高圧用コンデンサを提供する
ことを目的としている。
SUMMARY OF THE INVENTION In order to solve the above problems, the present invention improves the electrolytic solution to improve the initial
While keeping the tan δ value low,
It is an object of the present invention to provide a medium- and high-voltage capacitor which can suppress an increase in tanδ to be small over a long period of time and has improved withstand voltage.

【0004】[0004]

【課題を解決するための手段】本発明は上記の課題を解
決するため、多価アルコールを主溶媒とした電解コンデ
ンサ用電解液において、化2で示されるベンゼン基を有
するモノカルボン酸、またはその塩を溶解させたことを
特徴としている。即ち、エチレングリコール,1,3−
プロパンジオールを主体として用いた溶媒に、化1に示
した酸またはその塩(塩としてはアンモニウム塩が一般
的)のいずれか一種類以上を溶質として溶解させた電解
液である。
In order to solve the above-mentioned problems, the present invention provides a monocarboxylic acid having a benzene group represented by Chemical formula 2 in an electrolytic solution for an electrolytic capacitor using a polyhydric alcohol as a main solvent, or a compound thereof. It is characterized by dissolving salt. That is, ethylene glycol, 1,3-
This is an electrolytic solution obtained by dissolving one or more of the acid shown in Chemical formula 1 or a salt thereof (ammonium salt is generally used as a salt) as a solute in a solvent containing propanediol as a main component.

【0005】[0005]

【化2】 Embedded image

【0006】[0006]

【作用】ベンゼン環に付加しているカルボキシル基を含
む側鎖の炭素数が安息香酸より大きいことにより、電解
液の耐電圧が向上する。また、ベンゼン環がπ電子結合
により形成されていることから高温での電解液の安定性
が保持される。更に二塩基酸のアンモニウム塩のエステ
ル化反応が安息香酸による場合よりも緩和されるので、
アミド化した析出物による容量減少及びtanδ増大が抑
えられる。
Function: The side chain containing a carboxyl group added to the benzene ring has a carbon number larger than that of benzoic acid, so that the withstand voltage of the electrolytic solution is improved. Further, since the benzene ring is formed by the π-electron bond, the stability of the electrolytic solution at high temperature is maintained. Furthermore, since the esterification reaction of ammonium salt of dibasic acid is more relaxed than that by benzoic acid,
A decrease in capacity and an increase in tan δ due to amidated precipitates can be suppressed.

【0007】[0007]

【実施例】以下、本発明の具体的実施例について記す。
表1は本発明の実施例及び従来例の中高圧用電解液の組
成、比抵抗および火花発生電圧について比較した結果を
示す。表1において、電解液試料記号Aは従来例、B,
C,D,Eは本発明の実施例、Fは参考例である。
EXAMPLES Specific examples of the present invention will be described below.
Table 1 shows the results of comparison of the composition, the specific resistance and the spark generation voltage of the medium and high voltage electrolytic solutions of the examples of the present invention and the conventional example. In Table 1, electrolyte sample symbol A is a conventional example, B,
C, D and E are examples of the present invention, and F is a reference example.

【0008】[0008]

【表1】 [Table 1]

【0009】表1から明らかなように、従来例に使用し
た安息香酸アンモニウムとほぼ等モルの化1に示すアン
モニウム塩を用いると、比抵抗の変化はごくわずかであ
るのに対して、耐電圧の向上は大きい。
As is apparent from Table 1, when the ammonium benzoate used in the conventional example and the ammonium salt shown in Chemical formula 1 in an approximately equimolar amount are used, the change in the specific resistance is very small, while the withstand voltage is small. Is greatly improved.

【0009】このように、本発明における好ましい実施
態様は、中圧用ではエチレングリコールを主体とし、水
分を1重量%から8重量%含む溶媒に、アゼライン酸の
塩類あるいはセバシン酸等の高級二塩基酸の塩類ととも
に、本発明による化1に示した酸あるいはそのアンモニ
ウム塩を溶解させた電解液である。また必要に応じて、
ホウ酸、マンニット、亜燐酸、次亜リン酸もしくはその
塩を添加すると、更に特性を改善することができる。
As described above, the preferred embodiment of the present invention is such that a solvent mainly containing ethylene glycol for medium pressure and containing 1 wt% to 8 wt% of water is used, and a salt of azelaic acid or a higher dibasic acid such as sebacic acid is used. It is an electrolytic solution in which the acid shown in Chemical formula 1 according to the present invention or its ammonium salt is dissolved together with the salts of. Also, if necessary,
The properties can be further improved by adding boric acid, mannite, phosphorous acid, hypophosphorous acid or a salt thereof.

【0010】化1に示した酸あるいはその塩の溶解量
は、0.5wt%から10wt%の範囲が良い。0.5
wt%未満の場合には耐電圧を向上させる効果を奏せ
ず、また10wt%を超えると火花発生電圧が低下して
しまう。
The amount of the acid or its salt shown in Chemical formula 1 dissolved is preferably in the range of 0.5 wt% to 10 wt%. 0.5
If it is less than wt%, the effect of improving the withstand voltage is not exerted, and if it exceeds 10 wt%, the spark generation voltage is reduced.

【0011】なお、これらの実施例以外にも、他の溶質
との混合、あるいは低温特性の改善のためエチレングリ
コールの一部を2−エチル−1,3−ヘキサンジオール
に置き換えるなど、多枝にわたる応用が可能である。
In addition to these examples, there are many branches such as mixing with other solutes or substituting 2-ethyl-1,3-hexanediol for a part of ethylene glycol in order to improve low temperature characteristics. It can be applied.

【0012】[0012]

【発明の効果】以上のように、多価アルコールを主溶媒
とした電解コンデンサ用電解液において、本発明による
前記の一般式で表されるベンジル基を有するモノカルボ
ン酸またはその塩を溶質とした電解液は、電解液の耐電
圧を向上させることが可能であり、また、高温での電解
液の安定性を保持することができるので、工業的ならび
に実用的価値の大なるものである。
INDUSTRIAL APPLICABILITY As described above, in the electrolytic solution for electrolytic capacitors using a polyhydric alcohol as a main solvent, the monocarboxylic acid having a benzyl group represented by the above general formula according to the present invention or a salt thereof is used as a solute. Since the electrolytic solution can improve the withstand voltage of the electrolytic solution and can maintain the stability of the electrolytic solution at high temperature, it has great industrial and practical value.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 多価アルコールを主溶媒とした電解コン
デンサ駆動用電解液において、化1で示されるベンジル
基を有するモノカルボン酸、またはその塩を溶解するこ
とを特徴とする電解コンデンサ駆動用電解液。 【化1】
1. An electrolysis solution for driving an electrolytic capacitor, wherein a monocarboxylic acid having a benzyl group represented by Chemical formula 1 or a salt thereof is dissolved in an electrolytic solution for driving an electrolysis capacitor using a polyhydric alcohol as a main solvent. liquid. Embedded image
JP06452695A 1995-03-23 1995-03-23 Electrolyte for driving electrolytic capacitors Expired - Fee Related JP3499639B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP06452695A JP3499639B2 (en) 1995-03-23 1995-03-23 Electrolyte for driving electrolytic capacitors

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP06452695A JP3499639B2 (en) 1995-03-23 1995-03-23 Electrolyte for driving electrolytic capacitors

Publications (2)

Publication Number Publication Date
JPH08264388A true JPH08264388A (en) 1996-10-11
JP3499639B2 JP3499639B2 (en) 2004-02-23

Family

ID=13260759

Family Applications (1)

Application Number Title Priority Date Filing Date
JP06452695A Expired - Fee Related JP3499639B2 (en) 1995-03-23 1995-03-23 Electrolyte for driving electrolytic capacitors

Country Status (1)

Country Link
JP (1) JP3499639B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003059771A (en) * 2001-08-10 2003-02-28 Nichicon Corp Driving electrolyte for electrolytic capacitor
WO2011124554A2 (en) 2010-04-06 2011-10-13 Bayer Cropscience Ag Use of 4-phenylbutyric acid and/or the salts thereof for enhancing the stress tolerance of plants

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003059771A (en) * 2001-08-10 2003-02-28 Nichicon Corp Driving electrolyte for electrolytic capacitor
WO2011124554A2 (en) 2010-04-06 2011-10-13 Bayer Cropscience Ag Use of 4-phenylbutyric acid and/or the salts thereof for enhancing the stress tolerance of plants

Also Published As

Publication number Publication date
JP3499639B2 (en) 2004-02-23

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