JPS62219327A - Solid additive for magnetic recording medium and magnetic recording medium using such additive - Google Patents
Solid additive for magnetic recording medium and magnetic recording medium using such additiveInfo
- Publication number
- JPS62219327A JPS62219327A JP61063168A JP6316886A JPS62219327A JP S62219327 A JPS62219327 A JP S62219327A JP 61063168 A JP61063168 A JP 61063168A JP 6316886 A JP6316886 A JP 6316886A JP S62219327 A JPS62219327 A JP S62219327A
- Authority
- JP
- Japan
- Prior art keywords
- magnetic
- powder
- magnetic recording
- additive
- recording 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.)
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- Paints Or Removers (AREA)
- Magnetic Record Carriers (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
〔産業上の利用分野〕
この発明は磁気記録媒体用固形添加剤およびこの固形添
加剤を用いた磁気記録媒体に関し、さらに詳しくは、分
散性に優れた磁気記録媒体用固形添加剤およびこの固形
添加剤を用いて得られる耐久性および表面平滑性に優れ
た磁気記録媒体に関する。[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to a solid additive for magnetic recording media and a magnetic recording medium using this solid additive, and more specifically, to a solid additive for magnetic recording media with excellent dispersibility. The present invention relates to a solid additive and a magnetic recording medium with excellent durability and surface smoothness obtained using the solid additive.
一般に、ポリエステルフィルムなどの基体上に磁性粉末
、結合剤成分、有機溶剤およびその他の必要成分からな
る磁性塗料を塗着してつくられる磁気記録媒体は、記録
再生時に磁気ヘッドなどと激しく摺接するため磁性層が
摩耗され易く、磁性層の摩耗が少なくて耐久性に優れた
ものが要求される。In general, magnetic recording media, which are made by coating a magnetic paint consisting of magnetic powder, a binder component, an organic solvent, and other necessary components on a substrate such as a polyester film, come into violent sliding contact with magnetic heads, etc. during recording and playback. The magnetic layer is easily abraded, and a magnetic layer with low abrasion and excellent durability is required.
このため、磁性層の耐摩耗性を改善する方策として、磁
性層中に比較的硬い非磁性粉末からなる固形添加剤を混
入することが行われており、たとえば、at−Fe20
3粉末、Al2O3粉末、Cr2O3粉末、TiN粉末
およびSiC粉末などの非磁性粉末を磁性層中に混入し
たものが提案されている。(特公昭58−45088号
、特開昭56−13525号)
〔発明が解決しようとする問題点〕
ところが、これらの非磁性粉末からなる固形添加削は磁
性層中の結合剤樹脂中における分散性が悪いため、磁性
層の耐摩耗性を充分に改善しようとして比較的多量磁性
層中に混入させると、磁性層の表面平滑性を充分良好に
できないという難点があり、特に、記録密度を向上させ
るため非常に微細な磁性粉末を使用し、磁性層の表面を
可及的に平滑にすることが望まれる場合は、分散性に劣
るこれらの固形′添加剤により磁性層の表面平滑性が低
下して電気的特性に悪影響を及ぼすという難点がある。Therefore, as a measure to improve the wear resistance of the magnetic layer, solid additives made of relatively hard non-magnetic powder are mixed into the magnetic layer. For example, at-Fe20
3 powder, Al2O3 powder, Cr2O3 powder, TiN powder, and SiC powder are mixed into the magnetic layer. (Japanese Patent Publication No. 58-45088, JP-A No. 56-13525) [Problems to be Solved by the Invention] However, these solid additive cuttings made of non-magnetic powder have poor dispersibility in the binder resin in the magnetic layer. Therefore, if a relatively large amount is mixed into the magnetic layer in an attempt to sufficiently improve the wear resistance of the magnetic layer, there is a problem that the surface smoothness of the magnetic layer cannot be sufficiently improved, and in particular, it is difficult to improve the recording density. Therefore, when using very fine magnetic powder and desiring to make the surface of the magnetic layer as smooth as possible, these solid additives with poor dispersibility may reduce the surface smoothness of the magnetic layer. However, the disadvantage is that it has a negative effect on the electrical characteristics.
この発明は、かかる現状に鑑み鋭意研究を重ねた結果な
されたもので、磁性層中に、配向性形状を有し、最大粒
子径が0.01〜2.0μmで、単位表面積への単分子
層水分子吸着量が2〜4分子/nm′の非磁性粉末から
なる固形添加剤を含有させることによって、固形添加剤
の結合剤樹脂中における分散性を充分に向上させ、特に
微細な磁性粉末が使用される磁性層の表面平滑性を良好
にして、電気的特性に悪影響を及ぼすことなく、磁性層
の耐摩耗性を充分に向上させたものである。This invention was made as a result of intensive research in view of the current situation, and the magnetic layer has an oriented shape, a maximum particle size of 0.01 to 2.0 μm, and a single molecule per unit surface area. By including a solid additive made of non-magnetic powder with an adsorption amount of layer water molecules of 2 to 4 molecules/nm', the dispersibility of the solid additive in the binder resin can be sufficiently improved, and particularly fine magnetic powder can be obtained. The surface smoothness of the magnetic layer used in the magnetic layer is improved, and the wear resistance of the magnetic layer is sufficiently improved without adversely affecting the electrical characteristics.
この発明において使用される固形添加剤は、配向性形状
を有し、最大粒子径が0.01〜2.0μmで、かつ単
位表面積への単分子層水分子吸着量が2〜4分子/ n
lの非磁性粉末であることが好ましく、このような微粒
子で単位表面積への単分子層水分子吸着量が2〜4分子
/ n mの非磁性粉末からなる固形添加剤を磁性層中
に含有させると、この固形添加剤粒子表面の、たとえば
、O)を基等の結合剤樹脂との結着力の担い手となる親
水性基と結合剤樹脂中の極性基とが、適度な量にコント
ロールされ、これらが適当な割合で互いに良好に結合す
る。従って、固形添加剤は結合剤樹脂中に良好に捕捉さ
れ、結合剤樹脂と良好に結着して分散性が充分に向上さ
れ、磁性層の表面平滑性が充分に向上される。また、こ
の微細な非磁性粉末によって、充分に良好な研磨作用が
発揮され、電気的特性に悪影響を及ぼすことなく、耐久
性が充分に向上される。The solid additive used in this invention has an oriented shape, a maximum particle size of 0.01 to 2.0 μm, and an adsorption amount of monolayer water molecules per unit surface area of 2 to 4 molecules/n.
The magnetic layer contains a solid additive made of non-magnetic powder, which is preferably a non-magnetic powder with a monolayer water molecule adsorption amount of 2 to 4 molecules/nm per unit surface area with such fine particles. As a result, the amount of hydrophilic groups on the surface of the solid additive particles, such as O)-based groups, which are responsible for the binding force with the binder resin, and the polar groups in the binder resin are controlled to an appropriate amount. , these bond well with each other in appropriate proportions. Therefore, the solid additives are well captured in the binder resin and bonded well to the binder resin, thereby sufficiently improving the dispersibility and the surface smoothness of the magnetic layer. Moreover, this fine non-magnetic powder exhibits a sufficiently good polishing action, and the durability is sufficiently improved without adversely affecting the electrical characteristics.
特に、このように磁性層中の結合剤樹脂中に分散されて
使用される固形添加剤は、微粒子化されるほどその粒子
表面への水分子吸着量が多(なり、結合剤樹脂との結着
にも重大な影響を与えるようになるため、微細な磁性粉
末とともに微細な固形添加剤を使用するときこの効果が
大きく、このような最大粒子径が0.O1〜2.0μm
の微細な固形添加剤の単位表面積への単分子層水分子吸
着量を、4分子/ n rdより多くすると、塗料化の
ために多量の溶剤を消費して、充分な混線条件が得られ
ず、分散性が低下して磁性層の表面平滑性を劣化し、電
磁変換特性に悪影響を及ぼす。また、固形添加剤の単位
表面積への単分子層水分子吸着量を2分子/ n、?よ
り少なくすると結合剤樹脂との相互作用が弱くなり、磁
性層の表面平滑性を劣化させる。In particular, the finer the solid additives used as dispersed in the binder resin in the magnetic layer, the more water molecules are adsorbed to the surface of the particles (and the more water molecules are bound to the binder resin). This effect is greater when fine solid additives are used together with fine magnetic powder, and the maximum particle size is 0.01 to 2.0 μm.
If the amount of water molecules adsorbed in a monomolecular layer per unit surface area of a fine solid additive exceeds 4 molecules/nrd, a large amount of solvent will be consumed to form a coating, and sufficient crosstalk conditions will not be obtained. , the dispersibility decreases, the surface smoothness of the magnetic layer deteriorates, and the electromagnetic conversion characteristics are adversely affected. Also, the amount of water molecules adsorbed in a monomolecular layer per unit surface area of the solid additive is 2 molecules/n, ? When the amount is less, the interaction with the binder resin becomes weaker and the surface smoothness of the magnetic layer deteriorates.
また、固形添加剤の最大粒子径は2.0μmより大きい
場合には、単位表面積への単分子層水分子吸着量が4分
子/ndより多くても、それほど混練への影響は顕著で
はなく、問題にはならないが、粒子径が大きすぎて磁性
層の表面平滑性を充分に良好にできず、0.01μmよ
り小さいと研磨効果が充分に発揮されず、磁性層の耐摩
耗性を充分に向上することができないため、0.01〜
2.0μmの範囲内のものを使用するのが好ましい。さ
らに、このように結合剤樹脂との結着性の強い固形添加
剤を用いても、球状、サイコロ状のような無配向性のも
のでは、磁性層中での充填性が劣り、磁性層の表面量滑
性にも悪影響を及ぼすため、板状、針状等の配向性の形
状を有することが好ましい。In addition, when the maximum particle size of the solid additive is larger than 2.0 μm, even if the amount of monolayer water molecules adsorbed to the unit surface area is more than 4 molecules/nd, the effect on kneading is not so significant. Although this is not a problem, if the particle size is too large, the surface smoothness of the magnetic layer cannot be sufficiently improved, and if the particle size is smaller than 0.01 μm, the polishing effect cannot be sufficiently exhibited, and the wear resistance of the magnetic layer cannot be sufficiently improved. Since it cannot be improved, 0.01~
It is preferable to use one within the range of 2.0 μm. Furthermore, even if solid additives with strong binding properties with the binder resin are used, non-oriented additives such as spherical or dice-shaped additives have poor filling properties in the magnetic layer. Since the surface amount also has a negative effect on lubricity, it is preferable to have an oriented shape such as a plate shape or a needle shape.
このように、微粒子で単位表面積への単分子層水分子吸
着量が2〜4分子/ n’fの固形添加剤は、固形添加
剤が微細なほど粒子表面に水吸着量が多いことから、通
常、固形添加剤の粒子表面の一部を疎水性化することに
よって、表面水吸着量を減らし、最適化して得られる。In this way, solid additives that are fine particles and have a monomolecular layer water molecule adsorption amount of 2 to 4 molecules/n'f per unit surface area, because the finer the solid additive is, the greater the amount of water adsorption on the particle surface. Usually, by making part of the particle surface of the solid additive hydrophobic, the amount of surface water adsorption is reduced and optimized.
このような固形添加剤の粒子表面の疎水性化の方法とし
ては、■有機カップリング剤で表面処理する方法、ある
いは■たとえば高温で処理されたシリカ被膜などの無機
物疎水性被膜による表面処理などがあり、基本的にはど
のような方法をとってもよいが、一般的には固形添加剤
の粒子表面から容易に離脱することのない表面処理剤お
よび表面処理方法を採用することが好ましい。Methods for making the particle surface of such solid additives hydrophobic include (1) surface treatment with an organic coupling agent, and (2) surface treatment with an inorganic hydrophobic coating such as a silica coating treated at high temperature. Basically, any method may be used, but it is generally preferable to use a surface treatment agent and a surface treatment method that do not easily separate from the particle surface of the solid additive.
このようにして、最大粒子径が0.01〜2.0μmで
、単位表面積への単分子層水分子吸着量を2〜4分子/
n mの範囲内にする固形添加剤としては、たとえば
、Al2O3粉末、Cr2O3粉末、T i 02粉末
、5i02粉末、ct−Fe203粉末等の酸化物粉末
、SiC粉末等の炭化物粉末、TiN粉末等の窒化物粉
末などが好適なものとして使用される。このような、最
大粒子径が0.01〜2.0μmで、単位表面積への単
分子層水分子吸着量が2〜4分子/nMの固形添加剤の
使用量は、磁性粉末に対して0.5重量%より少ないと
耐摩耗性が充分に改善されず、20重量%より多くする
と磁性層の表面平滑性の劣化を招(おそれがあるため、
0.5〜20重量%の範囲内で磁性層中に含有させて使
用するのが好ましく、1〜10重量%の範囲内で磁性層
中に含有させるのがより好ましい。In this way, the maximum particle size is 0.01 to 2.0 μm, and the amount of monolayer water molecules adsorbed to a unit surface area is 2 to 4 molecules per unit surface area.
Examples of solid additives that are within the nm range include oxide powders such as Al2O3 powder, Cr2O3 powder, Ti02 powder, 5i02 powder, and ct-Fe203 powder, carbide powders such as SiC powder, and TiN powder. Nitride powders and the like are preferably used. The amount of solid additives with a maximum particle diameter of 0.01 to 2.0 μm and a monomolecular layer water molecule adsorption amount of 2 to 4 molecules/nM per unit surface area is 0. If it is less than .5% by weight, the abrasion resistance will not be sufficiently improved, and if it is more than 20% by weight, it may lead to deterioration of the surface smoothness of the magnetic layer.
It is preferably contained in the magnetic layer in an amount of 0.5 to 20% by weight, more preferably 1 to 10% by weight.
この発明の磁気記録媒体を製造するには常法に準じて行
えばよく、たとえば、配向性形状を有し、最大粒子径が
0.01〜2.0μmで、単位表面積への単分子層水分
子吸着量が2〜4分子/ n mの非磁性粉末からなる
固形添加剤を、磁性粉末、結合剤樹脂、有機溶剤等とと
もに混合分散して磁性塗料を調製し、これをポリエステ
ルフィルムなどの基体上にロールコータ−など任意の塗
布手段によって塗布し、乾燥すればよい。The magnetic recording medium of the present invention may be manufactured according to a conventional method. A magnetic paint is prepared by mixing and dispersing a solid additive made of non-magnetic powder with a molecular adsorption amount of 2 to 4 molecules/nm together with magnetic powder, binder resin, organic solvent, etc., and this is applied to a substrate such as a polyester film. What is necessary is just to apply|coat on top by arbitrary coating means, such as a roll coater, and to dry.
ここで、磁性粉末としては、たとえば、r−Fe203
粉末、Fe3O4粉末、Co含有r−Fe203粉末、
CO含有Fe3O4粉末、CrO2粉末の他、Fe粉末
、Co粉末、Fe−Ni粉末、バリウムフェライト粉末
など従来公知の各種磁性粉末が広く使用される。Here, as the magnetic powder, for example, r-Fe203
powder, Fe3O4 powder, Co-containing r-Fe203 powder,
In addition to CO-containing Fe3O4 powder and CrO2 powder, various conventionally known magnetic powders such as Fe powder, Co powder, Fe-Ni powder, and barium ferrite powder are widely used.
また、結合剤成分としては塩化ビニル−酢酸ビニル系共
重合体、繊維素系樹脂、ポリウレタン系樹脂、ポリエス
テル系樹脂、エポキシ系樹脂、ポリアミド系樹脂、アク
リル系樹脂、イソシアネート化合物、放射線硬化型樹脂
など、通常磁性粉末の結合剤成分として使用されるもの
が広く使用される。In addition, binder components include vinyl chloride-vinyl acetate copolymers, cellulose resins, polyurethane resins, polyester resins, epoxy resins, polyamide resins, acrylic resins, isocyanate compounds, radiation-curable resins, etc. , which are commonly used as binder components in magnetic powders, are widely used.
さらに、有機溶剤としては、メチルイソブチルケトン、
メチルエチルケトン、シクロヘキサノン等のケトン系溶
剤、酢酸エチル等のエステル系溶剤、イソプロピルアル
コール等のアルコール系溶剤、トルエン等の芳香族炭化
水素系溶剤など、一般に使用される有機溶剤がそれぞれ
単独で、あるいは二種以上混合して使用され、基体とし
ては、ポリエステル、ポリアミドセルロース誘導体など
の合成樹脂、非磁性金属、紙等のフィルム、やシートな
ど、通常、一般に使用されるものが、いずれも使用され
る。Furthermore, as organic solvents, methyl isobutyl ketone,
Commonly used organic solvents such as ketone solvents such as methyl ethyl ketone and cyclohexanone, ester solvents such as ethyl acetate, alcohol solvents such as isopropyl alcohol, and aromatic hydrocarbon solvents such as toluene may be used alone or in combination. The above-mentioned mixtures are used, and as the substrate, any commonly used substrate can be used, such as synthetic resins such as polyester and polyamide cellulose derivatives, non-magnetic metals, films such as paper, and sheets.
なお、磁性塗料中には通常使用されている各種添加剤、
たとえば、カーボンブラックなどの帯電防止剤や、潤滑
剤、分散剤などを任意に添加使用してもよい。In addition, various additives commonly used in magnetic paints,
For example, an antistatic agent such as carbon black, a lubricant, a dispersant, etc. may be optionally added.
次に、この発明の実施例について説明する。 Next, embodiments of the invention will be described.
実施例1〜4
第1表に示す磁性粉末および非磁性粉末を使用し、
磁性粉末 100重量部VACH
(U、C,C社製、塩化ビ 10〃ニル−酢酸ビニル−
ビニルア
ルコール共重合体)
パンデックスT−5201(大 6 〃日本インキ化
学工業社製、ポ
リウレタン樹脂、分子量2〜
3万)
ミリスチン酸 5 〃H3−5
00(旭電化社製、力 1 〃−ボンブラソク)
非磁性粉末 1〜シクロへキサノ
ン 85〃トルエン
85〃の組成物を31容量のスチール製ボールミル
中に入れ、これを72時間回転させ、よく分散させて磁
性ペーストを作製した。その後、この磁性ペーストにト
ルエン40重量部とコロネートしく武田薬品工業社製、
三官能性低分子量イソシアネート化合物)2重量部をさ
らに加え、磁性塗料を開裂した。この磁性塗料を厚さ1
2μmのポリエステルベースフィルム上に乾燥後の塗布
厚が4μmとなるように塗布し、乾燥して磁性層を形成
した。Examples 1 to 4 Using magnetic powder and non-magnetic powder shown in Table 1, magnetic powder 100 parts by weight VACH
(Manufactured by U, C, C, vinyl chloride 10-vinyl acetate-
(vinyl alcohol copolymer) Pandex T-5201 (large 6 〃manufactured by Nippon Ink Chemical Industry Co., Ltd., polyurethane resin, molecular weight 20,000 to 30,000) myristic acid 5 〃H3-5
00 (manufactured by Asahi Denka Co., Ltd., force 1〃-Bonburasoku) Non-magnetic powder 1~Cyclohexanone 85〃Toluene
The composition No. 85 was placed in a 31-capacity steel ball mill and rotated for 72 hours to ensure good dispersion to prepare a magnetic paste. Thereafter, this magnetic paste was coronated with 40 parts by weight of toluene, and
2 parts by weight of a trifunctional low molecular weight isocyanate compound (trifunctional low molecular weight isocyanate compound) was further added to cleave the magnetic paint. Apply this magnetic paint to a thickness of 1
It was coated on a 2 μm polyester base film to a coating thickness of 4 μm after drying, and dried to form a magnetic layer.
次いで、鏡面加工処理した後、1/2インチ幅に裁断し
て磁気テープをつくった。Next, the tape was mirror-finished and cut into 1/2-inch widths to produce magnetic tapes.
比較例1〜8
実施例1〜4における磁性塗料の組成において、第1表
に示す磁性粉末および非磁性粉末に代えて、第2表に示
す磁性粉末および非磁性粉末を同量使用した以外は実施
例1〜4と同様にして磁気テープをつくった。Comparative Examples 1 to 8 In the composition of the magnetic paint in Examples 1 to 4, the same amounts of magnetic powder and nonmagnetic powder shown in Table 2 were used instead of the magnetic powder and nonmagnetic powder shown in Table 1. Magnetic tapes were made in the same manner as in Examples 1-4.
各実施例および比軟例で得られた磁気テープについて、
耐久性および表面平滑性を調べた。耐久性は、市販VT
Rを使用し、−5°Cの恒温室中で静止画像再生を行っ
た時の出力が3dB低下するまでの時間を測定して判定
した。また表面平滑性は、触針式粗さ計を使用し、触針
速度0.06cm / sec、カットオフ0.08m
mの条件で磁性層の表面粗さくC,L、A )を測定し
、実施例1の磁気テープを基準′として下記の式に従っ
て算出される相対値で判断した。Regarding the magnetic tape obtained in each example and comparative example,
Durability and surface smoothness were examined. Durability is commercially available VT
The determination was made by measuring the time until the output decreases by 3 dB when still images are reproduced in a constant temperature room at −5° C. using R. In addition, the surface smoothness was measured using a stylus roughness meter with a stylus speed of 0.06 cm/sec and a cutoff of 0.08 m.
The surface roughness (C, L, A) of the magnetic layer was measured under the conditions of m, and the relative values calculated according to the following formula using the magnetic tape of Example 1 as a reference were determined.
下記第3表はその結果である。Table 3 below shows the results.
第3表
〔発明の効果〕
上記第3表から明らかなように、実施例1〜4で得られ
た磁気テープは、いずれも比較例1ないし8で得られた
磁気テープに比し、耐久性および表面平滑性がよく、こ
のことからこの発明の固形添加剤は結合剤樹脂中での分
散性がよく、その結果、この固形添加剤を使用して得ら
れる磁気記録媒体は、磁性層の表面平滑性が良好で、電
気的特性および耐久性が向上されていることがわかる。Table 3 [Effects of the Invention] As is clear from Table 3 above, the magnetic tapes obtained in Examples 1 to 4 have higher durability than the magnetic tapes obtained in Comparative Examples 1 to 8. As a result, the solid additive of the present invention has good dispersibility in the binder resin, and as a result, the magnetic recording medium obtained using this solid additive has a surface smoothness of the magnetic layer. It can be seen that the smoothness is good and the electrical properties and durability are improved.
Claims (1)
μmで、単位表面積への単分子層水分子吸着量が2〜4
分子/nm^2の非磁性粉末からなる磁気記録媒体用固
形添加剤 2、磁性層中に、配向性形状を有し、最大粒子径が0.
01〜2.0μmで、単位表面積への単分子層水分子吸
着量が2〜4分子/nm^2の非磁性粉末からなる磁気
記録媒体用固形添加剤を含ませたことを特徴とする磁気
記録媒体[Claims] 1. Has an oriented shape and has a maximum particle size of 0.01 to 2.0
In μm, the amount of water molecules adsorbed in a monomolecular layer per unit surface area is 2 to 4.
Solid additive 2 for magnetic recording media made of non-magnetic powder of molecule/nm^2, which has an oriented shape in the magnetic layer and has a maximum particle size of 0.
A magnetic material characterized by containing a solid additive for magnetic recording media consisting of a non-magnetic powder having a diameter of 01 to 2.0 μm and an adsorption amount of monolayer water molecules per unit surface area of 2 to 4 molecules/nm^2. recoding media
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61063168A JPS62219327A (en) | 1986-03-20 | 1986-03-20 | Solid additive for magnetic recording medium and magnetic recording medium using such additive |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61063168A JPS62219327A (en) | 1986-03-20 | 1986-03-20 | Solid additive for magnetic recording medium and magnetic recording medium using such additive |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS62219327A true JPS62219327A (en) | 1987-09-26 |
Family
ID=13221449
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP61063168A Pending JPS62219327A (en) | 1986-03-20 | 1986-03-20 | Solid additive for magnetic recording medium and magnetic recording medium using such additive |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS62219327A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6488917A (en) * | 1987-09-29 | 1989-04-03 | Matsushita Electric Industrial Co Ltd | Magnetic recording medium |
| JPH01102730A (en) * | 1987-10-15 | 1989-04-20 | Matsushita Electric Ind Co Ltd | Magnetic recording medium |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60129971A (en) * | 1983-12-16 | 1985-07-11 | Toshiba Corp | Reproduction waveform equalization method |
| JPS60129927A (en) * | 1983-12-19 | 1985-07-11 | Tdk Corp | Magnetic recording medium |
-
1986
- 1986-03-20 JP JP61063168A patent/JPS62219327A/en active Pending
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60129971A (en) * | 1983-12-16 | 1985-07-11 | Toshiba Corp | Reproduction waveform equalization method |
| JPS60129927A (en) * | 1983-12-19 | 1985-07-11 | Tdk Corp | Magnetic recording medium |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6488917A (en) * | 1987-09-29 | 1989-04-03 | Matsushita Electric Industrial Co Ltd | Magnetic recording medium |
| JPH01102730A (en) * | 1987-10-15 | 1989-04-20 | Matsushita Electric Ind Co Ltd | Magnetic recording medium |
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