JPS5829126A - Magnetic recording medium - Google Patents

Magnetic recording medium

Info

Publication number
JPS5829126A
JPS5829126A JP12800781A JP12800781A JPS5829126A JP S5829126 A JPS5829126 A JP S5829126A JP 12800781 A JP12800781 A JP 12800781A JP 12800781 A JP12800781 A JP 12800781A JP S5829126 A JPS5829126 A JP S5829126A
Authority
JP
Japan
Prior art keywords
magnetic
powder
coupling agent
magnetic powder
oligomer
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
JP12800781A
Other languages
Japanese (ja)
Inventor
Atsutaka Yamaguchi
山口 温敬
Masaaki Yasui
安井 正昭
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 JP12800781A priority Critical patent/JPS5829126A/en
Publication of JPS5829126A publication Critical patent/JPS5829126A/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
    • G11B5/7013Record 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 dispersing agent

Landscapes

  • Lubricants (AREA)
  • Paints Or Removers (AREA)
  • Magnetic Record Carriers (AREA)

Abstract

PURPOSE:To obtain a magnetic recording medium having superior magnetic characteristics and superior surface smoothness of the magnetic layer and contg. magnetic powder with high dispersibility and fillability by hardening a coated film contg. a specified coupling agent, a specified oligomer and magnetic powder under radiation so as to produce the magnetic layer. CONSTITUTION:A coated film contg. a titanium coupling agent represented by the general formula, an oligomer obtd. by bonding acrylic acid or methacrylic acid to a terminal of oligoester consisting of phthalic acid and alkylene glycol by esterification, and magnetic powder, is formed on a substrate and hardened by irradiation to produce a magnetic layer. The perferred amount of the coupling agent to be used is 0.1-10wt% of the amount of the magnetic powder in the magnetic layer, and that of the oligomer to be used is 20-60wt% of the total amount of the powder and the coupling agent.

Description

【発明の詳細な説明】 この発明は磁気記録媒体に関し、その目的とすると仁ろ
は磁性粉末の分散性および充填性が良好で磁気特性およ
び磁性層の表面平滑性に優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 its purpose is to provide a magnetic recording medium with good dispersibility and filling properties of magnetic powder, and excellent magnetic properties and surface smoothness of the magnetic layer. It's about doing.

磁気記録媒体は、通常、磁性粉末、結合剤成分、有機溶
剤およびその他の必要成分からなる磁性塗料をポリエス
テルフィルムなどの基体上に塗布、乾燥してつくられ、
磁気特性および表面平滑性に優れるとともに耐久性に優
れたものが要求される。
Magnetic recording media are usually made by applying a magnetic paint consisting of magnetic powder, a binder component, an organic solvent, and other necessary components onto a substrate such as a polyester film, and drying the coating.
It is required to have excellent magnetic properties and surface smoothness, as well as excellent durability.

そのため磁性粉末の分散性に優れた結合剤成分を選定し
たり、あるいは磁性粉末をたとえばアルキルチタネート
などの分散剤等で処理するなどの方法で磁性粉末の分散
性を改善することによって、磁気特性および磁性層の表
面平滑性を向上し、また耐摩耗性を改善する試みがなさ
れているが、未だ充分に満足できるものではなく、その
上この方法では磁性塗料調製時に結合剤成分を溶解する
有害な有機溶剤を大量に使用するため公害上の問題があ
る。
Therefore, the magnetic properties and Attempts have been made to improve the surface smoothness and abrasion resistance of the magnetic layer, but they are still not fully satisfactory, and furthermore, this method involves the harmful effects of dissolving binder components during the preparation of magnetic coatings. There are pollution problems because large amounts of organic solvents are used.

そこで、これを改善する方法として、近年、ウレタンア
クリレートオリゴマーなどの種々のオリゴマーを磁性粉
末およびその他の必要成分とともに混合分散して磁性塗
料を調製し、この磁性塗料−を基体上に塗布後、放射線
を照射しオリゴマーを放射線重合させて磁性層を形成す
る方法が提案されているが、この方法では公害上の問題
は改善されるものの、磁性粉末の分散性の改善および充
填性はいまひとつ充分ではなく、未だ充分に満足できる
結果は得られていない。
Therefore, as a method to improve this, in recent years, various oligomers such as urethane acrylate oligomers are mixed and dispersed with magnetic powder and other necessary components to prepare magnetic paint, and after coating this magnetic paint on a substrate, radiation A method has been proposed in which a magnetic layer is formed by irradiating the oligomer with radiation and polymerizing the oligomer, but although this method improves the pollution problem, it is still insufficient in improving the dispersibility and filling properties of the magnetic powder. However, fully satisfactory results have not yet been obtained.

この発明者らはかかる現状に鑑み種々検討を行なった結
果、基体上に、一般式 %式%) (但し、式中8は炭化水素基、Xは一〇〇またはsag
eあるいは−PO(OH)−0−PO。
The inventors conducted various studies in view of the current situation, and found that the general formula (%) (%) (in the formula, 8 is a hydrocarbon group, and X is 100 or sag
e or -PO(OH)-0-PO.

Yは炭化水素基または→0−ILt)tであってB1は
アルキル基である。) で示されるチタンカップリング剤と、フタル酸とアルキ
レングリコールからなるオリゴエステルの末端にアクリ
ル酸またはメタクリル酸をエステル結合させたオリゴマ
ーと、磁性粉末と卆含む磁性塗料を塗布し、次いで放射
線を照射し前記オリゴマーを重合硬化して磁性層を形成
すると、公害上の問題もなく、磁性粉末の分散性および
充填性が充分に改善されて磁気特性および磁性層の表面
平滑性が一段と向上することを見いだし、この発明をな
すに至った。
Y is a hydrocarbon group or →0-ILt)t, and B1 is an alkyl group. ), a magnetic paint containing a titanium coupling agent shown in the formula, an oligomer consisting of phthalic acid and alkylene glycol with acrylic acid or methacrylic acid ester bonded to the terminal end, and magnetic powder, and then irradiated with radiation. However, if the above oligomer is polymerized and cured to form a magnetic layer, there will be no pollution problems, and the dispersibility and filling properties of the magnetic powder will be sufficiently improved, and the magnetic properties and surface smoothness of the magnetic layer will be further improved. I discovered this and came up with this invention.

この発明で使用される前記一般式のチタンカップリング
剤は、磁性粉末と接すると粉末粒子表両上の水酸基と強
力に反応し、チタン原子と−ORとの結合が切れてチタ
ン原子が磁性粉末の表面に酸素を介して強固に結合する
。従ってこの種のテ、タンカップリング剤が′磁性層中
に含有されると磁性粉末の粒子表面に強固に被着し、被
膜が形成されて磁性粉末の分散性が充分に改善され、ま
たこの種のチタンカップリング剤は特に磁性塗料の粘度
を低下する作用が優れているため磁性粉末の充填性も充
分に改善されて磁気特性および磁性層の表面平滑性が一
段と向上する。仁のようなチタンカップリング剤の具体
例としては、たとえば下記の構造式で表わされるケンリ
ツヒペトロケミカル社製プレンアクトTTS、ブレンア
クト98、ブレンアクト888等が挙げられる。
When the titanium coupling agent of the general formula used in this invention comes into contact with magnetic powder, it reacts strongly with the hydroxyl groups on both sides of the powder particle surface, and the bond between the titanium atom and -OR is broken and the titanium atom is transferred to the magnetic powder. It is strongly bonded to the surface of the substance via oxygen. Therefore, when this kind of coupling agent is contained in the magnetic layer, it will firmly adhere to the surface of the magnetic powder particles, forming a film and sufficiently improving the dispersibility of the magnetic powder. The titanium coupling agent has a particularly excellent effect of lowering the viscosity of the magnetic coating material, so that the filling properties of the magnetic powder are sufficiently improved, and the magnetic properties and surface smoothness of the magnetic layer are further improved. Specific examples of such titanium coupling agents include PlenAct TTS, BlenAct 98, and BlenAct 888 manufactured by Kenritzhi Petrochemical Co., Ltd., which are represented by the following structural formulas.

ブレンアクトT’I’8(イソプロピルトリイソステア
ロイルチタネート) ブレンアクト9S(イソプロピルトリデシルベンゼンス
ルホニルチタネート) ブレンアクト88S〔イソプロピルトリス(ジオクチル
パイロホスフェート)チタネート〕これらのチタンカッ
プリング剤は、これらを適当な溶剤中に溶解させ、この
溶解によって得られた溶液を磁性塗料の調製時に添加す
るか、あるいはこの溶液中に磁性粉末を浸漬して予め磁
性粉末の表面処理を行ない、この磁性粉末を使用して磁
性塗料を調製するなどの方法で磁性塗料中に含有され、
使用される。使用量は磁性層中の磁性粉末に対して0.
1重量%より少ないと所期の効果が得られず、10′M
Jii%を越えるとブリードアウトするおそれがあるた
め0.1〜10重量%の範囲内であることが好ましく、
0.5〜5重量%の範囲内で使用するのがより好ましい
BlenAct T'I'8 (isopropyl triisostearoyl titanate) BlenAct 9S (isopropyl tridecylbenzenesulfonyl titanate) BlenAct 88S [isopropyl tris (dioctyl pyrophosphate) titanate] These titanium coupling agents Either dissolve it in a solvent and add the solution obtained by this dissolution when preparing magnetic paint, or immerse the magnetic powder in this solution to pre-treat the surface of the magnetic powder, and use this magnetic powder. Contained in magnetic paint by methods such as preparing magnetic paint,
used. The amount to be used is 0.0% based on the magnetic powder in the magnetic layer.
If it is less than 1% by weight, the desired effect cannot be obtained, and 10'M
If it exceeds Jii%, there is a risk of bleed-out, so it is preferably within the range of 0.1 to 10% by weight.
It is more preferable to use it within the range of 0.5 to 5% by weight.

また、この発明において使用されるフタル酸とアルキレ
ングリコールからなるオリゴエステルの末端にアクリル
酸またはメタクリル酸をエステル結合させたオリゴマー
リ、一般式 %式% ( 0((!H,) −000−1R,は炭化水素基、nは
1〜20の整数である。) で示されるオリゴマーで、分子量500〜20,000
のものが好適なものとして使用される。この種のオリゴ
エステルアクリレート′およびオリゴエステルメタクリ
レートは低粘度で磁性粉末の充填性がよく、前記のチタ
ンカップリング剤と併用されるとさらに粘度が低くなる
ため磁性粉末の充填性が充分に改善され、また磁性粉末
および前記のチタンカップリング剤とともに基体上に塗
布された後放射線の照射を受けると、末端あるいは両末
端の二重結合が開いて重合または架橋結合し、磁性粉末
の充填性に優れるとともに適度に重合硬化された磁性層
が形成されて磁気特性および磁性層の表面平滑性が一段
と向上されるとともに耐摩耗性も改善される。使用量は
磁性粉末との合計量に対して20〜60重量%の範囲内
であることが好ましく、少なすぎると所期の効果が得ら
れず、多すぎると磁性粉末の含率が低くなりすぎ良好な
電磁変換特性が得られない。
In addition, the oligomer used in this invention, which has acrylic acid or methacrylic acid ester bonded to the end of the oligoester consisting of phthalic acid and alkylene glycol, has the general formula % formula % (0((!H,) -000-1R , is a hydrocarbon group, and n is an integer of 1 to 20.) with a molecular weight of 500 to 20,000.
are preferably used. This type of oligoester acrylate' and oligoester methacrylate has a low viscosity and has good filling properties for magnetic powder, and when used in combination with the titanium coupling agent mentioned above, the viscosity becomes even lower and the filling property for magnetic powder is sufficiently improved. Also, when it is applied to a substrate together with magnetic powder and the titanium coupling agent and then irradiated with radiation, the double bond at the end or both ends opens and polymerizes or crosslinks, giving the magnetic powder excellent filling properties. At the same time, a suitably polymerized and hardened magnetic layer is formed, and the magnetic properties and surface smoothness of the magnetic layer are further improved, and the wear resistance is also improved. The amount used is preferably within the range of 20 to 60% by weight based on the total amount of magnetic powder. If it is too small, the desired effect cannot be obtained, and if it is too large, the content of magnetic powder will be too low. Good electromagnetic conversion characteristics cannot be obtained.

前記のオリゴマーを重合および架橋結合させるに際して
使用される放射線は、電子線などのβ線、および紫外線
、X線などのγ線などがいずれも・好適に使用され、紫
外線を使用するときは照射による効果をより効率的にす
るため増感剤が同時に使用される。このような放射線の
照射は加速電圧150〜750KVの放射線を用い、吸
収線量が8〜15Mr&11  となるように照射する
のが好ましく、吸収線量が少なすぎると前記オリゴマー
の架橋結合が不充分で所期の効果が得られな・い。
The radiation used to polymerize and crosslink the oligomers mentioned above is preferably beta rays such as electron beams, and gamma rays such as ultraviolet rays or X-rays. Sensitizers are used simultaneously to make the effect more efficient. It is preferable to irradiate such radiation using radiation with an accelerating voltage of 150 to 750 KV so that the absorbed dose is 8 to 15 Mr&11. If the absorbed dose is too small, the crosslinking of the oligomers will be insufficient and the desired result will not be achieved. I can't get the desired effect.

この発明に使用する磁性粉末としては、たとえば1−F
egO@粉末、Fe@04粉末、CO含有r  Fe1
on粉末、CO含4iiFe@04粉末、0r02粉末
の他、Fe粉末、Co粉末、Fe−N1Hj末などの金
属粉末など従来公知の各種磁性粉末が広く包含され、特
に金属粉末は表面に薄い酸郵膜層を形成させて用いると
、前記のチタンカップリング剤を併用した効果が大きく
なる。
Examples of the magnetic powder used in this invention include 1-F
egO@ powder, Fe@04 powder, CO containing r Fe1
In addition to on powder, CO-containing 4iiFe@04 powder, and 0r02 powder, various conventionally known magnetic powders such as Fe powder, Co powder, and metal powder such as Fe-N1Hj powder are widely included. When a film layer is formed and used, the effect of using the titanium coupling agent in combination becomes greater.

この発明の磁性層を基体上に形成するには、前記のオリ
ゴマー中に、磁性粉末と溶剤中に溶解した前記のチタン
カップリング剤とを分散混合するか、または前記のチタ
ンカップリング剤で予め表面処理した磁性粉末を分散混
合して磁性塗料を調製し、これをポリエステルフィルム
などの基体上に塗布した後、放射線を照射して重合硬化
させるか、あるいは前記のオリゴマーを有機溶剤に溶解
し、この溶波に前記と同様にして磁性粉末とチタンカッ
プリング剤またはチタンカップリング剤で表面処理した
磁性粉末を分散混合して磁性塗料を調製し、これをポリ
エステルフィルムなどの基体上に塗布し、予備加熱を行
なって磁性塗料中に含まれる有機溶剤を除去した後、放
射線を照射して重合硬化することによって行なわれる。
To form the magnetic layer of the present invention on a substrate, magnetic powder and the titanium coupling agent dissolved in a solvent are dispersed and mixed in the oligomer, or the titanium coupling agent is preliminarily mixed with the titanium coupling agent. A magnetic paint is prepared by dispersing and mixing the surface-treated magnetic powder, and after coating this on a substrate such as a polyester film, it is polymerized and cured by irradiation with radiation, or the oligomer is dissolved in an organic solvent, Magnetic powder and a titanium coupling agent or magnetic powder whose surface has been treated with a titanium coupling agent are dispersed and mixed in this melt wave in the same manner as described above to prepare a magnetic paint, and this is applied onto a substrate such as a polyester film. This is done by preheating to remove the organic solvent contained in the magnetic paint and then irradiating it with radiation to polymerize and harden it.

この際有機溶剤を使用する場合には磁性塗料の粘度がよ
り低くなるため磁性粉末の充填性がさらに向上し、磁気
特性および磁性層の表面平滑性はさらに一段と向上され
る。このような有機溶剤としては、メチルイソブチルケ
トン、シクロヘキサノン、トルエン、ジメチルホルムア
ミドなど従来一般に磁性塗料を調製する際に使用される
溶剤をいずれも好適に使用できるが、前記のオリゴマー
は有機溶剤に対する溶解性が良好なため、エタノール、
n −へブタン、n−ヘキサンなどの低沸点で毒性の弱
い溶剤も好適に使用することができ、従ってこれらの低
沸点で毒性の低い溶剤を使用すれば公害上の問題も解消
され、また磁性塗料塗布後の予備加熱によってこれら低
沸点の溶剤は容易に除去されるため溶剤の回収も容易に
なる。
In this case, when an organic solvent is used, the viscosity of the magnetic paint becomes lower, so that the filling properties of the magnetic powder are further improved, and the magnetic properties and surface smoothness of the magnetic layer are further improved. As such an organic solvent, any of the solvents conventionally used in preparing magnetic paints, such as methyl isobutyl ketone, cyclohexanone, toluene, and dimethylformamide, can be suitably used. Because ethanol is good,
Solvents with low boiling points and low toxicity such as n-hebutane and n-hexane can also be suitably used. Therefore, if these low boiling point and low toxicity solvents are used, pollution problems will be solved, and magnetic These low boiling point solvents can be easily removed by preheating after coating the paint, making it easy to recover the solvent.

なお、磁性塗料中には必要に応じて通常使用されている
各種添加剤、たとえば分散剤、研磨剤、帯電防止剤など
を適宜に添加使用してもよい。
In addition, various commonly used additives such as dispersants, abrasives, antistatic agents, etc. may be appropriately added to the magnetic coating material as necessary.

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1 構造式 で表わされるオリゴエステルアクリルオリゴマーを使用
し、 CO含有1−FegO1磁性粉末      60重量
部オリゴエステルアクリルオリゴマー    40 々
ブレンアクト98(ケンリツヒペトロケミカノ→m、2
  #イソブロビルトリデシルベンゼンスルカニルチタ
ネート)エチルアルコール/メチルエチルケトン 25
 ケ混合溶剤(混合比1/1) の組成からなる組成物をボールミルで72時間混合分散
して磁性塗料を調製し、この磁性塗料を厚さ15μのポ
リエステルベースフィルム上に塗膜厚が4μとなるよう
に塗布した。次いで90℃で1 分間予備加熱を行なっ
てエチルアルコール/メチルエチルケトン配合溶剤を除
去した後、日新ハイボルテージ社製EPS−750を用
い、7Mraclの照射線量で電子線を照射して硬化し
、カレンダー処理後所定の巾に裁断して磁気テープをつ
くった。
Example 1 Using an oligoester acrylic oligomer represented by the structural formula, CO-containing 1-FegO1 magnetic powder 60 parts by weight Oligoester acrylic oligomer 40
#Isobrobyl tridecylbenzenesulcanyl titanate) ethyl alcohol/methyl ethyl ketone 25
A magnetic paint was prepared by mixing and dispersing a composition consisting of a mixed solvent (mixing ratio 1/1) in a ball mill for 72 hours, and this magnetic paint was coated on a 15μ thick polyester base film to a coating thickness of 4μ. I applied it to make it look like this. Next, after preheating at 90°C for 1 minute to remove the ethyl alcohol/methyl ethyl ketone mixed solvent, the resin was cured by irradiation with an electron beam at a dose of 7 Mracl using Nissin High Voltage EPS-750, and then calendered. After that, it was cut to a specified width to make magnetic tape.

実施例2 実施例1における磁性塗料の組成において、エチルアル
コール/メチルエチルケトン混合溶剤を省き、オリゴエ
ステルアクリルオリゴマーの使用量を40M量部から4
5重量部に変更し、さらに予備加熱を省略した以外は実
施例1と同様にして磁気テープをつくった。
Example 2 In the composition of the magnetic paint in Example 1, the ethyl alcohol/methyl ethyl ketone mixed solvent was omitted, and the amount of oligoester acrylic oligomer used was changed from 40M parts to 4 parts.
A magnetic tape was produced in the same manner as in Example 1 except that the amount was changed to 5 parts by weight and the preheating was omitted.

比較例1 実施例1における磁性塗料の組成において、プレンアク
ト9Sを省いた以外は実施例1と同様にして磁気テープ
をつ(つた。
Comparative Example 1 A magnetic tape was prepared in the same manner as in Example 1 except that Preact 9S was omitted from the composition of the magnetic paint in Example 1.

比較例2 実施例1における磁性塗料の組成薯こおし)で、ブレン
アクト9Sに代えてテトラステアリルチタネート(Ti
 (001sHs丁)4〕を同量使用した以外番よ実施
例1と同様にして磁気テープをつくった。
Comparative Example 2 The composition of the magnetic paint in Example 1 was changed to tetrastearyl titanate (Ti) instead of Blenact 9S.
A magnetic tape was prepared in the same manner as in Example 1 except that the same amount of (001sHs 4) was used.

各実施例および各比較例で得られた磁気テープについて
、ビデオSN比およびカラー8N比を測定した。ビデオ
8N比およびカラー8N比は得られた磁気テープをビデ
オデツキ(日立製作所社製V’I’−5000)に装填
して記録再生を行な0、シバツク社製カラービデオノイ
ズメーター9260で測定し、比較例1で得られた磁気
テープのビデオ8N比およびカラーSN比を0としてそ
れとの差で表わした。
The video S/N ratio and color 8N ratio were measured for the magnetic tapes obtained in each Example and each Comparative Example. The video 8N ratio and the color 8N ratio were measured by loading the obtained magnetic tape into a video deck (V'I'-5000 manufactured by Hitachi, Ltd.) and performing recording and playback, and using a color video noise meter 9260 manufactured by Sibaku Corporation. The video 8N ratio and color SN ratio of the magnetic tape obtained in Comparative Example 1 were assumed to be 0, and the difference therebetween was expressed.

上表から明らかなように、この発明で得られた磁気テー
プ(実施例1および2)は、従来の磁気。
As is clear from the above table, the magnetic tapes obtained by this invention (Examples 1 and 2) are different from conventional magnetic tapes.

テープ(比較例1および2)に比し、ビデオ8N比およ
びカラー8N比がいずれも高く、このことからこの発明
によって得られる磁気記録媒体番よ磁性粉末の分散性お
よび充填性に優れ、磁気特性および磁性層の表面平滑性
が一段と向上されてt)ることかわかる。
Compared to the tape (Comparative Examples 1 and 2), both the video 8N ratio and the color 8N ratio are higher, which indicates that the magnetic recording medium obtained by the present invention has excellent dispersibility and filling properties of the magnetic powder, and has excellent magnetic properties. It can be seen that the surface smoothness of the magnetic layer is further improved.

Claims (1)

【特許請求の範囲】 1、基体上に、一般式 %式%) (但し、式中凰は炭化水素基、Xは−coまた1t−8
0,イ)あるい1i−PO(OR)−0−PO,。 Yは炭化水素基または→0−Rl)、であってR1はア
ルキル基である。) で示されるチタンカップリング剤と、フタル酸とアルキ
レングリコールからなるオリゴエステルの末端にアクリ
ル酸またはメタクリル酸をエステル結合させたオリゴマ
ーと、磁性粉末とを含む塗膜を形成し、これに放射線を
照射して硬化された磁性層を設けたことを特徴とする磁
気記録媒体
[Claims] 1. On the substrate, the general formula %) (However, in the formula, 凰 is a hydrocarbon group, and X is -co or 1t-8
0, a) or 1i-PO(OR)-0-PO,. Y is a hydrocarbon group or →0-Rl), and R1 is an alkyl group. ), a coating film containing a titanium coupling agent shown by the formula, an oligomer made of an oligoester consisting of phthalic acid and alkylene glycol with acrylic acid or methacrylic acid ester bonded to the end, and magnetic powder is formed, and this is exposed to radiation. A magnetic recording medium characterized by having a magnetic layer hardened by irradiation.
JP12800781A 1981-08-15 1981-08-15 Magnetic recording medium Pending JPS5829126A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12800781A JPS5829126A (en) 1981-08-15 1981-08-15 Magnetic recording medium

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12800781A JPS5829126A (en) 1981-08-15 1981-08-15 Magnetic recording medium

Publications (1)

Publication Number Publication Date
JPS5829126A true JPS5829126A (en) 1983-02-21

Family

ID=14974160

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12800781A Pending JPS5829126A (en) 1981-08-15 1981-08-15 Magnetic recording medium

Country Status (1)

Country Link
JP (1) JPS5829126A (en)

Similar Documents

Publication Publication Date Title
DE1929171A1 (en) Layer magnetogram carrier
DE1929931C3 (en) Magnetic recording medium
DE2834760C3 (en) Thermosetting liquid mass
JPS5829126A (en) Magnetic recording medium
JPH065575B2 (en) Method of manufacturing magnetic recording medium
JPS5829129A (en) Magnetic recording medium
JPS5829133A (en) Magnetic recording medium
JPS5829125A (en) Magnetic recording medium
JPS5829139A (en) Magnetic recording medium
JPS5829130A (en) Magnetic recording medium
JPS5829140A (en) Magnetic recording medium
JPS5829127A (en) Magnetic recording medium
DE3727197C2 (en) Magnetic recording medium and method for its production
JPS5829132A (en) Magnetic recording medium
JPS5829141A (en) Magnetic recording medium
JPS5829134A (en) Magnetic recording medium
JPS5829144A (en) Magnetic recording medium
JPS5829128A (en) Magnetic recording medium
JPS5829136A (en) Magnetic recording medium
JPS5829135A (en) Magnetic recording medium
JPS5829131A (en) Magnetic recording medium
JPS5829137A (en) Magnetic recording medium
JPS5829143A (en) Magnetic recording medium
JPS5829124A (en) Magnetic recording medium
JPS5829138A (en) Magnetic recording medium