JPH02108240A - Production of magnetic recording medium - Google Patents
Production of magnetic recording mediumInfo
- Publication number
- JPH02108240A JPH02108240A JP26176388A JP26176388A JPH02108240A JP H02108240 A JPH02108240 A JP H02108240A JP 26176388 A JP26176388 A JP 26176388A JP 26176388 A JP26176388 A JP 26176388A JP H02108240 A JPH02108240 A JP H02108240A
- Authority
- JP
- Japan
- Prior art keywords
- film
- vapor deposition
- magnetic recording
- crucible
- recording medium
- 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 description 18
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 230000005294 ferromagnetic effect Effects 0.000 claims abstract description 8
- 238000001704 evaporation Methods 0.000 claims abstract description 7
- 230000008020 evaporation Effects 0.000 claims abstract description 7
- 229920006254 polymer film Polymers 0.000 claims abstract description 7
- 238000010884 ion-beam technique Methods 0.000 claims abstract description 5
- 239000010409 thin film Substances 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 7
- 229910052751 metal Inorganic materials 0.000 claims description 7
- 238000000034 method Methods 0.000 abstract description 6
- 229910020630 Co Ni Inorganic materials 0.000 abstract description 4
- 229910002440 Co–Ni Inorganic materials 0.000 abstract description 4
- 239000000956 alloy Substances 0.000 abstract description 4
- 229910045601 alloy Inorganic materials 0.000 abstract description 4
- 229910021385 hard carbon Inorganic materials 0.000 abstract description 4
- 238000007740 vapor deposition Methods 0.000 abstract description 4
- 229910052804 chromium Inorganic materials 0.000 abstract description 3
- 239000000463 material Substances 0.000 abstract description 3
- 239000004734 Polyphenylene sulfide Substances 0.000 abstract description 2
- 230000006698 induction Effects 0.000 abstract description 2
- 229920000069 polyphenylene sulfide Polymers 0.000 abstract description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 229910002804 graphite Inorganic materials 0.000 abstract 1
- 239000010439 graphite Substances 0.000 abstract 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 abstract 1
- 239000007789 gas Substances 0.000 description 12
- 239000010408 film Substances 0.000 description 11
- 239000010410 layer Substances 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 3
- 229910020676 Co—N Inorganic materials 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 239000011241 protective layer Substances 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- WGGNJZRNHUJNEM-UHFFFAOYSA-N 2,2,4,4,6,6-hexamethyl-1,3,5,2,4,6-triazatrisilinane Chemical compound C[Si]1(C)N[Si](C)(C)N[Si](C)(C)N1 WGGNJZRNHUJNEM-UHFFFAOYSA-N 0.000 description 1
- 229910020517 Co—Ti Inorganic materials 0.000 description 1
- 239000004696 Poly ether ether ketone Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000005566 electron beam evaporation Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 239000000696 magnetic material Substances 0.000 description 1
- 230000005415 magnetization Effects 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229920002530 polyetherether ketone Polymers 0.000 description 1
- -1 polyethylene terephthalate Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 238000007738 vacuum evaporation Methods 0.000 description 1
Landscapes
- Manufacturing Of 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の製造方法に関する。DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a method of manufacturing a magnetic recording medium having a magnetic recording layer made of a ferromagnetic metal thin film suitable for high-density magnetic recording.
従来の技術
高密度記録を実現するには、G o −N i −0斜
め蒸着膜〔アイイーイーイー トランザクションズオフ
?f ネf イp ス(IEEE TRANSAC
TIONSON MAGNETIC3)Vo4 MAG
−20,P、P、824〜82θ(1984))や、C
o −Cr−Nb垂直磁化膜〔特開昭61−77128
号公報〕等の強磁性金属薄膜を磁気記録層とした磁気記
録媒体と、回転磁気ヘッドによるヘリカルスキャンを組
み合わせるのが最も優れているが、この組み合わせは、
磁気記録媒体に求められる耐久性能を満足させる構成を
必要とすることから、現在も各種の改善検討がなされて
いる。これらは、プラズマ重合膜(特開昭61−151
837号公報)、酸化膜、窒化膜(特開昭61−151
830号公報、特開昭61−131231号公報)、硬
質カーボン膜と潤滑剤層の組み合せ(特開昭61−12
6627号公報、特開昭61−233412号公報)等
のように、Co−Cr 、Co−Ti 、Co−Ta
、Co−Ni 、Co −N i −0、Co −N
i−P等の強磁性金属薄膜の形成とは別工程で保護層、
潤滑層を形成するものでスペーシング損失との兼ね合い
で、膜厚が余シ厚くできないことから、強磁性金属薄膜
に微細な凹凸を形成するようなベースを用いて接触面積
を低減して一層の改善を図る試みがなされている〔特開
昭59−207422号公報、特開昭59−12163
1号公報〕。Conventional technology In order to realize high-density recording, a G o -N i -0 obliquely deposited film is required. IEEE TRANSAC
TIONSON MAGNETIC3) Vo4 MAG
-20, P, P, 824-82θ (1984)), C
o -Cr-Nb perpendicular magnetization film [JP-A-61-77128
The best method is to combine a magnetic recording medium with a magnetic recording layer made of a ferromagnetic metal thin film, such as the one disclosed in [No.
Since there is a need for a structure that satisfies the durability required for magnetic recording media, various improvements are currently being studied. These are plasma polymerized films (Japanese Patent Laid-Open No. 61-151
No. 837), oxide film, nitride film (JP-A-61-151)
No. 830, JP-A No. 61-131231), combination of hard carbon film and lubricant layer (JP-A No. 61-12
Co-Cr, Co-Ti, Co-Ta, etc.
, Co-Ni, Co-N i -0, Co-N
A protective layer,
Since the film forms a lubricating layer and cannot be made too thick due to spacing loss, the contact area is reduced by using a base that forms fine irregularities on the ferromagnetic metal thin film. Attempts have been made to improve the results [JP-A-59-207422, JP-A-59-12163]
Publication No. 1].
発明が解決しようとする課題
しかし上記したような別工程で保護潤滑層を配したもの
は、均一性の面での改善が望まれているのは勿論のこと
、合金系のヘッドでの狭トラツク化に対応するには良好
なエンベロープを得ることが十分行えないことから改善
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、合金系のヘッドでの狭トラツクC/N と耐
久性を兼ね備えた磁気記録媒体を製造できる方法を提供
するものである。Problems to be Solved by the Invention However, in the case where the protective lubricant layer is applied in a separate process as described above, not only is it desired to improve the uniformity, but also the narrow track of the alloy head is desired. Improvements have been desired since it is not possible to obtain a good envelope sufficiently to cope with the current situation. The present invention has been made in view of the above-mentioned circumstances, and provides a method for manufacturing a magnetic recording medium that has both a narrow track C/N and durability in an alloy head.
課題を解決するための手段
本発明の磁気記録媒体の製造方法は、上記した課題を解
決するため、移動する高分子フィルムにクラスターイオ
ンビーム蒸着法で強磁性金属薄膜を形成する際、有機ガ
スを放電ガスとしたプラズマを通過させるようにしたも
のである。Means for Solving the Problems In order to solve the above-mentioned problems, the method for manufacturing a magnetic recording medium of the present invention uses an organic gas when forming a ferromagnetic metal thin film on a moving polymer film by cluster ion beam evaporation. This is designed to allow plasma, which is a discharge gas, to pass through.
作 用
本発明の磁気記録媒体の製造方法は、強磁性金属微粒子
結晶を非磁性材料が覆うように働くことから、従来の保
護層が強磁性金属薄膜上に積層された場合と異なり、耐
久性が改善されるのと、充てん率が高くなシかつ結晶性
もよいことも加わって角型比、飽和磁束量も大きくなり
、C/N も改善された磁気記録媒体が製造できる。Function: Since the method for manufacturing a magnetic recording medium of the present invention works so that the non-magnetic material covers the ferromagnetic metal fine particle crystals, unlike the conventional case where a protective layer is laminated on a ferromagnetic metal thin film, durability is improved. In addition to the improved filling ratio and good crystallinity, it is possible to manufacture a magnetic recording medium with a large squareness ratio, a large amount of saturation magnetic flux, and an improved C/N ratio.
又高分子フィルム上にイオン化された状態で蒸着しても
クラスター状で荷電の対質量比が極めて小さいことから
静電的なバラツキによるノイズ増加も防げる効果もある
。Furthermore, even if it is deposited on a polymer film in an ionized state, it forms a cluster and has an extremely small charge-to-mass ratio, which also has the effect of preventing an increase in noise due to electrostatic variations.
実施例
以下、図面を参照しながら本発明の一実施例について説
明する。図は本発明を実施するのに用いた巻取り蒸着装
置の要部構成図である。図で1はポリエチレンテレフタ
レート、ポリフェニレンサルファイド、ポリエーテルエ
ーテルケトン、ポリイミド等の高分子フィルムで、必要
ならば下塗υ層、下地層、軟磁性層をあらかじめ配した
ものを用いてもよい。2は円筒キャンで、絶縁し、電位
を加えられるように構成する。3は巻出し軸、4は巻取
υ軸、5はルツボで、eはCo−Cr、Co−Ni、C
o−3n、Co−Ta等の蒸着材料、7は高周波誘導コ
イルで、8は高周波グロー放電電極で、有機ガスを導入
するノズルを兼ねるのが好ましい。Embodiment Hereinafter, an embodiment of the present invention will be described with reference to the drawings. The figure is a configuration diagram of the main parts of a winding vapor deposition apparatus used to carry out the present invention. In the figure, 1 is a polymer film made of polyethylene terephthalate, polyphenylene sulfide, polyether ether ketone, polyimide, etc., and if necessary, a subbing layer, a base layer, and a soft magnetic layer may be provided in advance. 2 is a cylindrical can, which is insulated and constructed so that a potential can be applied to it. 3 is an unwinding shaft, 4 is a winding υ axis, 5 is a crucible, and e is Co-Cr, Co-Ni, C
7 is a high frequency induction coil, 8 is a high frequency glow discharge electrode, which preferably also serves as a nozzle for introducing organic gas.
9は絶縁導入端子、1oは真空容器、11は真空排気系
である。図の装置で、円筒キャンの直径を5ocrnと
し、絶縁抵抗を1500Vで800(MΩ)とし、キャ
ンの直下25crnに0.1Hの孔をもったZ ro2
ルツボを配し、2ターンの高周波グロー放電電極に0.
5φのガス導入孔を20ケ配して実施した。9 is an insulation introduction terminal, 1o is a vacuum container, and 11 is a vacuum exhaust system. In the device shown in the figure, the diameter of the cylindrical can is 5ocrn, the insulation resistance is 800 (MΩ) at 1500V, and a Z ro2 with a 0.1H hole 25crn directly below the can.
A crucible is placed on the 2-turn high frequency glow discharge electrode.
The test was carried out by arranging 20 gas introduction holes of 5φ.
厚み10μmのポリエチレンテレフタレートフィルム上
に最小入射角40度でCo−Cr (Coニア92wt
%)を電子ビーム蒸着し0.14μmの斜め蒸着膜を4
X 10−7(Torr) の真空度で形成し、そ
の上にグラファイトをターゲットにしてAr+H2=o
、i (Torr)Ar ; H2=i : s、a
、 13.58 (MHz ) 。Co-Cr (CoNia 92wt
%) by electron beam evaporation to form a 0.14 μm obliquely deposited film of 4
It is formed at a vacuum degree of
, i (Torr)Ar; H2=i: s, a
, 13.58 (MHz).
940 (W)の条件でスパッタ蒸着しダイアモンド状
硬質炭素膜を150人配し、更に真空蒸着法でステアリ
ン酸を40人配し8ミリ幅の磁気テープを製造し比較例
として準備した。実施例は同じフィルムを用いて、最小
入射角30度でCo −Cr(Co : 79.2 w
t%)をクラスターイオンビーム蒸着して0.14μm
の薄膜を形成した。その際CH4ガスを0.2 (l
/IJJI)導入し、13.56 (MHz ) 、
520(W)の高周波グローを発生させて、キャンには
500■の負の電圧を印加した。A magnetic tape having a width of 8 mm was prepared by depositing 150 diamond-like hard carbon films by sputter deposition under the conditions of 940 (W) and then depositing stearic acid by vacuum evaporation for 40 people, and prepared this as a comparative example. The example uses the same film with a minimum incident angle of 30 degrees and Co-Cr(Co: 79.2 w
t%) by cluster ion beam evaporation to a thickness of 0.14 μm.
A thin film was formed. At that time, CH4 gas was added to 0.2 (l
/IJJI), 13.56 (MHz),
A high frequency glow of 520 (W) was generated, and a negative voltage of 500 μ was applied to the can.
0.14μm の薄膜上にダイアモンド状硬質炭素薄膜
を90人、ステアリン酸膜を40人配し、同じく8ミリ
幅の磁気テープを製造した(実施例A)。A magnetic tape having a width of 8 mm was similarly manufactured by disposing a diamond-like hard carbon thin film on a 0.14 μm thin film by 90 people and a stearic acid film by 40 people (Example A).
又、有機ガスとして、ヘキサメチルシクロトリシラザン
を0.121/am 導入し、13.56 (MHz
) 。In addition, as an organic gas, hexamethylcyclotrisilazane was introduced at a rate of 0.121/am, and a rate of 13.56 (MHz
).
41o (W)の高周波グローを発生させ、キャンに4
60 (V)の負の電圧を印加した以外は実施例Aと同
じ条件で8ミリテープを製造した(実施例B)。Generates a high frequency glow of 41o (W) and
An 8 mm tape was manufactured under the same conditions as Example A except that a negative voltage of 60 (V) was applied (Example B).
次に有機ガスとしてアリルアルコールをO,Oa(17
m)、キャノンガスを0.02 (71!/III方)
導入し、2 o O(KHz)、 800 (W)の高
周波グローを発生させ、キャンには710 (V)の負
の電圧を印加した以外は実施例Aと同じ条件で製造した
(実施例C)。Next, allyl alcohol was added as an organic gas to O, Oa (17
m), Cannon gas 0.02 (71!/III way)
It was manufactured under the same conditions as Example A, except that a high-frequency glow of 800 (W) at 2 o O (KHz) was generated, and a negative voltage of 710 (V) was applied to the can (Example C). ).
これらのテープを用い、トラックピッチ7μm。Using these tapes, the track pitch was 7 μm.
記録波長0.47μm の高密度磁気記録をアモルファ
スヘッドによシ行い、Cハ を比較した。比較例をo(
dB)とした時、実施例Aは+2.9 (dB)。High-density magnetic recording at a recording wavelength of 0.47 μm was performed using an amorphous head, and Cc was compared. Comparative example o(
dB), Example A is +2.9 (dB).
実施例Bは+2.8 (dB) 、実施例Cは+3.3
(dB)であった。Example B is +2.8 (dB), Example C is +3.3
(dB).
又夫々のテープを5巻ずつ用意して、C/N を比較
したところ、比較例は平均値が0(dB)で2.1 (
dB)〜+0.9 (dB)のバラツキがあったが実施
例はAが平均値2.9 (dB)、 2.65〜2.9
9(dB)、Bが平均値2.8 (dB)、 2.64
〜2.91 (dB)、Cは平均値3.3 (dB)、
3.06〜3.41 (dB)で夫々雑音が場所ムラ
が小さいことを示している。In addition, when we prepared 5 rolls of each tape and compared the C/N, the comparative example had an average value of 0 (dB) and 2.1 (
dB) to +0.9 (dB), but in the example, A had an average value of 2.9 (dB), 2.65 to 2.9
9 (dB), B average value 2.8 (dB), 2.64
~2.91 (dB), C is average value 3.3 (dB),
3.06 to 3.41 (dB), respectively, indicating that the noise has little local unevenness.
又夫々のテープを、40’C88%RH、5,7ppm
5o2ガスの環境に1ケ月放置し、前後のり変化を比較
した結果、比較例が初期値に対し、 −6,7(dB)
と低下が大きかったのに対し、実施例はAが−1,1(
dB) 、 Bが−0,2(dB) 、 Cが−0
,7(dB)と良好であった。Also, each tape was 40'C88%RH, 5.7ppm.
As a result of leaving it in a 5o2 gas environment for one month and comparing the change in slope before and after, the comparison example showed -6.7 (dB) compared to the initial value.
In contrast, in the example, A decreased by -1, 1 (
dB), B is -0,2(dB), C is -0
, 7 (dB), which was good.
尚ステル状態でも比較例は33分、実施例A。In addition, even in the stealth state, the comparative example was 33 minutes, and the example A.
B、Cは夫々36分、34分、38分後に初期出力から
1(dB)出力がさがるだけといった耐久性も確認した
。The durability of B and C was also confirmed, with the output only decreasing by 1 (dB) from the initial output after 36 minutes, 34 minutes, and 38 minutes, respectively.
上記した以外でCo−Ni、Co−Ndでも類似の改善
ができたがco −N iについては、有機ガスに酸素
を流量で有機ガスに対して10%から26%の割合で混
合させることで有機ガス単独よりも改善がはかれること
がわかった。Similar improvements could be made with Co-Ni and Co-Nd other than those mentioned above, but for co-Ni, by mixing oxygen with organic gas at a flow rate of 10% to 26% of the organic gas. It was found that the improvement was better than using organic gas alone.
最適条件では出力は殆んど変らず雑音が約1(dB )
改善された。Under optimal conditions, the output hardly changes and the noise is about 1 (dB)
Improved.
発明の効果
以上のように本発明によれば、高密度記録を合金系ヘッ
ドで行った時に良好なC/N を与えることのできる、
耐久性を兼ね備えた磁気記録媒体を製造できるといった
すぐれた効果がある。Effects of the Invention As described above, according to the present invention, it is possible to provide a good C/N ratio when high-density recording is performed with an alloy head.
This has the excellent effect of making it possible to manufacture a magnetic recording medium that has both durability.
図は、本発明の実施に用いたクラスターイオンビーム蒸
着装置の要部構成図である。
1・・・・・・高分子フィルム、6・・・・・・蒸発源
容器、6・・・・・・蒸着材料、8・・・・・・高周波
グロー放電電極。The figure is a configuration diagram of main parts of a cluster ion beam evaporation apparatus used to implement the present invention. DESCRIPTION OF SYMBOLS 1... Polymer film, 6... Evaporation source container, 6... Evaporation material, 8... High frequency glow discharge electrode.
Claims (1)
法で強磁性金属薄膜を形成する際、有機ガスを放電ガス
としたプラズマを通過させることを特徴とする磁気記録
媒体の製造方法。A method for producing a magnetic recording medium, which comprises passing plasma using an organic gas as a discharge gas when forming a ferromagnetic metal thin film on a moving polymer film by cluster ion beam evaporation.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP26176388A JPH02108240A (en) | 1988-10-18 | 1988-10-18 | Production of magnetic recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP26176388A JPH02108240A (en) | 1988-10-18 | 1988-10-18 | Production of magnetic recording medium |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH02108240A true JPH02108240A (en) | 1990-04-20 |
Family
ID=17366355
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP26176388A Pending JPH02108240A (en) | 1988-10-18 | 1988-10-18 | Production of magnetic recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02108240A (en) |
-
1988
- 1988-10-18 JP JP26176388A patent/JPH02108240A/en active Pending
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