JPS60726A - Method of producing anode foil for aluminum electrolytic condenser - Google Patents

Method of producing anode foil for aluminum electrolytic condenser

Info

Publication number
JPS60726A
JPS60726A JP10791883A JP10791883A JPS60726A JP S60726 A JPS60726 A JP S60726A JP 10791883 A JP10791883 A JP 10791883A JP 10791883 A JP10791883 A JP 10791883A JP S60726 A JPS60726 A JP S60726A
Authority
JP
Japan
Prior art keywords
foil
anode foil
aluminum electrolytic
product
boiling
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
JP10791883A
Other languages
Japanese (ja)
Inventor
原川 順弘
鈴木 繁男
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.)
NEC Platforms Ltd
Original Assignee
Nitsuko Corp
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 Nitsuko Corp filed Critical Nitsuko Corp
Priority to JP10791883A priority Critical patent/JPS60726A/en
Publication of JPS60726A publication Critical patent/JPS60726A/en
Pending legal-status Critical Current

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  • Electrolytic Production Of Metals (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、At電解コンデンサの高圧用陽極箔の製造方
法に係り、特にCV積(陽極箔の単位面積当たりの静電
容量とその箔のもつ耐電圧値の積)を改良する製造方法
に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for manufacturing a high-voltage anode foil for an At electrolytic capacitor, particularly the CV product (the product of the capacitance per unit area of the anode foil and the withstand voltage value of the foil). The present invention relates to a manufacturing method for improving.

一般に、At電解コンデンサ用の陽極箔は、まずA4箔
をエツチングして表面な粗面化し、表面積を拡大する処
理を施した後、該エツチング箔上にA4の酸化皮膜Az
2o3を形成させる化成工程を経て製造される。
In general, anode foil for At electrolytic capacitors is made by first etching the A4 foil to roughen the surface and expand the surface area, and then forming an oxide film Az on the etched foil.
It is manufactured through a chemical conversion process that forms 2o3.

この化成工程は、大別して第1図に示す如く前処理工程
1と酸化皮膜形成工程2より成り、前処理工程において
は、高圧用(16oWV以上)陽極箔を製造する場合は
、エツチング箔6を通常純水中でボイルし、該エツチン
グ箔の表面に水酸化アルミAL(OH)3の皮膜を形成
したのち、次の酸化皮膜形成工程では、化成液と呼ばれ
る電解液中で該箔に化成電圧を印加して、電解酸化を行
ない、前記AL(OH)sをAz2o3に変換形成させ
、陽極箔4が製造されている。ところでこのように製造
される陽極箔のCV積は、その値が大きい程、該陽極箔
を使用したA4電解コンデンザを小型にできるので、C
V積を太き(するだめの研究が11々行なわれている。
This chemical conversion process is roughly divided into a pretreatment process 1 and an oxide film formation process 2 as shown in FIG. Usually, after boiling in pure water to form a film of aluminum hydroxide AL(OH)3 on the surface of the etching foil, in the next oxide film forming step, the foil is heated to a chemical formation voltage in an electrolytic solution called chemical liquid. is applied to perform electrolytic oxidation to convert the AL(OH)s into Az2o3, thereby manufacturing the anode foil 4. By the way, the larger the CV product of the anode foil manufactured in this way, the more compact the A4 electrolytic capacitor using the anode foil can be.
Eleven studies have been conducted on increasing the V product.

CV積を大きくする方法は、二法あり、第一の方法は前
記エツチング箔のエツチング倍率を大きくすること即ち
、At箔の表面の粗面化度合云いかえれば表面積の拡大
率を大きくする方法であり、第二の方法は、エツチング
箔上に均一にムラな(A42o 3の皮膜を化成によっ
て形成させることである。後者の方法では、A42o3
の皮膜を能率良(形成させるために、前記前処理工程で
、できるだけ多くのAt(OH)3を形成させることが
重要であるが、前記純水中でのエツチング箔のボイル処
理時間を長くしても、成る限度以上は該箔の重量増加が
みられずAt(OH)3が形成されないことがわかって
おり、従って、該箔を一定の化成電圧で化成して酸化皮
膜XZ、、O3を形成した後の該陽極箔のCV積もその
増大に限界がある。第6図は、純水中のボイル処理を行
なわず化成した後の陽極箔のCViを100とした場合
の純水ホイル処理時間とCV積の関係を示したもので、
ボイル処理時間を長くしてもCV積は一定値で飽和傾向
を示している。従って、従来ホイル時間は10分程度が
一般的である。
There are two methods to increase the CV product. The first method is to increase the etching magnification of the etching foil, that is, to increase the degree of roughening of the surface of the At foil, or in other words, to increase the expansion rate of the surface area. The second method is to form a uniform and uneven film of A42o3 on the etching foil by chemical conversion.
In order to form a film efficiently, it is important to form as much At(OH)3 as possible in the pretreatment process, but it is important to increase the boiling time of the etched foil in pure water. However, it is known that the weight of the foil does not increase and At(OH)3 is not formed beyond a certain limit. Therefore, the foil is anodized at a certain anodizing voltage to form an oxide film XZ, O3. There is a limit to the increase in the CV product of the anode foil after formation. Figure 6 shows the pure water foil treatment when the CVi of the anode foil after chemical conversion without boiling in pure water is 100. This shows the relationship between time and CV product.
Even if the boiling time is increased, the CV product remains constant and shows a tendency to saturate. Therefore, conventional foiling time is generally about 10 minutes.

本発明は、前記化成工程の前処理工程を改良し、酸化皮
膜形成後の陽極箔のCV積を従来工法による陽極箔より
増大、改良する高圧用陽極箔の製造方法を提供すること
を目的とする。以下、本発明について詳細に説明する。
An object of the present invention is to provide a method for manufacturing a high-pressure anode foil, which improves the pretreatment step of the chemical conversion step and increases and improves the CV product of the anode foil after forming an oxide film compared to anode foils produced by conventional methods. do. The present invention will be explained in detail below.

第2図は、本発明の製造方法の工程図で、11.12は
前処理工程で11は従来性なわれている純水ボイル工程
、12は本発明の特徴である有機酸水溶液によるボイル
工程(以下有機酸ボイル工程と云う)である。
FIG. 2 is a process diagram of the manufacturing method of the present invention, where 11 and 12 are pretreatment steps, 11 is a conventional pure water boiling step, and 12 is a boiling step using an organic acid aqueous solution, which is a feature of the present invention. (hereinafter referred to as organic acid boiling process).

即ち、本発明は、従来の化成工程の前処理工程に純水ボ
イル工程の外に有機酸ボイル工程を加えたことである。
That is, the present invention adds an organic acid boiling process to the pretreatment process of the conventional chemical conversion process in addition to the pure water boiling process.

以下本発明を、実施例に基づいて述べる。Atのエツチ
ング箔を前処理として純水中で10分間ボイル処理した
後、有機酸水溶液として濃度Q、5 w t%の安息香
酸水溶液を調製し、該水溶液中で該箔を更に2〜10分
間ボイル処理を行ない、有機酸ボイル処理後の該箔を酸
化皮膜形成工程で化成し、この工程で完成した陽極箔の
CV積を測定して、従来の前処理すなわち、純水ボイル
処理のみの陽極箔のCV積と比較したところ、本発明の
有機酸ボイル処理した陽極箔のCV積が約10%増大す
ることを見出した。このCV積の増大の結果を第4図に
示す。これから、有機酸ボイル処理時間は5分で充分で
ある。次いで他の有機酸としてフェニン酸等の水溶液を
用いて、前記と同様の処理を行い、CV積を比較し、そ
の増大効果が各々あることを確認できた。これらの有機
酸処理の及ぼす作用は、酸化皮膜(At203)の形成
の促進と均一性の増大に寄与しているものと思考され、
その機構はまだ充分解明できないが、エツチング箔表面
の界面活性化作用が、At2°3の形成に好影響を与え
ているものと考えられる。また有機酸水溶液の濃度につ
いて考察するに、 4・安息香酸とクエン酸について、
各種の濃度の水溶液を用いて、純水ボイル処理を10分
間行なった後のエツチング箔を、各々5分間有機酸ホイ
ル処理を行ない、該箔を化成して得た陽極箔のC÷積を
純水ボイル処理のみをした時のCV積を100として、
示したのが第5図である。CV積の増加度合は、濃度が
低いと小さく、また濃度が高くなるとその度合′は増加
するが、ある濃度以上になると再び小さくなる傾向を示
し、実用範囲としては、001〜1.0wt%の濃度範
囲が、この発明の目的から適当である。
The present invention will be described below based on examples. After boiling the At etching foil in pure water for 10 minutes as a pretreatment, a benzoic acid aqueous solution with a concentration of Q and 5 wt% was prepared as an organic acid aqueous solution, and the foil was further boiled in the aqueous solution for 2 to 10 minutes. The foil after boiling with organic acid is chemically converted in an oxide film forming process, and the CV product of the completed anode foil is measured in this process. When compared with the CV product of the foil, it was found that the CV product of the anode foil treated with organic acid boiling of the present invention increases by about 10%. The result of this increase in CV product is shown in FIG. From this, it can be seen that 5 minutes is sufficient for the organic acid boil treatment time. Next, the same treatment as above was performed using an aqueous solution of phenic acid or the like as another organic acid, and the CV products were compared, and it was confirmed that each had an increasing effect. The effects of these organic acid treatments are thought to contribute to promoting the formation of the oxide film (At203) and increasing its uniformity.
Although the mechanism has not yet been fully elucidated, it is thought that the surface activation effect of the etching foil surface has a favorable effect on the formation of At2°3. Also, considering the concentration of organic acid aqueous solution, 4. Regarding benzoic acid and citric acid,
The etched foils were boiled in pure water for 10 minutes using aqueous solutions of various concentrations, then treated with an organic acid foil for 5 minutes each, and the product of the anode foil obtained by chemically converting the etched foils was calculated as follows: Assuming that the CV product when only water boiling treatment is performed is 100,
This is shown in FIG. The degree of increase in the CV product is small when the concentration is low, and increases when the concentration is high, but it tends to decrease again when the concentration exceeds a certain level. A range of concentrations is suitable for the purposes of this invention.

以上述べたように、前処理手段として、従来の純水ボイ
ル処理に加えて、有機酸ボイル処理を更に付加すること
によって、得られる陽極箔のCV積を増大かつ改善する
ことが可能であり、従来の製造法では得られない優れた
At電解コンデンサ用陽極箔を提供することができる。
As described above, by adding an organic acid boiling treatment in addition to the conventional pure water boiling treatment as a pretreatment means, it is possible to increase and improve the CV product of the obtained anode foil. It is possible to provide an excellent anode foil for At electrolytic capacitors that cannot be obtained by conventional manufacturing methods.

CV積の増大した分だけ、電解コンデンサに使用する陽
極箔の量が従来より節減でき、且つ、小形1軒量化する
効果が生じ、経済的にも実用的にも、有用である。
The amount of anode foil used in the electrolytic capacitor can be reduced by the increase in the CV product compared to the conventional method, and the capacitor can be made smaller in size, which is useful both economically and practically.

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

第1図は、従来の製造方法を示す工程図。第2図は本発
明の製造方法を示す工程図。第6図は、従来の製造方法
による陽極箔の特性図。第4図および第5図は、本発明
の一実施例による陽極箔の特性図。 1:前処理工程、2:酸化皮膜形成工程、6:エノチン
グ箔4:陽極箔、11:純水ボイル処理工程。 12:有機酸ボイル処理工程 特許出願人 61図 菫2図 Y 3 図 、、、、 ¥14図 芦
FIG. 1 is a process diagram showing a conventional manufacturing method. FIG. 2 is a process diagram showing the manufacturing method of the present invention. FIG. 6 is a characteristic diagram of the anode foil produced by the conventional manufacturing method. 4 and 5 are characteristic diagrams of an anode foil according to an embodiment of the present invention. 1: Pretreatment step, 2: Oxide film formation step, 6: Enoting foil 4: Anode foil, 11: Pure water boiling step. 12: Organic acid boil treatment process patent applicant Fig. 61 Sumire 2 Fig. Y 3 Fig. ¥14 Fig.

Claims (2)

【特許請求の範囲】[Claims] (1)アルミノエツチング箔を化成してアルミ電解コン
デンサ用陽極箔を製造する工程において、前機酸ボイル
処理を行うことを特徴とするアルミ電解コンデンサ用陽
極箔の製造方法。
(1) A method for manufacturing an anode foil for an aluminum electrolytic capacitor, characterized in that in the process of chemically converting the alumino etched foil to produce the anode foil for an aluminum electrolytic capacitor, a pre-acid boiling treatment is performed.
(2)有機酸が安息香酸、クエン酸のいずれが1種で、
且つその水溶液濃度が0.01〜1.0wt%であるこ
とを特徴とする特許請求の範囲第(1)項記載のアルミ
電解コンデンサ用陽極箔の製造方法。
(2) The organic acid is either benzoic acid or citric acid,
The method for manufacturing an anode foil for an aluminum electrolytic capacitor according to claim 1, wherein the aqueous solution concentration is 0.01 to 1.0 wt%.
JP10791883A 1983-06-17 1983-06-17 Method of producing anode foil for aluminum electrolytic condenser Pending JPS60726A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10791883A JPS60726A (en) 1983-06-17 1983-06-17 Method of producing anode foil for aluminum electrolytic condenser

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10791883A JPS60726A (en) 1983-06-17 1983-06-17 Method of producing anode foil for aluminum electrolytic condenser

Publications (1)

Publication Number Publication Date
JPS60726A true JPS60726A (en) 1985-01-05

Family

ID=14471345

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10791883A Pending JPS60726A (en) 1983-06-17 1983-06-17 Method of producing anode foil for aluminum electrolytic condenser

Country Status (1)

Country Link
JP (1) JPS60726A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0243717A (en) * 1988-08-03 1990-02-14 Shinei Tsushin Kogyo Kk Manufacture of electrode foil for aluminum electrolytic capacitor

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0243717A (en) * 1988-08-03 1990-02-14 Shinei Tsushin Kogyo Kk Manufacture of electrode foil for aluminum electrolytic capacitor

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