JPS61184809A - Electrolytic liquid for driving electrolytic capacitor - Google Patents

Electrolytic liquid for driving electrolytic capacitor

Info

Publication number
JPS61184809A
JPS61184809A JP2478685A JP2478685A JPS61184809A JP S61184809 A JPS61184809 A JP S61184809A JP 2478685 A JP2478685 A JP 2478685A JP 2478685 A JP2478685 A JP 2478685A JP S61184809 A JPS61184809 A JP S61184809A
Authority
JP
Japan
Prior art keywords
electrolytic
corrosion
capacitor
solvent
driving
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.)
Granted
Application number
JP2478685A
Other languages
Japanese (ja)
Other versions
JPH0347567B2 (en
Inventor
仁 井二
匡司 松田
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.)
Sanyo Electric Co Ltd
Original Assignee
Sanyo Electric Co Ltd
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 Sanyo Electric Co Ltd filed Critical Sanyo Electric Co Ltd
Priority to JP2478685A priority Critical patent/JPS61184809A/en
Publication of JPS61184809A publication Critical patent/JPS61184809A/en
Publication of JPH0347567B2 publication Critical patent/JPH0347567B2/ja
Granted legal-status Critical Current

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  • Primary Cells (AREA)
  • Electrical Discharge Machining, Electrochemical Machining, And Combined Machining (AREA)
  • Secondary Cells (AREA)
  • Preventing Corrosion Or Incrustation Of Metals (AREA)
  • Fixed Capacitors And Capacitor Manufacturing Machines (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 U)産業上の利用分野 本発明a′(解コンデンサの駆動用電解液(以下、電解
液という。)l二関する。
DETAILED DESCRIPTION OF THE INVENTION U) Field of Industrial Application The present invention relates to a' (electrolytic solution for driving an electrolytic capacitor (hereinafter referred to as electrolytic solution) l2).

(ロ)従来の技術 近年プリント基板実装の高密度化、高信頼性化1:伴な
いi、1,1−)リクロルエタン又はフロンなどの塩素
系溶剤で基板洗浄が行なわれている。そして、かかる溶
剤は高い浸透性のため、溶剤がゴムバッキング中を透過
、拡散してコンデンサ内部まで浸入する可能性がある。
(b) Prior art In recent years, printed circuit board mounting has become more dense and reliable. Since such a solvent has high permeability, there is a possibility that the solvent may permeate and diffuse through the rubber backing and penetrate into the capacitor.

この浸入した溶剤は分解して塩化物イオンとなり、コン
デンサの高温負荷時に腐食を発生させ、特性の劣化をも
たらす。この腐食による劣化を防止するため、特公昭5
B−62989公報C;見られる如く、腐食防止剤とし
て酸化ホウ素を電解液C;添加する方法も提案されてい
るが、ある程度防止効果にあるものの高温負荷試験(二
2ける特性の悪化が大きかった。また、特公昭58−1
538号公報のように銀化合物を添加する方法も提案さ
れているが、溶媒C;対する溶解度が小さく、腐食防止
の十分な効果げ得られていなかった。
This infiltrated solvent decomposes into chloride ions, which cause corrosion when the capacitor is loaded at high temperatures, resulting in deterioration of its characteristics. In order to prevent deterioration due to this corrosion,
B-62989 Publication C; As can be seen, a method of adding boron oxide as a corrosion inhibitor to electrolyte C; has also been proposed, but although it has some degree of prevention effect, the high temperature load test (deterioration of the properties by 22 was significant) .Also, special public service 1986-1
Although a method of adding a silver compound has been proposed as in Japanese Patent No. 538, the solubility in solvent C is low and a sufficient effect of preventing corrosion has not been obtained.

(ハ)発明が解決しようとする問題点 従来の電解液では、塩素系溶剤でコンデンサを洗浄した
場合に、高温負荷中に腐食を引き起こすなどの問題があ
った。
(c) Problems to be Solved by the Invention Conventional electrolytes have problems such as corrosion during high-temperature loads when capacitors are cleaned with chlorinated solvents.

に)問題点を解決するための手段 本発明は溶媒と溶質とからなる電解液に、マンデン酸ま
たはその塩を添加し、溶解させたことを特徴とする。
B) Means for Solving the Problems The present invention is characterized in that mandic acid or a salt thereof is added to and dissolved in an electrolytic solution consisting of a solvent and a solute.

(ホ)作用 マンデル酸(CaHsCH(OH)COOH〕またにマ
ンデル酸塩は腐食の原因となる塩化物イオンと錯化合物
を形成し、塩化物イオンを腐食の反応系外(:取り出丁
ことにより、腐食を防止すると思われる。
(e) Action Mandelic acid (CaHsCH(OH)COOH) Also, mandelic acid salt forms a complex compound with chloride ions that cause corrosion, and removes chloride ions from the corrosion reaction system (by removing them). , which appears to prevent corrosion.

(へ)実 施 例 本発明C二於いて、溶媒としては、エチレンブト リコールやエチレングリコールとメチルカルビー外 ルの混合溶媒、また、メチルセロソルブやN−エチルホ
ルムアミド、ジエチレングリコール、ジメチルホルアミ
ド等の混合物などが用いられる。
(F) Example In the present invention C2, the solvent may be ethylene butrycol, a mixed solvent of ethylene glycol and methylcarbyl, or a mixture of methylcellosolve, N-ethylformamide, diethylene glycol, dimethylformamide, etc. etc. are used.

不発11C;於いて、溶質としては、アジピン酸、ギ酸
、安息香酸などの有機酸のアンモニウム塩、あるいC−
ホウ酸、マレイン酸、アゼライン酸等の各アンモニウム
塩やアミン塩が用いられる。
In the case of unexploded 11C, the solute is an ammonium salt of an organic acid such as adipic acid, formic acid, or benzoic acid, or C-
Ammonium salts and amine salts such as boric acid, maleic acid, and azelaic acid are used.

本発明は上述した溶媒と溶質からなる電解液【:マンデ
ル酸またはその塩?添加し、溶解させるものである。こ
のマンデル酸の添加量に好ましくは、0.1y以上20
y以下である。以下、本発明を具体的な実施例(:於て
g!、1;詳述する。第1表6二本発明の典型的実施例
としての5覆類の電解液(8)〜■と比較のための従来
の電解液(ト)〜閲を示す。
The present invention provides an electrolytic solution consisting of the above-mentioned solvent and solute [: mandelic acid or its salt? It is added and dissolved. The amount of mandelic acid added is preferably 0.1y or more and 20
It is less than or equal to y. Hereinafter, the present invention will be described in detail with specific examples (g!, 1). Conventional electrolyte solutions (g) to (b) are shown.

第   1   表 第2表は上記各電解液(A)〜@を用い、定格50V、
47μFの素子に含浸してなるアルミニウム電解コンデ
ンサを夫々試作した後、1,1.1−トリクロルエタン
に10分間浸漬し、105℃の加速高温負荷試験を行っ
た結果を示す。尚、試料コンデンサの構造は、周知の構
造であり、化成したエツチドアルミニウム箔と陰甑箔を
セパレータ紙’kHさんで巻回したコンデンサ素子C:
電解液を含浸し、この素子をゴムバッキングを用いてア
ルミニウムケース内に収納したものである。
Table 1 Table 2 uses each of the above electrolytes (A) to @, with a rating of 50V,
The results of aluminum electrolytic capacitors impregnated with 47 μF elements were prototyped, immersed in 1,1,1-trichloroethane for 10 minutes, and subjected to an accelerated high temperature load test at 105°C. The structure of the sample capacitor is a well-known structure, and consists of a capacitor element C made of chemically etched aluminum foil and shaded foil wrapped with separator paper 'kH':
The device is impregnated with electrolyte and housed in an aluminum case with a rubber backing.

第   2   表 105℃定格電圧印加 第2表から明らかなように、105℃500時間の定格
電圧印加■;おけるコンデンサの加速高温負荷試験C:
於いて、従来の電解液では、試験中I:腐食、所感とい
りた異常が見られる。ここで腐食−ド部分が断線状態に
至ったものをいう。一方不発明C:係る電解液(8)乃
至(E)−二おいては、この様な異常は全くみられず、
マンデル酸またげその塩の腐食防止効果が認められる。
Table 2: Application of rated voltage at 105°C As is clear from Table 2, accelerated high-temperature load test of capacitors under application of rated voltage for 500 hours at 105°C C:
With the conventional electrolyte, abnormalities such as I: Corrosion and impressions were observed during the test. This refers to a situation where the corroded portion has become disconnected. On the other hand, in non-inventive C: such electrolytes (8) to (E)-2, no such abnormality was observed.
The anti-corrosion effect of mandelic acid and its salts has been recognized.

また、本発明の他の実施例として第3表【:示すよう(
二、2種類の電解液CI)(J)と比較のための従来の
電解液(へ)を準備し、前述と同様C;腐食防止効果を
確認した。
In addition, as shown in Table 3 [: (
2. Two types of electrolytic solution CI) (J) and a conventional electrolytic solution (J) for comparison were prepared, and C: Corrosion prevention effect was confirmed in the same manner as described above.

@3表 第4表は上記各電解液(I)〜(へ)を用い、定格50
V、470μFの素子C二含浸してなるアルミニウム電
解コンデンサを夫々試作した後、フロン系溶剤で10分
間浸漬洗浄を行い、85℃の高温負荷試験を行った結果
を示す。尚、コンデンサの形態は前述のものと同様であ
る。
@Table 3 Table 4 uses each of the above electrolytes (I) to (F), and the rating is 50.
The results of aluminum electrolytic capacitors impregnated with V and C of 470 μF were fabricated as prototypes, and then immersed in a fluorocarbon solvent for 10 minutes and subjected to a high-temperature load test at 85° C. The results are shown below. Note that the form of the capacitor is the same as that described above.

第   4   表 85℃定格電圧印加 第4表に示すようC:、従来の電解液でに、腐食という
異常が見られたのに対して、マンデル酸およびその塩を
添加した本発明C:よる電解液では腐食などの異常に全
く見られず腐食防止効果があることが判る。
Table 4: Rated voltage application at 85°C As shown in Table 4, an abnormality of corrosion was observed with the conventional electrolyte, but the electrolysis of the present invention with C: in which mandelic acid and its salts were added. In the liquid, no abnormalities such as corrosion were observed, indicating that it has a corrosion-preventing effect.

次C二、マンデル酸またはその塩の添加量を第5表≦二
示すよう(;種々変更した電解液(Q〜0を準備した。
Next, the amount of mandelic acid or its salt added was as shown in Table 5≦2 (; Various electrolytes (Q~0) were prepared.

第   5   表 第6表μm上記各電解液0〜0を、第2表1:おけると
同様(;シて、定格50’/、47μFの素子C二含浸
してなるアルミニウム電解コンデンサを夫々試作した後
、1t1*1−トリクロルエタン(−10分間浸漬し、
105℃の加速高温負荷試験蓋を行ツタ結果を示す。尚
、コンデンサの形態は前述のものと同様である。
Table 5 Table 6 μm Each of the above electrolytes 0 to 0 was applied in the same manner as shown in Table 2 1. Aluminum electrolytic capacitors impregnated with element C2 each having a rating of 50'/47 μF were prototyped. After that, 1t1*1-trichloroethane (soaked for -10 minutes,
The lid was subjected to an accelerated high temperature load test at 105°C and the results are shown below. Note that the form of the capacitor is the same as that described above.

以下余白 第   6   表 105℃定格電圧印加 第6表から、105℃500時間の定格電圧印加におけ
るコンデンサの加速高温負荷試験蓋;於いて、マンデル
酸の添加量を溶媒100m1!に対して0.1y以上の
電解液でに、腐食防止I:対して有効な効果があること
が分った。ただ、マンデル酸の添加量が溶媒100ff
i/に対して20yを越えると、防食効果はあるものの
tan  σの増加などコンデンサ特性が劣化して好ま
しくない。従つて、マンデル酸の添加量に溶媒100m
1!c対して011y以上209以下が好ましいことが
判る。
Below is the margin No. 6 Table 105℃ rated voltage application From Table 6, accelerated high temperature load test of capacitor at 105℃ rated voltage application for 500 hours. It was found that an electrolytic solution of 0.1y or more has an effective effect on corrosion prevention I:. However, the amount of mandelic acid added is 100ff of the solvent.
If it exceeds 20y with respect to i/, although there is an anti-corrosion effect, capacitor characteristics such as an increase in tan σ deteriorate, which is not preferable. Therefore, 100ml of solvent is added to the amount of mandelic acid added.
1! It can be seen that c is preferably 011y or more and 209 or less.

(ト)発明の詳細 な説明したように、本発明C二係る電解液C;よれば、
塩素系溶剤で洗浄したを5合には腐食作用等を有効C;
防止することができる。また、長期の高温負荷に二対し
ても特性の変化が少ないので、電解コンデンサの長寿命
化を図ることができる。従って、本発明(:より電解コ
ンデンサの性能が飛躍的C二改善される。
(G) As described in detail of the invention, according to the present invention C2, the electrolyte C;
5. Effective against corrosion, etc. after cleaning with chlorinated solvents C;
It can be prevented. Furthermore, since the characteristics of the electrolytic capacitor do not change much even under long-term high-temperature loads, it is possible to extend the life of the electrolytic capacitor. Therefore, the performance of electrolytic capacitors is dramatically improved by the present invention.

Claims (2)

【特許請求の範囲】[Claims] (1)溶媒と溶質とからなる電解液に、マンデル酸また
はその塩を添加し、溶解させたことを特徴とする電解コ
ンデンサの駆動用電解液。
(1) An electrolytic solution for driving an electrolytic capacitor, characterized in that mandelic acid or a salt thereof is added and dissolved in an electrolytic solution consisting of a solvent and a solute.
(2)前記マンデン酸またはその塩の添加量が溶媒10
0mlに対して0.1g以上20g以下であることを特
徴とする特許請求の範囲第1項に記載の電解コンデンサ
の駆動用電解液。
(2) The amount of the mandic acid or its salt added is 10% of the solvent.
The electrolytic solution for driving an electrolytic capacitor according to claim 1, characterized in that the amount is 0.1 g or more and 20 g or less per 0 ml.
JP2478685A 1985-02-12 1985-02-12 Electrolytic liquid for driving electrolytic capacitor Granted JPS61184809A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2478685A JPS61184809A (en) 1985-02-12 1985-02-12 Electrolytic liquid for driving electrolytic capacitor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2478685A JPS61184809A (en) 1985-02-12 1985-02-12 Electrolytic liquid for driving electrolytic capacitor

Publications (2)

Publication Number Publication Date
JPS61184809A true JPS61184809A (en) 1986-08-18
JPH0347567B2 JPH0347567B2 (en) 1991-07-19

Family

ID=12147865

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2478685A Granted JPS61184809A (en) 1985-02-12 1985-02-12 Electrolytic liquid for driving electrolytic capacitor

Country Status (1)

Country Link
JP (1) JPS61184809A (en)

Also Published As

Publication number Publication date
JPH0347567B2 (en) 1991-07-19

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