JPS5951737B2 - Manufacturing method of solid electrolytic capacitor - Google Patents
Manufacturing method of solid electrolytic capacitorInfo
- Publication number
- JPS5951737B2 JPS5951737B2 JP13209179A JP13209179A JPS5951737B2 JP S5951737 B2 JPS5951737 B2 JP S5951737B2 JP 13209179 A JP13209179 A JP 13209179A JP 13209179 A JP13209179 A JP 13209179A JP S5951737 B2 JPS5951737 B2 JP S5951737B2
- Authority
- JP
- Japan
- Prior art keywords
- anode lead
- semiconductor layer
- capacitor element
- organic solvent
- solid 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.)
- Expired
Links
- 239000003990 capacitor Substances 0.000 title description 28
- 239000007787 solid Substances 0.000 title description 7
- 238000004519 manufacturing process Methods 0.000 title description 4
- 239000004065 semiconductor Substances 0.000 description 22
- 239000003960 organic solvent Substances 0.000 description 16
- 239000000243 solution Substances 0.000 description 16
- 239000007788 liquid Substances 0.000 description 11
- 229910052751 metal Inorganic materials 0.000 description 8
- 239000002184 metal Substances 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 6
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 5
- 230000007547 defect Effects 0.000 description 4
- 230000005484 gravity Effects 0.000 description 4
- 238000007598 dipping method Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000003466 welding Methods 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical compound FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 239000012452 mother liquor Substances 0.000 description 2
- 229910052758 niobium Inorganic materials 0.000 description 2
- 239000010955 niobium Substances 0.000 description 2
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- 229910052715 tantalum Inorganic materials 0.000 description 2
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- QOSATHPSBFQAML-UHFFFAOYSA-N hydrogen peroxide;hydrate Chemical compound O.OO QOSATHPSBFQAML-UHFFFAOYSA-N 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000005476 soldering Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
Landscapes
- Fixed Capacitors And Capacitor Manufacturing Machines (AREA)
Description
【発明の詳細な説明】
本発明は固体電解コンデンサの製造方法に関し、特に半
導体層形成工程においてコンデンサエレメントの陽極リ
ード部分に形成された不所望の半導体層を除去する方法
に関するも:のである計一般に、この種固体電解コンデ
ンサは例えば第1図に示すように、タンタル、ニオブ、
アルミニウムなどのように弁作用を有する金属粉末を円
柱状に加圧成形し焼結してなるコンデンサエレメントA
に予め弁作用を有する金属線を陽極リードBとして植立
し、この陽極リードBの突出部分に第1の外部リード部
材Cを溶接すると共に、第2の外部リード部材りをコン
デンサエレメントAの周面に酸化層、半導体層を介して
形成された電極引出し層に半田付けし、然る後、コンデ
ンサニレメン)Aの全周面を樹脂材Eにて被覆した構成
されている。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for manufacturing a solid electrolytic capacitor, and more particularly to a method for removing an undesired semiconductor layer formed on an anode lead portion of a capacitor element during a semiconductor layer forming process. , this type of solid electrolytic capacitor is made of tantalum, niobium, tantalum, niobium,
Capacitor element A made by press-forming metal powder with valve action, such as aluminum, into a cylindrical shape and sintering it.
A metal wire having a valve action is installed in advance as an anode lead B, a first external lead member C is welded to the protruding part of this anode lead B, and a second external lead member is attached around the capacitor element A. It is constructed by soldering to an electrode lead layer formed on the surface via an oxide layer and a semiconductor layer, and then covering the entire circumferential surface of the capacitor (A) with a resin material E.
ところで、このコンデンサエレメントAはそれより導出
された陽極リードBの突出部分に第1の外部リード部材
Cを溶接するに先立って、陽極リードBど共に化成処理
によりその表面に酸化層が形成され、さらにコンデンサ
エレメントAのみを半導体母液に一定時間浸漬し充分に
含浸させた後、高温雰囲気中において熱分解反応を起さ
せ酸化層上に半導体層が形成されている。By the way, before the first external lead member C is welded to the protruding portion of the anode lead B led out from the capacitor element A, an oxide layer is formed on the surface of the anode lead B by chemical conversion treatment. Further, only the capacitor element A is immersed in the semiconductor mother liquor for a certain period of time to fully impregnate it, and then a thermal decomposition reaction is caused in a high temperature atmosphere to form a semiconductor layer on the oxide layer.
しかし乍ら、□陽極リードBの表面には軸方向に多くの
ダイス傷が存在している関係で、コンデンサエレメント
A′に含浸された半導体母液がこのダイ・ス傷を通って
陽極リードBのコンデンサニレメン)Aがらの突出部分
(導出部分)に付着し、熱分解されていわゆる半導体層
の這い上りを生ずる。However, since there are many die scratches in the axial direction on the surface of the anode lead B, the semiconductor mother liquid impregnated in the capacitor element A' passes through these die scratches and forms the anode lead B. It adheres to the protruding part (lead-out part) of the capacitor A and is thermally decomposed to cause what is called a creep-up of the semiconductor layer.
通常、半導体母液の含浸−熱分解操作はコンデンサニレ
メン)Aが多孔質であることに鑑み数回以上繰り返され
る関係で、半導体層の這い上りもさらに進行する傾向に
ある。Normally, the impregnation-pyrolysis operation of the semiconductor mother liquor is repeated several times or more in view of the porous nature of the capacitor A, and the creeping-up of the semiconductor layer tends to progress further.
従って、陽極リードBの突出部分に第1の外部リード部
材Cに・溶接する際に、第1の外部リード部材Cと這い
上った半導体層とが接触して漏洩電流が増加したり、時
には陰極と陽極とが短絡されてしまいコンデンサとして
の機能を奏し得なくなるという・欠点がある。Therefore, when welding the first external lead member C to the protruding portion of the anode lead B, the first external lead member C and the semiconductor layer that has climbed up may come into contact and leakage current may increase. There is a drawback that the cathode and anode are short-circuited and cannot function as a capacitor.
・本発明はこのような点に鑑み、コンデンサエレメン
ト面から導出された陽極リード部分における不所望の半
導体層を除去することによってコンテンサとしての品位
を高めうる固体電解コンデンサの製造方法を提供するも
ので、以下その一製造方法について第2図〜第3図を参
照して説明する。- In view of these points, the present invention provides a method for manufacturing a solid electrolytic capacitor that can improve the quality of the capacitor by removing the undesired semiconductor layer in the anode lead portion led out from the surface of the capacitor element. Hereinafter, one manufacturing method will be explained with reference to FIGS. 2 and 3.
まず、第2図に示すように、弁作用を有する金属粉末を
円柱状に加圧成形し焼結してなるコンデンサエレメント
1に予め弁作用を有する金属線を陽極リード2として植
立する。First, as shown in FIG. 2, a metal wire having a valve function is installed in advance as an anode lead 2 on a capacitor element 1 which is formed by press-forming metal powder having a valve function into a cylindrical shape and sintering it.
そして、この陽極リード2のコンデンサエレメント面1
aからの導出端を帯状の金属板3に一定のピッチ間隔に
て接続して帯状部品を形成する。Then, the capacitor element surface 1 of this anode lead 2
The lead-out ends from a are connected to the band-shaped metal plate 3 at regular pitch intervals to form a band-shaped component.
そして、コンデンサエレメント1の表面に通常の方法に
よって酸化層、半導体層を形成する。Then, an oxide layer and a semiconductor layer are formed on the surface of the capacitor element 1 by a conventional method.
次に第3図に示すように、帯状部品を浸漬槽4に、金属
板3が下方に、コンデンサエレメント1が上方に位置す
るように収納し固定する。Next, as shown in FIG. 3, the strip-shaped component is housed and fixed in the dipping tank 4 with the metal plate 3 at the bottom and the capacitor element 1 at the top.
そして、浸漬槽4に、下方に配設した供給系路5より例
えば水に不溶でかつ比重が1.3〜1.4以上の有機溶
剤6を供給する。Then, an organic solvent 6 that is insoluble in water and has a specific gravity of 1.3 to 1.4 or more is supplied to the dipping tank 4 from a supply line 5 disposed below.
引続き、浸漬槽4の上方に配設された供給系路7より有
機溶剤6より比重が小さく、かつ酸と酸化剤を含む溶解
液8を、それの液面がコンデンサエレメント面1aより
例えば1〜2mm下方に位置するように供給する。Subsequently, a solution 8 having a specific gravity lower than that of the organic solvent 6 and containing an acid and an oxidizing agent is supplied from a supply line 7 disposed above the immersion tank 4 so that the liquid level thereof is lower than the capacitor element surface 1a, for example, by 1 to 1. Supplied so that it is located 2 mm below.
この状態で一定時間放置すると、陽極リード2のコンデ
ンサエレメント面1aからの導出部分に形成された半導
体層は溶解液8によって溶解除去される。When left in this state for a certain period of time, the semiconductor layer formed on the portion of the anode lead 2 extending from the capacitor element surface 1a is dissolved and removed by the dissolving solution 8.
次に帯状部品を若干上方に持上げた後、供給系路5より
有機溶剤6を徐々に浸漬槽4に補充し、それの液面を高
めると、溶解液8はオーバーフローして補助槽9に排除
される。Next, after lifting the strip part slightly upward, the organic solvent 6 is gradually replenished into the dipping tank 4 through the supply line 5 to raise the liquid level, and the solution 8 overflows and is drained into the auxiliary tank 9. be done.
然る後帯状部分を有機溶剤6.より引上げ純水にて洗浄
し、以下通常の方法にて固体電解コンデンサを製造する
。After that, the band-shaped portion was treated with an organic solvent 6. The capacitor is then pulled up and washed with pure water, and a solid electrolytic capacitor is then manufactured using the usual method.
このように陽極リード2のコンデンサエレメント面1a
からの導出部分は有機溶剤6及び溶解液8の2液層に浸
漬することによって、陽極リード2に形成されている不
所望の半導体層を確実に除去することができるので、例
えば陽極リード2に第1の外部リード部材を溶接する際
の半導体層との接触に起因する漏洩電流の増力出電極短
絡を皆無にできる。In this way, the capacitor element surface 1a of the anode lead 2
By immersing the lead-out portion in the two-liquid layer of the organic solvent 6 and the dissolving solution 8, it is possible to reliably remove the undesired semiconductor layer formed on the anode lead 2. Short-circuiting of the leakage current boosting output electrode due to contact with the semiconductor layer when welding the first external lead member can be completely eliminated.
しかも、陽極リード2における不所望の半導体層を除去
するに際し、陽極リード2は有機溶剤6と溶解液8との
2液層に浸漬されるのであるが、特に金属板3は有機溶
剤6にて覆われていることもあって、溶解液8による腐
食を防止できる。Moreover, when removing the undesired semiconductor layer on the anode lead 2, the anode lead 2 is immersed in a two-liquid layer of the organic solvent 6 and the solution 8. In particular, the metal plate 3 is immersed in the organic solvent 6. Since it is covered, corrosion caused by the solution 8 can be prevented.
さらには有機溶剤6は水に溶けず、比重が溶解液8より
大きいものが選定されている関係で、溶解液8との2液
層に構成しても必ず溶解液8が有機溶剤6上に浮上位置
するので、陽極リード2の所望部分にのみ溶解液8を接
触させることができ、不所望の半導体層を確実に除去で
きる。Furthermore, since the organic solvent 6 is not soluble in water and has a higher specific gravity than the dissolving liquid 8, the dissolving liquid 8 will always be on top of the organic solvent 6 even if it is configured as a two-liquid layer with the dissolving liquid 8. Since the anode lead 2 is in a floating position, the solution 8 can be brought into contact with only a desired portion of the anode lead 2, and an undesired semiconductor layer can be reliably removed.
次に具体的実施例について説明する。Next, specific examples will be described.
実施例 1
第3図の状態において、有機溶剤としてトリクレンを、
溶解液として塩酸(ECI)8容量%。Example 1 In the state shown in Figure 3, trichlene was used as an organic solvent,
Hydrochloric acid (ECI) 8% by volume as a dissolving solution.
過酸化水素(H2O2) 10容量%、水の混合液を使
用し陽極リードを溶解液中に25秒間浸漬し、引上げ後
、純水洗浄し通常の方法にて固体電解コンデンサを製作
し、漏洩電流、電極短絡不良の発生率について検討した
処、従来法によるものでは3%も不良が発生したが、本
発明法によるものでは全く不良が発生しなかった。Using a mixture of hydrogen peroxide (H2O2) 10% by volume and water, the anode lead was immersed in the solution for 25 seconds, pulled out, washed with pure water, and a solid electrolytic capacitor was manufactured using the usual method, and the leakage current was measured. When examining the incidence of electrode short-circuit defects, it was found that 3% of defects occurred with the conventional method, but no defects occurred with the method of the present invention.
実施例 2
有機溶剤としてダイキン株式会社より発売されている商
品名ダイフロンS3(比重1.565)を、溶解液とし
て実施例1と同様のものを使用した処、陽極リードにお
ける不所望の半導体層(二酸化マンガン)は完全に除去
でき、実施例1と同様の結果が得られた。Example 2 By using the same organic solvent as in Example 1 and using the product name Daiflon S3 (specific gravity 1.565) sold by Daikin Corporation as a dissolving solution, an undesired semiconductor layer ( Manganese dioxide) could be completely removed, and the same results as in Example 1 were obtained.
実施例 3
有機溶剤としてトリクレンを、溶解液として硫酸(H2
SO4)12容量%、過酸化水素(H2O2)10容量
%、水の混合液を使用した処、陽極リードに形成されて
いる不所望の半導体層(二酸化マンガン)を1分間程度
で除去できた。Example 3 Trichlene was used as an organic solvent and sulfuric acid (H2
When a mixture of 12% by volume of SO4), 10% by volume of hydrogen peroxide (H2O2), and water was used, the undesired semiconductor layer (manganese dioxide) formed on the anode lead could be removed in about 1 minute.
尚、金属板に対する影響は皆無であった。Note that there was no effect on the metal plate.
実施例 4 ・
有機溶剤として四塩化炭素を、溶解液として硝酸(HN
O3)10容量%、過酸化水素(H2O2)10容量%
、水の混合液を使用した処、陽極リードの半導体層(二
酸化ヤンガン)は30秒程度で完全に除去できた。Example 4 ・ Carbon tetrachloride was used as an organic solvent and nitric acid (HN) was used as a dissolving liquid.
O3) 10% by volume, hydrogen peroxide (H2O2) 10% by volume
When a water mixture was used, the semiconductor layer (Yangan dioxide) on the anode lead could be completely removed in about 30 seconds.
又、溶解液を常時オーバーフローさせた処、溶解速度は
さらに早くなり、作業時間を短縮できた。Furthermore, by constantly overflowing the dissolving solution, the dissolution rate became even faster and the working time could be shortened.
実施例 5
有機溶剤として実施例2のダイフロンS3を、溶解液ど
して実施例4の混合液を使用し、溶解液の厚みを4〜5
mmに設定した処、陽極リードにおける不所望の半導体
層(二酸化マンガン)は完全に除去できた。Example 5 Using Daiflon S3 of Example 2 as an organic solvent and the mixed solution of Example 4 as a dissolving solution, the thickness of the dissolving solution was 4 to 5.
mm, the undesired semiconductor layer (manganese dioxide) on the anode lead could be completely removed.
又、溶解液の有機溶剤上での厚みが薄く使用量を最小限
に抑えることができたので、溶解液を頻繁に交換しても
その使用量は少く、反面、溶解能力は常に高く保つこと
ができた。In addition, since the thickness of the dissolving solution on the organic solvent was thin, the amount used could be kept to a minimum, so even if the dissolving solution was replaced frequently, the amount used was small, and on the other hand, the dissolving ability could always be kept high. was completed.
尚、本発明において、溶解液における酸化剤は過酸化水
素にのみ制約されないし、有機溶剤も上記実施例以外の
ものも使用できる。In the present invention, the oxidizing agent in the solution is not limited to hydrogen peroxide, and organic solvents other than those in the above examples can also be used.
以上のように本発明によれば、コンデンサエレメント面
から導出された陽極リード部分における不所望の半導体
層を効果的に除去でき、例えば外部リード部材の溶接に
起因する漏洩電流、電極短絡などの不良発生率を著しく
減少できる。As described above, according to the present invention, it is possible to effectively remove the undesired semiconductor layer in the anode lead portion led out from the surface of the capacitor element, and to prevent defects such as leakage current and electrode short circuit caused by welding of the external lead member. The incidence can be significantly reduced.
第1図は従来の固体電解コンデンサの側断面図、第2図
〜第3図は本発明方法を説明するための側断面図であっ
て、第2図は帯状部品の状態を示す図、第3図は帯状部
品を2液層に浸漬した状態を示す図である。FIG. 1 is a side sectional view of a conventional solid electrolytic capacitor, FIGS. 2 and 3 are side sectional views for explaining the method of the present invention, and FIG. FIG. 3 is a diagram showing a state in which the strip-shaped component is immersed in the two liquid layers.
Claims (1)
と共に焼結し、:かつそれより:予め弁作用を有する金
属線を陽極リードとして導出したコンデンサエレメント
に酸化層、半導体層を形成した後に、陽極リードのコン
デンサエレメント面からの導出部分のみを、酸及び酸化
剤を含む溶解液ど溶解液より比重の大きい有機溶剤との
2液層に浸漬することによって陽極リード部分め半導体
層を除去することを特徴とする固体電解コンデンサの製
造方法。1 Pressure-forming metal powder with valve action into a desired shape and sintering: And then: After forming an oxide layer and a semiconductor layer on a capacitor element from which a metal wire with valve action has been led out in advance as an anode lead. , remove the semiconductor layer from the anode lead portion by immersing only the portion of the anode lead leading out from the surface of the capacitor element into a two-liquid layer of a solution containing an acid and an oxidizing agent, or an organic solvent having a higher specific gravity than the solution. A method for manufacturing a solid electrolytic capacitor, characterized by:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13209179A JPS5951737B2 (en) | 1979-10-12 | 1979-10-12 | Manufacturing method of solid electrolytic capacitor |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13209179A JPS5951737B2 (en) | 1979-10-12 | 1979-10-12 | Manufacturing method of solid electrolytic capacitor |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5655033A JPS5655033A (en) | 1981-05-15 |
| JPS5951737B2 true JPS5951737B2 (en) | 1984-12-15 |
Family
ID=15073271
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP13209179A Expired JPS5951737B2 (en) | 1979-10-12 | 1979-10-12 | Manufacturing method of solid electrolytic capacitor |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5951737B2 (en) |
-
1979
- 1979-10-12 JP JP13209179A patent/JPS5951737B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5655033A (en) | 1981-05-15 |
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