JPH06290996A - Electrolyte for electrolytic capacitor - Google Patents
Electrolyte for electrolytic capacitorInfo
- Publication number
- JPH06290996A JPH06290996A JP9724093A JP9724093A JPH06290996A JP H06290996 A JPH06290996 A JP H06290996A JP 9724093 A JP9724093 A JP 9724093A JP 9724093 A JP9724093 A JP 9724093A JP H06290996 A JPH06290996 A JP H06290996A
- Authority
- JP
- Japan
- Prior art keywords
- salt
- acid
- driving
- electrolytic capacitor
- electrolytic
- 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
Links
Landscapes
- Electric Double-Layer Capacitors Or The Like (AREA)
Abstract
Description
【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、特に中高圧用電解コンデンサの
特性改善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 improving the characteristics of a medium- and high-voltage electrolytic capacitor.
【0002】[0002]
【従来の技術】一般に、電解コンデンサの駆動用電解液
において、特に中高圧用として、エチレングリコールを
溶媒とし、ホウ酸又はホウ酸アンモニウムを溶質とした
ものが用いられていた。しかし、この種の駆動用電解液
は、エチレングリコールとホウ酸の間で起こるエステル
化反応によって生ずる水分のため、100℃を超える電
解コンデンサに使用すると、駆動用電解液中の水分が水
蒸気となり、電解コンデンサのパッケージ内圧が上昇
し、これを破壊させてしまうという問題があった。2. Description of the Related Art Generally, an electrolytic solution for driving an electrolytic capacitor has been used for medium and high pressure, in which ethylene glycol is used as a solvent and boric acid or ammonium borate is a solute. However, since this kind of driving electrolyte is water generated by the esterification reaction between ethylene glycol and boric acid, when used in an electrolytic capacitor having a temperature above 100 ° C, the water in the driving electrolyte becomes water vapor, There is a problem in that the package internal pressure of the electrolytic capacitor rises and destroys it.
【0003】そのため、このような問題を解決するため
にエチレングリコールにアゼライン酸又はオクタンジカ
ルボン酸又はブチルオクタン二酸などの有機カルボン酸
の塩を用いることも試みられている。Therefore, in order to solve such a problem, it has been attempted to use a salt of an organic carboxylic acid such as azelaic acid, octanedicarboxylic acid or butyloctanedioic acid for ethylene glycol.
【0004】しかしながら、これらの塩を用いた駆動用
電解液ではエステル化による水分の発生は抑制できるも
のの、溶解度が低いために低い比抵抗が得られず、化成
性も悪いと言う欠点を有していた。However, although the generation of water due to esterification can be suppressed in the driving electrolytic solution using these salts, it has a drawback that low specific resistance cannot be obtained due to its low solubility and the chemical conversion is poor. Was there.
【0005】また、溶解度を上げるために、有機カルボ
ン酸の側鎖にアルキル基を有する溶質も考案されている
が、比抵抗は下がるものの、火花発生電圧も下がってし
まい、中高圧用としては問題があった。Further, solutes having an alkyl group in the side chain of an organic carboxylic acid have been devised in order to increase the solubility, but although the specific resistance is lowered, the spark generation voltage is also lowered, which is a problem for medium and high pressure applications. was there.
【0006】[0006]
【発明が解決しようとする課題】以上述べたように、エ
チレングリコールにホウ酸やホウ酸アンモニウムを溶質
として用いた駆動用電解液では、100℃を超える高温
での化学的安定性に問題があり、また、アゼライン酸,
オクタンジカルボン酸又はブチルオクタン二酸などの有
機カルボン酸の塩又は側鎖に有機カルボン酸の塩を用い
た駆動用電解液では、化成性が悪く、高温における火花
電圧が十分でないという欠点を有し、実用上解決すべき
課題をもつものであった。As described above, the driving electrolyte using boric acid or ammonium borate as a solute in ethylene glycol has a problem in chemical stability at a high temperature exceeding 100 ° C. , Azelaic acid,
A driving electrolyte solution using a salt of an organic carboxylic acid such as octanedicarboxylic acid or butyloctanedioic acid or a salt of an organic carboxylic acid in the side chain has poor chemical conversion and has a drawback that the spark voltage at high temperature is not sufficient. , Had a problem to be solved practically.
【0007】本発明は、上記の問題を解決するために成
されたものであり、高温時における電解コンデンサの内
圧上昇を抑制し、且つ、比抵抗を上げることなく、火花
発生電圧を高め、且つ、化成性も向上させた中高圧用に
適した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 has been made to solve the above problems, suppresses an increase in the internal pressure of an electrolytic capacitor at high temperatures, and increases the spark generation voltage without increasing the specific resistance, and It is an object of the present invention to provide an electrolytic solution for driving an electrolytic capacitor, which is suitable for medium and high voltage and has improved chemical conversion.
【0008】[0008]
【課題を解決するための手段】本発明による電解コンデ
ンサ駆動用電解液は、エチレングリコールを主体とした
溶媒に、オクタンジカルボン酸又は側鎖にアルキル基を
有するオクタンジカルボン酸の塩を溶質として溶解し、
且つ、無水ケイ酸とニトロ化合物を添加することを特徴
とするものである。The electrolytic solution for driving an electrolytic capacitor according to the present invention is prepared by dissolving octanedicarboxylic acid or a salt of octanedicarboxylic acid having an alkyl group in its side chain as a solute in a solvent mainly composed of ethylene glycol. ,
Moreover, it is characterized in that silicic acid anhydride and a nitro compound are added.
【0009】また、塩がアンモニウム塩又は二級アミン
塩又は三級アミン塩又は四級アンモニウム塩であること
を特徴とするものである。The salt is characterized in that it is an ammonium salt, a secondary amine salt, a tertiary amine salt or a quaternary ammonium salt.
【0010】また、側鎖のアルキル基がメチル基又はエ
チル基であることを特徴とするものである。Further, the side chain alkyl group is a methyl group or an ethyl group.
【0011】また、ニトロ化合物がパラニトロフェノー
ル又はパラニトロ安息香酸であることを特徴とするもの
である。The nitro compound is para-nitrophenol or para-nitrobenzoic acid.
【0012】[0012]
【作用】以上のように構成された電解コンデンサ駆動用
電解液によれば、オクタンジカルボン酸の側鎖にアルキ
ル基をつけることにより、溶解度を上げ、無水ケイ酸と
ニトロ化合物の存在によって比抵抗を上げることなく、
火花電圧の上昇,化成性の向上化,水素ガス発生の抑制
に大きく作用する。According to the electrolytic capacitor driving electrolytic solution configured as described above, the solubility is increased by adding an alkyl group to the side chain of octanedicarboxylic acid, and the specific resistance is increased by the presence of silicic acid anhydride and a nitro compound. Without raising
It greatly increases the spark voltage, improves the chemical conversion, and suppresses the generation of hydrogen gas.
【0013】[0013]
【実施例】以下、本発明の実施例について説明する。す
なわち、本発明になる駆動用電解液は、エチレングリコ
ールを主体とした溶媒に、オクタンジカルボン酸又は側
鎖にアルキル基を有するオクタンジカルボン酸の塩を溶
質とし、且つ、無水ケイ酸とニトロ化合物を添加してな
るものであり、側鎖にアルキル基を有するオクタンジカ
ルボン酸としては、1−メチル−1,8−オクタンジカ
ルボン酸、1−エチル−1,8−オクタンジカルボン
酸、2−メチル−1,8−オクタンジカルボン酸、2−
エチル−1,8−オクタンジカルボン酸、3−メチル−
1,8−オクタンジカルボン酸、3−エチル−1,8−
オクタンジカルボン酸、4−メチル−1,8−オクタン
ジカルボン酸、4−エチル−1,8−オクタンジカルボ
ン酸であり、この場合、側鎖のアルキル基がエチル基以
上のプロピル基,ブチル基になると溶解度が低下するた
め、側鎖はメチル基,エチル基が望ましい。EXAMPLES Examples of the present invention will be described below. That is, the driving electrolytic solution according to the present invention, in a solvent mainly composed of ethylene glycol, octanedicarboxylic acid or a salt of octanedicarboxylic acid having an alkyl group in the side chain as a solute, and silicic anhydride and a nitro compound. The octanedicarboxylic acid having an alkyl group in the side chain is 1-methyl-1,8-octanedicarboxylic acid, 1-ethyl-1,8-octanedicarboxylic acid, 2-methyl-1. , 8-octanedicarboxylic acid, 2-
Ethyl-1,8-octanedicarboxylic acid, 3-methyl-
1,8-octanedicarboxylic acid, 3-ethyl-1,8-
Octanedicarboxylic acid, 4-methyl-1,8-octanedicarboxylic acid, and 4-ethyl-1,8-octanedicarboxylic acid. In this case, when the side chain alkyl group becomes a propyl group or a butyl group which is an ethyl group or more, The side chain is preferably a methyl group or an ethyl group because the solubility decreases.
【0014】また、上記した塩としてはアンモニウム
塩,二級アミン塩,三級アミン塩と四級アンモニウム塩
があり、二級アミン塩の具体例としては、ジメチルアミ
ン塩,ジエチルアミン塩などが挙げられ、三級アミン塩
の具体例としてはトリメチルアミン塩,トリエチルアミ
ン塩などが挙げられ、四級アンモニウム塩の具体例とし
ては、テトラメチルアンモニウム塩,テトラエチルアン
モニウム塩などが挙げられる。無水ケイ酸は火花電圧の
上昇及び化成性の向上に用いられ、濃度としては0.1
〜10重量%が望ましい。ニトロ化合物はパラニトロフ
ェノール又はパラニトロ安息香酸であり、水素を酸化し
てガス発生を抑制するために用いられ、0.1〜5重量
%が望ましい。The above-mentioned salts include ammonium salts, secondary amine salts, tertiary amine salts and quaternary ammonium salts, and specific examples of the secondary amine salts include dimethylamine salt and diethylamine salt. Specific examples of the tertiary amine salt include trimethylamine salt and triethylamine salt, and specific examples of the quaternary ammonium salt include tetramethylammonium salt and tetraethylammonium salt. Silicic anhydride is used to increase the spark voltage and improve the chemical conversion, and its concentration is 0.1
10% by weight is desirable. The nitro compound is para-nitrophenol or para-nitrobenzoic acid, which is used to oxidize hydrogen and suppress gas generation, and preferably 0.1 to 5% by weight.
【0015】以上のように構成してなる駆動用電解液に
よれば、溶質としてオクタンジカルボン酸又は側鎖にア
ルキル基を有するオクタンジカルボン酸の塩をつけるこ
とにより溶質としての溶解度を上げ、添加する無水ケイ
酸とニトロ化合物の存在によって、比抵抗を上げること
なく火花発生電圧の上昇、化成性の向上化、水素ガス発
生の抑制に大きく貢献し、これらの駆動用電解液を用い
た電解コンデンサは、中高圧用に適すると同時に、高温
時における電解コンデンサの内圧上昇を抑制できる優れ
た効果を有する。According to the driving electrolyte solution constructed as described above, the solubility as a solute is increased by adding octanedicarboxylic acid or a salt of octanedicarboxylic acid having an alkyl group in the side chain as a solute. The presence of silicic acid anhydride and nitro compounds greatly contributes to the increase of spark generation voltage, the improvement of chemical conversion, and the suppression of hydrogen gas generation without increasing the specific resistance, and electrolytic capacitors using these driving electrolytes Also, it has an excellent effect that it is suitable for medium and high voltage and at the same time, it can suppress an increase in internal pressure of the electrolytic capacitor at high temperature.
【0016】以下、具体的な実施例に基づき、本発明と
従来例との特性比較について述べる。まず、表1に本発
明に係る駆動用電解液の実施例1〜9と従来技術に係る
駆動用電解液の従来例1〜3の組成構成と、それぞれの
25℃の比抵抗と火花発生電圧を示す。The characteristic comparison between the present invention and the conventional example will be described below based on specific examples. First, Table 1 shows the composition configurations of Examples 1 to 9 of the driving electrolyte solution according to the present invention and Conventional Examples 1 to 3 of the driving electrolyte solution according to the related art, the specific resistance at 25 ° C., and the spark generation voltage. Indicates.
【0017】表1から明らかなように、従来例1〜2の
ものは火花発生電圧が低く、また、従来例3のものは比
抵抗は下がるものの火花発生電圧も低くなるのに対し
て、実施例のもは、比抵抗を上昇させることなく高い火
花発生電圧を得ることができることがわかる。As is apparent from Table 1, the spark generation voltage of the conventional examples 1 and 2 is low, and the spark generation voltage of the conventional example 3 is low, but the spark generation voltage is low. In the example, it can be seen that a high spark generation voltage can be obtained without increasing the specific resistance.
【0018】次に、表1に示した従来例1〜3と、実施
例1〜9の駆動用電解液を使用して製作したアルミニウ
ム電解コンデンサの初期値と高温負荷試験(105℃
1000時間)後の特性を比較した結果、表2,表3に
示す通りであった。Next, the initial values and high temperature load test (105 ° C.) of aluminum electrolytic capacitors manufactured using the conventional electrolytic solutions 1 to 3 shown in Table 1 and the driving electrolytic solutions of Examples 1 to 9 were performed.
As a result of comparing the characteristics after 1000 hours, the results are shown in Tables 2 and 3.
【0019】なお、定格は実施例及び従来例とも400
V−150μFである。The rating is 400 in both the embodiment and the conventional example.
V-150 μF.
【0020】[0020]
【表1】 [Table 1]
【0021】 [0021]
【0022】 [0022]
【0023】[0023]
【表2】 [Table 2]
【0024】[0024]
【表3】 [Table 3]
【0025】表2,表3から明らかなように、本発明の
駆動用電解液を用いた実施例1〜9のものは、従来の駆
動用電解液を用いた従来例1〜2と比較して、初期段階
での特性差はさほどないが、高温負荷試験後において
は、静電容量変化率、tanδ変化、漏れ電流変化が大
幅に少なく、且つ、従来例1〜2のものが弁ふくれとな
ったのに対して、実施例のもの全て弁ふくれ現象は皆無
で、本発明の顕著な効果を実証した。As is clear from Tables 2 and 3, Examples 1 to 9 using the driving electrolytic solution of the present invention are compared with Conventional Examples 1 to 2 using the conventional driving electrolytic solution. Although there is not much characteristic difference in the initial stage, after the high temperature load test, the capacitance change rate, tan δ change, and leakage current change are significantly small, and the conventional examples 1 and 2 are bulged. On the other hand, in all the examples, there was no blistering phenomenon, demonstrating the remarkable effect of the present invention.
【0026】なお、従来例3のものはエージング中防爆
弁が動作し実用上問題であることかわかった。It was found that the conventional example 3 has a practical problem because the explosion-proof valve operates during aging.
【0027】[0027]
【発明の効果】以上述べたように、本発明の電解コンデ
ンサ駆動用電解液は、無水ケイ酸の存在で比抵抗を上昇
させることなく、火花電圧を上昇させることができ、且
つ、ニトロ化合物を添加しているため、高温でのガス発
生が抑制され、高温で長寿命の電解コンデンサを得るこ
とができる。As described above, the electrolytic solution for driving an electrolytic capacitor of the present invention can increase the spark voltage without increasing the specific resistance in the presence of silicic acid anhydride, and can increase the nitro compound content. Since it is added, gas generation at high temperature is suppressed, and an electrolytic capacitor having a long life at high temperature can be obtained.
Claims (4)
に、オクタンジカルボン酸又は側鎖にアルキル基を有す
るオクタンジカルボン酸の塩を溶質として溶解し、且
つ、無水ケイ酸とニトロ化合物を添加することを特徴と
する電解コンデンサ駆動用電解液。1. A solvent comprising mainly ethylene glycol, wherein octanedicarboxylic acid or a salt of octanedicarboxylic acid having an alkyl group in a side chain is dissolved as a solute, and silicic anhydride and a nitro compound are added. An electrolytic solution for driving electrolytic capacitors.
は三級アミン塩又は四級アンモニウム塩であることを特
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 salt is an ammonium salt, a secondary amine salt, a tertiary amine salt or a quaternary ammonium salt.
基であ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。3. The electrolytic solution for driving an electrolytic capacitor according to claim 1, wherein the alkyl group of the side chain is a methyl group or an ethyl group.
はパラニトロ安息香酸であ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。4. The nitro compound is para-nitrophenol or para-nitrobenzoic acid.
The electrolytic solution for driving the electrolytic capacitor described.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9724093A JPH06290996A (en) | 1993-03-30 | 1993-03-30 | Electrolyte for electrolytic capacitor |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9724093A JPH06290996A (en) | 1993-03-30 | 1993-03-30 | Electrolyte for electrolytic capacitor |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH06290996A true JPH06290996A (en) | 1994-10-18 |
Family
ID=14187094
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9724093A Pending JPH06290996A (en) | 1993-03-30 | 1993-03-30 | Electrolyte for electrolytic capacitor |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH06290996A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20030087326A (en) * | 2002-05-08 | 2003-11-14 | 삼화전기주식회사 | An Electrolyte Having Low Resistance for Aluminium Electrolysis Condenser |
-
1993
- 1993-03-30 JP JP9724093A patent/JPH06290996A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20030087326A (en) * | 2002-05-08 | 2003-11-14 | 삼화전기주식회사 | An Electrolyte Having Low Resistance for Aluminium Electrolysis Condenser |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPH06290996A (en) | Electrolyte for electrolytic capacitor | |
JPH06290997A (en) | Electrolyte for electrolytic capacitor | |
JP3749913B2 (en) | Electrolytic solution for electrolytic capacitor drive | |
JPH07249547A (en) | Driving electrolyte of electrolytic capacitor | |
JP4570804B2 (en) | Electrolytic capacitor drive electrolyte | |
JP2624710B2 (en) | Electrolytic capacitor | |
JP3075789B2 (en) | Electrolyte for electrolytic capacitors | |
JPH0351285B2 (en) | ||
JP3612671B2 (en) | Electrolytic solution for electrolytic capacitor drive | |
JPH09251933A (en) | Electrolyte soln. for driving electrolytic capacitor | |
JPH05152163A (en) | Driving electrolyte for electrolytic capacitor | |
JP3212322B2 (en) | Electrolyte for driving electrolytic capacitors | |
JPH05144673A (en) | Electrolytic solution for electrolytic capacitor | |
JP3376750B2 (en) | Electrolyte for driving electrolytic capacitors | |
JPH0371616A (en) | Electrolyte for driving electrolytic capacitor | |
JPH05315194A (en) | Electrolyte for driving electrolytic capacitor | |
JPH05315195A (en) | Electrolyte for driving electrolytic capacitor | |
JPH07120615B2 (en) | Electrolytic solution for driving electrolytic capacitors | |
JPH07249546A (en) | Driving electrolyte of electrolytic capacitor | |
JPH07335497A (en) | Electrolyte for driving electrolytic capacitor | |
JPH01293609A (en) | Electrolytic solution for driving electrolytic capacitor | |
JPH0969471A (en) | Capacitor electrolyte for electrolytic solution | |
JP2004186188A (en) | Electrolyte for driving electrolytic capacitor | |
JP2003068585A (en) | Electrolyte for driving electrolytic capacitor | |
JPS6054768B2 (en) | Electrolyte for electrolytic capacitors |