JPS60219632A - Magnetic recording medium - Google Patents
Magnetic recording mediumInfo
- Publication number
- JPS60219632A JPS60219632A JP7391584A JP7391584A JPS60219632A JP S60219632 A JPS60219632 A JP S60219632A JP 7391584 A JP7391584 A JP 7391584A JP 7391584 A JP7391584 A JP 7391584A JP S60219632 A JPS60219632 A JP S60219632A
- Authority
- JP
- Japan
- Prior art keywords
- magnetic
- magnetic powder
- resin
- maleic anhydride
- paint
- 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
Landscapes
- Paints Or Removers (AREA)
- Magnetic Record Carriers (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、例えば磁気テープ、フロッピーディスク、ハ
ードディスクといった磁気記録媒体、特にコンピュータ
等の磁気ディスク装置に用いられる磁気記録媒体に関す
るものである。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to magnetic recording media such as magnetic tapes, floppy disks, and hard disks, and particularly to magnetic recording media used in magnetic disk devices such as computers.
従来、例えば磁気ディスク装置等の情報記録装置に用い
られる磁気記録媒体は、磁性粉末を、例えばエポキシ樹
脂、フェノール樹脂、メラミン樹脂、尿素樹脂、アクリ
ル樹脂、ブチラール樹脂等のバインダーを含む溶剤に分
散させた磁性塗料を、非硼性基板上に塗布し、そして焼
付硬化することによって構成されている。Conventionally, magnetic recording media used in information recording devices such as magnetic disk drives have been produced by dispersing magnetic powder in a solvent containing a binder such as epoxy resin, phenol resin, melamine resin, urea resin, acrylic resin, or butyral resin. It is constructed by applying a magnetic coating material on a non-borous substrate and curing it by baking.
そして、情報記録装置の高性能化に伴ない、上記の磁気
記録媒体には高密度化が要求されてきておシ、このよう
な要求を満たす為に、磁気記録層をよシ薄くすること、
その表面性を向上させるとと、磁気記録層中の磁性粉末
を均一に分散させておくこと、高保磁力の磁性粉末、例
えばCo改改良型−Fe203硲性粉末、Cr−0s硼
性粉末、金属磁性粉末等を用いること等が提案されてい
る。As the performance of information recording devices increases, the magnetic recording medium described above is required to have higher density.In order to meet such demands, it is necessary to make the magnetic recording layer thinner.
In order to improve the surface properties, it is necessary to uniformly disperse the magnetic powder in the magnetic recording layer, and to use magnetic powder with high coercive force, such as Co improved type-Fe203 boron powder, Cr-0s boron powder, metal It has been proposed to use magnetic powder or the like.
ところが、例えば磁気記録層を単に薄くするのみでは磁
性粉末量が少なくなることより、磁性粉末量を減らすの
ではなくその他の成分、例えばノζインダー量を減らす
ことが重要となるが、これではバインダー効果が乏しく
なり、耐久性が大きな問題となる。However, simply making the magnetic recording layer thinner will reduce the amount of magnetic powder, so it is important to reduce the amount of other components, such as the amount of binder, rather than reducing the amount of magnetic powder. It becomes less effective and durability becomes a major problem.
又、高保磁力の磁性粉末は、一般に粒子が小さ ′く、
しかも針状比が大きいことよシ、比表面積が大きく、こ
の為従来のγ−pet03磁性粉末に比べると分散しに
くいものとなっている。そこで、磁性粉末の分散性を向
上させる為、磁性塗料を長時間混合分散する必要がある
が、このような長時間の混合分散が行なわれると、磁性
粉末が折損し、保磁力の低下といった磁気特性が低下す
る問□題がある。In addition, magnetic powder with high coercive force generally has small particles;
Moreover, in addition to having a large acicular ratio, it also has a large specific surface area, which makes it difficult to disperse compared to conventional γ-PET03 magnetic powder. Therefore, in order to improve the dispersibility of the magnetic powder, it is necessary to mix and disperse the magnetic paint for a long time. However, if such a long time mixing and dispersion is carried out, the magnetic powder may break and magnetic problems such as a decrease in coercive force may occur. There is a problem of deterioration of characteristics □.
本発明者は、磁性粉末をバインダー樹脂中に分散せしめ
て焼付硬化してなるタイプの磁気記録媒体において、バ
インダー樹脂の少なくとも一部として塩化ビニルと無水
マレイン酸とより導かれる共重合体を用いていると、長
時間の混線をせずとも磁性塗料中における磁性粉末の分
散性が良く、従って磁気特性を低下せしめることもなく
、又、磁気記録層を薄くしても機械的強度に優れている
ことを見い出した。The present inventor has proposed a type of magnetic recording medium in which magnetic powder is dispersed in a binder resin and hardened by baking, using a copolymer derived from vinyl chloride and maleic anhydride as at least a part of the binder resin. This allows the magnetic powder to be dispersed well in the magnetic paint without long-term cross-talk, so the magnetic properties do not deteriorate, and the magnetic recording layer has excellent mechanical strength even if it is made thinner. I discovered that.
この分散性向上は、磁性粉末の折損による保磁力や角型
比の低下を防ぐといった効果をもたらすのみではなく、
磁性塗料の混線時間の大巾な短縮が可能となり、例えば
従来の磁気記録媒体の表面特性と同等の表面特性のもの
でよいとすれば混練時間は従来の半分以下ですみ、従っ
て製造時間の大巾な短縮化及び製造コストの大巾な低廉
化が行なえ、又、磁性粉末の折損が起きない程度まで比
較的長く磁性塗料の混線を行なえば保磁力等の低下もな
く表面特性は著しく向上することになる。This improved dispersibility not only has the effect of preventing a decrease in coercive force and squareness due to breakage of the magnetic powder, but also
It is possible to significantly shorten the mixing time of magnetic paint. For example, if the surface characteristics are equivalent to those of conventional magnetic recording media, the mixing time will be less than half of the conventional one, and therefore the manufacturing time will be greatly reduced. The width can be shortened and the manufacturing cost can be reduced significantly, and if the magnetic paint is mixed for a relatively long time to the extent that the magnetic powder does not break, the surface characteristics can be significantly improved without decreasing the coercive force etc. It turns out.
又、上記機械的強度の優秀性は、磁気記録層の密着性、
耐摩耗性及び耐溶剤性等に優れていることであり、耐摩
耗性は、例えば磁気ディスクの場合にはコンタクトスタ
ートアンドストップ(C8S)の回数で評価され、IS
OのTC97/5C1ON228で10000回以上と
いった規格があるが、本発明による磁気ディスクはこの
規格値を大きく止まり、又、磁性粉末の粉落ちといった
ことも極めて少なく、さらには磁気ディスクの表面洗浄
に使用されるアルコール等の溶剤に対する抵抗性が強く
、磁気記録層が変性を受けに<<、極めて耐久性に富む
ことになる。Moreover, the above-mentioned superiority of mechanical strength is due to the adhesion of the magnetic recording layer,
It has excellent abrasion resistance and solvent resistance. For example, in the case of magnetic disks, abrasion resistance is evaluated by the number of contact start and stop (C8S), and IS
Although there is a standard for TC97/5C1ON228 of O, it can be used more than 10,000 times, but the magnetic disk according to the present invention far exceeds this standard value, and there is extremely little chance of magnetic powder falling off, and furthermore, it can be used for surface cleaning of magnetic disks. It has strong resistance to solvents such as alcohol, and the magnetic recording layer is extremely durable against denaturation.
尚、上記塩化ビニルと無水マレイン酸とより導かれる共
重合体は、その分子針か約500〜5ooo。The copolymer derived from vinyl chloride and maleic anhydride has a molecular needle size of approximately 500 to 500 mm.
の範囲内、より望ましくは約1ooo〜10000の範
囲内のものであることが相溶性等の面から好ましい。From the viewpoint of compatibility, etc., it is preferable that the number is within the range of , more preferably within the range of about 100 to 10,000.
又、上記共重合体における無水マレイン酸の割合は、モ
ル比率で約5〜80%、より望ましくは約20〜50%
のものであることが磁性粉末に対する分散性等の面から
好ましい。Further, the proportion of maleic anhydride in the above copolymer is about 5 to 80% in molar ratio, more preferably about 20 to 50%.
It is preferable from the viewpoint of dispersibility in the magnetic powder.
又、上記塩化ビニルと無水マレイン酸とより導かれる共
重合体のみをバインダー樹脂として用いるよりも、この
共重合体と、例えばエポキシ樹脂、フェノール樹脂、メ
ラミン樹脂、尿素樹脂、アクリル樹脂、ブチラール樹脂
、その他のバインダー効果を有する樹脂とを併用して用
いることが好ましく、すなわち磁性塗料を調整する際添
加する全バインダー樹脂のうち塩化ビニルと無水マレイ
ン酸とより導かれる共重合体の割合は約1〜50重量係
の範囲内のものとすることが表面特性等の面から望まし
い。Moreover, rather than using only the copolymer derived from vinyl chloride and maleic anhydride as the binder resin, this copolymer and, for example, epoxy resin, phenol resin, melamine resin, urea resin, acrylic resin, butyral resin, It is preferable to use the resin in combination with another resin having a binder effect. That is, the proportion of the copolymer derived from vinyl chloride and maleic anhydride out of all the binder resins added when preparing the magnetic paint is about 1 to 1. It is desirable to use a material within the range of 50% by weight from the viewpoint of surface characteristics and the like.
特に、塩化ビニルと無水マレイン酸とより導かれる共重
合体を、エポキシ樹脂、より望ましくはエポキシ樹脂と
フェノール樹脂系、エポキシ樹脂とアクリル樹脂系又は
エポキシ樹脂とアクリル樹脂とフェノール樹脂系(いず
れもエポキシ樹脂が主体)のバインダー樹脂と共に用い
ることが好捷しい。In particular, a copolymer derived from vinyl chloride and maleic anhydride may be used in an epoxy resin, more preferably an epoxy resin and a phenol resin system, an epoxy resin and an acrylic resin system, or an epoxy resin, an acrylic resin, and a phenol resin system (all of which are epoxy resins and phenolic resins). It is preferable to use it together with a binder resin (mainly consisting of resin).
又、塩化ビニルと無水マレイン酸とよシ導かれる共重合
体等の全バインダーは、磁性粉末100重量部に対して
約30〜200重量部、より望ましくは約50〜120
重量部の範囲内であることが好ましい。The total amount of the binder such as a copolymer derived from vinyl chloride and maleic anhydride is about 30 to 200 parts by weight, more preferably about 50 to 120 parts by weight, based on 100 parts by weight of the magnetic powder.
It is preferably within the range of parts by weight.
〔実施例1〕
Co被着型γ−Fe203磁性粉末100重量部、α−
A L 203 粉末10重量部、エポキシ樹脂(シェ
ル化学社のエピコー) 1007 )45重量部、フェ
ノール樹脂(住友ベークライト社のスミラックPC−2
5)20重量部、塩化ビニル−無水マレイン酸共重合体
(交互共重合体、塩化ビニル/無水マレイン酸=50
/ 50、Mw= 5000 ) 10重量部、混合溶
剤620重量部の組成物をボールミルに入れ、24時間
混線を行なって磁性塗料を調整する。[Example 1] 100 parts by weight of Co-coated γ-Fe203 magnetic powder, α-
10 parts by weight of A L 203 powder, 45 parts by weight of epoxy resin (Epicor 1007, manufactured by Shell Chemical Co., Ltd.), 45 parts by weight of phenolic resin (Sumilac PC-2, manufactured by Sumitomo Bakelite Co., Ltd.)
5) 20 parts by weight, vinyl chloride-maleic anhydride copolymer (alternating copolymer, vinyl chloride/maleic anhydride = 50
/50, Mw=5000) A composition containing 10 parts by weight and 620 parts by weight of a mixed solvent was placed in a ball mill and mixed for 24 hours to prepare a magnetic coating material.
そして、上記磁性塗料をアルミニウム合金基板上に塗布
し、200℃で1時間の焼付硬化を行ない、その後研磨
処理を施して磁気ディスクを製作する。Then, the magnetic paint is applied onto an aluminum alloy substrate, baked and hardened at 200° C. for 1 hour, and then polished to produce a magnetic disk.
〔実施例2〕
実施例1において、ボールミルでの混練時間を半分の1
2時間とし、その他は同様にして磁気ディスクを製作す
る。[Example 2] In Example 1, the kneading time in the ball mill was reduced to 1/2.
The magnetic disk was produced in the same manner except for 2 hours.
〔実施例3〕
Co被着型7−Fe2O3磁性粉末100重量部、・−
A t 203粉末10重量部、エポキシ樹脂(シェル
化学社のエピコー) 1001 )35重量部、アクリ
ル樹脂(三菱レーヨン社のダイヤナール5E−5437
)25重量部、塩化ビニル−無水マレイン酸共重合体(
無水マレイン酸同士は結合していない形のランダム共重
合体、塩化ビニル/無水マレイン酸−60/ 40 、
Mw= 2000 ) 15重量部、混合溶剤620重
量部の組成物を用いて、実施例1と同様にして磁気ディ
スクを製作する。[Example 3] Co-coated type 7-Fe2O3 magnetic powder 100 parts by weight, -
10 parts by weight of At 203 powder, 35 parts by weight of epoxy resin (Epicor 1001, manufactured by Shell Chemical Co., Ltd.), acrylic resin (Dianal 5E-5437, manufactured by Mitsubishi Rayon Co., Ltd.)
) 25 parts by weight, vinyl chloride-maleic anhydride copolymer (
Random copolymer in which maleic anhydride is not bonded to each other, vinyl chloride/maleic anhydride-60/40,
A magnetic disk was manufactured in the same manner as in Example 1 using a composition containing 15 parts by weight of Mw=2000) and 620 parts by weight of a mixed solvent.
Co被着型γ−1i”e203磁性粉末100重量部、
a’−A220g粉末10重量部、エピコート1007
50重量部、スミラックPC−2525重量部、混合
溶剤620重量部を用いて、実施例1と同様にして磁気
ディスクを製作する。100 parts by weight of Co-coated γ-1i”e203 magnetic powder,
a'-A220g powder 10 parts by weight, Epicote 1007
A magnetic disk was manufactured in the same manner as in Example 1 using 50 parts by weight of SUMILAC PC-2525 and 620 parts by weight of the mixed solvent.
上記実施例1〜3及び比較例で製作した磁気ディスクに
ついて、磁気特性(保磁力、角型比)、表面欠陥及び耐
摩耗性を調べると表1に示す通りである。The magnetic properties (coercive force, squareness ratio), surface defects, and wear resistance of the magnetic disks manufactured in Examples 1 to 3 and Comparative Example were examined as shown in Table 1.
表 1
すなわち、本発明のものは、磁性塗料の混線時磁性粉末
の損傷が少なく、磁気特性の低下は少なく、つまり保磁
力は比較例のものよりも大きく、又、角型比は大きく、
分散性が良いことより磁気特性の良い記録媒体であるこ
とがわかる。Table 1 In other words, in the case of the present invention, there is less damage to the magnetic powder when the magnetic paint is crossed, and there is less deterioration of the magnetic properties.In other words, the coercive force is larger than that of the comparative example, and the squareness ratio is large.
It can be seen that it is a recording medium with good magnetic properties because of its good dispersibility.
又、表面欠陥の数も大巾に少なくなっており、又、耐摩
耗性に関しては実用上半永久的といってもよい位優れて
いる。Furthermore, the number of surface defects is greatly reduced, and the wear resistance is so excellent that it can be said to be semi-permanent in practical terms.
又、磁性塗料の混線時間を従来の半分にしても優れた記
録媒体が得られており、すなわち実施例2と比較例とを
比べると実施例2の方がはるかに優れており、このよう
なことより現在の規格程度のものを単に満足する程度の
ものでよいとするならば混線時間は著しく短縮化でき、
製造コストも低置なものとなり、しかも磁性粉末等に対
する制約も緩和でき、選択範囲は極めて広いものとなる
。Furthermore, an excellent recording medium was obtained even when the crosstalk time of the magnetic paint was reduced to half of the conventional one.In other words, when comparing Example 2 and the comparative example, Example 2 is far superior; In particular, if it were sufficient to simply satisfy the current standards, crosstalk time could be significantly reduced.
The manufacturing cost is also low, and restrictions on magnetic powder etc. can be relaxed, and the range of selection is extremely wide.
特許出願人 日本ビクター株式会社〜Patent applicant: Victor Japan Co., Ltd.
Claims (1)
共重合体を含むことを特徴とする磁気記録媒体。A magnetic recording medium characterized in that a magnetic layer contains a copolymer of vinyl chloride and maleic anhydride.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7391584A JPS60219632A (en) | 1984-04-14 | 1984-04-14 | Magnetic recording medium |
US06/722,663 US4689269A (en) | 1984-04-14 | 1985-04-12 | Magnetic recording medium comprising a specific type of copolymer binder |
DE19853513208 DE3513208A1 (en) | 1984-04-14 | 1985-04-12 | MAGNETIC RECORDING MEDIUM CONTAINING A SPECIAL COPOLYMER BINDING AGENT |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7391584A JPS60219632A (en) | 1984-04-14 | 1984-04-14 | Magnetic recording medium |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS60219632A true JPS60219632A (en) | 1985-11-02 |
Family
ID=13531936
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP7391584A Pending JPS60219632A (en) | 1984-04-14 | 1984-04-14 | Magnetic recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60219632A (en) |
-
1984
- 1984-04-14 JP JP7391584A patent/JPS60219632A/en active Pending
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