JPH0399416A - Electrolyte for electrolytic capacitor - Google Patents
Electrolyte for electrolytic capacitorInfo
- Publication number
- JPH0399416A JPH0399416A JP23650989A JP23650989A JPH0399416A JP H0399416 A JPH0399416 A JP H0399416A JP 23650989 A JP23650989 A JP 23650989A JP 23650989 A JP23650989 A JP 23650989A JP H0399416 A JPH0399416 A JP H0399416A
- Authority
- JP
- Japan
- Prior art keywords
- butyrolactone
- water
- gamma
- 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
Links
- 239000003990 capacitor Substances 0.000 title claims description 17
- 239000003792 electrolyte Substances 0.000 title abstract description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims abstract description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 17
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 claims abstract description 16
- 125000005265 dialkylamine group Chemical group 0.000 claims abstract description 8
- 239000002904 solvent Substances 0.000 claims abstract description 6
- OWCLRJQYKBAMOL-UHFFFAOYSA-N 2-butyloctanedioic acid Chemical compound CCCCC(C(O)=O)CCCCCC(O)=O OWCLRJQYKBAMOL-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000008151 electrolyte solution Substances 0.000 claims description 10
- 238000004140 cleaning Methods 0.000 abstract description 12
- 239000007788 liquid Substances 0.000 abstract description 6
- 229910052801 chlorine Inorganic materials 0.000 abstract description 4
- 239000000460 chlorine Substances 0.000 abstract description 4
- 230000007062 hydrolysis Effects 0.000 abstract description 4
- 238000006460 hydrolysis reaction Methods 0.000 abstract description 4
- -1 chlorine ions Chemical class 0.000 abstract description 3
- 238000005406 washing Methods 0.000 abstract description 3
- 230000006866 deterioration Effects 0.000 abstract description 2
- 238000000034 method Methods 0.000 abstract description 2
- 230000007797 corrosion Effects 0.000 description 13
- 238000005260 corrosion Methods 0.000 description 13
- 239000011888 foil Substances 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 5
- 239000000243 solution Substances 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 230000002401 inhibitory effect Effects 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
- AJDIZQLSFPQPEY-UHFFFAOYSA-N 1,1,2-Trichlorotrifluoroethane Chemical compound FC(F)(Cl)C(F)(Cl)Cl AJDIZQLSFPQPEY-UHFFFAOYSA-N 0.000 description 1
- OARDBPIZDHVTCK-UHFFFAOYSA-N 2-butyloctanoic acid Chemical compound CCCCCCC(C(O)=O)CCCC OARDBPIZDHVTCK-UHFFFAOYSA-N 0.000 description 1
- OTLNPYWUJOZPPA-UHFFFAOYSA-N 4-nitrobenzoic acid Chemical compound OC(=O)C1=CC=C([N+]([O-])=O)C=C1 OTLNPYWUJOZPPA-UHFFFAOYSA-N 0.000 description 1
- BTJIUGUIPKRLHP-UHFFFAOYSA-N 4-nitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C=C1 BTJIUGUIPKRLHP-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000012459 cleaning agent Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical compound [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229940100890 silver compound Drugs 0.000 description 1
- 150000003379 silver compounds Chemical class 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Landscapes
- Detergent Compositions (AREA)
Abstract
Description
【発明の詳細な説明】 (産業上の利用分野) 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 application field) The present invention relates to an electrolytic solution for electrolytic capacitors.
(従来の技術)
従来のアルミ電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
した構造になっている。(Prior technology) Conventional electrolytic capacitors such as aluminum electrolytic 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 and then wrapped in a case. It has a structure in which it is stored and sealed by attaching a lid to this case.
陽極箔と1114箔とは、エツ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。The anode foil and the 1114 foil are etched aluminum foils, and the former is particularly 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[口に含まれるフ
ラックスや汚れを除去するために、1.1.1−トリク
ロ0エタンや1.1.2−トリク00−1.212−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, in order to remove flux and dirt contained in the half-coat used for connection, 1.1.1-trichloroethane or 1.1. The cleaning process is performed using a halogen-based cleaning agent such as 2-Trifluoroethane (Freon 113).
(発明が解決しようとする課題)
しかし、従来の41I造の電解コンデンサでは、洗浄液
がケースと蓋の隙間から侵入することがある。(Problem to be Solved by the Invention) However, in the conventional 41I electrolytic capacitor, cleaning liquid may enter through the gap between the case and the lid.
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するが、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
解コンデンサの電気特性が著しく省電しあるいはコンデ
ンサ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 foil and cathode foil. As a result, defects such as the electrical characteristics of the electrolytic capacitor are significantly reduced or the capacitor function is lost occur.
この欠点を防止するために、蓋の外表面にエポキシ樹脂
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、¥J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 coated on the outer surface of the lid, but this requires coating the resin and curing it, making the J-manufacturing process complicated and time-consuming. There are drawbacks.
また、電解液に、P−ニトルフェノールやP−二トロ安
息香酸等のニトロ化合物や銀化合物等の腐食防止剤を添
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、ケースや作業者の手等に
付着して着色し、作業性に問題がある。そしてP−ニド
O安息香酸は、染色性の問題はないが少量を添加した場
合にも火花電圧が低下し、耐圧が低い欠点がある。また
、従来の腐食防止剤は、塩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−トリクロロエタンに対してはその効果が低い欠
点がある。Further, a corrosion inhibitor such as a nitro compound such as P-nitrphenol or P-nitrobenzoic acid, or a silver compound may be added to the electrolytic solution. However, P-nitrophenol has an extremely strong yellow staining property, and it adheres to and stains the case and the hands of workers, causing problems in workability. Although P-nido-O benzoic acid does not have any dyeing problems, it has the disadvantage that even when added in a small amount, the spark voltage decreases and the withstand voltage is low. In addition, conventional corrosion inhibitors include Freon 11, which has less dissociation of chlorine.
3 shows a relatively good corrosion inhibiting effect, but 1,
1.1-Trichloroethane has the drawback of being less effective.
本発明は、以上の欠点を改良し、ハロゲン系炭化水素系
の洗浄液による洗浄によって発生する特性劣化等を防止
しうる電解コンデンサ用電解液を提供することを目的と
するものである。An object of the present invention is to provide an electrolytic solution for an electrolytic capacitor that can improve the above-mentioned drawbacks and prevent property deterioration caused by cleaning with a halogenated hydrocarbon-based cleaning solution.
(課題を解決するための手段)
本発明は上記の目的を達成するために、γ−ブチロラク
トンを主成分とし、エチレングリコールを15wt%以
下、水を0.1〜8wt%含む溶媒中に、ブチルオクタ
ン2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てPHを4〜7.
5にした電解コンデンサ用電解液を提供するものである
。(Means for Solving the Problems) In order to achieve the above-mentioned object, the present invention has provided a solution containing γ-butyrolactone as a main component, ethylene glycol of 15 wt% or less, and water of 0.1 to 8 wt%. While dissolving octanoic acid as a solute, monoalkylamine or dialkylamine is dissolved to adjust the pH to 4-7.
The present invention provides an electrolytic solution for electrolytic capacitors according to No. 5.
(作用)
溶媒中の主成分であるT−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
るのを防止し、加水分解を抑制する作用がある。(Function) T-butyrolactone, which is the main component in the solvent, surrounds the halogen-based cleaning liquid molecules, 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.
電解液の溶媒は、γ−ブチロラクトンを主成分とし、エ
チレングリコールを15wt%以下、水を0.1〜8w
t%とじた成分からなる。The solvent of the electrolytic solution is mainly composed of γ-butyrolactone, 15 wt% or less of ethylene glycol, and 0.1 to 8 w of water.
Consists of t% components.
溶質としてはブチルオクタン2Mを溶解する。As a solute, 2M of butyl octane is dissolved.
また、PHを4〜7.5に調整するために、モア1アル
キルアミンやジアルキルアミンを添加する。Further, in order to adjust the pH to 4 to 7.5, a MoI alkylamine or a dialkylamine is added.
モノアルキルアミンにはモノメチルアミンやモノエチル
アミン、モノプロピルアミンを用いる。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、ジプロピルア
ミンを用いる。Monomethylamine, monoethylamine, or monopropylamine is used as the monoalkylamine. Dimethylamine, diethylamine, or dipropylamine is used as the dialkylamine.
次に、本発明の実施例、比較例及び従来例の電解液を含
浸して、定格400V−220μFのアルミ電解コンデ
ンサを製造する。そしてこれらのコンデンサを、洗浄槽
に入れて温度50℃の1゜1.1−トリクロロエタンを
注入し、15分間洗テした後、温度110℃の1&瀉槽
内に入れ、電圧400■を印加して高温負荷試験を行い
、腐食の発生状況を調べた。試料数は、実施例、比較例
及び従来例とも30個とし、試験時間500hr後に1
0個を解体し、試験時間1000hr11に残りの20
11を解体し、各々腐食の発生状況を調査した。Next, an aluminum electrolytic capacitor having a rating of 400V-220 μF is manufactured by impregnating the electrolytic solution of the example of the present invention, the comparative example, and the conventional example. Then, these capacitors were placed in a cleaning tank, and 1°1.1-trichloroethane at a temperature of 50°C was injected, and after washing for 15 minutes, they were placed in a cleaning tank at a temperature of 110°C, and a voltage of 400 μ was applied. A high-temperature load test was conducted to investigate the occurrence of corrosion. The number of samples was 30 for each example, comparative example, and conventional example, and after 500 hours of testing time, 1
0 pieces were disassembled, and the remaining 20 pieces were completed in 11 hours after the test time of 1000 hours.
11 were dismantled and the occurrence of corrosion was investigated.
結果は表の通りとなった。The results were as shown in the table.
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、500hr後及び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1000
hlには全数に腐食が発生していた。また、比較例1及
び比較例2から明らかな通り、エチレングリクールの含
有率が15wt%を越えると1000hr後には各々9
0%及び50%腐食が発生し、腐食抑制の効果が低下す
る。また、比較例3及び比較例4から明らかな通り、水
を含ま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, whereas in Conventional Example 1 and Conventional Example 2, the corrosion was 1000 hr.
Corrosion had occurred in all of the hls. Furthermore, as is clear from Comparative Example 1 and Comparative Example 2, when the content of ethylene glycol exceeds 15 wt%, after 1000 hr, each
0% and 50% corrosion occurs, reducing the effectiveness of corrosion inhibition. Further, as is clear from Comparative Examples 3 and 4, the specific resistance increases when water is not included, and the specific resistance can be lowered by containing water as in the present invention.
また、溶媒がγ−ブチロラクトン75wt%、エチレン
グリコール10wt%、水、溶質としてブチルオクタン
2酸1011%、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, in an electrolytic solution consisting of 75 wt% γ-butyrolactone, 10 wt% ethylene glycol, and water as a solvent, 1011% butyloctanoic acid as a solute, and 5 wt% diethylamine, we investigated the change in specific resistance when the water content was changed. Shown in the figure.
図から明らかな通り、水の含有量が6wt%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
量が多くなるとガス発生量が多くなり、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
量は0.1〜8wt%が適当である。As is clear from the figure, when the water content exceeds 6 wt%, the specific resistance hardly changes. Furthermore, it is generally known that when the amount of water added increases, the amount of gas generated increases and the life of the capacitor becomes shorter. 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 8 wt%.
(発明の効果)
以上の通り、本発明によれば、γ−ブチロラクトンを主
成分とし、モ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、またブチル
オクタン2酸を溶解することにより火花電圧を高くでき
、さらに、エチレングリコールを15wt%以下、水を
0.1〜Qwt%の範囲で添加することにより比抵抗の
低い電解コンデンサ用電解液が得られる。(Effects of the Invention) As described above, according to the present invention, since γ-butyrolactone is the main component and monoalkylamine and dialkylamine are dissolved, the corrosion inhibiting effect can be improved, and butyloctane dioic acid is dissolved. By doing so, the spark voltage can be increased, and by adding ethylene glycol in an amount of 15 wt% or less and water in a range of 0.1 to Qwt%, an electrolytic solution for an electrolytic capacitor with a low specific resistance can be obtained.
図は本発明の実施例において水の含有量を変えたときの
比抵抗のグラフを示す。The figure shows a graph of specific resistance when the water content is changed in an example of the present invention.
Claims (1)
コールを15wt%以下、水を0.1〜8wt%含む溶
媒中に、ブチルオクタン2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
解してPH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 the main component, 15 wt% or less of ethylene glycol, and 0.1 to 8 wt% of water, dissolve butyloctane dioic acid as a solute and dissolve monoalkylamine or dialkylamine. An electrolytic solution for electrolytic capacitors with a pH of 4 to 7.5.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP23650989A JPH0399416A (en) | 1989-09-12 | 1989-09-12 | Electrolyte for electrolytic capacitor |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP23650989A JPH0399416A (en) | 1989-09-12 | 1989-09-12 | Electrolyte for electrolytic capacitor |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0399416A true JPH0399416A (en) | 1991-04-24 |
Family
ID=17001769
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP23650989A Pending JPH0399416A (en) | 1989-09-12 | 1989-09-12 | Electrolyte for electrolytic capacitor |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0399416A (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6265406A (en) * | 1985-09-18 | 1987-03-24 | ニチコン株式会社 | Electrolyte for driving aluminum electrolytic condenser |
JPH01128418A (en) * | 1987-11-12 | 1989-05-22 | Hitachi Condenser Co Ltd | Electrolytic solution for electrolytic capacitor |
-
1989
- 1989-09-12 JP JP23650989A patent/JPH0399416A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6265406A (en) * | 1985-09-18 | 1987-03-24 | ニチコン株式会社 | Electrolyte for driving aluminum electrolytic condenser |
JPH01128418A (en) * | 1987-11-12 | 1989-05-22 | Hitachi Condenser Co Ltd | Electrolytic solution for electrolytic capacitor |
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