JPH025810B2 - - Google Patents

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Publication number
JPH025810B2
JPH025810B2 JP61073959A JP7395986A JPH025810B2 JP H025810 B2 JPH025810 B2 JP H025810B2 JP 61073959 A JP61073959 A JP 61073959A JP 7395986 A JP7395986 A JP 7395986A JP H025810 B2 JPH025810 B2 JP H025810B2
Authority
JP
Japan
Prior art keywords
plating
defects
substrate
adhesion
amount
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 - Lifetime
Application number
JP61073959A
Other languages
Japanese (ja)
Other versions
JPS62230947A (en
Inventor
Teruo Uno
Seiichi Hirano
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.)
Sumitomo Light Metal Industries Ltd
Original Assignee
Sumitomo Light Metal Industries 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 Sumitomo Light Metal Industries Ltd filed Critical Sumitomo Light Metal Industries Ltd
Priority to JP7395986A priority Critical patent/JPS62230947A/en
Publication of JPS62230947A publication Critical patent/JPS62230947A/en
Publication of JPH025810B2 publication Critical patent/JPH025810B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

[産業上の利用分野] 本発明は磁気デイスク用アルミニウム合金、特
に、メツキ性に優れた磁気デイスク用アルミニウ
ム合金に関するものである。 [従来の技術] 磁気デイスクは一般にアルミニウム合金基板の
表面を精密研磨した後に磁性体薄膜を被覆させた
ものであり、この磁性体薄膜を磁化させることに
より信号を記録する。 この磁気デイスク用基板には以下のような特性
が要求される。 (1) 精密研磨あるいは切削後の表面精度が良好な
こと、 (2) 磁性体薄膜の欠陥の原因となる基板表面の突
起や穴が少なく、かつ小さいこと、 (3) ある程度の強度を有し、基板製作時の機械加
工、使用時の高速回転にも耐え得ること、 (4) 軽量、非磁性であり、ある程度の耐食性を有
すること、 従来、このような特性を有する磁気デイスク用
基板としてAl−Mg−Mn−Cr系の5086合金やそ
の改良合金が使用されてきた。 近年、磁気デイスクに対する高密度化、大容量
化等の要求が高まり、この基板に適したアルミニ
ウム合金や基板に対する磁性体薄膜の被覆法の開
発が望まれている。 磁性体を基板表面に被覆する方法として、これ
までは塗付法が主体であつたが、近年、メツキ
法、スパツター法等が開発され、高密度磁気デイ
スクへの適用が進められている。 メツキ型磁気デイスクを製造するには、磁性体
を形成する以前に基板の平滑性をより向上させる
ため、基板上にNi−P系の中間層メツキを形成
させた後に再度研磨する。しかし、アルミニウム
基板上に直接中間層メツキ処理すると、メツキ層
の密着性が悪いために、良質な中間層メツキを施
すにはアルミニウム基板の前処理が必要である。 そのため、一般には酸性溶液により基板表面を
エツチングにより均一粗面化し、Zn置換法によ
るZnメツキが施され、その上にNi−P系の中間
層がメツキされる。 従つて、メツキ型磁気デイスクの性能は、下地
処理である均一粗面化の程度、Znメツキ性、Ni
−P中間層のメツキ性に左右されるので、欠陥が
なく、しかも密着性にすぐれたNi−Pメツキを
行う必要がある。そのためには、基板となるアル
ミニウム素材についても、メツキ性を考慮した合
金組成や製造方法を検討する必要がある。 [発明が解決しようとする問題点] この発明は、Ni−Pメツキ処理時に欠陥が少
なく、Ni−Pメツキ層の密着性が良好で、しか
も製造の容易な磁気デイスク用アルミニウム合金
を提供するものである。 [問題点を解決するための手段] 上記問題点を解決するためのこの発明の構成は
下記のとおりである。 Zn4〜7%、Mg1.5〜3.5%、Cu0.1〜0.7%、
Ti0.001〜0.05%を含み、さらにMn0.05〜0.5%、
Cr0.05〜0.25%、Zr0.05〜0.25%の1種以上を含
み残りアルミニウム不純物よりなり、不純物とし
てのFe、SiがFe≦0.15%、Si≦0.10%であるメツ
キ性に優れた磁気デイスク用アルミニウム合金。 上記構成に記載の各成分の含有量の限定理由は
下記のとおりである。 Zn:ZnはMgと共存してMgZn2化合物を形成し、
この化合物が前処理酸洗により溶解して均一微
細なエツチピツトを形成し、適当な粗さを基板
に付与し、メツキ層の密着性を向上させるばか
りでなく、ジンケート層を基板に均一に付着さ
せ、その後のNi−Pメツキ層の密着性の向上
に有効である。下限未満ではこの効果が少な
く、上限を越えると熱間加工性が低下する。 Mg:Mgは強度の向上に寄与するばかりでなく、
ZnとMgZn2化合物を形成し、前処理酸洗によ
る均一微細なエツチピツトの形成に寄与し、
Ni−Pメツキ層の密着性や欠陥の防止に有効
である。 下限未満ではこの効果が小さく、上限を越え
ると熱間加工性が低下する。 Cu:CuはZnやMgと同様に強度を向上させると
共にAlZnMgCu系化合物を形成し、前処理酸
洗によるエツチピツトの形成に寄与する。 また、本系合金のようなAl−Zn−Mg−Cu系
合金では、粒界にMgZn2が優先析出し、この部
分が前処理酸洗時に優先的にエツチングされ、顕
著な粒界エツチングを生じることがある。このよ
うな場合はNi−Pメツキが不均一となり、メツ
キ欠陥を生じやすくなる。 Cuを添加するとその一部は粒界に析出して粒
界の電位を貴にする作用がある。そのためCuの
添加は粒界エツチングを抑制して、前処理酸洗時
に板面を均一に粗面化させる作用がある。下限未
満ではこの効果が少なく、上限を越えるとこの効
果は飽和する。 一方、Cuを添加すると鋳塊割れが生じ易くな
るため現行の半連続鋳造法で大型鋳塊を製作する
ことが難しい。従つて、Cu量の高い合金はメツ
キ性は良好であるが、鋳造割れを起こすため、素
材の製造が極めて難しい問題がある。Cu量を上
限以下とした場合にはこの問題を解消して低コス
トの素材を製造することが可能となる。 また、Cu量が上限を越えると晶出する
AlZnMgCu系化合物が粗大化して前処理エツチ
ング時に粗大なエツチピツトを形成し、Ni−P
メツキ層が不均一となり、メツキ欠陥を生じるこ
とがある。 以上の理由から、Cu量は0.1〜0.7%とする必要
がある。 Ti:鋳造組織を微細にして、鋳造割れの防止に
寄与する。下限未満ではこの効果が不十分であ
り、上限を越えてもこの効果が飽和する。 Mn、Cr、Zr:これらの元素は均質化処理時に微
細な金属間化合物として析出し、結晶粒の微細
化に寄与する。下限未満ではこの効果が不十分
であり、上限を越えると巨大な金属間化合物が
晶出するので好ましくない。 Fe、Si:Fe、Siはアルミニウム中にほとんど固
溶せず、金属間化合物として析出するが、Fe、
Si量が多い場合には、Al−Fe系、Al−Fe−Si
系等の粗大な金属間化合物が多数存在し、メツ
キ欠陥の原因となるため、不純物量としての
Fe、SiはFe≦0.15%、Si≦0.10%とする。 その他の不純物はおのおの0.05%以下である。 本発明における前処理酸洗は50%HNO3液に50
g/の酸性フツ化アンモンを添加した30℃の溶
液中に50秒浸漬することにより行つた。 Znメツキ法は、例えばNaOH300g/、
ZnO80g/を溶解した20℃の水溶液中に90秒浸
漬することにより基板表面にZnを析出させる方
法により行われる。 また、Ni−Pメツキ法は次亜リン酸を環元剤
とする無電解Ni−Pメツキ法であり、通常80〜
90℃で2〜4hr処理することにより15〜30μmのメ
ツキ層が形成される。Ni−Pメツキ後の皮膜に
は欠陥がないこと、密着性がよいこと等が必要で
ある。 アルミニウム中に粗大な金属間化合物が存在す
ると、化合物がメツキ後まで残存したり、あるい
は前処理酸洗時に粗大なピツトを形成してNi−
Pメツキ欠陥となるため、良好なメツキ面は得ら
れない。 また、前処理酸洗時に均一に粗面化されない場
合やジンケートの密着性が悪いとNi−Pメツキ
層の密着性が低下したり、メツキ欠陥を生じるこ
とがある。 この発明は、Zn、Mg、Cu等を適度に添加する
ことにより前処理酸洗時に均一粗面化をはかると
共にジンケートの密着性を向上させ、Ni−Pメ
ツキ層の密着性の向上を目的としている。さら
に、Mn、Cr、Zrの添加による結晶粒の制御や
Fe、Si等の不純物元素の制御による粗大な金属
間化合物の減少によりメツキ欠陥を減少させたも
のである。また、本合金はCu量を抑制している
ため大型鋳塊の製造が容易であり、低コストの素
材の製作が可能となる。 以下、実施例によつて、本発明を具体的に説明
する。なお、実施例に記載の各化学成分の量
(%)は重量%である。 実施例 1 第1表に示す化学成分を有する400mm厚の大型
鋳塊を半連続鋳造により製作した。この鋳塊を
480℃で24hrの均質化処理後に430℃で熱間圧延を
開始し、板厚6mmに圧延した。熱間圧延板を370
℃で焼鈍し、冷間圧延して2mm板とし、その後
220℃で2hr焼鈍して半硬材とした。 この材料について、荒切削、歪取り焼鈍(380
℃)後にダイヤモンド仕上切削により鏡面仕上
し、ZnメツキとNi−Pメツキを行つた場合の諸
特性を第2表に示す。 ただし、Ni−Pメツキは市販の無電解Ni−P
メツキ液の90℃のものに3時間浸漬して実施し
た。また、第1表、第2表ともNo.1〜7は本発明
の実施例の合金、No.8以降は比較例の合金であ
る。
[Industrial Field of Application] The present invention relates to an aluminum alloy for magnetic disks, and particularly to an aluminum alloy for magnetic disks with excellent plating properties. [Prior Art] A magnetic disk is generally an aluminum alloy substrate whose surface is precisely polished and coated with a magnetic thin film, and signals are recorded by magnetizing the magnetic thin film. This magnetic disk substrate is required to have the following characteristics. (1) The surface accuracy after precision polishing or cutting is good; (2) there are few and small protrusions and holes on the substrate surface that can cause defects in the magnetic thin film; and (3) there is a certain degree of strength. (4) It is lightweight, non-magnetic, and has a certain degree of corrosion resistance. Conventionally, aluminum has been used as a magnetic disk substrate with these characteristics. -Mg-Mn-Cr alloy 5086 and its improved alloys have been used. In recent years, demands for higher density, larger capacity, etc. for magnetic disks have increased, and it is desired to develop an aluminum alloy suitable for this substrate and a method for coating the substrate with a magnetic thin film. Up until now, the main method for coating a substrate surface with a magnetic material has been a coating method, but in recent years, plating methods, sputtering methods, etc. have been developed, and their application to high-density magnetic disks is progressing. To manufacture a plating-type magnetic disk, in order to further improve the smoothness of the substrate before forming the magnetic material, a Ni--P intermediate layer plating is formed on the substrate and then polishing is performed again. However, when intermediate layer plating is directly performed on an aluminum substrate, the adhesion of the plating layer is poor, so pretreatment of the aluminum substrate is required to perform high-quality intermediate layer plating. Therefore, generally, the surface of the substrate is uniformly roughened by etching with an acidic solution, Zn plating is performed by a Zn substitution method, and a Ni--P intermediate layer is plated thereon. Therefore, the performance of a plated magnetic disk depends on the degree of uniform surface roughening used in the surface treatment, Zn plating properties, and Ni
Since it depends on the plating properties of the -P intermediate layer, it is necessary to perform Ni-P plating with no defects and excellent adhesion. To this end, it is necessary to consider the alloy composition and manufacturing method of the aluminum material that will serve as the substrate, taking plating properties into consideration. [Problems to be Solved by the Invention] The present invention provides an aluminum alloy for magnetic disks that has few defects during Ni-P plating, has good adhesion of the Ni-P plating layer, and is easy to manufacture. It is. [Means for Solving the Problems] The structure of the present invention for solving the above problems is as follows. Zn4~7%, Mg1.5~3.5%, Cu0.1~0.7%,
Contains Ti0.001~0.05%, further Mn0.05~0.5%,
A magnetic disk with excellent plating properties, containing one or more of 0.05 to 0.25% Cr and 0.05 to 0.25% Zr, and remaining aluminum impurities, and the impurities Fe and Si are Fe≦0.15% and Si≦0.10%. Aluminum alloy for. The reason for limiting the content of each component described in the above structure is as follows. Zn: Zn coexists with Mg to form MgZn 2 compound,
This compound dissolves during pre-treatment pickling to form fine and uniform etching pits, imparting appropriate roughness to the substrate, not only improving the adhesion of the plating layer, but also allowing the zincate layer to adhere uniformly to the substrate. This is effective in improving the adhesion of the subsequent Ni-P plating layer. Below the lower limit, this effect is small, and above the upper limit, hot workability decreases. Mg: Mg not only contributes to improving strength, but also
Forms a compound of Zn and MgZn , which contributes to the formation of uniform and fine etch pits by pretreatment pickling.
It is effective in improving the adhesion of the Ni-P plating layer and preventing defects. Below the lower limit, this effect is small, and above the upper limit, hot workability decreases. Cu: Like Zn and Mg, Cu improves strength, forms AlZnMgCu compounds, and contributes to the formation of etch pits during pretreatment pickling. In addition, in Al-Zn-Mg-Cu alloys such as this alloy, MgZn 2 preferentially precipitates at grain boundaries, and this region is preferentially etched during pretreatment pickling, resulting in significant grain boundary etching. Sometimes. In such a case, the Ni--P plating becomes non-uniform and plating defects are likely to occur. When Cu is added, some of it precipitates at grain boundaries and has the effect of increasing the potential at the grain boundaries. Therefore, the addition of Cu has the effect of suppressing grain boundary etching and uniformly roughening the board surface during pretreatment pickling. Below the lower limit, this effect is small, and above the upper limit, this effect is saturated. On the other hand, when Cu is added, ingot cracks tend to occur, making it difficult to produce large ingots using the current semi-continuous casting method. Therefore, although alloys with a high Cu content have good plating properties, they cause casting cracks, making it extremely difficult to manufacture the material. When the amount of Cu is kept below the upper limit, this problem can be solved and a low-cost material can be manufactured. In addition, if the amount of Cu exceeds the upper limit, crystallization will occur.
AlZnMgCu-based compounds become coarse and form coarse etch pits during pretreatment etching, and Ni-P
The plating layer may become non-uniform and plating defects may occur. For the above reasons, the amount of Cu needs to be 0.1 to 0.7%. Ti: Makes the casting structure finer and helps prevent casting cracks. Below the lower limit, this effect is insufficient, and even above the upper limit, this effect is saturated. Mn, Cr, Zr: These elements precipitate as fine intermetallic compounds during homogenization treatment and contribute to grain refinement. If it is less than the lower limit, this effect will be insufficient, and if it exceeds the upper limit, a huge intermetallic compound will crystallize, which is not preferable. Fe, Si: Fe and Si hardly form a solid solution in aluminum and precipitate as intermetallic compounds.
When the amount of Si is large, Al-Fe system, Al-Fe-Si
Since there are many coarse intermetallic compounds such as metals, which cause plating defects, the amount of impurities is
Fe and Si should be Fe≦0.15% and Si≦0.10%. Other impurities are each less than 0.05%. Pretreatment pickling in the present invention is 50% HNO 3 solution
This was carried out by immersing the sample in a solution at 30° C. to which g/g of acidic ammonium fluoride was added for 50 seconds. In the Zn plating method, for example, 300g of NaOH/
Zn is deposited on the surface of the substrate by immersing it in an aqueous solution of 80 g of ZnO at 20° C. for 90 seconds. In addition, the Ni-P plating method is an electroless Ni-P plating method that uses hypophosphorous acid as a ring agent.
A plating layer of 15 to 30 μm is formed by treatment at 90° C. for 2 to 4 hours. The film after Ni-P plating must be free of defects and have good adhesion. If coarse intermetallic compounds exist in aluminum, the compounds may remain after plating, or they may form coarse pits during pretreatment pickling and cause Ni-
Since this results in P plating defects, a good plating surface cannot be obtained. Furthermore, if the surface is not uniformly roughened during pretreatment pickling or the adhesion of zincate is poor, the adhesion of the Ni--P plating layer may decrease or plating defects may occur. This invention aims to uniformly roughen the surface during pretreatment pickling and improve the adhesion of zincate by adding appropriate amounts of Zn, Mg, Cu, etc., with the aim of improving the adhesion of the Ni-P plating layer. There is. Furthermore, we can control crystal grains by adding Mn, Cr, and Zr.
Plating defects are reduced by reducing coarse intermetallic compounds by controlling impurity elements such as Fe and Si. Furthermore, since this alloy suppresses the amount of Cu, it is easy to manufacture large ingots, making it possible to manufacture low-cost materials. Hereinafter, the present invention will be specifically explained with reference to Examples. In addition, the amount (%) of each chemical component described in the examples is weight %. Example 1 A large ingot with a thickness of 400 mm having the chemical components shown in Table 1 was produced by semi-continuous casting. This ingot
After homogenization treatment at 480°C for 24 hours, hot rolling was started at 430°C, and the sheet was rolled to a thickness of 6 mm. 370 hot rolled plates
It was annealed at ℃, cold rolled into a 2mm plate, and then
It was annealed at 220℃ for 2 hours to produce a semi-hard material. For this material, rough cutting, strain relief annealing (380
Table 2 shows the various properties when the specimens were mirror-finished by diamond-finish cutting, followed by Zn plating and Ni-P plating. However, Ni-P plating is commercially available electroless Ni-P
The test was carried out by immersing it in a plating solution at 90°C for 3 hours. Further, in both Tables 1 and 2, Nos. 1 to 7 are alloys of examples of the present invention, and Nos. 8 and after are alloys of comparative examples.

【表】【table】

【表】【table】

【表】 上記結果およびその他の所見を要約すると下記
のとおりである。 No.1〜7:メツキ欠陥が少なく、密着性が良好で
ある。 No.8:Cuの量が少なく、メツキ欠陥が多い。 No.9:Cuの量が多く、鋳塊割れが生じた。 No.10:Feの量が多く、メツキ欠陥が多い。 No.11〜12:メツキ欠陥が多く、密着性も悪い。
又、強度も低い。 実施例 2 第3表に示す化学成分を有する400mm厚の大型
鋳塊を半連続鋳造により製作し、実施例1と同じ
方法で板厚2mmの半硬材とした。この材料に実施
例1と同じ方法でNi−Pメツキを行つた場合の
特性を第4表に示す。 ただし、Ni−Pメツキ条件、評価法等は実施
例1と同じである。No.1〜7が実施例、No.8以降
は比較例である。
[Table] The above results and other findings are summarized as follows. No. 1 to 7: Few plating defects and good adhesion. No. 8: The amount of Cu is small and there are many plating defects. No. 9: The amount of Cu was large, and cracks occurred in the ingot. No. 10: Large amount of Fe and many plating defects. No. 11 to 12: Many plating defects and poor adhesion.
Also, the strength is low. Example 2 A large ingot with a thickness of 400 mm having the chemical components shown in Table 3 was produced by semi-continuous casting, and was made into a semi-hard material with a thickness of 2 mm using the same method as in Example 1. Table 4 shows the properties when this material was plated with Ni--P in the same manner as in Example 1. However, the Ni-P plating conditions, evaluation method, etc. are the same as in Example 1. Nos. 1 to 7 are examples, and Nos. 8 and after are comparative examples.

【表】【table】

【表】【table】

【表】 以上の結果およびその他の所見を要約すると下
記のとおりである。 No.1〜7:メツキ欠陥が少なく、密着性が良好で
ある。 No.8:Cuの量が少なく、メツキ欠陥が多い。 No.9:Cuの量が多く、鋳塊割れが生じた。 No.10:Feの量が多く、メツキ欠陥が多い。 No.11〜12:メツキ欠陥が多く、密着性も悪い。
又、強度も低い。 [発明の効果] 以上説明したように、本発明によれば、前処理
酸洗によつて均一な粗面化ができ、その結果Ni
−Pメツキの密着性が向上する。 また、粗大な金属間化合物の生成を抑制できる
のでメツキ欠陥が少なくなる。 一方、素材の鋳塊割れが防止されるので歩留り
がよく、製造加工が容易な低コスト材を提供でき
る。
[Table] The above results and other findings are summarized as follows. No. 1 to 7: Few plating defects and good adhesion. No. 8: The amount of Cu is small and there are many plating defects. No. 9: The amount of Cu was large, and cracks occurred in the ingot. No. 10: Large amount of Fe and many plating defects. No. 11 to 12: Many plating defects and poor adhesion.
Also, the strength is low. [Effects of the Invention] As explained above, according to the present invention, uniform surface roughening can be achieved by pretreatment pickling, and as a result, Ni
- The adhesion of P plating is improved. Furthermore, since the formation of coarse intermetallic compounds can be suppressed, plating defects are reduced. On the other hand, since cracking of the ingot of the material is prevented, it is possible to provide a low-cost material that has a high yield and is easy to manufacture and process.

Claims (1)

【特許請求の範囲】[Claims] 1 Zn4〜7%、Mg1.5〜3.5%、Cu0.1〜0.7%、
Ti0.001〜0.05%を含み、さらにMn0.05〜0.5%、
Cr0.05〜0.25%、Zr0.05〜0.25%の1種以上を含
み、残りアルミニウムと不純物よりなり、不純物
としてのFe、SiがFe≦0.15%、Si≦0.10%である
メツキ性に優れた磁気デイスク用アルミニウム合
金。
1 Zn4~7%, Mg1.5~3.5%, Cu0.1~0.7%,
Contains Ti0.001~0.05%, further Mn0.05~0.5%,
Contains one or more of Cr0.05~0.25% and Zr0.05~0.25%, and the remainder consists of aluminum and impurities, and Fe and Si as impurities are Fe≦0.15% and Si≦0.10%. Excellent plating properties. Aluminum alloy for magnetic disks.
JP7395986A 1986-03-31 1986-03-31 Aluminum alloy for magnetic disk Granted JPS62230947A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7395986A JPS62230947A (en) 1986-03-31 1986-03-31 Aluminum alloy for magnetic disk

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7395986A JPS62230947A (en) 1986-03-31 1986-03-31 Aluminum alloy for magnetic disk

Publications (2)

Publication Number Publication Date
JPS62230947A JPS62230947A (en) 1987-10-09
JPH025810B2 true JPH025810B2 (en) 1990-02-06

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Family Applications (1)

Application Number Title Priority Date Filing Date
JP7395986A Granted JPS62230947A (en) 1986-03-31 1986-03-31 Aluminum alloy for magnetic disk

Country Status (1)

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JP (1) JPS62230947A (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2015040320A (en) * 2013-08-21 2015-03-02 株式会社Uacj High strength aluminum alloy, and method for producing the same
JP6344923B2 (en) 2014-01-29 2018-06-20 株式会社Uacj High strength aluminum alloy and manufacturing method thereof
CN107109543B (en) * 2014-10-31 2019-07-16 株式会社Uacj Aluminium alloy base plate for magnetic disk

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5156719A (en) * 1974-11-15 1976-05-18 Furukawa Aluminium Seikeikakosei oyobi kokiseinosuguretakoryokuaruminiumugokin
JPS5369606A (en) * 1976-12-02 1978-06-21 Fujitsu Ltd Magnetic disc substrate
JPS6047901A (en) * 1983-08-26 1985-03-15 Yokogawa Hokushin Electric Corp Angle converter
JPS61266548A (en) * 1985-05-21 1986-11-26 Furukawa Alum Co Ltd Aluminum alloy for substrate of magnetic disc

Also Published As

Publication number Publication date
JPS62230947A (en) 1987-10-09

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