JPS6052931A - Method for manufacturing magnetic recording media - Google Patents
Method for manufacturing magnetic recording mediaInfo
- Publication number
- JPS6052931A JPS6052931A JP58161331A JP16133183A JPS6052931A JP S6052931 A JPS6052931 A JP S6052931A JP 58161331 A JP58161331 A JP 58161331A JP 16133183 A JP16133183 A JP 16133183A JP S6052931 A JPS6052931 A JP S6052931A
- Authority
- JP
- Japan
- Prior art keywords
- ion
- coercive force
- kinetic energy
- magnetic recording
- support
- 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.)
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- 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CO系合金から成る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 the Invention The present invention relates to a method of manufacturing a magnetic recording medium in which a thin film made of a CO-based alloy is used as a magnetic recording layer.
従来例の構成とその問題点
磁気記録に於て高密度化?図るために媒体に要求される
点は薄い磁気記録層で大きい抗磁力を有するものである
ことは良く知られることである。Conventional configuration and its problems High density in magnetic recording? It is well known that the media required for this purpose are a thin magnetic recording layer and a large coercive force.
この要求に生産規模でこたえていくことは必ずしも容易
ではない。Meeting this demand on a production scale is not necessarily easy.
特に媒体の表面と直交する方向の磁化を利用するいわゆ
る垂直磁化記録に用いる媒体の磁気記録層を高速で得て
しかも大きい抗磁力に制御するのは容易ではない。In particular, it is not easy to obtain a magnetic recording layer of a medium used for so-called perpendicular magnetization recording, which utilizes magnetization in a direction perpendicular to the surface of the medium, at high speed and to control it to a large coercive force.
現状で大きい抗磁力を確実に制御できるのはグロー放電
によって生じた陽イオンf Co −Cr合金等のター
ゲットに射突させ、ターゲットよりCo。At present, the only way to reliably control a large coercive force is to inject cations f generated by glow discharge into a target such as a Co--Cr alloy.
Cr原子を叩き出して所定の支持体に付着せしめるいわ
ゆるスパッタリング法であるが、前記したメカニズムよ
り予測できるように膜形成速度は高々1o入/secと
極めて遅い。This is a so-called sputtering method in which Cr atoms are ejected and attached to a predetermined support, but as expected from the mechanism described above, the film formation rate is extremely slow at most 10/sec.
一方真空蒸着法では支持体の温度’i 2.、O0℃以
上の高温にすることで初めて垂直方向の抗磁力が1KO
ei越える条件が現れるが、用いられる支持体の耐熱性
に制約があるのと蒸着時の支持体の温度を精度良く、例
えば±6℃に制御するのは難かしく長尺の支持体上に連
続して一定の特性の垂直磁化膜を得るのは困難である。On the other hand, in the vacuum evaporation method, the temperature of the support 'i2. , the perpendicular coercive force becomes 1KO only when the temperature is raised to 00°C or higher.
However, there are restrictions on the heat resistance of the support used, and it is difficult to accurately control the temperature of the support during vapor deposition to, for example, ±6°C, so it is difficult to continuously control the temperature of the support on a long support. It is difficult to obtain a perpendicularly magnetized film with constant characteristics.
しかしながらこの方法は膜形成速度としては200人/
sec 〜2,000人/secと大きくとれル+7)
でこの方法の改良として支持体温度を下げるためにイオ
ンブレーティン命法が鋭意検討されている。However, this method has a film formation rate of 200 people/
sec ~ 2,000 people/sec, which is large +7)
As an improvement to this method, the ion-blading method is being intensively studied in order to lower the support temperature.
イオンブレーティング法は、支持体上に形成された膜と
支持体との付着力が大きくなる。支持体の温度i100
℃以下でも大きい抗磁力が得られる傾向をもつ等の利点
はあるが例えば1000(0θ〕の抗磁力を得る場合膜
形成速度は第1図に示したように5グロー放電のパワー
に依存する。In the ion blating method, the adhesion between the film formed on the support and the support is increased. Support temperature i100
Although there are advantages such as a tendency to obtain a large coercive force even at temperatures below .degree. C., for example, when obtaining a coercive force of 1000 (0.theta.), the film formation rate depends on the power of the 5 glow discharge as shown in FIG.
グロー放電のパワーを大きくしていくと膜形成速度は途
中まで大きくできるが、パワーを大きくしていっても逆
に抗磁力が下がってし甘う現象があることがわかる。It can be seen that by increasing the power of the glow discharge, the film formation rate can be increased to a certain extent, but even if the power is increased, the coercive force decreases.
第1図の結果は、厚さが20μmのポリエチレンテレフ
タレートヲ直径50 cmの回転ドラムに沿って移動さ
せ、ドラム直下2f5cmに配した電子ビーム蒸発源よ
り蒸発させたCo −’Cr fドラム2Cm離れた位
置にポリエチレンテレフタレートの移動方向に開孔部と
して2.5(:@のスリノトヲ有する遮へい板を配して
イオンブレーティングした場合である。The results shown in Figure 1 show that polyethylene terephthalate with a thickness of 20 μm was moved along a rotating drum with a diameter of 50 cm, and Co-'Cr was evaporated from an electron beam evaporation source placed 2 cm directly below the drum. This is a case in which a shielding plate having an opening of 2.5 (:@) was placed in the direction of movement of the polyethylene terephthalate and ion blating was performed.
グロー放電は、2ターンの高周波コイルを遮へい板から
6Cmと16crnO間に配して、前記コイルに13.
56hh の高周波電力を投入するようにして発生させ
た。放電ガスは八■を用い、真空度は4.2 X 10
TORRの場合でありCrの含有量は18重量係で、
Co−Crの膜厚は0.2μm一定とした。Glow discharge is performed by placing a two-turn high-frequency coil between 6Cm and 16crnO from the shielding plate, and connecting the coil to 13.
It was generated by inputting 56hh of high frequency power. The discharge gas used was 8mm, and the degree of vacuum was 4.2 x 10.
In the case of TORR, the Cr content is 18% by weight,
The Co-Cr film thickness was kept constant at 0.2 μm.
従来のイオンブレーティング法による改良は第1図にみ
られるように限界がある。Improvements made by the conventional ion blating method have limitations, as shown in FIG.
この現象は、グロー放電のパワーを大きくするとイオン
ボンバードによる逆の作用効果である。This phenomenon is the opposite effect of ion bombardment when the power of glow discharge is increased.
結晶に欠陥を発生させる作用が支配的になってきてかえ
って結晶配向性が悪くなることによるもので大きい抗磁
力を得るには支持体温度をあげざるを得ないことになり
改良できる範囲は想像以上に狭いものであった。This is due to the fact that the effect of generating defects in the crystal becomes dominant, which actually worsens the crystal orientation, and in order to obtain a large coercive force, it is necessary to raise the temperature of the support, and the scope of improvement is beyond imagination. It was narrow.
発明の目的
本発明は、高速で高抗磁力OCO系合金から成る磁気記
録層を得る磁気記録媒体の製造方法全提供するものであ
る。OBJECTS OF THE INVENTION The present invention provides a complete method for manufacturing a magnetic recording medium that produces a magnetic recording layer made of a high coercive OCO alloy at high speed.
発明の構成
本発明は支持体の表面にイオンブレーティング法によっ
てGo系合金から成る磁気記録層を形成する際に、CO
に添加する元素のイオンの運動エネルギーがCOのイオ
ンの運動エネルギーより大きいことを特徴とするもので
ある。Structure of the Invention The present invention is directed to the use of CO
The kinetic energy of the ions of the element added to the carbon dioxide is larger than the kinetic energy of the ions of CO.
CO及びCOに添加する元素のうちイオンが占める割合
は高々10係程度である。The ratio of ions to CO and the elements added to CO is about 10 factors at most.
勿論1oo%イオンで構成することもできるが当然膜形
成速度はスパッタリング法と同程度であり、前記した程
度即ち10%程度のイオンを有効に利用するのが本発明
の特徴的な作用効果をもたらすポイントである。Of course, it can be composed of 10% ions, but the film formation rate is of course comparable to that of the sputtering method, and the effective use of ions at the above-mentioned level, that is, about 10%, brings about the characteristic effects of the present invention. That's the point.
即ちイオンf CoとCOに添加する元素の両者が同一
のエネルギーで構成された従来例と異なり、COに添加
する元素の方の運動エネルギーを大きくすることでCo
より添加元素の易動度が大きくなり結晶の表面に棟で移
動し易くなり、結果として粒子間の磁気的相互作用を弱
めることで抗磁力が大きくなるものと推察できる。That is, unlike the conventional example in which both the ion f Co and the element added to CO have the same energy, increasing the kinetic energy of the element added to CO increases the
It can be inferred that the mobility of the additive element increases, making it easier to move along the surface of the crystal, and as a result, the magnetic interaction between particles is weakened, thereby increasing the coercive force.
この作用効果を明確に得るには、支持体の温度にも依存
するが、COのイオンの運動エネルギーの1.2倍以上
から高々3倍の範囲に設定するのが好ましい。In order to clearly obtain this effect, it is preferable to set the kinetic energy to a range from 1.2 times or more to at most 3 times the kinetic energy of CO ions, although it depends on the temperature of the support.
一方エネルギーからみると高々2. KeVにおさえる
ことが好ましい。On the other hand, from an energy perspective, at most 2. It is preferable to suppress it to KeV.
これ以上になるとむしろ結晶配向性が悪化し、抗磁力の
分散が犬きくなり、磁気記録媒体として用いた時の記録
感度が下がる欠点が生じるからである。This is because if it exceeds this range, the crystal orientation deteriorates, the dispersion of coercive force becomes narrower, and the recording sensitivity decreases when used as a magnetic recording medium.
従ってエネルギーの選択はCoイオンを基礎にしての倍
率と、絶対値の両者で前記条件の範囲内で行われるもの
である。Therefore, the energy selection is made within the range of the above conditions, both in terms of magnification based on Co ions and in absolute value.
実施例の説明 J以下本発明の実施例を図面を参照しながら説明する。Description of examples Embodiments of the present invention will be described below with reference to the drawings.
第2図は、本発明の詳細な説明するために用いた蒸着装
置の基本構成を示すものである。FIG. 2 shows the basic configuration of a vapor deposition apparatus used to explain the present invention in detail.
支持体1は、図示してない巻取装置により巻取られる過
程で図示してない冷却装置で冷却されながら遮へい板2
の開孔部スリ・・ト3全通過した蒸気流にエリ磁気記録
層となる強磁性金属薄膜4の形成作用を受ける。In the process of being wound up by a winding device (not shown), the support 1 is cooled by a cooling device (not shown), and then the shielding plate 2 is rolled up.
The vapor flow that has completely passed through the opening slit 3 acts to form a ferromagnetic metal thin film 4 that will become a magnetic recording layer.
蒸発源5はCo用とCOに添加する元素(これ全Mと呼
ぶ)の両者を隣接してス’J 、ノド3直下に配置する
。Co 6 とM7は夫々所定の蒸発温度に制御され矢
印で模式的に示したようにCo蒸気流8゜M蒸気流9と
して支持体1の一部に向う。The evaporation source 5 is arranged adjacent to both the element for Co and the element to be added to CO (all referred to as M) directly below the throat 3. Co 6 and M7 are each controlled to a predetermined evaporation temperature and are directed toward a part of the support 1 as a Co vapor flow 8°M vapor flow 9, as schematically shown by the arrows.
CO蒸気流s、M蒸気流9には例えば加熱源が加速され
た電子ビームの時は一部イオンが含まれる。The CO vapor flow s and the M vapor flow 9 contain some ions, for example, when the heating source is an accelerated electron beam.
ここでは、この両者のイオンは1係以下にして且つ積極
的には加速しかいようにした。Here, both of these ions were made to have a coefficient of less than 1 and were actively accelerated.
イオン発生源は別々に配し、COイオン源1oより放出
されたイオンは所定の運動エネルギーを付与しCOイオ
ンビーム11とし偏向磁界12で偏向して、Co蒸気流
8のうち支持体1にスリット3を通過して向うものと同
じ方向に加速した。The ion sources are arranged separately, and the ions emitted from the CO ion source 1o are given a predetermined kinetic energy and turned into a CO ion beam 11, which is deflected by a deflection magnetic field 12. 3 and accelerated in the same direction as the one heading towards it.
同様にMイオンビーム14もMイオン源13より偏向磁
界15で偏向して支持体1に向わせた。Similarly, the M ion beam 14 was also deflected by the deflection magnetic field 15 from the M ion source 13 and directed toward the support 1 .
(実施例−1)
10.5μmのポリエチレンテレフタレートフィルムを
支持体として用い6℃の媒体を表面近くに循環させた2
重円筒構造の直径50 cmの円筒キャンに沿って前記
支持体f6.9m/minで移動させた。(Example-1) A 10.5 μm polyethylene terephthalate film was used as a support and a 6°C medium was circulated near the surface.
The support was moved at f6.9 m/min along a cylindrical can having a heavy cylindrical structure and a diameter of 50 cm.
スリット開孔部の支持体移動方向の幅は4.6cmで、
蒸発源は偏向型の電子ビーム蒸発源を一対用いた。イオ
ン源はマグネトロン放電型式の金属イオン源を用いた。The width of the slit opening in the support movement direction is 4.6 cm,
A pair of deflected electron beam evaporation sources were used as the evaporation sources. A magnetron discharge type metal ion source was used as the ion source.
イオンは偏向磁界(ポールピースの直径は10cm )
k調整(−てCo+、M+イオンのみを用いろように
した。Ions are deflected by a magnetic field (pole piece diameter is 10cm)
k adjustment (-) to use only Co+ and M+ ions.
第3図はCOと、MとしてCrを選んでイオンの割合f
Co 、Cr全体に占める割合を夫々8%として、C
o+のエネルギーを600 e V 、 1000 e
Vの2水準選び、CO+に対してM+のエネルギー?変
えて、薄膜形成速度を約5,000人/5ec一定とし
て0.2μmのCoCr膜の垂直抗磁力を示したもので
ある。Figure 3 shows CO and Cr selected as M, and the ion ratio f
Assuming that the proportions of Co and Cr in the total are 8% each, C
The energy of o+ is 600 e V, 1000 e
Choose two levels of V, energy of M+ for CO+? On the other hand, the perpendicular coercive force of a 0.2 μm CoCr film is shown with the thin film formation rate constant at about 5,000 people/5 ec.
(但しCrは18重量係である。)
第1図と比較しても明らかなように5,000八/se
cという高速で100Q〔083以上の大きい抗磁力を
もった垂直磁化膜が得られる利点がある。(However, Cr is 18 weight division.) As is clear from the comparison with Figure 1, 5,0008/se
There is an advantage that a perpendicularly magnetized film having a large coercive force of 100Q[083 or more] can be obtained at a high speed of c.
又、支持体は冷却していても垂直磁化膜が得られ磁気テ
ープ用として最も緒特性が優れたポリエチレンテレフタ
レートフィルムを支持体に選ぶことができる点も利点で
ある。Another advantage is that a perpendicularly magnetized film can be obtained even when the support is cooled, and a polyethylene terephthalate film, which has the best magnetic properties for magnetic tapes, can be selected as the support.
(実施例−2)
実施例−1′と同じ装置条件でCo−Moの垂直磁化膜
の試作を行った。(Example 2) A Co--Mo perpendicularly magnetized film was prototyped using the same equipment conditions as in Example 1'.
Co −Mo (Mo : 20.5重量%) 0.1
6 pm f約4,000 Cへμ〕の膜形成速度で得
た。Co-Mo (Mo: 20.5% by weight) 0.1
The film formation rate was 6 pm f about 4,000 C to μ].
夫々のイオンの割合を5%と1o%の2水準を選びco
”1eooev一定としMO+イオンのエネルギー ’
!z 1000 eV 、 1500 eV 、 2o
ooev の3条件設定して得たものの垂直抗磁力は次
表のよってあった。Select two levels of the proportion of each ion, 5% and 1o%.
``Energy of MO+ ion assuming 1 eooev constant''
! z 1000 eV, 1500 eV, 2o
The vertical coercive force obtained by setting the three conditions of ooev was as shown in the following table.
比較例として第1図の結果を得た装置で約40000八
/secで得たCo−Mo膜は6o6[0e:lが最大
の抗磁力であった。As a comparative example, a Co--Mo film obtained at a speed of about 40,000/sec using the apparatus that obtained the results shown in FIG. 1 had a maximum coercive force of 6o6[0e:l.
尚、本発明は、垂直磁化膜に限らず、面内磁化膜に於て
も大きい抗磁力を得ることのできるものでありCo −
Cr 、Co−Moに限らず、Co−Ti 、Co−3
i 。Note that the present invention is capable of obtaining a large coercive force not only in a perpendicularly magnetized film but also in an in-plane magnetized film.
Not limited to Cr and Co-Mo, but also Co-Ti and Co-3
i.
Co −Ni 、Co−Ru 、Co −W 、等OC
O系二元合金、C〇−Cr −Mo 、 Co −Ni
−Cr 、 Co −Cr−Rh等の三元合金であっ
ても効果は同じである。Co-Ni, Co-Ru, Co-W, etc.OC
O-based binary alloy, C〇-Cr-Mo, Co-Ni
-Cr, Co-Cr-Rh, and other ternary alloys have the same effect.
なお三元合金の場合はcoの磁性全一番希釈する元素の
イオンエネルギーfco+のエネルギーより大きくする
ようにして実施するものとする。In the case of a ternary alloy, it is assumed that the magnetic total of co is made larger than the ion energy fco+ of the element to be diluted the most.
発明の効果
以上のように本発明によれば支持体温度(i−2000
℃以上の高温にしなくても、極めて大きい膜形成速度で
大きい抗磁力の垂直磁化膜が得られる。Effects of the Invention As described above, according to the present invention, the support temperature (i-2000
A perpendicularly magnetized film with a large coercive force can be obtained at an extremely high film formation rate without raising the temperature to a temperature higher than °C.
従って耐熱性の高い特殊なフィルムを用いなくても垂直
磁化膜ヲ有する金属薄膜型磁気記録媒体が容易に高い生
産性でできるため、磁気ディスクのみに用途は留らず磁
気テープとしても短波長記録の要請にこたえることがで
きる。Therefore, metal thin film magnetic recording media with perpendicularly magnetized films can be easily produced with high productivity without using special films with high heat resistance, so their use is not limited to magnetic disks, but can also be used for short wavelength recording as magnetic tapes. can meet the demands of
第1図は従来のイオンブレーティング法によって得られ
た垂直磁化膜の特性図、第2図は本発明を実施するため
に用いたイオンブレーティング装置の基本構成を示す図
、第3図は本発明により得られる垂直磁化膜の特性図で
ある。
1・・・・・・支持体、2・・・・・・遮へい板、3・
・・・・・スリット、4・・・・・強磁性金属薄膜、6
・・・・・蒸発源、10゜13・・・・・・イオン源、
11.14・・・・・・イオンビーム。
代理人の氏名 弁理士 中 尾 敏 男 ほか1基筒
1 図
第2図
第3図
M+イオン又壬子ヤ”−Fig. 1 is a characteristic diagram of a perpendicularly magnetized film obtained by the conventional ion blating method, Fig. 2 is a diagram showing the basic configuration of the ion blating apparatus used to carry out the present invention, and Fig. 3 is a diagram of the present invention. FIG. 3 is a characteristic diagram of a perpendicularly magnetized film obtained by the invention. 1... Support body, 2... Shielding plate, 3.
...Slit, 4...Ferromagnetic metal thin film, 6
...Evaporation source, 10゜13...Ion source,
11.14...Ion beam. Name of agent: Patent attorney Toshio Nakao and 1 other person
1 Figure 2 Figure 3
Claims (1)
系合金から成る磁気記録層を形成する際に、COに添加
する元素のイオンの運動エネルギーがc。 のイオンの運動エネルギーより大きくすることを特徴と
する磁気記録媒体の製造方法。[Claims] CO is applied to the surface of the support by φ by the ion blating method.
When forming the magnetic recording layer made of the alloy, the kinetic energy of the ions of the element added to CO is c. A method for manufacturing a magnetic recording medium, characterized in that the kinetic energy of the magnetic recording medium is made larger than the kinetic energy of ions.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58161331A JPS6052931A (en) | 1983-09-01 | 1983-09-01 | Method for manufacturing magnetic recording media |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58161331A JPS6052931A (en) | 1983-09-01 | 1983-09-01 | Method for manufacturing magnetic recording media |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6052931A true JPS6052931A (en) | 1985-03-26 |
| JPH0450650B2 JPH0450650B2 (en) | 1992-08-14 |
Family
ID=15733049
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58161331A Granted JPS6052931A (en) | 1983-09-01 | 1983-09-01 | Method for manufacturing magnetic recording media |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6052931A (en) |
-
1983
- 1983-09-01 JP JP58161331A patent/JPS6052931A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0450650B2 (en) | 1992-08-14 |
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