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JPH0237606B2 - - Google Patents
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JPH0237606B2 - - Google Patents

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Publication number
JPH0237606B2
JPH0237606B2 JP56045188A JP4518881A JPH0237606B2 JP H0237606 B2 JPH0237606 B2 JP H0237606B2 JP 56045188 A JP56045188 A JP 56045188A JP 4518881 A JP4518881 A JP 4518881A JP H0237606 B2 JPH0237606 B2 JP H0237606B2
Authority
JP
Japan
Prior art keywords
magnetic
protective film
manufacturing
magnetic memory
metal
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
JP56045188A
Other languages
Japanese (ja)
Other versions
JPS57162133A (en
Inventor
Masahiro Yanagisawa
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 Corp
Original Assignee
Nippon Electric 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 Electric Co Ltd filed Critical Nippon Electric Co Ltd
Priority to JP56045188A priority Critical patent/JPS57162133A/en
Priority to DE3210866A priority patent/DE3210866C2/en
Publication of JPS57162133A publication Critical patent/JPS57162133A/en
Publication of JPH0237606B2 publication Critical patent/JPH0237606B2/ja
Granted legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G11INFORMATION STORAGE
    • G11BINFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
    • G11B5/00Recording by magnetisation or demagnetisation of a record carrier; Reproducing by magnetic means; Record carriers therefor
    • G11B5/62Record carriers characterised by the selection of the material
    • G11B5/72Protective coatings, e.g. anti-static or antifriction
    • G11B5/722Protective coatings, e.g. anti-static or antifriction containing an anticorrosive material

Landscapes

  • Magnetic Record Carriers (AREA)
  • Manufacturing Of Magnetic Record Carriers (AREA)

Description

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

本発明は磁気的記憶装置(磁気デイスク装置、
磁気ドラム装置など)に用いられる磁気記憶体、
特に磁性金属を記憶媒体とする磁気記憶体の製造
方法に関する。 一般に磁性金属を記憶媒体として使用する磁気
記憶体は主に次の2つの実用上の問題を有してい
る。 第1の問題は記録再生磁気ヘツド(以下ヘツド
と呼ぶ)と磁気記憶体とを構成部とする磁気記憶
装置の記録再生方法に伴なうものである。 操作開始時にヘツドと磁気記憶体面とを接触状
態でセツトした後、前記磁気記憶体に所要の回転
を与えることにより前記ヘツドと前記磁気記憶体
面との間に空気層分の空間を作り、この状態で記
録再生をする所謂コンタクト・スタート・ストツ
プ方式では操作終了時に磁気記憶体の回転が止ま
り、この時ヘツドと磁気記憶体面は操作開始時と
同様に接触摩擦状態にある。 これらの接触摩擦状態におけるヘツドと磁気記
憶体の間に生じる摩擦力は、ヘツドおよび磁気記
憶体を摩耗させついにはヘツドおよび金属磁性薄
膜媒体に傷を生じさせることがある。また前記接
触摩擦状態においてヘツドのわずかな姿勢の変化
がヘツドにかかる荷重を不均一にし、ヘツドおよ
び磁気記憶体表面に傷を作ることもある。また更
に記録再生中に突発的にヘツドが磁気記憶体に接
触しヘツドと磁気記憶体間に大きな摩擦力が働
き、ヘツドおよび磁気記憶体が破壊されることが
しばしば起こる。この様なヘツドと磁気記憶体と
の接触摩擦、接触摩耗および接触破壊からヘツド
および磁気記憶体を保護するために磁気記憶体の
表面に保護被膜を被覆することが必要である。 第2の問題は、磁性金属が腐食し易く、この腐
食により磁性金属の磁気特性が劣化又は消失し、
あるいは局部的な腐食によつてエラーの増加を招
く。 以上の2つの問題を解決する為に種々の保護膜
が提案されているが、耐摩耗性と耐食性両方共に
優れたものはまだ得られていない。 例えば特公昭52−17402号公報に見られる様な、
磁気記憶体表面をクロム酸又はその塩を含む酸化
剤で処理して作られる保護膜は耐摩耗性が十分で
ない上にクロム酸又はその塩の様な無機腐食抑制
剤はかえつて磁性金属を侵して磁性金属の膜厚の
不均一を招き、エラーを増加させる。この様に磁
性金属に過激に作用する腐食抑制剤は、磁気記憶
体の様な磁性金属の精密さが要求される用途には
適用が困難である。 本発明の目的は磁性金属への影響が無く、かつ
耐摩耗性および耐食性に優れた磁気記憶体の製造
方法を提供することにある。 すなわち、本発明の磁気記憶体の製造方法は鏡
面研磨された下地体の上に金属磁性媒体を被覆
し、この媒体の上に直接又は非磁性金属を介して
保護膜を被覆して磁気記憶体を形成し、この磁気
記憶体を有機腐食抑制剤溶液中に浸漬して前記保
護膜中に有機腐食抑制剤を含ませることを特徴と
している。 次に図面を参照して本発明を詳細に説明する。 図は本発明により製造された磁気記憶体の部分
断面図である。 第1図において磁気記憶体の基盤1としてアル
ミ合金が軽くて加工性が良く安価なことから最も
良く用いられるが、場合によつてはチタン合金が
用いられることもある。基盤表面は機械加工によ
り小さなうねり(円周方向で50μm以下、半径方
向で100μm以下)を有する面に仕上げられてい
る。 次にこの基盤1の上に下地体2としてニツケル
−燐合金がめつきにより被覆され、この下地体2
の表面は機械的研磨により最大表面粗さ0.03μm
以下に鏡面仕上げされる。次に上記下地体2の鏡
面研磨面上に金属磁性媒体3としてコバルト−ニ
ツケル−燐合金がめつきにより被覆され、この金
属磁性媒体3の上に有機腐食抑制剤を含む保護膜
4が被覆されている。 第2図においては上記金属磁性媒体3の上に非
磁性合金5としてニツケル−燐合金を介して有機
腐食抑制剤を含む保護膜4が被覆されている。 金属磁性媒体3はCo、Ni若しくはFeを含む金
属又は合金であればなんでも良い。 保護膜4もガラス、珪素酸化物、珪素窒化物、
珪酸ポリマー(ポリ珪酸)などの珪素化合物を初
めとし、Rh、Crなどの非磁性金属、NiPなどの
非磁性合金、Al、Co、Ni、Cr、Ti、Zr若しくは
Ceなどの金属またはこれらの合金の非磁性金属
酸化物が使用出来る。 有機腐食抑制剤としては1級、2級若しくは3
級アミン又はそれらの亜硝酸塩、安息香酸塩若し
くは炭酸塩が最も効果があり、例えばイソプロピ
ルアミン、ジイソプロピルアミン、トリエタノー
ルアミン、ジシクロヘキシルアミン、ジイソブチ
ルアミン、シクロヘキシルアミン、ジブチルアミ
ンまたはトリエチルアミンの亜硝酸塩、安息香酸
塩、又は炭酸塩がある。これら有機腐食抑制剤
は、アルコール類、ケトン類、エステル類などの
有機溶剤に溶解して溶液として用いる。但し、液
体の有機腐食抑制剤は有機溶剤で希釈することな
しにそのまま使用することが出来る。 液状にした有機腐食抑制剤液中に前記保護膜を
被覆した磁気記憶体を浸漬することにより、その
保護膜中に有機腐食抑制剤を含ませる。 本方法によれば、保護膜に腐食液(水など)が
最も侵入し易い部分にまず有機腐食抑制剤が侵入
する為、より一層防食効果を上げることが出来
る。 次に実施例および比較例により本発明の磁気記
憶体の製造方法を詳細に説明する。実施例 1 基板1として旋盤加工および熱矯正によつて十
分小さなうねり(円周方向で50μm以下および半
径方向で10μm以下)をもつた面に仕上げられた
デイスク状アルミニウム合金盤上に下地体2とし
てニツケル−燐合金を約50μmの厚さにめつきし、
このニツケル−燐めつき膜を最大表面粗さ
0.02μm、厚さ30μmまで鏡面研磨仕上げした。 次にこのニツケル−燐めつき膜の上に金属磁性
媒体3としてコバルト−ニツケル−燐合金を
0.05μmの厚さにめつきした。このコバルト−ニ
ツケル−燐めつき膜の上にテトラヒドロキシシラ
ンの2%n−ブチルアルコール溶液を0.1μmの厚
さに塗布、乾燥後200℃で5時間焼成して保護膜
4としてポリ珪酸を被覆した。次に全体を亜硝酸
ジシクロヘキシルアミンの23%無水メチルアルコ
ール溶液中に5時間浸漬して亜硝酸ジシクロヘキ
シルアミンを保護膜中に含ませて、第1図に示し
た構造の磁気デイスクを作つた。 実施例 2 実施例1と同様にして、但し、金属磁性媒体3
の上に非磁性合金5としてニツケル−燐合金を
0.02μmの厚さにめつきし、このニツケル−燐合
金の上に実施例1と同様にして有機腐食抑制剤を
含むポリ珪酸からなる保護膜を被覆して第2図に
示した構造の磁気デイスクを作つた。 実施例 3 実施例1と同様にして、但し、金属磁性媒体3
の上に保護膜4としてSiO2をスパツタにより
0.1μmの厚さに被覆し、その後、亜硝酸ジシクロ
ヘキシルアミンの2.2%イソプレピルアルフール
溶液中に24時間浸漬してSiO2保護膜中に有機腐
食抑制剤を十分含ませて磁気デイスクを作つた。 実施例 4 実施例2と同様にして、但し、金属磁性媒体3
としてCo−Mn−Pを用いて磁気デイスクを作つ
た。 実施例 5 実施例3と同様にして、但し、金属磁性媒体3
としてCo−Crを用いて磁気デイスクを作つた。 実施例 6 実施例1と同様にして、但し、金属磁性媒体3
の上に保護膜4としてニツケル−燐合金を0.1μm
の厚さにめつきし、その後亜硝酸ジシクロヘキシ
ルアミンの23%メチルアルコール溶液中に10時間
浸漬してニツケル−燐合金中に有機腐食抑制剤を
十分含ませて磁気デイスクを作つた。 実施例 7 実施例1と同様にして、但し、金属磁性媒体3
の表面を酸化してCo及びNiの酸化物からなる被
膜を形成して保護膜4となし、その後、亜硝酸ジ
シクロヘキシルアミンの9.2%エチルアルコール
溶液中に16時間浸漬して、Co及びNiの酸化物か
らなる保護膜中に有機腐食抑制剤を十分含ませて
磁気デイスクを作つた。 実施例 8 実施例7と同様にして、但し、金属磁性媒体3
の上にニツケル−燐合金を0.1μmの厚さにめつき
し、その表面を酸化してNiの酸化物からなる被
膜を形成して保護膜4となし、その後、亜硝酸ジ
シクロヘキシルアミンの7.9%ジオキサン溶液中
に4時間浸漬してNiの酸化物からなる保護膜中
に有機腐食抑制剤を十分含ませて磁気デイスクを
作つた。 実施例 9 実施例1と同様にして、但し、有機腐食抑制剤
として安息香酸ジイソブチルアミンの飽和イソプ
ロピルアルコール溶液を用いて磁気デイスクを作
つた。 実施例 10 実施例1と同様にして、但し、有機腐食抑制剤
としてジシクロヘキシルアミン(100%)を用い
て磁気デイスクを作つた。 比較例 1〜8 実施例1〜8に対応してそれらと同様にして、
但し、有機腐食抑制剤を用いずに磁気デイスクを
作り、それぞれを比較例1〜8とした。 実施例1〜10および比較例1〜8で示した各磁
気デイスクを用いて水中浸漬試験(120時間)お
よび環境試験(相対湿度90%、温度40℃、1ケ
月)を行ないそれぞれ腐食点の単位面積当りの個
数およびエラー数の増加率を調べた。 その結果下表の様な結果が得られた。
The present invention relates to a magnetic storage device (magnetic disk device,
magnetic storage bodies used in magnetic drum devices, etc.)
In particular, the present invention relates to a method of manufacturing a magnetic storage body using magnetic metal as a storage medium. Generally, magnetic storage bodies that use magnetic metal as a storage medium have the following two main practical problems. The first problem is associated with a recording/reproducing method for a magnetic storage device that includes a recording/reproducing magnetic head (hereinafter referred to as a head) and a magnetic storage body. After the head and the magnetic storage surface are set in contact at the start of operation, a space corresponding to an air layer is created between the head and the magnetic storage surface by giving the magnetic storage the required rotation, and this state is maintained. In the so-called contact start-stop method for recording and reproducing, the rotation of the magnetic storage body stops at the end of the operation, and at this time the head and the surface of the magnetic storage body are in the same frictional state as at the start of the operation. The frictional force generated between the head and the magnetic storage material under these contact friction conditions may wear out the head and the magnetic storage material, and may eventually cause scratches on the head and the metal magnetic thin film medium. Further, in the contact friction state, a slight change in the posture of the head makes the load applied to the head uneven, and may cause scratches on the surface of the head and the magnetic storage body. Furthermore, during recording and reproducing, the head suddenly comes into contact with the magnetic storage body, and a large frictional force acts between the head and the magnetic storage body, often resulting in destruction of the head and the magnetic storage body. In order to protect the head and the magnetic memory from such contact friction, contact wear and contact breakage between the head and the magnetic memory, it is necessary to coat the surface of the magnetic memory with a protective coating. The second problem is that magnetic metals are easily corroded, and this corrosion causes the magnetic properties of the magnetic metals to deteriorate or disappear.
Alternatively, localized corrosion may lead to increased errors. Various protective films have been proposed to solve the above two problems, but no one has yet been found that is excellent in both wear resistance and corrosion resistance. For example, as seen in Special Publication No. 52-17402,
A protective film made by treating the surface of a magnetic memory element with an oxidizing agent containing chromic acid or its salts does not have sufficient wear resistance, and inorganic corrosion inhibitors such as chromic acid or its salts may actually attack magnetic metals. This leads to non-uniformity in the film thickness of the magnetic metal and increases errors. Corrosion inhibitors that act radically on magnetic metals in this way are difficult to apply to applications that require precision of magnetic metals, such as magnetic storage bodies. An object of the present invention is to provide a method for manufacturing a magnetic memory body that does not affect magnetic metals and has excellent wear resistance and corrosion resistance. That is, the method for manufacturing a magnetic storage body of the present invention involves coating a mirror-polished base body with a metal magnetic medium, and covering this medium with a protective film either directly or through a non-magnetic metal to produce a magnetic storage body. The present invention is characterized in that the magnetic storage body is formed by immersing the magnetic memory in an organic corrosion inhibitor solution so that the organic corrosion inhibitor is included in the protective film. Next, the present invention will be explained in detail with reference to the drawings. The figure is a partial cross-sectional view of a magnetic memory body manufactured according to the present invention. In FIG. 1, aluminum alloy is most often used as the base 1 of the magnetic memory body because it is light, easy to work with, and inexpensive, but titanium alloy may also be used in some cases. The surface of the base is machined into a surface with small undulations (less than 50 μm in the circumferential direction and less than 100 μm in the radial direction). Next, a nickel-phosphorus alloy is coated on this base 1 as a base body 2 by plating, and this base body 2
The surface is mechanically polished to a maximum surface roughness of 0.03μm.
It will be mirror finished below. Next, a cobalt-nickel-phosphorus alloy is coated on the mirror-polished surface of the base body 2 as a metal magnetic medium 3 by plating, and a protective film 4 containing an organic corrosion inhibitor is coated on the metal magnetic medium 3. There is. In FIG. 2, the metal magnetic medium 3 is coated with a protective film 4 containing an organic corrosion inhibitor via a nickel-phosphorus alloy as a non-magnetic alloy 5. In FIG. The metal magnetic medium 3 may be any metal or alloy containing Co, Ni, or Fe. The protective film 4 is also made of glass, silicon oxide, silicon nitride,
Including silicon compounds such as silicic acid polymer (polysilicic acid), non-magnetic metals such as Rh and Cr, non-magnetic alloys such as NiP, Al, Co, Ni, Cr, Ti, Zr or
Nonmagnetic metal oxides of metals such as Ce or alloys thereof can be used. As an organic corrosion inhibitor, it is 1st class, 2nd class or 3rd class.
amines or their nitrites, benzoates or carbonates are the most effective, such as isopropylamine, diisopropylamine, triethanolamine, dicyclohexylamine, diisobutylamine, cyclohexylamine, dibutylamine or triethylamine nitrites, benzoic acid There are salts or carbonates. These organic corrosion inhibitors are used as a solution by dissolving them in organic solvents such as alcohols, ketones, and esters. However, the liquid organic corrosion inhibitor can be used as it is without diluting it with an organic solvent. By immersing the magnetic storage body coated with the protective film in a liquefied organic corrosion inhibitor solution, the organic corrosion inhibitor is included in the protective film. According to this method, the organic corrosion inhibitor first penetrates into the parts of the protective film where corrosive liquids (such as water) are most likely to penetrate, so that the anticorrosion effect can be further improved. Next, the method for manufacturing the magnetic storage body of the present invention will be explained in detail with reference to Examples and Comparative Examples. Example 1 The base body 2 was placed on a disk-shaped aluminum alloy disk whose surface had been finished with sufficiently small waviness (50 μm or less in the circumferential direction and 10 μm or less in the radial direction) by lathe processing and thermal straightening as the substrate 1. Nickel-phosphorus alloy is plated to a thickness of approximately 50μm,
This nickel-phosphorus plating film has the maximum surface roughness.
Mirror polished to a thickness of 0.02μm and 30μm. Next, a cobalt-nickel-phosphorus alloy is deposited on this nickel-phosphorus plating film as a metal magnetic medium 3.
It was plated to a thickness of 0.05 μm. On this cobalt-nickel-phosphorus plating film, a 2% n-butyl alcohol solution of tetrahydroxysilane was applied to a thickness of 0.1 μm, and after drying, it was baked at 200°C for 5 hours and polysilicic acid was coated as a protective film 4. did. Next, the whole was immersed in a 23% anhydrous methyl alcohol solution of dicyclohexylamine nitrite for 5 hours to incorporate dicyclohexylamine nitrite into the protective film, thereby producing a magnetic disk having the structure shown in FIG. Example 2 Same as Example 1, except that metal magnetic medium 3
A nickel-phosphorus alloy is placed on top of the non-magnetic alloy 5.
The nickel-phosphorus alloy was plated to a thickness of 0.02 μm, and a protective film made of polysilicate containing an organic corrosion inhibitor was coated on the nickel-phosphorus alloy in the same manner as in Example 1 to form a magnetic material having the structure shown in FIG. I made a disk. Example 3 Same as Example 1, except that metal magnetic medium 3
Sputter SiO 2 as a protective film 4 on top of the
The SiO 2 protective film was coated to a thickness of 0.1 μm, and then immersed in a 2.2% isoprepyl alfur solution of dicyclohexylamine nitrite for 24 hours to fully incorporate the organic corrosion inhibitor into the SiO 2 protective film to create a magnetic disk. Ivy. Example 4 Same as Example 2, except that metal magnetic medium 3
A magnetic disk was made using Co-Mn-P. Example 5 Same as Example 3, except that metal magnetic medium 3
A magnetic disk was made using Co-Cr. Example 6 Same as Example 1, except that metal magnetic medium 3
A nickel-phosphorus alloy with a thickness of 0.1 μm is applied as a protective film 4 on top.
The magnetic disk was then plated to a thickness of 100 ml, and then immersed in a 23% methyl alcohol solution of dicyclohexylamine nitrite for 10 hours to fully impregnate the organic corrosion inhibitor in the nickel-phosphorus alloy to produce a magnetic disk. Example 7 Same as Example 1, except that metal magnetic medium 3
was oxidized to form a film consisting of Co and Ni oxides to form the protective film 4, and then immersed in a 9.2% ethyl alcohol solution of dicyclohexylamine nitrite for 16 hours to oxidize Co and Ni. A magnetic disk was fabricated by sufficiently impregnating an organic corrosion inhibitor in a protective film made of a material. Example 8 Same as Example 7, except that metal magnetic medium 3
A nickel-phosphorus alloy was plated on top to a thickness of 0.1 μm, and the surface was oxidized to form a film made of Ni oxide to form the protective film 4. After that, 7.9% dicyclohexylamine nitrite was plated. A magnetic disk was prepared by immersing it in a dioxane solution for 4 hours to fully impregnate the organic corrosion inhibitor in the protective film made of Ni oxide. Example 9 A magnetic disk was made as in Example 1, but using a saturated isopropyl alcohol solution of diisobutylamine benzoate as the organic corrosion inhibitor. Example 10 A magnetic disk was made as in Example 1, but using dicyclohexylamine (100%) as the organic corrosion inhibitor. Comparative Examples 1 to 8 Corresponding to Examples 1 to 8, in the same manner as them,
However, magnetic disks were made without using an organic corrosion inhibitor, and Comparative Examples 1 to 8 were prepared. Using each of the magnetic disks shown in Examples 1 to 10 and Comparative Examples 1 to 8, an underwater immersion test (120 hours) and an environmental test (90% relative humidity, temperature 40°C, 1 month) were conducted to determine the unit of corrosion point. The number of pieces per area and the rate of increase in the number of errors were investigated. As a result, the results shown in the table below were obtained.

【表】【table】

【表】 以上の結果から本発明の製造方法によつて作ら
れた磁気記憶体は優れた耐環境性を有しているこ
とが分つた。 なお実施例1〜5および9,10の磁気デイスク
について2万回のCSS繰り返しテストを行なつた
が表面の傷および摩耗跡など全く異常は見られな
かつた。 以上のことから本発明により製造された磁気記
憶体は優れた信頼性を有していることが分つた。
[Table] From the above results, it was found that the magnetic memory produced by the production method of the present invention has excellent environmental resistance. The magnetic disks of Examples 1 to 5, 9, and 10 were subjected to CSS repetition tests 20,000 times, but no abnormalities such as scratches or wear marks on the surface were observed. From the above, it was found that the magnetic memory produced according to the present invention has excellent reliability.

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

第1図及び第2図はそれぞれ本発明により製造
された磁気記憶体の部分断面図である。 図において、1は基板、2は下地体、3は金属
磁性媒体、4は保護膜、5は非磁性合金である。
FIGS. 1 and 2 are partial cross-sectional views of magnetic storage bodies manufactured according to the present invention, respectively. In the figure, 1 is a substrate, 2 is a base body, 3 is a metal magnetic medium, 4 is a protective film, and 5 is a nonmagnetic alloy.

Claims (1)

【特許請求の範囲】 1 鏡面研磨された下地体の上に金属磁性媒体を
被覆し、この媒体の上に直接又は非磁性金属を介
して保護膜を被覆して磁気記憶体を形成し、この
磁気記憶体を1級、2級もしくは3級アミンまた
はそれらの亜硝酸塩、安息香酸塩もしくは炭酸塩
からなる有機腐食抑制剤溶液中に浸漬して前記保
護膜中にその有機腐食抑制剤を含ませることを特
徴とする磁気記憶体の製造方法。 2 前記保護膜が珪素化合物である特許請求の範
囲第1項に記載の磁気記憶体の製造方法。 3 前記珪素化合物がポリ珪酸である特許請求の
範囲第1項に記載の磁気記憶体の製造方法。 4 前記保護膜が非磁性金属又は合金である特許
請求の範囲第1項に記載の磁気記憶体の製造方
法。 5 前記非磁性金属又は合金がRh、Ni−P又は
Crである特許請求の範囲第4項に記載の磁気記
憶体の製造方法。 6 前記保護膜が金属酸化物である特許請求の範
囲第1項に記載の磁気記憶体の製造方法。 7 前記金属酸化物がAl、Co、Ni若しくはCr又
はこれらの酸化物である特許請求の範囲第6項に
記載の磁気記憶体の製造方法。 8 前記有機腐食抑制剤が亜硝酸ジシクロヘキシ
ルアミンである特許請求の範囲第1項に記載の磁
気記憶体の製造方法。
[Claims] 1. A metal magnetic medium is coated on a mirror-polished base body, and a protective film is coated on the medium directly or via a non-magnetic metal to form a magnetic storage body. The magnetic storage body is immersed in an organic corrosion inhibitor solution consisting of a primary, secondary, or tertiary amine or a nitrite, benzoate, or carbonate thereof, so that the organic corrosion inhibitor is included in the protective film. A method for manufacturing a magnetic memory body, characterized in that: 2. The method of manufacturing a magnetic memory body according to claim 1, wherein the protective film is a silicon compound. 3. The method for manufacturing a magnetic memory body according to claim 1, wherein the silicon compound is polysilicic acid. 4. The method of manufacturing a magnetic memory body according to claim 1, wherein the protective film is a nonmagnetic metal or an alloy. 5 The non-magnetic metal or alloy is Rh, Ni-P or
The method for manufacturing a magnetic memory body according to claim 4, wherein the magnetic memory body is made of Cr. 6. The method of manufacturing a magnetic memory body according to claim 1, wherein the protective film is a metal oxide. 7. The method of manufacturing a magnetic memory body according to claim 6, wherein the metal oxide is Al, Co, Ni, Cr, or an oxide thereof. 8. The method for manufacturing a magnetic memory according to claim 1, wherein the organic corrosion inhibitor is dicyclohexylamine nitrite.
JP56045188A 1981-03-24 1981-03-27 Manufacture of magnetic storage body Granted JPS57162133A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP56045188A JPS57162133A (en) 1981-03-27 1981-03-27 Manufacture of magnetic storage body
DE3210866A DE3210866C2 (en) 1981-03-24 1982-03-24 Magnetic recording medium and process for its manufacture

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56045188A JPS57162133A (en) 1981-03-27 1981-03-27 Manufacture of magnetic storage body

Publications (2)

Publication Number Publication Date
JPS57162133A JPS57162133A (en) 1982-10-05
JPH0237606B2 true JPH0237606B2 (en) 1990-08-27

Family

ID=12712286

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56045188A Granted JPS57162133A (en) 1981-03-24 1981-03-27 Manufacture of magnetic storage body

Country Status (1)

Country Link
JP (1) JPS57162133A (en)

Also Published As

Publication number Publication date
JPS57162133A (en) 1982-10-05

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