JPS622514A - Electrolytic capacitor - Google Patents

Electrolytic capacitor

Info

Publication number
JPS622514A
JPS622514A JP14198985A JP14198985A JPS622514A JP S622514 A JPS622514 A JP S622514A JP 14198985 A JP14198985 A JP 14198985A JP 14198985 A JP14198985 A JP 14198985A JP S622514 A JPS622514 A JP S622514A
Authority
JP
Japan
Prior art keywords
electrolytic capacitor
aluminum
salt
corrosion
electrolytic
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
JP14198985A
Other languages
Japanese (ja)
Other versions
JPH0334845B2 (en
Inventor
牧野 芳樹
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.)
SHINEI TSUSHIN KOGYO KK
Original Assignee
SHINEI TSUSHIN KOGYO KK
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 SHINEI TSUSHIN KOGYO KK filed Critical SHINEI TSUSHIN KOGYO KK
Priority to JP14198985A priority Critical patent/JPS622514A/en
Publication of JPS622514A publication Critical patent/JPS622514A/en
Publication of JPH0334845B2 publication Critical patent/JPH0334845B2/ja
Granted legal-status Critical Current

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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】 [産業上の利用分野] 本発明は、アルミニウム電解コンデンサに係り、特にハ
ロゲン系ITR溶剤の洗浄による陽極箔及び引き出しリ
ードタブ部の腐蝕を防Iしてさる電解液を用いた電解コ
ンデンサに関りるムのである。
[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to aluminum electrolytic capacitors, and in particular uses an electrolytic solution that prevents corrosion of the anode foil and pull-out lead tabs caused by cleaning with halogen-based ITR solvents. This is related to electrolytic capacitors.

[従来の技術と発明が解決しようとする問題点]ブ般に
、電解コンアン1ノは、高純度アルミニウム箔をエツチ
ングし、その表面を陽極酸化した陽極箔と、これに対向
するエツチングされたアルミ。
[Prior art and problems to be solved by the invention] In general, an electrolytic converter is made by etching a high-purity aluminum foil and using an anode foil whose surface is anodized, and an etched aluminum foil facing the anode foil. .

ニウム陰極箔との間に隔離紙を介在させて巻き取った構
造の素子に電解液を含浸し、この素子をアルミニウムケ
ースに収容して弾性封口体で密封し構成されている。
The device is constructed by impregnating an element with an electrolytic solution in a wound structure with a separator paper interposed between the aluminum cathode foil, housing the device in an aluminum case, and sealing it with an elastic sealing member.

近年、この電解コンデンサは、プリント基板に装着され
、半田付U後に半[1フラツクスの除去のため、1,1
.1−1−リクロロエタンや、トリクロロ1−リフロロ
エタンなどのハロゲン系有機溶剤により、基板洗浄が行
なわれている。
In recent years, this electrolytic capacitor is mounted on a printed circuit board, and after soldering U, half [1] is removed due to flux removal.
.. Substrate cleaning is performed using halogen-based organic solvents such as 1-1-lichloroethane and trichloro-1-lifluoroethane.

ところが、ハロゲン系有機溶剤は、電解コンデン1)゛
の封口体を拡散透過し、コンデンサ内の?tf解液中で
塩素イオンの解離を起こす。この解離した塩素イオンに
より、使用時に電解コンデンサの陽極箔及び、引き出し
り−ドタブ部が腐蝕を起こし、電解コンデンサの欠陥と
なっている。
However, halogen-based organic solvents diffuse through the sealing body of electrolytic condenser 1) and enter the capacitor. Dissociation of chloride ions occurs in the tf solution. These dissociated chlorine ions cause corrosion of the anode foil and lead-out tab portion of the electrolytic capacitor during use, resulting in defects in the electrolytic capacitor.

そのため従来番、L、弾性封口体表面に樹脂を塗イII
することにより、耐腐蝕性をもたせる方法が実施されて
いる。しかし、この方法では、小型化及びコス]・ダウ
ンの要求にそぐわない。
Therefore, it is necessary to apply resin on the surface of the conventional model, L, and the elastic sealing body II.
A method of imparting corrosion resistance has been implemented. However, this method does not meet the demands for miniaturization and cost reduction.

又、電解液にP−ニトロフェノールやP−ニトロ安息6
酸等の腐蝕防止剤を添加してハロゲン系6機溶剤に対し
、耐腐蝕性を向上さけることが知られているが、十分な
耐腐蝕性と言えず、1.1.1−トリクロロエタンによ
る洗浄に対しては、はとんど耐腐蝕性が得られでいない
In addition, P-nitrophenol or P-nitrobenz 6 is added to the electrolyte.
It is known to add corrosion inhibitors such as acids to improve corrosion resistance against halogen-based solvents, but it cannot be said that the corrosion resistance is sufficient, and cleaning with 1.1.1-trichloroethane is recommended. Corrosion resistance has not been achieved in most cases.

−・般に、塩素イ〕ンによるアルミニウムの腐蝕は次式 %式%] で表わされ、その腐蝕成長過程は、2つの段階に゛ 分
Gノられる。まず、第一段階では、塩素イオンがti接
アルミニウムの金属表面と反応してAj2cLaを生成
する。この第一段階は、アルミニウムの不fJJ態化ど
の競争反応であるため、反応速度はバい。
In general, the corrosion of aluminum by chlorine ions is expressed by the following formula: %, and the corrosion growth process can be divided into two stages. First, in the first step, chlorine ions react with the metal surface of aluminum in contact with Ti to generate Aj2cLa. Since this first step is a competitive reaction with the formation of aluminum into a non-fJJ state, the reaction rate is slow.

次の第二段階は、前記第一段階で9.成したΔff1c
f3の1度が増すことにJ:す、Aucf23が触媒ど
して働き、アルミニウムの金属表面を活性化してアルミ
ニウムの金属表面からΔ13+の溶出を容易に行うため
、塩素イオンと反応しやすくなり、腐蝕が急速に進行す
る。この第二段階の反応速度は、第一段階の反応に比べ
非常に速い。
The next second stage is 9. Δff1c
J: As f3 increases by 1 degree, Aucf23 acts as a catalyst, activates the metal surface of aluminum, and easily elutes Δ13+ from the metal surface of aluminum, making it easier to react with chlorine ions. Corrosion progresses rapidly. The reaction rate of this second stage is much faster than that of the first stage.

そこで、本発明者らは、金属イオン封鎖剤どして使用さ
れているエチレンジアミン四酢酸及び、ニトリロ三酢酸
又は、それらの塩が、前記第二段階の腐蝕にJ3いて、
八p3+の溶出を抑制する効果があり、腐蝕を防止でき
ることを見い出した。
Therefore, the present inventors discovered that ethylenediaminetetraacetic acid, nitrilotriacetic acid, or their salts, which are used as metal ion sequestering agents, are effective in the second stage of corrosion.
It has been found that it has the effect of suppressing the elution of 8p3+ and can prevent corrosion.

[発明の目的1 本発明は、これらの事情に鑑みてなされたもので、1,
1.1−1−リフし10エタンや、トリク[10トリフ
ロロエタン等のハロゲン系何重溶剤による電解コンデン
サの駐板洗浄に対して、電解液に十分な耐腐蝕性を与え
、陽極箔及び引き出しリードタブ部の腐蝕を防止し得る
ようにした電解コンデンIすを提供りることを目的とし
ている。
[Objective of the Invention 1 The present invention has been made in view of these circumstances, and includes the following:
1.1-1-It gives sufficient corrosion resistance to the electrolytic solution for cleaning the plate of electrolytic capacitors with halogen-based multi-layer solvents such as 10-ethane and trifluoroethane. An object of the present invention is to provide an electrolytic capacitor I which can prevent corrosion of a lead tab portion.

[問題点を解決するための手段及びその作用]前記目的
を達成づるため本発明による電解コンデンジは、エチレ
ングリコールを主溶媒とし、アジピン酸又は、その塩を
主電解質として溶解した電解液中に、エチレンジアミン
四酢酸又は、その塩及び二1〜リロ三酢酸又は、その塩
を添加溶解したしのである。
[Means for Solving the Problems and Their Effects] In order to achieve the above object, the electrolytic condenser according to the present invention contains ethylene glycol as the main solvent and adipic acid or a salt thereof as the main electrolyte in an electrolytic solution containing: Ethylenediaminetetraacetic acid or a salt thereof and di-1-lilotriacetic acid or a salt thereof are added and dissolved.

この電解コンデン勺では、前記第二段階の腐蝕にJ3い
て、アルミニウム金属表面からの八で34の溶出を抑制
し、陰極箔及び引き出しり−ドタブ部の腐蝕を防止り゛
ることができる。
In this electrolytic condenser, the second stage of corrosion can be suppressed, and the elution of aluminum from the surface of the aluminum metal can be suppressed, thereby preventing corrosion of the cathode foil and the lead-out tab.

[発明の実IM例] 以下、本発明に係る電解コンデンサの実施例を説明り゛
る。実施例は、一般の巻回構造のアルミニウム電解コン
デンサ“について説明されている。
[Practical IM Examples of the Invention] Examples of the electrolytic capacitor according to the present invention will be described below. The embodiment is described with respect to an aluminum electrolytic capacitor with a general wound structure.

実施例に用いられる電解コンデンサは、アルミニウム箔
を電気化学的にエツチング処理し、リン酸塩水溶液中に
て陽極酸化して表面に酸化皮膜を形成し、その後電極引
出し用リードタブを取りつりでアルミニウム陽極箔を作
成する。
The electrolytic capacitor used in the example is made by electrochemically etching aluminum foil, anodizing it in an aqueous phosphate solution to form an oxide film on the surface, and then attaching the lead tab for electrode extraction to the aluminum anode. Create foil.

一方、アルミニウム箔にエツチング処理を施した後、電
極引出し用リードタブを取り(=Jけてアルミニウム陰
極箔を作成し、上記陽+4i箔と上記陰極箔間にセパレ
ータ紙を重ね合わせて巻回することにより、コンデンサ
素子を製作する。そして、このコンデンサ素子に電解液
を含浸して例えば有底状アルミニウムケースに収容し、
該ケース開口を弾性封口体で密↑]して構成される。
On the other hand, after etching the aluminum foil, remove the lead tab for drawing out the electrode (=J) to create an aluminum cathode foil, overlap the separator paper between the positive +4i foil and the cathode foil, and wind it. Then, this capacitor element is impregnated with electrolyte and housed in, for example, a bottomed aluminum case.
The case opening is sealed with an elastic sealing member.

表−1に、エチレングリコールを主溶媒とし、アジピン
酸アンモニウムを主電解質として溶解した従来例の組成
と、これらの従来例に対しエチレンジアミン四酢酸及び
ニトリロ三WI酸を重量比にして0.1. 3.Owt
%添加溶解した電解液を用いる本発明実施例を示す。
Table 1 shows the composition of conventional examples in which ethylene glycol was used as the main solvent and ammonium adipate was dissolved as the main electrolyte, and the weight ratio of ethylenediaminetetraacetic acid and nitrilotriWI acid for these conventional examples was 0.1. 3. Owt
An example of the present invention using an electrolyte containing % added and dissolved is shown below.

以下余白 表−1に示ず本発明実施例及び従来例の電解コンデンυ
に用いられる電解液を使用し・て50W V −10μ
Fの電解コンデンサ゛を試作した。
The electrolytic condensers υ of the embodiments of the present invention and the conventional examples are not shown in the margin table-1 below.
50W V -10μ using the electrolyte used in
I made a prototype of an F electrolytic capacitor.

この供試コンデンサを、1,1.1−1−リクロロエタ
ン及びトリクロロトリフロロエタンの二種の溶剤につい
て、28K I−I Zの超音波洗浄を5分間行った。
This sample capacitor was subjected to 28K I-IZ ultrasonic cleaning for 5 minutes using two solvents: 1,1.1-1-lichloroethane and trichlorotrifluoroethane.

その後、105℃で定格電圧印加の高温負荷試験を行い
、500時間と 1,000時間後解体し、腐蝕発生率
(B蝕発生数/試験数)を調べた。
Thereafter, a high-temperature load test was conducted at 105° C. by applying a rated voltage, and after 500 hours and 1,000 hours, it was dismantled and the corrosion occurrence rate (number of B corrosion occurrences/number of tests) was investigated.

その結果を表−2に示す。The results are shown in Table-2.

以下余白 表−2に示した結果から、本発明の電解コンデンサは、
L+ 1.1−1−リクロロエタンによる洗浄に対シて
優れた耐腐蝕性を示し、トリクロロトリフロロエタンに
対しても優れた耐腐蝕効果がある。
From the results shown in Margin Table 2 below, the electrolytic capacitor of the present invention:
L+ 1. Shows excellent corrosion resistance when washed with 1-1-lichloroethane, and also has excellent corrosion resistance against trichlorotrifluoroethane.

尚、エチレンジアミン四酢酸及び、ニトリロ三酢酸の塩
についても同様の効果がある。
Incidentally, salts of ethylenediaminetetraacetic acid and nitrilotriacetic acid also have similar effects.

本発明のエチレンジアミン四酢酸又は、その塩及びニト
リロ三酢酸又はその塩の添加量は、重量化でo、iwt
%の微量においても、耐腐蝕性に効果があり、添加量が
増すほど耐腐蝕性を向上させることがわかった。即ら、
その添加量は■苗化で0.01〜10 wt%で良好で
ある。
The amount of ethylenediaminetetraacetic acid or its salt and nitrilotriacetic acid or its salt of the present invention is o, iwt by weight.
It has been found that even a small amount of % is effective for corrosion resistance, and as the amount added increases, corrosion resistance is improved. In other words,
The amount added is 0.01 to 10 wt% for seedling formation.

しかし、添加量をff1ffi比で10 wt%以上添
加しても、それに見合った効果が得られず、過飽和状態
となり、電解液に析出が起こり、良い特性が19られな
かっ!、:。
However, even if the addition amount is 10 wt% or more in terms of ff1ffi ratio, no commensurate effect can be obtained, a supersaturated state occurs, precipitation occurs in the electrolyte, and good characteristics cannot be obtained! , :.

[発明の効m] 以−り説明したように本発明によれば、1. L 1−
トリク0ロエタンや、]・]リクロロ1−リフロロエタ
ンのハロゲン系有機溶剤による電解]ンデン奢すの基板
洗浄に対して、′Fi解液に十分な耐病蝕性を与えるこ
とができ、陽極箔及び引き出しリードタブ部の腐蝕を防
1.でさる効果だある。
[Effects of the Invention] As explained below, according to the present invention, 1. L 1-
It is possible to provide sufficient corrosion resistance to the 'Fi solution for substrate cleaning using halogen-based organic solvents such as trichloroethane or ]. Prevents corrosion of lead tabs 1. It has a significant effect.

手記t’?r11.tlE’ii! (白R)昭和60
年 9J13日 昭和60年特gff願第141989号事件との関係 
  特許出願人 代表者 登  内  英  夫 5、拒絶理由通知のし1イ・1   自発1、明細お第
3ベニジ第14行の式が r [Au3+3ce−+Aid3] Jとあるをr[
/13++3cff−→AAd2allと補正しまづ。
Memo t'? r11. tlE'ii! (White R) Showa 60
9J13, 1985 Special GFF Application No. 141989
Representative Hideo Noboriuchi of the patent applicant 5, Notice of reasons for refusal 1 A. 1 Voluntary submission 1, the formula on the 14th line of the 3rd page of the specification is r [Au3+3ce-+Aid3] J is r [
/13++3cff-→AAd2all and corrected Shimazu.

以  上 手続?【11正書(自発) 昭和61年 9月18日that's all procedure? [11th official book (spontaneous) September 18, 1986

Claims (2)

【特許請求の範囲】[Claims] (1)アルミニウム電解コンデンサにおいて、エチレン
グリコールを主溶媒とし、アジピン酸又は、その1塩を
主電解質として溶解した電解液中に、エチレンジアミン
四酢酸又は、その塩及び、ニトリロ三酢酸又は、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。
(1) In an aluminum electrolytic capacitor, ethylenediaminetetraacetic acid or a salt thereof, and nitrilotriacetic acid or a salt thereof are added to an electrolytic solution containing ethylene glycol as the main solvent and adipic acid or a salt thereof as the main electrolyte. An electrolytic capacitor characterized by additive-dissolved.
(2)前記エチレンジアミン四酢酸又は、その塩及び、
ニトリロ三酢酸又は、その塩の添加量は、重量比0.0
1〜10wt%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。
(2) the ethylenediaminetetraacetic acid or a salt thereof;
The amount of nitrilotriacetic acid or its salt added is 0.0 by weight.
The electrolytic capacitor according to claim 1, wherein the content is 1 to 10 wt%.
JP14198985A 1985-06-27 1985-06-27 Electrolytic capacitor Granted JPS622514A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14198985A JPS622514A (en) 1985-06-27 1985-06-27 Electrolytic capacitor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14198985A JPS622514A (en) 1985-06-27 1985-06-27 Electrolytic capacitor

Publications (2)

Publication Number Publication Date
JPS622514A true JPS622514A (en) 1987-01-08
JPH0334845B2 JPH0334845B2 (en) 1991-05-24

Family

ID=15304804

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14198985A Granted JPS622514A (en) 1985-06-27 1985-06-27 Electrolytic capacitor

Country Status (1)

Country Link
JP (1) JPS622514A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0356798A1 (en) * 1988-08-12 1990-03-07 Bando Chemical Industries, Limited Flat belt and pulley transmission
US6288889B1 (en) 1998-12-01 2001-09-11 Rubycon Corporation Electrolytic solution for electrolytic capacitor and electrolytic capacitor using the same
JP4861983B2 (en) * 2004-08-04 2012-01-25 オーチス エレベータ カンパニー Sheaves used in elevator systems

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5892207A (en) * 1981-11-29 1983-06-01 日本ケミコン株式会社 Electrolyte for driving electrolytic condenser
JPS61191011A (en) * 1985-02-20 1986-08-25 三洋電機株式会社 Electrolytic liquid for driving electrolytic capacitor

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5892207A (en) * 1981-11-29 1983-06-01 日本ケミコン株式会社 Electrolyte for driving electrolytic condenser
JPS61191011A (en) * 1985-02-20 1986-08-25 三洋電機株式会社 Electrolytic liquid for driving electrolytic capacitor

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0356798A1 (en) * 1988-08-12 1990-03-07 Bando Chemical Industries, Limited Flat belt and pulley transmission
US6288889B1 (en) 1998-12-01 2001-09-11 Rubycon Corporation Electrolytic solution for electrolytic capacitor and electrolytic capacitor using the same
EP1006536A3 (en) * 1998-12-01 2003-01-15 Rubycon Corporation Electrolytic solution for electrolytic capacitor and electrolytic capacitor using the same
JP4861983B2 (en) * 2004-08-04 2012-01-25 オーチス エレベータ カンパニー Sheaves used in elevator systems

Also Published As

Publication number Publication date
JPH0334845B2 (en) 1991-05-24

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