Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JPH0357538B2 - - Google Patents
[go: Go Back, main page]

JPH0357538B2 - - Google Patents

Info

Publication number
JPH0357538B2
JPH0357538B2 JP56042963A JP4296381A JPH0357538B2 JP H0357538 B2 JPH0357538 B2 JP H0357538B2 JP 56042963 A JP56042963 A JP 56042963A JP 4296381 A JP4296381 A JP 4296381A JP H0357538 B2 JPH0357538 B2 JP H0357538B2
Authority
JP
Japan
Prior art keywords
magnetic
protective film
alloy
metal
magnetic memory
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
JP56042963A
Other languages
Japanese (ja)
Other versions
JPS57158033A (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 JP56042963A priority Critical patent/JPS57158033A/en
Priority to DE3210866A priority patent/DE3210866C2/en
Publication of JPS57158033A publication Critical patent/JPS57158033A/en
Publication of JPH0357538B2 publication Critical patent/JPH0357538B2/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)

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
録再生する方法であるコンタクト・スタート・ス
トツプ方式(以下CSS方式と呼ぶ)では操作終了
時に縦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動き
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、耐摩耗性と耐食性の両方共
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
耐食性に優れた保護膜を有する磁気記憶体を提供
することにある。 すなわち本発明の磁気記憶体は鏡面研磨された
下地体の上に金属磁性媒体が被覆され、この媒体
の上に直接又は非磁性合金を介して1級、2級若
しくは3級アミンの亜硝酸塩、安息香酸塩若しく
は炭酸塩からなる有機腐食抑制剤を含む保護膜が
被覆されてい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。 第1,2図は本発明の磁気記憶体の一実施例を
示す部分断面図である。 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)などの固定珪素化合物
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。 次に実施例および比較例により本発明の磁気記
憶体を詳細に説明する。 実施例 1 基盤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−燐めつき膜の上に下記の溶液をスピン塗
布法により塗布、乾燥した後、200℃で5時間焼
成して0.1μmの厚さの有機腐食抑制剤を含むポリ
珪酸からなる保護膜4を被覆して、第1図に示し
た構造の磁気デイスクを作つた。 テトラヒドロキシシラン2%イソプロピルアル
コール溶液 99.87g 亜硝酸ジシクロヘキシルアミン 0.13g 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4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%イソプロピルアルコール溶
液中に24時間浸漬してSiO2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 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、保護膜4を形成
する溶液として下記の溶液を用いて磁気デイスク
を作つた。 テトラヒドロキシシラン2%−ブチルアルコー
ル溶液 99.5g 亜硝酸ジシクロヘキシルアミン 0.5g 実施例 10 実施例1と同様にして、但し、保護膜4を形成
する溶液として下記の溶液を用いて磁気デイスク
を作つた。 テトラヒドロキシシラン2%−プロピルアルコ
ール溶液 99.5g 亜硝酸ジイソプロピルアミン 0.5g 実施例 11 実施例1と同様にして、但し、保護膜4を形成
する溶液として下記の溶液を用いて磁気デイスク
を作つた。 テトラヒドロキシシラン2%エチルアルコール
溶液 99.5g 安息香酸イソプロピルシクロヘキシルアミン
0.5g 比較例 1〜11 実施例1〜11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1〜11とした。 実施例1〜11および比較例1〜11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%、湿度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 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 contact start-stop method (hereinafter referred to as the CSS method), which is a recording and reproducing method, the rotation of the vertical air storage body stops at the end of the operation, and at this time, the head and magnetic storage surface are in the same contact friction state as at the beginning of the operation. It is in. 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 is generated 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 magnetic memory having a protective film that does not affect magnetic metals and has excellent corrosion resistance. That is, in the magnetic memory of the present invention, a metal magnetic medium is coated on a mirror-polished base body, and a nitrite of a primary, secondary, or tertiary amine is coated on this medium directly or via a nonmagnetic alloy. It is characterized by being coated with a protective film containing an organic corrosion inhibitor made of benzoate or carbonate. Next, the present invention will be explained in detail with reference to the drawings. 1 and 2 are partial cross-sectional views showing an embodiment of the magnetic storage body of 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 plated onto this base 1 as a base body 2, and the surface of this base body 2 is mechanically polished to a maximum surface roughness.
Mirror finish to 0.03μm or less. 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,
Fixed silicon compounds such as silicic acid polymers (polysilicic acid), non-magnetic metals such as Rh and Cr, non-magnetic alloys such as NiP, metals such as Al, Co, Ni, Cr, Ti, Zr or Ce, or metals such as these Alloyed non-magnetic metal oxides can be used. As an organic corrosion inhibitor, it is 1st class, 2nd class or 3rd class.
Nitrite, benzoate or carbonate of grade amines are most effective, such as isopropylamine,
diisopropylamine, triethanolamine,
dicyclohexylamine, diisobutylamine,
These include the nitrite, benzoate or carbonate salts of cyclohexylamine, dibutylamine or triethylamine. Next, the magnetic memory of the present invention will be explained in detail with reference to Examples and Comparative Examples. Example 1 As the substrate 1, the base body 2 was placed on a disk-shaped aluminum alloy plate whose surface was 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 heat straightening. 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. The following solution was applied onto this cobalt-nickel-phosphorus plating film by spin coating, dried, and then baked at 200°C for 5 hours to form a 0.1 μm thick polysilicic acid film containing an organic corrosion inhibitor. A protective film 4 was coated to produce a magnetic disk having the structure shown in FIG. Tetrahydroxysilane 2% isopropyl alcohol solution 99.87g Dicyclohexylamine nitrite 0.13g 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.
This nickel-phosphorus alloy was plated to a thickness of 0.02 μm, and a protective film 4 made of polysilicic acid containing an organic corrosion inhibitor was coated on the nickel-phosphorus alloy in the same manner as in Example 1 to obtain the structure shown in FIG. I made a magnetic 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 film was coated to a thickness of 0.1 μm, and then immersed in a 2.2% isopropyl alcohol solution of dicyclohexylamine nitrite for 24 hours to fully incorporate the organic corrosion inhibitor into the SiO 2 film to produce a magnetic disk. 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 sufficiently incorporate the organic corrosion inhibitor into the nickel-phosphorus alloy protective film. Example 7 Same as Example 1, except that metal magnetic medium 3
The surface of the protective film 4 is oxidized to form a film made of oxides of Co and Ni, which is then immersed in a 9.2% ethyl alcohol solution of dicyclohexylamine nitrite for 16 hours to form a film made of oxides of Co and Ni. A magnetic disk was manufactured by sufficiently impregnating an organic corrosion inhibitor in a protective film consisting of the following. 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% dioxane of dicyclohexylamine nitrite was plated. A magnetic disk was prepared by immersing it in a 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 manufactured in the same manner as in Example 1, except that the following solution was used as the solution for forming the protective film 4. 2% tetrahydroxysilane-butyl alcohol solution 99.5g Dicyclohexylamine nitrite 0.5g Example 10 A magnetic disk was produced in the same manner as in Example 1, except that the following solution was used as the solution for forming the protective film 4. 2% tetrahydroxysilane-propyl alcohol solution 99.5g Diisopropylamine nitrite 0.5g Example 11 A magnetic disk was produced in the same manner as in Example 1, except that the following solution was used as the solution for forming the protective film 4. Tetrahydroxysilane 2% ethyl alcohol solution 99.5g Isopropylcyclohexylamine benzoate
0.5g Comparative Examples 1-11 Magnetic disks were made in the same manner as Examples 1-11, but without using an organic corrosion inhibitor, and were designated as Comparative Examples 1-11, respectively. Using each of the magnetic disks shown in Examples 1 to 11 and Comparative Examples 1 to 11, an underwater immersion test (120 hours) and an environmental test (90% relative humidity, 40°C humidity, 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】 なお、実施例1〜5および9〜11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の磁気記憶体は優れた耐
環境性と耐摩耗性を有していることが分つた。
[Table] Incidentally, the magnetic disks of Examples 1 to 5 and 9 to 11 were subjected to CSS repetition tests 20,000 times, but no abnormality such as scratches or wear marks on the surface was observed. From the above, it was found that the magnetic memory of the present invention has excellent environmental resistance and wear resistance.

【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の磁気記憶
体の部分断面図である。 図において、1は基盤、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。
1 and 2 are partial cross-sectional views of the magnetic storage body of the present invention, respectively. In the figure, 1 is a base, 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が
被覆され、この媒体の上に直接又は非磁性合金を
介して1級、2級若しくは3級アミンの亜硝酸
塩、安息香酸塩若しくは炭酸塩からなる有機腐食
抑制剤を含み、硬質の固体材料からなる保護膜が
被覆されていることを特徴とする磁気記憶体。 2 前記保護膜が珪素化合物である特許請求の範
囲第1項記載の磁気記憶体。 3 前記珪素化合物がポリ珪酸である特許請求の
範囲第2項に記載の磁気記憶体。 4 前記保護膜が非磁性の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。 5 前記非磁性の金属又は合金が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。 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。 7 前記金属酸化物がAl、Co、Ni若しくはCr又
はこれらの合金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。 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。
[Scope of Claims] 1. A metal magnetic medium is coated on a mirror-polished base body, and a nitrite, benzoic acid of a primary, secondary or tertiary amine is coated on this medium directly or through a non-magnetic alloy. A magnetic memory comprising an organic corrosion inhibitor consisting of an acid salt or a carbonate and coated with a protective film made of a hard solid material. 2. The magnetic memory according to claim 1, wherein the protective film is a silicon compound. 3. The magnetic memory according to claim 2, wherein the silicon compound is polysilicic acid. 4. The magnetic memory according to claim 1, wherein the protective film is a nonmagnetic metal or alloy. 5. The magnetic storage body according to claim 4, wherein the non-magnetic metal or alloy is Rh, Ni-P or Cr. 6. The magnetic memory according to claim 1, wherein the protective film is a metal oxide. 7. The magnetic memory according to claim 6, wherein the metal oxide is an oxide of Al, Co, Ni, Cr, or an alloy thereof. 8. The magnetic memory according to claim 1, wherein the organic corrosion inhibitor is dicyclohexylamine nitrite.
JP56042963A 1981-03-24 1981-03-24 Magnetic storage body Granted JPS57158033A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP56042963A JPS57158033A (en) 1981-03-24 1981-03-24 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
JP56042963A JPS57158033A (en) 1981-03-24 1981-03-24 Magnetic storage body

Publications (2)

Publication Number Publication Date
JPS57158033A JPS57158033A (en) 1982-09-29
JPH0357538B2 true JPH0357538B2 (en) 1991-09-02

Family

ID=12650682

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56042963A Granted JPS57158033A (en) 1981-03-24 1981-03-24 Magnetic storage body

Country Status (1)

Country Link
JP (1) JPS57158033A (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0619802B2 (en) * 1984-05-31 1994-03-16 ティーディーケイ株式会社 Magnetic recording method
US4729924A (en) * 1984-12-21 1988-03-08 Minnesota Mining And Manufacturing Company Metallic thin film magnetic recording medium having a hard protective layer
US4803130A (en) * 1984-12-21 1989-02-07 Minnesota Mining And Manufacturing Company Reactive sputtering process for recording media
JPS62120630A (en) * 1985-11-20 1987-06-01 Nec Corp Magnetic memory medium and its production

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5120805A (en) * 1974-08-13 1976-02-19 Fuji Photo Film Co Ltd JIKIDEISUKUGATAKIROKUUTAI
JPS5140902A (en) * 1974-10-04 1976-04-06 Fujitsu Ltd JIKIKIROKUBAITAINOHOGOMAKU
JPS5440605A (en) * 1977-09-05 1979-03-30 Nec Corp Magnetic memory element
JPS5939808B2 (en) * 1977-02-10 1984-09-26 日本電気株式会社 Magnetic memory and its manufacturing method

Also Published As

Publication number Publication date
JPS57158033A (en) 1982-09-29

Similar Documents

Publication Publication Date Title
US6977030B2 (en) Method of coating smooth electroless nickel on magnetic memory disks and related memory devices
JPH0357538B2 (en)
JPH0419609B2 (en)
JPH0237606B2 (en)
JPH0237605B2 (en)
JPH079699B2 (en) Magnetic disk storage medium
JPH0237604B2 (en)
JPS6196512A (en) magnetic recording medium
JPH0241089B2 (en)
JPH0440782B2 (en)
JPS58179938A (en) Magnetic storage body
JP2924052B2 (en) Magnetic storage body and method of manufacturing the same
JPH0514325B2 (en)
JPS633378B2 (en)
JPH07225943A (en) Magnetic recording medium
JPS6288132A (en) magnetic recording medium
JPH02198001A (en) Magnetic recording and reproducing method, magnetic recording medium and floating type magnetic head
JPS6028053B2 (en) magnetic memory
JPH0467251B2 (en)
JPS5988807A (en) Magnetic storage body
JPH0450648B2 (en)
JPS62289913A (en) Magnetic recording medium
JPH0467249B2 (en)
JPH04109427A (en) Magnetic recording medium
JPS6313123A (en) Magnetic disk and its production