JPS60219628A - Magnetic recording medium - Google Patents
Magnetic recording mediumInfo
- Publication number
- JPS60219628A JPS60219628A JP7391184A JP7391184A JPS60219628A JP S60219628 A JPS60219628 A JP S60219628A JP 7391184 A JP7391184 A JP 7391184A JP 7391184 A JP7391184 A JP 7391184A JP S60219628 A JPS60219628 A JP S60219628A
- Authority
- JP
- Japan
- Prior art keywords
- magnetic
- resin
- maleic anhydride
- magnetic powder
- weight
- 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、例えば勝気テープ、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 Katsuki 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、非磁性基板上に塗布し、そして焼
付硬化すると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. The magnetic paint is coated on a non-magnetic substrate and cured 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仁と、勝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−pesos磁性粉末、Cr2O3磁
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 of the magnetic powder, it is necessary to uniformly disperse the magnetic powder in the recording layer. It has been proposed to use
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、例えばバ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 instead of reducing the amount of magnetic powder, it is important to reduce the amount of other components, such as the binder, but this will reduce the binder effect. Durability becomes a big 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−Fe20s磁性粉末に比べると分赦しにくい
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 powders with high coercive force generally have small particles and a large acicular ratio, as well as a large specific surface area, making them difficult to ablate compared to conventional γ-Fe20s magnetic powders. Therefore, in order to improve the dispersibility of magnetic powder, it is necessary to mix and disperse magnetic paint for a long time.
If such long-term mixing and dispersion is performed, there is a problem that the magnetic powder is broken and the magnetic properties are deteriorated, such as a decrease in coercive force.
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アクリル酸エステ
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 uses a copolymer derived from acrylic ester and maleic anhydride as at least a portion of the binder resin in a magnetic recording medium in which magnetic powder is dispersed in a binder resin and cured by baking. This allows the magnetic powder to be dispersed well in the magnetic coating material without long-term cross-talk, so the magnetic properties do not deteriorate, and even if the magnetic recording layer is made thinner, it has excellent mechanical strength. I found out that there is.
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、
磁性塗料の混練時間の大巾な短縮が可能となり、側えば
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
でよいとすれば混線−時間は従来の半分以下アすみ、従
って製造時間の大巾5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練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 drastically shorten the time required to mix the magnetic paint, and if the surface properties are the same as those of conventional magnetic recording media, the crosstalk time will be less than half that of the conventional magnetic recording medium, and therefore the manufacturing time will be reduced. It is possible to shorten the width 5 and reduce the manufacturing cost significantly, and if the magnetic paint is kneaded for a relatively long time to the extent that the magnetic powder does not break, the surface properties will be significantly improved without any decrease in coercive force etc. It will improve.
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(CSS)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 (CSS), 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.
伺、上記アクリル酸エステルと無水マレイン酸とより導
かれる共重合体は、その分子量が約500〜50000
の範囲内、より望1しくけ約1000〜10000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〇
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。The copolymer derived from the above acrylic ester and maleic anhydride has a molecular weight of about 500 to 50,000.
In terms of compatibility, the proportion of maleic anhydride in the above copolymer is preferably in the range of about 5 to 10,000, more preferably about 1,000 to 10,000. 80%, more preferably about 20-50%
It is preferable from the viewpoint of dispersibility in the magnetic powder.
又、上記ケクリル酸エステルと無水マレイン酸とより導
かれる共重合体のみをノくインダー樹脂として用いるよ
りも、との共重誉体と、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アクリル酸
エステ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%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 the above-mentioned queacrylic acid ester and maleic anhydride as the inder resin, a copolymer derived from the above-mentioned queacrylic acid ester and maleic anhydride, for example, an epoxy resin, a phenol resin, a melamine resin, a urea resin, etc. It is preferable to use acrylic resin, butyral resin, and other resins having a binder effect in combination.In other words, among all the binder resins added when preparing the magnetic paint, copolymer derived from acrylic ester and maleic anhydride is preferable. From the viewpoint of surface properties, etc., it is desirable that the proportion of coalescence be within the range of about 1 to 50% by weight.
特に、アクリル酸エステルζ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
シ樹脂とアクリル樹脂系、エポキシ樹脂とフェノール樹
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ましい。In particular, a copolymer derived from an acrylic acid ester ζ maleic anhydride is mixed with an epoxy resin, more preferably an epoxy resin and an acrylic resin system, an epoxy resin and a phenol resin system, or an epoxy resin, an acrylic resin, and a phenol resin system (both of which are It is preferable to use it together with a binder resin (mainly epoxy resin).
又、アクリル酸エステルと無水マレイン酸とより導かれ
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。Further, the total amount of the binder such as a copolymer derived from an acrylic ester and maleic anhydride is in the range of 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 preferable that it be within.
又、無水マレイン酸との共重合に用いられるアクリル酸
エステルCH2=CHC0ORは、Rが炭素数1〜18
、より望ましくは炭素数1〜8のアルキル基のものであ
ることが好ましい。そして、無水マレイン酸との共重合
に用いられるアクリル酸エステルは、一種類のものだけ
でなく、同時に二種類以上のアクリル酸エステルが用い
られてもよい。In addition, in the acrylic acid ester CH2=CHCOOR used for copolymerization with maleic anhydride, R has 1 to 18 carbon atoms.
, more preferably an alkyl group having 1 to 8 carbon atoms. The acrylic ester used in the copolymerization with maleic anhydride is not limited to one type, but two or more types of acrylic ester may be used at the same time.
〔実施例1〕
Co被着型γ−1?e203磁性粉末100重量部、α
−kt20s粉末10重量部、エポキシ樹脂(シェル化
〆
学社のエピコート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−25)2
0M量部、アクリル酸エステル−無水マレイン酸共重合
体(交互共重合体、アクリル酸エステルはアクリル酸ブ
チル、アクリル酸ブチル/無水マレイン酸−50/ 5
0 、 Mw= 500000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時間混練を行
なって磁性塗料を調整する。[Example 1] Co coated type γ-1? 100 parts by weight of e203 magnetic powder, α
- 10 parts by weight of kt20s powder, 45 parts by weight of epoxy resin (Epicoat 1007 manufactured by Shell Kajigakusha), 2 parts by weight of phenolic resin (Sumilac PC-25 manufactured by Sumitomo Bakelite Co., Ltd.)
0M parts, acrylic ester-maleic anhydride copolymer (alternating copolymer, acrylic ester is butyl acrylate, butyl acrylate/maleic anhydride-50/5
0, Mw=500000 parts by weight, mixed solvent 620
Parts by weight of the composition are placed in a ball mill and kneaded 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、ボールミルでの混線時間を半分の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 crosstalk time in the ball mill was halved.
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
A403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、アクリル酸エステル−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、アクリル酸エステルはアクリル酸エチル、アクリ
ル酸エチル/無水マレイン酸=60/40、Mw=20
00) 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] 100 parts by weight of Co-coated 7-Fe2O3 magnetic powder, a
10 parts by weight of A403 powder, 35 parts by weight of epoxy resin (Epicor 1001, manufactured by Shell Chemical Co., Ltd.), acrylic resin (
25 parts by weight of Dianaru 5E-5437 (manufactured by Mitsubishi Rayon Co., Ltd.), 25 parts by weight of acrylic ester-maleic anhydride copolymer (
Maleic anhydride is a random copolymer with no bonds, acrylic ester is ethyl acrylate, ethyl acrylate/maleic anhydride = 60/40, Mw = 20
00) A magnetic disk is manufactured in the same manner as in Example 1 using a composition containing 15 parts by weight of the mixed solvent and 620 parts by weight of the mixed solvent.
Co被着型7 Fe20s磁性粉末100重量部、a−
At*Os粉末10重量部、エピコー) 100750
重量部、スミラックPC−2525重量部、混合溶剤6
20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。Co-coated type 7 Fe20s magnetic powder 100 parts by weight, a-
At*Os powder 10 parts by weight, Epicor) 100750
Parts by weight, Sumilac PC-2525 parts by weight, mixed solvent 6
A magnetic disk is manufactured in the same manner as in Example 1 using 20 parts by weight.
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に示す通りでおる。 71
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″iiシ
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。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. 71 In other words, the product of the present invention has less damage to the magnetic powder when the magnetic paint is crossed, less deterioration of magnetic properties, and has a larger coercive force than the comparative example, and a larger squareness ratio. It can be seen that it is a recording medium with good magnetic properties due to its good dispersibility.
又、表面欠陥の数も犬rJi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。In addition, the number of surface defects is also reduced compared to dog rJi, and
In terms of abrasion resistance, it 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シ、このよう
なことよシ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練時間は著しく短縮化でき、
製造コストも低置なものとなシ、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 was far superior. In fact, if it were sufficient to simply meet the current standards, the kneading time could be significantly shortened.
The manufacturing cost is also low, and the 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 代 理 人 宇 高 克 l(b′);、:>、、、。Patent applicant: Victor Japan Co., Ltd. Representative Uko Katsu l(b');, :>,,,.
Claims (1)
導かれる共重合体を含むことを特徴とするr6気記録媒
体。An R6 recording medium characterized in that the magnetic layer contains a copolymer of acrylic acid ester and maleic anhydride.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7391184A JPS60219628A (en) | 1984-04-14 | 1984-04-14 | Magnetic recording medium |
DE19853513208 DE3513208A1 (en) | 1984-04-14 | 1985-04-12 | MAGNETIC RECORDING MEDIUM CONTAINING A SPECIAL COPOLYMER BINDING AGENT |
US06/722,663 US4689269A (en) | 1984-04-14 | 1985-04-12 | Magnetic recording medium comprising a specific type of copolymer binder |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7391184A JPS60219628A (en) | 1984-04-14 | 1984-04-14 | Magnetic recording medium |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS60219628A true JPS60219628A (en) | 1985-11-02 |
Family
ID=13531829
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP7391184A Pending JPS60219628A (en) | 1984-04-14 | 1984-04-14 | Magnetic recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60219628A (en) |
-
1984
- 1984-04-14 JP JP7391184A patent/JPS60219628A/en active Pending
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