JPS6256574B2 - - Google Patents
Info
- Publication number
- JPS6256574B2 JPS6256574B2 JP56210519A JP21051981A JPS6256574B2 JP S6256574 B2 JPS6256574 B2 JP S6256574B2 JP 56210519 A JP56210519 A JP 56210519A JP 21051981 A JP21051981 A JP 21051981A JP S6256574 B2 JPS6256574 B2 JP S6256574B2
- Authority
- JP
- Japan
- Prior art keywords
- magnetic
- recording medium
- concentration
- magnetic recording
- solution
- 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
Links
Classifications
-
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B5/00—Recording by magnetisation or demagnetisation of a record carrier; Reproducing by magnetic means; Record carriers therefor
- G11B5/62—Record carriers characterised by the selection of the material
- G11B5/68—Record carriers characterised by the selection of the material comprising one or more layers of magnetisable material homogeneously mixed with a bonding agent
- G11B5/70—Record carriers characterised by the selection of the material comprising one or more layers of magnetisable material homogeneously mixed with a bonding agent on a base layer
- G11B5/71—Record carriers characterised by the selection of the material comprising one or more layers of magnetisable material homogeneously mixed with a bonding agent on a base layer characterised by the lubricant
Landscapes
- Lubricants (AREA)
- Magnetic Record Carriers (AREA)
- Manufacturing Of Magnetic Record Carriers (AREA)
Description
(1) 発明の技術分野
本発明は磁気記録媒体の製造方法、特に磁性層
表面に塗布する潤滑剤にパーフロロアルキルポリ
エーテルを沸点が90℃以上の高ふつ化溶液中に希
釈したものを用いる方法に関する。
(2) 技術の背景
最近磁気媒体は記録密度向上の要請に応じて、
磁気ヘツドの浮上量の低減化が図られ、更に、始
動開始時と停止時は磁気ヘツドと媒体とが接触摺
動するいわゆるコンタクト・スタート・ストツプ
方式(CSS方式)が採用されるに至り、媒体の磨
耗に対する耐久性を向上させる目的で、パーフロ
ロアルキルポリエーテル〔デユポン社によりクラ
イトツクスなる商品名で市販されているもので分
子式は
(1) Technical Field of the Invention The present invention relates to a method for manufacturing a magnetic recording medium, and in particular to a lubricant applied to the surface of a magnetic layer in which perfluoroalkyl polyether is diluted in a high fluoride solution with a boiling point of 90°C or higher. Regarding the method. (2) Background of technology Recently, magnetic media has been
Efforts were made to reduce the flying height of the magnetic head, and the so-called contact start-stop method (CSS method), in which the magnetic head and the medium slide in contact with each other when starting and stopping, was adopted. For the purpose of improving the durability against abrasion, perfluoroalkyl polyether [commercially available under the trade name Krytxx by DuPont, whose molecular formula is
【式】などの潤滑剤を媒体
の磁性層表面に塗布することが行なわれている。
上記クライトツクスの塗布には、スピンコーテ
イング法(回転塗布法)、媒体をクライトツクス
中につける浸漬法、適当なスプレーガンなどを用
いてなされるスプレー法などが提案されている
が、各方法ともクライトツクスを原液(100%)
のまま用いることはほとんどなく、トリクロロト
リフロロエタン(商品名はフレオンTF)、または
フレオンTFとイソプロピルアルコールの混合液
などの溶剤中にクライトツクスを希釈して得られ
る懸濁液を使用している。
(3) 従来技術と問題点
上記したクライトツクスはフレオンTF中に完
全に溶解するので塗布量の微妙な制御を行なうに
は便利であるが、フレオンTFの沸点が約48℃と
きわめて低いので、クライトツクス溶解液の濃度
維持が難かしい。例えばクライトツクスの塗布に
前記した浸漬法を用いるとき、溶解液が多量で容
器の開口部が広いので、濃度維持はより深刻な問
題となる。また、スピンコート法においても、フ
レオンTFの蒸発が早いので、溶解液を媒体上に
滴下させてもそれを全面に均一に拡散させて塗布
することが難しく、ほとんどの場合均一化をはか
るためスピンコーテイングの後に拭き取り(バツ
フイング)、または熱拡散工程が必要となる。こ
れらの事情はすべて磁気媒体の製造工程の増加と
なり、ひいては歩留りを低下させる一因となつて
いる。
(4) 発明の目的
本発明は上記従来技術の問題点に鑑み、クライ
トツクスの溶解液の濃度維持が簡便でかつ均一塗
布性が優れた磁気媒体の製造方法を提供すること
を目的とする。
(5) 発明の構成
そしてこの目的は本発明によれば、磁性鉄粉体
を結合剤中に分散せしめてなる磁気塗料を非磁性
基体に塗布し磁性層を形成した後に磁性層表面に
潤滑剤を塗布してなる磁気記録媒体製造方法であ
つて、前記潤滑剤は、パーフロロアルキルポリエ
ーテルを分子式がC7F16またはC8F16Oの何れかの
単独または、これらの混合液からなる高フツ化希
釈液中に希釈した状態で塗布されることを特徴と
する磁気記録媒体の製造方法を提供する。
またこの溶液中のパーフロロアルキルポリエー
テルの希釈濃度は0.2〜5%である。
(6) 発明の実施例
以下本発明実施例を図面によつて詳述する。
本願の発明者は、現在市販のフレオンTFを使
用したとき経験される問題が、フレオンの蒸発速
度の早さに起因すると判断し、前記した問題点を
解決すべく沸点の異なる各種溶剤で実験を重ね、
第1図に示される沸点とクライトツクス溶解液濃
度変化の時間経過の関係を確定した。同図におい
て横軸は溶液の沸点温度(℃)を、縦軸は1日当
りの濃度変化率を%で示す。
図に矢印で示す範囲は合格範囲であるが、その
判定に際し、濃度変化率が3%/日以上のものは
実用上管理困難と判定し、3%/日未満を合格と
した。同図座標の左上方の丸に矢印を付したとこ
ろはフレオンTFを用いた場合を示し、濃度変化
率は50%/日以上である。なおこの実験は50cm立
方の容器に各溶剤とも5%のクライトツクスを溶
解したものを満たし、25℃で1日放置したときの
濃度変化を実測した。前記矢印範囲内の3点は本
発明の方法によるものについてのデータである。
次に、塗布性の評価結果を第2図に示す。この
評価は、スピンコーテイング法および浸漬法の双
方で行なつた。同図の縦軸に点数で示す塗布性に
関しては、9点以下は品質の安定性に欠けると
か、次工程にバツフイング工程または熱拡散工程
を要するという理由で不適当と判定し、9点を超
えるものを合格とした。
具体的に説明すると、溶剤が蒸発した後、クラ
イトツクスが連続膜に見え均一性良好であれば10
点、クライトツクスが均一に粒状に見えるときは
5点(後工程で拭き取りまたは熱拡散処理が必要
であるため)、クライトツクスが均一に塗布され
ていなければ3点とした。なお、これら点数分配
の中間値は適宜判定した。なお同図において、横
軸は溶液の沸点温度を(℃)、矢印で示す範囲は
合格を、角印は浸漬法によるものを、丸印はスピ
ンコート法によるものを示す。
スピンコート法、浸漬法ともに、径が約36cm
(14インチ)のデイスクに1枚当り30mgを塗布す
べく、溶液濃度、塗布条件(例えばスピンコーテ
イングにおける回転数、浸漬法におけるデイスク
引上速度)を最適化して塗布し評価した。
次いで、本発明による沸点約100℃の溶剤を使
用した場合の濃度とウインチエスタ型ヘツドの
CSS(コンタクト・スタート・ストツプ)の耐久
回数の関係を第3図に示す。デイスクへのクライ
トツクスの塗布は、スピンコーテイング法および
浸漬法の両方で行ない、各々最適と判定される塗
布条件を選んで塗布した。従つて、拭き取りおよ
び熱拡散処理は行なわない。同図において横軸は
クライトツクス溶液濃度(%)、縦軸は耐久回数
を万単位で示し、矢印で示す範囲は合格であり、
角印は浸漬法、丸印はスピンコーテイング法によ
るものを示す。耐久回数の合格ラインは1万回以
上とした。
更に、前記したデイスクの上に、加圧力約10g
のウインチエスタ型ヘツドを、24時間、24℃、湿
度70%の条件下に放置した後、ヘツドとデイスク
の間に生ずる吸着力〔ヘツド・ステイツク(ヘツ
ドとデイスクとのくつつき)〕を測定した結果を
第4図に示す。同図で横軸はクライトツクス溶液
濃度(%)、縦軸は吸着力(g)、矢印で示す範囲
は吸着力5g以下の合格を示す。角印、丸印は第
3図の場合と同様である。合格ラインについて
は、吸着力5g以下では、ヘツドとデイスクの双
方に傷が認められなかつたので、5g以下を合格
とした。
以上に説明した結果から、本発明による溶剤を
使用してクライトツクスを塗布する場合の安定な
品質が得られる実用的使用濃度は0.2〜0.5%であ
ると判定した。すなわち、この範囲より希釈度が
うすい場合、十分な耐久性を与える塗布条件が得
られず、逆に濃い場合は吸着力が大になりすぎて
実用上不適当である。
(7) 発明の効果
以上説明したように、本発明の方法によるとき
は、濃度変化率の低いクライトツクスの溶液が得
られ、この溶液を用いるときは、高品質の、耐久
性の高い、吸着力小なる潤滑剤層が得られ、磁気
媒体の信頼性向上に寄与するところ大である。A lubricant such as [Formula] is applied to the surface of the magnetic layer of the medium. Various methods have been proposed for applying the above-mentioned Klytux, including a spin coating method (rotary coating method), a dipping method in which a medium is placed in the Klytux, and a spray method using an appropriate spray gun. Stock solution (100%)
It is rarely used as is, but instead a suspension obtained by diluting Krytx in a solvent such as trichlorotrifluoroethane (trade name Freon TF) or a mixture of Freon TF and isopropyl alcohol is used. (3) Prior art and problems The Krytox mentioned above completely dissolves in Freon TF, so it is convenient for delicately controlling the amount of application. It is difficult to maintain the concentration of the solution. For example, when using the above-described dipping method for coating Krytox, maintaining concentration becomes a more serious problem because of the large volume of solution and the wide opening of the container. In addition, in the spin coating method, Freon TF evaporates quickly, so even if the solution is dropped onto the medium, it is difficult to spread and coat it uniformly over the entire surface.In most cases, spinning is used to achieve uniformity. A buffing or thermal diffusion step is required after coating. All of these circumstances result in an increase in the number of manufacturing steps for magnetic media, which in turn becomes a factor in lowering the yield. (4) Purpose of the Invention In view of the above-mentioned problems of the prior art, an object of the present invention is to provide a method for manufacturing a magnetic medium in which the concentration of a solution of Krytox is easily maintained and the uniform coating property is excellent. (5) Structure of the Invention According to the present invention, a magnetic paint made by dispersing magnetic iron powder in a binder is applied to a non-magnetic substrate to form a magnetic layer, and then a lubricant is applied to the surface of the magnetic layer. A method for manufacturing a magnetic recording medium comprising coating a perfluoroalkyl polyether with a molecular formula of C 7 F 16 or C 8 F 16 O alone or a mixture thereof. Provided is a method for producing a magnetic recording medium, characterized in that the magnetic recording medium is coated in a diluted state in a high-fluoride diluent. The diluted concentration of perfluoroalkyl polyether in this solution is 0.2 to 5%. (6) Examples of the invention Examples of the invention will be described in detail below with reference to the drawings. The inventor of this application determined that the problems experienced when using currently commercially available Freon TF were caused by the rapid evaporation rate of Freon, and conducted experiments using various solvents with different boiling points in order to solve the above-mentioned problems. Overlapping,
The relationship between the boiling point and the change in the concentration of Krytox solution over time shown in FIG. 1 was established. In the figure, the horizontal axis shows the boiling point temperature (°C) of the solution, and the vertical axis shows the concentration change rate per day in %. The range indicated by the arrow in the figure is an acceptable range, but when making this determination, a concentration change rate of 3%/day or more was determined to be practically difficult to manage, and a concentration change rate of less than 3%/day was determined to be acceptable. The area with an arrow attached to the circle in the upper left of the coordinates in the figure indicates the case where Freon TF is used, and the concentration change rate is 50%/day or more. In this experiment, a 50 cm cubic container was filled with 5% Krytx dissolved in each solvent, and the changes in concentration were measured when the solvents were left at 25°C for one day. The three points within the arrow range are data based on the method of the present invention. Next, the evaluation results of the coating properties are shown in FIG. This evaluation was performed using both the spin coating method and the dipping method. Regarding the applicability, which is indicated by a score on the vertical axis of the figure, a score of 9 or less is judged to be unsuitable because the quality lacks stability or the next process requires a buffing process or a thermal diffusion process, and a score above 9 is judged to be unsuitable. The item was passed. Specifically, after the solvent evaporates, if the Krytox appears as a continuous film and has good uniformity, it is 10
A score of 5 was given if the Krytox appeared uniformly granular (because wiping or heat diffusion treatment was required in a subsequent step), and a score of 3 was given if the Krytox was not uniformly applied. Note that the intermediate value of these score distributions was determined as appropriate. In the figure, the horizontal axis indicates the boiling point temperature of the solution (° C.), the range indicated by the arrow indicates a pass, square marks indicate those obtained by the dipping method, and circles indicate those obtained by the spin coating method. The diameter is approximately 36cm for both spin coating and dipping methods.
The solution concentration and coating conditions (for example, rotation speed in spin coating, disk pulling speed in dipping method) were optimized to coat 30 mg per 14-inch disk, and the coating was evaluated. Next, the concentration and winchiesta type head when using the solvent with a boiling point of about 100°C according to the present invention are determined.
Figure 3 shows the relationship between the number of CSS (contact start and stop) durability cycles. Krytx was applied to the disk by both a spin coating method and a dipping method, and coating conditions determined to be optimal were selected for each method. Therefore, wiping and heat diffusion treatments are not performed. In the figure, the horizontal axis shows the concentration of Krytox solution (%), the vertical axis shows the number of durability in tens of thousands, and the range shown by the arrow is the pass.
Square marks indicate the dipping method, and circle marks indicate the spin coating method. The passing line for durability was set at 10,000 times or more. Furthermore, apply a pressure of about 10g on the disk mentioned above.
A winchiesta-type head was left for 24 hours at 24°C and 70% humidity, and the adsorption force (head stay (sticking between the head and disk)) generated between the head and disk was measured. The results are shown in Figure 4. In the figure, the horizontal axis is the Krytox solution concentration (%), the vertical axis is the adsorption force (g), and the range indicated by the arrow indicates a passing grade with an adsorption force of 5 g or less. The square marks and round marks are the same as in Fig. 3. Regarding the pass line, since no scratches were observed on either the head or the disk when the suction force was 5 g or less, a value of 5 g or less was considered acceptable. From the results explained above, it was determined that the practical concentration at which stable quality can be obtained when coating Krytox using the solvent according to the present invention is 0.2 to 0.5%. That is, if the degree of dilution is less than this range, coating conditions that provide sufficient durability cannot be obtained, whereas if it is diluted more than this range, the adsorption force becomes too large and is not suitable for practical use. (7) Effects of the Invention As explained above, when the method of the present invention is used, a Klytox solution with a low concentration change rate can be obtained, and when this solution is used, it is possible to obtain a solution of high quality, high durability, and adsorption power. A small lubricant layer can be obtained, which greatly contributes to improving the reliability of the magnetic medium.
第1図は沸点とクライトツクス溶解液濃度変化
時間経過の関係を示す線図、第2図は前記溶解液
の塗布性を示す線図、第3図は本発明の溶剤を用
いた場合の濃度とCSSヘツドの耐久回数の関係を
示す線図、第4図は本発明の溶剤とCSSヘツドの
吸着力との関係を示す線図である。
Fig. 1 is a diagram showing the relationship between the boiling point and the change in concentration of the Krytox solution over time, Fig. 2 is a diagram showing the coatability of the solution, and Fig. 3 is a diagram showing the relationship between the concentration and the time when the solvent of the present invention is used. FIG. 4 is a diagram showing the relationship between the durability of the CSS head and the adsorption power of the CSS head.
Claims (1)
気塗料を非磁性基体に塗布し磁性層を形成した後
に磁性層表面に潤滑剤を塗布してなる磁気記録媒
体製造方法であつて、 前記潤滑剤は、パーフロロアルキルポリエーテ
ルを分子式がC7F16またはC8F16Oの何れかの単独
または、これらの混合液からなる高フツ化希釈液
中に希釈した状態で塗布されることを特徴とする
磁気記録媒体の製造方法。 2 前記高フツ化希釈液中へのパーフロロアルキ
ルポリエーテルの希釈濃度が0.2%〜5%である
ことを特徴とする特許請求の範囲第1項記載の磁
気記録媒体製造方法。[Claims] 1. Manufacture of a magnetic recording medium by applying a magnetic paint made by dispersing magnetic iron powder in a binder to a non-magnetic substrate to form a magnetic layer, and then applying a lubricant to the surface of the magnetic layer. In the method, the lubricant is prepared by diluting perfluoroalkyl polyether in a highly fluorinated diluted solution having a molecular formula of either C 7 F 16 or C 8 F 16 O alone or a mixture thereof. A method for manufacturing a magnetic recording medium, characterized in that the magnetic recording medium is coated in a state in which the magnetic recording medium is coated. 2. The method of manufacturing a magnetic recording medium according to claim 1, wherein the diluted concentration of perfluoroalkyl polyether in the high fluoride diluent is 0.2% to 5%.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP21051981A JPS58114331A (en) | 1981-12-26 | 1981-12-26 | Production of magnetic recording medium |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP21051981A JPS58114331A (en) | 1981-12-26 | 1981-12-26 | Production of magnetic recording medium |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58114331A JPS58114331A (en) | 1983-07-07 |
| JPS6256574B2 true JPS6256574B2 (en) | 1987-11-26 |
Family
ID=16590709
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP21051981A Granted JPS58114331A (en) | 1981-12-26 | 1981-12-26 | Production of magnetic recording medium |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58114331A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61126627A (en) * | 1984-11-26 | 1986-06-14 | Hitachi Ltd | Magnetic recording medium |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5379502A (en) * | 1976-12-24 | 1978-07-14 | Hitachi Ltd | Manufacture of magnetic disk |
| JPS53141003A (en) * | 1977-05-16 | 1978-12-08 | Hitachi Ltd | Production of magnetic disc |
-
1981
- 1981-12-26 JP JP21051981A patent/JPS58114331A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58114331A (en) | 1983-07-07 |
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