JPS61284830A - Magnetic recording medium - Google Patents

Magnetic recording medium

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Publication number
JPS61284830A
JPS61284830A JP12534985A JP12534985A JPS61284830A JP S61284830 A JPS61284830 A JP S61284830A JP 12534985 A JP12534985 A JP 12534985A JP 12534985 A JP12534985 A JP 12534985A JP S61284830 A JPS61284830 A JP S61284830A
Authority
JP
Japan
Prior art keywords
film
electron beam
magnetic recording
layer
curing resin
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
Application number
JP12534985A
Other languages
Japanese (ja)
Inventor
Koichi Shinohara
紘一 篠原
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial 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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP12534985A priority Critical patent/JPS61284830A/en
Publication of JPS61284830A publication Critical patent/JPS61284830A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To obtain a medium which decreases the wear of a magnetic head and decreases the medium noise by disposing an electron beam curing resin layer in which metallic atoms are partially disposed on a high-polymer film and providing a magnetic recording layer consisting of a thin ferromagnetic metallic film thereon. CONSTITUTION:This magnetic recording medium has the high-polymer film 1 consisting of a PE terephthalate film, the electron beam curing resin layer 2, a partially oxidized layer 3 obtd. by the formation of the thin ferromagnetic metallic film 4 and a stearic acid film 5 which is a protective lubricating film formed by a vacuum deposition method. A soln. prepd. by dissolving a dipentaerythritol hexaacrylate as the electron beam curing resin in a toluene is coated on the above-mentioned film and is dried; thereafter, the film is conducted from the run along a cylindrical can in the oxygen partial pressure and is subjected to diagonal vapor deposition of No-Ni by a vapor deposition method at the continuously changing incident angles to form the thin ferromagnetic metallic film thereon. An electron beam is irradiated on the film right after such formation to cure the resin film by the electron beam.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は高密度磁気記録に利用できる磁気記録媒体に関
する。
DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a magnetic recording medium that can be used for high-density magnetic recording.

従来の技術 従来磁気記録層として広く実用に供されているものは1
− Fe 203、Goをドープした1 −ve2o3
、CrO2、或いは、鉄等の強磁性金属又は合金微小粉
末磁性材料を塩化ビニル、酢酸ビニル共重合体、スチレ
ンブタジェン共重合体、エポキシ樹脂等の有機バインダ
中に分散させて高分子フィルム等の基板上に塗布乾燥さ
せた塗布型磁性層である。
Conventional technology The conventional magnetic recording layer that has been widely used in practical use is 1.
- Fe203, Go doped 1-ve2o3
A ferromagnetic metal such as , CrO2, or iron or an alloy fine powder magnetic material is dispersed in an organic binder such as vinyl chloride, vinyl acetate copolymer, styrene-butadiene copolymer, or epoxy resin to form a polymer film or the like. This is a coated magnetic layer that is coated and dried on a substrate.

近年高密度記録への要求の高まりと共に高密度域で優れ
た信号対雑音比(S/Nと以下記す)を与えつる期待の
大きい、強磁性金属薄膜を磁気記録層とするいわゆる金
属薄膜型磁気記録媒体が注目され、実用化に向けて努力
が続けられている。
In recent years, as the demand for high-density recording has increased, so-called metal thin film magnetism, in which a ferromagnetic metal thin film is used as the magnetic recording layer, has great expectations for providing an excellent signal-to-noise ratio (hereinafter referred to as S/N) in the high-density range. Recording media are attracting attention, and efforts are being made to put them into practical use.

〔例えば外国論文誌:アイイーイーイー磁気学会報(X
 EK K Transaction on Ma(n
etics )ToI!、MAG−10、NO−2、P
 P 36カ473(1974)参照〕 かかる磁気記録媒体の改良の主眼は、優れた電磁変換特
性を保ちながら、磁気記録層の耐久性を向上させること
にある。従ってこれに関する提案も多くなされ、一般に
、磁気記録層として用いられるGo−P、Co −Ni
 −P% Go  −Ni −0膜等の強磁性金属薄膜
上に保護膜を用いて、磁気ヘッドや走行系の機構材料と
の摩擦を少なくする方法〔例えば特開昭52−1537
07号、特開昭63−88704号、特開昭59−17
1026号の公報参照〕や高分子フィルム上に微細な凹
凸を設け、その上に強磁性金属薄膜を設は真実接触面積
を減少させることで、耐すり偏性や走行性能の改良を図
る上で一部で成功を収めている。〔例えば特開昭59−
84928号公報、特開昭59−121631号の公報
参照〕。
[For example, foreign journal: IEEI Magnetics Society Bulletin (X
EK K Transaction on Ma(n
etics)ToI! , MAG-10, NO-2, P
See P. 36 Ka. 473 (1974)] The main objective of improving such magnetic recording media is to improve the durability of the magnetic recording layer while maintaining excellent electromagnetic conversion characteristics. Therefore, many proposals have been made regarding this, and Go--P, Co--Ni, which are generally used as magnetic recording layers.
A method of using a protective film on a ferromagnetic metal thin film such as -P% Go -Ni -0 film to reduce friction with the mechanical material of a magnetic head or a traveling system [for example, JP-A-52-1537
No. 07, JP-A-63-88704, JP-A-59-17
1026] or by forming fine irregularities on a polymer film and placing a ferromagnetic metal thin film on top of it, it is possible to reduce the contact area and improve the abrasion resistance and running performance. It has been successful in some cases. [For example, JP-A-59-
84928 and Japanese Patent Application Laid-open No. 121631/1984].

発明が解決しようとする問題点 しかしながら上記したような構成では、磁気ヘッドが合
金系で特にスパッタ法で一部磁路を形成したタイプのヘ
ッドになった時に良好なS/Nを保つことができないと
いった問題が有った。
Problems to be Solved by the Invention However, with the above-mentioned configuration, it is not possible to maintain a good S/N ratio when the magnetic head is an alloy-based head, especially one in which a part of the magnetic path is formed by sputtering. There was a problem.

本発明は上記問題点に鑑み、磁気ヘッド摩耗の少ないか
つ媒体雑音の少ない磁気記録媒体を提供するものである
In view of the above-mentioned problems, the present invention provides a magnetic recording medium with less wear on the magnetic head and less media noise.

問題点を解決するための手段 上記問題点を解決するために本発明の磁気記録媒体は高
分子フィルム上に金属原子の部分拡散した電子ビーム硬
化樹脂層を配し、その上に強磁性金属薄膜からなる磁気
記録層を備えたものである。
Means for Solving the Problems In order to solve the above-mentioned problems, the magnetic recording medium of the present invention includes an electron beam-cured resin layer in which metal atoms are partially diffused on a polymer film, and a ferromagnetic metal thin film on top of the electron beam-cured resin layer in which metal atoms are partially diffused. It is equipped with a magnetic recording layer consisting of.

作用 本発明の磁気記録媒体は上記した構成によって磁気ヘッ
ドと高速で摺動した時に電子ビーム硬化樹脂が硬化する
時に磁気記録層との相互作用で微細な凹凸が出来るよう
に収縮してできた表面形状の作用効果と、部分拡散層が
あるため応力伝達の包配が連続性を帯びることで応力分
散がうまく行われる作用効果と相まって、ヘッドに対す
る衝撃力も平均化され摩耗が少なくできるのと、表面の
凹凸は極めて微細なので、S/Nも良好にできることに
なる。
Function The magnetic recording medium of the present invention has the above-described structure, and when it slides with a magnetic head at high speed, the electron beam-cured resin hardens and interacts with the magnetic recording layer to form a surface that shrinks to form fine irregularities. The effect of the shape and the effect of the partial diffusion layer, which makes the stress transmission envelope continuous and effectively disperses stress, equalizes the impact force on the head and reduces wear. Since the irregularities are extremely fine, the S/N ratio can also be improved.

実施例 以下、本発明の実施例の磁気記録媒体について、図面を
参照しながら説明する。
EXAMPLES Below, magnetic recording media according to examples of the present invention will be described with reference to the drawings.

第1図は本発明の第1の実施例の磁気記録媒体の拡大断
面図である。
FIG. 1 is an enlarged sectional view of a magnetic recording medium according to a first embodiment of the present invention.

第1図で1は厚み7.2μmのポリエチレンテレフタレ
ートフィルムから成る高分子フィルムで2は電子ビーム
硬化樹脂層で3は強磁性金属薄膜4を形成することで出
来る部分酸化層である。5は保護潤滑膜で真空蒸着法で
形成した厚み約60Xのステアリン酸膜である。
In FIG. 1, 1 is a polymer film made of polyethylene terephthalate film having a thickness of 7.2 μm, 2 is an electron beam cured resin layer, and 3 is a partially oxidized layer formed by forming a ferromagnetic metal thin film 4. 5 is a protective lubricating film, which is a stearic acid film with a thickness of about 60× formed by vacuum deposition.

電子ビーム硬化樹脂としてジペンタエリスリトールヘキ
サアクリレートをトルエンに1.0重量%の濃度で溶解
したものを塗布し、乾燥したのち、大気より真空蒸着機
内に導き、まずI X 10−’(’rorr)の酸素
分圧中でco −Ni (Ni ; 20重量%)を直
径1mの円筒もヤンに沿わせて、連続入射角変化蒸着法
で最大90度最小40度の入射角成分で斜め蒸着を行い
0.16μmの強磁性金属薄膜を形成し、その直後に1
00KVの電子ビームを5Mrad照射して電子ビーム
硬化させた。このようにすることで、Go−Niが0.
9μmの電子ビーム硬化樹脂の表層部370Xに部分拡
散した層ができ、かつ磁気記録層表面が硬化収縮の影響
で高分子フィルムの平均粗さをRaとすると(2,0〜
4.3)xRaとなる。この実施例ではRaを6OAに
選んで具体化したので200ムの磁気記録層表面を得る
ことができた。
Dipentaerythritol hexaacrylate dissolved in toluene at a concentration of 1.0% by weight was coated as an electron beam curing resin, and after drying, it was introduced into a vacuum evaporator from the atmosphere and first I X 10-'('rorr). Co-Ni (Ni; 20 wt%) was deposited obliquely on a cylinder with a diameter of 1 m along the yang in an oxygen partial pressure of A ferromagnetic metal thin film of 0.16 μm was formed, and immediately after that, 1
It was irradiated with an electron beam of 00 KV and 5 Mrad for electron beam curing. By doing this, Go-Ni becomes 0.
A partially diffused layer is formed on the surface layer 370X of the electron beam cured resin with a thickness of 9 μm, and the surface of the magnetic recording layer is affected by curing shrinkage. Assuming that the average roughness of the polymer film is Ra (2,0~
4.3) xRa. In this example, since Ra was selected to be 6OA, a magnetic recording layer surface of 200 μm could be obtained.

なお、このRaの倍率関係は、樹脂厚と電子線の単位時
間当りの照射エネルギーで変えることができ、S/Nを
みながら調整し、最適化すればよいものである。
Note that this magnification relationship of Ra can be changed by the resin thickness and the irradiation energy per unit time of the electron beam, and can be adjusted and optimized while looking at the S/N ratio.

本発明と比較するだめの比較例として、特開昭59−1
21631号公報に開示されたものでRaをほぼ同一の
20OAに設計したポリエチレンテレフタレートフィル
ムを用いて実施例と同一の蒸着を行い、強磁性金属薄膜
0.15μm、ステアリン酸(60人)膜を形成して磁
気テープを得た。
As a comparative example to be compared with the present invention, JP-A-59-1
Using a polyethylene terephthalate film disclosed in Japanese Patent Publication No. 21631 and designed to have almost the same Ra of 20OA, the same vapor deposition as in the example was performed to form a ferromagnetic metal thin film of 0.15 μm and a stearic acid (60%) film. and obtained a magnetic tape.

この両者をギャップ部にスパッタ法でセンダスト合金膜
を形成した、いわゆるメタルインギャップヘッドを用い
て(ギャップ長0.2μm)、エンベロープが80%以
下になるまでの時間を比較した。その結果は表に示した
ようであった。記録波長はo、49μmである。
Using a so-called metal-in-gap head in which a sendust alloy film was formed in the gap by sputtering (gap length 0.2 μm), the time required for the envelope to decrease to 80% or less was compared. The results were as shown in the table. The recording wavelength is o, 49 μm.

以上のように本実施例によれば、高分子フィルム上に金
属原子の部分拡散した電子ビーム硬化樹脂層を配して、
その上に磁気記録層として強磁性金属薄膜を設けること
により、メタルインギャッ ゛プヘッドを用いての短波
長記録再生で良好な再生エンベロープを長時間に渡り、
各種の環境で保持することができる。
As described above, according to this embodiment, an electron beam-cured resin layer in which metal atoms are partially diffused is arranged on a polymer film.
By providing a ferromagnetic metal thin film as a magnetic recording layer on top of this, a good reproduction envelope can be maintained for a long time during short wavelength recording and reproduction using a metal-in-gap head.
Can be maintained in various environments.

以下本発明の第2の実施例について図面を参照しながら
説明する。
A second embodiment of the present invention will be described below with reference to the drawings.

第2図は本発明の第2の実施例の磁気記録媒体の拡大断
面図である。第2図において、6は厚み11μmのポリ
アミドフィルムである。7は電子ビーム硬化樹脂層8は
Wbの部分拡散層9はNbの650ムの蒸着下地層であ
る。7.8.9の形成及び電子ビーム硬化樹脂は実施例
1と同一の材料を用いたものをムとし、電子ビーム硬化
樹脂として、エチレングリコールとコハク酸とへキサメ
チレンジイソシアネートとアクリル酸エステルの反応化
合物で、その架橋点間平均分子量が約230のものを用
いたものをBとした。
FIG. 2 is an enlarged sectional view of a magnetic recording medium according to a second embodiment of the present invention. In FIG. 2, 6 is a polyamide film with a thickness of 11 μm. Reference numeral 7 is an electron beam hardening resin layer 8, a Wb partial diffusion layer 9, and a Nb evaporation base layer of 650 μm. 7.8.9 Formation and electron beam curing The resin used was the same material as in Example 1, and the electron beam curing resin was prepared by reacting ethylene glycol, succinic acid, hexamethylene diisocyanate, and acrylic ester. A compound having an average molecular weight between crosslinking points of about 230 was used as B.

Nb脂層を配したのち、直径6ocIxの表面温度18
0’Cの円筒キャンに沿わせて、はぼ垂直成分のみで、
Go −Cr (Or + 19.7wt%)を1x 
1o−7Torrの真空中で電子ビーム蒸着して厚み0
.2μmの垂直磁化Co−Cr膜から成る強磁性金属薄
膜10を配し、その上にムr分圧lX10−”Torr
中で、13.56MHzの高周波グロー放電を発生させ
た状態で、ミリスチン酸をイオンブレーティング法で約
60ム保護潤滑膜11として形成せしめた。表面粗さR
aはムテープ、Bテープ、それぞれ240ム、200ム
であった。
After placing the Nb fat layer, the surface temperature of the diameter 6ocIx was 18
Along the 0'C cylindrical can, there is only a vertical component,
1x Go-Cr (Or + 19.7wt%)
Thickness 0 by electron beam evaporation in a vacuum of 1o-7 Torr
.. A ferromagnetic metal thin film 10 made of a perpendicularly magnetized Co--Cr film of 2 μm is placed on top of the ferromagnetic metal thin film 10 with a partial pressure of 1×10−”Torr.
Inside, while a high frequency glow discharge of 13.56 MHz was generated, myristic acid was formed as a protective lubricant film 11 with a thickness of about 60 μm using an ion blasting method. Surface roughness R
A was 240 MU and 200 MU for Mu tape and B tape, respectively.

ギャップ長0.16μmのメタルインギャップタイプの
リング”型ヘッドで、0.36μmの記録再生を行い第
1の実施例と同じようにエンベロープが80q6をきる
時間を比較した結果、各環境でムテープは10%〜16
%増し、°Bテープは一6%から+5%の範囲でほぼ同
じ性能を確認し得た。
Using a metal-in-gap ring type head with a gap length of 0.16 μm, we performed recording and playback of 0.36 μm and compared the time it took for the envelope to exceed 80q6 in the same way as in the first embodiment. 10%~16
% increase, and the °B tape was able to confirm almost the same performance in the range of -6% to +5%.

又ドロップアウトの変化についても各環境で調べた結果
、夫々10oO時間後のヘッドテープ使用状態下で、初
期値の1.3倍までてらったが、実施例−1で用いた比
較例は500時間後で約6倍に増加していた。
Also, as a result of examining the change in dropout in each environment, it was found to be up to 1.3 times the initial value under the head tape usage condition after 10oO hours, but in the comparative example used in Example-1, it was 1.3 times the initial value after 500 hours. Later, it increased by about 6 times.

以上のように本実施例によれば、メタルインギャップタ
イプのリングヘッドを用いて極めて高い記録密度であり
ながら、良好なエンベロープ再生波形、ドロップアウト
性能を確保することが長時間に渡ってできる利点がある
As described above, this embodiment has the advantage of being able to maintain good envelope playback waveforms and dropout performance over a long period of time while achieving extremely high recording density using a metal-in-gap type ring head. There is.

第1の実施例、第2の実施例で高分子フィルムは夫々ポ
リエチレンテレフタレート、ポリアミドとしたがポリイ
ミド、ポリ塩化ビニル、ポリカーボネート、セルロース
トリアセテート、ポリエチレンナフタレート、ポリスル
フォン等としてもよい。
In the first and second embodiments, the polymer films were made of polyethylene terephthalate and polyamide, respectively, but they may also be made of polyimide, polyvinyl chloride, polycarbonate, cellulose triacetate, polyethylene naphthalate, polysulfone, or the like.

電子ビーム硬化樹脂は、実施例に示したように、ポリオ
ール、ジカルボン酸、ジイソシアネート、(メタ)アク
リル酸、(メタ)アクリル酸エステルとの反応物を包含
していて、その架橋点間平均分子量が約300以下であ
るものがあげられ、組み合わせは多く、例えば、ポリオ
ールと(メタ)アクリル酸との反応生成物、ポリオール
とジカルボン酸と(メタ)アクリル酸エステルとの反応
生成物等が挙げられる。
As shown in the examples, the electron beam curing resin includes a reaction product with a polyol, dicarboxylic acid, diisocyanate, (meth)acrylic acid, and (meth)acrylic acid ester, and the average molecular weight between the crosslinking points is There are many combinations, such as reaction products of polyols and (meth)acrylic acid, reaction products of polyols, dicarboxylic acids, and (meth)acrylic esters, and the like.

下地層はWbとしたが、他にSi、Ga、Ti。The base layer was made of Wb, but other materials were Si, Ga, and Ti.

Mo、Ta、Ru、Rh、入/。Cu等でもよい。Mo, Ta, Ru, Rh, in/. It may also be Cu or the like.

強磁性金属薄膜は、Go−Ni−0,co−Orとした
が、他にGo−Ni、Go−Fe+Go−0,co−O
s。
The ferromagnetic metal thin film was Go-Ni-0, co-Or, but also Go-Ni, Go-Fe+Go-0, co-O
s.

Go−3i 、 Go−Ga 、 Go−Ti 、 G
o−Mo 、 Go−Ta 。
Go-3i, Go-Ga, Go-Ti, G
o-Mo, Go-Ta.

Go−Ru、Go−Rh、Go−ムJIGO−Cu、G
O−W。
Go-Ru, Go-Rh, Go-mu JIGO-Cu, G
O-W.

Go−8m 、 Go−Ni−P 、 Go−M(−0
等でもよい。
Go-8m, Go-Ni-P, Go-M(-0
etc.

発明の効果 以上のように本発明によれば、高記録密度を行うのに有
用なメタルインヘッドタイプのリング型磁気ヘッドと組
み合わせて、初期の良好なS/N(再生エンベロープ波
形)、ドロップアウト性能を、各種の環境条件下でも長
時間係てるといったすぐれた効果を得ることができる。
Effects of the Invention As described above, according to the present invention, in combination with a metal-in-head type ring-shaped magnetic head useful for high recording density, good initial S/N (reproduction envelope waveform) and dropout can be achieved. It is possible to obtain excellent effects such as maintaining performance for a long time even under various environmental conditions.

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

第1図は本発明の第1の実施例の磁気記録媒体の拡大断
面図、第2図は本発明の第2の実施例の磁気記録媒体の
拡大断面図である。 1.6・・・・・・高分子フィルム、2.7・・・・・
・電子ビーム硬化樹脂、3,8・・・・・・部分拡散層
、9・・・・・・下地層、4,1o・・・−・・強磁性
金属薄膜。 代理人の氏名 弁理士 中 尾 敏 男 ほか1名/−
−−高分子フイルム 第  1  図                  
   2−一一電iヒーム硬化有4月a濁3−−一邦分
孤欣] 4−一一陳砥a全盛涛灰
FIG. 1 is an enlarged sectional view of a magnetic recording medium according to a first embodiment of the invention, and FIG. 2 is an enlarged sectional view of a magnetic recording medium according to a second embodiment of the invention. 1.6...Polymer film, 2.7...
- Electron beam curing resin, 3,8...partial diffusion layer, 9...base layer, 4,1o...ferromagnetic metal thin film. Name of agent: Patent attorney Toshio Nakao and 1 other person/-
--Polymer film Figure 1
2-11 Den I Heem Hardening April A Cloudy 3--Ippang Bunkoshin] 4-11 Chen Toa Heyday in full bloom

Claims (1)

【特許請求の範囲】[Claims] 高分子フィルム上に金属原子の部分拡散した電子ビーム
硬化樹脂層を配し、その上に強磁性金属薄膜からなる磁
気記録層を配したことを特徴とする磁気記録媒体。
A magnetic recording medium characterized in that an electron beam-cured resin layer in which metal atoms are partially diffused is arranged on a polymer film, and a magnetic recording layer made of a ferromagnetic metal thin film is arranged thereon.
JP12534985A 1985-06-10 1985-06-10 Magnetic recording medium Pending JPS61284830A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12534985A JPS61284830A (en) 1985-06-10 1985-06-10 Magnetic recording medium

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12534985A JPS61284830A (en) 1985-06-10 1985-06-10 Magnetic recording medium

Publications (1)

Publication Number Publication Date
JPS61284830A true JPS61284830A (en) 1986-12-15

Family

ID=14907920

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12534985A Pending JPS61284830A (en) 1985-06-10 1985-06-10 Magnetic recording medium

Country Status (1)

Country Link
JP (1) JPS61284830A (en)

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