JPS5979428A - Magnetic recording medium - Google Patents

Magnetic recording medium

Info

Publication number
JPS5979428A
JPS5979428A JP19019082A JP19019082A JPS5979428A JP S5979428 A JPS5979428 A JP S5979428A JP 19019082 A JP19019082 A JP 19019082A JP 19019082 A JP19019082 A JP 19019082A JP S5979428 A JPS5979428 A JP S5979428A
Authority
JP
Japan
Prior art keywords
magnetic recording
recording medium
polyurethane resin
resin
magnetic
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.)
Granted
Application number
JP19019082A
Other languages
Japanese (ja)
Other versions
JPH0456369B2 (en
Inventor
Tsumoru Ohata
積 大畠
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.)
Sony Corp
Original Assignee
Sony Corp
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 Sony Corp filed Critical Sony Corp
Priority to JP19019082A priority Critical patent/JPS5979428A/en
Publication of JPS5979428A publication Critical patent/JPS5979428A/en
Publication of JPH0456369B2 publication Critical patent/JPH0456369B2/ja
Granted 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
    • G11B5/702Record 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 bonding agent
    • G11B5/7021Record 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 bonding agent containing a polyurethane or a polyisocyanate

Abstract

PURPOSE:To eliminate deterioration in shape due to repeated uses in environments of various temps. by using a mixture of a polyurethane resin having hydrophilic groups introduced, especially such a resin having high glass transition point Tg and high dispersibility, and other specified binders mixed in a specified range. CONSTITUTION:The binder is composed of 10-40wt% cellulose deriv. 30- 70wt% polyurethane resin having hydrophilic groups, such as formula I , introduced (M is H, Li, Na, or K, and M' is M or alkyl CnH2n+1), and 5-20wt% butadiene-acrylonitrile copolymer. Especially, as highly dispersible polyurethane resin, the resin having many so-called hard segments in one molecule, and >=30 deg.C glass transition point are used. As a result, hardness of the coat and stiffness of the whole body of a magnetic recording medium are enhanced, deformation is reduced, and thermal stability is also raised.

Description

【発明の詳細な説明】 、42発明はヒデオ用或いはオーディオ用等の磁気記録
テープ、硝気ディスク等に用いられ゛ζ好適な(磁気記
録媒体に係り、特に優れた耐摩耗11tを有すと、と同
時に1lii分11&性で、繰り返し操作後の形状劣化
か小さい磁気記録媒体を提イハするものである。
[Detailed Description of the Invention] The 42 invention relates to a magnetic recording medium suitable for use in magnetic recording tapes for video or audio, nitric disks, etc., and has particularly excellent wear resistance. At the same time, the present invention proposes a magnetic recording medium that is 11 times smaller than the previous one and exhibits less deterioration in shape after repeated operations.

fX−;l:、その(1911層が磁性Hの塗119よ
りなるいわゆる塗布型磁気記録媒体における機械的及び
物理的特性の向にを図るために、これに用いられる結合
剤の組成には種々の研究開発がなされている。
fX-;l:, In order to improve the mechanical and physical properties of a so-called coated magnetic recording medium in which the (1911 layer is coated with magnetic H), various compositions of the binder used therein are used. Research and development is being carried out.

例えばその耐久性及び電磁変換特性を向」−さ−ける1
」的°乙セルロース誘導体、ボリウレクン樹脂及びブタ
ジエンーアクリロニトル共重合体を所定の範囲で混入し
゛C使使用]るごとか提案されている。
For example, to improve its durability and electromagnetic conversion properties.
It has been proposed that a cellulose derivative, a polyurethane resin, and a butadiene-acrylonitrile copolymer be mixed within a predetermined range.

しかしながら、磁気記録分野のイこ展と共に磁気媒体に
対し“ζ一層の晶性能化が求められ°Cいζ、その磁気
特性の向」―や苛酷な使用条件にお&Jる耐久性の向上
、史には磁気記録媒体のY+VH’A化に伴う形状劣化
等の機械的強度の向」二が大きな問題点となっている。
However, with the advancement of the magnetic recording field, there is a need for magnetic media to further improve its crystal performance and its magnetic properties, and to improve its durability under harsh usage conditions. Historically, the decline in mechanical strength, such as shape deterioration, has become a major problem with the Y+VH'A magnetic recording medium.

すなわち、このような形状劣化が起きると例えばビデオ
テープにおいては、テープ両側に記録されζいるCTL
信号やオーディオ信号に乱れ′が生じる。また、近年で
はステレオ化が標準となってき°ζいるので多少の形状
劣化でも左右のバランスが崩れるので大きな問題となる
In other words, when such shape deterioration occurs, for example, in a video tape, the CTL recorded on both sides of the tape
Disturbances occur in the signal or audio signal. In addition, in recent years, stereo has become the standard, so even slight deterioration in the shape can cause the left and right balance to collapse, which poses a major problem.

本発明は上述した要求に対する磁気記録媒体の磁性層の
分散性、耐久性の向上を図るものである。
The present invention aims to improve the dispersibility and durability of the magnetic layer of a magnetic recording medium in response to the above-mentioned requirements.

本発明においては、特に−3O3M 、’ −C00M
、の高い11″lf分11に性ポリウレタン樹脂と他の
特定したバインターとを+1♀定範囲で混合使用するこ
とにより前述した諸問題の解決化を図ったものである。
In the present invention, especially -3O3M,'-C00M
The above-mentioned problems are solved by mixing and using a polyurethane resin having a high 11''lf content and another specified binder in a +1♀ specific range.

ずなわぢ、本発明においζは、非磁性支持体」−に磁性
1′5)と結合剤を主成分とする磁性層を塗布形成゛4
′るものであるが、I侍に本発明においζはその等の親
水性見開を導入しノ、−ポリウレタン樹脂が30・〜・
マ(INlj IMI94(但しMはtl 、L ’+
 + N aまたはに、M’はIt、  Li、NB、
Kまたはアルキル基Cn”2n−+−+ )とツタジエ
ン−アクリIIに1〜リル共市合体5〜20ii’i 
j書%を含f+’ L、て成る。
Zunawaji, in the present invention, ζ is formed by coating a magnetic layer mainly composed of magnetic 1'5) and a binder on a non-magnetic support.
However, in the present invention, the polyurethane resin is 30...
M(INlj IMI94 (However, M is tl, L'+
+ Na or M' is It, Li, NB,
K or alkyl group Cn"2n-+-+) and 1 to lyl co-merged with tutadiene-acrylic II 5 to 20ii'i
It consists of f+' L, including J%.

ltlrに+1°I+’分子lk t!Iポリウレタン
樹1指としζは、好ましくは、分子・1″1格中にいわ
ゆるハードセクメントを多く含むカラス転移n;tTg
が30℃以十のらのを用いるもので、このとき塗I9の
硬度が高められ、磁気記録媒体全体のスティフネスが1
11.められ、変形の少ない、!;ハ的にも安定化が図
られる。
+1°I+' molecule lk t to ltlr! I polyurethane tree 1 finger ζ is preferably a crow transition n;tTg containing many so-called hard segments in the molecule 1″1 case.
The hardness of coating I9 is increased, and the stiffness of the entire magnetic recording medium is reduced to 1.
11. Less distortion and less deformation! ; C) Stabilization is also achieved.

■1ミた、ここにシタジエン−゛rクリ■二トル共合体
体を用いるのは、磁性層オー1のレースリンク性を改善
すると共に塗;防に柔軟性をイーj?−5−4ることが
できるためごあり、このブタジェン−アクリ11ニトル
共用合体を5へ・201[量%に選定するのは5市It
 %未ンAでは」二jホしたレー・リンク及び柔軟性の
改善の勿J果が表われ一4゛、またこれが20市量%を
越えると塗膜のhす!さが低士し過ぎるごとによる。ま
た、このフタソコーンー7クリロニ1−ル共車合体のア
クリロニ[−リルの含有量は35%へ・4596がポリ
ウレタンとの相溶111に1くれ”Cいて好ましい。
■1 Also, the use of the Citadiene-Crystalline nithole copolymer improves the race linking properties of the magnetic layer O1 and also provides flexibility for coating. -5-4 There is a possibility that this butadiene-acrylic 11 nitrile co-combination will be selected as 5 and 201 [amount%].
At %-A, the results of improved relay links and flexibility are visible, and when this exceeds 20%, the paint film deteriorates! It depends on whether you're being too low-key or not. Further, the content of acryloni[-lyl] in this futasocone-7-acrylonyl-1-lyl combination is preferably 35% since 4596 is compatible with polyurethane by 1% in 111%.

また、セル1コース誘導体を10〜40車早%に選定す
る理由は、10市晴%未満゛Cは商温湿度での形状劣化
が大きくなり、また40市戸%を)〜えると塗膜がもろ
くなっC傷つき易いなどのltl・1閉耗111゛が:
ltj くなることを見出したごとによる・ また親水性極性基を含有するポリウレタン樹脂は種々の
方法で得ることができるが、例えばボリウLノタンの合
成に用いるポリエステル、またはポリオールの原料とし
ζもらいるジカルボン酸成分の一τ(1−に5−すトリ
ウムスルホイソフタル酸等のスルポン酸金jボ塩基を有
するジカルボン酸を用いる方法、或い4.1末端または
側鎖に一011基を有するボリウし・タン樹脂とCg−
CH−C:H−0803M で2 表わされる化合物を反応さ−Vて脱塩酸反応により導入
する方法などが考えられる。またポリウレタン樹脂への
′jlL水14: Iに性基の導入晴は極性基1つあた
りの分子甲が2000〜50000の範囲であることが
好まし7い。面1、二こにポリウレタン樹脂の含有pを
30へ・707RjFt%に特定する理由は、3咀1%
未満では分11& 個の改善や耐久性の同士の効果が顕
著でC;1なく、70Iロm%を越えると塗膜の流動性
が増し、形状劣化を起こ′4−1二とになることを見出
したことによる。
In addition, the reason why the cell 1 course derivative is selected at 10 to 40% is that if it is less than 10%, the shape will deteriorate significantly at commercial temperature and humidity, and if it is less than 40%, the coating film LTL・1 wear and tear 111゛ such as becoming brittle and easily damaged:
In addition, polyurethane resins containing hydrophilic polar groups can be obtained by various methods, such as polyester used in the synthesis of polyurethane, or dicarboxylic acid used as a raw material for polyol. A method using a dicarboxylic acid having a 1011 group at the terminal or side chain of the acid component (method using a dicarboxylic acid having a sulfonic acid group such as 1-5-sulfoisulfoisophthalic acid, or Tan resin and Cg-
Possible methods include reacting a compound represented by CH-C:H-0803M and introducing it by dehydrochlorination reaction. Further, when introducing a polar group into the polyurethane resin, it is preferable that the molecular weight per polar group is in the range of 2,000 to 50,000. The reason for specifying the content p of polyurethane resin on the first and second surfaces to 30 and 707RjFt% is 3 Tsui 1%.
If it is less than 11%, the effect of improvement in 11% and durability will be remarkable, and if it exceeds 70%, the fluidity of the coating will increase and the shape will deteriorate, resulting in 4-12. This is due to the discovery of

7また本発明による磁気記録媒体の磁性塗腺中の両性本
体としては、従来周知のγ−Pe203、Fe3O4或
いし、1ごれらの中間体、及びこれらにCO化合物をそ
の表面に被着させたものや、強磁性CrO7、或いはF
e、 Fe−Co、 Fe−Co−Ni等の合金磁性層
を単独若しくは混合して用いることができる。
7 In addition, as the amphoteric body in the magnetic smear of the magnetic recording medium according to the present invention, conventionally well-known intermediates such as γ-Pe203, Fe3O4, or ferromagnetic CrO7 or F
Alloy magnetic layers such as e, Fe-Co, and Fe-Co-Ni can be used alone or in combination.

また、磁気記録媒体中には必要に応じて潤滑剤、1II
F磨剤、帯電防止剤、或いはう) fl&剤等を添加し
得る。
In addition, a lubricant, 1II
A polishing agent, an antistatic agent, a fl& agent, etc. may be added.

ここに潤111剤としては、例えは各種のシリニlンオ
イル、2硫化゛eリブデン、2硫化タンクステン等の固
形111剤、及び脂肪酸エステルや燐酸エステル等が使
用できるが、その添加晴は結合剤IC)0市は邪に対し
、0.1〜20市m部に制御されることが望まれる。
Here, as the moisturizing agent, for example, solid 111 agents such as various silicone oils, libden disulfide, tunksten disulfide, fatty acid esters, phosphoric acid esters, etc. can be used, but the addition method is a binder. IC) It is desired that 0 city is controlled to 0.1 to 20 city m part with respect to evil.

また、その(LI[磨削としては、従来公知の材料て熔
醐1アルミナ、炭化珪素、酸化り1:Iム、二1ランダ
ム等の比較的硬度の而い1)のを使用でき、これら材料
の平均粒子径は好ましくは277m以下である。
In addition, for grinding, conventionally known materials such as 1:1 alumina, silicon carbide, 1:1 aluminum oxide, 21 random, etc., which are relatively hard, can be used. The average particle size of the material is preferably 277 m or less.

また、帯電防11−刑としては、カーボンブラック及び
サポニン等の天然界面活性剤、アルキレンオキザイド系
、グリセリン系等のノニオン!/11面々言Ii剤、1
1°11級アルキルアミン類、第4級アンモニウム塩類
、ピリジンその他の複素環類等のカヂメン界面消性剤、
カルボン酸、スルホン酸、燐酸、硫酸エステル基、ν、
)酸エステル基等の酸性基を含むアこ一オン界面活性剤
、アミノ酸類、アミノスルポン酸頓、アミノアルこ!−
ルの硫酸または燐酸エステルq−c+等のi:ln I
’l界面店I11゛剤等が使用される。面、これらの界
面Z!1性剤は、単独もしくは混合して用いf’7る。
In addition, as anti-static agents, natural surfactants such as carbon black and saponin, nonions such as alkylene oxide type and glycerin type! /11 Men's Words Ii Agent, 1
Kadmen surfactants such as 1°11-class alkylamines, quaternary ammonium salts, pyridine and other heterocycles,
Carboxylic acid, sulfonic acid, phosphoric acid, sulfuric acid ester group, ν,
) Aconone surfactants containing acidic groups such as acid ester groups, amino acids, aminosulfonic acids, amino alcohols! −
i: ln I of sulfuric acid or phosphoric acid ester q-c+ etc.
Agents such as I11 are used. surface, these interfaces Z! Uniform agents can be used alone or in combination.

これらは帯電防■ト刑としζ用いられるものであるが、
時としてその目的が例えば分散、潤′/FUI性の改良
として使われる場合もある。
These are used as anti-static protection,
Sometimes the purpose is to improve dispersion, wettability/FUI properties, for example.

−・方、分11に剤としては、カプリン酸、ラメリン酸
、ミリスチン酸、オレイン酸、リノール酸等の炭素数1
2〜18の脂肪酸、この脂肪酸のアルカリ金属または“
?ルカリ十類金属からなる金属イ1鹸、レシチン等を使
用しi)Iる。尚、ごれらの分散剤は、結合剤100市
ft1部に対し1〜20市田部の範囲で添加される。
-, as agents for 11 carbon atoms, such as capric acid, lamelic acid, myristic acid, oleic acid, linoleic acid, etc.
2 to 18 fatty acids, alkali metals of this fatty acid or “
? i) I) using a metal oxide consisting of alkali metals, lecithin, etc.; Incidentally, the dispersant of Gorera is added in a range of 1 to 20 parts per 1 part of 100 parts of binder.

:1モた、非磁性支持体としては、ポリエチレンテレツ
タレート、ボリコニチレン2・6−ブーフタレート等の
ポリごニスチル類、ボリブしlピレン等のポリウレタン
in 、セルローストリアセテート、セルr1−スダイ
アセテー1−等のセル【二l−ス誘専体、ポリカーボネ
ート、ポリアミド、ボリイミ]−等が使用される。
Examples of non-magnetic supports include polyesters such as polyethylene teretulate and voriconyethylene 2,6-buphthalate, polyurethanes such as polypyrene, cellulose triacetate, cellulose diacetate, etc. Cells such as carbon dioxide dielectric, polycarbonate, polyamide, polyimide, etc. are used.

史に、(別i’l M上には潤i’si i’4f1り
の人二めに1−ツブ=+−)、或いは41シ電防11−
のためのハック層等を設しノるごとができる。
In history, (on another i'l M there are jun i'si i'4f1 people second 1-tsubu=+-), or 41 shidenbo 11-
You can set up a hack layer etc. for this purpose.

次に、本発明の実施例について説明−するがその組成及
び製造法等がごの実施例に1914定されるものζはな
いことは明らかである。
Next, embodiments of the present invention will be described, but it is clear that the composition, manufacturing method, etc. thereof are not defined in the embodiments described above.

実施例1 先ず、上記組成の磁性塗事・1を調整する。Example 1 First, magnetic coating 1 having the above composition is prepared.

ごれら4A料をボールミル中で24時間混練し、次いで
硬化用1とし゛この3官能イソシアネ一ト化合物例えば
−目、Iネート1.(11本ポリウレタン工業;商品名
)を20PIIR(parts per hundre
d  parLr、 ofre!(in )を添加した
後、1時間混合攪拌し、ポリエチレンテレツタレートフ
ィルムよりなる非磁性支持体」−に乾燥後の厚みが5/
!mになるように塗布した。その後、通常の塗布型磁気
記録媒体を得る場合の処理と同様に磁気配向処理、乾燥
処理、巻き取り処理、及びカレンター処理の順に原反磁
気テープを114′ζごれを1/2インチ幅に切IJi
l、て磁気記t・諺媒体を11−た。
These 4A materials were kneaded in a ball mill for 24 hours, and then the trifunctional isocyanate compound 1. (11 polyurethane industry; product name) to 20PIIR (parts per hundre)
d parLr, ofre! After adding (in), the mixture was mixed and stirred for 1 hour, and then the non-magnetic support made of polyethylene terevitrate film had a thickness of 5/2 after drying.
! It was applied so that the thickness was m. After that, the original magnetic tape is processed to have a 114'ζ stain and a width of 1/2 inch by magnetic orientation treatment, drying treatment, winding treatment, and calendaring treatment in the same manner as in the case of obtaining ordinary coated magnetic recording media. Cut IJi
1. The magnetic recording medium was 11-.

実施例2〜4 実施例1において結合剤の組成を変えて同様にし′ζ夫
々磁気記録媒体を得た。
Examples 2 to 4 Magnetic recording media were obtained in the same manner as in Example 1 except that the composition of the binder was changed.

表1に本発明による実施例1〜4と、これに対する比較
例と、従来例におりる各結合剤の組成と、これらによる
磁気記録媒体の夫々のカレンダー処理後におい゛ζζ時
特性測定した結果を表1に示す。
Table 1 shows Examples 1 to 4 according to the present invention, comparative examples, and the composition of each binder in the conventional example, and the results of measuring the time characteristics of magnetic recording media after calendering. are shown in Table 1.

ごごに従来例は、その結合剤の組成がニトロセルロース
を30市量部、親水性極性基を導入していない従来のポ
リウレタン樹脂のニスタン57+12 (グツドリッチ
社製)を50重量部、ブタジェン−アクリロニトリル共
重合体(アクリロニトリル分20%)を20′*FA部
を用いた場合である。また表1中、塗膜の硬さくスティ
フネス)は相対値とし゛(ポしたものでその値が大きい
方が硬いことを示す。表1から明らかなように、比較例
1におり)るブタジエンーアルリしジニトリル共重合体
を含ませなかったものは、カレンダー処理によっても圧
潰が殆どなくバンキング性が上がっていなか−、た。ま
た比較例によるものは塗膜の接着強度が小さいという欠
点が認められた。
In the conventional example, the composition of the binder is 30 parts by weight of nitrocellulose, 50 parts by weight of Nistan 57+12 (manufactured by Gutdrich), a conventional polyurethane resin that does not have a hydrophilic polar group introduced, and butadiene-acrylonitrile. This is a case where a 20'*FA portion of a copolymer (acrylonitrile content: 20%) is used. In addition, in Table 1, the hardness (stiffness) of the coating film is a relative value. The material that did not contain the lysyl-dinitrile copolymer showed almost no crushing even after calendering, and the banking property did not improve. Moreover, the defect of the comparative example was that the adhesive strength of the coating film was low.

本発明によれば、種りの温度の環境十での繰返し使用に
、1、っても形状劣化なくすくれた安定性をホU7、ヒ
デオテーブとしてずぐれた電磁変換特性、物理的諸’l
’!l’性を示すことが値かめられた。
According to the present invention, it is possible to repeatedly use the seeds under various environmental conditions including (1) excellent stability without deterioration in shape, and (3) excellent electromagnetic conversion characteristics and physical properties as a video tape.
'! It was valued for exhibiting l' properties.

尚、硬化剤の使用においては、結合剤100Htli’
iiに対して5へ・;((川【51部の添加が望ましい
In addition, when using a hardening agent, binder 100Htli'
ii to 5.;((River [It is desirable to add 51 parts.

而、表1中、粉落Iつ及び形状劣化の欄において、◎印
は、15)藷ちないしは形状劣化が全くめられなかった
4)の、(つ印を殆どのられなかったもの、△は多少の
られたもの、×は1.n 著にみられるものでjY)幻
、表面1ηの欄中◎は極め゛ζ良好なもの、(つはJ’
JJ+’なt)の、△はやや劣るもの、×はiq成り劣
るものを表わしたものである。
In Table 1, in the columns of powder drop and shape deterioration, ◎ indicates 15) No lumps or shape deterioration was observed, 4) (X indicates almost no appearance), △ ◎ in the column of surface 1η is extremely good, (J'
JJ+'t), △ indicates slightly inferior, and × indicates iq is inferior.

\ \ \23、 ゝ・1、 \\ \ \23, ゝ・1、 \

Claims (1)

【特許請求の範囲】[Claims] 月:磁性グ持体1−に、磁性粉及び結合剤を主成分とす
る(?ケ牲1?ツを形成し7て成る磁気記録媒体におい
C1」−記結合剤は、セル+1−ス銹専体が10〜40
市ン樹脂が30へ・7(川(量%、ブタジエン−アクリ
ロニトル共Y((合体が5〜20車甲%含有して成り、
上記M1..ill、  I、i、Nnまたは+<、M
’はIt 、  I−+、N alIくまたはアルキル
基ct+Hzn→−1である磁気記録媒体。
Month: In a magnetic recording medium consisting of a magnetic holding body 1-, a magnetic powder and a binder as main components, the binder C1 is a cell+1-spring. 10-40 dedicated
City resin is 30 to 7 (amount%, butadiene-acrylonitrile co-Y ((combined) contains 5 to 20% of vehicle armor,
Above M1. .. ill, I, i, Nn or +<, M
' is It, I-+, NalI, or an alkyl group ct+Hzn→-1.
JP19019082A 1982-10-29 1982-10-29 Magnetic recording medium Granted JPS5979428A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19019082A JPS5979428A (en) 1982-10-29 1982-10-29 Magnetic recording medium

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19019082A JPS5979428A (en) 1982-10-29 1982-10-29 Magnetic recording medium

Publications (2)

Publication Number Publication Date
JPS5979428A true JPS5979428A (en) 1984-05-08
JPH0456369B2 JPH0456369B2 (en) 1992-09-08

Family

ID=16253944

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19019082A Granted JPS5979428A (en) 1982-10-29 1982-10-29 Magnetic recording medium

Country Status (1)

Country Link
JP (1) JPS5979428A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994028544A1 (en) * 1993-05-24 1994-12-08 Tdk Corporation Magnetic recording medium

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS51118403A (en) * 1975-04-10 1976-10-18 Sony Corp Magnetic recording media
JPS5740743A (en) * 1980-08-23 1982-03-06 Sony Corp Magnetic recording medium

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS51118403A (en) * 1975-04-10 1976-10-18 Sony Corp Magnetic recording media
JPS5740743A (en) * 1980-08-23 1982-03-06 Sony Corp Magnetic recording medium

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994028544A1 (en) * 1993-05-24 1994-12-08 Tdk Corporation Magnetic recording medium
US5451464A (en) * 1993-05-24 1995-09-19 Tdk Corporation Magnetic recording medium having a magnetic layer comprising ferromagnetic powders and binder which is two polyurethane resins with specified glass transition temperatures

Also Published As

Publication number Publication date
JPH0456369B2 (en) 1992-09-08

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