JPH0969471A - Capacitor electrolyte for electrolytic solution - Google Patents

Capacitor electrolyte for electrolytic solution

Info

Publication number
JPH0969471A
JPH0969471A JP24679095A JP24679095A JPH0969471A JP H0969471 A JPH0969471 A JP H0969471A JP 24679095 A JP24679095 A JP 24679095A JP 24679095 A JP24679095 A JP 24679095A JP H0969471 A JPH0969471 A JP H0969471A
Authority
JP
Japan
Prior art keywords
ammonium
electrolytic
electrolytic solution
dissolved
nitropyrimidine
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
JP24679095A
Other languages
Japanese (ja)
Inventor
Takehiro Nakamura
雄大 中村
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.)
Lincstech Circuit Co Ltd
Original Assignee
Hitachi AIC Inc
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 Hitachi AIC Inc filed Critical Hitachi AIC Inc
Priority to JP24679095A priority Critical patent/JPH0969471A/en
Publication of JPH0969471A publication Critical patent/JPH0969471A/en
Pending legal-status Critical Current

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  • Fixed Capacitors And Capacitor Manufacturing Machines (AREA)

Abstract

PROBLEM TO BE SOLVED: To obtain an electrolytic solution which can be kept high in long-term properties of absorbing hydrogen gas generated in an electrolytic capacitor case by a method wherein a specific % by weight of 3-nitropyrimidine is dissolved into the electrolytic solution. SOLUTION: Ethylene glycol is used as polyvalent alcohol solvent. Ammonium boride, ammonium butyl octanodiate, ammonium sebacate, ammonium suberate, ammonium azelate, ammonium benzonate or ammonium adipdiate is used as solute. 0.01 to 2.0% by weight of 3-nitropyrimidine is dissolved into the solution composed of these solvent and solute. Hydrogen gas generated in an electrolytic capacitor is reduced to 13 to 30% of that generated in a conventional one, so that the capacitor can be prolonged in service life.

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用電解液
に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an electrolytic solution for electrolytic capacitors.

【0002】[0002]

【従来の技術】通信機器や計測機器などの高性能化に伴
い、これ等の機器に組み込む電解コンデンサは、電気特
性や寿命をより一層向上することが必要となってきた。
この電解コンデンサは、中高圧用であり、例えば、アル
ミケース等に、電解液を含浸したコンデンサ素子を収納
し、蓋を取り付けて密閉した構造になっている。そして
電解液は、例えばエチレングリコールなどの多価アルコ
ールを主溶媒とし、カルボン酸のアンモニウム塩を主溶
質として溶解した組成になっている。
2. Description of the Related Art As the performance of communication equipment and measuring equipment has improved, it has become necessary to further improve the electrical characteristics and life of electrolytic capacitors incorporated in such equipment.
This electrolytic capacitor is for medium and high voltage, and for example, has a structure in which a capacitor element impregnated with an electrolytic solution is housed in an aluminum case or the like, and a lid is attached and sealed. The electrolytic solution has a composition in which a polyhydric alcohol such as ethylene glycol is used as a main solvent and an ammonium salt of carboxylic acid is dissolved as a main solute.

【0003】ところで、この電解液は、電極箔と反応し
て水素ガスが発生する。そして水素ガスが発生すると、
ケース内部の圧力が上昇する。この内圧が所定値に達成
すると、蓋等に設けた防爆弁が作動する。これにより電
解コンデンサは不良品となる。従来、水素ガスの発生を
抑制して、上記のような防爆弁の作動を遅らせ、電解コ
ンデンサの寿命を改善する目的で、電解液に芳香族ニト
ロ化合物を溶解している。
By the way, this electrolytic solution reacts with the electrode foil to generate hydrogen gas. And when hydrogen gas is generated,
The pressure inside the case rises. When this internal pressure reaches a predetermined value, the explosion-proof valve provided on the lid or the like operates. As a result, the electrolytic capacitor becomes defective. Conventionally, an aromatic nitro compound is dissolved in an electrolytic solution for the purpose of suppressing the generation of hydrogen gas, delaying the operation of the above explosion-proof valve, and improving the life of the electrolytic capacitor.

【0004】[0004]

【発明が解決しようとする課題】しかし、芳香族ニトロ
化合物を溶解した電解液は、溶解量が多いと火花発生電
圧が低下し易い欠点がある。そのため、通常、芳香族ニ
トロ化合物の溶解量を少なくして用いているが、長時間
にわたって水素ガスを吸収する作用を持続できず、電解
コンデンサの寿命を改善する効果が低い欠点がある。
However, the electrolytic solution in which the aromatic nitro compound is dissolved has a drawback that the spark generation voltage is likely to be lowered when the dissolved amount is large. Therefore, although the amount of the aromatic nitro compound dissolved is usually reduced, it has a drawback that the action of absorbing hydrogen gas cannot be continued for a long time and the effect of improving the life of the electrolytic capacitor is low.

【0005】本発明の目的は、以上の欠点を改良し、発
生した水素ガスを長時間吸収でき、電解コンデンサの寿
命を改良できる電解コンデンサ用電解液を提供するもの
である。
An object of the present invention is to provide an electrolytic solution for an electrolytic capacitor, which is capable of absorbing the generated hydrogen gas for a long period of time and improving the life of the electrolytic capacitor by improving the above drawbacks.

【0006】[0006]

【課題を解決するための手段】本発明は、上記の目的を
達成するために、多価アルコール類を主溶媒とする電解
コンデンサ用電解液において、3−ニトロピリミジンを
0.01〜2.0wt%溶解することを特徴とする電解コ
ンデンサ用電解液を提供するものである。
[Means for Solving the Problems] In order to achieve the above-mentioned object, the present invention uses 0.01 to 2.0 wt% of 3-nitropyrimidine in an electrolytic solution for electrolytic capacitors containing polyhydric alcohols as a main solvent. % Electrolytic solution for electrolytic capacitors.

【0007】多価アルコールは、エチレングリコールや
ジエチレングリコール、プロピレングリコール、1,4
−ブタンジオール等を用いる。
Polyhydric alcohols include ethylene glycol, diethylene glycol, propylene glycol, 1,4
-Use butanediol or the like.

【0008】なお、3−ニトロピリミジンの溶解量は、
0.01wt%より少ないと水素ガスの発生を抑制する効
果が低く、2.0wt%より多くなると火花発生電圧が低
下し、電解コンデンサの耐電圧が低くなる。従って、3
−ニトロピリミジンの溶解量は0.01〜2.0wt%の
範囲が良い。
The amount of 3-nitropyrimidine dissolved is
If it is less than 0.01 wt%, the effect of suppressing the generation of hydrogen gas is low, and if it is more than 2.0 wt%, the spark generation voltage is lowered and the withstand voltage of the electrolytic capacitor is lowered. Therefore, 3
The amount of nitropyrimidine dissolved is preferably in the range of 0.01 to 2.0 wt%.

【0009】[0009]

【作用】電解液中の3−ニトロピリミジンは、電解コン
デンサのケース内に発生するガスのうち大部分をしめる
水素ガスを吸収する。そのため、電解コンデンサの内圧
が上昇するのを防止できる。
The 3-nitropyrimidine in the electrolytic solution absorbs hydrogen gas, which is the majority of the gas generated in the case of the electrolytic capacitor. Therefore, it is possible to prevent the internal pressure of the electrolytic capacitor from rising.

【0010】[0010]

【実施例】以下、本発明を実施例に基づいて説明する。
多価アルコールは、エチレングリコールを用い、これを
溶媒とする。また、溶質は、ホウ酸アンモニウムやブチ
ルオクタン二酸アンモニウム、セバシン酸アンモニウ
ム、スベリン酸アンモニウム、アゼライン酸アンモニウ
ム、安息香酸アンモニウム、アジピン酸二アンモニウム
を用いる。そしてこれらの溶媒及び溶質からなる溶液に
化1の構造式からなる3−ニトロピリミジンを溶解す
る。
EXAMPLES The present invention will be described below based on examples.
Ethylene glycol is used as the polyhydric alcohol, and this is used as the solvent. As the solute, ammonium borate, ammonium butyloctanedioate, ammonium sebacate, ammonium suberate, ammonium azelate, ammonium benzoate, and diammonium adipate are used. Then, 3-nitropyrimidine having the structural formula of Chemical formula 1 is dissolved in a solution containing these solvents and solutes.

【0011】[0011]

【化1】 Embedded image

【0012】次に、表1及び表2に示す組成の実施例、
従来例及び比較例の電解液について、温度30℃での比
抵抗及び温度85℃での火花発生電圧を測定した。
Next, examples of the compositions shown in Tables 1 and 2,
With respect to the electrolytic solutions of the conventional example and the comparative example, the specific resistance at a temperature of 30 ° C. and the spark generation voltage at a temperature of 85 ° C. were measured.

【0013】[0013]

【表1】 [Table 1]

【0014】[0014]

【表2】 [Table 2]

【0015】なお、従来例1〜従来例4に溶解したm−
ニトロ安息香酸やP−ニトロトルエン、O−ニトロフェ
ノールの構造式は〔化2〕〜〔化4〕の通りになる。
Incidentally, m-dissolved in Conventional Example 1 to Conventional Example 4
The structural formulas of nitrobenzoic acid, P-nitrotoluene, and O-nitrophenol are as shown in [Chemical formula 2] to [Chemical formula 4].

【0016】[0016]

【化2】 Embedded image

【0017】[0017]

【化3】 Embedded image

【0018】[0018]

【化4】 Embedded image

【0019】表1から明らかな通り、実施例1〜実施例
10は、比抵抗が350〜1000Ω・cm、火花発生電
圧が350〜440Vとなる。また、従来例1〜従来例
4は、比抵抗が350〜1000Ω・cm、火花発生電圧
が340〜430Vとなる。すなわち、実施例1〜実施
例10は、従来例1〜従来例4に比較して比抵抗は同一
であるが、火花発生電圧は高くなっている。なお、3−
ニトロビリミジンの溶解量を5.0wt%とした比較例2
は、火花発生電圧が280Vとなり実施例1〜実施例1
0に比較して4/5以下の大きさになっている。
As is apparent from Table 1, in Examples 1 to 10, the specific resistance was 350 to 1000 Ω · cm and the spark generation voltage was 350 to 440V. Further, in Conventional Example 1 to Conventional Example 4, the specific resistance is 350 to 1000 Ω · cm and the spark generation voltage is 340 to 430V. That is, in Examples 1 to 10, the specific resistance was the same as in Conventional Example 1 to Conventional Example 4, but the spark generation voltage was higher. In addition, 3-
Comparative Example 2 in which the amount of nitropyrimidine dissolved was 5.0 wt%
Has a spark generation voltage of 280 V, and the example 1 to example 1
The size is 4/5 or less compared to 0.

【0020】また、表1及び表2に示した組成の各電解
液を含浸した、定格400V、330μF、ケースサイ
ズφ30×45のアルミ電解コンデンサについて、ケー
ス内のガス発生量を測定した。測定方法は、実施例1〜
実施例4、従来例1並びに比較例1及び比較例2につい
ては温度85℃のそしてその他の実施例5〜実施例10
及び従来例2〜従来例4については温度105℃の各雰
囲気中に、定格電圧400Vを印加して、2000hr
放置した後のガス発生量を測定して行なう。試料数は各
々10個づつとする。そして測定量は平均値とする。
Further, the amount of gas generated in the case was measured for aluminum electrolytic capacitors having a rating of 400 V, 330 μF and a case size of φ30 × 45, which were impregnated with the electrolytic solutions having the compositions shown in Tables 1 and 2. The measurement method is from Example 1
For Example 4, Conventional Example 1 and Comparative Examples 1 and 2, the temperature was 85 ° C. and other Examples 5 to 10 were used.
For Conventional Example 2 to Conventional Example 4, a rated voltage of 400 V was applied to each atmosphere at a temperature of 105 ° C. for 2000 hours.
The amount of gas generated after standing is measured. The number of samples shall be 10 each. The measured amount is an average value.

【0021】表1及び表2から明らかな通り、ガス発生
量は、実施例1〜実施例10を含浸した電解コンデンサ
が1.3〜1.5ml、従来例1〜従来例4を含浸した電
解コンデンサが5.0〜10.0mlそして比較例1〜比
較例2を含浸した電解コンデンサが1.4〜18.0ml
となる。すなわち、実施例1〜実施例10は従来例1〜
従来例4に比較してガス発生が13〜30%の量になっ
ている。なお、比較例1は3−ニトロピリミジンの溶解
量を0.005wt%とした電解液であるが、この電解液
を用いた電解コンデンサのガス発生量は18.0mlとな
り、実施例1〜実施例10に比較して12倍になってい
る。
As is clear from Tables 1 and 2, the amount of gas generated was 1.3 to 1.5 ml for the electrolytic capacitors impregnated with Examples 1 to 10 and the electrolytic amount impregnated with Conventional Examples 1 to 4 was used. The capacitor is 5.0-10.0 ml and the electrolytic capacitor impregnated with Comparative Example 1-Comparative Example 2 is 1.4-18.0 ml.
Becomes That is, Examples 1 to 10 are conventional examples 1 to
The amount of gas generation is 13 to 30% as compared with Conventional Example 4. Comparative Example 1 is an electrolytic solution in which the amount of 3-nitropyrimidine dissolved is 0.005 wt%, but the amount of gas generated by an electrolytic capacitor using this electrolytic solution is 18.0 ml. It is 12 times that of 10.

【0022】[0022]

【発明の効果】以上の通り、本発明によれば、3−ニト
ロピリミジンを0.01〜2.0wt%溶解しているた
め、発生した水素ガスを長時間吸収でき、電解コンデン
サの寿命を改善できる電解コンデンサ用電解液が得られ
る。
As described above, according to the present invention, since 3-nitropyrimidine is dissolved in 0.01 to 2.0 wt%, the generated hydrogen gas can be absorbed for a long time and the life of the electrolytic capacitor is improved. An electrolytic solution for an electrolytic capacitor can be obtained.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 多価アルコール類を主溶媒とする電解コ
ンデンサ用電解液において、3−ニトロピリミジンを
0.01〜2.0wt%溶解することを特徴とする電解コ
ンデンサ用電解液。
1. An electrolytic solution for an electrolytic capacitor, wherein 0.01 to 2.0 wt% of 3-nitropyrimidine is dissolved in the electrolytic solution containing a polyhydric alcohol as a main solvent.
JP24679095A 1995-08-31 1995-08-31 Capacitor electrolyte for electrolytic solution Pending JPH0969471A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP24679095A JPH0969471A (en) 1995-08-31 1995-08-31 Capacitor electrolyte for electrolytic solution

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP24679095A JPH0969471A (en) 1995-08-31 1995-08-31 Capacitor electrolyte for electrolytic solution

Publications (1)

Publication Number Publication Date
JPH0969471A true JPH0969471A (en) 1997-03-11

Family

ID=17153717

Family Applications (1)

Application Number Title Priority Date Filing Date
JP24679095A Pending JPH0969471A (en) 1995-08-31 1995-08-31 Capacitor electrolyte for electrolytic solution

Country Status (1)

Country Link
JP (1) JPH0969471A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20020091964A (en) * 2001-06-01 2002-12-11 삼성전기주식회사 Electrolyte for intermediate voltage aluminium electrolysis condenser and aluminium electrolysis condenser having the electrolyte

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20020091964A (en) * 2001-06-01 2002-12-11 삼성전기주식회사 Electrolyte for intermediate voltage aluminium electrolysis condenser and aluminium electrolysis condenser having the electrolyte

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