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JPH0255848B2 - - Google Patents
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JPH0255848B2 - - Google Patents

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Publication number
JPH0255848B2
JPH0255848B2 JP59054531A JP5453184A JPH0255848B2 JP H0255848 B2 JPH0255848 B2 JP H0255848B2 JP 59054531 A JP59054531 A JP 59054531A JP 5453184 A JP5453184 A JP 5453184A JP H0255848 B2 JPH0255848 B2 JP H0255848B2
Authority
JP
Japan
Prior art keywords
monoglyceride
magnetic
acetylated
acetylated monoglyceride
sample
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.)
Expired - Lifetime
Application number
JP59054531A
Other languages
Japanese (ja)
Other versions
JPS60201525A (en
Inventor
Hitoshi Ogawa
Tomofumi Kaneko
Tooru Ishida
Ariake Shin
Hiroshi Myamura
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.)
Taiyo Yuden Co Ltd
Original Assignee
Taiyo Yuden Co 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 Taiyo Yuden Co Ltd filed Critical Taiyo Yuden Co Ltd
Priority to JP59054531A priority Critical patent/JPS60201525A/en
Publication of JPS60201525A publication Critical patent/JPS60201525A/en
Publication of JPH0255848B2 publication Critical patent/JPH0255848B2/ja
Granted legal-status Critical Current

Links

Landscapes

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

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は、例えば磁気録画用の磁気テープ等の
磁気記録媒体に関する。 従来、磁気テープ等の磁気記録媒体は、その走
行性を良くするために、磁気記録媒体の磁性粉
末、結合剤等から成る磁性層中に、鉱物油、シリ
コンオイル、金属石鹸、高級アルコール、脂肪酸
類、硅素化合物等の潤滑剤を配合するを一般とし
ているが、この種の潤滑剤を配合した磁気記録媒
体は、常温、常湿下での走行性やスチール耐久性
には支障がないが、高温、高湿な条件下で使用し
た場合には走行摩擦が大きくなつて走行性が悪く
なり、また静止画像も30分程度で鮮明度を失いス
チール耐久性に欠けるという不都合を有する。 本発明はかかる従来の磁気記録媒体の不都合
を、新規な潤滑剤の使用によつて解消した、高
温、高湿な条件下においても走行性、スチール耐
久性の優れた磁気記録媒体を提供することをその
目的とするもので、 磁性層中に、 一般式
The present invention relates to a magnetic recording medium such as a magnetic tape for magnetic recording, for example. Conventionally, magnetic recording media such as magnetic tapes contain mineral oil, silicone oil, metal soap, higher alcohol, fatty acid, etc. in the magnetic layer of the magnetic recording medium, which is made of magnetic powder, binder, etc., in order to improve its running properties. Generally, magnetic recording media containing lubricants such as silicon compounds, etc., are blended with lubricants such as silicon compounds, etc., but magnetic recording media containing this type of lubricant have no problems with runnability or steel durability at room temperature and humidity, but When used under high temperature and high humidity conditions, running friction increases, resulting in poor running performance, and still images lose sharpness after about 30 minutes, resulting in a lack of steel durability. The present invention solves the disadvantages of conventional magnetic recording media by using a new lubricant, and provides a magnetic recording medium that has excellent runnability and steel durability even under high temperature and high humidity conditions. The purpose is to have the following general formula in the magnetic layer:

【式】或いは[Formula] or

【式】 (但し、Rは炭素数11〜21のアルキル基を示
す。) で表わされるモノグリセライドを60〜100%アセ
チル化したアセチル化モノグリセライドを配合し
て成る。 かかる一般式で表わされるモノグリセライドの
式中Rを炭素数11〜21のアルキル基に限定したの
は、Rが炭素数10以下のアルキル基である場合に
は、アセチル化モノグリセライドが磁性層中に結
合剤として配合されている樹脂に可塑剤として作
用し、該樹脂の機械的強度を低下させてしまうか
らであり、Rが炭素数21を越えるアルキル基であ
る場合にはアセチル化モノグリセライドが前記樹
脂と分離して存在し、磁性層表面の粘着性を増
し、摩擦が大きくスチール耐久性を悪くするから
である。 又、かかるモノグリセライドをアセチル化して
得られるアセチル化モノグリセライドのアセチル
化率を60〜100%としてのは、アセチル化率が60
〜100%の場合には高温、高湿下での良好な走行
性並びにスチール耐久性が得られるが、アセチル
化率が60%未満ではかかる良好な走行性並びにス
チール耐久性が得られないからである。 ここでアセチル化モノグリセライドのアセチル
化率は前記モノグリセライドの水酸基の何パーセ
ントが酢酸によつてアセチル化されたかによつて
示される。 又、かかるアセチル化モノグリセライドの磁性
層中への配合量は一般的には該磁性層中の磁性粉
末重量に対して約0.4〜5重量%程度とするのが
好ましい。 前記磁気記録媒体は、例えばポリエチレンテレ
フタレート、ポリエステル等から成るベースフイ
ルム等の非磁性基材の表面に、磁性粉末、結合剤
等と共に前記のアセチル化モノグリセライドを含
んだ磁性塗料を塗布して磁性層を形成して得られ
る。 以下、本発明を実施例及び比較例に基づき説明
する。 実施例 1 ラウリン酸(C11H23COOH)でグリセリンを
モノエステル化したモノグリセライドを100%ア
セチル化してアセチル化モノグリセライドを得、
この2重量部を、 C0含有γ−Fe2O3 100重量部 Al2O3 3重量部 塩酢ビ共重合体(商品名VAGH) 11重量部 ポリウレタン 11重量部 カーボン 5重量部 レシチン 1重量部 メチルエチルケトン 130重量部 トルエン 130重量部 と混合して磁性塗料を得、巾12cm、厚さ14μmの
長尺なポリエステルフイルム上に巾10cm、乾燥後
厚4μmになるように該磁性塗料を塗布し、配向、
乾燥、カレンダー処理、細断等の工程を経て1/2
インチ巾の録画用磁気テープを得た。これを試料
No.1とした。 実施例 2 実施例1のアセチル化モノグリセライドに代え
て、実施例1のモノグリセライドを60%アセチル
化したアセチル化モノグリセライドを使用した以
外は実施例1と同様にして録画用磁気テープを
得、これを試料No.2とした。 実施例 3 実施例1のアセチル化モノグリセライドに代え
て、実施例1のモノグリセライドを70%アセチル
化したアセチル化モノグリセライドを使用した以
外は実施例1と同様にして録画用磁気テープを
得、これを試料No.3とした。 実施例 4 実施例1のアセチル化モノグリセライドに代え
て、ミリスチン酸(C13H27COOH)でグリセリ
ンをモノエステル化したモノグリセライドを100
%アセチル化したアセチル化モノグリセライドを
使用した以外は実施例1と同様にして録画用磁気
テープを得、これを試料No.4とした。 実施例 5 実施例1のアセチル化モノグリセライドに代え
て、パルミチン酸(C15H31COOH)でグリセリ
ンをモノエステル化したモノグリセライドを100
%アセチル化したアセチル化モノグリセライドを
使用した以外は実施例1と同様にして録画用磁気
テープを得、これを試料No.5とした。 実施例 6 実施例1のアセチル化モノグリセライドに代え
て、ベヘン酸(C21H43COOH)でグリセリンを
モノエステル化したモノグリセライドを100%ア
セチル化したアセチル化モノグリセライドを使用
した以外は実施例1と同様にして録画用磁気テー
プを得、これを試料No.6とした。 比較例 1 実施例1のアセチル化モノグリセライドに代え
て、実施例1のモノグリセライドを50%アセチル
化したアセチル化モノグリセライドを使用した以
外は実施例1と同様にして録画用磁気テープを
得、これを試料No.7とした。 比較例 2 実施例1のアセチル化モノグリセライドに代え
て、カプリン酸(C9H19COOH)でグリセリンを
モノエステル化したモノグリセライドを100%ア
セチル化したアセチル化モノグリセライドを使用
した以外は実施例1と同様にして録画用磁気テー
プを得、これを試料No.8とした。 比較例 3 実施例1のアセチル化モノグリセライドに代え
て、リグノリン酸(C23H47COOH)でグリセリ
ンをモノエステル化したモノグリセライドを100
%アセチル化したアセチル化モノグリセライドを
使用した以外は実施例1と同様にして録画用磁気
テープを得、これを試料No.9とした。このように
して得られた試料No.1〜9の夫々につき、23℃−
50%RH並びに40℃−85%RHの条件下における
摩擦係数(μ)とスチール耐久性(分)とを測定
した。その測定結果を下記の表に示す。
It is made by blending an acetylated monoglyceride which is 60-100% acetylated from the monoglyceride represented by the formula: (wherein R represents an alkyl group having 11 to 21 carbon atoms). The reason why R in the monoglyceride represented by this general formula is limited to an alkyl group having 11 to 21 carbon atoms is because when R is an alkyl group having 10 or less carbon atoms, the acetylated monoglyceride is bonded into the magnetic layer. This is because the acetylated monoglyceride acts as a plasticizer on the resin blended as an agent, reducing the mechanical strength of the resin, and if R is an alkyl group with more than 21 carbon atoms, the acetylated monoglyceride may not work with the resin. This is because they exist separately, increasing the adhesion of the magnetic layer surface, causing large friction, and impairing the durability of the steel. In addition, the acetylation rate of the acetylated monoglyceride obtained by acetylating such monoglyceride is 60 to 100%.
If the acetylation rate is ~100%, good runnability and steel durability under high temperature and high humidity conditions can be obtained, but if the acetylation rate is less than 60%, such good runnability and steel durability cannot be obtained. be. Here, the acetylation rate of the acetylated monoglyceride is indicated by what percentage of the hydroxyl groups of the monoglyceride are acetylated by acetic acid. The amount of acetylated monoglyceride to be incorporated into the magnetic layer is generally preferably about 0.4 to 5% by weight based on the weight of the magnetic powder in the magnetic layer. The magnetic recording medium is produced by applying a magnetic paint containing the acetylated monoglyceride together with magnetic powder, a binder, etc. to the surface of a non-magnetic substrate such as a base film made of polyethylene terephthalate, polyester, etc. to form a magnetic layer. Obtained by forming. Hereinafter, the present invention will be explained based on Examples and Comparative Examples. Example 1 Acetylated monoglyceride was obtained by 100% acetylation of monoglyceride obtained by monoesterifying glycerin with lauric acid (C 11 H 23 COOH),
Add this 2 parts by weight to 100 parts by weight of C0 -containing γ-Fe 2 O 3 3 parts by weight of Al 2 O 3 11 parts by weight of salt-vinyl acetate copolymer (trade name: VAGH) 11 parts by weight of polyurethane 5 parts by weight of carbon Lecithin 1 part by weight 130 parts by weight of methyl ethyl ketone and 130 parts by weight of toluene were mixed to obtain a magnetic paint, and the magnetic paint was applied onto a long polyester film 12 cm wide and 14 μm thick to a width of 10 cm and a thickness of 4 μm after drying. orientation,
1/2 after drying, calendering, shredding, etc.
An inch-wide recording magnetic tape was obtained. sample this
It was ranked No.1. Example 2 A recording magnetic tape was obtained in the same manner as in Example 1, except that an acetylated monoglyceride obtained by 60% acetylation of the monoglyceride of Example 1 was used in place of the acetylated monoglyceride of Example 1, and this was used as a sample. It was set as No.2. Example 3 A recording magnetic tape was obtained in the same manner as in Example 1, except that an acetylated monoglyceride obtained by 70% acetylation of the monoglyceride in Example 1 was used in place of the acetylated monoglyceride in Example 1, and this was used as a sample. It was set as No.3. Example 4 In place of the acetylated monoglyceride in Example 1, monoglyceride obtained by monoesterifying glycerin with myristic acid (C 13 H 27 COOH) was used at 100%
A recording magnetic tape was obtained in the same manner as in Example 1, except that acetylated monoglyceride with % acetylation was used, and this was designated as Sample No. 4. Example 5 In place of the acetylated monoglyceride of Example 1, monoglyceride obtained by monoesterifying glycerin with palmitic acid (C 15 H 31 COOH) was used at 100%
A recording magnetic tape was obtained in the same manner as in Example 1, except that acetylated monoglyceride having % acetylation was used, and this was designated as Sample No. 5. Example 6 Same as Example 1 except that instead of the acetylated monoglyceride of Example 1, an acetylated monoglyceride obtained by monoesterifying glycerin with behenic acid (C 21 H 43 COOH) was used, which was 100% acetylated. A recording magnetic tape was obtained, which was designated as Sample No. 6. Comparative Example 1 A recording magnetic tape was obtained in the same manner as in Example 1, except that instead of the acetylated monoglyceride in Example 1, an acetylated monoglyceride obtained by 50% acetylation of the monoglyceride in Example 1 was used, and this was used as a sample. It was set as No.7. Comparative Example 2 Same as Example 1 except that in place of the acetylated monoglyceride of Example 1, an acetylated monoglyceride obtained by 100% acetylation of monoesterified monoglyceride of glycerin with capric acid (C 9 H 19 COOH) was used. A recording magnetic tape was obtained, which was designated as Sample No. 8. Comparative Example 3 In place of the acetylated monoglyceride of Example 1, monoglyceride obtained by monoesterifying glycerin with lignophosphoric acid (C 23 H 47 COOH) was used at 100%
A recording magnetic tape was obtained in the same manner as in Example 1, except that acetylated monoglyceride with % acetylation was used, and this was designated as Sample No. 9. For each of the samples No. 1 to 9 obtained in this way, 23℃-
The friction coefficient (μ) and steel durability (minutes) were measured under the conditions of 50%RH and 40°C-85%RH. The measurement results are shown in the table below.

【表】 尚、摩擦係数は、各試料テープを引出しリール
と巻取リールとの間をそれらの間に介在される円
柱に接触角θで巻回させながら3.34cm/secの速
度で走行させ、引出し側のテープテンシヨンT1
と巻取り側のテープテンシヨンT2とを夫々測定
し、下記のオイラーの式により求めた。 μ=1/θlogT2/T1 又、スチール耐久性はVHSビデオテープレコ
ーダ(松下電器産業株式会社製、マクロードNV
−310型)を用いて、各試料テープに一定のビデ
オ信号を記録した後これを静止画像として再生
し、再生画像が鮮明さを失うまでの時間を以つて
スチール耐久性とした。 以上の実施例および比較例の各試料テープの摩
擦係数とスチール耐久性の測定結果を表わした上
記の表から明らかなように、本発明の磁気記録媒
体は23℃−50%RHという通常の条件下ばかりで
なく、40℃−85%RHという高温、高湿条件下に
おいても走行性並びにスチール耐久性に優れてい
ることが確認された。
[Table] The coefficient of friction was determined by running each sample tape at a speed of 3.34 cm/sec between a pull-out reel and a take-up reel while winding it around a cylinder interposed between them at a contact angle θ. Tape tension T 1 on drawer side
and the tape tension T 2 on the winding side were measured, respectively, and calculated using Euler's equation below. μ=1/θlogT 2 /T 1Also , steel durability is VHS video tape recorder (manufactured by Matsushita Electric Industrial Co., Ltd., McLeod NV
A constant video signal was recorded on each sample tape using a video camera (Model -310), which was then played back as a still image, and the time taken until the played image lost its sharpness was defined as the steel durability. As is clear from the above table showing the measurement results of the friction coefficient and steel durability of each sample tape of the Examples and Comparative Examples, the magnetic recording medium of the present invention can be used under the normal conditions of 23°C and 50% RH. It was confirmed that the steel has excellent runnability and steel durability not only under low temperature conditions, but also under high temperature and high humidity conditions of 40℃-85%RH.

Claims (1)

【特許請求の範囲】 1 磁性層中に、 一般式【式】或いは【式】 (但し、Rは炭素数11〜21のアルキル基を示
す。) で表わされるモノグリセライドを60〜100%アセ
チル化したアセチル化モノグリセライドを配合し
て成る磁気記録媒体。
[Claims] 1. A monoglyceride represented by the general formula [Formula] or [Formula] (wherein R represents an alkyl group having 11 to 21 carbon atoms) is acetylated by 60 to 100% in the magnetic layer. A magnetic recording medium containing acetylated monoglyceride.
JP59054531A 1984-03-23 1984-03-23 Magnetic recording medium Granted JPS60201525A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59054531A JPS60201525A (en) 1984-03-23 1984-03-23 Magnetic recording medium

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59054531A JPS60201525A (en) 1984-03-23 1984-03-23 Magnetic recording medium

Publications (2)

Publication Number Publication Date
JPS60201525A JPS60201525A (en) 1985-10-12
JPH0255848B2 true JPH0255848B2 (en) 1990-11-28

Family

ID=12973246

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59054531A Granted JPS60201525A (en) 1984-03-23 1984-03-23 Magnetic recording medium

Country Status (1)

Country Link
JP (1) JPS60201525A (en)

Also Published As

Publication number Publication date
JPS60201525A (en) 1985-10-12

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