JPH03102811A - Electrolyte for electrolytic capacitor - Google Patents
Electrolyte for electrolytic capacitorInfo
- 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
Links
- 239000003990 capacitor Substances 0.000 title claims description 16
- 239000003792 electrolyte Substances 0.000 title abstract description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims abstract description 24
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 claims abstract description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 17
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims abstract description 10
- 125000005265 dialkylamine group Chemical group 0.000 claims abstract description 8
- 239000002904 solvent Substances 0.000 claims abstract description 7
- 239000005711 Benzoic acid Substances 0.000 claims abstract description 5
- 235000010233 benzoic acid Nutrition 0.000 claims abstract description 5
- 239000008151 electrolyte solution Substances 0.000 claims description 5
- 238000004140 cleaning Methods 0.000 abstract description 10
- 229910052736 halogen Inorganic materials 0.000 abstract description 4
- -1 halogen hydrocarbon Chemical class 0.000 abstract description 4
- 230000007062 hydrolysis Effects 0.000 abstract description 4
- 238000006460 hydrolysis reaction Methods 0.000 abstract description 4
- 229910052801 chlorine Inorganic materials 0.000 abstract description 3
- 239000000460 chlorine Substances 0.000 abstract description 3
- 230000006866 deterioration Effects 0.000 abstract description 3
- 150000002367 halogens Chemical class 0.000 abstract description 3
- 239000002075 main ingredient Substances 0.000 abstract 3
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 230000007797 corrosion Effects 0.000 description 11
- 238000005260 corrosion Methods 0.000 description 11
- 239000000243 solution Substances 0.000 description 8
- 239000011888 foil Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 3
- 230000002401 inhibitory effect Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- UBOXGVDOUJQMTN-UHFFFAOYSA-N 1,1,2-trichloroethane Chemical compound ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 2
- OTLNPYWUJOZPPA-UHFFFAOYSA-N 4-nitrobenzoic acid Chemical compound OC(=O)C1=CC=C([N+]([O-])=O)C=C1 OTLNPYWUJOZPPA-UHFFFAOYSA-N 0.000 description 2
- BTJIUGUIPKRLHP-UHFFFAOYSA-N 4-nitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C=C1 BTJIUGUIPKRLHP-UHFFFAOYSA-N 0.000 description 2
- 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
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000001784 detoxification Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 238000000034 method Methods 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
- FJSRPVWDOJSWBX-UHFFFAOYSA-N 1-chloro-4-[1-(4-chlorophenyl)-2,2,2-trifluoroethyl]benzene Chemical compound C=1C=C(Cl)C=CC=1C(C(F)(F)F)C1=CC=C(Cl)C=C1 FJSRPVWDOJSWBX-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000012459 cleaning agent Substances 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 230000000694 effects Effects 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
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 150000008282 halocarbons Chemical class 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
- 235000012054 meals Nutrition 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- 229920000647 polyepoxide Polymers 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
- 229910000679 solder Inorganic materials 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001629 suppression Effects 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)
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.
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)
| 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 |
-
1989
- 1989-09-14 JP JP1239324A patent/JPH03102811A/en active Pending
Cited By (3)
| 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 |
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