JPS61110334A - Magnetic recording medium - Google Patents

Magnetic recording medium

Info

Publication number
JPS61110334A
JPS61110334A JP23156084A JP23156084A JPS61110334A JP S61110334 A JPS61110334 A JP S61110334A JP 23156084 A JP23156084 A JP 23156084A JP 23156084 A JP23156084 A JP 23156084A JP S61110334 A JPS61110334 A JP S61110334A
Authority
JP
Japan
Prior art keywords
magnetic
powder
binder
substrate
glycidyl
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
JP23156084A
Other languages
Japanese (ja)
Other versions
JPH0572652B2 (en
Inventor
Kosaburo Sato
佐藤 幸三郎
Yoshiharu Katsuta
勝田 善春
Toshihiko Tanabe
田辺 敏彦
Takezo Shimizu
清水 丈三
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 JP23156084A priority Critical patent/JPS61110334A/en
Publication of JPS61110334A publication Critical patent/JPS61110334A/en
Publication of JPH0572652B2 publication Critical patent/JPH0572652B2/ja
Granted legal-status Critical Current

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

Abstract

PURPOSE:To obtain a magnetic recording medium with which the dispersibility of magnetic powder is excellent and the electric resistance on the surface of the magnetic layer is substantially small and which has a high squareness ratio by providing a magnetic layer contg. a glycidyl type epoxy compd. as a binder component for the magnetic powder. CONSTITUTION:The magnetic soln, prepd. by dispersing magnetic oxide such as Co-contg. gamma-Fe2O3 powder or magnetic metallic powder of Co, Fe-Ni alloy, etc. into a binder soln. of the glycidyl type epoxy compd., more preferably the epoxy compd. contg. glycidyl ester having polyol in ht eskeleton structure or polycarboxylic acid in the skeleton structure combined with the other binder, more preferably resin binder such as vinyl chloride/vinyl acetate copolymer or polyurethane is coated on a substrate and is dried. After the coated substrate is subjected to a calender treatment, the substrate is cut to a prescribed width, by which a magnetic tape is obtd. The magnetic tape or the like having the excellent dispersibility of the magnetic powder and binding power with the bincer, good binding property between the magnetic layer and the substrate, small electric resistance on the surface of the magnetic layer, good running stability and high squareness ratio is thus obtd.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 この発明は磁気記録媒体に関し、さらに詳しくは磁性粉
末の分散性に優れ、かつ磁性層表面の電気抵抗が充分に
小さい磁気記録媒体に関する。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a magnetic recording medium, and more particularly to a magnetic recording medium in which magnetic powder has excellent dispersibility and the electrical resistance of the surface of the magnetic layer is sufficiently small.

〔従来の技術〕[Conventional technology]

磁気記録媒体は、通常、磁性粉末、結合剤成分、育機熔
剤およびその他の必要成分からなる磁性史料をポリエス
テルフィルムなどの基体上に塗布、乾燥してつくられる
。この際使用される結合剤成分としては、磁性粉末の分
散性に優れ、磁気記録媒体に優れた磁気特性ないし電磁
変換特性を付与できるとともに、耐久性に優れるものが
望まれこのため、従来から結合剤樹脂について種々の研
究開発がなされ、これらの特性が優れたものとして、塩
化ビニル−酢酸ビニル系共重合体、繊維素系樹脂および
ポリウレタン系41脂等が汎用されている。
A magnetic recording medium is usually made by applying a magnetic material consisting of magnetic powder, a binder component, a growth agent, and other necessary components onto a substrate such as a polyester film, and drying it. The binder component used in this case is desired to be one that has excellent dispersibility of the magnetic powder, can impart excellent magnetic properties or electromagnetic conversion properties to the magnetic recording medium, and has excellent durability. Various research and developments have been carried out on agent resins, and vinyl chloride-vinyl acetate copolymers, cellulose resins, polyurethane 41 resins, and the like have been widely used as having excellent properties.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

ところが、これらの結合剤樹脂は比較的これらの特性が
優れるものの、未だ磁性粉末との親和力が充分でなく、
また併用する+n脂同士の反応性もそれほど高くないた
め、磁性粉末の分散性はいまひとつ充分に満足できるも
のではなく、磁性層表面の電気抵抗も充分に小さくなら
ない。
However, although these binder resins have relatively excellent properties, they still do not have sufficient affinity with magnetic powder.
Furthermore, since the reactivity of the +n resins used together is not so high, the dispersibility of the magnetic powder is not quite satisfactory, and the electrical resistance of the surface of the magnetic layer is not sufficiently reduced.

〔問題点を解決するための手段〕[Means for solving problems]

この発明は、かかる現伏に鑑み結合剤樹脂について種々
検討を行った結果なされたもので、磁性層の結合剤成分
として、磁性粉末との親和性に優れ、かつ併用する結合
剤樹脂との反応性に優れたグリシジル型エポキシ化合物
を含有させることによって、磁性粉末の分散性を改善し
、磁性層表面の電気抵抗を充分に小さくしたものである
This invention was made as a result of various studies on binder resins in view of the current state of affairs. By containing a glycidyl-type epoxy compound with excellent properties, the dispersibility of the magnetic powder is improved and the electrical resistance of the surface of the magnetic layer is sufficiently reduced.

この発明において、結合剤成分として使用されるグリシ
ジル型エポキシ化合物は、分子の末端にエポキシ基を有
し、このエポキシ基が磁性層形成後の乾燥等における加
熱により開環して磁性粉末表面に存在するOH基と直接
に化学結合する。このため、このグリシジル型エポキシ
化合物は磁性粉末に対して非常に強い結合力を発揮して
磁性粉末の粒子表面に強固に結合する。またこの磁性粉
末の粒子表面に強固に結合したこの種のグリシジル型エ
ポキシ化合物は併用する結合剤樹脂とのなじみが非常に
よい、従って、磁性粉末の結合剤樹脂中における分散性
が充分に改善される。また、この種のグリシジル型エポ
キシ化合物は、電子密度が分子内部で局在するという特
育の性質ををしていることから磁性層表面の電気抵抗が
小さくなり、走行安定性も改善される。
In this invention, the glycidyl-type epoxy compound used as a binder component has an epoxy group at the end of the molecule, and this epoxy group is ring-opened by heating during drying after forming the magnetic layer and is present on the surface of the magnetic powder. chemically bonds directly with the OH group. Therefore, this glycidyl type epoxy compound exhibits a very strong bonding force to the magnetic powder and is firmly bonded to the particle surface of the magnetic powder. In addition, this type of glycidyl-type epoxy compound that is firmly bonded to the particle surface of this magnetic powder has very good compatibility with the binder resin used in combination, and therefore, the dispersibility of the magnetic powder in the binder resin is sufficiently improved. Ru. In addition, this type of glycidyl-type epoxy compound has a special property in that the electron density is localized within the molecule, which reduces the electrical resistance of the magnetic layer surface and improves running stability.

このようなグリシジル型エポキシ化合物としては、ポリ
オールを骨格構造として有し、分子中にグリシジルエー
テルを少なくとも1以上含むポリグリシジルエーテルを
主成分とする分子量が1000以下のグリシジル型エポ
キシ化合物、およびポリカルボン酸を骨格構造として有
し、分子中にグリシジルエステルを少なくとも1以上含
むポリグリシジルエステルを主成分とする分子量が10
00以下のグリシジル型エポキシ化合物が好ましく使用
され、たとえば、下記の構造式で表されるグリシジル型
エポキシ化合物が、好適なものとして、単独で、あるい
は二種以上混合して使用される。
Such glycidyl-type epoxy compounds include glycidyl-type epoxy compounds with a molecular weight of 1000 or less, which have a polyol as a skeleton structure and whose main component is polyglycidyl ether containing at least one glycidyl ether in the molecule, and polycarboxylic acids. as a skeleton structure, and whose main component is a polyglycidyl ester containing at least one glycidyl ester in the molecule, and whose molecular weight is 10.
Glycidyl type epoxy compounds having a molecular weight of 00 or less are preferably used. For example, glycidyl type epoxy compounds represented by the following structural formula are preferably used alone or in combination of two or more types.

1.6−ヘキサンシオールジグリシジルエーテルH2B
r ジブロモ不オベンチルグリコールジグリ0シジルエーテ
ル 0−フタル酸ジグリシジルエステル ソルビトールボリグリンジルエーテル ポリプロピレングリコールジグリシジルエーテルCH。
1.6-hexanethiol diglycidyl ether H2B
r Dibromoobentyl glycol diglycidyl ether 0-phthalic acid diglycidyl ester sorbitol polyglycidyl ether polypropylene glycol diglycidyl ether CH.

ツ ネオベンチルグリコールジグリシジルエーテルH20H ■ リ トリメチロールプロパンボリグリシジルエーテルアリル
グリシジルエーテル p−第3級ブチルフェニルグリシジルエーテル(但し、
Rは炭素数が12または13のアルキル基である。) アルキルアルコールグリンジルエーテルジブロモフェニ
ルグリシジルエーテル このようなグリシジル型エポキシ化合物の市販品の具体
例としては、たとえば、ナガセ化成社製テナコ−7L/
EX −212、デーJ−コールEX−221、デ+コ
ールEX−721,デ+コールEX−622、ブナコー
ルEX−931、ブナコールEX−211,ブナコール
EX−321、デナコーJl/EX−11Lデナ:l−
ルEX−121、ブナコールgX−141、デナ:y−
ルEX−146、ブナ:l−/L/EX−192、デナ
D−Jl/EX−147等が挙げられる。
Tsuneobentyl glycol diglycidyl ether H20H ■ Litrimethylolpropane polyglycidyl ether Allyl glycidyl ether p-tertiary butylphenyl glycidyl ether (However,
R is an alkyl group having 12 or 13 carbon atoms. ) Alkyl alcohol glycidyl ether dibromophenyl glycidyl ether Specific examples of commercially available glycidyl-type epoxy compounds include Tenaco-7L/manufactured by Nagase Kasei Co., Ltd.
EX-212, De J-Cole EX-221, De+Cole EX-721, De+Cole EX-622, Bunacole EX-931, Bunacole EX-211, Bunacole EX-321, Denaco Jl/EX-11L Dena:l −
Le EX-121, Bunacol gX-141, Dena:y-
Examples include LEX-146, Buna:l-/L/EX-192, and Dena D-Jl/EX-147.

このようなグリシジル型エポキシ化合物は、従来一般に
磁気記録媒体用として使用される結合剤樹脂と併用して
使用するのが好ましく、併用する結合剤樹脂としては、
塩化ビニル−酢酸ビニル系共重合体、繊維素系樹脂、ポ
リとニルアセクール系樹脂、ポリウレタン系樹脂、ポリ
エステル系樹脂、イソノアJ−ト化合物など従来一般に
磁気記録媒体用として使用される結合剤樹脂がいずれも
好適なものとして使用されるが、特に、塩化ビニル−酢
酸ビニル−ビニルアルコール共重合体およびポリウレタ
ン樹脂と併用すると良好な結果が得られる。これらの結
合剤樹脂と併用する場合、グリシジル型エポキシ化合物
の配合割合は、これらの結合剤樹脂との合計量に対して
5〜50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、多すぎると耐熱性に難点
がある。
Such glycidyl type epoxy compounds are preferably used in combination with binder resins conventionally generally used for magnetic recording media.
Binder resins conventionally used for magnetic recording media, such as vinyl chloride-vinyl acetate copolymers, cellulose resins, poly and nyl acecool resins, polyurethane resins, polyester resins, and isonorate compounds, are Although they are also preferably used, particularly good results are obtained when used in combination with vinyl chloride-vinyl acetate-vinyl alcohol copolymers and polyurethane resins. When used together with these binder resins, the blending ratio of the glycidyl-type epoxy compound is preferably within the range of 5 to 50% by weight based on the total amount with these binder resins, and if it is too small, it may not be possible to achieve the desired results. If the amount is too high, the heat resistance will be poor.

この発明の磁気記録媒体を製造するには常法に準じて行
えばよく、たとえば、ポリエステルフィルムなどの基体
上に、磁性粉末、グリシジル型エポキシ化合物および併
用する結合剤樹脂とからなる結合剤成分、有機溶剤およ
びその他の添加剤を含む磁性塗料を、吹きつけもしくは
ロール塗りなど任意の手段で塗布し、乾燥すればよい。
The magnetic recording medium of the present invention may be manufactured according to a conventional method. For example, a binder component consisting of a magnetic powder, a glycidyl-type epoxy compound, and a binder resin to be used together, on a substrate such as a polyester film, A magnetic paint containing an organic solvent and other additives may be applied by any means such as spraying or roll coating, and dried.

ここで使用される磁性粉末としては、たとえば、T−F
ezOz粉末、Fe、04粉末、r−Fe203粉末と
Fe3O4粉末の中間化合物粉末、CO含有r−Fe2
03粉末、Co含有Fed04粉末、CrO2粉末のl
11.Fe粉末、CO扮末、Fe−Ni粉末などの金属
粉末およびバリウムフェライトなど、従来公知の各種磁
性粉末が広く包含される。
As the magnetic powder used here, for example, T-F
ezOz powder, Fe, 04 powder, intermediate compound powder between r-Fe203 powder and Fe3O4 powder, CO-containing r-Fe2
03 powder, Co-containing Fed04 powder, CrO2 powder
11. A wide variety of conventionally known magnetic powders are included, such as metal powders such as Fe powder, CO powder, and Fe-Ni powder, and barium ferrite.

また、有vi溶剤としては、シクロヘキサノン、メチル
イソブチルケトン、メチルエチルケトンなどのケトン系
溶剤、酢酸エチル、酢酸ブチルなどのエステル系溶剤、
ベンゼン、キシレン、トルエンなどの芳香族炭化水素系
溶剤、ジメチルスルホキシドなどのスルホキシド系溶剤
、テトラヒドロフラン、ジオキサンなどのエーテル系溶
剤など、使用する結合剤樹脂を熔解するのに適した溶剤
が、特に限定されることなく、単独または二謹以上混合
して使用される。
In addition, examples of solvents include ketone solvents such as cyclohexanone, methyl isobutyl ketone, and methyl ethyl ketone; ester solvents such as ethyl acetate and butyl acetate;
Solvents suitable for melting the binder resin used are particularly limited, such as aromatic hydrocarbon solvents such as benzene, xylene, and toluene, sulfoxide solvents such as dimethyl sulfoxide, and ether solvents such as tetrahydrofuran and dioxane. They can be used alone or in a mixture of two or more.

なお、磁性塗料中には、通常使用されている各種添加剤
、たとえば、分散剤、1fIfk剤、研摩剤、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, 1fIf agents, abrasives, antistatic agents, etc. may be appropriately added to the magnetic paint.

〔実施例〕〔Example〕

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 CO含有r−Fe203粉末  800!量部VAGH
(米国U、C,C社製、塩  80#化ビニル−酢酸ビ
ニル−ビニル アルコール共重合体) バンプ7クスT−5201(大口 60〃インキ化学工
業社製、ウレタン エラストマー) ブナコールEX−622(ナガセ 60#化成社製、ソ
ルビトールテトラ グリンノルエーテル) レンチン            16#ラウリン酸 
          12  lメチルイソブチルケト
ン    550#トルエン           5
50#これらの組成物を容量31のボールミル中で72
時間混合分散した後、これにコロネートL(日本ポリウ
レタン工業社製、三官能性低分子量イソシアネート化合
物)を15重量部加え、さらに30分間混合分散して磁
性塗料を調製した。この磁性塗料を、厚さ12μのポリ
エステルフィルム上に乾燥厚が6μとなるようにヱ布、
乾燥して磁性層を形成し、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 CO-containing r-Fe203 powder 800! Volume part VAGH
(Manufactured by U, C, C, USA, salt 80# vinyl-vinyl acetate-vinyl alcohol copolymer) Bump 7x T-5201 (Oguchi 60, manufactured by Ink Chemical Industry Co., Ltd., urethane elastomer) Bunacol EX-622 (Nagase 60# Kasei Co., Ltd., Sorbitol Tetraglin Norether) Lentin 16# Lauric Acid
12 l Methyl isobutyl ketone 550# toluene 5
50# these compositions in a ball mill with a capacity of 72
After mixing and dispersing for a period of time, 15 parts by weight of Coronate L (manufactured by Nippon Polyurethane Industries, Ltd., a trifunctional low molecular weight isocyanate compound) was added thereto, and the mixture was further mixed and dispersed for 30 minutes to prepare a magnetic paint. This magnetic paint was spread on a polyester film with a thickness of 12μ so that the dry thickness was 6μ.
It was dried to form a magnetic layer, calendered, and then cut to a predetermined width to produce a magnetic tape.

実施F!42〜12 実施例1における磁性塗料の組成において、VAGH、
バンプ7クスT−5201およびブナコールEX−62
2の組成比率を下記第1表に示すように種々に変更して
使用した以外は実施例1と同様にして磁気テープをつく
った。なお、各結合剤樹脂の組成比率はこれら三種の結
合剤樹脂の合針量に対する重量%で表した。
Implementation F! 42-12 In the composition of the magnetic paint in Example 1, VAGH,
Bump 7x T-5201 and Bunacol EX-62
Magnetic tapes were prepared in the same manner as in Example 1, except that the composition ratio of Example 2 was varied as shown in Table 1 below. The composition ratio of each binder resin is expressed in weight % based on the total amount of needles of these three binder resins.

第1表 実施例13 実施例1における磁性塗料の組成において、デナコーJ
しEX−622に代えてブナコール巳X−211(ナガ
セ化成社製、ネオペンチルグリコールジグリシジルエー
テル)を同量使用した以外は実施例1と同様にして磁気
テープをつくった。
Table 1 Example 13 In the composition of the magnetic paint in Example 1, Denako J
A magnetic tape was prepared in the same manner as in Example 1, except that the same amount of Bunacol Mi X-211 (manufactured by Nagase Kasei Co., Ltd., neopentyl glycol diglycidyl ether) was used in place of EX-622.

比較例1 実施例1における磁性塗料の組成において、ブナコール
BX−622を省き、VAGH(1)使用量を80重量
部から100重量部に、またバンプ7クスT−5201
の使用量を60重量部から100重量部に変更した以外
は、実施例1と同様にして磁眞テープをつくった。
Comparative Example 1 In the composition of the magnetic paint in Example 1, Bunacol BX-622 was omitted, the amount of VAGH (1) was changed from 80 parts by weight to 100 parts by weight, and Bump 7x T-5201 was added.
A magnetic tape was produced in the same manner as in Example 1, except that the amount used was changed from 60 parts by weight to 100 parts by weight.

各実施例および比較例で得られた磁気テープについて、
角型比および表面電気抵抗を測定した。
Regarding the magnetic tapes obtained in each example and comparative example,
Squareness ratio and surface electrical resistance were measured.

下記第2表はその結果である。Table 2 below shows the results.

第2表 (発明の効果) 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1−13)は、いずれも従来の磁気テープ(
比較例1)に比し、角型比が高くて、表面電気抵抗が小
さく、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、磁性粉末の分散性に優れ、磁性層の表面電気抵
抗も充分に低減されていることがわかる。
Table 2 (Effects of the Invention) As is clear from the above table, the magnetic tapes obtained by the present invention (Examples 1-13) are all different from conventional magnetic tapes (Examples 1-13).
Compared to Comparative Example 1), the squareness ratio is high and the surface electrical resistance is small. Therefore, the magnetic recording medium obtained by this invention has excellent dispersibility of magnetic powder and has a sufficient surface electrical resistance of the magnetic layer. It can be seen that this has been reduced to .

Claims (1)

【特許請求の範囲】[Claims] 1、結合剤成分として、グリシジル型エポキシ化合物が
含まれてなる磁性層を有する磁気記録媒体
1. A magnetic recording medium having a magnetic layer containing a glycidyl-type epoxy compound as a binder component
JP23156084A 1984-11-01 1984-11-01 Magnetic recording medium Granted JPS61110334A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP23156084A JPS61110334A (en) 1984-11-01 1984-11-01 Magnetic recording medium

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP23156084A JPS61110334A (en) 1984-11-01 1984-11-01 Magnetic recording medium

Publications (2)

Publication Number Publication Date
JPS61110334A true JPS61110334A (en) 1986-05-28
JPH0572652B2 JPH0572652B2 (en) 1993-10-12

Family

ID=16925418

Family Applications (1)

Application Number Title Priority Date Filing Date
JP23156084A Granted JPS61110334A (en) 1984-11-01 1984-11-01 Magnetic recording medium

Country Status (1)

Country Link
JP (1) JPS61110334A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5082733A (en) * 1988-04-18 1992-01-21 Fuji Photo Film Co., Ltd. Magnetic recording medium containing magnetic particles surface treated with a glycidyl compound

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5188205A (en) * 1975-01-31 1976-08-02 JISEITORYONOSEIZOHOHO

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5188205A (en) * 1975-01-31 1976-08-02 JISEITORYONOSEIZOHOHO

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5082733A (en) * 1988-04-18 1992-01-21 Fuji Photo Film Co., Ltd. Magnetic recording medium containing magnetic particles surface treated with a glycidyl compound

Also Published As

Publication number Publication date
JPH0572652B2 (en) 1993-10-12

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