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JP3310690B2 - Electrolytic solution for electrolytic capacitors - Google Patents
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JP3310690B2 - Electrolytic solution for electrolytic capacitors - Google Patents

Electrolytic solution for electrolytic capacitors

Info

Publication number
JP3310690B2
JP3310690B2 JP08491592A JP8491592A JP3310690B2 JP 3310690 B2 JP3310690 B2 JP 3310690B2 JP 08491592 A JP08491592 A JP 08491592A JP 8491592 A JP8491592 A JP 8491592A JP 3310690 B2 JP3310690 B2 JP 3310690B2
Authority
JP
Japan
Prior art keywords
electrolytic
electrolytic solution
solvent
butanediol
capacitors
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.)
Expired - Fee Related
Application number
JP08491592A
Other languages
Japanese (ja)
Other versions
JPH05251278A (en
Inventor
修三 本合
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 JP08491592A priority Critical patent/JP3310690B2/en
Publication of JPH05251278A publication Critical patent/JPH05251278A/en
Application granted granted Critical
Publication of JP3310690B2 publication Critical patent/JP3310690B2/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)

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 an electrolytic capacitor.

【0002】[0002]

【従来の技術】従来より電解コンデンサの電解液には、
エチレングリコ−ルおよび水を主体とした溶媒に、有機
酸あるいはその塩を溶解した電解液が多用されていた。
しかし、エチレングリコ−ルおよび水を主体とした溶媒
を使用した電解コンデンサは、溶媒の融点との関係で、
低温雰囲気におけるコンデンサとしての信頼性が低いた
め、γ−ブチロラクトンやN,N−ジメチルホルムアミ
ドが使用されるようになった。
2. Description of the Related Art Conventionally, electrolytic solutions for electrolytic capacitors include:
An electrolytic solution in which an organic acid or a salt thereof is dissolved in a solvent mainly composed of ethylene glycol and water has been frequently used.
However, an electrolytic capacitor using a solvent mainly composed of ethylene glycol and water has a problem in relation to the melting point of the solvent.
Because of low reliability as a capacitor in a low-temperature atmosphere, γ-butyrolactone and N, N-dimethylformamide have been used.

【0003】[0003]

【発明が解決しようとする課題】しかし、ジメチルホル
ムアミドは人体に及ぼす影響が大きいために好ましくな
く、γ−ブチロラクトンも高温雰囲気中における蒸気圧
が高いために、電解コンデンサは、外観膨張を発生しや
すいという問題を有していた。
However, dimethylformamide is not preferable because it has a large effect on the human body, and γ-butyrolactone also has a high vapor pressure in a high-temperature atmosphere. Had the problem that

【0004】[0004]

【課題を解決するための手段】これらの問題を解決する
には、使用する溶媒を高沸点かつ低凝固点のものにすれ
ば良い。すなわち、有機酸あるいはその塩を溶質とした
電解コンデンサの電解液において、1,3−ブタンジオ
ールを主体とした溶媒中へ有機酸あるいはその塩を溶解
したことを特徴とする電解液である。
In order to solve these problems, the solvent used should have a high boiling point and a low freezing point. That is, the electrolytic solution of an electrolytic capacitor using an organic acid or a salt thereof as a solute is obtained by dissolving an organic acid or a salt thereof in a solvent mainly containing 1,3-butanediol.

【0005】[0005]

【作用】本発明の電解液に使用した1,3−ブタンジオ
ールは、低凝固点であると同時に高沸点かつ低蒸気圧で
あるため、電解液の気化による外観異常が発生せず、ま
た、低温においても電解液の凝固が起こりにくいため、
低温特性が向上する。さらに人体に及ぼす影響も無視で
きる程度であることから、非常に扱いやすい。
The 1,3-butanediol used in the electrolytic solution of the present invention has a low freezing point, a high boiling point and a low vapor pressure, so that no abnormal appearance due to vaporization of the electrolytic solution occurs, The solidification of the electrolyte is unlikely to occur even in
Low temperature characteristics are improved. Furthermore, since the effect on the human body is negligible, it is very easy to handle.

【0006】[0006]

【実施例】以下、本発明の具体的実施例について説明す
る。表1は、各種溶媒の沸点および凝固点を示した。表
2は、本発明の電解液と従来の電解液を用いて試作し
た、定格250V,330μFのアルミニウム電解コン
デンサ用の電解液組成と、−40℃における定格容量に
対する容量保持率を示す。表3は、表2中に示したアル
ミニウム電解コンデンサの115℃における高温負荷試
験の結果を示した。なお、表中電解液試料記号A,B,
Cは従来例、E,Fは本発明例であり、また、エチレン
グリコ−ルはEG、γ−ブチロラクトンはGBL、N,
N−ジメチルホルムアミドはDMF、2−エチル−1,
3−ヘキサンジオールはEHD、1,3−ブタンジオー
ルはBDと各々記号で示す。
DESCRIPTION OF THE PREFERRED EMBODIMENTS Hereinafter, specific embodiments of the present invention will be described. Table 1 shows the boiling points and freezing points of the various solvents. Table 2 shows the composition of the electrolytic solution for an aluminum electrolytic capacitor rated at 250 V and 330 μF, which was produced using the electrolytic solution of the present invention and a conventional electrolytic solution, and the capacity retention ratio at -40 ° C. with respect to the rated capacity. Table 3 shows the results of the high-temperature load test at 115 ° C. of the aluminum electrolytic capacitors shown in Table 2. The electrolyte sample symbols A, B, and
C is a conventional example, E and F are examples of the present invention, and ethylene glycol is EG, γ-butyrolactone is GBL, N,
N-dimethylformamide is DMF, 2-ethyl-1,
3-hexanediol is indicated by EHD, and 1,3-butanediol is indicated by BD.

【0007】[0007]

【表1】 [Table 1]

【0008】[0008]

【表2】 [Table 2]

【0009】[0009]

【表3】 [Table 3]

【0010】表から明かなように、本発明に係わる試料
記号E,Fの電解液は従来の電解液に比べ、高温雰囲気
中での電解液の気化による外観膨張が見られず、また、
信頼性の低下も見られない。さらに−40℃において
も、γ−ブチロラクトン、N,N−ジメチルホルムアミ
ドを溶媒とした従来例と比較しても容量変化率の点でほ
ぼ同等である。なお、1,3−ブタンジオールは、溶媒
全体に占める重量比で50%未満の場合には、エチレン
グリコールおよび水の影響により、特に低温特性の改善
効果が少なくなるため好ましくない。
As is clear from the table, the electrolytes of sample symbols E and F according to the present invention do not show any external expansion due to the vaporization of the electrolyte in a high-temperature atmosphere, as compared with the conventional electrolytes.
There is no decrease in reliability. Furthermore, even at -40 ° C, the capacity change rate is almost the same as in the conventional example using γ-butyrolactone and N, N-dimethylformamide as solvents. If the weight ratio of 1,3-butanediol to the entire solvent is less than 50%, it is not preferable because the effect of ethylene glycol and water to improve the low-temperature characteristics is particularly reduced.

【0011】[0011]

【発明の効果】以上のように、1,3−ブタンジオール
を主溶媒とする溶媒中に、有機酸あるいはその塩を溶解
したことを特徴とする電解液は、人体への影響も小さ
く、かつ高沸点、低凝固点であるため、この電解液を用
いた電解コンデンサは、広い温度範囲において良好な特
性を示すと同時に扱い易い。特に、広い温度範囲で使用
可能であることは、今後さらに重要視される項目であ
り、工業的ならびに実用的価値の大なるものである。
As described above, an electrolytic solution characterized by dissolving an organic acid or a salt thereof in a solvent containing 1,3-butanediol as a main solvent has a small effect on the human body, and Since it has a high boiling point and a low freezing point, an electrolytic capacitor using this electrolytic solution exhibits good characteristics over a wide temperature range and is easy to handle. In particular, the ability to be used in a wide temperature range is an item to be further emphasized in the future, and has great industrial and practical value.

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 有機酸あるいはその塩を溶質とした、電
解コンデンサの電解液において、1,3−ブタンジオー
ルを主溶媒とすることを特徴とする電解コンデンサの電
解液。
1. An electrolytic solution for an electrolytic capacitor comprising an organic acid or a salt thereof as a solute and 1,3-butanediol as a main solvent.
【請求項2】 上記1,3−ブタンジオールは、溶媒全
体に占める重量比で50〜100%であることを特徴と
する請求項1の電解コンデンサの電解液。
2. The electrolytic solution according to claim 1, wherein said 1,3-butanediol accounts for 50 to 100% by weight of the whole solvent.
JP08491592A 1992-03-06 1992-03-06 Electrolytic solution for electrolytic capacitors Expired - Fee Related JP3310690B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP08491592A JP3310690B2 (en) 1992-03-06 1992-03-06 Electrolytic solution for electrolytic capacitors

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP08491592A JP3310690B2 (en) 1992-03-06 1992-03-06 Electrolytic solution for electrolytic capacitors

Publications (2)

Publication Number Publication Date
JPH05251278A JPH05251278A (en) 1993-09-28
JP3310690B2 true JP3310690B2 (en) 2002-08-05

Family

ID=13844020

Family Applications (1)

Application Number Title Priority Date Filing Date
JP08491592A Expired - Fee Related JP3310690B2 (en) 1992-03-06 1992-03-06 Electrolytic solution for electrolytic capacitors

Country Status (1)

Country Link
JP (1) JP3310690B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2017228738A (en) * 2016-06-24 2017-12-28 ニチコン株式会社 Electrolytic solution and electrolytic capacitor

Also Published As

Publication number Publication date
JPH05251278A (en) 1993-09-28

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