JP3362789B2 - Magnetic recording media - Google Patents

Magnetic recording media

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Publication number
JP3362789B2
JP3362789B2 JP02265291A JP2265291A JP3362789B2 JP 3362789 B2 JP3362789 B2 JP 3362789B2 JP 02265291 A JP02265291 A JP 02265291A JP 2265291 A JP2265291 A JP 2265291A JP 3362789 B2 JP3362789 B2 JP 3362789B2
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JP
Japan
Prior art keywords
magnetic
particle size
head
magnetic recording
abrasive
Prior art date
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Expired - Fee Related
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JP02265291A
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Japanese (ja)
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JPH04248119A (en
Inventor
清人 福島
和志 田中
仁 畔上
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TDK Corp
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TDK Corp
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Priority to JP02265291A priority Critical patent/JP3362789B2/en
Publication of JPH04248119A publication Critical patent/JPH04248119A/en
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Publication of JP3362789B2 publication Critical patent/JP3362789B2/en
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Expired - Fee Related legal-status Critical Current

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  • Paints Or Removers (AREA)
  • Magnetic Record Carriers (AREA)
  • Manufacturing Of Magnetic Record Carriers (AREA)

Description

【発明の詳細な説明】 【0001】 【産業上の利用分野】本発明は、支持体上に磁性塗料を
塗布してなる磁気記録媒体に関し、本発明は前記磁性層
に研摩剤粒子を含有して、ヘッド付着を減少し、走行耐
久性、スチル等のテープ物性を改良する。 【0002】 【従来技術】オーディオ、ビデオ、フロッピーディス
ク、コンピュータ用テープ等の磁気記録媒体では磁気ヘ
ッドとの接触による磁性層の損傷を防ぐため、Al
23、Cr23、TiO2、SiO2、SiC、α−Fe
23、ZnO2等の非磁性無機材料を添加することが一
般に行われている。しかし添加する無機材料粒子の種
類、粒子サイズ、添加量を適切に選ばないと、磁気ヘッ
ドを損傷したり、磁気ヘッドの摩耗量を増大したり、電
磁変換特性を劣化させたりという不具合を生ずる。 【0003】このため、従来、上記無機材料を単独で、
または組み合わせて少量添加し磁性層を強化してきた。
本発明者は、塗膜補強剤としての無機材料として、予め
2種類の無機材料を含む粒子を添加することによって、
塗膜の補強効果を高めヘッド付着が少なく、かつヘッド
摩耗量も少ない磁気記録媒体を提供できるよう研究を行
った。これまで高硬度の非磁性無機粉末を混入すること
で塗膜の補強を行ってきたが、近年ビデオテープ及びデ
ジタル機器用テープにおいて要求性能の向上にともな
い、微粒子磁性粉の採用、高分散性結合剤(バインダ)
の採用、テープ表面性の平滑化などが進み、これらの施
策は磁性塗膜の耐久性や、摩擦の安定性、ヘッド付着に
は不利な方向にあり、より一層の塗膜の耐久性の強化、
ヘッドクリーニング効果の向上が望まれている。従来よ
り一般に使用されている無機材料粒子をこのような高性
能テープに使用すると、電磁変換特性が悪化したり、補
強効果が不十分なため、耐久走行でテープダメージが発
生したり、ヘッドクリーニング効果が不足するため、ヘ
ッド付着が増加し、出力が低下する等の問題が生ずる。
また摩擦の上昇によって走行不良が生ずる場合がある。 【0004】 【発明が解決すべき課題】そこで本発明者らは、塗膜補
強剤としての無機材料と添加量を適切に選定することに
より、高性能化に伴う問題を解決できるものと考えた。
本出願人は、無機材料としてTiO2とα−Al23
その他の無機材粒子を組み合わせて使用することによ
り、磁気ヘッドの損傷や、摩耗の減少、磁気テープの摩
耗の減少という相容れない要求を満足させることができ
ることを見いだした。しかし尚ヘッド摩耗、摩擦の安定
性の面では不十分であった。 【0005】本発明は、ヘッド付着が少なく、ヘッド摩
耗が少ない、物性が改良された磁気記録媒体を提供する
ことを目的とする。 【0006】 【課題を解決するための手段】現在一般に用いられてい
るα−Al23は単独で用いた場合磁性塗膜の補強効果
とヘッド付着の減少がむずかしい。また、2種以上の無
機粒子の組合せでも同様の問題が生じた。しかし、α−
Al23製造時にFe元素を有する化合物又はSi元素
を有する化合物及びFe元素を有する化合物をα−Al
2 3 の原料と混合し焼成してSiまたはFeまたは両者
を含有したα−Al23を使用することにより互いの欠
点を補いあいヘッド付着、ヘッド摩耗、磁性層の摩耗等
を少なくすることができた。 【0007】本発明は、平均粒径0.10μ〜0.30
μで、0.5〜3.0%のFe元素又は0.05〜0.
30%のSi元素及び0.5〜3.0%のFe元素を含
有しα−Al23を磁性粉等と共に結合剤中に分散せ
しめた磁性塗料を非磁性支持体に塗布してなる磁気記録
媒体である。 【0008】ここに平均粒径0.10μ〜0.30μの
Fe、又はSi及びFe元素を含有するα−Al23
製造する方法は、原料を焼成してα−Al23を製造す
る際に、焼成前にSiまたはFe元素を有する化合物を
混合し、焼成してFe、又はSi及びFe元素含有のα
−Al23とする工程からなる。Si添加量は0.05
〜0.30%、Fe添加量は0.5〜3.0%が好適で
ある。本書で%は重量%を意味する。 【0009】粒子径は0.10μ未満では磁性塗膜の補
強効果が不十分であり、0.30μを越えると磁性塗膜
の表面性を悪くし、電磁特性に悪影響を及ぼす。Si及
びFeの含有量は、下限未満では補強効果不足であり、
上限を越えても補強効果は不足する。 【0010】本発明に使用できる磁性層用の結合剤とし
てはポリウレタン系樹脂、塩化ビニル−酢酸ビニル−ビ
ニルアルコール共重合体等の熱硬化性樹脂、電子線に感
応する二重結合を有するアクリル酸等の電子線硬化性樹
脂等、周知の樹脂を使用し得る。特に熱硬化性樹脂及び
電子線硬化性樹脂は適している。本発明で使用できる磁
性粉としては従来周知の磁気記録媒体用の磁性粉が使用
できる。本発明の磁性塗料は結合剤に上記研磨剤の外、
周知の磁性粉、溶剤、潤滑剤を添加混合して製造される
もので、その方法は当業界に周知の方法の一つを採用で
きる。 【0011】本発明の磁性塗料に使用できる潤滑剤とし
てはミリスチン酸、ステアリン酸等の脂肪酸、ステアリ
ン酸ブチル、ミリスチン酸ブチル等の脂肪酸エステル
等、従来周知の任意のものが使用できる。 【0012】その他極く少量なら他の無機補強剤を含有
してもよい。 【0013】磁性塗料に添加する平均粒径0.10μ〜
0.30μのSiまたはFe元素含有α−Al23の量
は結合剤樹脂に対して0.5〜15.0重量%の割合で
添加できる。多過ぎると分散性に悪影響を与え、電磁特
性を低下させ、少な過ぎると効果がない。本発明で使用
できる非磁性支持体としてはオーディオ、ビデオ、フロ
ッピーディスク、コンピュータ用テープ等の磁気記録媒
体に従来から使用されているポリエステル等の合成樹
脂、その他の非磁性支持体を使用することができる。 【0014】 【実施例の説明】参考例1 下記に示す組成の磁性塗料を調製して乾燥後の厚さが3
μmになるように厚さ14μmのポリエステルベースに
塗布した後カレンダー加工し、熱処理した後、1/2イ
ンチの巾に裁断した。 ・磁性粉(BET45m2/gのCo−γ−Fe23) 100部 ・結合剤 塩酢ビ共重合体(VAGH)/ポリウレタン樹脂(N−2304) 20部 ・研摩剤(Si元素0.10%含有α−Al23粒径0.11μ) 10部 ・MEK 300部 ・カーボン 3部 ・添加剤等(脂肪酸類) 2部 【0015】参考例2 研摩材の粒径を0.22μに変更した他は、参考例1と
同様にして磁気テープを製造した。 【0016】参考例3 研摩材の粒径を0.28μに変更した他は、参考例1と
同様にして磁気テープを製造した。 【0017】実施例 研摩材を粒径0.18μのFe元素0.85%含有α−
Al23に変更した他は参考例2と同様にして磁気テー
プを製造した。 【0018】実施例 研摩材を粒径0.23μのSi 0.20%及びFe元
素1.15%含有α−Al23に変更した他は、参考
2と同様にして磁気テープを製造した。 【0019】比較例1 研摩材の粒径を0.07μに変更した他は、参考例1と
同様にして磁気テープを製造した。 【0020】比較例2 研摩材の粒径を0.35μに変更した他は、参考例1と
同様にして磁気テープを製造した。 【0021】比較例3 研摩材を粒径0.12μのα−Al23に変更した他
は、参考例1と同様にして磁気テープを製造した。 【0022】比較例4 研摩材の粒径を0.21μに変更した他は、比較例3と
同様にして磁気テープを製造した。 【0023】比較例5 研摩材の粒径を0.30μに変更した他は、比較例3と
同様にして磁気テープを製造した。 【0024】比較例6 α−Fe23 1.20%で被覆した粒径0.20μの
α−Al23とした他は、参考例2と同様にして磁気テ
ープを製造した。 【0025】上記、試作磁気記録媒体の諸特性の結果を
下記表1に示す。表中Brは残留磁束密度、Bmは飽和
磁束密度、ORはオリエンテーション比(縦方向/横方
向の磁束密度の比)、Y−S/N、C−S/Nの単位は
dBである。 【0026】 【表1】 【0027】表1から、次のことが確認できた。 【0028】Si元素有無の比較 参考例 1、2、3と比較例3、4、5を比較すると、各
粒径において、磁気特性、Y−S/N、C−S/Nに差
はほとんど見られないが、磁気ヘッド付着(目詰りパス
回数)、スチルライフ(磁気テープの耐久性)に大きな
効果が見られる。 【0029】Fe元素有無の比較 実施例と比較例4を比較すると、磁気特性、Y−S/
N、C−S/Nにも効果が見られ、又、目詰りパス回
数,スチルライフ(磁気テープの耐久性)にも効果が見
られる。 【0030】Si及びFe元素含有の場合 実施例2から分かるように 単独の場合と同様耐久性,ス
チルライフに顕著な効果がある。 【0031】SiO 2 を吸着させた場合の粒径について 粒径が0.07μの場合、SiまたはFe未吸着に比較
すると目詰りパス回数、スチルライフも良好であるが、
粒径0.10〜0.30μの物に比較すると劣ってい
る。 【0032】0.35μの場合は、目詰りパス回数,ス
チルライフとも良好であるが、Y−S/N、C−S/N
が0.10〜0.30μの物に比較して劣る。これは、
粒径が大きいため表面粗度が悪くなり、ヘッドとのスペ
ーシングロスが生じたためと考えられる。 【0033】Fe元素含有とα−Fe 2 3 被覆した場合の違いについ
実施例と比較例6を比較した。α−Fe23を被覆さ
せた場合、目詰りパス回数、スチルライフが含有させた
場合に比較して劣る。 【0034】 【発明の効果】以上のように、本発明によると磁気特性
を犠牲にしないで磁気ヘッド付着(目詰りパス回数)を
減じ、また磁気記録媒体のスチルライフ(磁気テープの
耐久性)を向上させることができる。
Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a magnetic recording medium comprising a support and a magnetic paint applied on the support. The present invention relates to a magnetic recording medium containing abrasive particles in the magnetic layer. Thus, head adhesion is reduced, and running properties and tape properties such as stills are improved. 2. Description of the Related Art In magnetic recording media such as audio, video, floppy disks, computer tapes, etc., in order to prevent a magnetic layer from being damaged by contact with a magnetic head, aluminum is used.
2 O 3 , Cr 2 O 3 , TiO 2 , SiO 2 , SiC, α-Fe
It is common practice to add non-magnetic inorganic materials such as 2 O 3 and ZnO 2 . However, if the type, particle size, and amount of the inorganic material particles to be added are not properly selected, problems such as damaging the magnetic head, increasing the wear amount of the magnetic head, and deteriorating the electromagnetic conversion characteristics occur. For this reason, conventionally, the above-mentioned inorganic materials have been used alone.
Alternatively, a small amount is added in combination to strengthen the magnetic layer.
The inventor has previously added particles containing two types of inorganic materials as an inorganic material as a coating film reinforcing agent,
Research has been conducted to provide a magnetic recording medium that enhances the effect of reinforcing the coating film, has less head adhesion, and has less head wear. Until now, coatings have been reinforced by mixing non-hard inorganic powders with high hardness.In recent years, however, with the improvement in performance required for video tapes and tapes for digital equipment, the use of fine magnetic powders and high dispersion bonding Agent (binder)
The adoption of tapes and the smoothing of the tape surface have progressed, and these measures are disadvantageous to the durability of the magnetic coating, the stability of friction, and the adhesion of the head, and further enhance the durability of the coating. ,
It is desired to improve the head cleaning effect. The use of inorganic material particles that have been generally used in the past for such high-performance tapes deteriorates the electromagnetic conversion characteristics and causes inadequate reinforcement, resulting in tape damage during durability running and head cleaning effects. Deficiency causes problems such as an increase in head adhesion and a decrease in output.
In addition, running failure may occur due to an increase in friction. [0004] Therefore, the present inventors thought that the problem associated with high performance can be solved by appropriately selecting the inorganic material and the amount of addition as a coating film reinforcing agent. .
The present applicant has proposed that TiO 2 and α-Al 2 O 3 as inorganic materials,
It has been found that the combined use of other inorganic particles can satisfy the conflicting requirements of damage to the magnetic head, reduction in wear, and reduction in wear of the magnetic tape. However, head wear and friction stability were not sufficient. SUMMARY OF THE INVENTION An object of the present invention is to provide a magnetic recording medium with reduced head adhesion, reduced head wear, and improved physical properties. [0006] When α-Al 2 O 3, which is generally used at present, is used alone, the reinforcing effect of the magnetic coating film and the decrease in head adhesion are difficult. Further, a similar problem occurred with a combination of two or more kinds of inorganic particles. However, α-
Compound having Fe element at the time of production of Al 2 O 3 or Si element
And a compound having an Fe element as α-Al
Reducing head mutually compensate for each other's shortcomings attachment, head wear, the wear of the magnetic layer by using the alpha-Al 2 O 3 containing were mixed with 2 O 3 raw material calcined to Si or Fe, or both I was able to. According to the present invention, the average particle size is 0.10 μm to 0.30 μm.
In μ , 0.5 to 3.0% of Fe element or 0.05 to 0.
A magnetic paint in which α-Al 2 O 3 containing 30% of Si element and 0.5 to 3.0% of Fe element is dispersed in a binder together with a magnetic powder or the like is applied to a non-magnetic support. Magnetic recording medium. [0008] Here, the average particle size of 0.10μ ~ 0.30μ
Fe, or a method of manufacturing the α-Al 2 O 3 containing Si and Fe elements, in manufacturing the α-Al 2 O 3 by firing a raw material, a compound having a Si or Fe element before firing Mix and fire to obtain Fe or α containing Si and Fe elements
-Al 2 O 3 . Si addition amount is 0.05
The content of Fe is preferably 0.5 to 3.0%. In this document,% means% by weight. When the particle diameter is less than 0.10 μm, the effect of reinforcing the magnetic coating film is insufficient, and when it exceeds 0.30 μm, the surface properties of the magnetic coating film are deteriorated, and the electromagnetic characteristics are adversely affected. If the content of Si and Fe is less than the lower limit, the reinforcing effect is insufficient,
Even if the upper limit is exceeded, the reinforcing effect is insufficient. Examples of the binder for the magnetic layer that can be used in the present invention include a polyurethane resin, a thermosetting resin such as vinyl chloride-vinyl acetate-vinyl alcohol copolymer, and an acrylic acid having a double bond sensitive to an electron beam. A well-known resin such as an electron beam curable resin can be used. In particular, thermosetting resins and electron beam curable resins are suitable. As the magnetic powder that can be used in the present invention, a conventionally known magnetic powder for a magnetic recording medium can be used. The magnetic paint of the present invention has a binder other than the above abrasive,
It is manufactured by adding and mixing a well-known magnetic powder, a solvent, and a lubricant, and one of the methods well-known in the art can be adopted as the method. As the lubricant that can be used in the magnetic paint of the present invention, any conventionally known lubricants such as fatty acids such as myristic acid and stearic acid, and fatty acid esters such as butyl stearate and butyl myristate can be used. In addition, other inorganic reinforcing agents may be contained in a very small amount. The average particle size added to the magnetic paint is 0.10 μm
The amount of α-Al 2 O 3 containing 0.30 μm of Si or Fe element can be added at a ratio of 0.5 to 15.0% by weight based on the binder resin. If the amount is too large, the dispersibility is adversely affected, and the electromagnetic characteristics are deteriorated. If the amount is too small, there is no effect. As the non-magnetic support that can be used in the present invention, there can be used synthetic resins such as polyester and other non-magnetic supports conventionally used for magnetic recording media such as audio, video, floppy disk, and computer tape. it can. DESCRIPTION OF THE PREFERRED EMBODIMENTS Reference Example 1 A magnetic paint having the following composition was prepared and dried to a thickness of 3
It was applied to a polyester base having a thickness of 14 μm to a thickness of 14 μm, calendered, heat-treated, and then cut to a width of イ ン チ inch. 100 parts of magnetic powder (BET 45 m 2 / g Co-γ-Fe 2 O 3 ) 20 parts of binder polyvinyl chloride copolymer (VAGH) / polyurethane resin (N-2304) 20 parts Abrasive (Si element 0.1. 10% content α-Al 2 O 3 particle size 0.11μ) 10 parts ・ MEK 300 parts ・ Carbon 3 parts ・ Additives (fatty acids) 2 parts Reference Example 2 The particle size of the abrasive is 0.22μ A magnetic tape was manufactured in the same manner as in Reference Example 1 except that the magnetic tape was changed. Reference Example 3 A magnetic tape was manufactured in the same manner as in Reference Example 1, except that the particle size of the abrasive was changed to 0.28 μm. Example 1 An abrasive was prepared by using an α-particle containing 0.85% of Fe element having a particle size of 0.18 μm.
The exception that the al 2 O 3 was prepared a magnetic tape in the same manner as in Reference Example 2. [0018] the exception that in Example 2 Si 0.20% of the abrasive particle size 0.23μ and Fe elements 1.15% containing α-Al 2 O 3, the magnetic tape in the same manner as in Reference Example 2 Manufactured. Comparative Example 1 A magnetic tape was manufactured in the same manner as in Reference Example 1, except that the particle size of the abrasive was changed to 0.07 μm. Comparative Example 2 A magnetic tape was manufactured in the same manner as in Reference Example 1, except that the particle size of the abrasive was changed to 0.35 μm. Comparative Example 3 A magnetic tape was produced in the same manner as in Reference Example 1, except that the abrasive was changed to α-Al 2 O 3 having a particle size of 0.12 μm. Comparative Example 4 A magnetic tape was manufactured in the same manner as in Comparative Example 3, except that the particle size of the abrasive was changed to 0.21 μm. Comparative Example 5 A magnetic tape was manufactured in the same manner as in Comparative Example 3 except that the particle size of the abrasive was changed to 0.30 μm. Comparative Example 6 A magnetic tape was produced in the same manner as in Reference Example 2, except that α-Al 2 O 3 having a particle size of 0.20 μm coated with 1.20% of α-Fe 2 O 3 was used. Table 1 below shows the results of the characteristics of the above-described prototype magnetic recording medium. In the table, Br is the residual magnetic flux density, Bm is the saturation magnetic flux density, OR is the orientation ratio (the ratio of the magnetic flux density in the vertical direction / horizontal direction), and the unit of YS / N and CS / N is dB. [Table 1] The following can be confirmed from Table 1. When Comparative Examples 1, 2, and 3 with and without Si element are compared with Comparative Examples 3, 4, and 5, there is almost no difference in the magnetic characteristics, YS / N, and CS / N for each particle size. Although not seen, significant effects are seen on the adhesion of the magnetic head (number of clogging passes) and still life (durability of the magnetic tape). Comparison of the Presence or Absence of Fe Element When comparing Example 1 and Comparative Example 4, the magnetic properties, YS /
N and C / S / N also have an effect, and the number of clogging passes and still life (durability of magnetic tape) are also effective. As can be seen from Example 2 when Si and Fe elements are contained, there is a remarkable effect on durability and still life as in the case of using Si alone. Regarding the particle size when SiO 2 is adsorbed When the particle size is 0.07 μm, the number of clogging passes and still life are good as compared with the case where Si or Fe is not adsorbed.
It is inferior to those having a particle size of 0.10 to 0.30 μm. In the case of 0.35 μm, the number of clogging passes and still life are good, but YS / N and CS / N
Is inferior to that of 0.10 to 0.30 μm. this is,
It is considered that the surface roughness was deteriorated due to the large particle size, and a spacing loss with the head occurred. Regarding the difference between Fe element containing and α-Fe 2 O 3 coating,
Comparing Comparative Example 6 Example 1 Te. When coated with α-Fe 2 O 3 , the number of clogging passes and inferior to the case where still life is included are inferior. As described above, according to the present invention, the adhesion of the magnetic head (the number of clogging passes) is reduced without sacrificing the magnetic characteristics, and the still life of the magnetic recording medium (the durability of the magnetic tape) is achieved. Can be improved.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 畔上 仁 東京都中央区日本橋一丁目13番1号ティ ーディーケイ株式会社内 (56)参考文献 特開 昭63−96732(JP,A) 特開 平3−86918(JP,A)   ────────────────────────────────────────────────── ─── Continuation of front page    (72) Inventor Hitoshi Kamigami               1-13-1 Nihonbashi, Chuo-ku, Tokyo               ー Decay Corporation                (56) References JP-A-63-96732 (JP, A)                 JP-A-3-86918 (JP, A)

Claims (1)

(57)【特許請求の範囲】 【請求項1】 平均粒径0.10μ〜0.30μで、
0.5〜3.0%のFe元素、又は0.05〜0.30
%のSi元素及び0.5〜3.0%のFe元素を含有す
るα−Al23を磁性粉と共に結合剤中に分散せしめた
磁性塗料を非磁性支持体に塗布してなる磁気記録体にお
いて、前記のFe元素又はSi元素及びFe元素を含有
するα−Al 2 3 は、Fe元素を有する化合物又はSi
元素を有する化合物及びFe元素を有する化合物をα−
Al 2 3 の原料と混合し、焼成して得たものであること
を特徴とする磁気記録媒体。
(57) [Claims 1] An average particle size of 0.10μ to 0.30μ,
0.5 to 3.0% Fe element, or 0.05 to 0.30
% Of Si element and 0.5 to 3.0% of Fe magnetism of α-Al 2 O 3 containing elemental formed by a magnetic coating material was dispersed in a binder with a magnetic powder is applied to the nonmagnetic support All the recording medium
Containing the Fe element or the Si element and the Fe element
Α-Al 2 O 3 is a compound having Fe element or Si
The compound having the element and the compound having the Fe element are referred to as α-
Must be obtained by mixing with the raw material of Al 2 O 3 and firing
A magnetic recording medium characterized by the above-mentioned.
JP02265291A 1991-01-24 1991-01-24 Magnetic recording media Expired - Fee Related JP3362789B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP02265291A JP3362789B2 (en) 1991-01-24 1991-01-24 Magnetic recording media

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP02265291A JP3362789B2 (en) 1991-01-24 1991-01-24 Magnetic recording media

Publications (2)

Publication Number Publication Date
JPH04248119A JPH04248119A (en) 1992-09-03
JP3362789B2 true JP3362789B2 (en) 2003-01-07

Family

ID=12088778

Family Applications (1)

Application Number Title Priority Date Filing Date
JP02265291A Expired - Fee Related JP3362789B2 (en) 1991-01-24 1991-01-24 Magnetic recording media

Country Status (1)

Country Link
JP (1) JP3362789B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2922771B2 (en) * 1993-12-22 1999-07-26 ティーディーケイ株式会社 Magnetic recording medium and method of manufacturing the same

Also Published As

Publication number Publication date
JPH04248119A (en) 1992-09-03

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