JPS58164029A - Magnetic recording medium - Google Patents

Magnetic recording medium

Info

Publication number
JPS58164029A
JPS58164029A JP57045145A JP4514582A JPS58164029A JP S58164029 A JPS58164029 A JP S58164029A JP 57045145 A JP57045145 A JP 57045145A JP 4514582 A JP4514582 A JP 4514582A JP S58164029 A JPS58164029 A JP S58164029A
Authority
JP
Japan
Prior art keywords
magnetic
magnetic layer
capric acid
recording medium
carbon black
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
JP57045145A
Other languages
Japanese (ja)
Inventor
Masaya Funabashi
正也 船橋
Akito Sakamoto
章人 酒本
Kunio Mizushima
水島 邦夫
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.)
Maxell Ltd
Original Assignee
Hitachi Maxell 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 Maxell Ltd filed Critical Hitachi Maxell Ltd
Priority to JP57045145A priority Critical patent/JPS58164029A/en
Publication of JPS58164029A publication Critical patent/JPS58164029A/en
Pending legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G11INFORMATION STORAGE
    • G11BINFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
    • G11B5/00Recording by magnetisation or demagnetisation of a record carrier; Reproducing by magnetic means; Record carriers therefor
    • G11B5/62Record carriers characterised by the selection of the material
    • G11B5/68Record carriers characterised by the selection of the material comprising one or more layers of magnetisable material homogeneously mixed with a bonding agent
    • G11B5/70Record carriers characterised by the selection of the material comprising one or more layers of magnetisable material homogeneously mixed with a bonding agent on a base layer
    • G11B5/71Record carriers characterised by the selection of the material comprising one or more layers of magnetisable material homogeneously mixed with a bonding agent on a base layer characterised by the lubricant

Landscapes

  • Pigments, Carbon Blacks, Or Wood Stains (AREA)
  • Paints Or Removers (AREA)
  • Magnetic Record Carriers (AREA)

Abstract

PURPOSE:To enhance the wear resistance of a magnetic layer by adding a liq. hydrocarbon and capric acid to the layer optionally together with carbon black. CONSTITUTION:To a magnetic layer are added a liq. hydrocarbon such as liq. paraffin, squalane, squalene, synthetic squalane, synthetic squalene or polymerized oil or alpha-olefin and capric acid in 99:1-50:50 weight ratio. Carbon black having 40mmu average single particle size and 400ml/100g DBP oil absorption may be added furthermore.

Description

【発明の詳細な説明】 この発明は磁気記録媒体に関し、その目的とするところ
は耐久性に擾れた磁気記録媒体を提供することにある。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a magnetic recording medium, and an object thereof is to provide a magnetic recording medium with excellent durability.

一般に、ポリエステルフィルムなどの基体上に磁性粉末
、結合剤樹脂、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#e体は、記
録再生時に磁気ヘッドおよびパッドなどと檄しく摺接す
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 bodies are made by coating a magnetic paint consisting of magnetic powder, binder resin, organic solvent, and other necessary components on a substrate such as a polyester film, and are used as magnetic heads and pads during recording and reproduction. Because of the delicate sliding contact, the magnetic layer is easily abraded, and a magnetic layer that is less abrasive and has excellent durability is required.

このため磁性層の耐摩耗性を改善する一方策として磁性
層中に種々の潤fft剤を混入することが行なわれてお
り、たとえば合成スクアランや流動パラフィンなどの液
状炭化水素さらにはこれらの液状炭化水素とステアリン
酸とを磁性層中に混入したものが提案されている。
Therefore, as a measure to improve the wear resistance of the magnetic layer, various lubricating agents have been mixed into the magnetic layer.For example, liquid hydrocarbons such as synthetic squalane and liquid paraffin, and liquid carbonized A magnetic layer in which hydrogen and stearic acid are mixed has been proposed.

ところが、これらの鯛滑剤の混入によって耐摩耗性はた
しかに改善されるものの充分ではなく、特に合成スクア
ラン単独の場合には揮発し易く長時間良好な間滑効朱を
持続でさない難点がある。
However, although the abrasion resistance is certainly improved by the addition of these sea bream lubricants, it is not sufficient. In particular, when synthetic squalane is used alone, it easily volatizes and has the disadvantage that a good lubricating effect cannot be maintained for a long period of time.

この発明者らはかかる事情に鑑み種々検討を行なった結
果、液状炭化水素とカプリン酸とを磁性層中に含有させ
ると磁性層の耐摩耗性を充分に向上することができ、さ
らにこれらの液状炭化水素およびカプリン酸とともに平
均単一粒子径が40m、izでかつDBPI&油量が4
00 rnll / 100jFのカーボンブラックを
含有させると磁性層の摩擦係数が低下してさらに一段と
磁性層の耐摩耗性が向上されることを見いだし、この発
明をなすに至った。
The inventors conducted various studies in view of the above circumstances, and found that the abrasion resistance of the magnetic layer can be sufficiently improved by containing liquid hydrocarbons and capric acid in the magnetic layer. With hydrocarbon and capric acid, average single particle size is 40m, iz and DBPI & oil amount is 4
It was discovered that the inclusion of carbon black of 00 rnll / 100 jF lowers the friction coefficient of the magnetic layer and further improves the wear resistance of the magnetic layer, leading to the present invention.

この発明において使用する液状炭化水素とし一〇は、た
とえば、流動パラフィン、スクアラン、スクアレン、合
成スクアラン、ば成スクアレン、αオレフイン重合油な
どが好適なものとして使用される。この種の液状炭化水
素はいずれも常温で液状の膨化水素油で、優れた潤滑能
を有し、磁性層の耐摩耗性を向上する。
The liquid hydrocarbon used in this invention is preferably, for example, liquid paraffin, squalane, squalene, synthetic squalane, virgin squalene, α-olefin polymerized oil, or the like. All of these types of liquid hydrocarbons are expanded hydrogen oils that are liquid at room temperature, and have excellent lubrication ability and improve the wear resistance of the magnetic layer.

また、液状炭化水素と併用するカプリン酸は炭素数が1
0の飽和脂肪酸で、揮発性が低くて優れた潤滑持続効果
を有し、液状炭化水素と併用するとこの効果が発揮され
て磁性層の耐摩耗性が一段と向上されるとともに擾れた
耐摩耗性が長期にわたって持続される。
In addition, capric acid used in combination with liquid hydrocarbon has a carbon number of 1.
0 saturated fatty acid, has low volatility and excellent long-lasting lubrication effect, and when used in combination with liquid hydrocarbon, this effect is exhibited, further improving the wear resistance of the magnetic layer and reducing wear resistance. is sustained over a long period of time.

このようなカプリン酸の液状炭化水素に対する配合割合
は重量比(液状炭化水素対カプリン酸)で99対1〜5
0対50の範囲内となるようにするのが好ましく、カプ
リン酸の配合割合が少なすぎると充分な潤滑持続効果が
発揮されず、多すぎると耐久性が低下してくる。またこ
のような配合割合で配合した液状炭化水素とカプリン酸
の使用量は両者合わせて磁性粉末に対して0.1〜20
重指%の範囲内にするのが好ましく、少なすぎると所期
の効果が得られず、多すぎると磁性層表面にブリードア
ウトして磁気ヘッドを汚染し、出力を低下させるおそれ
がある。
The blending ratio of capric acid to liquid hydrocarbon is 99:1 to 5 by weight (liquid hydrocarbon to capric acid).
It is preferable to keep the ratio within the range of 0:50; if the blending ratio of capric acid is too small, sufficient lubrication sustaining effect will not be exhibited, and if it is too large, durability will decrease. In addition, the combined amount of liquid hydrocarbon and capric acid blended in this proportion is 0.1 to 20% of the magnetic powder.
It is preferable to keep the amount within the range of %. If it is too small, the desired effect cannot be obtained, and if it is too large, it may bleed out onto the surface of the magnetic layer, contaminating the magnetic head, and reducing the output.

液状炭化水素およびカプリン酸とともに併用するカーボ
ンブラックは、平均単一粒子径が40rrLμでかつD
BP吸油量が400 mfl/ 100&のものが好ま
しく使用され、このようなカーボンブラックの具体例と
しては、たとえば旭カーボン社製H5−500等が挙げ
られる。この種のカーボンプラッタは潤滑能を有し、磁
性層中に含有されると磁性層表面の摩擦係数を小さくし
て磁性層の耐摩耗性を向上する。従ってこの種のカーボ
ンブラックが、液状炭化水素およびカプリン酸とともに
併用されると磁性層の耐摩耗性が一段と向上され、耐久
性にしれた磁気記録媒体が得られる。使用量は磁性粉末
に対して3〜15重社%の範囲内で使用     +1
するのが好ましく、少なすぎると磁性層表面の摩擦係数
を充分に小さくして耐摩耗性を充分に向上することがで
きず、多すぎると相対的に磁性粉末の含有率が低下して
磁気特性に悪影響を及ぼすおそれがある。
The carbon black used together with the liquid hydrocarbon and capric acid has an average single particle size of 40rrLμ and D
A carbon black having a BP oil absorption of 400 mfl/100& is preferably used, and specific examples of such carbon black include H5-500 manufactured by Asahi Carbon Co., Ltd., and the like. This type of carbon platter has a lubricating ability, and when contained in the magnetic layer, reduces the coefficient of friction on the surface of the magnetic layer and improves the wear resistance of the magnetic layer. Therefore, when this type of carbon black is used together with a liquid hydrocarbon and capric acid, the wear resistance of the magnetic layer is further improved, and a durable magnetic recording medium can be obtained. The amount used is within the range of 3 to 15% of the magnetic powder +1
If it is too small, the coefficient of friction on the surface of the magnetic layer cannot be sufficiently reduced and the wear resistance cannot be sufficiently improved, and if it is too large, the content of magnetic powder will be relatively reduced and the magnetic properties will be deteriorated. may have an adverse effect on

液状炭化水素およびカプリン酸を磁性層中に含有させる
には、これらをノルマルヘキサンなどの適当な溶剤に溶
解し、溶解によって得られた溶液を予め形成した磁性層
に塗布もしくは噴霧するか、或いは逆に磁性層を上記溶
液中に浸漬して行なえばよく、またこれらを磁性粉末お
よび結合剤樹脂とともに混練して磁性層を形成すること
により含有させてもよい。また前記のカーボンブラック
は磁性粉末および結合剤樹脂とともに混練して磁性層を
形成することによって磁性層中に含有される。
In order to incorporate liquid hydrocarbons and capric acid into the magnetic layer, they can be dissolved in a suitable solvent such as n-hexane, and the resulting solution can be applied or sprayed onto a previously formed magnetic layer, or vice versa. This may be carried out by immersing the magnetic layer in the above solution, or it may be incorporated by kneading these together with magnetic powder and binder resin to form a magnetic layer. Further, the above-mentioned carbon black is incorporated into the magnetic layer by kneading it with a magnetic powder and a binder resin to form a magnetic layer.

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I Co含有r −Fe、O,磁性粉末  270重量部V
AGH(米国U 、C−C社製、塩化  80 〃ビニ
ル−酢醗ビニルービニ/レアル コール共重合体) N1432J  (日本ゼオン社製、  15 〃アク
リロニトリルーブタジェン 共重合体) コロネートしく日本ポリウレタン  10重量部工業社
製、三官能性低分子量イソ シアネート化合物) H8−500(旭カーボン社製、   34  〃カー
ボンブラック、平均単一粒子 径40rrLμ、DBP吸油亀400 rrLl/100F) α−Fe203粉末        11 〃メチルイ
ソブチルケトン    420 〃トルエン     
     420 〃この組成物をボールミル中で混合
分散して磁性塗料を調製し、この磁性塗料を厚さ75μ
のポリエステルフィルム両面に乾燥厚が3μとなるよう
に塗布、乾燥して磁性層を形成した。次いでこれを合成
スクアラン45重量部、カプリン酸5重量部、ノルマル
ヘキサン1000型針部からなる含浸溶液に短時間浸漬
し、乾燥後円板状に打ち抜いて磁気ディスクをつくった
Example I Co-containing r-Fe, O, magnetic powder 270 parts by weight V
AGH (manufactured by U.S.A., C-C, chloride 80 Vinyl-acetyl vinyl/real alcohol copolymer) N1432J (manufactured by Nippon Zeon Co., Ltd., 15 acrylonitrile-butadiene copolymer) Coronate Japan Polyurethane 10 parts by weight (manufactured by Kogyo Co., Ltd., trifunctional low molecular weight isocyanate compound) H8-500 (manufactured by Asahi Carbon Co., Ltd., 34 〃Carbon black, average single particle size 40rrLμ, DBP oil absorption turtle 400 rrLl/100F) α-Fe203 powder 11 〃Methyl isobutyl ketone 420 Toluene
420 This composition was mixed and dispersed in a ball mill to prepare a magnetic paint, and the magnetic paint was coated in a 75μ thick layer.
A magnetic layer was formed by coating both sides of the polyester film to a dry thickness of 3 μm and drying. Next, this was immersed for a short time in an impregnating solution consisting of 45 parts by weight of synthetic squalane, 5 parts by weight of capric acid, and a 1000-type n-hexane needle, and after drying, it was punched out into a disk shape to produce a magnetic disk.

実施例2 実施例1における磁性塗料の組成において、VA G 
Hの使用針を80重置部から40重鎖部に変更し、N1
432Jを省き、新たにバンデツクスT−5201(大
日本インキ化学工業社製、ウレタンエラストマー)を4
0重量部加え、さらにコロネー )Lの使用量を10重
量部から20重量部に変更した以外は実施例1と同様に
して磁気ディスクをつくった。
Example 2 In the composition of the magnetic paint in Example 1, VA G
Change the needle used for H from 80 overlapped part to 40 heavy chain part, and use N1
432J was omitted, and 4 new Bandex T-5201 (manufactured by Dainippon Ink & Chemicals Co., Ltd., urethane elastomer) was added.
A magnetic disk was produced in the same manner as in Example 1, except that 0 parts by weight was added and the amount of Coronae) L used was changed from 10 parts by weight to 20 parts by weight.

実施例3 実施例1における含浸溶液の組成において、合成スクア
ランに代えて流動パラフィンを同量使用した以外は実施
例1と同様にして磁気ディスクをつくった。
Example 3 A magnetic disk was produced in the same manner as in Example 1 except that the same amount of liquid paraffin was used in place of the synthetic squalane in the composition of the impregnating solution in Example 1.

実施例4 実施例1における磁性塗料の組成において、N5−50
0を省いた以外は実施例1と同様にして磁気ディスクを
つくった。
Example 4 In the composition of the magnetic paint in Example 1, N5-50
A magnetic disk was produced in the same manner as in Example 1 except that 0 was omitted.

比較例1 実施例1における含浸溶液の組成において、カプリン酸
を省いた以外は実施例1と同様にして磁気ディスクをつ
くった。
Comparative Example 1 A magnetic disk was produced in the same manner as in Example 1 except that capric acid was omitted from the composition of the impregnating solution in Example 1.

比較例2 実施例1における含浸溶液の組成において、合成スクア
ランを省いた以外は実施例1と同様にして磁気ディスク
をつくった。
Comparative Example 2 A magnetic disk was produced in the same manner as in Example 1 except that synthetic squalane was omitted from the composition of the impregnating solution in Example 1.

比較例3 実施例3における含浸溶液の組成において、カプリン酸
に代えてステアリン酸を同量使用した以外は実施例3と
同様にして磁気ディスクをっくった。
Comparative Example 3 A magnetic disk was prepared in the same manner as in Example 3 except that the same amount of stearic acid was used instead of capric acid in the composition of the impregnating solution in Example 3.

各実施例および各比較例で得られた磁気ディスクについ
て耐久性を調べるため、各磁気ディスクを汚れ防止用ジ
ャケットに挿入して記録再生装置に装填し、磁気ヘッド
をパッド圧251 / cm2で接触させて周速10m
/secで摺接させながら再生出力が初期出力の50%
になるまでの走行時間やよ、定、え。        
               ゛下表はその結果であ
る。
In order to examine the durability of the magnetic disks obtained in each example and each comparative example, each magnetic disk was inserted into a dirt prevention jacket and loaded into a recording/reproducing device, and the magnetic head was brought into contact with a pad pressure of 251/cm2. peripheral speed 10m
The playback output is 50% of the initial output while sliding at /sec.
The driving time until it becomes fixed, eh.
゛The table below shows the results.

上表から明らかなように、この発明によって得られた磁
気ディスク(実施例1〜4)はいずれも従来の磁気ディ
スク(比較例1〜3)に比し、走行時間が長く、このこ
とからこの発明によって得られる磁気記録媒体は耐久性
に優れていることがわかる。
As is clear from the table above, all of the magnetic disks obtained by the present invention (Examples 1 to 4) have longer running times than conventional magnetic disks (Comparative Examples 1 to 3), and therefore, this It can be seen that the magnetic recording medium obtained by the invention has excellent durability.

特許出願人  日立マクセル株式会社 代理人 高岡−春Patent applicant: Hitachi Maxell, Ltd. Agent Takaoka-Haru

Claims (1)

【特許請求の範囲】 1、液状炭化水素とカプリン酸とが含まれてなる磁性層
を有する磁気記録媒体 2、液状炭化水素と、カプリン酸と、平均単一粒子径が
40惜μでかつDBP吸油量が400m1/100fI
のカーボンブラックとが含まれてなる磁性層を有する磁
気記録媒体
[Scope of Claims] 1. A magnetic recording medium having a magnetic layer containing a liquid hydrocarbon and capric acid 2. A magnetic recording medium containing a liquid hydrocarbon, capric acid, and an average single particle size of 40 μm and DBP Oil absorption amount is 400m1/100fI
A magnetic recording medium having a magnetic layer containing carbon black.
JP57045145A 1982-03-20 1982-03-20 Magnetic recording medium Pending JPS58164029A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57045145A JPS58164029A (en) 1982-03-20 1982-03-20 Magnetic recording medium

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57045145A JPS58164029A (en) 1982-03-20 1982-03-20 Magnetic recording medium

Publications (1)

Publication Number Publication Date
JPS58164029A true JPS58164029A (en) 1983-09-28

Family

ID=12711107

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57045145A Pending JPS58164029A (en) 1982-03-20 1982-03-20 Magnetic recording medium

Country Status (1)

Country Link
JP (1) JPS58164029A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59186125A (en) * 1983-04-08 1984-10-22 Fuji Photo Film Co Ltd Magnetic recording medium
JPS59191133A (en) * 1983-04-13 1984-10-30 Fuji Photo Film Co Ltd Magnetic recording medium

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59186125A (en) * 1983-04-08 1984-10-22 Fuji Photo Film Co Ltd Magnetic recording medium
JPH0479061B2 (en) * 1983-04-08 1992-12-14 Fuji Photo Film Co Ltd
JPS59191133A (en) * 1983-04-13 1984-10-30 Fuji Photo Film Co Ltd Magnetic recording medium
JPH0479062B2 (en) * 1983-04-13 1992-12-14 Fuji Photo Film Co Ltd

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