JPS61107527A - Magnetic recording medium - Google Patents

Magnetic recording medium

Info

Publication number
JPS61107527A
JPS61107527A JP22941684A JP22941684A JPS61107527A JP S61107527 A JPS61107527 A JP S61107527A JP 22941684 A JP22941684 A JP 22941684A JP 22941684 A JP22941684 A JP 22941684A JP S61107527 A JPS61107527 A JP S61107527A
Authority
JP
Japan
Prior art keywords
magnetic recording
recording medium
group
oxygen
carbon atoms
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
JP22941684A
Other languages
Japanese (ja)
Inventor
Takashi Suzuki
貴志 鈴木
Masaru Odagiri
優 小田桐
Yoshiaki Kai
義昭 貝
Hisayo Kitamaki
北牧 久代
Akio Hogo
蓬郷 章郎
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 JP22941684A priority Critical patent/JPS61107527A/en
Priority to US06/791,075 priority patent/US4647507A/en
Priority to DE19853538836 priority patent/DE3538836A1/en
Publication of JPS61107527A publication Critical patent/JPS61107527A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To provide a magnetic recording medium having a long and stable still reproduction life at a low temp. by forming a thin layer contg. a specific org. compd. on a thin ferromagnetic metallic film contg. oxygen. CONSTITUTION:The thin layer contg. the org. compd. having respectively one fluoroalkyl group of >=3C, aliphat. alkyl group of >=8C and mercapto group at the molecular terminal is formed on the thin ferromagnetic metallic film contg. oxygen. The still reproduction life at the low temp. is improved by the synergistic effect of the stable lubricating effect possessed by the fluoroalkyl group and aliphat. alkyl group and the strong reactive power of the mercapto group to the oxide layer on the surface of the thin ferromagnetic metallic film.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、磁気テープ、磁気ディスクなどの磁気記録媒
体に適したもので、とくに回転ヘッド型ビデオテープレ
コーダーに最適の磁気記録媒体に関するものである。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention is suitable for magnetic recording media such as magnetic tapes and magnetic disks, and particularly relates to a magnetic recording medium suitable for rotary head type video tape recorders.

従来例の構成とその問題点 鉄、コバルト、ニッケルまたはそれらを主成分とする合
金を真空蒸着、スパッタリング、イオンブレーティング
などの真空中製膜法によりポリエステルフィルム、ポリ
イミドフィルムなどの高分子フィルムや非磁性金属薄板
などから成る基板上に形成して成る強磁性金属落莫型磁
気記録媒体は、従来の塗布型磁気記録媒体に比べて記録
密度を飛躍的に向上せしめることが可能であるが、この
高密度化のためには、磁気記録媒体の表面を極力平担化
して磁気ヘッド・磁気記録媒体間のスペーシングロスを
極力減少せしめることが必要である。
Structures of conventional examples and their problems Iron, cobalt, nickel, or alloys containing these as main components are used in vacuum film forming methods such as vacuum evaporation, sputtering, and ion blasting to produce polymer films such as polyester films, polyimide films, and A ferromagnetic metal drop type magnetic recording medium formed on a substrate made of a magnetic thin plate or the like can dramatically improve recording density compared to conventional coating type magnetic recording media. In order to increase the density, it is necessary to make the surface of the magnetic recording medium as flat as possible to reduce the spacing loss between the magnetic head and the magnetic recording medium as much as possible.

しかしあまり表面を平担化しすぎるとヘッドタッチ、走
行性に支障をきたすため表面を微細に粗面化すると同時
に各種有機滑剤を含む表面被覆を設けることによりこn
を解決する必要がある。従来このような有機滑剤として
、各種の脂肪酸、脂肪酸エステル、脂肪酸アミド、シリ
コンオイル、フッ素オイル等が単独あるいは種々複合化
さnた形で使用されてきた。しかし、スチル再生寿命を
みた場合、とnらのものは常温〜高温(10C〜3゜C
)においては、寿命は通常30分以上であるが、気温が
5C以下になると、寿命が30分以下、ときには数分以
下に低下することが本発明者らの検討の結果間らかにな
った。
However, if the surface is made too flat, it will interfere with the head touch and running performance, so it is necessary to finely roughen the surface and at the same time provide a surface coating containing various organic lubricants.
need to be resolved. Conventionally, as such organic lubricants, various fatty acids, fatty acid esters, fatty acid amides, silicone oils, fluorine oils, etc. have been used singly or in various composite forms. However, when looking at the still playback life, those of Ton et al.
), the lifespan is usually 30 minutes or more, but as a result of the inventors' studies, it has been found that when the temperature drops below 5C, the lifespan decreases to less than 30 minutes, and sometimes less than a few minutes. .

発明の目的 本発明は、上記の問題を解決したものであって・低温下
におけるスチル再生寿命の長い磁気記録媒体を提供する
ものである。
OBJECTS OF THE INVENTION The present invention solves the above problems and provides a magnetic recording medium that has a long still playback life at low temperatures.

発明の構成 本発明は、分子末端に炭素数3以上のフロロアルキル基
と炭素数8以上の脂肪族アルキル基とメルカプト基とを
そnぞjL1個以上有する有機化合物を含む薄層を、酸
素を含む強磁性金属薄膜上に形成せしめたことを特徴と
する磁気記録媒体に関するものであシ、フロロアルキル
基と脂肪族アルキル基のもつ安定した滑性作用とメルカ
プト基の強磁性金属薄膜表面の酸化層への強い反応力と
の相乗効果によシ、低温下におけるスチル再生寿命を向
上せしめるものである。
Structure of the Invention The present invention provides a thin layer containing an organic compound each having at least one fluoroalkyl group having 3 or more carbon atoms, an aliphatic alkyl group having 8 or more carbon atoms, and 1 or more mercapto groups at the molecular terminal, by removing oxygen. The present invention relates to a magnetic recording medium formed on a ferromagnetic metal thin film containing a stable lubricating effect of fluoroalkyl groups and aliphatic alkyl groups and oxidation of the surface of the ferromagnetic metal thin film of mercapto groups. The synergistic effect with the strong reaction force to the layer improves the life of still playback at low temperatures.

実施例の説明 本発明に使用するフロロアルキル基(Rfと記g   
   す。)、脂肪族アルキル基(Rと記す。)、並び
K、メルカプト基を有する有機化合物としては、たとえ
ば、多価アルコールエステル誘導体、メルカプト脂肪酸
誘導体。
Description of Examples Fluoroalkyl group (denoted as Rf) used in the present invention
vinegar. ), an aliphatic alkyl group (denoted as R), K, and a mercapto group, such as polyhydric alcohol ester derivatives and mercapto fatty acid derivatives.

チオカルボン酸(チオジンゴ酸、α−メチルチオリンゴ
酸、チオコへり酸、チオ7タル酸等)誘導体。
Thiocarboxylic acid (thiodingic acid, α-methylthiomalic acid, thiocoheriic acid, thioheptatalic acid, etc.) derivatives.

OOR 5−CH CM2C0OCH2CH2R。OOR 5-CH CM2C0OCH2CH2R.

(+;12しり(JI: M 2CM 2 N (J 
S CJ kL fR ■ HCOOR CH2Co0CH2CH2Rf メルカプトアミノカルボン酸(システィン等、)誘導体
、 −R HSCH2−CH−Co○CH2CH2Rf 。
(+; 12 Shiri (JI: M 2CM 2 N (J
S CJ kL fR ■ HCOOR CH2Co0CH2CH2Rf Mercaptoaminocarboxylic acid (cystine, etc.) derivative, -R HSCH2-CH-Co○CH2CH2Rf.

等がある。フロロアルキル基としては、炭素数3以上、
さらに好ましくは5以上の直鎖または分枝パーフロロア
ルキル基、または炭素数3以上、さらに好ましくは6以
上の末端炭素に水素原子を1個有する直鎖フロロアルキ
ル基(たとえば、HCF2CF2CF2CF2CF2−
)が適しており、炭素数が2以下の場合にはスチル寿命
が短かくなる。
etc. The fluoroalkyl group has 3 or more carbon atoms,
More preferably, a linear or branched perfluoroalkyl group having 5 or more carbon atoms, or a linear fluoroalkyl group having one hydrogen atom at the terminal carbon having 3 or more carbon atoms, and more preferably 6 or more carbon atoms (for example, HCF2CF2CF2CF2CF2-
) is suitable, and if the number of carbon atoms is 2 or less, the still life will be shortened.

脂肪族アルキル基としては、炭素数8以上さらに好まし
くは10以上の直鎖または分枝アルキル基が適しており
、炭素数7以下の場合にもスチル寿命が低下する。本発
明に用いる前記有機化合物としては同一分子内に上記フ
ロロアルキル基と脂肪族アルキル基とメルカプト基とを
少なくとも各1個以上末端基として有していることが必
要であ担いずれか1種類、または2種類の末端基を有す
る有機化合物を混合して混合状態において上記3種の末
端基を取り揃えたとしても本発明と同様の効果を得るこ
とは困難である。上記の各基は同一分子中に複数個存在
させることが可能であシ、また上記以外の末端基(たと
えば、CH3−、C2H6−。
As the aliphatic alkyl group, a straight chain or branched alkyl group having 8 or more carbon atoms, more preferably 10 or more carbon atoms is suitable, and even if the carbon number is 7 or less, the still life is reduced. The organic compound used in the present invention must have at least one of each of the fluoroalkyl group, aliphatic alkyl group, and mercapto group as a terminal group in the same molecule; Alternatively, even if organic compounds having two types of terminal groups are mixed and the three types of terminal groups described above are arranged in a mixed state, it is difficult to obtain the same effect as the present invention. A plurality of each of the above groups can be present in the same molecule, and terminal groups other than the above (for example, CH3-, C2H6-).

等の炭素数が7以下の炭化水素基、HCF2−。A hydrocarbon group having 7 or less carbon atoms such as HCF2-.

02F、−、等の炭素数2以下のフロロアルキル基。A fluoroalkyl group having 2 or less carbon atoms, such as 02F, -, etc.

等)を存在せしめることも可能である。etc.) can also exist.

本発明に使用する前記有機化合物の分子量としては、3
,000以下、さらに好ましくは2,000以下が適当
である。分子量が3,000以上であると、スチル時の
出力が不安定となる。
The molecular weight of the organic compound used in the present invention is 3.
,000 or less, more preferably 2,000 or less. If the molecular weight is 3,000 or more, the output during stilling becomes unstable.

前記有機化合物中における各末端基の比率としては、分
子量比率で、炭素数5以上のフロロアルキル基が10〜
80%、炭素数8以上の脂肪族アルキル基が10〜8o
%、メルカプト基が2〜16チが適当である。この範囲
以外では、低温のスチル寿命改善効果が得られ難い。
As for the ratio of each terminal group in the organic compound, the molecular weight ratio is 10 to 5 fluoroalkyl groups having 5 or more carbon atoms.
80%, aliphatic alkyl group having 8 or more carbon atoms is 10-8o
%, and 2 to 16 mercapto groups are suitable. Outside this range, it is difficult to obtain the effect of improving the life of the still at low temperatures.

強磁性金属薄膜上には、前記有機化合物を、表面1rr
?当り0.1〜60omg 、あらに好ましくは0.5
〜200■の割合で、それ単独、あるいは、他方剤、防
鎖剤、樹脂等との複合体として薄層状に存在せしめるの
が良い。また、それを存在せしめる′方法としては、強
磁性金属薄膜表面に直接塗布、あるいは蒸着する方法以
外に磁気記録媒体の裏面に塗布あるいは蒸着せしめてお
き磁気記録媒体の」 積層(捲回)時に強磁性金属薄膜表面へ転写せしめる方
法も可能である。
On the ferromagnetic metal thin film, the organic compound is applied to the surface 1rr.
? 0.1-60omg, more preferably 0.5
It is preferable to make it exist in a thin layer at a ratio of ~200 cm, either alone or as a composite with other agents, anti-chain agents, resins, etc. In addition, methods for making it exist include coating or vapor-depositing it directly on the surface of the ferromagnetic metal thin film, or coating or vapor-depositing it on the back side of the magnetic recording medium so that it is strong during stacking (winding) of the magnetic recording medium. A method of transferring it to the surface of a magnetic metal thin film is also possible.

強磁性金属薄膜としては、例えば斜め蒸着あるいは垂直
蒸着法にて形成さnるC o 、 N i 、 F e
等を主体とする金属薄膜それらの合金を主体とする金属
薄膜(例えばCoNi、CoCr等)であって成膜時の
雰囲気を酸素ガスが支配的となる雰囲気としたときに得
らnる酸素を含むものが適当である。酸素の含有量とし
ては、強磁性金属に対する原子数比で少くとも3%以上
、好ましくは5%以上が適当である。3%以下であると
、低温でのスチル寿命改善効果が得らn難い。
As the ferromagnetic metal thin film, for example, C o , N i , Fe formed by oblique evaporation or vertical evaporation method is used.
A metal thin film mainly composed of alloys of these metals (e.g. CoNi, CoCr, etc.), which is obtained when the atmosphere during film formation is dominated by oxygen gas. It is appropriate to include. The oxygen content is suitably at least 3% or more, preferably 5% or more in terms of atomic ratio to the ferromagnetic metal. If it is less than 3%, it is difficult to obtain the effect of improving still life at low temperatures.

強磁性金属薄膜を形成すべき基板としては、巨視的には
表面平滑度良好であり、かつ、微細な突起を有するもの
が適当で、たとえば、表面に高さ5.0〜600人で1
−当シ平均1X1o4〜188個の波状あるいは山伏突
起を有するポリエステルフィルムは、とくに好ましいも
のである。
As the substrate on which the ferromagnetic metal thin film is to be formed, it is appropriate to use one that has good macroscopic surface smoothness and has minute protrusions.
- Polyester films having an average of 1×104 to 188 wavy or convex protrusions are particularly preferred.

(実 施 例ン 重合触媒残査に起因する微粒子をほとんど含まないポリ
エステルフィルムの表面に延伸製膜途上      ′
で増粘剤を含む変性シリコーンエマルジョン液を塗布硬
化させることによシ得らnた波状突起(高さ10OA密
度1X106個)を形成せしめたものの上に連続真空斜
め蒸着法によf)CoNi強磁性金属薄膜(N i =
 20%、膜厚1oOo人)を微量の酸素の存在下で形
成せしめた。皮膜中の酸素含量は原子数比で5%であっ
た。この試料をAとする。
(Example: In the process of forming a stretched film on the surface of a polyester film that contains almost no particulates caused by polymerization catalyst residue.
f) CoNi strength was formed by continuous vacuum oblique vapor deposition on the wavy protrusions (height: 10 OA density: 1 x 106 pieces) obtained by coating and curing a modified silicone emulsion containing a thickener. Magnetic metal thin film (N i =
20%, film thickness 100%) was formed in the presence of a trace amount of oxygen. The oxygen content in the film was 5% in terms of atomic ratio. This sample is designated as A.

ポリエステルフィルム内に添加されたシリカ微粒子によ
る勾配のゆるやかな粒状突起(平均高さ70人平均直径
1μm)が表面100μm′当り数個存在し、しかも重
合触媒残査に起因する微粒子による比較的大きな突起を
極力低減せしめたポリエステルフィルムの表面に直径1
50人のシリカコロイド粒子を核とし紫外線硬化エポキ
シ樹脂を結合剤とする急峻な山状突起を1×107個形
成せしめた基板上に上記と同様の条件でCo N i膜
(N i = 20チ、膜厚1000人、酸素含量7%
)を形成せしめたものをBとする。また、比較例として
Bにおいて蒸着時に酸素の導入を行わなかったもの(B
において酸素含量のみ2%以下としたもの〉をCとする
。これらの蒸着膜上にあらかじめ合成試作した各種の有
機化合物溶液を塗布したのち所定巾に切断して磁気テー
プを作シ、こnらを、−5C中で、試作ビデオデツキに
掛けてステル再生特性を測定した。スチル再生寿命は、
出力が初期値から10dB低下するまでの時間とした。
There are several granular protrusions with a gentle slope (average height: 70 people, average diameter: 1 μm) per 100 μm' of surface due to silica fine particles added to the polyester film, and relatively large protrusions due to fine particles caused by polymerization catalyst residue. The surface of the polyester film has a diameter of 1
A Co Ni film (N i = 20 cm) was formed under the same conditions as above on a substrate on which 1 x 10 7 steep mountain-like protrusions were formed using silica colloid particles as cores and UV-curable epoxy resin as a binder. , film thickness 1000, oxygen content 7%
) is formed as B. In addition, as a comparative example, in B, no oxygen was introduced during vapor deposition (B
C) in which only the oxygen content is 2% or less. Various organic compound solutions synthesized and prototyped in advance were coated on these vapor-deposited films, and then cut into predetermined widths to make magnetic tapes.These tapes were hung on a prototype video deck in -5C to test the stealth playback characteristics. It was measured. The still playback life is
The time required for the output to decrease by 10 dB from the initial value was taken as the time.

そnらの結果を第1表にまとめて記す。なお、比較例と
して、フロロアルキル基のないもの・・・(9)。
The results are summarized in Table 1. In addition, as a comparative example, one without fluoroalkyl group...(9).

脂肪族アルキル基のないもの・・・(10)、メルカプ
ト基のないもの・・・(11) p磁性膜の酸素含量の
低いもの・・・(7)等、を加えている。
Those without an aliphatic alkyl group (10), those without a mercapto group (11), those with a low oxygen content in the p magnetic film (7), etc. are added.

以   下   余   白 発明の効果 以上の結果から明らかなように本発明の磁気記録媒体は
、低温におけるスチル再生寿命が長く安定しているため
実用的価値の非常に高いものである。
Effects of the Invention As is clear from the above results, the magnetic recording medium of the present invention has a long and stable still playback life at low temperatures, and therefore has extremely high practical value.

Claims (1)

【特許請求の範囲】[Claims] 分子末端に炭素数3以上のフロロアルキル基と炭素数8
以上の脂肪族アルキル基とメルカプト基とをそれぞれ1
個以上有する有機化合物を含む薄層を1酸素を含む強磁
性金属薄膜上に形成せしめたことを特徴とする磁気記録
媒体。
Fluoroalkyl group with 3 or more carbon atoms and 8 carbon atoms at the end of the molecule
1 each of the above aliphatic alkyl groups and mercapto groups
1. A magnetic recording medium characterized in that a thin layer containing an organic compound having at least one oxygen is formed on a ferromagnetic metal thin film containing one oxygen.
JP22941684A 1984-10-31 1984-10-31 Magnetic recording medium Pending JPS61107527A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP22941684A JPS61107527A (en) 1984-10-31 1984-10-31 Magnetic recording medium
US06/791,075 US4647507A (en) 1984-10-31 1985-10-24 Magnetic recording material
DE19853538836 DE3538836A1 (en) 1984-10-31 1985-10-31 MAGNETIC RECORDING MATERIAL

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP22941684A JPS61107527A (en) 1984-10-31 1984-10-31 Magnetic recording medium

Publications (1)

Publication Number Publication Date
JPS61107527A true JPS61107527A (en) 1986-05-26

Family

ID=16891883

Family Applications (1)

Application Number Title Priority Date Filing Date
JP22941684A Pending JPS61107527A (en) 1984-10-31 1984-10-31 Magnetic recording medium

Country Status (1)

Country Link
JP (1) JPS61107527A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6399066A (en) * 1986-07-29 1988-04-30 ア  タ Novel compound polyhydroxylated and highly fluorinated, production thereof and use thereof as surfactant
US5188747A (en) * 1990-09-04 1993-02-23 Matsushita Electric Industrial Co., Ltd. Fluorine-containing lubricant compounds
US5252400A (en) * 1990-11-13 1993-10-12 Matsushita Electric Industrial Co., Ltd. Fluorine-containing compounds
US5266724A (en) * 1990-09-04 1993-11-30 Matsushita Electric Industrial Co., Ltd. Fluorine-containing compounds

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6399066A (en) * 1986-07-29 1988-04-30 ア  タ Novel compound polyhydroxylated and highly fluorinated, production thereof and use thereof as surfactant
US5188747A (en) * 1990-09-04 1993-02-23 Matsushita Electric Industrial Co., Ltd. Fluorine-containing lubricant compounds
US5266724A (en) * 1990-09-04 1993-11-30 Matsushita Electric Industrial Co., Ltd. Fluorine-containing compounds
US5252400A (en) * 1990-11-13 1993-10-12 Matsushita Electric Industrial Co., Ltd. Fluorine-containing compounds

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