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JPH031818B2 - - Google Patents
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JPH031818B2 - - Google Patents

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Publication number
JPH031818B2
JPH031818B2 JP9072185A JP9072185A JPH031818B2 JP H031818 B2 JPH031818 B2 JP H031818B2 JP 9072185 A JP9072185 A JP 9072185A JP 9072185 A JP9072185 A JP 9072185A JP H031818 B2 JPH031818 B2 JP H031818B2
Authority
JP
Japan
Prior art keywords
electrolytic
adipate
electrolytic capacitors
corrosion
symbol
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
Application number
JP9072185A
Other languages
Japanese (ja)
Other versions
JPS6150322A (en
Inventor
Kyoshi Sakamoto
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.)
Marcon Electronics Co Ltd
Original Assignee
Marcon Electronics 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 Marcon Electronics Co Ltd filed Critical Marcon Electronics Co Ltd
Priority to JP9072185A priority Critical patent/JPS6150322A/en
Publication of JPS6150322A publication Critical patent/JPS6150322A/en
Publication of JPH031818B2 publication Critical patent/JPH031818B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Primary Cells (AREA)
  • Secondary Cells (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は電解コンデンサをハロゲン化炭化水素
で洗浄した場合に、コンデンサ内部にハロゲン化
炭化水素が透過して生ずるコンデンサ素子の腐蝕
を防止することによつて、コンデンサの寿命特性
を向上せしめる電解コンデンサ用電解液に関す
る。 従来電極箔とスペーサーとを巻回してコンデン
サ素子を構成し、該コンデンサ素子をケースに収
凾してゴム栓により封口する電解コンデンサで、
コンデンサ素子に含浸する駆動用電解液にはエチ
レングリコール(以下EGと称する)−硼酸アンモ
ン系やEG−アジピン酸アンモニウム系などが用
いられていた。しかしながら、電解コンデンサの
洗浄工程や印刷基板へ取着するときに用いるハン
ダフラツクスの除去工程で洗浄剤として使用され
るハロゲン化炭化水素、例えば1.1.1トリクロロ
エタンは該ハロゲン化炭化水素への浸漬あるいは
蒸気浴などによつてゴム栓を透過してコンデンサ
内部へ浸入し分解して塩素イオンを生成してい
た。 このようにして生成された塩素イオンはコンデ
ンサ素子の電極箔および引出端子を腐蝕せしめる
が、この腐蝕は電解コンデンサに電圧を印加した
ときとくに著しく、ときには引出端子の断線を招
く欠点があつた。 本発明は上記の点に鑑みてなされたもので、洗
浄に使用するハロゲン化炭化水素がケース内部に
浸入しても腐蝕の発生を防止できる電解コンデン
サ用電解液を提供するもので、これによつて電解
コンデンサの寿命を向上せしめようとするもので
ある。以下実施例により説明する。 本発明になる電解液は水−アジピン酸アンモニ
ウム−エタノールアミンアジペート−残部がEG
からなるもので、その実施例の組成を表に示す。、
従来例1はEG−アジピン酸アンモニウム、従来
例2は若干の水を含んだ電解液で、特開昭54−
91754号公報に記載されているものである。
The present invention is for use in electrolytic capacitors that improve the life characteristics of capacitors by preventing corrosion of capacitor elements caused by penetration of halogenated hydrocarbons into the capacitors when electrolytic capacitors are cleaned with halogenated hydrocarbons. Regarding electrolyte. Conventional electrolytic capacitors consist of a capacitor element formed by winding an electrode foil and a spacer, and the capacitor element is housed in a case and sealed with a rubber stopper.
Ethylene glycol (hereinafter referred to as EG)-ammonium borate, EG-ammonium adipate, and the like have been used as driving electrolytes to impregnate capacitor elements. However, halogenated hydrocarbons, such as 1.1.1 trichloroethane, which are used as cleaning agents in the process of cleaning electrolytic capacitors and the process of removing solder flux used when attaching them to printed circuit boards, cannot be used by dipping them in the halogenated hydrocarbons or When exposed to steam baths, it penetrated the rubber plug and entered the capacitor, where it decomposed and produced chlorine ions. The chlorine ions thus generated corrode the electrode foils and lead terminals of the capacitor element, but this corrosion is particularly severe when voltage is applied to the electrolytic capacitor, and sometimes leads to disconnection of the lead terminals. The present invention has been made in view of the above points, and provides an electrolytic solution for electrolytic capacitors that can prevent corrosion even if halogenated hydrocarbons used for cleaning penetrate into the case. The aim is to improve the lifespan of electrolytic capacitors. This will be explained below using examples. The electrolyte of the present invention is water - ammonium adipate - ethanolamine adipate - the balance is EG.
The compositions of the examples are shown in the table. ,
Conventional Example 1 is EG-ammonium adipate, Conventional Example 2 is an electrolytic solution containing some water,
This is described in Publication No. 91754.

【表】 なお、表に記載されたモノ,ジ,トリエタノー
ルアミンアジペートはエタノールアミンアジペー
トの1種であり、アジピン酸とエタノールアミン
とを混合し加熱またはEG中で該混合を行うこと
により生成できるが、これらは40wt%を越える
とエチレングリコールに溶解しなくなる。またア
ジピン酸アンモニウムも同様20wt%を越えると
溶解しない。この表に示した組成からなる電解液
を電極箔とスペーサとを巻回して構成したコンデ
ンサ素子に含浸し、該コンデンサ素子をアルミニ
ウムからなるケースに収凾してゴム栓で封口した
定格50WV−1μFのリード線端子同一方向形電解
コンデンサを作り、該電解コンデンサを1.1.1ト
リクロロエタンの蒸気中に10分間浸漬したもの
各々50個を試料として105℃中に50V電圧印加し
て放置したときの特性を第1図〜第4図に示す。
すなわち第1図な放置時間と防爆弁動作数との関
係を示す曲線図であるが、1000hでは全数分解の
上確認した腐蝕数を示してある。第2図は放置時
間と静電容量変化率との関係、第3図は放置時間
とtanδとの関係、第4図は放置時間と漏れ電流と
の関係をそれぞれ示す曲線図である。なお第1図
〜第4図の曲線に付した記号は表に示したA〜J
の記号を用いたもので電解液の種別を表わしたも
のである。この結果によれば第1図の弁動作数に
おいて従来例1(記号A)、従来例2(記号B)で
は全数弁動作し、参考例3(記号I)では1000h
において7個の腐蝕が発生している。そして前記
曲線A,Bは分解調査結果、腐蝕現象が顕著であ
り腐蝕によつて内部圧力が上昇し防爆弁が動作し
たものである。また参考例1(記号G)は第2図
および第3図に示した静電容量変化率およびtanδ
が電解液の中に含む水によつて電解箔がベーマイ
ト反応を生ずるために変化が大きくなるものであ
り、参考例2(記号H)は電解液に水を全く含ま
ないので初期から比抵抗が大きいものである。ま
た参考例4(J)はアジピン酸ンモニウムを含まない
ので初期から非抵抗が大なるものである。 したがつて本発明になる電解液は水27〜5wt
%、アジピン酸アンモニウム20〜1wt%、エタノ
ールアミンアジペート40〜5wt%、残部がEGか
らなるということができる。 以下述べたように、本発明になる電解コンデン
サ用電解液を用いた電解コンデンサでは、ハロゲ
ン化炭化水素を洗浄液に使用してもコンデンサ内
部の腐蝕が発生せず、静電容量、tanδ、漏れ電流
の安定したものを得ることができる。勿論洗浄剤
としてハロゲン化炭化水素を使用しない場合でも
同様な特性を得ることができるのは述べるまでも
ないことである。
[Table] Mono-, di-, and triethanolamine adipate listed in the table is a type of ethanolamine adipate, and can be produced by mixing adipic acid and ethanolamine and heating or mixing in EG. However, these become insoluble in ethylene glycol when the amount exceeds 40 wt%. Similarly, ammonium adipate does not dissolve if it exceeds 20 wt%. A capacitor element made by winding electrode foil and a spacer was impregnated with an electrolytic solution having the composition shown in this table, and the capacitor element was housed in an aluminum case and sealed with a rubber plug. 1.1.1 Electrolytic capacitors with lead wire terminals in the same direction were made. 1.1.1 The electrolytic capacitors were immersed in trichloroethane vapor for 10 minutes. 50 pieces of each were used as samples to evaluate the characteristics when a voltage of 50 V was applied and left at 105°C. It is shown in FIGS. 1 to 4.
That is, FIG. 1 is a curve diagram showing the relationship between the standing time and the number of explosion-proof valve operations, and at 1000 hours, the number of corrosion confirmed after complete disassembly is shown. FIG. 2 is a curve diagram showing the relationship between the standing time and the capacitance change rate, FIG. 3 is a curve diagram showing the relationship between the standing time and tan δ, and FIG. 4 is a curve diagram showing the relationship between the standing time and leakage current. The symbols attached to the curves in Figures 1 to 4 are A to J shown in the table.
This symbol uses the symbol to represent the type of electrolyte. According to the results, all valves operated in conventional example 1 (symbol A) and conventional example 2 (symbol B) at the number of valve operations shown in Fig. 1, and in reference example 3 (symbol I), all valves operated for 1000 hours.
There were 7 areas of corrosion. As a result of the disassembly investigation, the curves A and B indicate that the corrosion phenomenon was remarkable, and the internal pressure rose due to the corrosion, causing the explosion-proof valve to operate. Reference example 1 (symbol G) has the capacitance change rate and tanδ shown in FIGS. 2 and 3.
However, the electrolytic foil undergoes a boehmite reaction due to the water contained in the electrolytic solution, resulting in a large change.In reference example 2 (symbol H), the electrolytic solution does not contain any water, so the specific resistance changes from the beginning. It's big. Further, since Reference Example 4 (J) does not contain ammonium adipate, it has a large non-resistance from the initial stage. Therefore, the electrolyte of the present invention contains 27 to 5 wt of water.
%, ammonium adipate 20-1 wt%, ethanolamine adipate 40-5 wt%, and the balance consists of EG. As described below, in the electrolytic capacitor using the electrolytic solution for electrolytic capacitors according to the present invention, corrosion does not occur inside the capacitor even when halogenated hydrocarbon is used as a cleaning solution, and the capacitance, tanδ, leakage current You can get a stable result. Of course, it goes without saying that similar characteristics can be obtained even when no halogenated hydrocarbon is used as the cleaning agent.

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

図面はいずれも本発明および従来例、参考例に
なる電解液を含浸した電解コンデンサを105℃中
に電圧印加して放置したときの放置時間と各特性
との関係を示す曲線図で、第1図は防爆弁動作
数、第2図は静電容量変化率、第3図はtanδ、第
4図は漏れ電流を示したものである。
The drawings are all curve diagrams showing the relationship between the standing time and each characteristic when electrolytic capacitors impregnated with an electrolyte according to the present invention, a conventional example, and a reference example are left with a voltage applied at 105°C. The figure shows the number of explosion-proof valve operations, Fig. 2 shows the capacitance change rate, Fig. 3 shows tan δ, and Fig. 4 shows the leakage current.

Claims (1)

【特許請求の範囲】[Claims] 1 水27〜5wt%、アジピン酸アンモニウム20〜
1wt%、エタノールアミンアジペート40〜5wt%、
残部がエチレングリコールからなる電解コンデン
サ用電解液。
1 Water 27~5wt%, ammonium adipate 20~
1wt%, ethanolamine adipate 40~5wt%,
Electrolyte for electrolytic capacitors, the remainder of which is ethylene glycol.
JP9072185A 1985-04-25 1985-04-25 Electrolyte for electrolytic condenser Granted JPS6150322A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9072185A JPS6150322A (en) 1985-04-25 1985-04-25 Electrolyte for electrolytic condenser

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9072185A JPS6150322A (en) 1985-04-25 1985-04-25 Electrolyte for electrolytic condenser

Publications (2)

Publication Number Publication Date
JPS6150322A JPS6150322A (en) 1986-03-12
JPH031818B2 true JPH031818B2 (en) 1991-01-11

Family

ID=14006411

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9072185A Granted JPS6150322A (en) 1985-04-25 1985-04-25 Electrolyte for electrolytic condenser

Country Status (1)

Country Link
JP (1) JPS6150322A (en)

Also Published As

Publication number Publication date
JPS6150322A (en) 1986-03-12

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