JPH07120615B2 - Electrolytic solution for driving electrolytic capacitors - Google Patents
Electrolytic solution for driving electrolytic capacitorsInfo
- Publication number
- JPH07120615B2 JPH07120615B2 JP62096571A JP9657187A JPH07120615B2 JP H07120615 B2 JPH07120615 B2 JP H07120615B2 JP 62096571 A JP62096571 A JP 62096571A JP 9657187 A JP9657187 A JP 9657187A JP H07120615 B2 JPH07120615 B2 JP H07120615B2
- Authority
- JP
- Japan
- Prior art keywords
- electrolytic solution
- electrolytic
- salt
- driving
- 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.)
- Expired - Fee Related
Links
Landscapes
- Electric Double-Layer Capacitors Or The Like (AREA)
- Primary Cells (AREA)
- Control Of Indicators Other Than Cathode Ray Tubes (AREA)
Description
【発明の詳細な説明】 産業上の利用分野 本発明は電解コンデンサに関するものであり、詳しく言
えば、アルミ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 capacitor, and more specifically to an electrolytic solution for driving an aluminum electrolytic capacitor.
従来の技術 従来、電解コンデンサ駆動用電解液としては、エチレン
グリコールにイオノゲンを溶解した電解液が用いられて
いる。この種の電解コンデンサは低温における特性を悪
化させる。以上のような欠点を改良するため、特開昭61
−70711号公報にみられるように、γ−ブチロラクトン
を溶媒とし、フタル酸のトリエチルアミン塩を用いる例
や、特開昭54−7564号公報にみられるように、γ−ブチ
ロラクトンとエチレングリコールの混合溶媒にマレイン
酸のアミン塩を用いる例がある。2. Description of the Related Art Conventionally, as an electrolytic solution for driving an electrolytic capacitor, an electrolytic solution in which ionogen is dissolved in ethylene glycol has been used. This type of electrolytic capacitor deteriorates the characteristics at low temperatures. In order to improve the above drawbacks, JP-A-61
As disclosed in JP-A-70711, an example using γ-butyrolactone as a solvent and a triethylamine salt of phthalic acid, and, as seen in JP-A-54-7564, a mixed solvent of γ-butyrolactone and ethylene glycol. There is an example of using an amine salt of maleic acid.
発明が解決しようとする問題点 しかし、従来の問題点として、γ−ブチロラクトンを溶
媒とし、フタル酸のトリエチルアミン塩を用いた場合、
比電導度が低く、また105℃中では高い安定性を示す
が、125℃中ではあまり安定でないという欠点である。
また、γ−ブチロラクトンとエチレングリコールの混合
溶媒にマレイ酸のアミン塩を用いた場合、比電導度は十
分高い値が得られるが、高温での安定性に欠け105℃中
でも安定性は低いという欠点がある。Problems to be Solved by the Invention However, as a conventional problem, when γ-butyrolactone is used as a solvent and a triethylamine salt of phthalic acid is used,
It has a low specific conductivity and high stability at 105 ° C, but is not very stable at 125 ° C.
Further, when the amine salt of maleic acid is used as the mixed solvent of γ-butyrolactone and ethylene glycol, the specific electric conductivity can be obtained at a sufficiently high value, but the stability at high temperature is poor and the stability is low even at 105 ° C. There is.
本発明はこのような従来の欠点を解決するもので、高導
電度で、高温劣化の小さい電解液を提供し、電解コンデ
ンサの損失特性の改善、並びに高温で長寿命化を図るこ
とを目的とする。The present invention solves such conventional drawbacks, and an object thereof is to provide an electrolytic solution having high conductivity and little deterioration at high temperature, aiming at improvement of loss characteristics of an electrolytic capacitor and at the same time prolonging its life at high temperature. To do.
問題点を解決するための手段 上記問題点を解決するために、本発明はγ−ブチロラク
トンを主体とする溶媒に、マレイン酸のテトラメチルア
ンモニウム塩あるいは、テトラエチルアンモニウム塩を
溶解して溶質とし、さらにアルキルリン酸エステルもし
くはその塩および/またはP−ニトロ安息香酸もしくは
その塩を添加剤として用いる電解コンデンサ駆動用電解
液である。Means for Solving the Problems In order to solve the above problems, the present invention, in a solvent containing γ-butyrolactone as a main component, a tetramethylammonium salt of maleic acid or a tetraethylammonium salt as a solute, An electrolytic solution for driving an electrolytic capacitor, which uses an alkyl phosphate ester or a salt thereof and / or P-nitrobenzoic acid or a salt thereof as an additive.
アルキルリン酸エステルのアルキル基はどのようなもの
を用いても効果は認められるが、好ましくは、モノエチ
ルリン酸エステル,モノプロピルリン酸エステル,モノ
ブチルリン酸エステル,モノペンチルリン酸エステル,
ジエチルリン酸エステル,ジプロピルリン酸エステル,
ジブチルリン酸エステル,ジペンチルリン酸エステルお
よびこれらの塩である。Although the effect can be recognized by using any alkyl group of the alkyl phosphate ester, preferably, monoethyl phosphate ester, monopropyl phosphate ester, monobutyl phosphate ester, monopentyl phosphate ester,
Diethyl phosphate ester, dipropyl phosphate ester,
Dibutyl phosphate ester, dipentyl phosphate ester and salts thereof.
アルキルリン酸エステルもしくはその塩の添加量は、電
解液量に対して0.01〜5.0重量%が好ましい。これは0.0
1重量%以下では効果がなく、5.0重量%を越えると電導
度低下が大きくなるからである。The addition amount of the alkyl phosphate or its salt is preferably 0.01 to 5.0% by weight with respect to the amount of the electrolytic solution. This is 0.0
This is because if the amount is less than 1% by weight, there is no effect, and if the amount exceeds 5.0% by weight, the decrease in electrical conductivity becomes large.
P−ニトロ安息香酸もしくはその塩の添加量は電解液量
に対して0.01〜5.0重量%が好ましい。これは0.01重量
%以下では効果がなく、5.0重量%を越えると火花電圧
が低下するからである。The amount of P-nitrobenzoic acid or its salt added is preferably 0.01 to 5.0% by weight based on the amount of the electrolytic solution. This is because if the amount is less than 0.01% by weight, there is no effect, and if the amount exceeds 5.0% by weight, the spark voltage decreases.
作用 γ−ブチロラクトンを主体とする溶媒に、マレイン酸の
テトラメチルアンモニウム塩あるいは、テトラエチルア
ンモニウム塩を溶質として組合わせた場合非常に高い電
寿度が得られる。Action When a solvent mainly composed of γ-butyrolactone is combined with a tetramethylammonium salt of maleic acid or a tetraethylammonium salt as a solute, an extremely high degree of electrical life can be obtained.
γ−ブチロラクトンを主体とする溶媒の時、マレイン酸
は高温中で比較的分解しにくく、またテトラメチルアン
モニウムあるいはテトラエチルアンモニウムとの反応も
起こりにくい。このため高温中での特性変化がきわめて
低い電解液が得られると考えられる。When the solvent is mainly composed of γ-butyrolactone, maleic acid is relatively hard to decompose at high temperature, and the reaction with tetramethylammonium or tetraethylammonium hardly occurs. Therefore, it is considered that an electrolytic solution with extremely low characteristic changes at high temperatures can be obtained.
さらにアルキルリン酸エステル、あるいはP−ニトロ安
息香酸がアルミニウム電解箔表面に吸着し、誘電体酸化
皮膜を保護することにより、静電容量の減少及びtanδ
の増加が大幅に抑制できるものと考えられる。Further, alkyl phosphate or P-nitrobenzoic acid is adsorbed on the surface of the aluminum electrolytic foil to protect the dielectric oxide film, thereby reducing the capacitance and increasing tan δ.
It is considered that the increase of the can be significantly suppressed.
実施例 以下、本発明による実施例について述べる。Examples Hereinafter, examples according to the present invention will be described.
表1に本発明の実施例及び従来の電解液組成例、並びに
常温における比電導度を示す。Table 1 shows examples of the present invention, conventional electrolytic solution composition examples, and specific electric conductivity at room temperature.
表1から明らかなように、従来の電解液と比較して高い
比電導度を得ることができる。 As is clear from Table 1, a higher specific electric conductivity can be obtained as compared with the conventional electrolytic solution.
表2に、表1の従来例1、従来例2、実施例1、実施例
2、実施例3および実施例6の電解液を用いたコンデン
サの初期特性を示す。試料コンデンサは6.3V1000μF
(φ10×12.5)のアルミ電解コンデンサである。Table 2 shows initial characteristics of capacitors using the electrolytic solutions of Conventional Example 1, Conventional Example 2, Example 1, Example 2, Example 3 and Example 6 of Table 1. Sample capacitor is 6.3V 1000μF
(Φ10 × 12.5) aluminum electrolytic capacitor.
表2から明らかなように、実施例は従来例と比較してta
nδを低くすることができる。 As is clear from Table 2, the embodiment has a ta
nδ can be lowered.
第1図〜第3図に、表2で示したアルミ電解コンデンサ
の125℃における特性経時変化を示している、第1図は
定格電圧印加における静電容量変化、第2図は定格電圧
印加における損失角の正接変化、第3図は電圧印加なし
における漏れ電流変化を示す図である。Figures 1 to 3 show the changes over time in the characteristics of the aluminum electrolytic capacitors shown in Table 2 at 125 ° C. Figure 1 shows the change in capacitance when rated voltage is applied, and Figure 2 shows when the rated voltage is applied. Change in tangent of loss angle, and FIG. 3 is a view showing change in leakage current without application of voltage.
この第1図〜第3図から明らかなように、高温中におい
ても特性変化はきわめて小さく、信頼性の高いコンデン
サを得ることができる。As is apparent from FIGS. 1 to 3, the change in characteristics is extremely small even at high temperatures, and a highly reliable capacitor can be obtained.
発明の効果 以上のように本発明によれば、従来の電解液と比較し
て、損失特性を改善でき、しかも125℃という高温中で
もきわめて安定な信頼性の高い電解コンデンサを提供で
き、工業的価値の大なるものである。EFFECTS OF THE INVENTION As described above, according to the present invention, loss characteristics can be improved as compared with conventional electrolytic solutions, and an extremely stable and highly reliable electrolytic capacitor can be provided even at a high temperature of 125 ° C. Is a great thing.
第1図〜第3図はそれぞれ従来の電解液および本発明の
電解液を用いた定格6.3V1000μF(φ10×12.5)のアル
ミ電解コンデンサの125℃における特性経時変化を示し
たものであり、第1図は定格電圧印加における静電容量
変化、第2図は定格電圧印加における損失角の正接変
化、第3図は電圧印加なしにおける漏れ電流変化を示し
た特性図である。FIGS. 1 to 3 show characteristics of the aluminum electrolytic capacitors rated at 6.3V and 1000 μF (φ10 × 12.5) using the conventional electrolytic solution and the electrolytic solution of the present invention with time at 125 ° C., respectively. FIG. 2 is a characteristic diagram showing a change in capacitance when a rated voltage is applied, FIG. 2 is a characteristic diagram showing a tangent change in loss angle when a rated voltage is applied, and FIG.
Claims (4)
マレイン酸のテトラメチルアンモニウム塩あるいはテト
ラエチルアンモニウム塩を溶質とし、アルキルリン酸エ
ステルもしくはその塩、および/またはP−ニトロ安息
香酸もしくはその塩を添加溶解したことを特徴とする電
解コンデンサ駆動用電解液。1. A solvent containing γ-butyrolactone as a main component,
An electrolytic solution for driving an electrolytic capacitor, characterized in that a tetramethylammonium salt or a tetraethylammonium salt of maleic acid is used as a solute, and an alkyl phosphate ester or a salt thereof and / or P-nitrobenzoic acid or a salt thereof is added and dissolved.
(B)のような化学構造のものである特許請求の範囲第
1項記載の電解コンデンサ駆動用電解液。 2. An alkyl phosphoric acid ester having the following (A),
The electrolytic solution for driving an electrolytic capacitor according to claim 1, which has a chemical structure as shown in (B).
添加量が電解液重量に対して0.01〜5.0重量%であるこ
とを特徴とする特許請求の範囲第2項記載の電解コンデ
ンサ駆動用電解液。3. The electrolytic solution for driving an electrolytic capacitor according to claim 2, wherein the addition amount of the alkyl phosphate or its salt is 0.01 to 5.0% by weight based on the weight of the electrolytic solution.
量が電解液重量に対して0.01〜5.0重量%であることを
特徴とする特許請求の範囲第1項記載の電解コンデンサ
駆動用電解液。4. The electrolytic solution for driving an electrolytic capacitor according to claim 1, wherein the added amount of P-nitrobenzoic acid or its salt is 0.01 to 5.0% by weight based on the weight of the electrolytic solution. .
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62096571A JPH07120615B2 (en) | 1987-04-20 | 1987-04-20 | Electrolytic solution for driving electrolytic capacitors |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62096571A JPH07120615B2 (en) | 1987-04-20 | 1987-04-20 | Electrolytic solution for driving electrolytic capacitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63261822A JPS63261822A (en) | 1988-10-28 |
| JPH07120615B2 true JPH07120615B2 (en) | 1995-12-20 |
Family
ID=14168685
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62096571A Expired - Fee Related JPH07120615B2 (en) | 1987-04-20 | 1987-04-20 | Electrolytic solution for driving electrolytic capacitors |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH07120615B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0754790B2 (en) * | 1987-06-02 | 1995-06-07 | ニチコン株式会社 | Electrolytic solution for driving aluminum electrolytic capacitors |
-
1987
- 1987-04-20 JP JP62096571A patent/JPH07120615B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPS63261822A (en) | 1988-10-28 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |