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JPS6350849B2 - - Google Patents
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JPS6350849B2 - - Google Patents

Info

Publication number
JPS6350849B2
JPS6350849B2 JP17136679A JP17136679A JPS6350849B2 JP S6350849 B2 JPS6350849 B2 JP S6350849B2 JP 17136679 A JP17136679 A JP 17136679A JP 17136679 A JP17136679 A JP 17136679A JP S6350849 B2 JPS6350849 B2 JP S6350849B2
Authority
JP
Japan
Prior art keywords
foil
capacitance
manganese
silicon
aluminum
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
Application number
JP17136679A
Other languages
Japanese (ja)
Other versions
JPS5694724A (en
Inventor
Kozo Arai
Takao Suzuki
Shozo Umetsu
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.)
Altemira Co Ltd
Original Assignee
Showa Aluminum 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 Showa Aluminum Corp filed Critical Showa Aluminum Corp
Priority to JP17136679A priority Critical patent/JPS5694724A/en
Publication of JPS5694724A publication Critical patent/JPS5694724A/en
Publication of JPS6350849B2 publication Critical patent/JPS6350849B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • 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 この発明は、電解コンデンサ陰極用アルミニウ
ム合金箔に関する。 この明細書において「%」は「重量%」を示す
ものとする。 従来技術とその問題点 電解コンデンサの性能を向上させるためには、
陽極用箔の静電容量だけでなく、陰極用箔の静電
容量を増大させることが必要である。箔の静電容
量を増大させるためには、箔にエツチングを施し
て箔の表面に微細な凹部を高密度に形成すること
により、その表面積を増大させることが有効であ
るが、エツチングが過度になると、腐食減量も過
度になり、結果的に箔の静電容量は低下し、また
機械的強度も低下する。また、コンデンサの小型
軽量化のために箔の厚さを薄くする必要があり、
そのためには箔の強度を大きくしなければならな
い。したがつて、電解コンデンサ陰極用アルミニ
ウム合金箔の具備すべき条件は、静電容量が大き
いこと、エツチングのさいの腐食減量が過度にな
らず適量であること、および機械的強度が大きい
ことである。 従来から電解コンデンサ陰極用アルミニウム合
金箔は種々存在するが、上記3条件をすべて満た
す箔は存在しなかつたのが実情である。 この発明の目的は、上記条件をすべて満足しう
る電解コンデンサ陰極用アルミニウム合金箔を提
供することにある。 問題点を解決するための手段 この発明による電解コンデンサ陰極用アルミニ
ウム合金箔は、ケイ素を0.5%を越えかつ1.0%以
下、マンガンを0.2〜2.0%、および不純物として
の鉄を0.5%以下含有し、残部アルミニウムおよ
び不可避不純物からなることを特徴とするもので
ある。 ケイ素およびマンガンは、これらをともにアル
ミニウム中に含有せしめることにより、アルミニ
ウム合金箔の静電容量を増大させる性質を有する
が、ケイ素の含有量が0.5%以下、マンガンの含
有量が0.2%未満では上記効果は得られず、ケイ
素の含有量が1.0%を越え、マンガンの含有量が
2.0%を越えると微細なエツチング組織を得られ
ないので箔の静電容量は小さくなり、腐食減量も
過度になる。したがつて、ケイ素の含有量を0.5
%を越えかつ1.0%以下、マンガンの含有量を0.2
〜2.0%とするべきである。 ケイ素およびマンガンをともに含有せしめるこ
とによりアルミニウム合金箔の静電容量が増大す
るのは、次の理由による。すなわち、周知の如
く、アルミニウム合金箔の静電容量は箔の表面積
と比例し、箔の表面積を増大させるためには、エ
ツチングによつて箔の表面に微細な凹部を均一か
つ高密度に生じさせる必要がある。アルミニウム
中にケイ素を0.5%を越えて含有せしめるととも
に、マンガンを0.2%以上含有せしめると、微細
なAl―Si―Mn化合物がアルミニウム・マトリツ
クス中に多数分散した組織を得ることができる。
Al―Si―Mn化合物は、電位的に貴であつてアル
ミニウム・マトリツクスと大きな電極電位差を有
するので、エツチングのさいにアルミニウム・マ
トリツクスが優先的に腐食されて、箔の表面に微
細な凹部が均一かつ高密度に形成され、その表面
積が増大する。しかしながら、ケイ素の含有量が
1.0%を越え、マンガンの含有量が2.0%を越える
と、Al―Si―Mn化合物が粗大になり合金箔中に
均一に分散されなくなるために、微細なエツチン
グ組織が得られず、静電容量が低下する。 この発明によるアルミニウム合金箔には、鉄な
どの製造上不可避の不純物が含まれているが、不
純物の中で、とくに鉄の場合は、その含有量が
0.5%を越えると鋳造時に粗大なAl―Si―Mn―
Fe化合物を晶出し、上述したようなケイ素およ
びマンガンを添加することにより得られる効果を
阻害するので、不純物中鉄の含有量は0.5%以下
にすべきである。 実施例 以下、この発明の実施例を対照例とともに説明
する。 下表に示す組成の16種のアルミニウム合金から
通常の製箔法によつて箔を製造した後、これらの
合金箔を液温60℃の3%塩酸および0.5%シユウ
酸水溶液中に浸漬し、電流密度30A/dm2の交流電
流を通じて1分30秒間エツチングを行い、静電容
量を測定した。その結果は下表の通りであつた。
INDUSTRIAL APPLICATION FIELD This invention relates to an aluminum alloy foil for an electrolytic capacitor cathode. In this specification, "%" refers to "% by weight". Conventional technology and its problems In order to improve the performance of electrolytic capacitors,
It is necessary to increase not only the capacitance of the anode foil but also the capacitance of the cathode foil. In order to increase the capacitance of foil, it is effective to increase the surface area by etching the foil and forming minute depressions on the surface of the foil at a high density. In this case, the corrosion loss becomes excessive, and as a result, the capacitance of the foil decreases, and the mechanical strength also decreases. Additionally, in order to make capacitors smaller and lighter, it is necessary to reduce the thickness of the foil.
To achieve this, the strength of the foil must be increased. Therefore, the conditions that an aluminum alloy foil for an electrolytic capacitor cathode must meet are that it has a large capacitance, that the amount of corrosion loss during etching is not excessive but is an appropriate amount, and that it has a high mechanical strength. . Although various aluminum alloy foils for electrolytic capacitor cathodes have conventionally existed, the reality is that there has been no foil that satisfies all of the above three conditions. An object of the present invention is to provide an aluminum alloy foil for an electrolytic capacitor cathode that can satisfy all of the above conditions. Means for Solving the Problems The aluminum alloy foil for an electrolytic capacitor cathode according to the present invention contains more than 0.5% and less than 1.0% silicon, 0.2 to 2.0% manganese, and less than 0.5% iron as an impurity, It is characterized in that the remainder consists of aluminum and unavoidable impurities. Silicon and manganese have the property of increasing the capacitance of aluminum alloy foil when they are both contained in aluminum, but if the silicon content is less than 0.5% and the manganese content is less than 0.2%, the above-mentioned No effect was obtained, and the silicon content exceeded 1.0% and the manganese content
If it exceeds 2.0%, a fine etched structure cannot be obtained, so the capacitance of the foil becomes small and the weight loss due to corrosion becomes excessive. Therefore, the silicon content should be reduced to 0.5
% and 1.0% or less, manganese content 0.2%
Should be ~2.0%. The reason why the capacitance of aluminum alloy foil increases by containing both silicon and manganese is as follows. In other words, as is well known, the capacitance of aluminum alloy foil is proportional to the surface area of the foil, and in order to increase the surface area of the foil, fine recesses are uniformly and densely created on the surface of the foil by etching. There is a need. When aluminum contains more than 0.5% silicon and 0.2% or more manganese, it is possible to obtain a structure in which a large number of fine Al--Si--Mn compounds are dispersed in the aluminum matrix.
Since the Al--Si--Mn compound is potentially noble and has a large electrode potential difference with the aluminum matrix, the aluminum matrix is preferentially corroded during etching, resulting in uniform fine depressions on the surface of the foil. Moreover, it is formed with high density and its surface area increases. However, the silicon content
If the manganese content exceeds 1.0% and the manganese content exceeds 2.0%, the Al-Si-Mn compound becomes coarse and not uniformly dispersed in the alloy foil, making it impossible to obtain a fine etched structure and reducing the capacitance. decreases. The aluminum alloy foil according to the present invention contains impurities such as iron that are unavoidable during manufacturing.
If it exceeds 0.5%, coarse Al―Si―Mn― will form during casting.
The content of iron among impurities should be 0.5% or less, since it crystallizes Fe compounds and inhibits the effects obtained by adding silicon and manganese as described above. Examples Examples of the present invention will be described below along with comparative examples. After manufacturing foils from 16 types of aluminum alloys having the compositions shown in the table below using a normal foil manufacturing method, these alloy foils were immersed in an aqueous solution of 3% hydrochloric acid and 0.5% oxalic acid at a temperature of 60°C. Etching was performed for 1 minute and 30 seconds using an alternating current with a current density of 30 A/dm 2 to measure the capacitance. The results were as shown in the table below.

【表】 上表から明らかなように、合金L〜Pでは、合
金A〜Kに比べて静電容量が大きくなつている。 発明の効果 この発明の電解コンデンサ陰極用アルミニウム
合金箔は、ケイ素を0.5%を越えかつ1.0%以下お
よびマンガンを0.2〜2.0%含有しているので、微
細なAl―Si―Mn化合物がアルミニウム・マトリ
ツクス中に多数分散した組織を得ることができ
る。そして、Al―Si―Mn化合物は、電位的に貴
であつてアルミニウム・マトリツクスと大きな電
極電位差を有するので、エツチングのさいにアル
ミニウム・マトリツクスが優先的に腐蝕され、箔
の表面に微細な凹部が均一かつ高密度に形成され
てその表面積が増大し、その結果静電容量が著し
く増大する。しかも、腐食減量も過度にならな
い。また、不純物としての鉄を0.5%以下含有す
るので、製箔工程中スラブの鋳造時に粗大なAl
―Si―Mn―Fe化合物が晶出するのを防止するこ
とができ、上述したようなケイ素およびマンガン
を添加することにより得られる効果を阻害するこ
とはない。
[Table] As is clear from the above table, alloys L to P have a larger capacitance than alloys A to K. Effects of the Invention The aluminum alloy foil for an electrolytic capacitor cathode of the present invention contains more than 0.5% silicon and less than 1.0% silicon, and 0.2 to 2.0% manganese, so that fine Al--Si--Mn compounds form an aluminum matrix. It is possible to obtain a large number of tissues dispersed inside. Since the Al--Si--Mn compound is potentially noble and has a large electrode potential difference with the aluminum matrix, the aluminum matrix is preferentially corroded during etching, resulting in minute depressions on the surface of the foil. It is formed uniformly and densely, increasing its surface area and, as a result, significantly increasing its capacitance. Moreover, the corrosion loss does not become excessive. In addition, since it contains less than 0.5% iron as an impurity, coarse Al
-Si--Mn--Fe compounds can be prevented from crystallizing, and the effects obtained by adding silicon and manganese as described above are not inhibited.

Claims (1)

【特許請求の範囲】[Claims] 1 ケイ素を0.5%を越えかつ1.0%以下、マンガ
ンを0.2〜2.0%、および不純物としての鉄を0.5%
以下含有し、残部アルミニウムおよび不可避不純
物からなる電解コンデンサ陰極用アルミニウム合
金箔。
1 Silicon more than 0.5% and less than 1.0%, manganese 0.2-2.0%, and impurity iron 0.5%
An aluminum alloy foil for an electrolytic capacitor cathode containing the following, with the balance being aluminum and unavoidable impurities.
JP17136679A 1979-12-28 1979-12-28 Aluminum alloy foil for electrolytic condenser cathode Granted JPS5694724A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17136679A JPS5694724A (en) 1979-12-28 1979-12-28 Aluminum alloy foil for electrolytic condenser cathode

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17136679A JPS5694724A (en) 1979-12-28 1979-12-28 Aluminum alloy foil for electrolytic condenser cathode

Publications (2)

Publication Number Publication Date
JPS5694724A JPS5694724A (en) 1981-07-31
JPS6350849B2 true JPS6350849B2 (en) 1988-10-12

Family

ID=15921839

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17136679A Granted JPS5694724A (en) 1979-12-28 1979-12-28 Aluminum alloy foil for electrolytic condenser cathode

Country Status (1)

Country Link
JP (1) JPS5694724A (en)

Also Published As

Publication number Publication date
JPS5694724A (en) 1981-07-31

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