JPS6334719A - Magnetic recording medium - Google Patents
Magnetic recording mediumInfo
- Publication number
- JPS6334719A JPS6334719A JP17694586A JP17694586A JPS6334719A JP S6334719 A JPS6334719 A JP S6334719A JP 17694586 A JP17694586 A JP 17694586A JP 17694586 A JP17694586 A JP 17694586A JP S6334719 A JPS6334719 A JP S6334719A
- Authority
- JP
- Japan
- Prior art keywords
- layer
- magnetic
- recording medium
- magnetic recording
- films
- 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
Links
- 230000005291 magnetic effect Effects 0.000 title claims abstract description 33
- 239000010409 thin film Substances 0.000 claims abstract description 8
- 230000005294 ferromagnetic effect Effects 0.000 claims abstract description 7
- 229920000642 polymer Polymers 0.000 claims abstract description 6
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 238000000926 separation method Methods 0.000 claims description 4
- 239000010408 film Substances 0.000 abstract description 12
- 230000007797 corrosion Effects 0.000 abstract description 9
- 238000005260 corrosion Methods 0.000 abstract description 9
- 238000003475 lamination Methods 0.000 abstract description 3
- 230000003247 decreasing effect Effects 0.000 abstract description 2
- 238000006056 electrooxidation reaction Methods 0.000 abstract description 2
- 239000010410 layer Substances 0.000 description 35
- 230000000052 comparative effect Effects 0.000 description 7
- -1 polyethylene terephthalate Polymers 0.000 description 6
- 229920006254 polymer film Polymers 0.000 description 6
- 238000005566 electron beam evaporation Methods 0.000 description 5
- 239000010419 fine particle Substances 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000011651 chromium Substances 0.000 description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 description 4
- 239000005020 polyethylene terephthalate Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 238000007740 vapor deposition Methods 0.000 description 3
- ZTSDOGSKTICNPQ-UHFFFAOYSA-N 2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,13,13,14,14,15,15,16,16,17,17,18,18,18-pentatriacontafluorooctadecanoic acid Chemical compound OC(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F ZTSDOGSKTICNPQ-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000007885 magnetic separation Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- TWJNQYPJQDRXPH-UHFFFAOYSA-N 2-cyanobenzohydrazide Chemical compound NNC(=O)C1=CC=CC=C1C#N TWJNQYPJQDRXPH-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 229910020630 Co Ni Inorganic materials 0.000 description 1
- 229910002440 Co–Ni Inorganic materials 0.000 description 1
- 229910020515 Co—W Inorganic materials 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Natural products CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- 235000021360 Myristic acid Nutrition 0.000 description 1
- 239000004962 Polyamide-imide Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004734 Polyphenylene sulfide Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- BCCOBQSFUDVTJQ-UHFFFAOYSA-N octafluorocyclobutane Chemical compound FC1(F)C(F)(F)C(F)(F)C1(F)F BCCOBQSFUDVTJQ-UHFFFAOYSA-N 0.000 description 1
- 235000019407 octafluorocyclobutane Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920003207 poly(ethylene-2,6-naphthalate) Polymers 0.000 description 1
- 229920002312 polyamide-imide Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 239000011112 polyethylene naphthalate Substances 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910000702 sendust Inorganic materials 0.000 description 1
- 238000000992 sputter etching Methods 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
Landscapes
- Magnetic Record Carriers (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は高密度磁気記録に適する強磁性金属薄膜を磁気
記録層とする磁気記録媒体に関する。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a magnetic recording medium whose magnetic recording layer is a ferromagnetic metal thin film suitable for high-density magnetic recording.
従来の技術
高分子フィルム上に直接又は下地層を介して電子ビーム
蒸着法でCo−Niを斜め蒸着した、いわゆる蒸着テー
プは、蒸着時に酸素ガスを導入し部分酸化を最適化する
ことで、保磁力の制御は勿論のこと、耐久性、耐食性の
向上をはかり、実用性を高めている〔外国論文誌:アイ
イーイーイートランザクションズオンマグネティクス(
IEEETRANSACTIONS ON MAG
NETIC3)Vol。Conventional technology The so-called vapor deposition tape, in which Co-Ni is obliquely vapor-deposited by electron beam evaporation directly or through an underlayer on a polymer film, can be preserved by introducing oxygen gas during vapor deposition and optimizing partial oxidation. Not only does it control magnetic force, but it also improves durability and corrosion resistance, making it more practical.
IEEETRANS ACTIONS ON MAG
NETIC3) Vol.
MAG−20,黒−5P、P、824〜826(198
4))。MAG-20, black-5P, P, 824-826 (198
4)).
更に、耐食性の向上や微粒子化により雑音を改良するた
めに積層化する試みがなされている。第2図は、従来の
磁気記録媒体の一例の拡大断面図で、第2図で1はポリ
エチレンテレフタレートフィルム等の高分子フィルムで
、2.4は電子ビーム蒸着法で形成したCr蒸着層で、
厚み0.05μmで、3,6はCo −Cr 斜め蒸
着膜で、Crは19wt%含むもので、保磁力1000
(○e)で、厚みは夫々0.07μmであるu6はパー
フロロシクロブタンのプラズマ重合膜150人と、ミリ
スチン酸のCo塩の40人の蒸着膜の積層構成の保護膜
である。Furthermore, attempts have been made to stack layers in order to improve corrosion resistance and reduce noise by making particles finer. FIG. 2 is an enlarged cross-sectional view of an example of a conventional magnetic recording medium. In FIG. 2, 1 is a polymer film such as a polyethylene terephthalate film, and 2.4 is a Cr vapor deposition layer formed by electron beam evaporation.
The thickness is 0.05 μm, 3 and 6 are Co-Cr obliquely deposited films, which contain 19 wt% of Cr, and have a coercive force of 1000.
(◯e) and u6, each having a thickness of 0.07 μm, is a protective film having a laminated structure of a plasma polymerized film of perfluorocyclobutane of 150 layers and a vapor-deposited film of Co salt of myristic acid of 40 layers.
非磁性層との積層で、雑音は改良される傾向にあるが、
電気化学的に腐食が進行する場合があり、材料に限定を
受けている。Lamination with non-magnetic layers tends to improve noise, but
Corrosion may progress electrochemically, and there are limitations to the materials used.
発明が解決しようとする問題点
しかしながら上記した構成では、記録波長の短波長化が
進むと、十分な信号出力対雑音化(以下、C/N と記
す)が得られにくいため改良が望まれていた。本発明は
上記した事情に鑑みなされたもので、十分なC/Nと耐
食性の良好な磁気記録媒体を提供するものである。Problems to be Solved by the Invention However, with the above configuration, as the recording wavelength becomes shorter, it becomes difficult to obtain a sufficient signal output to noise ratio (hereinafter referred to as C/N), so improvements are desired. Ta. The present invention was made in view of the above-mentioned circumstances, and provides a magnetic recording medium with sufficient C/N and good corrosion resistance.
問題点を解決するだめの手段
上記問題点を解決するだめに本発明の磁気記録媒体は、
部分酸化された強磁性金属薄膜の積層構成にあって、積
層界面に酸化層をもたずに、高分子分離層を配したもの
である。Means for Solving the Problems In order to solve the above problems, the magnetic recording medium of the present invention comprises:
It has a laminated structure of partially oxidized ferromagnetic metal thin films, but has no oxidized layer at the laminated interface, but a polymer separation layer.
作 用
本発明の磁気記録媒体は上記した構成により、積層した
夫々の薄膜間の磁気的分離が、良好になり、かつ、磁気
ヘッドからみて、中間の非磁性層の酸化層がないので、
磁気ヘッドから遠くなる側の薄膜のスペーシングが小さ
くなることから、出力が大きくなり雑音が下がるので、
C/Nが改良され、さらに積層構成をとっても電気化学
的腐食は無視できるので、部分酸化された強磁性金属薄
膜は腐食しにくい状態で構成されることになり耐食性も
良好になるのである。Function: The magnetic recording medium of the present invention has the above-described structure, and the magnetic separation between the laminated thin films is good, and when viewed from the magnetic head, there is no oxidized layer in the intermediate nonmagnetic layer.
Since the spacing of the thin film on the side far from the magnetic head is smaller, the output is larger and the noise is lower.
Since the C/N ratio is improved and electrochemical corrosion can be ignored even in a laminated structure, the partially oxidized ferromagnetic metal thin film is constructed in a state where it is difficult to corrode, and its corrosion resistance is also improved.
実施例
以下、図面を参照しながら、本発明の実施例について説
明する。第1図は本発明の実施例の磁気記録媒体の拡大
断面図である。、、7は厚みが1o、4μmのポリエチ
レンテレフタレートフィルムのごとき高分子フィルムで
、8は直径1mの円筒キャンに沿わせて、最小入射角3
6度で、2x 10−’ (Torr)の酸素中でCo
を○、066μm電子ビーム蒸着した後、Ar イオン
でスパッタエツチングを行い、上部表面酸化層を除去し
た、第1磁性薄膜で、9は直径100へのシリカ微粒子
を含む厚み40人のポリエステル樹脂層からなる高分子
分離層で、1゜は第1磁性層と同じ装置で最小入射角4
7度で、1 x 10−’ (Torr )の酸素中で
Co 8O−Ni 20 を0.07μm 電子ビー
ム蒸着して得だ第2磁性層である。第2磁性層も9との
界面は9からの微量の脱ガスで酸化層をなくすことがで
きるのである。Embodiments Hereinafter, embodiments of the present invention will be described with reference to the drawings. FIG. 1 is an enlarged sectional view of a magnetic recording medium according to an embodiment of the present invention. ,, 7 is a polymer film such as a polyethylene terephthalate film with a thickness of 10 and 4 μm, and 8 is a polymer film such as a cylindrical can with a diameter of 1 m, with a minimum incidence angle of 3
Co in oxygen at 2x 10-' (Torr) at 6 degrees
○, 066 μm electron beam evaporation, followed by sputter etching with Ar ions to remove the upper surface oxide layer, is the first magnetic thin film, 9 is from a polyester resin layer with a thickness of 40 μm containing silica fine particles to a diameter of 100 μm. 1° is the minimum incidence angle of 4 with the same device as the first magnetic layer.
The second magnetic layer was obtained by electron beam evaporation of Co 8 O-Ni 20 to a thickness of 0.07 μm in oxygen at 7° C. and 1×10 −′ (Torr). The interface between the second magnetic layer and the magnetic layer 9 can be freed from an oxidized layer by a small amount of gas degassing from the magnetic layer 9.
11は真空蒸着法で形成した厚み約40人のパーフロロ
ステアリン酸から成る潤滑剤層である。Reference numeral 11 denotes a lubricant layer made of perfluorostearic acid and having a thickness of approximately 40 μm formed by vacuum deposition.
比較例として、厚み1o、4μmのポリエチレンテレフ
タレートフィルム上に直径150人のシリカ微粒子を含
む厚み40人のポリエステル樹脂層を配し、その上に上
記した第2磁性層を、2層積層しその上にパーフロロス
テアリン酸40人を配したものを比較例A、磁性層間に
厚み400人のクロムを電子ビーム蒸着して配したもの
を比較例Bとして準備した。As a comparative example, a 40-layer polyester resin layer containing 150-layer diameter silica fine particles was placed on a polyethylene terephthalate film with a thickness of 1.0 mm and 4 μm, and the above-mentioned second magnetic layer was laminated in two layers on top of the layer. Comparative Example A was prepared in which 40 layers of perfluorostearic acid were placed between the magnetic layers, and Comparative Example B was prepared in which chromium was deposited by electron beam evaporation to a thickness of 400 layers between the magnetic layers.
実施例と比較例A、Bを用い、ギャップ長0.14μm
のセンダストヘッドにより、相対速度3 、4m1se
c 、周波数6@を記録した時、6川でのノイズからみ
だC/Nを比較した。実施例を0(dB)とすると、比
較例A、Bは夫々−2,1(dB)、−3,9(dB)
であった。夫々のテープを60℃85SRHの環境に2
週間放置後のC/Nは、実施例、比較例Aが変化しなか
ったのに比し、比較例Bは初期値から2、edB低下し
た。Using Example and Comparative Examples A and B, gap length 0.14 μm
With the sendust head, the relative speed is 3,4mlse
c. When recording frequency 6@, we compared the noise C/N at 6 rivers. If the example is 0 (dB), comparative examples A and B are -2, 1 (dB) and -3, 9 (dB), respectively.
Met. Place each tape in an environment of 60°C and 85SRH.
The C/N after being left for a week remained unchanged in Examples and Comparative Example A, whereas Comparative Example B decreased by 2 edB from the initial value.
実施例として、高分子フィルムはポリエチレンテレフタ
レートフィルムを用いたが他に、ポリイミド、ポリフェ
ニレンサルファイド、ポリアミドイミド、ポリエチレン
ナフタレート、ポリカーボネート等でもよく、必要に応
じて微粒子塗布層を配したものでもよい。In the example, a polyethylene terephthalate film was used as the polymer film, but other materials such as polyimide, polyphenylene sulfide, polyamideimide, polyethylene naphthalate, polycarbonate, etc. may be used, and a fine particle coating layer may be provided as necessary.
磁性層は、他にCo −Fe−0、Co−Cr −0。The magnetic layer is also made of Co-Fe-0 and Co-Cr-0.
Co−Ti−0,Co−W’−(J、Co−NLo−0
,Co−Pt −0。Co-Ti-0, Co-W'-(J, Co-NLo-0
, Co-Pt-0.
Co−Ni−Pr−0,Co−NL−B−0等の単−又
は複、合でもよい。Co-Ni-Pr-0, Co-NL-B-0 and the like may be used alone or in combination.
高分子分離層は、樹脂として、他にエポキシ樹脂、ポリ
ウレタン樹脂、多くの電子ビーム硬化樹脂などでもよく
、微粒子は、他にA l 203. CaOO3゜B
a S O4,Ca O、T iO2、F e 304
等でもよいし。The polymer separation layer may be made of other resins such as epoxy resins, polyurethane resins, and many electron beam cured resins, and the fine particles may also be made of Al 203. CaOO3゜B
a S O4, Ca O, TiO2, Fe 304
etc. is fine.
微粒子を含まないとしても磁気的分離と耐食性の向上は
十分得られるもので適宜選択すればよい。Even if it does not contain fine particles, magnetic separation and corrosion resistance can be sufficiently improved, so it may be selected as appropriate.
樹脂層厚みは20八から2oo人、好ましくは3o入〜
100人が適当といえる。The resin layer thickness is 208 to 20 mm, preferably 30 mm to 300 mm.
100 people would be appropriate.
発明の効果
以上のように本発明によれば、短波長記録を行った時の
テープのC/Nが良好で、かつ耐食性が良好で、高湿環
境下で保存しても、C/Nの劣化のない磁気記録媒体が
得られるといったすぐれた効果がある。Effects of the Invention As described above, according to the present invention, the C/N of the tape is good when short wavelength recording is performed, the corrosion resistance is good, and the C/N remains unchanged even when stored in a high humidity environment. This has an excellent effect in that a magnetic recording medium without deterioration can be obtained.
第1図は本発明の実施例に係る磁気記録媒体の拡大断面
図、第2図は従来の磁気記録媒体の拡大断面図である。
7・・・・・・高分子フィルム、8・・・・・・第1磁
性層、9・・・・・高分子分離層、10・・・・・・第
2磁性層。
代理人の氏名 弁理士 中 尾 敏 男 ほか1名7−
−〜17i分)フィル/;
第2図FIG. 1 is an enlarged sectional view of a magnetic recording medium according to an embodiment of the present invention, and FIG. 2 is an enlarged sectional view of a conventional magnetic recording medium. 7... Polymer film, 8... First magnetic layer, 9... Polymer separation layer, 10... Second magnetic layer. Name of agent: Patent attorney Toshio Nakao and 1 other person7-
-~17i minutes) Fill/; Figure 2
Claims (1)
層界面に酸化層をもたずに、高分子分離層を配して成る
磁気記録層を有することを特徴とする磁気記録媒体。1. A magnetic recording medium having a laminated structure of partially oxidized ferromagnetic metal thin films, and having a magnetic recording layer having a polymer separation layer without an oxidized layer at the laminated interface.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17694586A JPS6334719A (en) | 1986-07-28 | 1986-07-28 | Magnetic recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17694586A JPS6334719A (en) | 1986-07-28 | 1986-07-28 | Magnetic recording medium |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6334719A true JPS6334719A (en) | 1988-02-15 |
Family
ID=16022483
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP17694586A Pending JPS6334719A (en) | 1986-07-28 | 1986-07-28 | Magnetic recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6334719A (en) |
-
1986
- 1986-07-28 JP JP17694586A patent/JPS6334719A/en active Pending
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