JPH03102811A - Electrolyte for electrolytic capacitor - Google Patents

Electrolyte for electrolytic capacitor

Info

Publication number
JPH03102811A
JPH03102811A JP1239324A JP23932489A JPH03102811A JP H03102811 A JPH03102811 A JP H03102811A JP 1239324 A JP1239324 A JP 1239324A JP 23932489 A JP23932489 A JP 23932489A JP H03102811 A JPH03102811 A JP H03102811A
Authority
JP
Japan
Prior art keywords
water
cleanser
butyrolactone
dialkylamine
monoalkylamine
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
JP1239324A
Other languages
Japanese (ja)
Inventor
Kenichi Iida
飯田 謙一
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.)
Lincstech Circuit Co Ltd
Original Assignee
Hitachi AIC Inc
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 Hitachi AIC Inc filed Critical Hitachi AIC Inc
Priority to JP1239324A priority Critical patent/JPH03102811A/en
Publication of JPH03102811A publication Critical patent/JPH03102811A/en
Pending legal-status Critical Current

Links

Landscapes

  • Detergent Compositions (AREA)

Abstract

PURPOSE:To prevent deterioration of characteristic due to cleaning with cleanser of halogen hydrocarbon by dissolving benzoic acid as solute in solvent containing gamma-butyrolactone as a main ingredient, ethylene glycol and water, dissolving monoalkylamine or dialkylamine, and specifying its pH. CONSTITUTION:Solvent of electrolyte contains gamma-butyrolactone as a main ingredient, 25wt.% or less of ethylene glycol and 0.1-8wt.% of water. Benzoic acid is dissolved as salute. In order to adjust its pH to 4-7.5, monoalkylamine or dialkylamine is added. The gamma-butyrolactone of the main ingredient in the solvent surrounds the halogen cleanser molecules to prevent the cleanser from being brought into contact with the water so as to suppress hydrolysis. The monoalkylamine or dialkylamine traps chlorine ions generated through the hydrolysis of the cleanser and exhibits strong correction suppressing action.

Description

【発明の詳細な説明】 (産業上の利用分腎) 本発明は電解コンデンサ用電解液に関する。[Detailed description of the invention] (Industrial use portion) The present invention relates to an electrolytic solution for electrolytic capacitors.

(従米の技術) 従来のアルミ雷解コンデンサ等の電解コンデンサは、リ
ード線を接続した陽極箔とセパレータと陰極箔とを重ね
巻回してコンデンサ素子を形成し、これに電解液を含浸
してケースに収納し、このケースに蓋を取り付けて密封
した構造になって(Xる。
(Junior's technology) Conventional electrolytic capacitors such as aluminum lightning capacitors are made by winding an anode foil connected to a lead wire, a separator, and a cathode foil in layers to form a capacitor element, which is then impregnated with an electrolytic solution to form a case. It is stored in a case, and a lid is attached to the case to create a sealed structure (Xu).

陽#1箔と陰極箔とは、エッチングしたアルミニウム箔
を用い、特に前者は化成して誘電体酸化皮膜を形成して
いる。
Etched aluminum foils are used for the positive #1 foil and the negative electrode foil, and in particular, the former is chemically converted to form a dielectric oxide film.

ところで、プリント基板に電解コンデンサ等の電子部品
を接続した場合、接続に用いられた半田に含まれるフラ
ックスや汚れを除去するために、1,1.1−トリクロ
ロエタ゛ンや1,1.2−トリクロロー1,2.2−ト
リフロロエタン(フロン113)などのハロゲン系の洗
浄剤を用いて洗浄処理を行なっている。
By the way, when electronic components such as electrolytic capacitors are connected to a printed circuit board, 1,1,1-trichloroethane or 1,1,2-trichloroethane is used to remove flux and dirt contained in the solder used for connection. The cleaning process is performed using a halogen-based cleaning agent such as 1,2,2-trifluoroethane (Freon 113).

(発明が解決しようとする課題) しかし、従来の構造の毘解コンデンサでは、洗浄液がケ
ースと益の隙間から侵入することがある。
(Problem to be Solved by the Invention) However, in the permeation capacitor having the conventional structure, cleaning liquid may sometimes enter through the gap between the case and the case.

ケース内に洗浄液が侵入すると、電解液中に含まれる水
分と反応して塩素イオンが遊離づるが、この塩素イオン
のために陽極箔や陰極箔が腐食を起こす。その結果、電
解コンデンサの毒気特性が著しく劣化しあるいはコンデ
ンザとしての機能が失われる等の不良が生じる。
When the cleaning solution enters the case, it reacts with the water contained in the electrolyte to liberate chlorine ions, which cause corrosion of the anode and cathode foils. As a result, defects such as significant deterioration of the electrolytic capacitor's gas characteristics or loss of its function as a capacitor occur.

この欠点を防止するために、蓋の外表面にエボキシ樹脂
を塗布する構造とした電解コンデンサもあるが、樹脂の
塗布及びその硬化処理が必要で、製造工程が複雑になり
、時間がかかる欠点がある。
In order to prevent this drawback, some electrolytic capacitors have a structure in which epoxy resin is applied to the outer surface of the lid, but this requires the application of the resin and its curing process, making the manufacturing process complicated and time-consuming. be.

また、電解液に、P−ニトロフェノールやP二トロ安息
香酸等のニトロ化合物や銀化合物等のgf!防止剤を添
加する場合もある。しかし、P二トロフェノールは黄色
で極めて強い染色性があり、ケースや作業名の手等に付
肴して着色し、作業性に問題がある。そしてP−ニトロ
安息香酸は、染色性の問題はないが少量を添加した場合
にも火花定圧が低下し、耐圧が低い欠点がある。また、
従来の腐食防止剤は、FA素の解離の少ないフロン11
3に対しては比較的良好な腐食抑制効果を示すが、1.
1.1−トリクロ口エタンに対してはその効果が低い欠
点がある。
In addition, gf! such as nitro compounds such as P-nitrophenol and P-nitrobenzoic acid, and silver compounds are added to the electrolyte. Inhibitors may also be added. However, P-nitrophenol is yellow and has an extremely strong staining property, which causes problems in workability as it stains cases, hands, etc. P-nitrobenzoic acid does not have any dyeing problems, but even when added in a small amount, the constant spark pressure decreases and the pressure resistance is low. Also,
Conventional corrosion inhibitors are Freon 11, which has less dissociation of FA elements.
It shows a relatively good corrosion inhibiting effect against 1.
1.1-Trichloroethane has the disadvantage of low effectiveness.

本発明は、以上の欠点を改良し、ハロゲン系炭化水木系
の洗浄液による洗浄によって発生づる特性劣化等を防止
しうる毒解コンデンサ用電解液を捉仇することを目的と
するものである。
The object of the present invention is to improve the above-mentioned drawbacks and to provide an electrolytic solution for detoxification capacitors that can prevent the deterioration of characteristics caused by cleaning with a halogenated hydrocarbon-based cleaning solution.

(課題を解決するための手段) 本允明は上記の目的を辻成するために、γ−ブチロラク
トンを主成分とし、エチレングリコールを25wt%以
下、水を0.1〜3wt%含む溶媒中に、安息香酸を溶
質として溶解するとともに、モノアルキルアミンまたは
ジアルキルアミンを溶解し、PHを4〜7.5にした電
解コンデンサ用毒解液を提供するものである。
(Means for Solving the Problems) In order to achieve the above-mentioned objectives, Masaaki Moto developed a solution containing γ-butyrolactone as a main component, 25 wt% or less of ethylene glycol, and 0.1 to 3 wt% of water. The present invention provides a detoxification solution for electrolytic capacitors, which has benzoic acid as a solute and monoalkylamine or dialkylamine dissolved therein to have a pH of 4 to 7.5.

(作用) 溶媒中の主成分であるγ−ブチロラクトンは、ハロゲン
系洗浄液分子のまわりを取り囲み、洗浄液が水と接触す
るのを訪止し、加水分解を抑制する作用がある。
(Function) γ-Butyrolactone, which is the main component in the solvent, surrounds the molecules of the halogen-based cleaning liquid, prevents the cleaning liquid from coming into contact with water, and has the effect of suppressing hydrolysis.

また、モノアルキルアミンやジアルキルアミンは、洗浄
液が加水分解して発生する塩素イオンをトラップし、強
い腐食抑制作用を示す。
Furthermore, monoalkylamines and dialkylamines trap chlorine ions generated by hydrolysis of the cleaning solution, and exhibit a strong corrosion inhibiting effect.

(実施例) 以下、本発明を実施例に基づいて説明する。(Example) Hereinafter, the present invention will be explained based on examples.

霜解液の溶媒は、γ−ブチロラクトンを主成分とし、エ
チレングリコールを25wt%以下、水を0.1〜8w
t%とじた成分からなる。
The solvent for the defroster solution is mainly composed of γ-butyrolactone, 25 wt% or less of ethylene glycol, and 0.1 to 8 w of water.
Consists of t% components.

溶質としては安息香酸を溶解する。Dissolves benzoic acid as a solute.

また、PHを4〜7.5に調整する!こめに、七ノアル
キルアミンやジアルギルアミンを添加する●モノアルギ
ルアミンにはモノメチルアミンやモノエチルアミン、モ
ノブロビルアミンを用いる。ジアルキルアミンにはジメ
チルアミンやジエチルアミン、ジブロピルアミンを用い
る。
Also, adjust the pH to 4-7.5! Then, add heptanoalkylamine or dialgylamine. ●For monoargylamine, use monomethylamine, monoethylamine, or monobrobylamine. Dimethylamine, diethylamine, or dibropylamine is used as the dialkylamine.

次に、本発明の実施例、比較例及び従来例の雷解液を含
浸して、定格250V−470μFのアルミ雷解コンデ
ンサを′!J造する。そしてこれらのコンデン→ノを、
洗浄槽に入れて温度50℃の1,1, ”L−トリクロ
ロエタンを注入し、15分間洗浄した後、温度110℃
の高温Igt〜に入れ、泪圧250Vを印加して高温負
荷試験を行い、腐食の介生状況を調べた。試料数は、実
施例、比較例及び従来例とも30lI!Iとし、試験時
間500hr後に10側を解体し、試験時間1000h
r後に残りの20個を解体し、各々腐食の允生状況を調
査した。
Next, an aluminum lightning capacitor with a rating of 250V-470 μF was made by impregnating it with the lightning solution of the embodiment of the present invention, the comparative example, and the conventional example! J-build. And these condensation→ノ,
Pour 1,1,"L-trichloroethane at a temperature of 50℃ into a cleaning tank, wash for 15 minutes, and then reduce the temperature to 110℃.
A high-temperature load test was conducted by placing the specimen in a high-temperature Igt ~ and applying a pressure of 250 V to investigate the state of corrosion. The number of samples is 30lI for the example, comparative example, and conventional example! After the test time of 500 hours, the 10th side was disassembled and the test time was 1000 hours.
After that, the remaining 20 pieces were dismantled and the corrosion status of each piece was investigated.

結果は表の通りとなった。The results were as shown in the table.

以下衆白。Below is the crowd.

表から明らかな通り、本発明の実施例1〜実施例4によ
れば、5 0 0 hrl及び1000hr後も腐食は
零であるのに対して、従来例1及び従来例2によれば1
000hr後には全数にr94食が発生していた.また
、比較例1及び比較例2がら明らかな通り、エチレング
リコールの含有率が25w【%を越えると1000hr
後には各々8問及び12個腐食が発生し、腐食抑制の効
果が低下する。また、比較@3及び比較例4から明らか
な通り、水が含まれないと,比抵抗が増加し、本発明の
通り、水を含有する方が比抵抗を下げることができる。
As is clear from the table, according to Examples 1 to 4 of the present invention, there was no corrosion even after 500 hr and 1000 hr, while in Conventional Example 1 and Conventional Example 2, the corrosion was 1.
After 000 hours, r94 meals had occurred in all the animals. Furthermore, as is clear from Comparative Example 1 and Comparative Example 2, if the content of ethylene glycol exceeds 25w%, the
Afterwards, corrosion occurs in 8 and 12 cases, respectively, and the corrosion suppression effect decreases. Further, as is clear from Comparison @ 3 and Comparative Example 4, when water is not included, the specific resistance increases, and as per the present invention, when water is included, the specific resistance can be lowered.

また、溶媒がγ−ブチロラクトン75Wt%、エチレン
グリコールiQwt%、水、溶質として安息香M10w
t%、そしてジエチルアミン5wt%からなる電解液に
おいて、水の含有量を変えたときの比抵抗の変化を図に
示した。
In addition, the solvent was γ-butyrolactone 75wt%, ethylene glycol iQwt%, water, and the solute was benzoin M10w.
The figure shows the change in specific resistance when the water content is changed in an electrolytic solution consisting of 5 wt % of diethylamine and 5 wt % of diethylamine.

図から明らかな通り、水の含有堡がBwt%を越えると
ほとんど比抵抗が変化しない。また、一般に、水の添加
吊が多くなるとガス発生童が多くなり、コンデンサの寿
命が短かくなることが知られている。さらに、水を添加
しないと、化成性が非常に悪くなる。従って、水の添加
生は0.1〜8w1%が適当である。
As is clear from the figure, when the water content exceeds Bwt%, the specific resistance hardly changes. Furthermore, it is generally known that the more water is added, the more gases are generated and the life of the capacitor is shortened. Furthermore, if water is not added, the chemical formation properties will be very poor. Therefore, the appropriate amount of water to be added is 0.1 to 8w1%.

《介明の効宋冫 以上の通り、本発明によれば、γ〜プチロラクトンを主
成分とし、七ノアルキルアミンやジアルキルアミンを溶
解しているために腐食抑制効果を向上でき、また、安息
香酸を溶解することにより火花電圧を高くでき、さらに
、エヂレングリコールを25W【%以下、水を0.1〜
8Wt%の範囲で添加することにより比抵抗の低い竜解
コンデンサ用用解液が得られる。
As described above, according to the present invention, the corrosion inhibiting effect can be improved because the main component is γ-butyrolactone and heptanoalkylamine and dialkylamine are dissolved. By dissolving ethylene glycol, the spark voltage can be increased by dissolving
By adding in a range of 8 wt%, a solution for a dragon capacitor with low resistivity can be obtained.

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

図は電解液中の水の含有坐を変えたときの比抵抗の変化
のグラフを示す。
The figure shows a graph of changes in specific resistance when the content of water in the electrolyte is changed.

Claims (1)

【特許請求の範囲】[Claims] (1) γ−ブチロラクトンを主成分とし、エチレング
リコールを25wt%以下、水を0.1〜8wt%含む
溶媒中に、安息香酸を溶質として溶解するとともに、モ
ノアルキルアミンまたはジアルキルアミンを溶解し、P
Hを4〜7.5にした電解コンデンサ用電解液。
(1) In a solvent containing γ-butyrolactone as a main component, 25 wt% or less of ethylene glycol, and 0.1 to 8 wt% of water, benzoic acid is dissolved as a solute, and monoalkylamine or dialkylamine is dissolved, P
An electrolytic solution for electrolytic capacitors with H of 4 to 7.5.
JP1239324A 1989-09-14 1989-09-14 Electrolyte for electrolytic capacitor Pending JPH03102811A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1239324A JPH03102811A (en) 1989-09-14 1989-09-14 Electrolyte for electrolytic capacitor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1239324A JPH03102811A (en) 1989-09-14 1989-09-14 Electrolyte for electrolytic capacitor

Publications (1)

Publication Number Publication Date
JPH03102811A true JPH03102811A (en) 1991-04-30

Family

ID=17043024

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1239324A Pending JPH03102811A (en) 1989-09-14 1989-09-14 Electrolyte for electrolytic capacitor

Country Status (1)

Country Link
JP (1) JPH03102811A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007223648A (en) * 2006-02-23 2007-09-06 Otsuka Hoso Kogyo Kk Article storage box
JPWO2023276589A1 (en) * 2021-06-28 2023-01-05

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007223648A (en) * 2006-02-23 2007-09-06 Otsuka Hoso Kogyo Kk Article storage box
JPWO2023276589A1 (en) * 2021-06-28 2023-01-05
WO2023276589A1 (en) * 2021-06-28 2023-01-05 三洋化成工業株式会社 Electrolyte for electrolytic capacitor and electrolytic capacitor and hybrid electrolytic capacitor using said electrolyte

Similar Documents

Publication Publication Date Title
JPH03102811A (en) Electrolyte for electrolytic capacitor
JP2561323B2 (en) Electrolytic solution for driving electrolytic capacitors
JPH0399416A (en) Electrolyte for electrolytic capacitor
JP2598094B2 (en) Electrolyte for driving electrolytic capacitors
JPH031817B2 (en)
JP2960153B2 (en) Electrolyte for driving electrolytic capacitors
JPH05205978A (en) Electrolyte of electrolytic capacitor
JPH03127812A (en) Electrolyte for electrolytic capacitor
JPH01173615A (en) Electrolyte for electrolytic condenser
JP3612671B2 (en) Electrolytic solution for electrolytic capacitor drive
JPH0364905A (en) Electrolyte for driving electrolytic capacitor
JPH0410515A (en) Electrolyte for electrolytic capacitor
JPH0215610A (en) Driving electrolyte of electrolytic condenser
JPH0355820A (en) Electrolyte for electrolytic capacitor
JP2612021B2 (en) Electrolyte for driving electrolytic capacitors
JPH0370116A (en) Electrolyte for driving electrolytic capacitor
JP2948252B2 (en) Electrolyte for driving electrolytic capacitors
JPS6094719A (en) Electrolyte for driving electrolytic condenser
JPH08264389A (en) Electrolyte for driving electrolytic capacitor
JPH0334845B2 (en)
JP2567418B2 (en) Electrolytic solution for driving electrolytic capacitors
JPH031818B2 (en)
JPS6130727B2 (en)
JPH0268914A (en) Electrolytic solution for driving electrolytic capacitor
JPH0199209A (en) Driving electrolyte for electrolytic capacitor