JPS59179749A - Amorphous alloy for magnetic head - Google Patents

Amorphous alloy for magnetic head

Info

Publication number
JPS59179749A
JPS59179749A JP58053766A JP5376683A JPS59179749A JP S59179749 A JPS59179749 A JP S59179749A JP 58053766 A JP58053766 A JP 58053766A JP 5376683 A JP5376683 A JP 5376683A JP S59179749 A JPS59179749 A JP S59179749A
Authority
JP
Japan
Prior art keywords
amorphous alloy
alloy
magnetic
amorphous
magnetic head
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
Application number
JP58053766A
Other languages
Japanese (ja)
Inventor
Hiroshi Tateishi
浩史 立石
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Toshiba Corp
Original Assignee
Toshiba Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Toshiba Corp filed Critical Toshiba Corp
Priority to JP58053766A priority Critical patent/JPS59179749A/en
Publication of JPS59179749A publication Critical patent/JPS59179749A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To provide an amorphous alloy for a magnetic head having a high crystallization temp. and an excellent magnetic characteristic and wear resistance by incorporating a specific amt. of Y and B in a Co-Fe-Ni alloy consisting essentially of Co and making the alloy amorphous. CONSTITUTION:The melt of a Co-Fe-Ni alloy consisting essentially of Co expressed by the formula (1) is quickly cooled at an extremely high cooling rate and is made amorphous. The amt. (m) of the Y to be added in the formula (1) is set within a range of 2<=m<=10 in atom concn. The amorphous alloy for a magnetic head which does not crystallize at the melting temp. of glass in the stage of adhering securely the amorphous alloy as a magnetic head material to the glass and has excellent wear resistance against friction with a magnetic medium and an excellent magnetic characteristic is obtd.

Description

【発明の詳細な説明】 〔発明の技術分野〕 本発明は磁気ヘット用非晶質合金に係わり、更に詳しく
は、高い結晶化温度を示し、且つ磁気媒体との摩擦に対
して優れた摩耗特性を示す磁気ヘッド用非晶信合金に係
わるものでt・る。
[Detailed Description of the Invention] [Technical Field of the Invention] The present invention relates to an amorphous alloy for a magnetic head, and more specifically, an amorphous alloy having a high crystallization temperature and excellent wear characteristics against friction with a magnetic medium. This relates to an amorphous alloy for magnetic heads showing the following characteristics.

〔発明の技術的背景とその間4゛・点〕従来、磁気記録
装置等にセける磁気ヘッドには、例えば、Fe−Ni合
金(パーマロイ) F”e−8i −k1合金(センダ
スト)、或いはMn−Zn フェライト増の結晶構造を
有する歿性村料が使用されている。
[Technical background of the invention and 4 points] Conventionally, magnetic heads used in magnetic recording devices, etc. have been made of, for example, Fe-Ni alloy (permalloy), F”e-8i-k1 alloy (sendust), or Mn. -Zn A perishable material having a ferrite-rich crystal structure is used.

しかしながら、Fe−Ni合金は、6磁4−が高い反面
、耐摩耗性に劣り、Fe−8i−AI3合金は、飽和磁
束密度は筒いものの、帖・(渣的5虫+1:、か弱く、
もろいだめに塑性加工が極めて困難で2・)す、父、M
n=Znフェライトは、耐歴耗性は做れているものの、
飽和磁束密度が低いという間:)−q点を有しでいる。
However, although the Fe-Ni alloy has a high 6 magnetism, it has poor wear resistance, and the Fe-8i-AI3 alloy has a high saturation magnetic flux density, but is weak and
It is extremely difficult to perform plastic processing due to its brittle nature.2) Father, M.
Although n=Zn ferrite has poor wear resistance,
While the saturation magnetic flux density is low, it has a -q point.

これらに対し、結晶(71造を持だ力、い非晶質合金が
、近年、優れた磁気的特性をイ]していることが見い出
されただめ、新たな磁気ヘット用材料として注目されて
いる。
In contrast, it has recently been discovered that amorphous alloys with crystalline properties have excellent magnetic properties, and are attracting attention as new materials for magnetic heads. There is.

しかしながら、一般にVTR鍋に使用される磁気ヘッド
に於いては、安定で強+r1′fr、括病がリタ求芒れ
、特にガラスによる接着が望号しいとされている。しか
し、ガラス接着には400℃以上の+n IJI−での
熱処理とその後の徐冷が必要である。この点で、非晶質
合金は必ず結晶化温度(T x)を有しており、その温
度の近傍で熱処理をした後、徐冷をすると緒特性、特に
実効透磁率が劣化するという欠点があるため、実用上大
きな問題となっている。従って、優れた磁気ヘッド用非
晶質合金としては、高い結晶化温度を示し、ガラス接着
後の緒特性が劣化しない材質であることが望捷れている
However, in general, magnetic heads used in VTR pans are stable, strong, and free from stiffness, and bonding with glass is particularly desirable. However, glass bonding requires heat treatment at +n IJI- of 400° C. or higher and subsequent slow cooling. In this respect, amorphous alloys always have a crystallization temperature (T This poses a major problem in practice. Therefore, as an excellent amorphous alloy for a magnetic head, it is desirable to have a material that exhibits a high crystallization temperature and that does not deteriorate its properties after bonding to glass.

又同時に、磁気媒体と合金系の磁気ヘッドの高速での摩
擦に於いてヘッドの媒体摺動面上に縞状の模様が発生し
、これが原因となってヘッドの再生出力が低下すること
が、本発明渚による研究の結果判明し、実用上大きな問
題となっている。従って優れた磁気ヘッド用非晶賀合金
としては、如何なる条件で磁気媒体を走行させても、縞
状WASが発生しない材質であることが望ましい。
At the same time, due to high-speed friction between the magnetic medium and the alloy magnetic head, a striped pattern is generated on the medium sliding surface of the head, which causes a reduction in the reproduction output of the head. This was discovered as a result of research by Nagisa, the inventor of the present invention, and has become a major problem in practice. Therefore, it is desirable that an excellent amorphous alloy for a magnetic head be a material that does not cause striped WAS no matter what conditions the magnetic medium is run on.

〔発明の目的〕[Purpose of the invention]

本発明の目的は、上記した問題点を解消し、睡気特性に
優れ、高い結晶化温度を示し、徐冷を伴なう熱処理を処
しても品持性、肋に実効透磁率が低下せず、月つ如何な
るΦ件でのz類4ハlム体十行に対しても縞状模様が発
生し〃い:l−J ノp↓の磁気ヘット用非晶質合金を
提供することにある。
The purpose of the present invention is to solve the above-mentioned problems, have excellent sleep properties, exhibit a high crystallization temperature, maintain good quality even when subjected to heat treatment accompanied by slow cooling, and exhibit low effective magnetic permeability in the ribs. Firstly, to provide an amorphous alloy for a magnetic head of 1-J nop↓, which causes a striped pattern even in 10 rows of z-class 4-halm bodies under any Φ condition. be.

〔発明の朽、要〕[Decay of invention, essential]

本発明の磁気ヘッド用非晶質c金は、(COI−a−b
 Fe a Ni b )  + oo −m−n Y
m BnO≦ a ≦ 0.20 0 ≦ b ≦0.15 05 ≦m≦ 10 3 S n ≦ 25 で示されること’c %徴とするものである。
The amorphous c-gold for magnetic heads of the present invention is (COI-a-b
Fe a Ni b ) + oo -m-n Y
m BnO≦ a ≦ 0.20 0 ≦ b ≦ 0.15 05 ≦ m ≦ 10 3 S n ≦ 25.

又、本発明の磁気ヘラl−’用非晶質合金は、特に上式
に於いて示きれるYの添加イSf: I+:が原子濃度
で、2≦m≦ 10 であることを特徴とするものである1、以下に於いて本
発明をif:i、に評しく説明する。
In addition, the amorphous alloy for magnetic spatula l-' of the present invention is particularly characterized in that the addition of Y, Sf:I+: shown in the above formula, satisfies 2≦m≦10 in terms of atomic concentration. 1. The present invention will be described below in terms of if:i.

本発明に示される非晶質合金において、谷元素の添加理
由2組成比並びにその限父■゛、1′!1!由は以下の
とおりである。
In the amorphous alloy shown in the present invention, the reasons for the addition of the valley element, the two composition ratios, and their limiters ゛, 1'! 1! The reason is as follows.

本発明の非晶質合金はコバルト((?0)を主体とする
ものである。Coを主体とした理由は、磁歪が小さく透
磁率が品いものであるために磁気ヘッド用材料として最
適であることによる。
The amorphous alloy of the present invention is mainly composed of cobalt ((?0). The reason why it is mainly composed of Co is that it has low magnetostriction and high magnetic permeability, making it optimal as a material for magnetic heads. It depends.

本発明の非晶質合金に於いて、添加元素について説明す
ると、鉄(F e)は、非晶質合金の透磁率を高める作
用をなすものであるが、ナくても良く0≦a≦0.20
の範囲である。aが0.2を越えると透磁率が逆にイ氏
ドする。
Regarding the additive elements in the amorphous alloy of the present invention, iron (Fe) has the effect of increasing the magnetic permeability of the amorphous alloy, but it may be omitted and 0≦a≦ 0.20
is within the range of When a exceeds 0.2, the magnetic permeability goes up.

ニッケル(Nj)はFeと共に非晶質合金の透磁率を高
める作用をなすものであるが含まない場合でも高い透磁
率を得ることができ、0≦b≦0.15の範囲である。
Nickel (Nj) acts to increase the magnetic permeability of the amorphous alloy together with Fe, but even when it is not included, high magnetic permeability can be obtained, and the range is 0≦b≦0.15.

bが0.15を越えると飽和磁束密度が低くなる。When b exceeds 0.15, the saturation magnetic flux density becomes low.

イツトvウム(Y)は、本発明非晶質合金の結晶化温度
の上昇に大きく寄与するものであり、mで示される合金
中に於ける原子濃度は、0.5≦m≦10の範囲である
。n】が0.5未満であると添加効果が充分でない。又
、同時に、Yは^11記の縞状模様の発生を抑制する効
果が肩り、特にmが2≦m6r)範囲で、その効果が顕
著となる。一方mが10を越えると、高温で酸化し易く
なり、非晶質合金の作製が困かIGになる。
Yield (Y) greatly contributes to increasing the crystallization temperature of the amorphous alloy of the present invention, and the atomic concentration in the alloy, represented by m, is in the range of 0.5≦m≦10. It is. If n] is less than 0.5, the effect of the addition will not be sufficient. At the same time, Y has an even greater effect of suppressing the occurrence of the striped pattern described in ^11, and this effect becomes particularly noticeable in the range of m=2≦m6r). On the other hand, when m exceeds 10, it becomes easy to oxidize at high temperatures, making it difficult to produce an amorphous alloy or resulting in IG.

次に、非金属元素であるホウ素(B)について説明する
と、Bは、本発明の合金の非晶質化に有効な作用をなす
ものである。nで示される合金中に於ける原子濃度は、
3≦n≦25の範囲である。
Next, boron (B), which is a nonmetallic element, will be explained. B has an effective effect on making the alloy of the present invention amorphous. The atomic concentration in the alloy denoted by n is
The range is 3≦n≦25.

nが3未満で心ると非晶質化が困難であシ、25を越え
ると耐錆性が劣化するので好ましくない。
If n is less than 3, it will be difficult to make it amorphous, and if it exceeds 25, the rust resistance will deteriorate, which is not preferable.

又、ケイ素(Si)も非晶質化に有効な作用をなす非金
属元素として一般に知られているが、Siは、Bを添加
した場合に比べて飽和磁束密度の低下が犬きく、シかも
、縞状模様の発生を促進する作用があるので、好ましく
欧い。
In addition, silicon (Si) is also generally known as a nonmetallic element that has an effective effect on amorphization, but Si has a significantly lower saturation magnetic flux density than when B is added. , is preferable because it has the effect of promoting the formation of striped patterns.

本発明の磁気ヘッド用非晶質合金は、上記したCO、F
e、Ni、Y、13の各成分を所定の割合で混合した後
、溶融し、これを、例えば、液体急冷法、或いは、スパ
ッタ法叫によって非晶質合金化し、必要に応じて熱処理
を施すことにより、容易に製造することができるもので
おる。
The amorphous alloy for magnetic heads of the present invention includes the above-mentioned CO, F,
After mixing each component of e, Ni, Y, and 13 in a predetermined ratio, it is melted, and this is made into an amorphous alloy by, for example, a liquid quenching method or a sputtering method, and heat treatment is performed as necessary. This makes it easy to manufacture.

〔発明の実施例〕[Embodiments of the invention]

実施例 第1表に示した組成の非晶質合金5種類(試料番号1〜
5)を、それぞれ液体急冷法により作製した。即ち、上
記組成の溶融合金を、アルゴン雰囲気中で高速回転する
単ロール表面上に、石英管ノズルからアルゴンガス圧(
1,0〜2.2 kg / cm″)で噴出はせ、得ら
れた薄帯を急冷して胛さ30μm1幅12mmの非晶質
合金薄帯試料として、それぞれ得た。得られた5種類の
薄帯試料を、外径10mmφ、内径8 mmφを有する
リング状にす]ち抜き、層間絶縁物を介在をせて、それ
ぞれ10枚積層した。次いで、この積層物に、550℃
で30分間熱処理を施した後、毎分3℃の割合で徐冷し
、積層コアを得た。それぞれの非晶質合金を用いた積層
コアについて、−次コイル及び二次コイルを巻きつけて
、実効透磁率、保磁力及び飽和磁束密度を測定した。
Examples Five types of amorphous alloys with compositions shown in Table 1 (sample numbers 1 to 1)
5) were each produced by a liquid quenching method. That is, a molten alloy having the above composition is placed on the surface of a single roll rotating at high speed in an argon atmosphere, and is heated by argon gas pressure (
1.0 to 2.2 kg/cm''), and the resulting ribbons were rapidly cooled to obtain amorphous alloy ribbon samples with a ridge of 30 μm and a width of 12 mm.The five types obtained. A thin strip sample was punched out into a ring shape having an outer diameter of 10 mmφ and an inner diameter of 8 mmφ, and 10 sheets of each were laminated with an interlayer insulator interposed.Then, this laminate was heated at 550°C.
After performing heat treatment for 30 minutes, the core was slowly cooled at a rate of 3° C. per minute to obtain a laminated core. A secondary coil and a secondary coil were wound around a laminated core using each amorphous alloy, and the effective magnetic permeability, coercive force, and saturation magnetic flux density were measured.

尚、実効透磁率μ′は、インピーダンス計を用いて測定
し、計算により求めた。保磁力及び飽和磁束密度につい
ては、自動自記磁束側を用いて直流磁化曲線を測定し、
計算により求めた。
Note that the effective magnetic permeability μ' was measured using an impedance meter and determined by calculation. For coercive force and saturation magnetic flux density, measure the DC magnetization curve using the automatic self-recording magnetic flux side,
Obtained by calculation.

次いで、それぞれの非晶質合金薄帯試料に対して切削加
工を施し、VTR用磁気へラドコアを形成し、磁気ヘッ
ドを試作して、血1摩耗性を測定した。耐摩耗性の評価
は、試作ヘッドを市販のv′v几に実装して、γ−Fe
2eg塗布のV’l’R用カセットテープを500時間
走行させ、その前後におけるヘッドのテープ摺動面の変
化を側面から光学顕微鏡を用いて測定し、摩耗量を求め
、これを100時間当りに換算して行なった。
Next, each amorphous alloy ribbon sample was cut to form a magnetic rad core for a VTR, a prototype magnetic head was manufactured, and its abrasion resistance was measured. Wear resistance was evaluated by mounting the prototype head on a commercially available v′v
A V'l'R cassette tape coated with 2eg was run for 500 hours, and the change in the tape sliding surface of the head before and after was measured using an optical microscope from the side to determine the amount of wear, and this was measured per 100 hours. I did the conversion.

又、結晶化温度は、示差熱分析計を用いて測定し、昇温
中、最初に現われる発熱ピークの発熱開始の温度とした
The crystallization temperature was measured using a differential thermal analyzer, and was defined as the temperature at which the first exothermic peak that appeared during heating started.

これらの結果を、第1表に組成と共に示す。尚、実効透
磁率は5MHzにおける値である。
These results are shown in Table 1 along with the composition. Note that the effective magnetic permeability is a value at 5 MHz.

比較例 組成が異なる他は実施例1と同様の操作にて、3種類(
試料番号6〜8)の非晶質合金薄帯試料を得た。
Comparative Example Three types (
Amorphous alloy ribbon samples of sample numbers 6 to 8) were obtained.

尚、試料番号6及び7はYを全く含まず、Slを含むも
のである。試料番号8もYを全く含ますSiも全く含寸
ないものである。
Note that sample numbers 6 and 7 do not contain Y at all, but contain Sl. Sample No. 8 also contains no Y and no Si at all.

これらの試料について、実施例1と同様の方法にて実効
透磁率、保磁力、飽和磁束密度、摩耗量及び結晶化温度
をそれぞれ測定した。それらの組成及び試験結果を第1
表に実施例と共に示す。
Regarding these samples, effective magnetic permeability, coercive force, saturation magnetic flux density, wear amount, and crystallization temperature were measured in the same manner as in Example 1. Their composition and test results are
It is shown in the table together with examples.

又、試料番号9は、現在の家庭用VTRに使用されてい
るヘッド材料のMn−Znフェライトである。結晶化温
度を除く一般的なデータを比較例として第1表に示す。
Sample number 9 is Mn-Zn ferrite, which is a head material used in current home VTRs. General data excluding crystallization temperature are shown in Table 1 as a comparative example.

k′人干、#臼 f・rから明r・かなように、Yを含寸ない非晶り合金
の結晶化温度に比べて本発明の非晶質合金の結晶化渦r
is−は、約130℃〜380℃も高いことが確認され
た。しかも徐冷を伴なう熱処理を施し/こ後の磁気特性
、 14−′fに実効透磁率μ’  (5MHz )の
値に関しては、比較例のものに対し本発明の非晶質合金
は劣化がみられないことがわかる。
As shown by k′ and kana, the crystallization vortex r of the amorphous alloy of the present invention is higher than the crystallization temperature of the amorphous alloy that does not contain Y.
is- was confirmed to be as high as about 130°C to 380°C. Moreover, after heat treatment with slow cooling, the magnetic properties of the amorphous alloy of the present invention deteriorated compared to those of the comparative example in terms of the effective magnetic permeability μ' (5 MHz) at 14-'f. It can be seen that this is not seen.

又、Yを含オず、Slを含む比較例(試料6I号6及び
7)の摩耗量に比べて、本発明の非晶質合金の摩耗量は
少ないことがわかる。こわは、ヘット摺動面上の縞1f
s 4M様の発生が抑制訟れたヨ1トによる。
Furthermore, it can be seen that the amount of wear of the amorphous alloy of the present invention is smaller than that of the comparative examples (Samples 6I No. 6 and 7) containing no Y but containing Sl. The stiffness is the stripes 1f on the head sliding surface.
s This is due to the fact that the outbreak of 4M was suppressed.

〔発明の効七に〕[7 Effects of invention]

本発明の悩気ヘット用非晶ノe1合金は、イツトリウム
を添加することにより、結晶化温度75” 4N シ<
向上したものであり、且つ、徐冷を伴なう熱処理を施し
ても、晶面性 特に実効透磁率が低化(2ないものであ
る。又、イツトリウムの添加と、ケイ素を含まない事の
相乗効果により、ヘッドの磁気媒体Ji”i動面−ヒの
縞状模様の発生が抑制され、優れた摩耗特性を示すもの
である。この効果は、イツトリウムの添加量が原子ンに
?、后で2%以上で1.’lJR著なものとなる。
By adding yttrium, the amorphous e1 alloy for hot gas heads of the present invention has a crystallization temperature of 75" 4N
Moreover, even if heat treatment with slow cooling is performed, the crystal orientation, especially the effective magnetic permeability, will not decrease (2). Due to the synergistic effect, the occurrence of striped patterns on the moving surface of the magnetic medium of the head is suppressed, and excellent wear characteristics are exhibited. If it is 2% or more, it becomes 1.'lJR.

本発明の磁気ヘッド用非晶質合<、′;は、i34気ヘ
ット用材料として、侵れた適性をイ1するものである。
The amorphous alloy for magnetic heads of the present invention has excellent suitability as a material for I34 heads.

Claims (2)

【特許請求の範囲】[Claims] (1) (Co+ −a−b Pe a N1b)to
o −m−n Ym BnO≦ a ≦0.20 0≦ b≦ 0.15 0.5 ≦m≦ 10 3≦n ≦ 25 で示されることを特徴とする磁気ヘッド用非晶質合金。
(1) (Co+ -a-b Pe a N1b)to
o −m−n Ym BnO≦a≦0.20 0≦b≦0.15 0.5≦m≦10 3≦n≦25 An amorphous alloy for a magnetic head.
(2)Yの添加量mが原子濃度で 2≦m≦ 10 であることを特徴とする特許稍求の範囲第1項記載の磁
気ヘッド用非晶質合金。
(2) The amorphous alloy for a magnetic head according to item 1 of the claimed patent application, characterized in that the amount m of Y added satisfies 2≦m≦10 in terms of atomic concentration.
JP58053766A 1983-03-31 1983-03-31 Amorphous alloy for magnetic head Pending JPS59179749A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
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Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58053766A JPS59179749A (en) 1983-03-31 1983-03-31 Amorphous alloy for magnetic head

Publications (1)

Publication Number Publication Date
JPS59179749A true JPS59179749A (en) 1984-10-12

Family

ID=12951932

Family Applications (1)

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Country Status (1)

Country Link
JP (1) JPS59179749A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6436740A (en) * 1987-07-31 1989-02-07 Kazuaki Fukamichi Amorphous alloy and its production

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5751237A (en) * 1980-09-11 1982-03-26 Akai Electric Co Ltd Amorphous alloy
JPS5757854A (en) * 1980-09-19 1982-04-07 Hitachi Ltd Metal-metal type ferromagnetic amorphous alloy and magnetic core using it
JPS5943837A (en) * 1982-09-06 1984-03-12 Hitachi Ltd Amorphous alloy with high saturation magnetic flux density

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5751237A (en) * 1980-09-11 1982-03-26 Akai Electric Co Ltd Amorphous alloy
JPS5757854A (en) * 1980-09-19 1982-04-07 Hitachi Ltd Metal-metal type ferromagnetic amorphous alloy and magnetic core using it
JPS5943837A (en) * 1982-09-06 1984-03-12 Hitachi Ltd Amorphous alloy with high saturation magnetic flux density

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6436740A (en) * 1987-07-31 1989-02-07 Kazuaki Fukamichi Amorphous alloy and its production

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