JPH05258281A - Magnetic recording medium and magnetic recorder - Google Patents

Magnetic recording medium and magnetic recorder

Info

Publication number
JPH05258281A
JPH05258281A JP5476092A JP5476092A JPH05258281A JP H05258281 A JPH05258281 A JP H05258281A JP 5476092 A JP5476092 A JP 5476092A JP 5476092 A JP5476092 A JP 5476092A JP H05258281 A JPH05258281 A JP H05258281A
Authority
JP
Japan
Prior art keywords
magnetic
powder
recording medium
magnetic recording
coating
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
JP5476092A
Other languages
Japanese (ja)
Inventor
Katsuyoshi Chiba
克義 千葉
Yasutaro Kamisaka
保太郎 上坂
Masayuki Katsumoto
正之 勝本
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.)
Hitachi Ltd
Original Assignee
Hitachi 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 Hitachi Ltd filed Critical Hitachi Ltd
Priority to JP5476092A priority Critical patent/JPH05258281A/en
Publication of JPH05258281A publication Critical patent/JPH05258281A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To prevent the reflocculation of magnetic powder in a magnetic coating material, to enhance the squareness ratio (Br/Bm) of a magnetic recording medium and to further enhance electromagnetic characteristics such as S-N ratio. CONSTITUTION:When a magnetic coating material is produced, 36g powder of polyvinyl butyral resin, 130g powder of epoxy resin and 500g acicular metal powder are charged into a kneader and kneaded for about 15min, 200g cellosolve acetate is slowly added to the kneaded material and 1.5g organically synthesized functional polymer having polyoxyalkylene glycol and acid anhydride structures in the skeleton and 472g cellosolve acetate are further added. They are kneaded for about 4hr in the kneader.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、記憶装置等に用いる塗
布型の磁気ディスク等の磁気記録媒体及び大容量の磁気
記録装置に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a magnetic recording medium such as a coating type magnetic disk used for a storage device and the like and a large capacity magnetic recording device.

【0002】[0002]

【従来の技術】従来の塗布型磁気ディスクの製造は、磁
性粉をバインダ(高分子結合剤)又はその溶液中にサン
ドミル,ニーダ,ボールミル等を用いて分散させて磁気
塗料とし、これを基板上に塗布し、必要に応じて配向さ
せ、熱硬化し、研摩する等により行なっている。さらに
必要なら製造した塗膜に潤滑剤を塗布している。バイン
ダは通常熱硬化性樹脂が使用されるので熱硬化するが、
単に加熱のみで用いる場合もある。また、通常磁気塗料
は磁性粉の再凝集を防ぐために保存中は撹拌される。
2. Description of the Related Art A conventional coating type magnetic disk is manufactured by dispersing magnetic powder in a binder (polymer binder) or a solution thereof using a sand mill, a kneader, a ball mill or the like to prepare a magnetic paint, which is applied on a substrate. It is applied by applying it to, and if necessary, orienting it, thermosetting it, and polishing it. If necessary, a lubricant is applied to the produced coating film. The binder is usually a thermosetting resin, so it is thermoset,
It may be used only by heating. Further, the magnetic paint is usually agitated during storage to prevent reaggregation of the magnetic powder.

【0003】近年、磁気記録装置の大容量化、高密度化
が進むにつれて、より微粒子の磁性粉が用いられるよう
になった。このような磁性粉を用いた磁気塗料は再凝集
し易く、撹拌だけでは再凝集を完全に防ぐことは困難で
ある。このような問題を解決するために、特開平2−239
424 号公報に記載の技術は、金属磁性粉末の平均長軸長
が0.35μm 以下、針状比6〜9であるものを使用し
ている。また、エポキシ−フェノール系に於てはスチレ
ンアリルアルコール樹脂,ブロック化酸触媒及び各種の
添加剤から製造する磁気記録媒体が特公平2−56728号公
報に記載されている。
In recent years, as the capacity and density of magnetic recording devices have increased, finer magnetic powder has come to be used. A magnetic coating material using such magnetic powder easily re-aggregates, and it is difficult to completely prevent re-aggregation only by stirring. In order to solve such a problem, JP-A-2-239
The technique described in Japanese Patent No. 424 uses a magnetic metal powder having an average major axis length of 0.35 μm or less and an acicular ratio of 6 to 9. Further, in the epoxy-phenol system, a magnetic recording medium produced from a styrene allyl alcohol resin, a blocked acid catalyst and various additives is described in JP-B-2-56728.

【0004】[0004]

【発明が解決しようとする課題】特開平2−239424 号公
報に記載の従来技術は、面内配向の磁気記録媒体として
の高密度化した磁気ディスクの製造については十分考慮
されておらず、優れた電磁気特性を持つ、例えば、S/
N比や角形比が良好な、高密度化した磁気記録媒体及び
装置を提供することが困難であるという問題があった。
すなわち上記従来技術は、2μm程度以上と厚い塗膜を
有する磁気テープの製造に関するものである。
The prior art disclosed in Japanese Patent Application Laid-Open No. 2-239424 is not sufficiently considered in the production of a high density magnetic disk as an in-plane oriented magnetic recording medium, and is excellent. With electromagnetic characteristics such as S /
There is a problem that it is difficult to provide a high density magnetic recording medium and device having a good N ratio and squareness ratio.
That is, the above-mentioned prior art relates to the production of a magnetic tape having a thick coating film of about 2 μm or more.

【0005】このような塗膜を製造するための磁気塗料
は、例えば、1000cp程度の高粘度である。それ
故、金属磁性粉をより高分散化した塗料は短時間では再
凝集しないので、分散した直後に磁場配向すれば容易に
配向することができる。それに対して高密度化した磁気
ディスクの塗膜は1μm以下と薄い。それ故、このよう
な塗膜を製造するための磁気塗料は低粘度のものを用い
る必要がある。低粘度(50〜500cp)の塗料は再
凝集し易いので、各種の処理してから磁場配向を行なう
までに時間があると、たとえ短時間でもその分だけ磁性
粉の再凝集が生じる。そのため、製造した磁気ディスク
は、種々の電磁気特性、例えば、角形比(B−H特性)
等が劣化するという問題があった。
The magnetic paint for producing such a coating film has a high viscosity of, for example, about 1000 cp. Therefore, since the coating material in which the magnetic metal powder is highly dispersed does not re-aggregate in a short time, it can be easily oriented by magnetic field orientation immediately after dispersing. On the other hand, the coating film of a magnetic disk having a high density is as thin as 1 μm or less. Therefore, it is necessary to use a magnetic paint having a low viscosity for producing such a coating film. Since a low-viscosity (50 to 500 cp) coating material is likely to re-aggregate, if there is time between various treatments and magnetic field orientation, re-aggregation of the magnetic powder will occur correspondingly even for a short time. Therefore, the manufactured magnetic disk has various electromagnetic characteristics, for example, a squareness ratio (B-H characteristic).
However, there was a problem of deterioration of the quality.

【0006】また、特公平2−56728号公報に記載された
スチレンアリルアルコール樹脂,有機金属触媒オクタン
酸第1スズ,ブロック化酸触媒イソプロパノール・ブロ
ックP−トルエンスルホン酸等のものは磁気塗料製造後
の安定性が困難である。すなわち、樹脂の性質や触媒と
しての反応性のため、電磁気特性として、S/N比が劣
化し、さらに欠陥が発生したり、出力がおちる等の問題
があった。
The styrene allyl alcohol resin, the organometallic catalyst stannous octoate, the blocked acid catalyst isopropanol / block P-toluenesulfonic acid, etc. described in Japanese Patent Publication No. 2-56728 are used after the magnetic coating is manufactured. The stability of is difficult. That is, due to the properties of the resin and the reactivity as a catalyst, there are problems in that the S / N ratio deteriorates as electromagnetic characteristics, further defects occur, and the output falls.

【0007】本発明の目的は、少なくとも磁性粉を分散
させた磁気塗料を用い、磁性粉の再凝集を防止し高配向
せしめた、電磁気特性に優れた高密度な面内配向磁気デ
ィスク並びに媒体を用いた大容量磁気ディスク装置を提
供することにある。
An object of the present invention is to provide a high-density in-plane oriented magnetic disk and medium excellent in electromagnetic characteristics, in which at least a magnetic coating material in which magnetic powder is dispersed is used to prevent re-aggregation of the magnetic powder and highly oriented. It is to provide a large-capacity magnetic disk device used.

【0008】[0008]

【課題を解決するための手段】上記目的は、高分子結合
剤中に少なくとも有機合成可能な骨格内にポリオキシア
ルキレングリコール構造と酸無水物構造を持つ機能性高
分子で分散させた磁気塗料を非磁性基板上に塗布して得
られた磁気記録膜の未乾燥の状態を維持しつつ、磁性粉
を配向させ磁気記録膜を製造することによって達せられ
る。
The above-mentioned object is to provide a magnetic coating material in which a functional polymer having a polyoxyalkylene glycol structure and an acid anhydride structure is dispersed in a polymer binder in at least an organically synthesizable skeleton. This can be achieved by manufacturing the magnetic recording film by orienting the magnetic powder while maintaining the undried state of the magnetic recording film obtained by coating on the non-magnetic substrate.

【0009】本発明において、得られた磁性塗料の機能
性高分子に磁場を印加し、磁気ディスクを回転させるこ
とにより、磁性粉の分散配向をより高めることができ
る。さらに、微粉で高配向が得られるため磁気ディスク
としての電磁気特性を向上させるものである。
In the present invention, by applying a magnetic field to the functional polymer of the obtained magnetic paint and rotating the magnetic disk, the dispersion orientation of the magnetic powder can be further enhanced. Furthermore, since fine powder can obtain high orientation, the electromagnetic characteristics of the magnetic disk are improved.

【0010】磁気ディスクは膜厚1μm以下、より好ま
しくは、円板の内周部で約0.55±0.05μm 、又
は、それ以下の膜厚に、外周部で約0.65±0.05μ
m又はそれ以下の膜厚に少なくとも高分子材料と磁性粉
から成る塗膜を形成して後、塗膜を熱硬化し、内周部で
約0.35μm以下、外周部で0.45μm以下になるよ
うに研削して得る。このようにして、例えば、記録密度
30,000BPI 以上の磁気ディスクが得られる。
The magnetic disk has a film thickness of 1 μm or less, more preferably about 0.55 ± 0.05 μm or less on the inner peripheral portion of the disk, and about 0.65 ± 0. 05μ
After forming a coating film consisting of at least a polymer material and magnetic powder to a film thickness of m or less, the coating film is heat-cured to about 0.35 μm or less at the inner peripheral portion and 0.45 μm or less at the outer peripheral portion. Grind to obtain. Thus, for example, a magnetic disk having a recording density of 30,000 BPI or more can be obtained.

【0011】[0011]

【作用】磁性塗料にポリオキシアルキレングリコール等
の機能性高分子を含有することにより、磁性粉の結合が
弱められ塗膜中の磁性粉は分散、配向される。磁性粉の
分散、配向の方法は、例えば、直径5.25 インチ,厚
さ2mmのアルミニウム円板を用い、磁石の磁極をN(又
はS)極とN(又はS)極、間隙5mm、同極を合せた通
常の反発磁界を印加(約3500 Oe)することによっ
て達成される。また、再分散・配向時のディスク回転数
は20〜60RPMの範囲がより効果があった。塗膜の
膜厚が1μm以下のときに配高度が高く、角形比が0.
85 以上となった。
By including a functional polymer such as polyoxyalkylene glycol in the magnetic paint, the binding of the magnetic powder is weakened and the magnetic powder in the coating film is dispersed and oriented. The method of dispersing and orienting the magnetic powder is, for example, using an aluminum disc having a diameter of 5.25 inches and a thickness of 2 mm, and the magnetic poles of the magnet are N (or S) poles and N (or S) poles, a gap of 5 mm, and the same. It is achieved by applying a normal repulsive magnetic field with the poles aligned (about 3500 Oe). Further, the disk rotation speed during re-dispersion / orientation was more effective in the range of 20 to 60 RPM. When the thickness of the coating film is 1 μm or less, the gradient is high and the squareness ratio is 0.
It was over 85.

【0012】また、磁性粉が微粉末のとき、例えば、平
均粒径が0.4μm 以下、より好ましくは0.2μm 以
下のような微粉末のとき、磁性粉が塗膜中で移動,回転
する抵抗が小さいため、より有効性が得られた。なお、
機能性高分子材はポリオキシアルキレングリコール構造
と無無水物構造を有する高分子材などが分散性を高める
上で有効である。本媒体により大容量の装置と提供でき
る。
When the magnetic powder is a fine powder, for example, the average particle size is 0.4 μm or less, more preferably 0.2 μm or less, the magnetic powder moves and rotates in the coating film. Due to the low resistance, more effectiveness was obtained. In addition,
As the functional polymer material, a polymer material having a polyoxyalkylene glycol structure and an anhydrous structure is effective for enhancing dispersibility. This medium can provide a large-capacity device.

【0013】[0013]

【実施例】【Example】

〈実施例1〉ポリビニルブチラール樹脂の粉末36g,
エポキシ樹脂の粉末130gと針状メタル粉(平均粒
径:0.17×0.02μm,抗磁力Hc:1300 O
e,残留磁束密度δs:120emu/g,比表面積B
ET:54m2/g)500gをニーダ混練機に投入し、
約15分間混練を行なう。次に酢酸セロソルブ200g
を徐々に添加し、さらに、有機合成した骨格内にポリオ
キシアルキレングリコール構造と酸無水物構造を持つ機
能性高分子1.5g と酢酸セロソルブ472gを加えて
ニーダ混練を約4時間行なう。
<Example 1> Polyvinyl butyral resin powder 36 g,
130 g of epoxy resin powder and acicular metal powder (average particle size: 0.17 x 0.02 μm, coercive force Hc: 1300 O
e, residual magnetic flux density δs: 120 emu / g, specific surface area B
ET: 54 m 2 / g) 500 g was put into a kneader kneader,
Knead for about 15 minutes. Next, 200 g of cellosolve acetate
Is gradually added, and 1.5 g of a functional polymer having a polyoxyalkylene glycol structure and an acid anhydride structure in the organically synthesized skeleton and 472 g of cellosolve acetate are added, and kneading is performed for about 4 hours.

【0014】この混練物887gをとり、アルミナ3
g,酢酸セロソルブ700gを共に、31のボールミル
ポットに入れ、7日間ボールミル混練を行ない磁性粉,
アルミナを良好に分散させる。つぎにフェノール樹脂8
6g,ブチルセロソルブ500gを添加混合し、磁気塗
料を調合する。次にこの塗料を、予め表面を清浄にした
ディスク径1″,1.5″,2.5″,3.5″,5.2
5″,8.8″,10.5″のアルミニウム円板にそれぞ
れ回転塗布し、直ちに通常の磁気ディスク配向装置で面
内磁場配向し、窒素中210℃で硬化した。得られた磁
気記録膜(7mm角に切断して測定)のB−H曲線(角形
比:Br/Bm)との関係は図1の曲線aに示す通りで
ある。なお、従来法(機能性高分子のないもの)は図の
曲線bであり、磁場配向のないもの(未配向)は図の曲
線Cで示すとおりである。
887 g of this kneaded material was taken and alumina 3
g and cellosolve 700g together in a 31 ball mill pot and kneaded with a ball mill for 7 days to obtain a magnetic powder,
Disperses the alumina well. Next is phenol resin 8
6 g and butyl cellosolve 500 g are added and mixed to prepare a magnetic paint. Next, this paint was applied to a disk whose surface had been cleaned in advance, and had disk diameters of 1 ", 1.5", 2.5 ", 3.5", 5.2.
5 ″, 8.8 ″, and 10.5 ″ aluminum discs were spin-coated, immediately subjected to in-plane magnetic field orientation with a conventional magnetic disk orientation apparatus, and cured at 210 ° C. in nitrogen. The relation with the BH curve (square ratio: Br / Bm) of (cut to 7 mm square) is as shown by the curve a in Fig. 1. Conventional method (without functional polymer) Is the curve b in the figure, and the one without magnetic field orientation (unoriented) is as shown by the curve C in the figure.

【0015】ここでの角形比(Br/Bm)は0.85
(a:本発明),0.55(b:従来)、0.52(c:
未配向)である。また、抗磁力は1410 Oe(a:本
発明)、1310 Oe(b:従来),1260 Oe
(c:未配向)であった。いずれも本発明のものは特性
の向上が大であった。
The squareness ratio (Br / Bm) here is 0.85.
(A: present invention), 0.55 (b: conventional), 0.52 (c:
(Unoriented). Moreover, the coercive force is 1410 Oe (a: the present invention), 1310 Oe (b: conventional), 1260 Oe.
(C: unoriented). In all cases, the products of the present invention showed a great improvement in characteristics.

【0016】こうして得られた磁気記録膜の内周部の膜
厚を0.27μm とした磁気ディスクの記録再生特性を
ギャップ長0.3μm のメタルインギャップ型ヘッドに
より測定したところ、従来の磁気ディスクのそれに対
し、S/N比が32%向上した。
The recording / reproducing characteristics of the magnetic disk having the inner peripheral portion of the magnetic recording film thus obtained of 0.27 μm were measured by a metal-in-gap type head having a gap length of 0.3 μm. However, the S / N ratio was improved by 32%.

【0017】〈実施例2〉ポリビニルブチラールの粉末
70gと針状γ−Fe23磁性粉(平均粒径:0.35
×0.06μm,抗磁力Hc:330 Oe、比表面積B
ET:22m2/g)700gをニーダ混練機に投入
し、約15分間混練を行なう。次に酢酸セロソルブ25
0gを徐々に添加し、ニーダ混練を約4時間行なう。こ
の混練物480gをとり、アルミナ3g、有機合成した骨
格内にポリオキシアルキレングリコール構造と酸無水物
構造を持つ機能性高分子1.5g ,酢酸セロソルブ70
0gを共に、31のボールミルポットに入れ、7日間ボ
ールミル混練を行ない磁性粉,アルミナを良好に分散さ
せる。つぎにフェノール樹脂120g,40%のエポキ
シ樹脂のブチルセロソルブ溶液300g,ブチルセロソ
ルブ500gを添加混合し、磁気塗料を調合する。次に
この塗料を、予め表面を清浄にしたディスク径5.2
5″ のアルミニウム円板に回転塗布し、通常の磁気デ
ィスク配向装置で面内磁場配向し、210℃で硬化し
た。得られた磁気記録膜の角形比(Br/Bm)との関係
は表1の(2)に示す通りである。
Example 2 70 g of polyvinyl butyral powder and acicular γ-Fe 2 O 3 magnetic powder (average particle size: 0.35)
× 0.06 μm, coercive force Hc: 330 Oe, specific surface area B
ET: 22 m 2 / g) 700 g is put into a kneader kneader and kneading is performed for about 15 minutes. Next, cellosolve acetate 25
0 g is gradually added and kneading is performed for about 4 hours. Taking 480 g of this kneaded material, 3 g of alumina, 1.5 g of a functional polymer having a polyoxyalkylene glycol structure and an acid anhydride structure in the organically synthesized skeleton, and 70 cellosolve acetate.
Both 0 g are put in a ball mill pot 31 and kneaded by a ball mill for 7 days to satisfactorily disperse the magnetic powder and alumina. Next, 120 g of phenolic resin, 300 g of butyl cellosolve solution of 40% epoxy resin, and 500 g of butyl cellosolve are added and mixed to prepare a magnetic paint. Next, apply this paint to a disk whose surface has been cleaned in advance.
It was spin-coated on a 5 ″ aluminum disk, subjected to in-plane magnetic field orientation with a normal magnetic disk orientation apparatus, and cured at 210 ° C. The relation to the squareness ratio (Br / Bm) of the obtained magnetic recording film is shown in Table 1. It is as shown in (2) of.

【0018】[0018]

【表1】 [Table 1]

【0019】こうして得られた磁気記録膜の内周部の膜
厚を0.32μm とした磁気ディスクの記録再生特性を
ギャップ長0.5μm のMnZnフェライトヘッドによ
り測定したところ、従来の磁気ディスクのそれに対し、
S/N比が7%向上した。
The recording / reproducing characteristics of the magnetic disk having an inner peripheral portion of the magnetic recording film thus obtained of 0.32 μm were measured by an MnZn ferrite head having a gap length of 0.5 μm. On the other hand,
The S / N ratio was improved by 7%.

【0020】〈実施例3〉針状Co−γ−Fe23磁性
粉(平均粒径:0.40×0.07μm,抗磁力Hc:6
50 Oe,比表面積BET:22.5m2/g)を用いた
外は実施例2と同様の処理を行なった。その結果は表1
の(3)に示す通りである。またS/N比は従来のそれ
に対して9%向上した。
Example 3 Needle-like Co-γ-Fe 2 O 3 magnetic powder (average particle size: 0.40 × 0.07 μm, coercive force Hc: 6)
The same treatment as in Example 2 was performed except that 50 Oe and specific surface area BET: 22.5 m 2 / g) were used. The results are shown in Table 1.
It is as shown in (3) of. Moreover, the S / N ratio was improved by 9% as compared with the conventional one.

【0021】〈実施例4〉針状微粉Co−γ−Fe23
磁性粉(平均粒径:0.2×0.02μm,抗磁力Hc:
770 Oe,比表面積BET:50m2/g)を用いた
外は実施例2と同様の処理を行なった。その結果は表1
の(4)に示す通りである。またS/N比は従来のそれ
に対して12%向上した。
<Example 4> Needle-like fine powder Co-γ-Fe 2 O 3
Magnetic powder (average particle size: 0.2 × 0.02 μm, coercive force Hc:
770 Oe, specific surface area BET: 50 m 2 / g) was used, and the same treatment as in Example 2 was performed. The results are shown in Table 1.
It is as shown in (4). Further, the S / N ratio was improved by 12% as compared with the conventional one.

【0022】〈実施例5〉粉末状のエポキシ樹脂25重
量部と板状六方晶系バリウムフェライト磁性粉(直径約
0.1μm,抗磁力Hc:655 Oe,比表面積BE
T:30m2/g)100重量部、有機合成した骨格内に
ポリオキシアルキレングリコール構造と酸無水物構造を
持つ機能性高分子1g及び単結晶アルミナ5重量部を十
分混合した後、シクロヘキサノン10重量部を添加し
て、ニーダ混練機中でさらに混合を行なった。その後、
さらにシクロヘキサノン5重量部を添加して約4時間混
練を続けた。
Example 5 25 parts by weight of powdery epoxy resin and plate-like hexagonal barium ferrite magnetic powder (diameter about 0.1 μm, coercive force Hc: 655 Oe, specific surface area BE)
T: 30 m 2 / g) 100 parts by weight, 1 g of a functional polymer having a polyoxyalkylene glycol structure and an acid anhydride structure in an organically synthesized skeleton and 5 parts by weight of single crystal alumina are thoroughly mixed, and then 10 parts by weight of cyclohexanone Parts were added and further mixed in a kneader kneader. afterwards,
Further, 5 parts by weight of cyclohexanone was added and kneading was continued for about 4 hours.

【0023】この混練物をボールミルポットに入れ、シ
クロヘキサノンとイサホロンの混合溶媒140重量部を
加え、3日間ボールミル混練を行ない、磁性粉を分散さ
せた。つぎに、フェノール樹脂25重量部とビニル樹脂
6重量部をシクロヘキサノン・イソホロン・ジオキサン
の混合溶媒490重量部に溶解した溶液を加えて磁気塗
料を調整した。つぎに、予め表面を清浄にした5.25
インチのアルミニウム基板上にこの塗料を回転塗布し、
通常の配向装置で配向を行なった。
This kneaded product was put in a ball mill pot, 140 parts by weight of a mixed solvent of cyclohexanone and isaphorone was added, and ball mill kneading was carried out for 3 days to disperse the magnetic powder. Next, a magnetic coating material was prepared by adding a solution prepared by dissolving 25 parts by weight of a phenol resin and 6 parts by weight of a vinyl resin in 490 parts by weight of a mixed solvent of cyclohexanone / isophorone / dioxane. Next, the surface was cleaned in advance 5.25
Spin coating this paint on an inch aluminum substrate,
Alignment was performed with a normal aligner.

【0024】さらに塗膜を210℃で硬化し、表面加工
して磁気記録膜を0.3μm の厚みとし、フッ素系液体
潤滑剤を塗布し磁気ディスクとした。この磁気ディスク
の電気特性をギャップ長0.3μm の薄膜磁気ヘッドを
用いて測定したところ、従来の配向した磁気ディスク
(表1の(5))のそれに対して、機能性高分子を含有
せしめ、配向したものはS/N比が10%向上した。
Further, the coating film was cured at 210 ° C. and surface-treated to make a magnetic recording film having a thickness of 0.3 μm, and a fluorine-based liquid lubricant was applied to obtain a magnetic disk. The electrical characteristics of this magnetic disk were measured using a thin film magnetic head with a gap length of 0.3 μm. In contrast to that of a conventional oriented magnetic disk ((5) in Table 1), a functional polymer was added, The oriented material had an improved S / N ratio of 10%.

【0025】〈実施例6〉実施例1〜5の磁気ディスク
とギャップ長0.4μm の薄膜ヘッドとを組み合わせて
磁気ディスク装置化することで、従来の装置に比べ1.
2〜1.5倍の大容量化が実現できた。
<Embodiment 6> By combining the magnetic disks of Embodiments 1 to 5 with a thin film head having a gap length of 0.4 μm to form a magnetic disk device, the magnetic disk device can be made 1.
We achieved a 2-1.5 times larger capacity.

【0026】〈実施例7〉実施例1〜5の磁気ディスク
とギャップ長0.35μm の録再分離型磁気ヘッドと組
み合わせて磁気ディスク装置とすることで、従来の装置
に比べて2〜3倍の大容量装置が実現できた。
<Embodiment 7> By combining the magnetic disk of Embodiments 1 to 5 with the recording / reproducing separated magnetic head having a gap length of 0.35 μm to form a magnetic disk device, the magnetic disk device is 2-3 times as large as the conventional device. It was possible to realize a large capacity device.

【0027】[0027]

【発明の効果】本発明の磁気ディスク及び製造方法は、
磁気塗料中の磁性粉の再凝集を防止し、磁気記録媒体の
角形比(Br/Bm)の向上、さらにはS/N比等の電
磁気特性に優れた磁気ディスク及び磁気記録装置を得る
ことができる。
The magnetic disk and manufacturing method of the present invention are
(EN) A magnetic disk and a magnetic recording device which prevent re-aggregation of magnetic powder in a magnetic paint, improve the squareness ratio (Br / Bm) of a magnetic recording medium, and have excellent electromagnetic characteristics such as S / N ratio. it can.

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

【図1】本発明の磁性膜の角形比(Br/Bm)を示す
B−H曲線の特性図。
FIG. 1 is a characteristic diagram of a BH curve showing the squareness ratio (Br / Bm) of a magnetic film of the present invention.

【符号の説明】[Explanation of symbols]

a…磁気記録膜のB−H曲線との関係、b…従来法、c
…磁場配向のないもの。
a ... Relation with BH curve of magnetic recording film, b ... Conventional method, c
… Those without magnetic field orientation.

Claims (6)

【特許請求の範囲】[Claims] 【請求項1】複数種の高分子材料と磁性粉を含有してな
る磁性層の膜厚が1μm以下であり、磁気ヘッド走行方
向の角形比が0.85 以上であることを特徴とする塗布
型磁気記録媒体。
1. A coating characterized in that a film thickness of a magnetic layer containing a plurality of kinds of polymer materials and magnetic powder is 1 μm or less, and a squareness ratio in a magnetic head traveling direction is 0.85 or more. Type magnetic recording medium.
【請求項2】請求項1において磁性粉の大きさが0.4
μm 以下である磁気記録媒体。
2. The size of magnetic powder according to claim 1, which is 0.4.
A magnetic recording medium having a size of μm or less.
【請求項3】請求項1において、前記磁性粉の大きさが
0.2μm 以下である磁気記録媒体。
3. The magnetic recording medium according to claim 1, wherein the size of the magnetic powder is 0.2 μm or less.
【請求項4】請求項1において前記高分子材料中に機能
性高分子材料としてポリオキシアルキレングリコールを
含有せしめた磁気記録媒体。
4. A magnetic recording medium according to claim 1, wherein the polymer material contains polyoxyalkylene glycol as a functional polymer material.
【請求項5】高分子結合剤中に少なくとも有機合成可能
な骨格内にポリオキシアルキレングリコール構造と酸無
水物構造を持つ機能性高分子で磁性分を分散させた磁気
塗料を非磁性基板上に塗布して得られた磁気記録膜の未
乾燥の状態を維持しつつ、前記磁性粉を配向せしめて前
記磁気記録膜を製造することを特徴とする磁気ディス
ク。
5. A magnetic coating material comprising a functional binder having a polyoxyalkylene glycol structure and an acid anhydride structure in a polymer binder in which at least an organically synthesizable skeleton has a magnetic component dispersed on a non-magnetic substrate. A magnetic disk, wherein the magnetic powder is orientated to produce the magnetic recording film while maintaining the undried state of the magnetic recording film obtained by coating.
【請求項6】主成分の高分子を微粉砕化し、少なくとも
ポリビニルブチラール粉末樹脂とエポキシ粉末樹脂に磁
性粉を混入し、さらに溶剤と必要に応じて添加剤を含有
してニーダ混練を行い、所定の組成比を保持せしめるこ
とを特徴とする磁気ディスク用磁気塗料の製造方法。
6. A main component polymer is finely pulverized, at least polyvinyl butyral powder resin and epoxy powder resin are mixed with magnetic powder, and a kneader is kneaded by kneading with a solvent and, if necessary, additives. A method for producing a magnetic paint for a magnetic disk, characterized in that the composition ratio of the above is maintained.
JP5476092A 1992-03-13 1992-03-13 Magnetic recording medium and magnetic recorder Pending JPH05258281A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5476092A JPH05258281A (en) 1992-03-13 1992-03-13 Magnetic recording medium and magnetic recorder

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5476092A JPH05258281A (en) 1992-03-13 1992-03-13 Magnetic recording medium and magnetic recorder

Publications (1)

Publication Number Publication Date
JPH05258281A true JPH05258281A (en) 1993-10-08

Family

ID=12979730

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5476092A Pending JPH05258281A (en) 1992-03-13 1992-03-13 Magnetic recording medium and magnetic recorder

Country Status (1)

Country Link
JP (1) JPH05258281A (en)

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