JPS59215716A - Method of compounding electrode foil for electrolytic condenser - Google Patents

Method of compounding electrode foil for electrolytic condenser

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Publication number
JPS59215716A
JPS59215716A JP9168783A JP9168783A JPS59215716A JP S59215716 A JPS59215716 A JP S59215716A JP 9168783 A JP9168783 A JP 9168783A JP 9168783 A JP9168783 A JP 9168783A JP S59215716 A JPS59215716 A JP S59215716A
Authority
JP
Japan
Prior art keywords
electrode foil
tank
foil
chemical
forming
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
JP9168783A
Other languages
Japanese (ja)
Inventor
菅原 昌宏
船越 明
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.)
Marcon Electronics Co Ltd
Original Assignee
Marcon Electronics Co Ltd
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 Marcon Electronics Co Ltd filed Critical Marcon Electronics Co Ltd
Priority to JP9168783A priority Critical patent/JPS59215716A/en
Publication of JPS59215716A publication Critical patent/JPS59215716A/en
Pending legal-status Critical Current

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  • Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)

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】 本発明は竜野コンデン+j用電極冶の化成方法、待に陰
極酸化皮膜生成の際′i、極箔に電圧印加するときの順
電手段に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for forming an electrode for Tatsuno condensate +j, and firstly to a forward current means for applying a voltage to the electrode foil during the formation of a cathode oxide film.

従来、たとえば粗面化さ扛fc屯解コンデンサ用アルミ
ニウム箔に@極鹸化皮膜をル成するために電解液を入れ
た化成槽中に悶漬した粗面化済U箔に電圧を印加するこ
とが行われている。その一般的な化成方法を第1図によ
シ説明するとCu々どの金属ローラー(1)には直施電
m (2)から陽極が、また化F7y、槽(3)中の3
個の電極(4)には陽極がそれぞれ接続されている。□
前記金属ローラー(1)に接触して粗面化されたU箔(
5)が走行し化成槽(3)中の電解M(6)に配された
2個の電極(4)の間を皿り、化成槽(3)下部に位簡
した液中絶縁ローラー(7)で反転して再び2個の電極
(4)の関を通って液面に出、絶縁ローラー(8)に接
して走行していた。しかしながらこのように金属ローラ
ー(1)に粗面化済” 箔(5)を接触させることによ
って該M箔(5)に饋電する方式ではA/箔(5)の接
触が金属ローラー(1)の1・部に限定され接触面積が
小ざいこと、さらにAt i (5)tIL面化されて
いるために実効接触面積は妊らに小さくなること、また
U胎(5)衣面は粗面化にょシ絶縁状態にちかくこのよ
りを状態から金属ローラー(IJとの接触時の抵抗によ
って発熱し、特に大電流を饋電のときには発熱によって
U箭(5〕が高温になシ” Ifi(5)が溶断するな
どの事故を生ずる場合もめった。そしてhIJ記発熱に
よって金為ローラー(1)表面に畿化皮映か生成さ扛る
ためスパークや部分的な溶練なとも生ずる場合もあるの
で、これらを防止するfcめに金属ローラー(IJの研
磨を常に行っておがなけ扛ばならないなどの作業上の問
題点もあり1.上述の槓々の事項よ多金属ローラー(1
)に饋電する電流値を低く制限することも実施されてい
たが低塩流しが饋篭できないのでU箔(5)の走行速度
を上げることができなかった◎ 本発明は上記の点に鑑みてなされたもので粗面化済U箔
に@極戯化皮膜を生成する化成工程においてU箔への饋
電方式を陽、陰極とも電極から電解液を介して行うこと
にょル従来における金属ロ−ラーとU陥との接触による
スパーク、を谷融、溶断などをなくし化成工程における
At箔の走行速度を上け、特性の陵れた化成済ム1泊を
晶りし率に得ようとするものである。以下実hI8I例
によシ説明する。
Conventionally, for example, in order to form a saponified film on roughened aluminum foil for use in fc capacitors, a voltage is applied to roughened U foil that has been soaked in a chemical bath containing an electrolyte. is being carried out. The general chemical formation method is explained with reference to Fig. 1. Direct electricity is applied to the Cu metal roller (1) from m (2) to the anode;
An anode is connected to each of the electrodes (4). □
The U foil (which has been roughened by contacting the metal roller (1))
5) runs between the two electrodes (4) arranged on the electrolysis M (6) in the chemical conversion tank (3), and the submerged insulating roller (7) placed at the bottom of the chemical conversion tank (3). ), it was turned over again, passed through the barrier between the two electrodes (4), came out onto the liquid surface, and was running in contact with an insulated roller (8). However, in this method of feeding the M foil (5) by bringing the roughened foil (5) into contact with the metal roller (1), the contact of the foil (5) with the metal roller (1) The contact area is small because it is limited to one part of the (5) tIL surface, and the effective contact area is small due to the surface of the (5) tIL surface. When the metal roller (IJ) comes into contact with the metal roller (IJ), it generates heat due to the resistance when it comes into contact with the insulating state, and when a large current is being fed, the heat generation causes the U-shape (5) to become hot. ) has rarely caused accidents such as melting.In addition, sparks and partial melting may occur due to the generation of heat generation on the surface of the metal roller (1). , There are also operational problems such as having to constantly polish the metal roller (IJ) to prevent these problems.1.
) has been implemented, but the running speed of the U-foil (5) could not be increased because the low-salt sink could not be fed.◎ The present invention was developed in view of the above points. In the chemical conversion process that produces a polarized film on roughened U-foil, the feeding method to U-foil is carried out from the positive and negative electrodes through an electrolyte, unlike conventional metal foils. - In order to increase the running speed of the At foil in the chemical formation process by eliminating sparks, melting, melting, etc. caused by the contact between the metal and the U-depression, and to obtain a high crystallization rate of chemically formed aluminum with rough characteristics. It is something to do. This will be explained below using an actual hI8I example.

第2図に示すように直N、電源(11〕の陽極は絶縁さ
れ7C通゛亀IvI(12)の電解液(13)中に設れ
した例えばステンL/ス、 Pb 、 Sn 、 Pt
 、 C’71どの3個の陽極電極(14015)(1
6)に接続され、陰極は化成槽(171の化成液(18
)中に設置した例えはステンレス。
As shown in Figure 2, the anode of the power supply (11) is insulated and placed in the electrolyte (13) of the 7C IvI (12), for example, stainless steel, Pb, Sn, Pt.
, C'71 which three anode electrodes (14015) (1
6), and the cathode is connected to the chemical conversion tank (171 chemical liquid (18
) The example installed inside is stainless steel.

I’b 、 Sn 、 Pt 、 Cなどの3個の陰m
′a焔t193+203(21)k: ha t&され
る。上記mh7a(J3)は導電率を萬くするために1
〜20wt%のアジピン師アンモン水浴液または該水溶
液に例えば0.01−0.1wt% のリン酸を加えた
アジピン敞アンモンーリン酸水だ液などが用いられ、化
成液(1日)も同じ組成のものを用いるのが好ましい。
Three shades such as I'b, Sn, Pt, C etc.
'a flame t193+203(21)k: ha t&. The above mh7a (J3) is 1 to increase the conductivity.
~20 wt% adipine ammonium water bath solution or an adipine ammonium phosphoric acid bath solution prepared by adding, for example, 0.01-0.1 wt% phosphoric acid to the aqueous solution, etc. are used, and the chemical conversion solution (1 day) is also It is preferable to use

これは賄電檀(12)内を走行した粗面化済At箔(2
2)が絶縁ローラー (23)、液中絶縁ローラー+2
43.絶縁ローラー+253[261を紅て化成槽(1
7)内の化成液(18)に入シ走行するとき、通電借(
12胸の電解液(13)を当然化成槽(17)に持ち込
むわけで化成欣(18)の組成に変化を%+7’Cらす
からである。なお(27)は化成槽(173内の液中絶
縁り一う−、(28)は樵り四−ラーであ、!11 (
29)および(3o)は空気中に目出しているM箔(2
2]の発熱を防止するためにth IW液(13」を噴
出させる冷却用のシャワーである。このシャワー(29
)および(3o)から噴出させるのに゛屯1)ト液(1
3)を使用するのは削述の電解液(13)と化成液(1
8)との関係と同様、水などでは化成液(18]の組成
に醍化をもたらしJ′jT期の目的を達成で@ないから
である。
This is the roughened At foil (2) that ran inside the power bank (12).
2) is an insulated roller (23), submerged insulated roller +2
43. Turn the insulated roller +253 [261] into the chemical conversion tank (1
7) When entering the chemical liquid (18) and running, energize (
This is because the electrolyte solution (13) of 12 parts is naturally brought into the chemical conversion tank (17), and the composition of the chemical conversion tank (18) changes by %+7'C. In addition, (27) is a chemical conversion tank (submerged insulation in 173), (28) is a woodcutter four-lar, and !11 (
29) and (3o) are M foils (2) exposed in the air.
This is a cooling shower that spouts th IW liquid (13) to prevent heat generation in the shower (29).
) and (3o).
3) uses the electrolytic solution (13) and chemical solution (1) described in the description.
Similar to the relationship with 8), this is because water or the like will not bring about an intensification of the composition of the chemical liquid (18) and will not achieve the purpose of the J'jT period.

上記の構成からなる化成製置に屯惚晶例えばね血止した
At箔(22)をセントし走行さぜるとAt箔(22)
には直流電源(11)の@極に接続された陽極電極+1
4015)から電解液(18)を介しそ藺電されるが、
At箔(22)と電極との接触面積は電解液(1日)中
の陽極電極+14)(15)の対向面となるので非常に
大きくな勺、したがって電流密度は大幅に軽減されるか
ら発熱による箔の変形や従来0.5%(長さまたは重量
比)程度発生していたスパーク不良は皆無となシスムー
ズに走行させることができるはか、従来のような金)6
40−ラーの定期的ω[磨も不要となる効果がろる0菫
た屯施蕃吸か軽減されるため従来に比して鎖電できるi
I−呑亀五値が大幅にアップし、これによって化成工程
のU箔(22)走行速度を高めることができる。
For example, when At foil (22) that has stopped bleeding is placed in a chemical processing machine with the above-mentioned configuration and run, At foil (22) is formed.
is an anode electrode +1 connected to the @ pole of the DC power supply (11).
4015) through the electrolyte (18),
The contact area between the At foil (22) and the electrode is the opposite surface of the anode electrode + 14) (15) in the electrolyte (1 day), so it has a very large area, so the current density is significantly reduced, so no heat is generated. There is no deformation of the foil or spark defects that conventionally occurred at around 0.5% (length or weight ratio), and the system can run smoothly.
40-ra periodic ω [The effect of not requiring polishing is that it reduces the need for 0-sum ta-ton application, so it is possible to chain electricity compared to the conventional method.
The I-Nonki five-point value is significantly increased, and as a result, the running speed of the U foil (22) in the chemical conversion process can be increased.

発明者の実縮2によれば第1図に示したr[米例にょる
化成方法と比軟し下表のような走行速度を伶ることかで
さる。
According to the inventor's actual reduction 2, the comparison of the chemical conversion method shown in FIG. 1 with the chemical conversion method shown in FIG.

走行速度 (ひ!ヅmi、n ) 上記の結果から明らかなように本発明になる化成方法で
は電箆密度が大fI’hiに軽減ちれるから発熱やスパ
ークによる不良を皆無にできるほか金属ローラーのef
塵が不要となシ、さらにν箔の走行M度を従来の約2倍
に高めることができ、これによって約2倍の生産性を得
ることができる。
Running speed (hi!zumi, n) As is clear from the above results, the chemical formation method of the present invention reduces the electric knife density to a large fI'hi, which eliminates defects caused by heat generation and sparks, and also eliminates metal rollers. ef
Dust is not required, and the running degree of the ν foil can be increased to approximately twice that of the conventional method, thereby achieving approximately twice the productivity.

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

第1図は従来の化成方法゛を説す1するための断面41
1成因、第2図は本如明になる化成方法を説明するため
の〜1面構成図でめる。 +11−−−一直五゛h1.源 (12)−−−−−一
進電榴(13)−−−−−−@酢液 (14H15)(
16)−−−−一陽執電極(:17 )−−−−一化成
檜 IIBト−−一化成液119)(20)(21)−
−−一陰他電極(22)−−−−一粗血止済U箔 +233(25N26028J−−−−−・絶縁ローラ
ー+243 (271−−−−−一液中絶はローラー+
293 (30)−−−−シャワー 特  許  出  願  人 マルコン電子株式会社 手  続  補  正  書 (自発)特許庁長官 若
杉和夫 殿 1、事件の表示 昭和58年特許願第  91687号 2、発明の名称 電解コンデンサ用電極箔の化成方法 3、補正をする者 事件との関係  特許出願人 住所 山形系r′五笛讐1560番地 電話 長井(0238B) 4−2131 (大代表)
郵便番号  993 自発的 5、補正の対象 明細書の「発明の詳細な説明」の檎 へ補正の内容 (1)明細書5頁14行 [電解液(18) Jとあるを[電解液(13) Jと
訂正する。 (21明細曹5頁15行 「電解液(18)Jとあるを「電解液(13)Jと訂正
する。 以  上
Figure 1 shows a cross section 41 for explaining the conventional chemical formation method.
FIG. 2 is a first-page structural diagram for explaining the chemical conversion method disclosed herein. +11---One straight five h1. Source (12)-----Ishin Electric Copper (13)-----@Vinegar Solution (14H15)(
16)----Ichiyotsu electrode (:17)----Ichikasei Hinoki IIBto---Ichikasei liquid 119) (20) (21)-
--- One cathode and other electrode (22) --- One rough hemostatic U foil + 233 (25N26028J --- Insulated roller + 243 (271 --- One liquid abort is roller +
293 (30)---Shower Patent Applicant Marukon Electronics Co., Ltd. Procedural Amendment (Spontaneous) Commissioner of the Patent Office Kazuo Wakasugi 1, Indication of Case Patent Application No. 91687 of 1982 2, Title of Invention Chemical Formation Method for Electrode Foil for Electrolytic Capacitors 3, Relationship with the Case of Person Who Makes Amendment Patent Applicant Address: Yamagata-kei R'Gofuei 1560 Telephone: Nagai (0238B) 4-2131 (Main Representative)
Postal code 993 Voluntary 5, Contents of amendment to the "Detailed Description of the Invention" of the specification to be amended (1) Page 5, line 14 of the specification [Electrolyte (18) J] [Electrolyte (13) ) Correct it as J. (21 Specification, page 5, line 15, “Electrolyte (18) J” should be corrected to “Electrolyte (13) J.”)

Claims (1)

【特許請求の範囲】 (1)直tlt′a源に接続さ7’した陰極電極を電解
液中に有する通電槽と、該通電槽の後に直流*源に接続
された陰極電極を化成液中に有する化成槽を配し、前記
通電槽中を電極箔を走行させたのち化成槽中を走行させ
ることを特徴とする電解コンデンサ用電極箔の化成方法
。 (2〕電解液および化成液が1〜2 Q wt%アジピ
ン酸アンモン水溶液または該アジピン醗アンモン水溶液
に0.O1〜0.1wt%のリン酸を加えた水溶液から
なることを特徴とする特許請求の柁囲第(1)項記載の
電解コンデンサ用電極箔の化成方法0 (3)通電槽と化成槽との間で空気中に露出している電
極箔に電解液を噴出させて冷却することを特徴とする特
許請求の軛囲第(1)項または第(2)項記載の゛電解
コンデンサ用電極箔の化成方法。
[Scope of Claims] (1) An energizing tank having a cathode electrode connected to a direct tlt'a source in an electrolytic solution, and a cathode electrode connected to a direct current* source after the energizing tank in a chemical solution. 1. A method for chemically forming an electrode foil for an electrolytic capacitor, the method comprising disposing a chemically forming tank having a chemical forming tank, and running the electrode foil through the current-carrying tank, and then running the electrode foil through the chemically forming tank. (2) A patent claim characterized in that the electrolytic solution and the chemical solution consist of a 1-2 Q wt% ammonium adipate aqueous solution or an aqueous solution in which 0.01-0.1 wt% phosphoric acid is added to the adipic ammonium aqueous solution. Method for forming an electrode foil for an electrolytic capacitor as described in Clause (1) of Section 0 (3) Cooling the electrode foil exposed in the air between the energizing tank and the chemical forming tank by spouting an electrolyte onto the electrode foil. ``A method for forming an electrode foil for an electrolytic capacitor,'' as set forth in paragraph (1) or (2) of the claim.
JP9168783A 1983-05-24 1983-05-24 Method of compounding electrode foil for electrolytic condenser Pending JPS59215716A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9168783A JPS59215716A (en) 1983-05-24 1983-05-24 Method of compounding electrode foil for electrolytic condenser

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9168783A JPS59215716A (en) 1983-05-24 1983-05-24 Method of compounding electrode foil for electrolytic condenser

Publications (1)

Publication Number Publication Date
JPS59215716A true JPS59215716A (en) 1984-12-05

Family

ID=14033412

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9168783A Pending JPS59215716A (en) 1983-05-24 1983-05-24 Method of compounding electrode foil for electrolytic condenser

Country Status (1)

Country Link
JP (1) JPS59215716A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62202513A (en) * 1986-02-28 1987-09-07 松下電器産業株式会社 Formation of electrode foil for aluminum electrolytic capacitor
JP2010245065A (en) * 2009-04-01 2010-10-28 Nippon Chemicon Corp Electrode material for electrolytic capacitor

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62202513A (en) * 1986-02-28 1987-09-07 松下電器産業株式会社 Formation of electrode foil for aluminum electrolytic capacitor
JP2010245065A (en) * 2009-04-01 2010-10-28 Nippon Chemicon Corp Electrode material for electrolytic capacitor

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