JPH0590079A - Electrolytic capacitor driving electrolyte - Google Patents
Electrolytic capacitor driving electrolyteInfo
- Publication number
- JPH0590079A JPH0590079A JP3276962A JP27696291A JPH0590079A JP H0590079 A JPH0590079 A JP H0590079A JP 3276962 A JP3276962 A JP 3276962A JP 27696291 A JP27696291 A JP 27696291A JP H0590079 A JPH0590079 A JP H0590079A
- Authority
- JP
- Japan
- Prior art keywords
- electrolytic capacitor
- benzene
- salt
- tetraalkylammonium
- electrolyte
- 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 electrolytic solution).
【0002】[0002]
【従来の技術】従来より低圧用電解コンデンサの電解液
としては、エチレングリコールを主溶媒として、アジピ
ン酸塩を溶解した電解液が多用されていたが、近年、電
解コンデンサの低インピーダンス化、高信頼化への対応
に伴い、γ−ブチロラクトンを主溶媒として、フタル酸
あるいはマレイン酸のテトラアルキルアンモニウム塩を
溶解した電解液が一般的に使用されている。2. Description of the Related Art Conventionally, as an electrolytic solution for a low-voltage electrolytic capacitor, an electrolytic solution containing ethylene glycol as a main solvent and adipate dissolved therein has been widely used. Along with the adaptation to the change, an electrolytic solution in which γ-butyrolactone is used as a main solvent and a tetraalkylammonium salt of phthalic acid or maleic acid is dissolved is generally used.
【0003】[0003]
【発明が解決しようとする課題】電解コンデンサの電解
液として、γ−ブチロラクトンへフタル酸のテトラメチ
ルアンモニウム塩を溶解したものは、高温雰囲気中にお
ける信頼性が非常に高いものの、溶解度の限界より比抵
抗値としては80Ω・cmが限度であった。一方、マレイン
酸のテトラエチルアンモニウム塩を溶解したものは、比
抵抗値としては70Ω・cmが可能な反面、マレイン酸の転
位、脱水などにより、高温雰囲気中における信頼性が非
常に低いという欠点を有していた。The electrolytic solution of the electrolytic capacitor in which tetramethylammonium salt of phthalic acid is dissolved in γ-butyrolactone is very reliable in a high temperature atmosphere, but its ratio is lower than the solubility limit. The resistance value was limited to 80 Ω · cm. On the other hand, the one obtained by dissolving the tetraethylammonium salt of maleic acid has a specific resistance value of 70 Ω · cm, but on the other hand, it has a drawback that the reliability is extremely low in a high temperature atmosphere due to maleic acid rearrangement and dehydration. Was.
【0004】[0004]
【発明が解決しようとする課題】本発明は上述の問題点
を解決するもので、低比抵抗ながら高温雰囲気中におけ
る信頼性も確保するものである。SUMMARY OF THE INVENTION The present invention solves the above-mentioned problems and ensures reliability in a high temperature atmosphere while having a low specific resistance.
【0005】[0005]
【課題を解決するための手段】すなわち、γ−ブチロラ
クトンを主溶媒として、ベンゼン−1,2,4,5,−テトラカ
ルボン酸のテトラアルキルアンモニウム塩あるいはテト
ラアルキルホスホニウム塩を溶解したことを特徴とする
電解液である。That is, γ-butyrolactone is used as a main solvent, and tetraalkylammonium salt or tetraalkylphosphonium salt of benzene-1,2,4,5, -tetracarboxylic acid is dissolved. It is an electrolytic solution.
【0006】[0006]
【作用】本発明の電解液は、溶質の転位、脱水が起こり
にくいため、高温度雰囲気中での信頼性も十分に確保す
ることができ、かつ、4塩基酸のため電解液の低比抵抗
化が可能となる。In the electrolytic solution of the present invention, since solute rearrangement and dehydration do not easily occur, the reliability in a high temperature atmosphere can be sufficiently ensured, and since the tetrabasic acid has a low specific resistance. Can be realized.
【0007】[0007]
【実施例】以下、本発明の実施例について説明する。表
1は、溶質量25重量%の際の本発明の電解液と従来の電
解液の組成、比抵抗および火花発生電圧についての比較
例を示す。なお、表1中電解液試料記号A,B は従来例、
C,D は本発明例であり、また、γ−ブチロラクトンはGB
L と略した。EXAMPLES Examples of the present invention will be described below. Table 1 shows comparative examples of the composition, the specific resistance and the spark generation voltage of the electrolytic solution of the present invention and the conventional electrolytic solution when the dissolved mass is 25% by weight. In addition, the electrolyte sample symbols A and B in Table 1 are conventional examples,
C and D are examples of the present invention, and γ-butyrolactone is GB
Abbreviated as L.
【0008】[0008]
【表1】 [Table 1]
【0009】表1から明らかなように、本発明に係わる
試料記号C,D の電解液は従来の電解液に比べ、低比抵抗
化が可能である。表2は、表1に示す電解液を用いて試
作した定格 25 V 3300μFの電解コンデンサによる、
105 ℃ 2000 時間 高温負荷試験を行なった結果を示
す。As is apparent from Table 1, the electrolytic solutions of the sample symbols C and D according to the present invention can have a lower specific resistance than the conventional electrolytic solutions. Table 2 shows electrolytic capacitors with a rated voltage of 25 V and 3300 μF, which were prototyped using the electrolytic solution shown in Table 1.
The results of high temperature load test at 105 ℃ for 2000 hours are shown below.
【0010】[0010]
【表2】 [Table 2]
【0011】表2 から明らかなように、本発明に係わる
試料記号C,D の電解液を用いた電解コンデンサは、長時
間の高温雰囲気中における試験においても全ての特性に
問題がない。また、これら実施例以外にも4級塩のアル
キル基がプロピル基,ブチル基などで構成されたもの、
あるいは、各種アルキル基の混成によって構成されたも
のなどについても評価を行なったが、同様な結果が得ら
れた。なお、今回の実施例では示さなかったが、他の溶
質との混合も可能であるため、飽和濃度を越えない範囲
であれば配合量は任意であるが、混合溶媒100gに対しベ
ンゼン−1,2,4,5,−テトラカルボン酸のテトラアルキル
アンモニウム塩あるいはテトラアルキルホスホニウム塩
が5g未満では電解液の低比抵抗化が不可能であり、ま
た、30g を越えた場合は溶質の析出がみられる。As is clear from Table 2, all characteristics of the electrolytic capacitors using the electrolytic solutions of sample symbols C and D according to the present invention have no problem even in a test in a high temperature atmosphere for a long time. In addition to these examples, those in which the alkyl group of the quaternary salt is composed of a propyl group, a butyl group, or the like,
Alternatively, the evaluation was also performed on those composed of various alkyl groups, and similar results were obtained. Although not shown in this example, since it is possible to mix with other solutes, the blending amount is arbitrary as long as it does not exceed the saturation concentration, but benzene-1, 100 g of the mixed solvent, If the tetraalkylammonium salt or tetraalkylphosphonium salt of 2,4,5, -tetracarboxylic acid is less than 5 g, it is impossible to lower the specific resistance of the electrolytic solution, and if it exceeds 30 g, solute precipitation is observed. Be done.
【0012】[0012]
【発明の効果】以上のように、γ−ブチロラクトンを主
溶媒として、ベンゼン−1,2,4,5,−テトラカルボン酸の
テトラアルキルアンモニウム塩あるいはテトラアルキル
ホスホニウム塩を溶解したことを特徴とする電解液は、
低比抵抗ながら、高温雰囲気中においても高い信頼性を
有し、工業的かつ実用的価値の大なるものである。As described above, γ-butyrolactone is used as the main solvent, and the tetraalkylammonium salt or tetraalkylphosphonium salt of benzene-1,2,4,5, -tetracarboxylic acid is dissolved. The electrolyte is
It has low specific resistance and high reliability even in a high temperature atmosphere, and has great industrial and practical value.
Claims (2)
ンゼン−1,2,4,5,−テトラカルボン酸のテトラアルキル
アンモニウム塩あるいはテトラアルキルホスホニウム塩
を溶解したことを特徴とする電解コンデンサの駆動用電
解液。1. For driving an electrolytic capacitor, characterized in that a tetraalkylammonium salt or a tetraalkylphosphonium salt of benzene-1,2,4,5, -tetracarboxylic acid is dissolved using γ-butyrolactone as a main solvent. Electrolyte.
ン酸のテトラアルキルアンモニウム塩あるいはテトラア
ルキルホスホニウム塩は、混合溶媒100gに対し 5〜30g
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. The tetraalkylammonium salt or tetraalkylphosphonium salt of benzene-1,2,4,5, -tetracarboxylic acid is 5 to 30 g per 100 g of the mixed solvent.
The electrolytic solution for driving the electrolytic capacitor according to claim 1, which is present.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3276962A JPH0590079A (en) | 1991-09-26 | 1991-09-26 | Electrolytic capacitor driving electrolyte |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3276962A JPH0590079A (en) | 1991-09-26 | 1991-09-26 | Electrolytic capacitor driving electrolyte |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0590079A true JPH0590079A (en) | 1993-04-09 |
Family
ID=17576839
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3276962A Pending JPH0590079A (en) | 1991-09-26 | 1991-09-26 | Electrolytic capacitor driving electrolyte |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0590079A (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62272512A (en) * | 1986-05-20 | 1987-11-26 | 三菱化学株式会社 | Electrolyte for electrolytic capacitor |
JPS6369211A (en) * | 1986-09-11 | 1988-03-29 | 旭硝子株式会社 | Electrolytic capacitor |
-
1991
- 1991-09-26 JP JP3276962A patent/JPH0590079A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62272512A (en) * | 1986-05-20 | 1987-11-26 | 三菱化学株式会社 | Electrolyte for electrolytic capacitor |
JPS6369211A (en) * | 1986-09-11 | 1988-03-29 | 旭硝子株式会社 | Electrolytic capacitor |
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