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JPH0237604B2 - - Google Patents
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JPH0237604B2 - - Google Patents

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Publication number
JPH0237604B2
JPH0237604B2 JP56042964A JP4296481A JPH0237604B2 JP H0237604 B2 JPH0237604 B2 JP H0237604B2 JP 56042964 A JP56042964 A JP 56042964A JP 4296481 A JP4296481 A JP 4296481A JP H0237604 B2 JPH0237604 B2 JP H0237604B2
Authority
JP
Japan
Prior art keywords
magnetic
corrosion inhibitor
magnetic storage
metal
medium
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
JP56042964A
Other languages
Japanese (ja)
Other versions
JPS57158034A (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 JP56042964A priority Critical patent/JPS57158034A/en
Priority to DE3210866A priority patent/DE3210866C2/en
Publication of JPS57158034A publication Critical patent/JPS57158034A/en
Publication of JPH0237604B2 publication Critical patent/JPH0237604B2/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
    • 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
    • G11B5/726Two or more protective coatings
    • G11B5/7262Inorganic protective coating

Landscapes

  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • 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
優れたものはまず得られていない。 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有機
腐食抑制剤を含むテトラヒドロキシシランの溶液
を塗布し、焼成することにより有機腐食抑制剤を
含むポリ珪酸からなる保護膜を被覆することを特
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
多く用いられるが、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ポリ珪
酸からなる保護膜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
腐食抑制剤を含むポリ珪酸からなる保護膜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は腐食抑制剤を含むテトラヒドロキシ
シランの有機溶剤、特にアルコール類、ケトン
類、又はエステル類の溶液を磁気記憶体を回転さ
せながら塗布(スピンコーテイング)した後、焼
成して作られる、腐食抑制剤を含むポリ珪酸であ
る。このポリ珪酸は有機腐食抑制剤を良く吸着
し、焼成によつても取り除かれることが無い。 非磁性合金5はNi−P、Cr、Rhなど非磁性で
あればなんでも良い。 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。 次に実施例および比較例により本発明の磁気記
憶媒体の製造方法を詳細に説明する。 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(周周方向で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
布により塗布し、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%、イソブ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、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%n−ブチルアルコー
ル溶液 99g 亜硝酸ジシクロヘキシルアミン 1g 実施例 3 実施例1と同様にして、但し、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 安息香酸ジイソブチルアミン 0.5g 実施例 4 実施例1と同様にして、但し、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%トリエチルアミン
溶液 実施例 5 実施例1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。 比較例 1 実施例1と同様にして、但し、有機腐食抑制剤
を含まずに磁気デイスクを作つた。 比較例 2 実施例5と同様にして、但し、有機腐食抑制剤
を含まずに磁気デイスクを作つた。 比較例 3 実施例6と同様にして、但し、有機腐食抑制剤
を含まずに磁気デイスクを作つた。 実施例1〜6および比較例1〜3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 of 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 state of contact friction as at the start of the operation. The frictional force generated between the head and the magnetic storage body in this state can wear out the head and the magnetic storage body, and may eventually cause scratches on the head and the metal magnetic thin film medium. Changes in posture may make the load applied to the head uneven, causing scratches on the head and magnetic storage surface.Furthermore, the head may suddenly come into contact with the magnetic storage during recording and playback, causing damage between the head and the magnetic storage. A large frictional force acts on the head and magnetic storage, often resulting in destruction of the head and magnetic storage.In order to protect the head and magnetic storage from such contact friction, contact wear, and contact destruction between the head and magnetic storage. It is necessary to coat the surface of the magnetic memory with a protective film.The second problem is that magnetic metals are prone to corrosion, and this corrosion deteriorates or eliminates the magnetic properties of the magnetic metals.
Alternatively, localized corrosion may lead to increased errors. Various protective films have been proposed to solve the above two problems, but none that has both excellent wear resistance and corrosion resistance has yet to be obtained. For example, a protective film made by treating the surface of a magnetic memory with an oxidizing agent containing chromic acid or its salt, as seen in Japanese Patent Publication No. 52-17402, does not have sufficient abrasion resistance, and also contains chromic acid or its salt. Such inorganic corrosion inhibitors actually attack the magnetic metal, causing non-uniformity in the film thickness of the magnetic metal and increasing 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 includes coating a metal magnetic medium on a mirror-polished base body;
The medium is coated with a protective film made of polysilicate containing an organic corrosion inhibitor by applying a solution of tetrahydroxysilane containing an organic corrosion inhibitor directly or via a non-magnetic metal and baking the medium. It is said that 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 made of polysilicate containing an organic corrosion inhibitor is formed on the metal magnetic medium 3. is covered. In FIG. 2, the metal magnetic medium 3 is coated with a protective film 4 made of polysilicate containing an organic corrosion inhibitor via a nickel-phosphorus alloy as a non-magnetic alloy 5. As shown in FIG. The metal magnetic medium 3 may be any metal or alloy containing Co, Ni, or Fe. The protective film 4 is made by coating (spin coating) a solution of tetrahydroxysilane in an organic solvent containing a corrosion inhibitor, especially alcohols, ketones, or esters while rotating the magnetic storage body (spin coating), and then firing the coating. It is a polysilicic acid containing a corrosion inhibitor. This polysilicic acid adsorbs organic corrosion inhibitors well and is not removed even by firing. The nonmagnetic alloy 5 may be any nonmagnetic alloy such as Ni-P, Cr, Rh, etc. 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. Next, the method for manufacturing a magnetic storage medium 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 plate 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 heat straightening as the base 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. The following solution was applied by spin coating onto this cobalt-nickel-phosphorus plating film, 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 was coated to produce a magnetic disk having the structure shown in FIG. 2% tetrahydroxysilane, isopropyl alcohol solution
99.87g, dicyclohexylamine nitrite 0.13g Example 2 A magnetic disk was made in the same manner as in Example 1, but using the following solution. Tetrahydroxysilane 2% n-butyl alcohol solution 99g Dicyclohexylamine nitrite 1g Example 3 A magnetic disk was made in the same manner as in Example 1, except that the following solutions were used. Tetrahydroxysilane 2% ethyl alcohol solution 99.5g Diisobutylamine benzoate 0.5g Example 4 A magnetic disk was made in the same manner as in Example 1, except that the following solutions were used. Tetrahydroxysilane 2% triethylamine solution Example 5 Same as Example 1, 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 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. Comparative Example 1 A magnetic disk was made in the same manner as in Example 1, but without the organic corrosion inhibitor. Comparative Example 2 A magnetic disk was made in the same manner as in Example 5, but without the organic corrosion inhibitor. Comparative Example 3 A magnetic disk was made in the same manner as in Example 6, but without the organic corrosion inhibitor. Using each of the magnetic disks shown in Examples 1 to 6 and Comparative Examples 1 to 3, 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】 以上の結果から本発明の製造方法によつて作ら
れた磁気記憶媒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1〜6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
憶媒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 storage medium manufactured by the manufacturing method of the present invention has excellent environmental resistance. Regarding the magnetic disks of Examples 1 to 6, 2
After repeated CSS tests 10,000 times, no abnormalities such as surface scratches or wear marks were observed. From the above, it was found that the magnetic storage medium manufactured 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。
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 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を
被覆し、この媒体の上に直接又は非磁性金属を介
して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
有機腐食抑制剤を含むテトラヒドロキシシランの
溶液を塗布し、焼成することにより前記有機腐食
抑制剤を含むポリ珪酸からなる保護膜を被覆する
ことを特徴とする磁気記憶体の製造方法。 2 前記有機腐食抑制剤として亜硝酸ジシクロヘ
キシルアミンを用い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 primary, secondary or tertiary amines or their nitrites are coated on this medium directly or via a non-magnetic metal. , a magnetic material characterized in that a solution of tetrahydroxysilane containing an organic corrosion inhibitor such as benzoate or carbonate is coated and baked to cover a protective film made of polysilicic acid containing the organic corrosion inhibitor. A method for manufacturing a memory body. 2. The method for manufacturing a magnetic memory according to claim 1, wherein dicyclohexylamine nitrite is used as the organic corrosion inhibitor.
JP56042964A 1981-03-24 1981-03-24 Manufacture of magnetic storage body Granted JPS57158034A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP56042964A JPS57158034A (en) 1981-03-24 1981-03-24 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
JP56042964A JPS57158034A (en) 1981-03-24 1981-03-24 Manufacture of magnetic storage body

Publications (2)

Publication Number Publication Date
JPS57158034A JPS57158034A (en) 1982-09-29
JPH0237604B2 true JPH0237604B2 (en) 1990-08-27

Family

ID=12650712

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56042964A Granted JPS57158034A (en) 1981-03-24 1981-03-24 Manufacture of magnetic storage body

Country Status (1)

Country Link
JP (1) JPS57158034A (en)

Also Published As

Publication number Publication date
JPS57158034A (en) 1982-09-29

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