JPS5894131A - Metallic thin film type magnetic recording medium - Google Patents

Metallic thin film type magnetic recording medium

Info

Publication number
JPS5894131A
JPS5894131A JP56191435A JP19143581A JPS5894131A JP S5894131 A JPS5894131 A JP S5894131A JP 56191435 A JP56191435 A JP 56191435A JP 19143581 A JP19143581 A JP 19143581A JP S5894131 A JPS5894131 A JP S5894131A
Authority
JP
Japan
Prior art keywords
surface active
active agent
thin film
molecular surface
type high
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
JP56191435A
Other languages
Japanese (ja)
Other versions
JPH0258687B2 (en
Inventor
Kunio Hibino
邦男 日比野
Mikio Murai
幹夫 村居
Takashi Fujita
藤田 隆志
Masatoshi Takao
高尾 正敏
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial 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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP56191435A priority Critical patent/JPS5894131A/en
Publication of JPS5894131A publication Critical patent/JPS5894131A/en
Publication of JPH0258687B2 publication Critical patent/JPH0258687B2/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
    • G11B5/72Protective coatings, e.g. anti-static or antifriction
    • G11B5/722Protective coatings, e.g. anti-static or antifriction containing an anticorrosive material
    • 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
    • G11B5/72Protective coatings, e.g. anti-static or antifriction
    • G11B5/725Protective coatings, e.g. anti-static or antifriction containing a lubricant, e.g. organic compounds

Landscapes

  • Lubricants (AREA)
  • Preventing Corrosion Or Incrustation Of Metals (AREA)
  • Magnetic Record Carriers (AREA)

Abstract

PURPOSE:To improve the anticorrosion and lubricating properties of titled medium, by making high-molecular surface active agents adsorbed on a ferromagnetic metallic thin film. CONSTITUTION:After an aqueous solution of an ionic high-molecular surface active agent such as a carboxylic acid type high-molecular surface active agent, a sulfate type high-molecular surface active agent, a sulfonic acid type high- molecular surface active agent, an amine type high-moleacular surface active agent and a quat. ammonium salt type high-molecular surface active agent is applied on a ferromagnetic metallic thin film, this substance is washed with a large quantity of pure water to wash away the high-molecular surface active agent which is not adsorbed. Polyvinyl potassium sulfate, sodium naphthalenesulfonate-formalin condensate, sodium alpha-olefin-sulfonate and sodium polyacrylate etc. are used actually used as surface active agents.

Description

【発明の詳細な説明】 本発明は金属薄膜型磁気記録媒体、特に磁性層表面の改
質を行ない、耐食性および滑性を向上させた金属薄膜型
磁気記録媒体に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a metal thin film magnetic recording medium, and particularly to a metal thin film magnetic recording medium in which the surface of the magnetic layer is modified to improve corrosion resistance and slipperiness.

真空蒸着法またはメッキ法で作製した金属薄膜型磁気記
録媒体は高密度記録に適しているといわれている。特に
、近年はオーディオ用テープやビデオ用テープとしての
用途が期待されている。しかし、一般的に、強磁性金属
薄膜は、腐食し易く、これ?避けるために磁性体自体の
合金化の方法や磁性層上に高分子化合物などの被膜を形
成する方法などが採用されている。しかし合金化の場合
、磁気特性の観点からは、耐食性の良い合金が必ずしも
良い特性をもっていると言えないのが普通である。また
、磁性層表面に高分子化合物などの耐食性のある被膜を
形成することは、効果はあるが、電磁変換特性の観点か
らは、被膜層が厚くなるため好ましいとは言えない。被
膜層の厚みの許され得る範囲は、たかだか500八であ
り、望ましくは2oO人程度である。この程度の膜厚を
有する耐食性被膜を均一にしかも量産性良く形成するこ
とは、非常な困難を伴う。また、この程度の厚みでは完
全に水分の侵入を妨げることは困難である。
Metal thin film magnetic recording media manufactured by vacuum evaporation or plating are said to be suitable for high-density recording. In particular, in recent years, it has been expected to be used as audio tapes and video tapes. However, in general, ferromagnetic metal thin films are easily corroded. In order to avoid this, methods such as alloying the magnetic material itself or forming a film of a polymer compound or the like on the magnetic layer have been adopted. However, in the case of alloying, from the viewpoint of magnetic properties, an alloy with good corrosion resistance cannot necessarily be said to have good properties. Further, although forming a corrosion-resistant coating such as a polymer compound on the surface of the magnetic layer is effective, it is not preferable from the viewpoint of electromagnetic conversion characteristics because the coating layer becomes thick. The permissible range of the thickness of the coating layer is at most 500 mm, preferably about 20 mm. It is extremely difficult to uniformly form a corrosion-resistant coating having such a thickness and with good mass productivity. Further, with such a thickness, it is difficult to completely prevent moisture from entering.

また、金属薄膜型磁気記録媒体においては、金士 属同恣の接触のために、滑性が不十分であり、さらに、
ヘッドとの間で、スムーズな接触を得ることが困難であ
り、出力変動が大きくなるなどの欠点を持っている。
In addition, thin metal film magnetic recording media have insufficient lubricity due to random metal-metal contact;
It is difficult to obtain smooth contact with the head, and it has drawbacks such as large fluctuations in output.

本発明では、このような従来品の問題点を水溶性の高分
子界面活性剤を強磁性金属からなる磁性層に吸着させる
ことによって解決したもので、これにより十分な耐食性
と滑性を持った金属薄膜型磁気記録媒体を得ることがで
きたものである。
The present invention solves these problems with conventional products by adsorbing a water-soluble polymeric surfactant to a magnetic layer made of ferromagnetic metal, which has sufficient corrosion resistance and lubricity. It was possible to obtain a metal thin film type magnetic recording medium.

本発明でいう水溶性の高分子界面活性剤とは、イオン性
高分子界面活性剤、すなわち、陰イオン性高分子界面性
剤、陽イオン性高分子界面活性剤をいう。たとえばポリ
アクリル酸、あるいは、スチレン、エチレン、インブチ
レンなどとの共重合ル塩など硫酸エステル型高分子界面
活性剤、ナフタレンスルフオン酸ホルマリン縮合物* 
ホ)スチレ/スルフォン酸、σ−オレフィンスルフォン
酸などのスルフォン酸塩などのスルフォン酸型高分子界
面活性剤、ポリビニルアミンなどのアミン型高分子界面
活性剤、ポリビニルピリジンの4級アンモニウム塩など
の4級アンモニウム塩型高分子界面活性剤などが本発明
に適用できる。
The water-soluble polymeric surfactant in the present invention refers to an ionic polymeric surfactant, that is, an anionic polymeric surfactant and a cationic polymeric surfactant. For example, polyacrylic acid, sulfate ester type polymeric surfactants such as copolymer salts with styrene, ethylene, imbutylene, etc., naphthalene sulfonate formalin condensates *
e) Sulfonic acid type polymeric surfactants such as sulfonic acid salts such as styrene/sulfonic acid and σ-olefin sulfonic acid, amine type polymeric surfactants such as polyvinylamine, quaternary ammonium salts of polyvinylpyridine, etc. Grade ammonium salt type polymeric surfactants and the like can be applied to the present invention.

本発明における水溶性高分子界面活性剤は、水溶液の濃
度として、10 F / 42〜0 、0001 y/
j!0.001F/ρである。高分子界面活性剤の濃度
が10y/ρを超えると、高分子界面活性剤を吸着させ
たあとの水洗工程で未吸着の高分子界面活性剤を十分に
洗い流すことができなくなり、ミセル状態で残存するこ
とになる。未吸着の高分子部活けでなく、テープ走行時
において容易にはがれやすく、はがれたものが磁気ヘッ
ド部にたまるなどして、目づまりやドロップアウトの原
因となる。
The water-soluble polymer surfactant in the present invention has an aqueous solution concentration of 10 F/42 to 0,0001 y/
j! It is 0.001F/ρ. If the concentration of the polymeric surfactant exceeds 10y/ρ, the unadsorbed polymeric surfactant will not be sufficiently washed away in the water washing process after adsorbing the polymeric surfactant, and it will remain in a micellar state. I will do it. The unadsorbed polymer parts tend to peel off when the tape is running, and the peeled off parts accumulate in the magnetic head, causing clogging and dropouts.

また、濃度が0.0o01y/!未満になると磁性金属
薄膜上に均一な吸着被膜の形成ができず、不十分な耐食
性しか得られない。
Also, the concentration is 0.0o01y/! If it is less than that, a uniform adsorption film cannot be formed on the magnetic metal thin film, and only insufficient corrosion resistance can be obtained.

つぎに本発明の製造方法について説明する。Next, the manufacturing method of the present invention will be explained.

1oy/1〜o、ooo1y/I!、(7)高分子界面
活性剤の水溶液を、磁性金属薄膜上に各種のコーティン
グ方法によって、塗布する。つぎに、浸漬法、流下法。
1oy/1~o, ooo1y/I! , (7) Applying an aqueous solution of a polymeric surfactant onto a magnetic metal thin film using various coating methods. Next, the immersion method and the flowing method.

スプレー法などによって、多量の純水で水洗し、未吸着
の高分子界面活性剤を洗い流す。コーテイング液の10
倍以上の水で洗うことが望ましい。
Rinse with a large amount of pure water using a spray method to wash away unadsorbed polymer surfactant. Coating liquid 10
It is recommended to wash with more than twice as much water.

また、水洗を完全にするため、水洗工程を繰り返しても
良い。水洗後、各種ブレードで水分を除く磁性薄膜表面
に傷などをつけないため、エアーナイフ方式が有効であ
る。水切りを行なった後、乾燥を行なう。
Furthermore, the washing process may be repeated to ensure complete washing. After washing with water, the air knife method is effective because it does not damage the surface of the magnetic thin film, which removes moisture using various blades. After draining, dry.

このようにして、磁性金属薄膜上に、良好な滑性と耐食
性をもった高分子界面活性剤の被膜が得られる。
In this way, a polymer surfactant coating having good lubricity and corrosion resistance is obtained on the magnetic metal thin film.

つぎに、本発明の実施例について説明する。Next, examples of the present invention will be described.

実施例1 ポリエチレンテレフタレートフィルム(以下、PETフ
ィルムと称す)上に強制的に酸素を導入し、コバルト(
80%’)ニッケル(20%)の強磁性合金薄膜を真空
蒸着法で作製した。この強磁性合金薄膜にポリビニル硫
酸カリウム(和光紬薬工業■製)の0.05f/flの
濃度の水溶液をディッピング法によって塗布した。その
後、多量の純水で洗浄してから乾燥空気を吹きつけ、洗
浄水を除き、80Cの熱風で乾燥させた。得られた磁性
薄膜を試料Aとする。
Example 1 Oxygen was forcibly introduced onto a polyethylene terephthalate film (hereinafter referred to as PET film), and cobalt (
A ferromagnetic alloy thin film of nickel (80%') (20%) was fabricated by vacuum evaporation. An aqueous solution of potassium polyvinyl sulfate (manufactured by Wako Pongyaku Kogyo ■) having a concentration of 0.05 f/fl was applied to this ferromagnetic alloy thin film by dipping. Thereafter, it was washed with a large amount of pure water and then blown with dry air, the washing water was removed, and it was dried with hot air at 80C. The obtained magnetic thin film is referred to as sample A.

実施例2 強制的に酸素を導入し、PETフィルム上に真空蒸着法
で作製したコバルト(80%)ニッケル(20%)の強
磁性合金薄膜に、高分子界面活性剤であるす7タレンス
7オン酸ナトリウムホルマリン縮合物(花王アトラス■
製「デモールNJ)の1.oy7ρの濃度の水溶液をデ
ィッピング法によって塗布し、多量の純水で洗浄した後
、乾燥空気を吹きつけ、洗浄水を除き、8oCの熱風で
乾燥させた。得られた磁性薄膜を試料Bとする。
Example 2 Oxygen was forcibly introduced into a ferromagnetic alloy thin film of cobalt (80%) and nickel (20%) produced by vacuum evaporation on a PET film, and the polymeric surfactant Su7talence7on was applied to it. acid sodium formalin condensate (Kao Atlas■
An aqueous solution with a concentration of 1.oy7ρ (manufactured by Demol NJ) was applied by the dipping method, washed with a large amount of pure water, and then blown with dry air to remove the washing water and dried with hot air at 8oC. Sample B is the magnetic thin film prepared by the above method.

実施例3 強制的に酸素を導入し、PETフィルム上に真空蒸着法
で作製したコバルト(80%)ニッケル(20%)の強
磁性合金薄膜に高分子界面活性削土 であるカルボン酸型高分子活性剤(花六アトラス■製「
デモールPJ)の0.1f/ρの濃度の水溶液をディッ
ピング法によって塗布し、多量の純水で実施例4 強制的に酸素を導入し、PETフィルム上に真空蒸着法
で作製したコバルト(80%)−ニッケル(20%)の
強磁性合金薄膜に高分子界面活性剤であるα−オレフィ
ンスルホン酸ナトリウム(ライオン油脂■製「リポラン
1400 J )の0.03y/2の濃度の水溶液をデ
ィッピング法によって塗布し、多量の純水で純水で洗浄
した後、乾燥空気を吹きつけ、洗浄水を除き、80Cの
熱風で乾燥させた。得られた磁性薄膜を試料りとする。
Example 3 Oxygen was forcibly introduced into a ferromagnetic alloy thin film of cobalt (80%) and nickel (20%) produced by vacuum evaporation on a PET film. Activator (manufactured by Hanaroku Atlas ■)
An aqueous solution of 0.1 f/ρ of Co (80% ) - A ferromagnetic alloy thin film of nickel (20%) was coated with an aqueous solution of sodium α-olefin sulfonate (Liporan 1400 J manufactured by Lion Oil Co., Ltd.), a polymeric surfactant, at a concentration of 0.03y/2 by dipping. After coating and washing with a large amount of pure water, dry air was blown to remove the washing water and the film was dried with hot air at 80 C. The obtained magnetic thin film was used as a sample.

実施例5 強制的に酸素を導入し、PETフィルム上に真空蒸着法
で作製したコバルト(8Q%)−ニッケル(20%)の
強磁性合金薄膜に、高分子界面活性剤であるa−オレフ
ィンスルホン酸ナトリウム(花王アトラス■製「ソフト
デタージエントWJ)のo、o○29/flの濃度の水
溶液をディッピング法によって塗布し1多量の純水で洗
浄した後、乾燥空気を吹きつけ、洗浄水を除き、80C
の熱風で乾燥させた。得られた磁性薄膜を試料Eとする
Example 5 Oxygen was forcibly introduced and a-olefin sulfone, a polymeric surfactant, was applied to a cobalt (8Q%)-nickel (20%) ferromagnetic alloy thin film produced by vacuum evaporation on a PET film. An aqueous solution of sodium chloride (Soft Detergent WJ manufactured by Kao Atlas ■) with a concentration of o, o○29/fl was applied by the dipping method, washed with a large amount of pure water, and then blown with dry air and washed with washing water. 80C except
dried with hot air. The obtained magnetic thin film is designated as sample E.

実施例6 強制的に酸素を導入し、PETフィルム上に真空蒸着法
で作製したコバルト(80%)−ニッケル(20%)の
強磁性金属薄膜に、ポリアクリル酸ソーダ(ラジカル重
合法で合成したポリアクリル酸をケン化して得たもの)
の○、o6y/犯の濃度の水溶液をディッピング法によ
って塗布し、多量の純水で洗浄した後、乾燥空気を吹き
つけ、洗浄水を除き、8oCの熱風で乾燥させた。得ら
れた磁性薄膜を試料Fとする。
Example 6 A ferromagnetic metal thin film of cobalt (80%) - nickel (20%) produced by vacuum evaporation on a PET film with forced introduction of oxygen was coated with sodium polyacrylate (synthesized by radical polymerization). obtained by saponifying polyacrylic acid)
An aqueous solution with a concentration of ○, o6y/min was applied by a dipping method, washed with a large amount of pure water, and dried air was blown to remove the washing water, followed by drying with hot air at 8oC. The obtained magnetic thin film is designated as sample F.

実施例1〜6で作製した試料A−Fの撥水性。Water repellency of samples AF produced in Examples 1 to 6.

耐食性、滑性を調べた。比較のため未処理試料にC9相
対湿度90%における環境試験、滑性は鏡面仕上げした
ステンレス鋼5US304のブロック上での10y荷重
下での摩擦係数を測定した。
Corrosion resistance and lubricity were investigated. For comparison, an untreated sample was subjected to an environmental test at a C9 relative humidity of 90%, and lubricity was measured by measuring the coefficient of friction under a 10y load on a mirror-finished stainless steel 5US304 block.

結果を下表に示す。The results are shown in the table below.

(以   下    余   白 ) 本発明によれば、強磁性金属からなる磁性層の性が向上
している。また、その摩擦係数も低下しており、滑性の
すぐれた磁気記録媒体を得ることができる。
(Margin below) According to the present invention, the properties of the magnetic layer made of ferromagnetic metal are improved. In addition, the coefficient of friction is also reduced, making it possible to obtain a magnetic recording medium with excellent lubricity.

Claims (1)

【特許請求の範囲】 気配録媒体。 (2)°  高分子界面活性剤が水溶性であることを特
徴とする特許請求の範囲第1項記載の金属薄膜型磁気記
録媒体。
[Claims] Sense recording medium. (2) The metal thin film magnetic recording medium according to claim 1, wherein the polymeric surfactant is water-soluble.
JP56191435A 1981-11-28 1981-11-28 Metallic thin film type magnetic recording medium Granted JPS5894131A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56191435A JPS5894131A (en) 1981-11-28 1981-11-28 Metallic thin film type magnetic recording medium

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56191435A JPS5894131A (en) 1981-11-28 1981-11-28 Metallic thin film type magnetic recording medium

Publications (2)

Publication Number Publication Date
JPS5894131A true JPS5894131A (en) 1983-06-04
JPH0258687B2 JPH0258687B2 (en) 1990-12-10

Family

ID=16274565

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56191435A Granted JPS5894131A (en) 1981-11-28 1981-11-28 Metallic thin film type magnetic recording medium

Country Status (1)

Country Link
JP (1) JPS5894131A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6350914A (en) * 1986-08-20 1988-03-03 Matsushita Electric Ind Co Ltd Vapor deposition type thin film recording medium

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54143114A (en) * 1978-04-27 1979-11-08 Matsushita Electric Ind Co Ltd Magnetic recording medium
JPS5589375A (en) * 1978-12-27 1980-07-05 Asahi Glass Co Ltd Antistatic agent for reproducing and recording material
JPS5589376A (en) * 1978-12-27 1980-07-05 Asahi Glass Co Ltd Antistaic agent composition for reproducing and recording material
JPS55144079A (en) * 1979-04-27 1980-11-10 Asahi Glass Co Ltd Surface-treating agent for record-reproductive material

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54143114A (en) * 1978-04-27 1979-11-08 Matsushita Electric Ind Co Ltd Magnetic recording medium
JPS5589375A (en) * 1978-12-27 1980-07-05 Asahi Glass Co Ltd Antistatic agent for reproducing and recording material
JPS5589376A (en) * 1978-12-27 1980-07-05 Asahi Glass Co Ltd Antistaic agent composition for reproducing and recording material
JPS55144079A (en) * 1979-04-27 1980-11-10 Asahi Glass Co Ltd Surface-treating agent for record-reproductive material

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6350914A (en) * 1986-08-20 1988-03-03 Matsushita Electric Ind Co Ltd Vapor deposition type thin film recording medium

Also Published As

Publication number Publication date
JPH0258687B2 (en) 1990-12-10

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