JPH0294111A - Magnetic recording medium - Google Patents
Magnetic recording mediumInfo
- Publication number
- JPH0294111A JPH0294111A JP24758588A JP24758588A JPH0294111A JP H0294111 A JPH0294111 A JP H0294111A JP 24758588 A JP24758588 A JP 24758588A JP 24758588 A JP24758588 A JP 24758588A JP H0294111 A JPH0294111 A JP H0294111A
- Authority
- JP
- Japan
- Prior art keywords
- magnetic recording
- photosetting
- recording medium
- synthetic resin
- film
- 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.)
- Pending
Links
- 239000000758 substrate Substances 0.000 claims abstract description 48
- 229920003002 synthetic resin Polymers 0.000 claims abstract description 26
- 239000000057 synthetic resin Substances 0.000 claims abstract description 26
- 229920005989 resin Polymers 0.000 claims abstract description 15
- 239000011347 resin Substances 0.000 claims abstract description 15
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 8
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 8
- 239000011248 coating agent Substances 0.000 claims description 35
- 238000000576 coating method Methods 0.000 claims description 35
- 239000000428 dust Substances 0.000 abstract description 8
- 230000005611 electricity Effects 0.000 abstract description 6
- 230000003068 static effect Effects 0.000 abstract description 6
- 238000001179 sorption measurement Methods 0.000 abstract description 2
- 238000006748 scratching Methods 0.000 abstract 2
- 230000002393 scratching effect Effects 0.000 abstract 2
- 230000001070 adhesive effect Effects 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 21
- 238000000034 method Methods 0.000 description 17
- 239000000203 mixture Substances 0.000 description 5
- 229910000838 Al alloy Inorganic materials 0.000 description 4
- 239000011651 chromium Substances 0.000 description 4
- 239000003973 paint Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 229910045601 alloy Inorganic materials 0.000 description 3
- 239000000956 alloy Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 230000007547 defect Effects 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 238000007747 plating Methods 0.000 description 3
- 238000005498 polishing Methods 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 239000004697 Polyetherimide Substances 0.000 description 2
- HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000005389 magnetism Effects 0.000 description 2
- 229920001601 polyetherimide Polymers 0.000 description 2
- 229920001721 polyimide Polymers 0.000 description 2
- 239000011241 protective layer Substances 0.000 description 2
- 229910052814 silicon oxide Inorganic materials 0.000 description 2
- BNGXYYYYKUGPPF-UHFFFAOYSA-M (3-methylphenyl)methyl-triphenylphosphanium;chloride Chemical compound [Cl-].CC1=CC=CC(C[P+](C=2C=CC=CC=2)(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 BNGXYYYYKUGPPF-UHFFFAOYSA-M 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229910018487 Ni—Cr Inorganic materials 0.000 description 1
- 229910001096 P alloy Inorganic materials 0.000 description 1
- 239000004695 Polyether sulfone Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004734 Polyphenylene sulfide Substances 0.000 description 1
- 229910001069 Ti alloy Inorganic materials 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- MPIAGWXWVAHQBB-UHFFFAOYSA-N [3-prop-2-enoyloxy-2-[[3-prop-2-enoyloxy-2,2-bis(prop-2-enoyloxymethyl)propoxy]methyl]-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(COC(=O)C=C)(COC(=O)C=C)COCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C MPIAGWXWVAHQBB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- 150000001721 carbon Chemical class 0.000 description 1
- 229910001567 cementite Inorganic materials 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 239000006247 magnetic powder Substances 0.000 description 1
- 238000001755 magnetron sputter deposition Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229910001120 nichrome Inorganic materials 0.000 description 1
- WHOPEPSOPUIRQQ-UHFFFAOYSA-N oxoaluminum Chemical compound O1[Al]O[Al]1 WHOPEPSOPUIRQQ-UHFFFAOYSA-N 0.000 description 1
- 229920001643 poly(ether ketone) Polymers 0.000 description 1
- 229920001230 polyarylate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 239000009719 polyimide resin Substances 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- -1 scales Substances 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、磁気記録媒体に関し、特に、合成樹脂製基板
を用いたCSS特性に優れた磁気記録媒体に係る。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a magnetic recording medium, and particularly to a magnetic recording medium using a synthetic resin substrate and having excellent CSS characteristics.
[従来の技術]
(技術背景)
従来、磁気記録媒体としては、アルミ合金製基板の表面
をアルマイト処理または金属メツキし、さらにその表面
を鏡面研磨仕上した磁気ディスク基板を用いたものか知
られている。[Prior Art] (Technical Background) Conventionally, magnetic recording media have been known to use magnetic disk substrates made of aluminum alloy substrates whose surfaces are alumite-treated or metal-plated, and whose surfaces are mirror-polished. There is.
しかるに、近時、磁気記録媒体にも軽量化、加工容易性
か強く要請されており、かかる要請に基づぎ、アルミ合
金製基板よりも軽量で加工が容易な合成樹脂製基板が提
案されている。しかし、合成樹脂製基板はアルミ合金製
基板に比べ硬度が十分ではなく、そのため、合成樹脂製
基板を用いた磁気記録媒体のCSS特性は不十分なもの
となってしまう。そこで、十分なC8S特性を有する磁
気記録媒体が探究され、いくつかの試みがなされている
。However, in recent years, there has been a strong demand for magnetic recording media to be lighter and easier to process, and based on these demands, synthetic resin substrates that are lighter and easier to process than aluminum alloy substrates have been proposed. There is. However, synthetic resin substrates do not have sufficient hardness compared to aluminum alloy substrates, and as a result, the CSS characteristics of magnetic recording media using synthetic resin substrates are insufficient. Therefore, magnetic recording media having sufficient C8S characteristics are being sought, and several attempts have been made.
(直近の従来技術)
上記試みの1つとして、合成樹脂製基板上に、Ti、T
i合金またはT1化合物の被膜をイオンブレーティング
等の手段で形成した磁気ディスク基板か提案されている
(特開昭61−187117号公報)。(Latest prior art) As one of the above attempts, Ti, T
A magnetic disk substrate in which a film of i-alloy or T1 compound is formed by means such as ion blasting has been proposed (Japanese Patent Application Laid-open No. 187117/1983).
なお、硬度を高め、磁気記録媒体のCSS特性を向上さ
せ、その信頼性を高める技術としては、アルミ合金製基
板を用いたものついててはあるが次の技術か知られてい
る。Note that as a technique for increasing the hardness, improving the CSS characteristics of a magnetic recording medium, and increasing its reliability, the following technique is known, although one uses an aluminum alloy substrate.
■基板上に、N1−P合金を基本組成とする厚さ5〜2
0μmの被膜を湿式メツキ等の方法により施す技術。■Thickness 5 to 2 with basic composition of N1-P alloy on the substrate
A technology that applies a 0 μm film using methods such as wet plating.
■硝酸アルミニウムのメタノール溶液を基板上に塗布し
、これを高温で焼成することにより基板上にAl2O2
の被膜を形成する技術(特開昭62−252526号公
報)。■By applying a methanol solution of aluminum nitrate on the substrate and baking it at high temperature, Al2O2 is formed on the substrate.
(Japanese Unexamined Patent Publication No. 62-252526).
[発明か解決しようとする課題] しかし、上記従来技術には次のような課題が存在する。[Invention or problem to be solved] However, the above conventional technology has the following problems.
■特開昭61−187117号公報に開示されている、
T1、T1合金またはTI化合物の被膜を合成樹脂製基
板上に形成する技術は、必要にして十分な膜厚を得るこ
とが非常に困難である。ざらにTi、Ti合金またはT
1化合物の被膜は合成樹脂製基板との密着性に劣るため
、酸化シリコン等の中間層を設けねばならないという問
題点があり、酸化シリコン等の中間層を設けたとしても
必すしも十分な硬度か得られず、従って十分なCSS特
性か得らねない。■Disclosed in Japanese Patent Application Laid-open No. 187117/1983,
With the technique of forming a film of T1, T1 alloy, or TI compound on a synthetic resin substrate, it is extremely difficult to obtain a sufficient film thickness. Roughly Ti, Ti alloy or T
Since a single compound coating has poor adhesion to a synthetic resin substrate, there is a problem in that an intermediate layer such as silicon oxide must be provided, and even if an intermediate layer such as silicon oxide is provided, it does not necessarily have sufficient hardness. Therefore, sufficient CSS characteristics may not be obtained.
さらに、合成樹脂製基板を用いた上記従来技術において
は、摩擦等により容易に静電気を発生し、磁気ディスク
基板上に空気中の塵埃を吸着する。磁気ディスク基板上
に磁気記録層を形成する前段階において磁気ディスク基
板表面に塵埃が付着すると、その後に形成された磁気記
録層に信号欠陥か発生する原因となる。この塵埃は除去
することが容易ではなく、磁気記録媒体としての性能を
著しく低下させる。Furthermore, in the above-mentioned conventional technology using a synthetic resin substrate, static electricity is easily generated due to friction, etc., and dust in the air is attracted onto the magnetic disk substrate. If dust adheres to the surface of the magnetic disk substrate before forming the magnetic recording layer on the magnetic disk substrate, it may cause signal defects in the magnetic recording layer formed thereafter. This dust is not easy to remove and significantly degrades the performance of the magnetic recording medium.
■合成樹脂製基板に対して、N1−Pメツキにより基板
硬度を向上させる方法を適用した場合、メツキ層と合成
樹脂製基板とは密着性が悪いため、その界面で剥離か生
じ、実際上の使用が困難である。また、N1−Pを基本
組成とした合金被膜は組成のわずかな変化によって磁性
を持ち易くなり、かかる磁性は磁気記録媒体としての性
能を損なう原因と/lる。■When applying the method of improving the substrate hardness by N1-P plating to a synthetic resin substrate, the plating layer and the synthetic resin substrate have poor adhesion, so peeling occurs at the interface, which causes practical problems. Difficult to use. Further, an alloy film having a basic composition of N1-P becomes more likely to have magnetism due to a slight change in composition, and such magnetism may impair the performance as a magnetic recording medium.
■特開昭62−、252526号公報に開示されている
、焼成によりAj2203の被覆を得る方法は、500
℃という高温下での成膜処理が必要であるため、合成樹
脂製基板に対しては全く適用することかできない。■The method of obtaining Aj2203 coating by firing, which is disclosed in JP-A-62-252526, is
Since the film formation process is required at a high temperature of °C, it cannot be applied to synthetic resin substrates at all.
本発明は、上記課題を解決し、耐摩耗性、耐擦傷性に優
れ、静電気による塵埃の付着のない、合成樹脂製基板を
用いた磁気記録媒体を提供することを目的とし、かつ、
軽量かつ安価でC5S特性に優れ、信頼性に優れた磁気
記録媒体を提供することをも目的とする。An object of the present invention is to solve the above problems and provide a magnetic recording medium using a synthetic resin substrate, which has excellent wear resistance and scratch resistance, and does not attract dust due to static electricity, and
Another object of the present invention is to provide a magnetic recording medium that is lightweight, inexpensive, has excellent C5S characteristics, and has excellent reliability.
[問題点を解決するための手段コ
本発明の要旨は、合成樹脂製基板上に、電気抵抗値が1
09Ω/口以下となるようにカーボンを含有せしめた光
硬化性樹脂からなる光硬化性塗膜か形成され、該光硬化
性塗膜上に磁気記録層を有していることを特徴とする磁
気記録媒体に存在する。[Means for Solving the Problems] The gist of the present invention is to provide a synthetic resin substrate with an electric resistance value of 1.
A magnetic device comprising: a photocurable coating film made of a photocurable resin containing carbon such that the resistance is 0.09 Ω/min or less; and a magnetic recording layer is provided on the photocurable coating film. Exists on a recording medium.
本発明に使用される合成樹脂製基板としては、例えば、
アクリル系、ポリカーボネイト系、ポリイミド系、エポ
キシ系等の合成樹脂よりなる基板か使用できる。例えは
、ポリエーテルイミド、ポリエーテルサルホン、ポリフ
ェニレンサルファイド、ボリアリレート、ポリカーボネ
ート、ポリイミド、ポリエーテルケトン等の樹脂よりな
る基板を挙げることができる。さらに、必要に応じて、
上記合成樹脂中にガラス繊維、アルミナ粒子等の無機質
充填剤を適宜添加してもよい。なお、合成樹脂からなる
基板は、2層以上の多層構造でもよい。Examples of the synthetic resin substrate used in the present invention include:
Substrates made of synthetic resins such as acrylic, polycarbonate, polyimide, and epoxy resins can be used. Examples include substrates made of resins such as polyetherimide, polyethersulfone, polyphenylene sulfide, polyarylate, polycarbonate, polyimide, and polyetherketone. Furthermore, if necessary,
Inorganic fillers such as glass fibers and alumina particles may be appropriately added to the synthetic resin. Note that the substrate made of synthetic resin may have a multilayer structure of two or more layers.
本発明ではこの合成樹脂製基板上に光硬化製樹脂よりな
る光硬化性塗膜を形成してあり、この光硬化製塗膜は、
カーボンを、電気抵抗値が109Ω/口以下となるよう
に含有している。In the present invention, a photocurable coating film made of a photocurable resin is formed on this synthetic resin substrate, and this photocurable coating film is
Carbon is contained so that the electrical resistance value is 10 9 Ω/mouth or less.
電気抵抗値は、含有せしめるカーボン含有量、光硬化性
塗膜内における分布状況等によって変化するのて、10
9Ω/口以下とするには、予めこれらと電気抵抗値との
関係を求めておき適宜決定すればよい。−船釣には、光
硬化性樹脂100重量部に対し50〜150重量部含有
させればよい。The electrical resistance value varies depending on the carbon content contained, the distribution situation within the photocurable coating film, etc.
In order to set the resistance to 9Ω/mouth or less, the relationship between these values and the electrical resistance value may be determined in advance and determined as appropriate. - For boat fishing, the content may be 50 to 150 parts by weight per 100 parts by weight of the photocurable resin.
光硬化性塗膜を形成する方法としては、例えば、デイツ
プ法、スプレー法、スピンコーティング法その他の方法
を用いることか可能である。As a method for forming a photocurable coating film, for example, a dip method, a spray method, a spin coating method, and other methods can be used.
光硬化性塗膜の膜厚としては、2〜20μmが好ましく
、5〜10μmがより好ましい。The thickness of the photocurable coating film is preferably 2 to 20 μm, more preferably 5 to 10 μm.
光硬化性樹脂としては、例えば、ジペンタエリスリトー
ルへキサアクリレート、テトラメチロールメタントリア
クリレート、テトラメチロールメタンテトラアクリレー
トあるいはこれらの混合物が挙げられる。Examples of the photocurable resin include dipentaerythritol hexaacrylate, tetramethylolmethane triacrylate, tetramethylolmethanetetraacrylate, or mixtures thereof.
カーボンの形態には特に限定されず、例えは、粉状、粒
状、鱗片状、繊維状(ウィスカーを含む)あるいは塊状
のいずれであってもよい。また、膜内の分布についても
特に限定されないが、表面近傍を高密度とすることが好
ましい。さらに、表面にその一部が露出していてもよい
。The form of carbon is not particularly limited, and may be, for example, powder, granules, scales, fibers (including whiskers), or lumps. Further, the distribution within the film is not particularly limited either, but it is preferable to have a high density near the surface. Furthermore, a portion thereof may be exposed on the surface.
このカーボンは、磁気記録媒体の平面平滑性を維持する
上からは直径05μm以下の粒状、もしくは、直径1μ
m以下で厚さ03μm以下の鱗片状であることが望まし
い。In order to maintain the planar smoothness of the magnetic recording medium, this carbon should be in the form of particles with a diameter of 05 μm or less, or in the form of particles with a diameter of 1 μm.
It is desirable to have a scale-like shape with a thickness of 0.3 μm or less and a thickness of 0.3 μm or less.
なお、硬化後の光硬化性塗膜表面に、テープ研磨等の方
法で中心から同心円状に微細な凹凸を設けてもよい。Note that fine irregularities may be provided concentrically from the center on the surface of the photocurable coating film after curing by a method such as tape polishing.
また、硬化後の光硬化性塗膜表面に対し、コロナ放電、
プラズマ照射等の処理を行ってもよい。In addition, corona discharge,
Treatment such as plasma irradiation may also be performed.
光硬化性塗膜上の磁気記録層は、記録再生に関与する層
であり、かかる作用を奏するならばいかなるものでもよ
い。例えば、Co−Cr。The magnetic recording layer on the photocurable coating film is a layer involved in recording and reproduction, and any layer may be used as long as it exhibits this function. For example, Co-Cr.
Co−Ni−Cr、酸化鉄、酸化クロム等からなる場合
、磁性粉末(例えば、炭化鉄粉、γFe2O3粉等)を
樹脂で結合してなる場合等でもよい。なお、光硬化性塗
膜と磁気記録層との間には下地膜(例えばCr膜)を介
在させてもよい。It may be made of Co-Ni-Cr, iron oxide, chromium oxide, etc., or it may be made of magnetic powder (for example, iron carbide powder, γFe2O3 powder, etc.) bonded with a resin. Note that a base film (for example, a Cr film) may be interposed between the photocurable coating film and the magnetic recording layer.
[作 用] 以下に本発明の詳細な説明する。[Work] The present invention will be explained in detail below.
本発明では、樹脂製基板に被膜を設け、その被膜として
光硬化性塗膜を用いているので(すなわち、光硬化性樹
脂塗料を合成樹脂製基板上に塗布し光により硬化させる
ので)、光硬化性塗膜と合成樹脂製基板との間で良好な
密着性を得ることかてきる。さらに、硬化は光により行
なうことができるので、合成樹脂製基板に過大な熱を加
えることなく高硬度な被膜を形成することが可能である
。In the present invention, a coating is provided on a resin substrate and a photocurable coating is used as the coating (that is, a photocurable resin coating is applied onto a synthetic resin substrate and cured by light). It is possible to obtain good adhesion between the curable coating film and the synthetic resin substrate. Furthermore, since curing can be performed with light, it is possible to form a highly hard coating without applying excessive heat to the synthetic resin substrate.
さらに、本発明では、光硬化性樹脂中に、光硬化性塗膜
の表面電気抵抗値が109Ω/口以下となるように、カ
ーボンを含有せしめているため、光硬化性塗膜に導電性
が付与され、磁気記録媒体の帯電が防止される。Furthermore, in the present invention, since carbon is contained in the photocurable resin so that the surface electrical resistance value of the photocurable coating film is 109Ω/or less, the photocurable coating film has electrical conductivity. This prevents the magnetic recording medium from being charged.
なお、光硬化性塗膜の膜厚を2〜20μmとした場合に
は硬度か一層高くなり、また、膜厚を5〜10μmとし
た場合には硬度がより一層高くなり、C5S特性は一段
と向上する。In addition, when the film thickness of the photocurable coating film is 2 to 20 μm, the hardness becomes even higher, and when the film thickness is 5 to 10 μm, the hardness becomes even higher, and the C5S properties are further improved. do.
硬化後の光硬化性塗膜表面に、テープ研磨等の方法で中
心から同心円状に微細な凹凸を設けることで、磁気ヘッ
トの吸着か生じにくい磁気記録媒体を得ることも可能で
あり、光硬化性塗膜と磁気記録層(光硬化性塗膜と磁気
記録層との間に下地層か設りられている場合には、光硬
化性塗膜と下地層)との密着性も向上する。By creating fine irregularities concentrically from the center on the surface of the photocurable coating film after curing using a method such as tape polishing, it is possible to obtain a magnetic recording medium that is less prone to attracting magnetic heads. The adhesion between the magnetic coating film and the magnetic recording layer (or the photocurable coating film and the base layer if an underlayer is provided between the photocurable coating film and the magnetic recording layer) is also improved.
また、硬化後の光硬化性塗膜表面に対し、コロナ放電、
プラズマ照射等の処理を行うことにより、光硬化性塗膜
と磁気記録層(光硬化性塗膜と磁気記録層との間に下地
層が設けられている場合には、光硬化性塗膜と下地層)
との密着性をさらに向上させることが可能である。In addition, corona discharge,
By performing a treatment such as plasma irradiation, the photocurable coating film and the magnetic recording layer (if a base layer is provided between the photocurable coating film and the magnetic recording layer, the photocurable coating film and the magnetic recording layer) base layer)
It is possible to further improve the adhesion with.
[実施例] 以下、本発明の実施例を製造工程とともに説明する。[Example] Examples of the present invention will be described below along with manufacturing steps.
まずテトラメチロールメタントリアクリレートとテトラ
メチロールメタンテトラアクリレートの混合物(重量比
84 : 16)からなる光硬化性オリゴマー100重
量部に対し、光重合開始剤ベンゾフェノン5重量部、メ
チルメタクリレ−1・−ヒドロキシエチルメタクリレー
ト共重合体20重量部、粒径0.3μmのカーボン粉体
100重量部からなる光硬化性塗料を、メチルエチルケ
トン、エチルセロソルブを希釈剤として用いて、サンド
ミル型分散機により作製した。この塗料をスピンコード
法を用いて、ポリエーテルイミド製の5.25インチ樹
脂製基板3上に乾燥硬化後の膜厚か10μmになるよう
に塗布した。First, to 100 parts by weight of a photocurable oligomer consisting of a mixture of tetramethylolmethane triacrylate and tetramethylolmethanetetraacrylate (weight ratio 84:16), 5 parts by weight of photopolymerization initiator benzophenone and methyl methacrylate-1-hydroxy A photocurable paint consisting of 20 parts by weight of ethyl methacrylate copolymer and 100 parts by weight of carbon powder having a particle size of 0.3 μm was prepared using a sand mill type dispersing machine using methyl ethyl ketone and ethyl cellosolve as diluents. This paint was applied onto a 5.25-inch resin substrate 3 made of polyetherimide using a spin cord method so that the film thickness after drying and curing would be 10 μm.
光硬化性塗料を塗布したのち、60℃の熱風乾燥器を用
いて30分間乾燥を行なうことにより希釈剤の除去を行
い、続いて水銀ランプを用いて50J/cm2の光線を
照射して塗料を硬化させ光硬化性塗膜を形成して磁気デ
ィスク基板を得た。After applying the photocurable paint, the diluent was removed by drying it for 30 minutes using a hot air dryer at 60°C, and then the paint was irradiated with a light beam of 50 J/cm2 using a mercury lamp. A magnetic disk substrate was obtained by curing to form a photocurable coating film.
なお、本例ては、硬化後、光硬化性塗膜に対し、テープ
研磨機を用いて研磨テープで同心円状の微細な凹凸を施
した。このとき、磁気ディスク基板の半径方向の表面粗
さは8nmであった。また、この磁気ディスク基板の表
面電気抵抗は2×10−7Ω/口であった。In this example, after curing, the photocurable coating film was given concentric fine irregularities with a polishing tape using a tape polisher. At this time, the surface roughness of the magnetic disk substrate in the radial direction was 8 nm. Further, the surface electrical resistance of this magnetic disk substrate was 2×10 −7 Ω/hole.
以上の工程て得られた磁気ディスク基板に対して、Cr
下地層を厚さ200nmに、Co−NiCr6m気記録
層(Co+Ni :Cr=7515:10)を厚さ80
nmに、カーホン保護層を厚さ30nmに、D、Cマグ
ネトロン方式スパッタ装置により順次形成し、本発明に
係る磁気記録媒体を得た。この磁気記録媒体の表面には
フッ素樹脂系潤滑剤により潤滑処理を施した。For the magnetic disk substrate obtained through the above steps, Cr
The underlayer was 200 nm thick, and the Co-NiCr 6m recording layer (Co+Ni:Cr=7515:10) was 80 nm thick.
A carphone protective layer was sequentially formed to a thickness of 30 nm using a D and C magnetron sputtering apparatus to obtain a magnetic recording medium according to the present invention. The surface of this magnetic recording medium was lubricated with a fluororesin lubricant.
この6n気記録媒体に対してCSS試験を行い、再生出
力の低下を測定した。その結果を第1表に示す。比較の
ために、光硬化性塗膜を形成しない樹脂製基板上に上記
実施例と同じ下地層、磁気記録層、保護層を設は潤滑処
理を施した従来型磁気記録媒体の評価結果を併記する。A CSS test was conducted on this 6n recording medium to measure the decrease in reproduction output. The results are shown in Table 1. For comparison, the evaluation results of a conventional magnetic recording medium in which the same underlayer, magnetic recording layer, and protective layer as in the above example were provided on a resin substrate without a photocurable coating and were subjected to lubrication treatment are also listed. do.
CSS試験にはトラック幅24μm1荷重9.5gの3
370型ミニモノシリツクタイプヘツトを使用した。For CSS test, track width 24μm 1 load 9.5g 3
A 370 type mini monolithic type head was used.
第1表
第1表から明らかなように、従来型の磁気記録媒体では
、CSS回数10000回で既に出力か5%低下してい
るのに対し、本発明に係る磁気記録媒体ては20000
回てもまた出力の低下が生じず、40000回でようや
く5%の出力低下が測定された。すなわち、本発明に係
る磁気記録媒体では、CSS耐久性が著しく向上し、従
来の数倍の耐久性を得ることができる。Table 1 As is clear from Table 1, in the conventional magnetic recording medium, the output has already decreased by 5% after 10,000 CSS cycles, whereas the output of the magnetic recording medium according to the present invention has already decreased by 5% after 10,000 CSS cycles.
No decrease in output occurred even after 40,000 cycles, and a 5% decrease in output was finally measured after 40,000 cycles. That is, in the magnetic recording medium according to the present invention, the CSS durability is significantly improved, and the durability can be several times higher than that of the conventional magnetic recording medium.
また、上記の2種類の磁気記録媒体の信号欠陥個数を測
定した結果を第2表に示す。Further, Table 2 shows the results of measuring the number of signal defects of the above two types of magnetic recording media.
第2表
を付与することか可能であり、基板の平面性が良好であ
る。It is possible to provide Table 2, and the flatness of the substrate is good.
■光硬化性塗膜に、カーホンを含有させることにより導
電性が付与されており、摩擦等による静電気の発生、ひ
いては塵埃の吸着という、合成樹脂製基板を用いた場合
に生ずる特有の問題点を解決することができる。■Containing carphone in the photocurable coating gives it conductivity, which eliminates the unique problems that occur when using synthetic resin substrates, such as the generation of static electricity due to friction, etc., and the adsorption of dust. It can be solved.
■耐摩耗性、耐擦傷性に優れ、CSS特性に優れた、合
成樹脂製基板を用いた磁気記録媒体を実現することが可
能である。(2) It is possible to realize a magnetic recording medium using a synthetic resin substrate that has excellent wear resistance, scratch resistance, and CSS characteristics.
第2表から明かなように、本発明に係る磁気記録媒体は
、静電気の帯電を効果的に解消でき、塵埃のイ」着か全
く生じないため、これに起因する信号欠陥の発生を完全
に防止できる。As is clear from Table 2, the magnetic recording medium according to the present invention can effectively eliminate static electricity charging and does not cause any dust build-up, so it completely eliminates the occurrence of signal defects caused by this. It can be prevented.
[発明の効果] 本発明は、次に述へる諸々の効果を奏する。[Effect of the invention] The present invention provides various effects described below.
■光硬化性塗膜を形成しているため、合成樹脂製基板に
対して過大な熱を加えることなく高硬度特許出願人 積
水化学工業株式会社
代表者 廣 1) 馨■Because it forms a photocurable coating film, it has high hardness without applying excessive heat to the synthetic resin substrate Patent applicant Hiroshi, Representative of Sekisui Chemical Co., Ltd. 1) Kaoru
Claims (1)
となるようにカーボンを含有せしめた光硬化性樹脂から
なる光硬化性塗膜が形成され、該光硬化性塗膜上に磁気
記録層を有していることを特徴とする磁気記録媒体。A photocurable coating film made of a photocurable resin containing carbon is formed on a synthetic resin substrate so that the electrical resistance value is 10^9Ω/mouth or less, and a magnetic layer is applied on the photocurable coating film. A magnetic recording medium characterized by having a recording layer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP24758588A JPH0294111A (en) | 1988-09-30 | 1988-09-30 | Magnetic recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP24758588A JPH0294111A (en) | 1988-09-30 | 1988-09-30 | Magnetic recording medium |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0294111A true JPH0294111A (en) | 1990-04-04 |
Family
ID=17165694
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP24758588A Pending JPH0294111A (en) | 1988-09-30 | 1988-09-30 | Magnetic recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0294111A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998003972A1 (en) * | 1996-07-22 | 1998-01-29 | Matsushita Electric Industrial Co., Ltd. | Master information carrier, process for producing the carrier, and method and apparatus for recording master information signal on magnetic recording medium by using the carrier |
US6611388B1 (en) | 1998-03-23 | 2003-08-26 | Matsushita Electric Industrial Co., Ltd. | Master information magnetic recorder |
US6714367B1 (en) | 1998-10-29 | 2004-03-30 | Matsushita Electric Industrial Co., Ltd. | Master information medium and method of master information recording |
US6858328B1 (en) | 1998-03-20 | 2005-02-22 | Matsushita Electric Industrial Co., Ltd. | Master information support |
-
1988
- 1988-09-30 JP JP24758588A patent/JPH0294111A/en active Pending
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998003972A1 (en) * | 1996-07-22 | 1998-01-29 | Matsushita Electric Industrial Co., Ltd. | Master information carrier, process for producing the carrier, and method and apparatus for recording master information signal on magnetic recording medium by using the carrier |
US6347016B1 (en) | 1996-07-22 | 2002-02-12 | Matsushita Electric Industrial Co., Ltd. | Master information carrier, process for producing the carrier, and method and apparatus for recording master information signal on magnetic recording medium by using the carrier |
US6567227B2 (en) | 1996-07-22 | 2003-05-20 | Matsushita Electric Industrial Co., Ltd. | Master information carrier, method for producing the carrier, method and apparatus for writing information into magnetic record medium using the carrier |
US6587290B2 (en) | 1996-07-22 | 2003-07-01 | Matsushita Electric Industrial Co., Ltd. | Master information carrier, method for producing the carrier, and method apparatus for writing information into magnetic record medium using the carrier |
US6590727B2 (en) | 1996-07-22 | 2003-07-08 | Matsushita Electric Industrial Co., Ltd. | Master information carrier, method for producing the carrier, method and apparatus for writing information into magnetic record medium using the carrier |
US6606209B2 (en) | 1996-07-22 | 2003-08-12 | Matsushita Electric Industrial Co., Ltd. | Master information carrier, method for producing the carrier, method and apparatus for writing information into magnetic record medium using the carrier |
US6606208B2 (en) | 1996-07-22 | 2003-08-12 | Matsushita Electric Industrial Co., Ltd. | Master information carrier, method for producing the carrier, method and apparatus for writing information into magnetic record medium using the carrier |
US6961196B2 (en) | 1996-07-22 | 2005-11-01 | Matsushita Electric Industrial Co., Ltd. | Master information carrier, method for producing the carrier, method and apparatus for writing information into magnetic record medium using the carrier |
US6858328B1 (en) | 1998-03-20 | 2005-02-22 | Matsushita Electric Industrial Co., Ltd. | Master information support |
US6611388B1 (en) | 1998-03-23 | 2003-08-26 | Matsushita Electric Industrial Co., Ltd. | Master information magnetic recorder |
US6714367B1 (en) | 1998-10-29 | 2004-03-30 | Matsushita Electric Industrial Co., Ltd. | Master information medium and method of master information recording |
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