JPH06309665A - Method of manufacturing magnetic recording medium - Google Patents
Method of manufacturing magnetic recording mediumInfo
- Publication number
- JPH06309665A JPH06309665A JP5100939A JP10093993A JPH06309665A JP H06309665 A JPH06309665 A JP H06309665A JP 5100939 A JP5100939 A JP 5100939A JP 10093993 A JP10093993 A JP 10093993A JP H06309665 A JPH06309665 A JP H06309665A
- Authority
- JP
- Japan
- Prior art keywords
- magnetic layer
- polymer substrate
- oxygen
- magnetic
- 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
Links
Landscapes
- Manufacturing Of Magnetic Record Carriers (AREA)
- Thin Magnetic Films (AREA)
- Physical Vapour Deposition (AREA)
Abstract
(57)【要約】
【目的】 連続蒸着装置を用いた斜方蒸着において、蒸
気密度の小さい領域に存在する余剰酸素が、磁性層の特
性劣化に及ぼす影響を低減し、記録再生特性の向上を図
る。
【構成】 真空容器内に酸素を導入し、連続蒸着により
円筒状キャン8の周面上を走行する長尺の高分子基板上
5に磁性層を形成する斜方蒸着過程において、酸素の導
入部4を磁性層形成終期の蒸発原子の高分子基板5への
入射角を規制する遮蔽板3bと円筒状キャン8との間に
置き、かつ磁性層形成初期の蒸発原子が高分子基板5に
入射する近傍において、希土類原子、もしくはイットリ
ウム原子、またはこれらを混合したものを蒸発させる。
(57) [Abstract] [Purpose] In oblique vapor deposition using a continuous vapor deposition apparatus, it is possible to reduce the effect of excess oxygen existing in a region with a low vapor density on the characteristic deterioration of the magnetic layer and improve the recording / reproducing characteristics. Try. [Structure] Introducing oxygen into a vacuum container and forming a magnetic layer on a long polymer substrate 5 running on the circumferential surface of a cylindrical can 8 by continuous vapor deposition. 4 is placed between the cylindrical can 8 and the shielding plate 3b that regulates the incident angle of vaporized atoms at the end of the formation of the magnetic layer to the polymer substrate 5, and the vaporized atoms at the initial stage of magnetic layer formation are incident on the polymer substrate 5. The rare earth atom, the yttrium atom, or a mixture thereof is evaporated in the vicinity.
Description
【0001】[0001]
【産業上の利用分野】本発明は、高密度記録再生特性に
優れた磁気記録媒体の製造方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method of manufacturing a magnetic recording medium having excellent high density recording / reproducing characteristics.
【0002】[0002]
【従来の技術】現在、磁気記録再生装置は小型化、高密
度化の傾向にあり、従来の塗布型媒体の高密度化の限界
を越えるものとして金属薄膜型媒体が注目されている。
これに関しては、CoとNiとOを主成分とする金属薄
膜型媒体がVTR用の磁気テープとして実用化され市販
されている。このような磁気記録媒体を生産性良く形成
するためには、例えば円筒状キャンを用いた連続真空蒸
着装置などにより、長尺の高分子基板を移動させながら
その上に磁性層を連続して蒸着すればよい。2. Description of the Related Art At present, magnetic recording / reproducing devices tend to be smaller and have higher densities, and metal thin film type media have been attracting attention as exceeding the limit of high density of conventional coating type media.
In this regard, a metal thin film type medium containing Co, Ni and O as main components has been put to practical use as a magnetic tape for a VTR and is commercially available. In order to form such a magnetic recording medium with high productivity, for example, a continuous vacuum vapor deposition device using a cylindrical can is used to continuously deposit a magnetic layer on a long polymer substrate while moving it. do it.
【0003】この際、真空容器内に酸素を導入して磁性
層をCoとNiの部分酸化物よりなる強磁性薄膜にする
とともに、斜方蒸着の手法を用いることにより、磁性層
がその膜面に垂直方向の磁化成分を有するようにし、そ
の寄与によって従来の塗布型媒体に比べて高密度記録再
生特性を向上させている。上記技術による金属薄膜型磁
気テープは、次世代の家庭用小型ディジタルVTR、特
にハイビジョン対応ディジタルVTRに対応する磁気テ
ープとしても応用が期待されている。At this time, oxygen is introduced into the vacuum container to make the magnetic layer a ferromagnetic thin film of partial oxides of Co and Ni, and the oblique evaporation technique is used to make the magnetic layer have a film surface. Has a magnetization component in the perpendicular direction, and the contribution thereof improves the high density recording / reproducing characteristics as compared with the conventional coating type medium. The metal thin film type magnetic tape according to the above technique is expected to be applied as a magnetic tape corresponding to a next-generation home compact digital VTR, particularly a high-definition digital VTR.
【0004】[0004]
【発明が解決しようとする課題】上述の連続蒸着装置を
用いた製造方法により、酸素を導入して形成したCoと
O、あるいはCoとNiとOを主成分とする磁性層にお
いて、Co(Co及びNi)と酸素の組成比の磁性層厚
み方向のプロファイルを調べてみると、磁性層形成初期
部(Co等の蒸気密度が小である。)における酸素の割
合が他の部分よりも大きくなっており、特に顕著な例で
は、高分子基板面近傍でその組成比が1対1となってい
ることがわかった。In the magnetic layer mainly composed of Co and O or Co, Ni and O formed by introducing oxygen by the manufacturing method using the above continuous vapor deposition apparatus, Co (Co And a profile of the composition ratio of Ni) and oxygen in the thickness direction of the magnetic layer is examined, the proportion of oxygen in the initial portion of the magnetic layer formation (the vapor density of Co or the like is small) becomes larger than that in other portions. In a particularly remarkable example, it was found that the composition ratio was 1: 1 near the surface of the polymer substrate.
【0005】このことは、磁性層の初期形成部がほとん
ど非磁性になっていることを意味している。すなわち、
従来の製造方法では、磁性層の形成初期部である高分子
基板面近傍に磁気特性の劣る部分が存在し、磁性層表面
側に近づくほど磁気特性が改善されているものと考えら
れる。このような高分子基板表面近傍の部分の存在は、
磁性層全体としての磁気特性を劣化させる。また、磁性
層厚み方向において磁気特性が大きな差異をもって分布
することは、記録再生特性向上の観点から好ましいこと
ではない。上記観点から、磁性層形成初期部におけるC
o(Co及びNi)と酸素の組成比を磁性層表面近傍と
同等程度とし、磁性層厚み方向における酸素の組成分布
をほぼ一定とできる製造方法が必要とされている。This means that the initial formation portion of the magnetic layer is almost non-magnetic. That is,
In the conventional manufacturing method, it is considered that there is a portion having inferior magnetic properties near the surface of the polymer substrate, which is the initial portion of the formation of the magnetic layer, and the magnetic properties are improved as it approaches the surface side of the magnetic layer. The existence of such a portion near the surface of the polymer substrate is
It deteriorates the magnetic properties of the entire magnetic layer. Further, it is not preferable from the viewpoint of improving the recording / reproducing characteristics that the magnetic characteristics are distributed with a large difference in the thickness direction of the magnetic layer. From the above viewpoint, C in the initial portion of the magnetic layer formation
There is a need for a manufacturing method in which the composition ratio of o (Co and Ni) to oxygen is approximately the same as in the vicinity of the surface of the magnetic layer, and the compositional distribution of oxygen in the thickness direction of the magnetic layer is substantially constant.
【0006】[0006]
【課題を解決するための手段】本発明は、上記課題の観
点からより好ましい金属薄膜型磁気テープの製造方法を
提供するものであり、真空容器内に酸素を導入し、連続
蒸着により円筒状キャンの周面上を走行する長尺の高分
子基板上に磁性層を形成する斜方蒸着過程において、酸
素の導入部を磁性層形成終期の蒸発原子の高分子基板へ
の入射角を規制する遮蔽板と円筒状キャンとの間に置
き、かつ磁性層形成初期の蒸発原子が高分子基板に入射
する近傍において、希土類原子、もしくはイットリウム
原子、またはこれらを混合したものを蒸発させることを
特徴とする。SUMMARY OF THE INVENTION The present invention provides a method for producing a metal thin film magnetic tape which is more preferable from the viewpoint of the above-mentioned problems, in which oxygen is introduced into a vacuum container, and a cylindrical can is formed by continuous vapor deposition. In the oblique deposition process of forming a magnetic layer on a long polymer substrate running on the peripheral surface of the substrate, the oxygen introduction part is shielded to regulate the incident angle of vaporized atoms to the polymer substrate at the end of the magnetic layer formation. It is characterized by being placed between a plate and a cylindrical can, and vaporizing rare earth atoms, yttrium atoms, or a mixture thereof in the vicinity of the vaporized atoms in the initial stage of magnetic layer formation that are incident on the polymer substrate. .
【0007】[0007]
【作用】本発明によると、酸素の導入部を磁性層形成終
期側に配置して、Co等の蒸気密度が小である磁性層形
成初期側での酸素量をなるべく少なくなるようにしてい
る。また本発明によると、磁性層形成初期側に回り込ん
だ酸素を、磁性層を構成するCo等の金属原子より酸化
され易い希土類もしくはイットリウムの蒸発原子に優先
的に結合させることができるので、磁性層形成初期側の
層内に過剰の酸素が含有されることを防ぐことができ
る。According to the present invention, the oxygen introduction portion is arranged on the final side of the magnetic layer formation so that the oxygen amount on the initial side of the magnetic layer formation where the vapor density of Co or the like is low is as small as possible. Further, according to the present invention, the oxygen circulated to the initial side of the magnetic layer formation can be preferentially bonded to the vaporized atoms of rare earth or yttrium which are more easily oxidized than the metal atoms such as Co constituting the magnetic layer. It is possible to prevent excess oxygen from being contained in the layer on the initial side of layer formation.
【0008】[0008]
【実施例】図1に、本発明の製造方法を実現するための
連続蒸着装置の構成例を示す。この図において、5は長
尺の高分子基板であり、6、7はそれぞれ高分子基板5
の供給ロールおよび巻取りロールである。高分子基板5
には円筒状キャン8の周面上を矢印9の方向に走行する
間に、蒸発源1から蒸発したCoの蒸発原子が堆積され
る。蒸発原子の入射角は1対の遮蔽板3a、3bによっ
て規制される。また酸素導入管4により酸素を導入し
て、反応蒸着により部分酸化物よりなる強磁性層を形成
する構成となっている。EXAMPLE FIG. 1 shows an example of the structure of a continuous vapor deposition apparatus for realizing the manufacturing method of the present invention. In this figure, 5 is a long polymer substrate, and 6 and 7 are polymer substrates 5, respectively.
Supply roll and take-up roll. Polymer substrate 5
While traveling on the circumferential surface of the cylindrical can 8 in the direction of the arrow 9, evaporated atoms of Co evaporated from the evaporation source 1 are deposited. The incident angle of the vaporized atoms is regulated by the pair of shield plates 3a and 3b. Further, oxygen is introduced through the oxygen introduction tube 4 to form a ferromagnetic layer made of a partial oxide by reactive vapor deposition.
【0009】磁性層形成初期部の酸素のCoに対する組
成比が磁性層表面近傍よりも大きくなる原因として、以
下の点が考えられる。まず、図1のような連続蒸着装置
によって磁性層を形成する場合には、蒸発原子の高分子
基板5への入射角が初期形成部から終期形成部に至るま
で連続的に変化する。高分子基板面近傍の初期部を形成
する蒸発原子の入射角は高分子基板法線に対して高入射
角となる領域であり、蒸発原子の付着効率が低い上に、
蒸発源からの距離が大きいために蒸気密度が低くなって
いるので、相対的に膜中の酸素の割合が高くなるのであ
る。The following points can be considered as a cause of the composition ratio of oxygen to Co in the initial portion of the magnetic layer becoming larger than that in the vicinity of the surface of the magnetic layer. First, when the magnetic layer is formed by the continuous vapor deposition apparatus as shown in FIG. 1, the incident angle of the vaporized atoms to the polymer substrate 5 continuously changes from the initial formation portion to the final formation portion. The incident angle of the vaporized atoms forming the initial part in the vicinity of the polymer substrate surface is a region where the incident angle is high with respect to the polymer substrate normal, and the attachment efficiency of the vaporized atoms is low.
Since the distance from the evaporation source is large and the vapor density is low, the proportion of oxygen in the film is relatively high.
【0010】これを考慮して、図1の装置では、酸素導
入管4を磁性層の形成終期側において蒸発原子の高分子
基板5への入射角を規制する遮蔽板3bと円筒状キャン
8との間に置き、磁性層の形成初期側での酸素量をなる
べく少なくするように構成されている。しかしながら、
磁性層の形成終期側で導入された酸素はすべてCo等の
金属原子と結合するのではなく、一部は余剰となる。こ
の余剰酸素は、磁性層の形成終期側から高入射角領域の
磁性層形成初期側へも回り込んでしまう。In consideration of this, in the apparatus shown in FIG. 1, the oxygen introducing tube 4 is provided with a shielding plate 3b and a cylindrical can 8 for restricting the incident angle of vaporized atoms to the polymer substrate 5 at the final stage of formation of the magnetic layer. The oxygen amount on the initial side of formation of the magnetic layer is reduced as much as possible. However,
Oxygen introduced at the final stage of formation of the magnetic layer does not all bond with metal atoms such as Co, but a part thereof becomes an excess. This excess oxygen also wraps around from the final stage of formation of the magnetic layer to the initial stage of formation of the magnetic layer in the high incident angle region.
【0011】そこで本製造方法ではさらに、磁性層形成
初期の蒸発原子が高分子基板5に入射する近傍におい
て、希土類原子もしくはイットリウム原子を酸化用蒸発
源2から蒸発させる構成としている。これら希土類もし
くはイットリウムの蒸発原子は、磁性層を構成するCo
等の金属原子よりも酸化され易いため、磁性層形成初期
側に回り込んだ酸素と優先的に結合し、磁性層内に過剰
の酸素が含有されることを防ぐことができる。Therefore, in the present manufacturing method, the rare earth atoms or the yttrium atoms are evaporated from the evaporation source 2 for oxidation in the vicinity of the evaporated atoms at the initial stage of forming the magnetic layer, which are incident on the polymer substrate 5. These rare earth or yttrium vaporized atoms form Co that constitutes the magnetic layer.
Since it is more easily oxidized than the metal atoms such as the above, it preferentially bonds with oxygen that has circulated to the initial side of the magnetic layer formation, and can prevent excess oxygen from being contained in the magnetic layer.
【0012】次に本実施例をより具体的に説明する。Next, this embodiment will be described more specifically.
【0013】図1に示す装置を用い、磁性材料の蒸発源
1をCoとして高分子基板上にCoとOを主成分とする
磁性層を形成した。本実施例では、酸化用蒸発源2をG
dとした。図1の構成においては、酸化用蒸発源2より
蒸発した希土類もしくはイットリウムの蒸発原子が磁性
層内に混入しないよう、酸化用蒸発源2、磁性材料の蒸
発源1および遮蔽板3aの相対位置関係、また希土類も
しくはイットリウムの蒸気密度分布を十分に考慮しなけ
ればならない。この観点からは、必要に応じて、酸化用
蒸発源2と磁性材料の蒸発源1との間を遮蔽する遮蔽板
を設置すればさらに好ましい。本実施例では作製された
磁性層の組成分析を行った結果、磁性層内のGd原子の
組成比は0.2 原子% 以下であり、ほとんど混入が無いこ
とが確認された。Using the apparatus shown in FIG. 1, a magnetic layer containing Co and O as main components was formed on a polymer substrate using Co as the evaporation source 1 of the magnetic material. In the present embodiment, the oxidation evaporation source 2 is G
d. In the configuration of FIG. 1, the relative positional relationship between the evaporation source 2 for oxidation, the evaporation source 1 of the magnetic material, and the shield plate 3a is prevented so that the evaporated atoms of rare earth or yttrium evaporated from the evaporation source 2 for oxidation are not mixed in the magnetic layer. Also, the vapor density distribution of rare earths or yttrium must be fully considered. From this viewpoint, it is more preferable to install a shielding plate that shields between the evaporation source 2 for oxidation and the evaporation source 1 of the magnetic material, if necessary. As a result of composition analysis of the magnetic layer produced in this example, the composition ratio of Gd atoms in the magnetic layer was 0.2 atomic% or less, and it was confirmed that there was almost no mixing.
【0014】図2(a)に、本実施例において作製した
CoとOを主成分とする磁性層において、オージェ分光
分析により得られたCo、酸素、およびカーボンの磁性
層厚み方向の組成プロファイルの一例を示す。また比較
例として、酸化用蒸発源2によってGdを蒸発させずに
作製したCoとOを主成分とする磁性層における分析結
果例を同様に(b)に示す。なお、カーボンを分析した
のは、磁性層と高分子基板との境界面をより明瞭に把握
するためである。FIG. 2A shows a composition profile of Co, oxygen, and carbon in the thickness direction of the magnetic layer obtained by Auger spectroscopic analysis in the magnetic layer containing Co and O as main components manufactured in this example. An example is shown. Further, as a comparative example, an example of an analysis result of a magnetic layer containing Co and O as main components, which is produced without evaporating Gd by the oxidizing evaporation source 2, is also shown in (b). The carbon was analyzed in order to more clearly understand the boundary surface between the magnetic layer and the polymer substrate.
【0015】(b)に示す比較例において、磁性層の基
板側ほど酸素のCoに対する組成比が大きくなってお
り、磁性層厚み方向で酸素濃度分布が大きいことが分か
る。一方(a)に示す本実施例の製造方法による磁性層
では、磁性層の表面側から基板側にいたるまで酸素のC
oに対する組成比はほぼ一定となっており、(b)に比
べて磁性層厚み方向における酸素の濃度分布が改善され
ていることが分かる。In the comparative example shown in (b), it can be seen that the composition ratio of oxygen to Co is increased toward the substrate side of the magnetic layer, and the oxygen concentration distribution is large in the thickness direction of the magnetic layer. On the other hand, in the magnetic layer according to the manufacturing method of the present embodiment shown in (a), oxygen C
The composition ratio with respect to o is almost constant, and it can be seen that the oxygen concentration distribution in the thickness direction of the magnetic layer is improved as compared with (b).
【0016】また本実施例および比較例における磁性層
の膜面内において、磁性層形成時の高分子基板の走行方
向、すなわち磁気テープとしたときのテープ長手方向に
磁界を印加した際の磁化曲線を振動試料型磁力計により
測定した。その結果、比較例では角型比が0.85であった
のに対し、本実施例による磁性層では0.9 に向上した。
これは磁性層形成初期部の磁気特性が改善されることに
よって磁気特性の磁性層厚み方向分布が抑制され、磁性
層全体としての磁気特性が向上したものと考えられる。Further, in the film surface of the magnetic layer in the present example and the comparative example, a magnetization curve when a magnetic field is applied in the running direction of the polymer substrate when the magnetic layer is formed, that is, in the tape longitudinal direction when forming a magnetic tape. Was measured by a vibrating sample magnetometer. As a result, the squareness ratio was 0.85 in the comparative example, while it was improved to 0.9 in the magnetic layer according to the present example.
It is considered that this is because the magnetic properties in the initial portion of the magnetic layer formation were improved, and thus the distribution of the magnetic properties in the thickness direction of the magnetic layer was suppressed, and the magnetic properties of the entire magnetic layer were improved.
【0017】さらに本実施例および比較例によって磁性
層が形成された高分子基板を裁断して磁気テープとし、
ドラムテスタを用いて記録再生特性の測定を行った。そ
の結果、波長0.5 μm 記録において、本実施例による磁
性層を有する磁気テープのC/N は、比較例による磁性層
を有する磁気テープよりも2dB 程度高いことが確認され
た。Further, the polymer substrate having the magnetic layer formed according to the present embodiment and the comparative example is cut into a magnetic tape,
Recording and reproducing characteristics were measured using a drum tester. As a result, it was confirmed that the C / N of the magnetic tape having the magnetic layer according to this example was about 2 dB higher than that of the magnetic tape having the magnetic layer according to the comparative example at the wavelength of 0.5 μm.
【0018】なお、酸化用蒸発源2をGd以外の希土
類、あるいはイットリウム、あるいはこれらの少なくと
も2種を混合したものを用いた場合にも、Coよりも優
先的に酸素と結合することによる本発明の効果が確認さ
れた。一方、酸化用蒸発源2にMg、Ti等の材料を用
いた場合にも、Coよりも優先的に酸素と結合すること
により、磁性層形成初期部での過剰酸素含有を防止する
効果が得られる。しかしこれらの昇華によって気相とな
る材料を用いた場合には、これらの原子が磁性層内に数
原子% 以上の割合で混入し、かえって磁気特性を劣化さ
せる結果となった。Even when a rare earth element other than Gd, yttrium, or a mixture of at least two of them is used as the evaporation source 2 for oxidation, the present invention can be obtained by preferentially bonding with oxygen over Co. The effect of was confirmed. On the other hand, even when a material such as Mg or Ti is used for the oxidation evaporation source 2, the effect of preventing excess oxygen content in the initial portion of the magnetic layer formation is obtained by preferentially bonding with oxygen over Co. To be However, when a material that becomes a gas phase by sublimation is used, these atoms are mixed in the magnetic layer at a ratio of several atomic% or more, which rather deteriorates the magnetic properties.
【0019】また磁性材料の蒸発源1としてCoの他、
Fe、Niあるいはこれらの少なくとも2種を混合した
ものを用いた場合にも、上記と同様に磁性層厚み方向の
酸素濃度分布を改善する本発明の効果が得られた。In addition to Co as the evaporation source 1 of the magnetic material,
Even when Fe, Ni or a mixture of at least two of them is used, the effect of the present invention of improving the oxygen concentration distribution in the thickness direction of the magnetic layer was obtained as in the above.
【0020】[0020]
【発明の効果】本発明の製造方法によれば、真空容器内
に酸素を導入して連続蒸着により形成される磁性層の層
厚方向において、酸素濃度分布をほぼ一定にすることが
でき、磁性層形成初期部の酸素含有量過剰による磁気特
性の劣化を防止することができる。これにより、磁性層
厚み方向において磁気特性が大きな差異をもって分布す
ることを抑制することができ、記録再生特性の向上を図
ることができる。According to the manufacturing method of the present invention, the oxygen concentration distribution can be made substantially constant in the layer thickness direction of the magnetic layer formed by continuous vapor deposition by introducing oxygen into the vacuum container. It is possible to prevent deterioration of magnetic properties due to excess oxygen content in the initial portion of layer formation. As a result, it is possible to prevent the magnetic characteristics from being distributed with a large difference in the thickness direction of the magnetic layer, and it is possible to improve the recording / reproducing characteristics.
【図1】本発明の製造方法を実現するための連続蒸着装
置の構成例を示す概略図である。FIG. 1 is a schematic view showing a configuration example of a continuous vapor deposition apparatus for realizing the manufacturing method of the present invention.
【図2】オージェ分光分析により得られたCo、酸素、
およびカーボンの磁性層厚み方向の組成プロファイル
を、本実施例(a)と比較例(b)とを比較して示す図
である。FIG. 2 Co, oxygen, obtained by Auger spectroscopy
FIG. 3 is a diagram showing the composition profile of carbon in the thickness direction of the magnetic layer in comparison between the present example (a) and the comparative example (b).
1 磁性材料の蒸発源 2 希土類、もしくはイットリウム、またはこれらを混
合したものの蒸発源 3a遮蔽板 3b遮蔽板 4 酸素導入管 5 高分子基板 6 供給ロール 7 巻取りロール 8 円筒状キャン 9 円筒状キャンの回転方向1 evaporation source of magnetic material 2 evaporation source of rare earth, yttrium, or a mixture thereof 3a shielding plate 3b shielding plate 4 oxygen introducing pipe 5 polymer substrate 6 supply roll 7 winding roll 8 cylindrical can 9 cylindrical can Direction of rotation
Claims (1)
より円筒状キャンの周面上を走行する長尺の高分子基板
上に磁性層を形成する斜方蒸着過程において、酸素の導
入部を磁性層形成終期の蒸発原子の高分子基板への入射
角を規制する遮蔽板と円筒状キャンとの間に置き、かつ
磁性層形成初期の蒸発原子が高分子基板に入射する近傍
において、希土類原子、もしくはイットリウム原子、ま
たはこれらを混合したものを蒸発させることを特徴とす
る磁気記録媒体の製造方法。1. An oxygen introduction part in an oblique vapor deposition process in which oxygen is introduced into a vacuum container and a magnetic layer is formed on a long polymer substrate running on the circumferential surface of a cylindrical can by continuous vapor deposition. Is placed between the shield and the cylindrical can that regulates the incident angle of vaporized atoms at the end of the magnetic layer formation onto the polymer substrate, and in the vicinity of the vaporized atoms at the initial stage of magnetic layer formation on the polymer substrate A method of manufacturing a magnetic recording medium, which comprises vaporizing atoms, yttrium atoms, or a mixture thereof.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5100939A JPH06309665A (en) | 1993-04-27 | 1993-04-27 | Method of manufacturing magnetic recording medium |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5100939A JPH06309665A (en) | 1993-04-27 | 1993-04-27 | Method of manufacturing magnetic recording medium |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH06309665A true JPH06309665A (en) | 1994-11-04 |
Family
ID=14287328
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5100939A Pending JPH06309665A (en) | 1993-04-27 | 1993-04-27 | Method of manufacturing magnetic recording medium |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH06309665A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8435594B2 (en) | 2007-09-05 | 2013-05-07 | Sony Corporation | Evaporation apparatus, method of manufacturing anode using same, and method of manufacturing battery using same |
-
1993
- 1993-04-27 JP JP5100939A patent/JPH06309665A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8435594B2 (en) | 2007-09-05 | 2013-05-07 | Sony Corporation | Evaporation apparatus, method of manufacturing anode using same, and method of manufacturing battery using same |
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