JPS584917A - Electrolyte for driving aluminum electrolytic condenser - Google Patents

Electrolyte for driving aluminum electrolytic condenser

Info

Publication number
JPS584917A
JPS584917A JP10892982A JP10892982A JPS584917A JP S584917 A JPS584917 A JP S584917A JP 10892982 A JP10892982 A JP 10892982A JP 10892982 A JP10892982 A JP 10892982A JP S584917 A JPS584917 A JP S584917A
Authority
JP
Japan
Prior art keywords
electrolytic solution
capacitor
electrolyte
aluminum electrolytic
corrosion
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
JP10892982A
Other languages
Japanese (ja)
Other versions
JPS6258650B2 (en
Inventor
宇都宮 昭平
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
Sanyo Denki Co Ltd
Original Assignee
Sanyo Electric Co Ltd
Sanyo Denki 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, Sanyo Denki Co Ltd filed Critical Sanyo Electric Co Ltd
Priority to JP10892982A priority Critical patent/JPS584917A/en
Publication of JPS584917A publication Critical patent/JPS584917A/en
Publication of JPS6258650B2 publication Critical patent/JPS6258650B2/ja
Granted legal-status Critical Current

Links

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】 本発明はアルミニウム電解コンデンサ駆動用電解液の改
良に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to improvements in electrolytes for driving aluminum electrolytic capacitors.

従来、との櫨電解液として、エチレングリコールを主溶
媒とし、これに有機カルボン酸のアンモニウム塩を溶解
したものが知られている。
BACKGROUND ART Conventionally, a solution in which an ammonium salt of an organic carboxylic acid is dissolved in ethylene glycol as a main solvent is known as an electrolytic solution.

斯る電解液は、コンデンサの低温特性などに於て秀れた
効果をもたらすが、半面、コンデンサの高温負荷試験中
に腐蝕が発生する欠点を信する。
Such an electrolyte has excellent effects on the low-temperature characteristics of the capacitor, but on the other hand, it has the drawback of causing corrosion during a high-temperature load test of the capacitor.

即ち、rの腐蝕を、図の典型的アルミニウム電解コンデ
ンサに於て説明すると、コンデンサは、巻回素子(l、
該素子を収納するケース(2)、該ケースの開口を封口
し、合成樹脂板(4)及びゴム板(5)の合体からなる
封口板(3)、外部端子(6)、該外部端子とリード箔
(ηとを接続する内部端子(8)とから構成されるが、
高温負荷試験中に、特に9−ド箔(7)や内部端子(8
)K腐蝕が見られる。腐蝕は充放電やリップル電流を流
すことkより加速され、ついにはリード箔(ηなどが腐
蝕切断されるに至る。
That is, to explain the corrosion of r in the typical aluminum electrolytic capacitor shown in the figure, the capacitor has a wound element (l,
A case (2) that houses the element, a sealing plate (3) that seals the opening of the case and is made of a combination of a synthetic resin plate (4) and a rubber plate (5), an external terminal (6), and a sealing plate (3) that seals the opening of the case, an external terminal (6), and It consists of an internal terminal (8) that connects the lead foil (η),
During the high temperature load test, especially the 9-wire foil (7) and internal terminals (8)
) K corrosion is seen. Corrosion is accelerated by charging/discharging and flowing ripple current, and eventually lead foils (η, etc.) are corroded and cut.

従って本発明目的は、エチレングリコールと有機カルボ
ン酸のアンモニウム塩との組合せになる電解液に於て、
その秀れた特性を損うことなく、上記腐蝕の発生を防止
し得る改良されたアルミニウム電解コンデンサ駆動用電
解液を提供するKある。
Therefore, the object of the present invention is to provide an electrolytic solution that is a combination of ethylene glycol and an ammonium salt of an organic carboxylic acid.
An object of the present invention is to provide an improved electrolytic solution for driving an aluminum electrolytic capacitor that can prevent the above-mentioned corrosion without impairing its excellent properties.

即ち、本発明電解液は、主溶媒エチレングリコールにイ
オノーゲンとして有機カルボン酸のアンモニウム塩を溶
解した電解液に酸化ホウ素(B!05)を0.5〜10
重量%添加したことを特徴とする特のであり、これによ
り、特に、ポリプロピレン樹脂を内面とする封口板で封
口されたアルミニウム!解コンデンサに射いて、所期の
目的が有効に達せられる。
That is, the electrolytic solution of the present invention is prepared by dissolving an ammonium salt of an organic carboxylic acid as an ionogen in ethylene glycol as a main solvent, and adding 0.5 to 10% of boron oxide (B!05) to the electrolytic solution.
It is characterized by the addition of % by weight, which makes it especially suitable for aluminum sealed with a sealing plate whose inner surface is made of polypropylene resin! the intended purpose can be effectively achieved.

本発明電解液に於て、酸化ホウ素の添加量が0.5重量
係より少ない場合には腐蝕抑制または防止効果がほとん
ど認められず、一方10重量%を越えると腐蝕防止効果
は十分であるもの\、副作用として電解液の粘度が高く
なり、電導間も低くなるため、コンデンサの低湿特性に
於ける容量減少及び損失の増大を来たし好ましくない。
In the electrolytic solution of the present invention, when the amount of boron oxide added is less than 0.5% by weight, almost no corrosion suppression or prevention effect is observed, whereas when it exceeds 10% by weight, the corrosion prevention effect is sufficient. As a side effect, the viscosity of the electrolytic solution increases and the conductivity decreases, which is undesirable because it causes a decrease in capacity and an increase in loss in the low humidity characteristics of the capacitor.

従ってこれらの添加量範囲は本発明から除外される。Therefore, these addition amount ranges are excluded from the present invention.

又、本発明電解液に於て、有機カルボン酸のアンモニウ
ム塩としては、アジピン酸、スペリン酸、セパチン酸な
どの各アンモニウム塩が好適である。
In the electrolytic solution of the present invention, ammonium salts of organic carboxylic acids such as adipic acid, speric acid, and sepatic acid are suitable.

史に、本発明電解液に於て、溶媒としてのエチレングリ
コールと溶質としての何機カルボン酸のアンモニウム塩
との含有割合は任意であり、通常期る溶質は溶解量限度
内で使用される。
Historically, in the electrolytic solution of the present invention, the content ratio of ethylene glycol as a solvent and the ammonium salt of an organic carboxylic acid as a solute is arbitrary, and the solute is usually used within the solubility limit.

以下本発明実施例を述べる。Examples of the present invention will be described below.

本発明実施例に於て、添加剤である酸化ホウ素は溶媒に
100℃前後で良く溶解し、従って通常の手法で溶媒、
溶質及び添加剤が混合されて電解液が作成され、次いで
その電解液を用いて既述の図示せる形態のコンデンサが
作成された。以下の試験は斯るコンデンサによりなされ
たものである。
In the examples of the present invention, boron oxide, which is an additive, dissolves well in a solvent at around 100°C.
The solute and additives were mixed to form an electrolyte, which was then used to form a capacitor of the form described and illustrated. The following tests were conducted with such a capacitor.

尚コンデンサの定格は140v、680μFであり、又
リップル負荷試験は、温度85℃、リップル電流60t
h、2人、電流印加時間500時間の条件下で行なわれ
た。
The capacitor rating is 140V and 680μF, and the ripple load test was conducted at a temperature of 85℃ and a ripple current of 60t.
Testing was conducted under the conditions of 2 people and a current application time of 500 hours.

第1表 第1表に於て、Z/Z □は一25℃に於ける120−
でのインピーダンス(勾と千20℃に於ける120出で
のインピーダンス(zO)との比を表わし、この値が小
さいほど低温性が秀れている。又第1表の試験に供され
たコンデンサの封口板(3)を構成する合成樹脂板(4
)(図面参照)はフェノール樹脂からなる6 第1表から明らかな如く、エチレングリコールと有機カ
ルボン酸のアンモニウム塩からなる基本電解液に酸化ホ
ウ素を添加した場合、基本電解液の秀れた低温特性をほ
とんど損うことなく有効な腐蝕防止をなすことができる
Table 1 In Table 1, Z/Z □ is 120- at -25℃
It represents the ratio of the impedance (zO) at 120°C and the impedance (zO) at 1,200°C, and the smaller this value is, the better the low-temperature performance is. Synthetic resin plate (4) constituting the sealing plate (3) of
) (see drawing) is made of phenolic resin 6 As is clear from Table 1, when boron oxide is added to a basic electrolyte consisting of ethylene glycol and an ammonium salt of an organic carboxylic acid, the basic electrolyte has excellent low-temperature properties. Effective corrosion prevention can be achieved with almost no damage to the surface.

尚、ポリプロピレン樹脂はフェノール樹脂よりも電解液
による腐蝕が現われ錐く、従って合成樹脂板(4)をポ
リプロピレン樹脂で形成した場合にも、当然有効な腐蝕
防止効果を得ることができる。
It should be noted that polypropylene resin is more susceptible to corrosion by electrolyte than phenol resin, so even when the synthetic resin plate (4) is made of polypropylene resin, it is naturally possible to obtain an effective corrosion prevention effect.

斯る酸化ホウ素の添加効果はその添加量によって左右さ
れる。第2表に、基本電解液としてエチレングリコール
とアジピン酸アンモニウムを選んだ場合を典型例として
添加量効果を代表的に示す。
The effect of adding boron oxide depends on the amount added. Table 2 shows the additive amount effect as a typical example when ethylene glycol and ammonium adipate are selected as the basic electrolyte.

以下余白 第2表 第2表に於て、2μGは第1表と同義であり、又、ム及
びBは夫々、第2表の試験に供されたコンデンサの封口
板(3)の内面を構成する合成樹脂板(4)がフェノ−
少樹脂製である場合及びポリプロピレン樹脂製である場
合を系す。
Margin Table 2 In Table 2 below, 2μG has the same meaning as in Table 1, and M and B respectively constitute the inner surface of the sealing plate (3) of the capacitor subjected to the test in Table 2. The synthetic resin plate (4)
This includes cases where it is made of a small amount of resin and cases where it is made of polypropylene resin.

第2表から明らかな如く、合成樹脂板(4)がポリプロ
ピレン製の場合酸化ホウ素の添加量が0.5〜10重量
係重量器で有効である。
As is clear from Table 2, when the synthetic resin plate (4) is made of polypropylene, it is effective to add boron oxide in an amount of 0.5 to 10 by weight.

尚、本発明に於て、水素ガス発生によるコンデンサ内圧
上昇を防ぐための水素吸収剤を更に添加しても、斯る水
素吸収剤及び酸化ホウ素の夫々の効果は有効に生ずるこ
とが確認された。例えば、エチレングリコール1o o
 cc、アジピン酸アンモニウム5Pからなる基本電解
液に酸化ホウ素2重量%及び水素吸収剤としてのジニト
ロフェノール0.5Pを添加した電解液を用いて第1表
と同種の試験をなしたところ、2β0が1.16、腐蝕
発生がなく更にコンデンサ内圧の上昇も認められなかっ
た。
Furthermore, in the present invention, it has been confirmed that even if a hydrogen absorbent is further added to prevent an increase in the internal pressure of the capacitor due to the generation of hydrogen gas, the respective effects of the hydrogen absorbent and boron oxide are effectively produced. . For example, ethylene glycol 1o o
When the same type of test as shown in Table 1 was carried out using an electrolytic solution prepared by adding 2% by weight of boron oxide and 0.5P of dinitrophenol as a hydrogen absorbent to a basic electrolytic solution consisting of cc, ammonium adipate 5P, 2β0 was 1.16, no corrosion occurred, and no increase in the internal pressure of the capacitor was observed.

以上の説明より明らかな如く、本発明によれば、主溶媒
エチングリコールにイオノーゲンとして有機カルボン酸
のアンモニウム塩を溶解した電解液に酸化ホウ素を添加
することによりポリプロピレン樹脂を内面とする封口板
で封口されたコンデンサ内での腐蝕が防止されて信頼性
の高いアルミニウム電解コンデンサを得ることができる
As is clear from the above description, according to the present invention, boron oxide is added to an electrolytic solution in which an ammonium salt of an organic carboxylic acid as an ionogen is dissolved in ethyne glycol as a main solvent, and the sealing plate is sealed with a polypropylene resin inner surface. Corrosion within the capacitor is prevented and a highly reliable aluminum electrolytic capacitor can be obtained.

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

図は典型的なアルミニウム電解コンデ。ンサの断面図を
示し、(1)は巻回素子、(2)はケース、(3)は封
口板である。 63−
The figure shows a typical aluminum electrolytic capacitor. 1 shows a cross-sectional view of the sensor, in which (1) is a winding element, (2) is a case, and (3) is a sealing plate. 63-

Claims (1)

【特許請求の範囲】[Claims] (1)  ポリプロピレン樹脂を内面とする封口板で封
口されたアルミニウム電解コンデンサ用電解液であって
、主溶媒エチレングリコールにイオノーゲンとしてスペ
リン酸、アジピン酸又はセパチン酸のアンモニウム塩を
溶解した電解液に酸化ホウ素を0.5〜10重量係添加
したことを特徴とするアルミニウム電解コンデンサ駆動
用電解液。
(1) An electrolytic solution for aluminum electrolytic capacitors sealed with a sealing plate with a polypropylene resin inner surface, which is oxidized into an electrolytic solution in which ammonium salts of speric acid, adipic acid, or sepatic acid are dissolved as ionogen in ethylene glycol as the main solvent. An electrolytic solution for driving an aluminum electrolytic capacitor, characterized in that boron is added in a proportion of 0.5 to 10% by weight.
JP10892982A 1982-06-23 1982-06-23 Electrolyte for driving aluminum electrolytic condenser Granted JPS584917A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10892982A JPS584917A (en) 1982-06-23 1982-06-23 Electrolyte for driving aluminum electrolytic condenser

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10892982A JPS584917A (en) 1982-06-23 1982-06-23 Electrolyte for driving aluminum electrolytic condenser

Publications (2)

Publication Number Publication Date
JPS584917A true JPS584917A (en) 1983-01-12
JPS6258650B2 JPS6258650B2 (en) 1987-12-07

Family

ID=14497231

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10892982A Granted JPS584917A (en) 1982-06-23 1982-06-23 Electrolyte for driving aluminum electrolytic condenser

Country Status (1)

Country Link
JP (1) JPS584917A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04284614A (en) * 1991-03-13 1992-10-09 Hitachi Aic Inc Electrolyte for electrolytic capacitor

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7420381B2 (en) 2004-09-13 2008-09-02 Cascade Microtech, Inc. Double sided probing structures

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04284614A (en) * 1991-03-13 1992-10-09 Hitachi Aic Inc Electrolyte for electrolytic capacitor

Also Published As

Publication number Publication date
JPS6258650B2 (en) 1987-12-07

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