JPH08273985A - Electrolyte for driving electrolytic capacitor - Google Patents

Electrolyte for driving electrolytic capacitor

Info

Publication number
JPH08273985A
JPH08273985A JP9981395A JP9981395A JPH08273985A JP H08273985 A JPH08273985 A JP H08273985A JP 9981395 A JP9981395 A JP 9981395A JP 9981395 A JP9981395 A JP 9981395A JP H08273985 A JPH08273985 A JP H08273985A
Authority
JP
Japan
Prior art keywords
acid
driving
peroxide
butylperoxy
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.)
Pending
Application number
JP9981395A
Other languages
Japanese (ja)
Inventor
Shinichi Ohashi
伸一 大橋
Shuichi Tanno
修一 丹野
Kazuhiro Higuchi
和浩 樋口
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.)
Marcon Electronics Co Ltd
Original Assignee
Marcon Electronics 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 Marcon Electronics Co Ltd filed Critical Marcon Electronics Co Ltd
Priority to JP9981395A priority Critical patent/JPH08273985A/en
Publication of JPH08273985A publication Critical patent/JPH08273985A/en
Pending legal-status Critical Current

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Abstract

PURPOSE: To provide electrolytic capacitor driving electrolyte which does not color human organism nor machine even when it adheres to human organism or machine and prevents the spark generating voltage from reducing by using organic peroxide as gas absorbent for driving electrolyte. CONSTITUTION: Organic peroxide is added to electrolyte which is provided by adding organic carboxylic acid or boric acid or salt of these to a solvent. The organic peroxide is the mixture of one or two materials of the following: 1,1-di-t-butylperoxy-3,3,5-trimethylcyclohexane, di-t-butyl peroxide, t-butylcumyl peroxide, dicumyl peroxide, 2,5-dimethyl-2,5-di-(t-butylperoxy)hexane, 1,3-bis-(t- butylperoxyisopropyl)benzene, t-butylperoxyisopropyl carbonate. At least 0.5wt.% organic peroxide is to be added.

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、特にコンデンサ素子から発生するガスを吸収す
る新規な吸収剤を添加した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, and more particularly to an electrolytic solution for driving an electrolytic capacitor containing a novel absorbent for absorbing gas generated from a capacitor element.

【0002】[0002]

【従来の技術】従来、電解コンデンサの駆動用電解液と
しては、エチレングリコール、ジエチレングリコール、
γ−ブチロラクトン、モノメチルホルムアミド、ジメチ
ルホルムアミド等を溶媒とし、これに無機酸又はそのア
ンモニウム塩(ほう酸、ほう酸アンモニウムなど)を溶
解したものや、有機酸(セバシン酸、アゼライン酸、安
息香酸、1,6−デカンジカルボン酸、1−メチル−
1,7−ヘプタンジカルボン酸、1,3−ジメチル−
1,3,9−ノナントリカルボン酸など)又はその塩を
溶質として用い、これにコンデンサ素子から発生する水
素ガスを吸収するために、ガス吸収剤としてパラニトロ
フェノール、パラニトロ安息香酸、パラニトロアセトフ
ェノンなどのニトロ化合物を添加していた。
2. Description of the Related Art Conventionally, as an electrolytic solution for driving an electrolytic capacitor, ethylene glycol, diethylene glycol,
γ-butyrolactone, monomethylformamide, dimethylformamide and the like as a solvent, in which an inorganic acid or its ammonium salt (boric acid, ammonium borate, etc.) is dissolved, or an organic acid (sebacic acid, azelaic acid, benzoic acid, 1,6 -Decanedicarboxylic acid, 1-methyl-
1,7-Heptanedicarboxylic acid, 1,3-dimethyl-
1,3,9-nonanetricarboxylic acid or the like) or a salt thereof is used as a solute, and in order to absorb hydrogen gas generated from the capacitor element, paranitrophenol, paranitrobenzoic acid, paranitroacetophenone or the like is used as a gas absorbent. Nitro compound was added.

【0003】この水素ガスの発生メカニズムを説明する
と、駆動用電解液に含まれた水分が、コンデンサ素子に
流れる漏れ電流により電気分解されて陰極はくから水素
ガスとなって発生するものである。
Explaining the generation mechanism of this hydrogen gas, the water contained in the driving electrolyte is electrolyzed by the leakage current flowing through the capacitor element to generate hydrogen gas from the cathode foil.

【0004】[0004]

【発明が解決しようとする課題】しかしながら、前記の
ようなニトロ化合物は、黄色に発色する性質が強く、人
体や機械へ付着すると落ちにくく、また、電解液の火花
発生電圧を低下させる問題点があり、使用する電圧に限
度があった。
However, the above-mentioned nitro compounds have a strong property of developing a yellow color, are difficult to remove when they adhere to a human body or a machine, and have a problem of lowering the spark generation voltage of the electrolytic solution. Yes, there was a limit to the voltage used.

【0005】本発明は、上記のような欠点を解決するた
めに成されたもので、駆動用電解液のガス吸収剤として
ニトロ化合物に替え有機過酸化物を使用することによっ
て、人体や機械に付着しても発色せず、かつ、火花発生
電圧が低下しない電解コンデンサ駆動用電解液を提供す
るものである。
The present invention has been made to solve the above-mentioned drawbacks. By using an organic peroxide instead of a nitro compound as a gas absorbent of a driving electrolyte, the present invention can be applied to a human body or a machine. It is intended to provide an electrolytic solution for driving an electrolytic capacitor, which does not develop a color even when adhered and does not reduce the spark generation voltage.

【0006】[0006]

【課題を解決するための手段】本発明による電解コンデ
ンサ駆動用電解液において、請求項1記載の発明は、溶
媒に、有機カルボン酸又はほう酸或いはこれらの塩を溶
質として加えた駆動用電解液に、有機過酸化物を添加し
たことを特徴とする電解コンデンサ駆動用電解液であ
る。請求項2の発明は、前記請求項1における溶媒がエ
チレングリコール、ジエチレングリコール、γ−ブチロ
ラクトン、モノメチルホルムアミド、ジメチルホルムア
ミドの中の1種又は2種以上の混合物である駆動用電解
液、請求項3の発明は、前記有機カルボン酸がセバシン
酸、アゼライン酸、安息香酸、1,6−デカンジカルボ
ン酸、1−メチル−1,7−ヘプタンジカルボン酸、
1,3−ジメチル−1,3,9−ノナントリカルボン酸
の中の1種又は2種以上の混合物からなる駆動用電解
液、請求項4の発明は、有機過酸化物が1,1−ジ−t
−ブチルペルオキシ−3,3,5−トリメチルシクロヘ
キサン、ジ−t−ブチルペルオキシド、t−ブチルクミ
ルペルオキシド、ジクミルペルオキシド、2,5−ジメ
チル−2,5−ジ(t−ブチルペルオキシ)ヘキサン、
2,5−ジメチル−2,5−ジ(t−ブチルペルオキ
シ)ヘキセン、1,3ビス−(t−ブチルペルオキシ−
iso−プロピル)ベンゼン、t−ブチルペルオキシ−
iso−プロピルカーボネイトの中の1種又は2種以上
の混合物からなる駆動用電解液、請求項5は、この有機
過酸化物の添加量が少なくとも0.5重量%の駆動用電
解液である。
In the electrolytic solution for driving an electrolytic capacitor according to the present invention, the invention according to claim 1 provides a driving electrolytic solution in which an organic carboxylic acid or boric acid or a salt thereof is added as a solute to a solvent. The electrolytic solution for driving an electrolytic capacitor is characterized by adding an organic peroxide. The invention of claim 2 is a driving electrolyte solution in which the solvent in claim 1 is one kind or a mixture of two or more kinds of ethylene glycol, diethylene glycol, γ-butyrolactone, monomethylformamide and dimethylformamide. In the invention, the organic carboxylic acid is sebacic acid, azelaic acid, benzoic acid, 1,6-decanedicarboxylic acid, 1-methyl-1,7-heptanedicarboxylic acid,
A driving electrolytic solution comprising one or a mixture of two or more of 1,3-dimethyl-1,3,9-nonanetricarboxylic acid, wherein the organic peroxide is 1,1-dicarboxylic acid. -T
-Butylperoxy-3,3,5-trimethylcyclohexane, di-t-butyl peroxide, t-butylcumyl peroxide, dicumyl peroxide, 2,5-dimethyl-2,5-di (t-butylperoxy) hexane,
2,5-Dimethyl-2,5-di (t-butylperoxy) hexene, 1,3bis- (t-butylperoxy)-
iso-propyl) benzene, t-butylperoxy-
A driving electrolytic solution comprising one kind or a mixture of two or more kinds of iso-propyl carbonate. Claim 5 is a driving electrolytic solution containing at least 0.5% by weight of this organic peroxide.

【0007】[0007]

【作用】以上のように構成してなる電解コンデンサ駆動
用電解液によれば、有機過酸化物は、ニトロ化合物と同
様に駆動用電解液の水分とコンデンサ素子に流れる漏れ
電流によって生じる水素ガスを吸収する作用があるとと
もに、この過酸化物を添加した駆動用電解液は、火花発
生電圧の低下が見られない特徴を有し、かつ、無色透明
で人体や機械に付着しても着色することがないので、ニ
トロ化合物を添加した場合に比較して、その取扱いや作
業が格段に容易になるものである。
According to the electrolytic capacitor driving electrolytic solution configured as described above, the organic peroxide is similar to the nitro compound in that it contains hydrogen gas generated by the moisture of the driving electrolytic solution and the leakage current flowing through the capacitor element. In addition to having the function of absorbing, the driving electrolyte solution containing this peroxide has the characteristics that no decrease in the spark generation voltage is observed, and it is colorless and transparent and should be colored even if it adheres to the human body or machinery. Since there is no nitro compound, it is much easier to handle and work as compared with the case of adding a nitro compound.

【0008】[0008]

【実施例】以下、本発明に係る電解コンデンサ駆動用電
解液の実施例について説明する。
EXAMPLES Examples of the electrolytic solution for driving an electrolytic capacitor according to the present invention will be described below.

【0009】実施例A 表1に従来例、実施例、参考例の各駆動用電解液の組成
を示し、表2には、これらの駆動用電解液を使用して作
製した定格50V−2200μF、ケースサイズφ18
mm×L35mmのコンデンサ各20個について、高温
負荷試験(105℃中で50Vを印加して1000h)
後の外観と水素ガス量を示す。なお、この表2に示した
水素ガス量(ml)は試料20個の平均値であり、防爆
弁はアルミニウムケースに瑕疵を付与したものからな
る。
Example A Table 1 shows the composition of each driving electrolytic solution of the conventional example, the example, and the reference example, and Table 2 shows a rating of 50V-2200 μF produced using these driving electrolytic solutions. Case size φ18
High temperature load test (1000 h at 105 ° C with 50 V applied) for each 20 mm x L35 mm capacitors
The external appearance and the amount of hydrogen gas are shown below. The hydrogen gas amount (ml) shown in Table 2 is an average value of 20 samples, and the explosion-proof valve is made of an aluminum case with a flaw.

【0010】[0010]

【表1】 [Table 1]

【0011】[0011]

【表2】 [Table 2]

【0012】表2から明らかなように、有機過酸化物
(t−ブチルペルオキシ−iso−プロピルカーボネイ
ト)の添加量が0.3重量%の参考例1では、水素ガス
量が従来例や実施例に比較して約3〜6倍となり、全数
防爆弁膨れを生じた。同様の有機過酸化物を0.5重量
%添加した実施例8では、まったく異常がないことか
ら、有機過酸化物の添加量が少ない場合は、ガス吸収能
が不足することがあり、実施例の場合は、0.5重量%
異常の添加が必要である。また、ニトロ化合物や有機過
酸化物をまったく添加していない参考例2では、発生し
た水素ガスを吸収できないので、全数防爆弁が動作して
いる。
As is clear from Table 2, in Reference Example 1 in which the addition amount of the organic peroxide (t-butylperoxy-iso-propylcarbonate) was 0.3% by weight, the hydrogen gas amount was in the conventional example or the example. It was about 3 to 6 times as much as that of No. 1, and all explosion-proof valves swelled. In Example 8 in which the same organic peroxide was added by 0.5% by weight, there was no abnormality at all, so when the amount of the organic peroxide added was small, the gas absorption capacity might be insufficient. In case of, 0.5% by weight
Abnormal addition is required. Further, in Reference Example 2 in which no nitro compound or organic peroxide was added at all, the generated hydrogen gas could not be absorbed, so that all explosion-proof valves were operating.

【0013】この結果から、実施例の場合、従来からガ
ス吸収剤として使用されているニトロ化合物と同等のガ
ス吸収能を有していることがわかる。
From these results, it can be seen that the example has a gas absorption capacity equivalent to that of a nitro compound conventionally used as a gas absorbent.

【0014】実施例B 次に従来例1、2及び実施例1、2に示した駆動用電解
液について、火花発生電圧を調査したので、その結果を
表3に示す。この従来例と実施例は、添加したガス吸収
剤が従来例ではニトロ化合物、実施例では有機過酸化物
であることが相違するのみである。
Example B Next, the spark generation voltage was investigated for the driving electrolyte solutions shown in Conventional Examples 1 and 2 and Examples 1 and 2, and the results are shown in Table 3. The only difference between this conventional example and the example is that the added gas absorbent is a nitro compound in the conventional example and an organic peroxide in the example.

【0015】[0015]

【表3】 [Table 3]

【0016】表3に示されたように、有機過酸化物を添
加した実施例では、ニトロ化合物を添加した従来例に比
較し40〜50V上回り、ガス吸収剤添加による火花電
圧の低下を防止することができる。
As shown in Table 3, in the examples in which the organic peroxide was added, the voltage was 40 to 50 V higher than that in the conventional example in which the nitro compound was added, and the decrease in the spark voltage due to the addition of the gas absorbent is prevented. be able to.

【0017】なお、上記実施例では、溶媒としてエチレ
ングリコール、γ−ブチロラクトンを用いた場合につい
て述べたが、ジエチレングリコール、モノメエルホルム
アミド、ジメチルホルムアミドを単独で、又は2種異常
混合して用いても同様の効果を得ることができる。
In the above examples, the case where ethylene glycol or γ-butyrolactone was used as the solvent was described. However, the same applies when diethylene glycol, monomeerformamide, dimethylformamide are used alone or in an abnormal mixture of two kinds. The effect of can be obtained.

【0018】また、有機カルボン酸としては、実施例で
示したものの他に、アゼライン酸、1−メチル−1,7
−ヘプタンジカルボン酸、1,3−ジメチル−1,3,
9−ノナントリカルボン酸などを単独で、又は2種以上
を混合して使用しても良い。
As the organic carboxylic acid, in addition to those shown in the examples, azelaic acid and 1-methyl-1,7
-Heptanedicarboxylic acid, 1,3-dimethyl-1,3
You may use 9-nonane tricarboxylic acid etc. individually or in mixture of 2 or more types.

【0019】[0019]

【発明の効果】以上述べたように、本発明になる電解コ
ンデンサ駆動用電解液によれば、ガス吸収剤として有機
過酸化物を使用したことによって、従来使用されていた
ニトロ化合物と吸収能は同等で、ニトロ化合物の欠点と
されていた火花発生電圧の低下、及び人体や機械への色
の付着がないという作用効果を得ることができる。
As described above, according to the electrolytic capacitor driving electrolytic solution of the present invention, since the organic peroxide is used as the gas absorbent, the conventionally used nitro compound and the absorption capacity are In the same manner, it is possible to obtain the effect of reducing the spark generation voltage, which has been a drawback of nitro compounds, and preventing the adherence of color to the human body or machine.

Claims (5)

【特許請求の範囲】[Claims] 【請求項1】 溶媒に、有機カルボン酸又はほう酸或い
はこれらの塩を溶質として加えた駆動用電解液に、有機
過酸化物を添加したことを特徴とする電解コンデンサ駆
動用電解液。
1. An electrolytic solution for driving an electrolytic capacitor, wherein an organic peroxide is added to a driving electrolyte solution in which an organic carboxylic acid or boric acid or a salt thereof is added as a solute to a solvent.
【請求項2】 溶媒がエチレングリコール、ジエチレン
グリコール、γ−ブチロラクトン、モノメチルホルムア
ミド、ジメチルホルムアミドの中の1種又は2種以上の
混合物からなることを特徴とする請求項1記載の電解コ
ンデンサ駆動用電解液。
2. The electrolytic solution for driving an electrolytic capacitor according to claim 1, wherein the solvent comprises one kind or a mixture of two or more kinds among ethylene glycol, diethylene glycol, γ-butyrolactone, monomethylformamide and dimethylformamide. .
【請求項3】 有機カルボン酸がアジピン酸、セバシン
酸、アゼライン酸、安息香酸、1,6−デカンジカルボ
ン酸、1−メチル−1,7−ヘプタンジカルボン酸、
1,3−ジメチル−1,3,9−ノナントリカルボン
酸、マレイン酸、シトラコン酸、サリチル酸、フタル酸
の中の1種又は2種以上の混合物からなることを特徴と
する請求項1又は請求項2記載の電解コンデンサ駆動用
電解液。
3. The organic carboxylic acid is adipic acid, sebacic acid, azelaic acid, benzoic acid, 1,6-decanedicarboxylic acid, 1-methyl-1,7-heptanedicarboxylic acid,
The compound according to claim 1 or claim 1, which comprises one or a mixture of 1,3-dimethyl-1,3,9-nonanetricarboxylic acid, maleic acid, citraconic acid, salicylic acid and phthalic acid. 2. An electrolytic solution for driving an electrolytic capacitor as described in 2.
【請求項4】 有機過酸化物が1,1−ジ−t−ブチル
ペルオキシ−3,3,5−トリメチルシクロヘキサン、
ジ−t−ブチルペルオキシド、t−ブチルクミルペルオ
キシド、ジクミルペルオキシド、2,5−ジメチル−
2,5−ジ(t−ブチルペルオキシ)ヘキサン、2,5
−ジメチル−2,5−ジ(t−ブチルペルオキシ)ヘキ
セン、1,3ビス−(t−ブチルペルオキシ−iso−
プロピル)ベンゼン、t−ブチルペルオキシ−iso−
プロピルカーボネイトの中の1種又は2種以上の混合物
からなることを特徴とする請求項1〜請求項3のいずれ
かに記載の電解コンデンサ駆動用電解液。
4. The organic peroxide is 1,1-di-t-butylperoxy-3,3,5-trimethylcyclohexane,
Di-t-butyl peroxide, t-butyl cumyl peroxide, dicumyl peroxide, 2,5-dimethyl-
2,5-di (t-butylperoxy) hexane, 2,5
-Dimethyl-2,5-di (t-butylperoxy) hexene, 1,3 bis- (t-butylperoxy-iso-
Propyl) benzene, t-butylperoxy-iso-
The electrolytic solution for driving an electrolytic capacitor according to any one of claims 1 to 3, which is composed of one kind or a mixture of two or more kinds of propyl carbonate.
【請求項5】 有機過酸化物の添加量が少なくとも0.
5重量%であることを特徴とする請求項1〜請求項4の
いずれかに記載の電解コンデンサ駆動用電解液。
5. The amount of organic peroxide added is at least 0.
It is 5% by weight, and the electrolytic solution for driving an electrolytic capacitor according to any one of claims 1 to 4.
JP9981395A 1995-03-31 1995-03-31 Electrolyte for driving electrolytic capacitor Pending JPH08273985A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9981395A JPH08273985A (en) 1995-03-31 1995-03-31 Electrolyte for driving electrolytic capacitor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9981395A JPH08273985A (en) 1995-03-31 1995-03-31 Electrolyte for driving electrolytic capacitor

Publications (1)

Publication Number Publication Date
JPH08273985A true JPH08273985A (en) 1996-10-18

Family

ID=14257299

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9981395A Pending JPH08273985A (en) 1995-03-31 1995-03-31 Electrolyte for driving electrolytic capacitor

Country Status (1)

Country Link
JP (1) JPH08273985A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100467689B1 (en) * 2001-10-24 2005-01-24 삼성에스디아이 주식회사 Organic electrolyte solution and lithium battery adopting the same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100467689B1 (en) * 2001-10-24 2005-01-24 삼성에스디아이 주식회사 Organic electrolyte solution and lithium battery adopting the same

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