JPS61240624A - Driving electrolytic liquid for electrolytic capacitor - Google Patents

Driving electrolytic liquid for electrolytic capacitor

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Publication number
JPS61240624A
JPS61240624A JP8181285A JP8181285A JPS61240624A JP S61240624 A JPS61240624 A JP S61240624A JP 8181285 A JP8181285 A JP 8181285A JP 8181285 A JP8181285 A JP 8181285A JP S61240624 A JPS61240624 A JP S61240624A
Authority
JP
Japan
Prior art keywords
electrolytic
acid
corrosion
capacitor
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.)
Pending
Application number
JP8181285A
Other languages
Japanese (ja)
Inventor
仁 井二
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 JP8181285A priority Critical patent/JPS61240624A/en
Publication of JPS61240624A publication Critical patent/JPS61240624A/en
Pending legal-status Critical Current

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  • Primary Cells (AREA)
  • Electrical Discharge Machining, Electrochemical Machining, And Combined Machining (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】 (イ)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。
DETAILED DESCRIPTION OF THE INVENTION (a) Field of Industrial Application The present invention relates to an electrolytic solution for driving an electrolytic capacitor (hereinafter referred to as electrolytic solution).

初 従来の技術 従来、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、アジピン酸、ギ酸。
First Conventional technology Conventionally, the electrolyte for electrolytic capacitors uses ethylene glycol as the main solvent, adipic acid, and formic acid.

安息香酸などの有機酸やその塩類、あるいはホウ酸、リ
ン酸などの無機酸やその塩類などを溶質とするものが多
く用いられている。これら従来の電解液を用いたコンデ
ンサは5高温負荷中に腐食が発生し、特性劣化をもたら
すことがあった。この腐食による劣化を防止するため、
特公昭58−6298号公報に見られる如く、腐食防止
剤として酸化ホウ素を電解液に添加する方法も提案され
ているが、ある程度防止効果はあるものの高温負荷試験
における特性の悪化が大きかった。また、特公昭58−
1538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、溶媒に対する溶解度が小さく、腐食防止
の十分な効果は得られていなかった。
Many are used that have organic acids such as benzoic acid and their salts, or inorganic acids and their salts such as boric acid and phosphoric acid as solutes. In capacitors using these conventional electrolytes, corrosion may occur during high-temperature loads, resulting in deterioration of characteristics. In order to prevent deterioration due to this corrosion,
As seen in Japanese Patent Publication No. 58-6298, a method has been proposed in which boron oxide is added to the electrolytic solution as a corrosion inhibitor, but although this has a certain degree of prevention effect, the properties in high-temperature load tests are significantly deteriorated. In addition, special public service 58-
Although a method of adding a silver compound has been proposed as in Japanese Patent No. 1538, the solubility in a solvent 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、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 had problems such as corrosion during high-temperature loads.

に)問題点を解決するだめの手段 本発明は溶媒と溶質とからなる電解液に、ボロンサリチ
ル酸またはその塩を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 boron salicylic acid or a salt thereof is dissolved in an electrolytic solution consisting of a solvent and a solute.

(ホ)作 用 ボロジサリチル酸およびその塩は、腐食発生の原因であ
る塩化物イオンと錯化合物を形成し、塩化物イオンを腐
食の反応系外に取り出し、腐食防止効果が生じると思わ
れる。
(e) Effects Borodisalicylic acid and its salts form a complex with chloride ions, which are the cause of corrosion, and take out the chloride ions out of the corrosion reaction system, which is thought to produce a corrosion-preventing effect.

(へ)実施例 本発明に於いて、溶媒としてはエチレングリコールを主
溶媒として用い1例えばエチレングリコール溶媒、″!
、たエチレングリコールとメチルカルピトールの混合溶
媒、あるいはエチレングリコールとメチルセロソルブや
N−エチルポルムアミド。
(f) Example In the present invention, ethylene glycol is used as the main solvent.1 For example, ethylene glycol solvent,''!
, a mixed solvent of ethylene glycol and methylcarpitol, or a mixed solvent of ethylene glycol and methyl cellosolve or N-ethylpolamide.

ジエチレングリコール、ジメテルホルアミド等の混合溶
媒などが用いられる。
A mixed solvent such as diethylene glycol and dimeterformamide is used.

本発明に於いて、溶質としては、アジピン酸。In the present invention, the solute is adipic acid.

ギ酸、安息香酸などの有機酸のアンモニウム塩やアミン
塩あるいはホウ酸、マレイン酸、アービライン酸等の各
アンモニウム塩やアミン」急が用いられる。
Ammonium salts and amine salts of organic acids such as formic acid and benzoic acid, and ammonium salts and amine salts of boric acid, maleic acid, and arbilaic acid are used.

本発明は上述した溶質および溶媒からなる′巾;解液に
ボロジサリチル酸またはその塩を添加し溶解するもので
ある。このボロジサリチル酸またはその塩の添加量は溶
媒100 m、/に対して、好゛土しくはり、5!I以
上最も好ましくは0.5g〜2oyである。
In the present invention, borodisalicylic acid or a salt thereof is added to and dissolved in a solution consisting of the above-mentioned solute and solvent. The amount of this borodisalicylic acid or its salt added is preferably 5! It is most preferably 0.5 g to 2 oy.

以下1本発明を具体的な実施例に於て更に詳述する。第
1表に本発明の典型的実施例としての4種類の電解液(
、A)〜(TI)]と比較のだめの従来の電解液(ト)
)aP)(G)を示す。
The present invention will be explained in more detail below using specific examples. Table 1 shows four types of electrolytes (
, A) ~ (TI)] and a conventional electrolyte (G) for comparison.
)aP) (G) is shown.

第1表 第2表は、上記各電解液(A)〜(G)を用い定格16
QV、10μFの素子に含浸してかるアルミニウム電解
コンデンサを夫々20個づつ試作した後。
Table 1 and Table 2 show the rating of 16 using each of the above electrolytes (A) to (G).
After making prototypes of 20 aluminum electrolytic capacitors each impregnated with QV and 10μF elements.

135℃の加速高温負荷試験を行った結果を示す。The results of an accelerated high temperature load test at 135°C are shown.

尚、試料コンデンサの構造は1周知の構造であり化成し
たエツチドアルミニウム箔をセパレータ紙をはさんで巻
回したコンデンサ素子に電解液を含浸し、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。
The structure of the sample capacitor is a well-known structure in which a capacitor element is made by winding chemically etched aluminum foil with separator paper in between, impregnated with electrolyte, and this element is placed inside an aluminum case using a rubber backing. It is stored.

第2表 105℃定格電圧印加 である。Table 2 105℃ rated voltage applied It is.

第2表から明らかなように、105℃1000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に於
いて、従来の電解液では、試験中に腐食といつ九異常が
見られる。ここで腐食とはコンデンサ素子より封口部に
至るアルミリード部分の腐食をいう。一方本発明に係る
電解液体)乃至(D)に於いては、この様な異常は全く
見られず、ボロジサリチル酸およびその塩の腐食防止効
果が誌められる。
As is clear from Table 2, in the accelerated high-temperature load test of capacitors at 105° C. and 1000 hours of rated voltage application, corrosion and abnormalities were observed with the conventional electrolyte during the test. Corrosion here refers to corrosion of the aluminum lead portion extending from the capacitor element to the sealing portion. On the other hand, in the electrolytic liquids () to (D) according to the present invention, such abnormalities were not observed at all, indicating the corrosion-preventing effect of borodisalicylic acid and its salts.

また、ボロジサリチル酸またはその塩の添加量について
はボロジサリチル酸アンモニウムを例にとって説明する
。第1図は溶媒としてエチレングリコール100−に溶
質としてアジピン酸アンモニウム10.ft−溶解した
基本組成の電解液に対して、ボロジサリチル酸アンモニ
ウムの添加量を種々変化させた場合の耐化成電圧の関係
を示す特性図である。
Further, the amount of addition of borodisalicylic acid or its salt will be explained using ammonium borodisalicylate as an example. Figure 1 shows 100% of ethylene glycol as a solvent and 10% of ammonium adipate as a solute. FIG. 2 is a characteristic diagram showing the relationship between the chemical formation voltage resistance when the amount of ammonium borodisalicylate added to an electrolytic solution having a basic composition dissolved in ft- is varied.

一般に化成処理は定格電圧の20〜3oチ程度り、主電
圧klばて行うため、第1図より100WV(ワークボ
ルト)以上の定格′電圧のコンデンサに使用するために
は、添加量を溶媒1oo−に対して20.!i’以下に
することが好せしい。また1゜OW’ V未満の定格電
圧のものに対してはそれ以上に添加しても同様の効果を
有するものと思われる。
Generally, chemical conversion treatment is carried out at a main voltage of about 20 to 3 degrees of the rated voltage, so from Figure 1, in order to use it for capacitors with a rated voltage of 100 WV (work volts) or more, the amount of solvent added must be 10 to 30 degrees. -20. ! It is preferable to make it less than or equal to i'. Furthermore, for those with a rated voltage of less than 1° OW' V, it is thought that the same effect can be obtained even if a higher amount is added.

つぎに1本発明の他の実施例として第3表に示す電解液
但)(T)(J)と、前述の電解液(A)(B)(0)
およびP)(G3を準備し、高温負荷時のコンデンサ特
性を測定した。
Next, as another embodiment of the present invention, the electrolytes (T) (J) shown in Table 3 and the electrolytes (A) (B) (0) described above
and P) (G3 was prepared, and the capacitor characteristics under high temperature load were measured.

第5表 第4表は上記各電解液(Nの)(0)(ハ)(IIGT
)および□□□)側を前述と同様にして、試料コンデン
サ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、105℃の高温負荷試験を行った結果を示す
Table 5 Table 4 shows each of the above electrolytes (N) (0) (c) (IIGT
) and □□□) sides were made in the same manner as described above, and aluminum electrolytic capacitors were made by impregnating the sample capacitor, and then a high temperature load test at 105° C. was conducted. The results are shown below.

第4表 105℃定格電圧印加 第4表から明らかな如く、従来の電解液では。Table 4 105℃ rated voltage applied As is clear from Table 4, in the conventional electrolyte.

腐食の発生などコンデンサ特性の劣化が著しいのに対し
1本発明に係る′住解淑ではボロジリーリチル酸および
その堪の添lI[I量がM媒’+ 00 mlに対しで
0.59以上で腐食防出が図れ、高温負荷特性の向上が
認められ、寿命延長の効果があることが判る。
In contrast, the deterioration of capacitor characteristics such as the occurrence of corrosion is significant, whereas in the case of the present invention, borodilyrithylic acid and its tolerant addition lI [I amount is 0.59 or more per ml of M medium' + 00 ml, corrosion occurs. It can be seen that the product has the effect of prolonging the life of the product, as it has been found to be effective in preventing leakage and improving high-temperature load characteristics.

(ト)発明の詳細 な説明したように1本発明に糸る゛電解液は長期の高温
負荷に対してもコンデンサ特性の劣化紫はとんどなりシ
、電解コンデンサの長寿命化全図ることができる。
(G) As explained in detail about the invention, 1. The electrolytic solution according to the present invention hardly deteriorates the capacitor characteristics even under long-term high-temperature loads, and it is possible to extend the life of electrolytic capacitors. can.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は本発明の電解コンデンサの駆動用電解液におけ
るボロジサリチル酸アンモニクムの添加量と耐化成電圧
の関係を示す特性図である。
FIG. 1 is a characteristic diagram showing the relationship between the amount of ammonium borodisalicylate added to the driving electrolyte of the electrolytic capacitor of the present invention and the chemical formation voltage resistance.

Claims (1)

【特許請求の範囲】[Claims] (1)エチレングリコールを主体とする溶媒に、溶質と
して有機酸および無機酸またはそれらの塩の一種以上を
溶解した電解液に、ボロジサリチル酸またはその塩を溶
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 capacitor characterized in that borodisalicylic acid or its salt is dissolved in an electrolytic solution in which one or more organic acids, inorganic acids, or their salts are dissolved as solutes in a solvent mainly composed of ethylene glycol. driving electrolyte.
JP8181285A 1985-04-17 1985-04-17 Driving electrolytic liquid for electrolytic capacitor Pending JPS61240624A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8181285A JPS61240624A (en) 1985-04-17 1985-04-17 Driving electrolytic liquid for electrolytic capacitor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8181285A JPS61240624A (en) 1985-04-17 1985-04-17 Driving electrolytic liquid for electrolytic capacitor

Publications (1)

Publication Number Publication Date
JPS61240624A true JPS61240624A (en) 1986-10-25

Family

ID=13756907

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8181285A Pending JPS61240624A (en) 1985-04-17 1985-04-17 Driving electrolytic liquid for electrolytic capacitor

Country Status (1)

Country Link
JP (1) JPS61240624A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0291917A (en) * 1988-09-29 1990-03-30 Shinei Tsushin Kogyo Kk Electrolyte for driving electrolytic capacitor

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0291917A (en) * 1988-09-29 1990-03-30 Shinei Tsushin Kogyo Kk Electrolyte for driving electrolytic capacitor

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