JPH01292802A - Highly corrosion-resistant amorphous magnetic film - Google Patents
Highly corrosion-resistant amorphous magnetic filmInfo
- Publication number
- JPH01292802A JPH01292802A JP12171988A JP12171988A JPH01292802A JP H01292802 A JPH01292802 A JP H01292802A JP 12171988 A JP12171988 A JP 12171988A JP 12171988 A JP12171988 A JP 12171988A JP H01292802 A JPH01292802 A JP H01292802A
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- JP
- Japan
- Prior art keywords
- magnetic
- film
- corrosion resistance
- amorphous
- magnetic film
- 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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- Thin Magnetic Films (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薄膜ヘッド磁極に用
いる磁性膜に係り、特に高飽和磁束密度。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a magnetic film used in a thin-film head magnetic pole suitable for high-density magnetic recording, particularly a high saturation magnetic flux density.
高耐食性を有する高耐食性非晶質磁性膜に関する。The present invention relates to a highly corrosion-resistant amorphous magnetic film having high corrosion resistance.
磁気記録の高密度化、高性能化の進歩には目覚ましいも
のがある。大型コンピューター用の磁気ディスク装置の
分野に於いては、従来のフェライト型バルクヘッドに比
べてインダクタンスが小さく、高周波透磁率が大きくて
、狭トラツク幅加工の可能な薄膜磁気ヘッドの使用が必
須となっている。There has been remarkable progress in increasing the density and performance of magnetic recording. In the field of magnetic disk drives for large computers, it is essential to use thin-film magnetic heads, which have lower inductance and higher high-frequency magnetic permeability than conventional ferrite bulk heads, and can be processed into narrow track widths. ing.
薄膜磁気ヘッドに於いては、記録の高密度化にともなっ
て分解能を向上するために磁極を薄膜化する必要があり
、薄い磁極先端部で磁気飽和が起こり易く、このため高
飽和磁束密度の磁性膜を用いた薄膜磁気ヘッドが必要に
なっている。In thin-film magnetic heads, it is necessary to make the magnetic pole thinner to improve resolution as recording density increases, and magnetic saturation tends to occur at the tip of the thin magnetic pole. A thin film magnetic head using a film is now required.
また、磁気ディスク装置では、磁気ヘッドと記録媒体と
は、約0.1〜0.2μmのスペーシングを保ちながら
速度3600 m/seeで相対運動している。そこで
、磁気ヘッドの磁極磁性膜の腐食生成物が媒体上にある
と、磁気ヘッドと記録媒体はクラッシュを起こし、両者
とも損傷してしまう。Further, in a magnetic disk device, the magnetic head and the recording medium move relative to each other at a speed of 3600 m/see while maintaining a spacing of about 0.1 to 0.2 μm. Therefore, if corrosion products of the magnetic pole magnetic film of the magnetic head are present on the medium, the magnetic head and the recording medium will crash, and both will be damaged.
したがって、磁気ディスク用の磁性膜は、VTR用ヘッ
ドに使用される磁性膜よりも高耐蝕性が必須の条件とな
る。Therefore, a magnetic film for a magnetic disk must have higher corrosion resistance than a magnetic film used for a VTR head.
薄膜磁気ヘッドの磁性膜としては、従来、主にNi−F
e系合金膜(パーマロイ膜)が用いられてきた。Ni−
Fe系合金膜は、耐蝕性に優れているが、飽和磁束密度
は1.OTである。今後の高飽和磁束密度化には、N
i −F eでは対応しきれなくなってきている。Conventionally, the magnetic film of thin-film magnetic heads has mainly been made of Ni-F.
E-based alloy films (permalloy films) have been used. Ni-
The Fe-based alloy film has excellent corrosion resistance, but the saturation magnetic flux density is 1. It is OT. In order to increase the saturation magnetic flux density in the future, N
i-Fe is no longer able to handle the situation.
近年高飽和磁束密度で高性能の磁性膜として非晶質スパ
ッタ膜が開発されつつある。この中でも特にZr系非晶
質膜はガラス化元素がB、Si。In recent years, amorphous sputtered films have been developed as high-performance magnetic films with high saturation magnetic flux density. Among these, the vitrification elements of the Zr-based amorphous film are B and Si.
Pからなる非晶質合金に比較して、耐熱性に優れており
、磁気ヘッド用磁性膜としてすぐれた特性を有している
。このZr系非晶質膜の組成はMaTaZrの組成式で
表される。ここで、Mは磁気モーメントを有するGo、
Fe、Niなとの少なくとも一種であり、TはMおよび
Zr以外の遷移金属である。It has better heat resistance than an amorphous alloy made of P, and has excellent properties as a magnetic film for a magnetic head. The composition of this Zr-based amorphous film is represented by the composition formula of MaTaZr. Here, M is Go with a magnetic moment,
T is at least one of Fe and Ni, and T is a transition metal other than M and Zr.
このような、ガラス化元素が主にZrからなる非晶質合
金については特開昭55−138049並びに特開昭5
6−84439等に述べられている。これらのZr系非
晶質合金の中でもMがCOからなるC。Regarding such amorphous alloys in which the vitrifying element is mainly Zr, Japanese Patent Application Laid-open No. 55-138049 and Japanese Patent Application Laid-open No. 55-138
6-84439 etc. Among these Zr-based amorphous alloys, C is one in which M is CO.
−Zr系非晶質膜は、飽和磁束密度が高く、優れた磁性
材料である。しかし、この非晶質合金の磁歪定数は、2
〜4X10−”と大きな値を示すため、添加元素として
、非晶質合金の磁歪定数に負の寄与を与えるV、Nb、
Ta、Mo、Wなどの元素を用いる事により磁歪定数が
ほぼ0の非晶質合金が得られる。このような非晶質合金
は、第6回日本応用磁気学会学f講演概要集p 、93
(1982年)に示されているように、磁歪零に於い
て飽和磁束密度1.5Tが得られる事から、薄膜磁気ヘ
ッドとして、有望視されている。The -Zr-based amorphous film has a high saturation magnetic flux density and is an excellent magnetic material. However, the magnetostriction constant of this amorphous alloy is 2
V, Nb, and
By using elements such as Ta, Mo, and W, an amorphous alloy with a magnetostriction constant of approximately 0 can be obtained. Such amorphous alloys are described in the 6th Japanese Society of Applied Magnetics Lecture Abstracts, p. 93.
(1982), a saturation magnetic flux density of 1.5 T can be obtained at zero magnetostriction, so it is considered promising as a thin film magnetic head.
〔発明が解決しようとするiM)
上記従来技術は、飽和磁束密度、磁歪定数という観点か
らは優れた薄膜磁気ヘッド用材料であるが、耐蝕性に問
題がある。すなわち、CooCo組成0at%以上では
急激に耐蝕性が劣化する事が明らかになり、飽和磁束密
度が高いCoTaZr系非晶質膜は、磁気ヘッド材料と
して信頼性に欠けるという問題があった0本発明の目的
は、Co組成が90at%以上で、高飽和磁束密度と高
耐蝕性のCo系非晶質膜を得ることにあり、ひいてはこ
の膜を用いて高性能の磁気ヘッドを得ることにある。[iM to be Solved by the Invention] The above-mentioned prior art is an excellent material for a thin film magnetic head from the viewpoint of saturation magnetic flux density and magnetostriction constant, but it has a problem in corrosion resistance. In other words, it has become clear that the corrosion resistance deteriorates rapidly when the CooCo composition exceeds 0 at%, and the CoTaZr-based amorphous film, which has a high saturation magnetic flux density, has the problem of lacking reliability as a magnetic head material. The purpose of this method is to obtain a Co-based amorphous film having a Co composition of 90 at % or more, high saturation magnetic flux density, and high corrosion resistance, and further to obtain a high-performance magnetic head using this film.
CNMIを解決するための手段〕 上記問題を解決するために、発明者らは、G。Measures to resolve CNMI] In order to solve the above problem, the inventors developed G.
組成が90a t%以上のCoTaZr系非晶質膜に種
々の元素を添加して磁気特性、耐蝕性を調べた。その結
果、Au、Ag、Ptの添加元素をlat%程度以上添
加すれば、CoTaZr系非晶質膜の磁気特性を劣化さ
せる事無く耐蝕性を向上させる事を見出した。Various elements were added to a CoTaZr-based amorphous film having a composition of 90 at% or more, and its magnetic properties and corrosion resistance were investigated. As a result, it has been found that if the additive elements of Au, Ag, and Pt are added at lat% or more, the corrosion resistance of the CoTaZr-based amorphous film can be improved without deteriorating its magnetic properties.
以下、本発明を実施例により詳細に説明する。 Hereinafter, the present invention will be explained in detail with reference to Examples.
第2図に、CoTaZr系非晶質合金においてTaとZ
rの比を5:3と一定にしておいてCo組成を変えた時
のCo組成とCoTaZr系非晶質合金の耐蝕性との関
係を示す。耐蝕性は、試料を温度60℃、湿度80%の
恒温恒温炉に150時間放置し、飽和磁化の変化量で評
価した。すなわち、腐食率を(Ms(0)−Ms(15
0))/Ms(0)X100(%)で定義した。ここで
、M s (t )は、を時間後の飽和磁化である。C
o組成が90at%までは、CoTaZr非晶質合金は
腐食していないが、C。Figure 2 shows that Ta and Z in a CoTaZr amorphous alloy.
The relationship between the Co composition and the corrosion resistance of a CoTaZr-based amorphous alloy is shown when the Co composition is changed while keeping the ratio of r constant at 5:3. Corrosion resistance was evaluated by leaving the sample in a constant temperature oven at a temperature of 60° C. and a humidity of 80% for 150 hours, and evaluating the amount of change in saturation magnetization. That is, the corrosion rate is (Ms(0)-Ms(15
0))/Ms(0)X100(%). Here, M s (t) is the saturation magnetization after time. C
Although the CoTaZr amorphous alloy does not corrode up to 90 at% o composition, C.
組成が90%を越えると、急激に腐食率が増している。When the composition exceeds 90%, the corrosion rate increases rapidly.
すなわち、 CoTaZr非晶質合金に於いては、Co
組成が90at%以下では、磁気ヘッドとして十分な信
頼性を備えているが、Co組成が90at%以上では、
信頼性に問題がある事がわかる。That is, in the CoTaZr amorphous alloy, Co
When the Co composition is 90 at% or less, it has sufficient reliability as a magnetic head, but when the Co composition is 90 at% or more,
It turns out that there is a problem with reliability.
第1図には、 CoezTaxZrvMc (X +
Y + Z = 8 。In Figure 1, CoezTaxZrvMc (X +
Y + Z = 8.
X:Y=5:3)非晶質合金において、添加元素Mの添
加量と耐蝕性との関係を示す、なお、M=W、V、Pd
、Mo、Au、Ag、Pt、である。X:Y=5:3) Indicates the relationship between the addition amount of the additive element M and the corrosion resistance in an amorphous alloy, where M=W, V, Pd
, Mo, Au, Ag, and Pt.
試料は高周波2極スパツタ法により形成した。耐蝕性は
、第2図の例と同じように試料を温度60℃、湿度80
%の恒温恒温炉に150時間放置し、飽和磁化の変化量
で評価した。Co組成が90at%では、添加元素によ
って耐蝕性の程度が異なる。Au、Ag、Ptは、la
t%添加するだけで、耐蝕性が向上している。ところが
、W、V。The sample was formed by high frequency bipolar sputtering method. Corrosion resistance was measured at a temperature of 60°C and a humidity of 80°C as in the example in Figure 2.
% in a constant temperature oven for 150 hours, and evaluated by the amount of change in saturation magnetization. When the Co composition is 90 at%, the degree of corrosion resistance varies depending on the added elements. Au, Ag, Pt are la
Corrosion resistance is improved just by adding t%. However, W, V.
Pd、Moは数at%添加すると逆に耐蝕性が悪くなっ
ている。なお、これらの元素を添加しても。On the contrary, when Pd or Mo is added in an amount of several at%, the corrosion resistance deteriorates. Note that even if these elements are added.
添加していないときと同等の保磁力0.30eを示した
。It showed a coercive force of 0.30e, which is equivalent to when no addition was made.
CoezTasZrs非晶質膜の磁歪はほぼ零であるが
第4添加元索としてA u g A g I P tを
添加した時は磁歪は負の方に変化した。したがって。The magnetostriction of the CoezTasZrs amorphous film was almost zero, but when AugAgIPt was added as the fourth additive, the magnetostriction changed to the negative side. therefore.
CoTaZrMの磁歪を零にするにはM=Au、Ag。To make the magnetostriction of CoTaZrM zero, M=Au, Ag.
ptのときTa : Zr=5 : 3よりもZrの割
合を多くする必要があった。第1表には、CoTaZr
M非晶質膜の磁歪を零にする組成の代表例を示す。In the case of pt, it was necessary to increase the ratio of Zr than Ta:Zr=5:3. Table 1 shows CoTaZr
A representative example of a composition that makes the magnetostriction of the M amorphous film zero is shown.
また、TaとZrの比を変えても耐蝕性には変化がなか
った。Further, even if the ratio of Ta and Zr was changed, there was no change in corrosion resistance.
第 1 表
〔発明の効果〕
本発明によれば、Co組成が90a t%でも高耐蝕性
を有し、低保磁力で零磁歪のCoTaZrM系非晶質膜
が得られるので、飽和磁束の高い磁束を持ちかつ信頼性
の高い磁気ヘッドが得られる効果がある。Table 1 [Effects of the Invention] According to the present invention, a CoTaZrM amorphous film with high corrosion resistance, low coercive force, and zero magnetostriction can be obtained even when the Co composition is 90 at%. This has the effect of providing a magnetic head that has magnetic flux and is highly reliable.
Claims (1)
する高耐蝕性非晶質磁性膜。 Co_ATa_BZr_CM_D…(1) ただし、元素Mは M=Au,Ag,Pt の群より選ばれる1種もしくは2種以上の元素であり、 A≧90 D≧1 かつA+B+C+D:100 B/C<3/5 なる条件(単位はat%)を満足する。1. A highly corrosion-resistant amorphous magnetic film characterized by having a component composition represented by formula (1). Co_ATa_BZr_CM_D...(1) However, the element M is one or more elements selected from the group of M=Au, Ag, Pt, A≧90 D≧1 and A+B+C+D: 100 B/C<3/5 The following conditions (unit: at%) are satisfied.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12171988A JPH01292802A (en) | 1988-05-20 | 1988-05-20 | Highly corrosion-resistant amorphous magnetic film |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12171988A JPH01292802A (en) | 1988-05-20 | 1988-05-20 | Highly corrosion-resistant amorphous magnetic film |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH01292802A true JPH01292802A (en) | 1989-11-27 |
Family
ID=14818186
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP12171988A Pending JPH01292802A (en) | 1988-05-20 | 1988-05-20 | Highly corrosion-resistant amorphous magnetic film |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH01292802A (en) |
-
1988
- 1988-05-20 JP JP12171988A patent/JPH01292802A/en active Pending
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