JP2791392B2 - Aluminum foil for anode of electrolytic capacitor - Google Patents

Aluminum foil for anode of electrolytic capacitor

Info

Publication number
JP2791392B2
JP2791392B2 JP1094858A JP9485889A JP2791392B2 JP 2791392 B2 JP2791392 B2 JP 2791392B2 JP 1094858 A JP1094858 A JP 1094858A JP 9485889 A JP9485889 A JP 9485889A JP 2791392 B2 JP2791392 B2 JP 2791392B2
Authority
JP
Japan
Prior art keywords
aluminum foil
foil
anode
ppm
electrolytic capacitor
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 - Fee Related
Application number
JP1094858A
Other languages
Japanese (ja)
Other versions
JPH02274832A (en
Inventor
寿雄 斎藤
啓一 荒木
兼滋 山本
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.)
Nippon Foil Manufacturing Co Ltd
Original Assignee
Nippon Foil Manufacturing 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 Nippon Foil Manufacturing Co Ltd filed Critical Nippon Foil Manufacturing Co Ltd
Priority to JP1094858A priority Critical patent/JP2791392B2/en
Publication of JPH02274832A publication Critical patent/JPH02274832A/en
Application granted granted Critical
Publication of JP2791392B2 publication Critical patent/JP2791392B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Manufacture And Refinement Of Metals (AREA)
  • Fixed Capacitors And Capacitor Manufacturing Machines (AREA)

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION 【産業上の利用分野】[Industrial applications]

本発明は、高容量の電解コンデンサ陽極箔を得るのに
適したアルミニウム箔に関するものである。
The present invention relates to an aluminum foil suitable for obtaining a high capacity electrolytic capacitor anode foil.

【従来の技術】[Prior art]

従来より、高容量の電解コンデンサ陽極箔を得るのに
純度99.9%以上のアルミニウム箔が用いられてきた。そ
して、更に高容量の電解コンデンサ陽極箔が要求され、
純度99.99%以上のアルミニウム箔が用いられている。
しかし、高容量に対する要求は、更に厳しくなり、純度
99.999%以上の4アルミニウム箔を用いて電解コンデン
サ陽極箔を製造することが望まれている。 純度99.999%以上のアルミニウム箔を製造するために
は、当然に高純度のアルミニウム地金が必要となる。ア
ルミニウム地金は、アルミニウム含有鉱石を精製して作
成されるが、高純度のものを得ようとすると、精製工程
が複雑になり、アルミニウム地金が高価になってしま
う。特に、純度99.999%以上のアルミニウム地金は非常
に高価である。従って、この地金より得られる純度99.9
99%以上のアルミニウム箔は非常に高価なものになり、
この結果陽極箔として用いるには経済的に成立しない状
況となっている。
Conventionally, an aluminum foil having a purity of 99.9% or more has been used to obtain a high capacity electrolytic capacitor anode foil. And a higher capacity electrolytic capacitor anode foil is required,
Aluminum foil with a purity of 99.99% or more is used.
However, the demand for higher capacity has become more stringent,
It is desired to produce an electrolytic capacitor anode foil using 99.999% or more of 4 aluminum foil. In order to produce an aluminum foil having a purity of 99.999% or more, a high-purity aluminum metal is naturally required. Aluminum ingots are produced by refining ores containing aluminum. However, in order to obtain high-purity ones, the refining process becomes complicated and the aluminum ingots become expensive. In particular, aluminum ingot having a purity of 99.999% or more is very expensive. Therefore, the purity obtained from this metal is 99.9
More than 99% of aluminum foil becomes very expensive,
As a result, it is not economically feasible to use it as an anode foil.

【発明が解決しようとする課題】[Problems to be solved by the invention]

そこで、本発明は、アルミニウム箔中にある特定の元
素を特定量含有させることにより、純度99.99%程度の
アルミニウム箔であっても、純度99.999%以上のアルミ
ニウム箔を使用した場合と同程度の高容量の電解コンデ
ンサ陽極箔が得られるようにしたものである。
Accordingly, the present invention provides an aluminum foil having a purity of about 99.99% by including a specific element in the aluminum foil in a specific amount, so that the aluminum foil having a purity of about 99.999% or higher is used. An electrolytic capacitor anode foil having a capacity is obtained.

【課題を解決するための手段及び作用】Means and Action for Solving the Problems

即ち、本発明は、Fe4〜13ppm、Si4〜15ppm、Cu15〜65
ppm、不可避元素の総計35ppm以下、残部Alよりなり、Cu
とFeの量は、(80−5×Fe)≦Cu≦(85−5×Fe)〔但
し、単位はppm〕の関係を満たすことを特徴とする電解
コンデンサ陽極用アルミニウム箔に関するものである。 本発明に係る電解コンデンサ陽極用アルミニウム箔中
には、Al以外の必須の成分元素としてFe,Si,Cuが含有さ
れている。 Feは4〜13ppm含有されている。なお、1ppmは、%表
示では0.0001%である。Feを4ppm未満にすると、Al純度
を99.999%程度にしなければならず、アルミニウム地金
が高価になるため好ましくない。また、Feが13ppmを超
えると、アルミニウム箔のエッチング時に過溶解が生
じ、高容量の陽極箔が得られないので好ましくない。 Siは4〜15ppm含有されている。Siを4ppm未満にする
と、Al純度を99.999%程度にしなければならず、アルミ
ニウム地金が高価になるため好ましくない。また、Siが
15ppmを超えると、アルミニウム箔のエッチング時に過
溶解が生じ、高容量の陽極箔が得られないので好ましく
ない。 Cuは15〜65ppm含有されている。Cuを15ppm未満にする
と、アルミニウム箔のエッチング時に箔表面が溶解しに
くくなり、高容量の陽極箔が得られないので好ましくな
い。また、Cuが65ppmを超えると、アルミニウム箔のエ
ッチング時に過溶解が生じ、高容量の陽極箔が得られな
いので好ましくない。 不可避元素の総計は35ppmを超えて含有されてはいけ
ない。不可避元素としては、Mg,Mn,Ti,Zn,Ga等が挙げら
れる。不可避元素の総計が35ppmを超えると、アルミニ
ウム箔のエッチング時に過溶解が生じたり、アルミニウ
ム箔の引張強度が低下したりするので、好ましくない。 そして、本発明においては、FeとCuとの量が次の如き
関係にあることが必要である。即ち、(80−5×Fe)≦
Cu≦(85−5×Fe)〔但し、単位はppm〕の関係であ
る。Cu<(80−5×Fe)となると、アルミニウム箔のエ
ッチング時に箔表面が溶解しにくくなり、高容量の陽極
箔が得られないので好ましくない。Cu>(85−5×Fe)
となると、アルミニウム箔のエッチング時に過溶解が生
じ、高容量の陽極箔が得られないので好ましくない。 本発明に係る電解コンデンサ陽極用アルミニウム箔
は、従来公知の方法で製造することができる。即ち、上
記した如き成分組成の鋳塊を作成し、均熱化処理,熱間
圧延,冷間圧延,中間焼純,最終焼鈍を所望に応じて施
して製造することができる。
That is, the present invention, Fe4 ~ 13ppm, Si4 ~ 15ppm, Cu15 ~ 65
ppm, total of unavoidable elements 35 ppm or less, balance Al, Cu
And the amount of Fe satisfies the relationship of (80-5 × Fe) ≦ Cu ≦ (85-5 × Fe), where the unit is ppm. The aluminum foil for an anode of an electrolytic capacitor according to the present invention contains Fe, Si, and Cu as essential component elements other than Al. Fe is contained in an amount of 4 to 13 ppm. Note that 1 ppm is 0.0001% in%. If Fe is less than 4 ppm, the Al purity must be about 99.999%, which is not preferable because the aluminum base metal becomes expensive. On the other hand, when Fe exceeds 13 ppm, overdissolution occurs during etching of the aluminum foil, and a high-capacity anode foil cannot be obtained, which is not preferable. Si is contained at 4 to 15 ppm. If the content of Si is less than 4 ppm, the purity of Al must be about 99.999%, which is not preferable because the aluminum base metal becomes expensive. In addition, Si
If it exceeds 15 ppm, overdissolution occurs during etching of the aluminum foil, and a high-capacity anode foil cannot be obtained. Cu is contained in an amount of 15 to 65 ppm. If the Cu content is less than 15 ppm, the foil surface becomes difficult to dissolve during the etching of the aluminum foil, and a high-capacity anode foil cannot be obtained. On the other hand, if Cu exceeds 65 ppm, overdissolution occurs during etching of the aluminum foil, and a high-capacity anode foil cannot be obtained. The total amount of unavoidable elements must not exceed 35 ppm. Examples of inevitable elements include Mg, Mn, Ti, Zn, and Ga. If the total amount of the unavoidable elements exceeds 35 ppm, overdissolution occurs during the etching of the aluminum foil, and the tensile strength of the aluminum foil decreases, which is not preferable. In the present invention, it is necessary that the amounts of Fe and Cu have the following relationship. That is, (80−5 × Fe) ≦
Cu ≦ (85−5 × Fe) [where the unit is ppm]. If Cu <(80−5 × Fe), the foil surface becomes difficult to dissolve during etching of the aluminum foil, and a high-capacity anode foil is not obtained, which is not preferable. Cu> (85-5 × Fe)
In such a case, excessive melting occurs during etching of the aluminum foil, and a high-capacity anode foil cannot be obtained, which is not preferable. The aluminum foil for an anode of an electrolytic capacitor according to the present invention can be manufactured by a conventionally known method. That is, it can be produced by preparing an ingot having the above component composition and subjecting it to soaking treatment, hot rolling, cold rolling, intermediate annealing and final annealing as required.

【実施例】 第1表に示す如き成分組成の鋳塊を水冷鋳造によって
作成した。この鋳塊の寸法は、60mm厚さ×300mm巾×800
mm長さであった。この鋳塊を表面面削後、560℃で4時
間、更に480℃で8時間均熱化処理した。その後、出側
温度250℃で熱間圧延を行い、次いで1パスリダクショ
ン約50%で冷間圧延を繰り返し、厚さ90μのアルミニウ
ム箔を得た。そして、このアルミニウム箔を石油系溶剤
で脱脂処理し、更に不活性雰囲気で最終焼鈍し、電解コ
ンデンサ陽極用アルミニウム箔を得た。 この電解コンデンサ陽極用アルミニウム箔を、次のよ
うにしてエッチングした。即ち、硫酸:塩酸:蒸留水=
800:40:3160(体積比)の組成で、温度70〜85℃のエッ
チング液中にこのアルミニウム箔を浸漬し、直流4.0A/5
0×2cm2の電流を5分間与えてエッチングした。そし
て、このときの溶解減量を測定した。溶解減量は実施例
3のものを基準として、即ち1として相対評価を行っ
た。その結果は、第2表のとおりであった。なお、溶解
減量は0.95〜1.05の範囲にあるものが合格である。溶解
減量が0.95未満であると、アルミニウム箔表面が元の状
態で残っている部分が存在し、箔表面に微細な凹凸が十
分形成されずに、表面積の拡大が図れず、高容量の陽極
箔が得られない。また、溶解減量が1.05を超えると、超
溶解により箔表面に比較的大きな凹部が形成され、微細
な凹凸が十分形成されずに、表面積の拡大が図れず、高
容量の陽極箔が得られない。 以上の結果より明らかなとおり、実施例に係る電解コ
ンデンサ陽極用アルミニウム箔を用いれば、強度低下を
来すことなく、高容量の陽極箔が得られることが判る。
これに対し、比較例に係るアルミニウム箔を用いると、
高容量の陽極箔が得られないことが判る。
EXAMPLES Ingots having the component compositions shown in Table 1 were prepared by water-cooled casting. The dimensions of this ingot are 60mm thickness x 300mm width x 800
mm in length. After the surface of this ingot was ground, it was soaked at 560 ° C. for 4 hours and further at 480 ° C. for 8 hours. Thereafter, hot rolling was performed at an outlet temperature of 250 ° C., and then cold rolling was repeated at about 50% per pass reduction to obtain an aluminum foil having a thickness of 90 μm. Then, this aluminum foil was degreased with a petroleum-based solvent, and finally annealed in an inert atmosphere to obtain an aluminum foil for an anode of an electrolytic capacitor. The aluminum foil for an anode of an electrolytic capacitor was etched as follows. That is, sulfuric acid: hydrochloric acid: distilled water =
This aluminum foil is immersed in an etching solution having a composition of 800: 40: 3160 (volume ratio) and a temperature of 70 to 85 ° C., and a direct current of 4.0 A / 5
Etching was performed by applying a current of 0 × 2 cm 2 for 5 minutes. Then, the dissolution loss at this time was measured. Dissolution weight loss was evaluated relative to that of Example 3, that is, 1 as a relative evaluation. The results are as shown in Table 2. In addition, the thing whose dissolution loss is in the range of 0.95 to 1.05 passes. If the dissolution loss is less than 0.95, there is a portion where the aluminum foil surface remains in its original state, fine irregularities are not sufficiently formed on the foil surface, the surface area cannot be expanded, and a high capacity anode foil Can not be obtained. Also, when the dissolution loss exceeds 1.05, relatively large recesses are formed on the foil surface due to super-dissolution, fine irregularities are not sufficiently formed, the surface area cannot be increased, and a high capacity anode foil cannot be obtained. . As is evident from the above results, it is understood that the use of the aluminum foil for an anode of an electrolytic capacitor according to the example can provide a high-capacity anode foil without a decrease in strength.
In contrast, when the aluminum foil according to the comparative example is used,
It turns out that a high capacity anode foil cannot be obtained.

【発明の効果】【The invention's effect】

以上説明したように、本発明に係る電解コンデンサ陽
極用アルミニウム箔は、ある特定の成分組成からなって
いるので、Al純度を99.99%程度としても、エッチング
性が良好で、このアルミニウム箔を用いて高容量の陽極
箔を得ることができる。従って、Al純度99.999%以上の
高価なアルミニウム箔を用いなくても、比較的安価なAl
純度99.99%程度のアルミニウム箔を用いることによ
り、前者と同程度の高容量の陽極箔を得ることができ
る。依って、本発明は安価に高容量の陽極箔を提供しう
るという効果を奏するものである。
As described above, the aluminum foil for an anode of an electrolytic capacitor according to the present invention is composed of a specific component composition. Therefore, even if the Al purity is about 99.99%, the etching property is good. A high capacity anode foil can be obtained. Therefore, relatively inexpensive Al can be used without using expensive aluminum foil with an Al purity of 99.999% or more.
By using an aluminum foil having a purity of about 99.99%, it is possible to obtain an anode foil having the same high capacity as the former. Therefore, the present invention has an effect that an inexpensive high-capacity anode foil can be provided.

───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特許2657262(JP,B2) 特公 昭45−25978(JP,B1) (58)調査した分野(Int.Cl.6,DB名) C22C 21/00 H01G 9/042────────────────────────────────────────────────── ─── Continuation of front page (56) References Patent 2657262 (JP, B2) Japanese Patent Publication No. 45-25978 (JP, B1) (58) Fields investigated (Int. Cl. 6 , DB name) C22C 21/00 H01G 9/042

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】Fe4〜13ppm、Si4〜15ppm、Cu15〜65ppm、
不可避元素の総計35ppm以下、残部Alよりなり、CuとFe
の量は、(80−5×Fe)≦Cu≦(85−5×Fe)〔但し、
単位はppm〕の関係を満たすことを特徴とする電解コン
デンサ陽極用アルミニウム箔。
(1) Fe4 to 13 ppm, Si4 to 15 ppm, Cu15 to 65 ppm,
Total of 35 ppm or less of unavoidable elements, balance of Al, Cu and Fe
The amount of (80-5 × Fe) ≦ Cu ≦ (85-5 × Fe) [however,
The unit is ppm], an aluminum foil for an anode of an electrolytic capacitor.
JP1094858A 1989-04-14 1989-04-14 Aluminum foil for anode of electrolytic capacitor Expired - Fee Related JP2791392B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1094858A JP2791392B2 (en) 1989-04-14 1989-04-14 Aluminum foil for anode of electrolytic capacitor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1094858A JP2791392B2 (en) 1989-04-14 1989-04-14 Aluminum foil for anode of electrolytic capacitor

Publications (2)

Publication Number Publication Date
JPH02274832A JPH02274832A (en) 1990-11-09
JP2791392B2 true JP2791392B2 (en) 1998-08-27

Family

ID=14121732

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1094858A Expired - Fee Related JP2791392B2 (en) 1989-04-14 1989-04-14 Aluminum foil for anode of electrolytic capacitor

Country Status (1)

Country Link
JP (1) JP2791392B2 (en)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2657262B2 (en) 1987-10-14 1997-09-24 日本製箔株式会社 Aluminum alloy foil for anode of electrolytic capacitor

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2657262B2 (en) 1987-10-14 1997-09-24 日本製箔株式会社 Aluminum alloy foil for anode of electrolytic capacitor

Also Published As

Publication number Publication date
JPH02274832A (en) 1990-11-09

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