JPH0782616B2 - Non-magnetic substrate for magnetic head - Google Patents

Non-magnetic substrate for magnetic head

Info

Publication number
JPH0782616B2
JPH0782616B2 JP1214206A JP21420689A JPH0782616B2 JP H0782616 B2 JPH0782616 B2 JP H0782616B2 JP 1214206 A JP1214206 A JP 1214206A JP 21420689 A JP21420689 A JP 21420689A JP H0782616 B2 JPH0782616 B2 JP H0782616B2
Authority
JP
Japan
Prior art keywords
magnetic
hardness
substrate
head
magnetic substrate
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.)
Expired - Lifetime
Application number
JP1214206A
Other languages
Japanese (ja)
Other versions
JPH0380411A (en
Inventor
隆一 長瀬
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.)
Eneos Corp
Original Assignee
Japan Energy 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 Japan Energy Corp filed Critical Japan Energy Corp
Priority to JP1214206A priority Critical patent/JPH0782616B2/en
Publication of JPH0380411A publication Critical patent/JPH0380411A/en
Publication of JPH0782616B2 publication Critical patent/JPH0782616B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Compositions Of Oxide Ceramics (AREA)
  • Magnetic Heads (AREA)
  • Thin Magnetic Films (AREA)

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、金属性磁性膜を蒸着するための非磁性の磁気
ヘッド用非磁性基板に関するものである。
TECHNICAL FIELD The present invention relates to a non-magnetic substrate for a non-magnetic magnetic head for depositing a metallic magnetic film.

従来技術 従来この種の用途のものとしては、チタン酸バリウム、
チタン酸カルシウム、アルミナ等が使用されていた。し
かしながら、その熱膨張率が磁性膜構造体と大きく異な
っていたため、蒸着した磁性膜構造体が剥離しやすく、
また熱膨張率の差により応力が発生しクラックが発生す
ることがあった。
Conventional technology Conventionally, barium titanate,
Calcium titanate, alumina, etc. were used. However, since the coefficient of thermal expansion was greatly different from that of the magnetic film structure, the vapor-deposited magnetic film structure was easily peeled off,
Further, a stress may be generated due to the difference in the coefficient of thermal expansion and a crack may be generated.

さらに、従来の材料は硬さが低く、特に高保磁力テープ
(いわゆるメタルテープ)が使用された場合には、非磁
性基板が磁性膜構造体と硬度及び耐摩耗性が異なり、磁
気テープとの摺動により発生する摩擦のために偏摩耗等
を引き起こし、磁気特性に変化をきたすという問題があ
った。特に硬度が低い場合には、磁気ヘッドの寿命が短
くなること、あるいは非磁性基板の変形や割れ及び剥離
を引き起こすといった欠点が顕著であった。
Furthermore, the conventional material has low hardness, and especially when a high coercive force tape (so-called metal tape) is used, the non-magnetic substrate is different from the magnetic film structure in hardness and abrasion resistance, so that the non-magnetic substrate slides on the magnetic tape. There is a problem in that the friction generated by the movement causes uneven wear and the like, resulting in changes in the magnetic characteristics. Particularly when the hardness is low, the shortcomings of shortening the life of the magnetic head and causing deformation, cracking and peeling of the non-magnetic substrate are remarkable.

本発明者は、上記の欠点について解決すべく、多くの材
料を検討し、基本組成としてCoxNi2-xO2(ただし0.2≦
x≦1.8)なる組成の酸化物が有効であるとして既に開
示している。また、添加材の検討を行ない、MnO、Ti
O2、Al2O3あるいはCaOの0.1〜5wt%添加が有効であると
して、既に開示している。
The present inventor investigated many materials in order to solve the above-mentioned drawbacks, and as a basic composition, Co x Ni 2-x O 2 (however, 0.2 ≦
It has already been disclosed that an oxide having a composition of x ≦ 1.8) is effective. In addition, we examined the additive materials and found that MnO, Ti
It has already been disclosed that the addition of 0.1 to 5 wt% of O 2 , Al 2 O 3 or CaO is effective.

また、CoO、NiOを基本組成として添加材の検討を続けた
結果、1〜5wt%のY2O3、あるいは0.1〜1wt%のTiN、ま
たは0.3〜2wt%のB2O3を添加した場合でも上記の特性を
有するので、これも開示した。
In addition, as a result of continuing to study the additive material with CoO and NiO as the basic composition, when 1 to 5 wt% Y 2 O 3 or 0.1 to 1 wt% TiN, or 0.3 to 2 wt% B 2 O 3 was added However, since it has the above-mentioned characteristics, this is also disclosed.

発明が解決しようとする問題点 本発明は、上記の欠点を解決したもので、具体的には13
0〜150x10-7/℃の熱膨張率を有し、ビッカース硬度600
以上の特性を持ち、さらに他のヘッド構成材料間で過度
の化学的侵食反応を起こさない材料を提供することが目
的である。
Problems to be Solved by the Invention The present invention solves the above-mentioned drawbacks, and specifically,
Has a coefficient of thermal expansion of 0 ~ 150x10 -7 / ℃, Vickers hardness 600
It is an object of the present invention to provide a material that has the above characteristics and that does not cause an excessive chemical erosion reaction between other head constituent materials.

発明の構成 即ち、本発明は、CoxNi2-xO2(ただし0.2≦x≦1.8)を
基本組成として、該組成物100wt%に対し1〜5wt%のSi
O2を添加したことを特徴とする磁気ヘッド用非磁性基板
に関する。
Structure of the Invention That is, the present invention is based on Co x Ni 2 -x O 2 (where 0.2 ≦ x ≦ 1.8) as a basic composition, and 1 to 5 wt% of Si is used for 100 wt% of the composition.
The present invention relates to a non-magnetic substrate for a magnetic head, to which O 2 is added.

問題点を解決するための手段及び作用 本発明は、さらに、CoxNi2-xO2(ただし0.2≦x≦1.8)
を基本組成として添加材の検討を続けた結果、該組成物
100wt%に対し1〜5wt%のSiO2を添加した場合に密度及
び硬度の向上が観察されることを見い出した。
Means and Actions for Solving Problems The present invention further provides Co x Ni 2-x O 2 (where 0.2 ≦ x ≦ 1.8)
As a result of continuing to study the additive material with the basic composition of
It was found that when 1 to 5 wt% of SiO 2 was added to 100 wt%, an improvement in density and hardness was observed.

SiO2は、NiO、CoOとの濡れ性が良く、1wt%以上の添加
により密度は増加する。しかしながら5wt%より多量のS
iO2の添加は、粒界部分に偏析が生じるため硬度、熱膨
張率の低下をもたらすため好ましくない。
SiO 2 has a good wettability with NiO and CoO, and the density increases when 1 wt% or more is added. However, more than 5 wt% S
Addition of iO 2 is not preferable because it causes segregation at the grain boundary portion, resulting in a decrease in hardness and coefficient of thermal expansion.

添加は、単独あるいは各々の組み合わせでも良好であ
り、既に開示している添加材との組み合わせも有効であ
る。所望の硬度、熱膨張率に対応した組み合わせを採用
するのが望ましい。
The addition may be performed singly or in combination with each other, and the combination with the already disclosed additive is also effective. It is desirable to adopt a combination corresponding to the desired hardness and thermal expansion coefficient.

市販の各酸化物を原料として、所望組成になるよう秤量
し、ボールミルにより混合する。混合は例えばエタノー
ル中湿式ボールミルで10〜30時間行なう。
Each commercially available oxide is used as a raw material, weighed to have a desired composition, and mixed by a ball mill. Mixing is carried out, for example, in a wet ball mill in ethanol for 10 to 30 hours.

乾燥後、CIP成形し、例えばAr中850〜1100℃で仮焼し、
次いで粗砕機を用いて粉砕し、100〜200μmの篩で篩分
けを行なう。
After drying, CIP molding, calcination in Ar at 850-1100 ℃,
Then, it is crushed using a coarse crusher and sieved with a sieve of 100 to 200 μm.

仮焼粉はさらに例えばエタノール中湿式ボールミルで20
〜72時間処理し、1μm以下に微粉砕する。
The calcined powder can be further processed, for example, in a wet type ball mill in ethanol.
Treat for ~ 72 hours and pulverize to 1 μm or less.

これを造粒後、CIP成形し、例えばN2中1230〜1400℃で
焼結し、その後、HIP処理を行なう。HIP処理条件は、80
0〜1200kg/cm2、1200〜1350℃、1〜2時間が望まし
い。
After granulating this, it is CIP molded and sintered, for example, in N 2 at 1230 to 1400 ° C., and then subjected to HIP treatment. HIP processing condition is 80
0 to 1200 kg / cm 2 , 1200 to 1350 ° C., and 1 to 2 hours are desirable.

このようにして得られた焼結体は、緻密で岩塩型構造を
有し、テープの摺動により摩擦やエッヂ部の欠けが少な
く従来の材料よりも優れていることが確認できた。
It was confirmed that the thus-obtained sintered body had a dense and rock-salt structure, was less likely to cause friction and chipping at the edge portion due to the sliding of the tape, and was superior to conventional materials.

実施例 CoO、NiOを原料にCoxNi2-xO2(x=1.0)組成となるよ
うに調整し混合した。混合はエタノール中湿式ボールミ
ルで20時間行なった。
Example CoO and NiO were used as raw materials and adjusted so as to have a Co x Ni 2 -x O 2 (x = 1.0) composition and mixed. Mixing was carried out in ethanol with a wet ball mill for 20 hours.

これをAr中1000℃で仮焼後、粗砕して150μmで篩分け
した。さらにエタノールの湿式ボールミルで70時間微粉
砕した。
This was calcined in Ar at 1000 ° C., then roughly crushed and sieved at 150 μm. Further, it was finely pulverized for 70 hours with a wet ball mill of ethanol.

この微粉砕にSiO2を表1の割合で添加し、CIP成形後N2
中1400℃で焼結した。なお、HIP処理を行なわくとも焼
結体の密度は高い値であった。
SiO 2 was added to this pulverized powder in the ratio shown in Table 1, and after CIP molding, N 2 was added.
Sintered at 1400 ° C in medium. The density of the sintered body was a high value even if the HIP treatment was not performed.

焼結体の相対密度、ビッカース硬度(Hv)、熱膨張率
(α)を表1に示す。表中には、比較例としてチタン酸
バリウム(チタバリ)の特性を併記した。
Table 1 shows the relative density, Vickers hardness (Hv), and coefficient of thermal expansion (α) of the sintered body. In the table, the characteristics of barium titanate (Citabari) are also shown as a comparative example.

発明の効果 以上説明したように、(1)本組成の非磁性基板は、熱
膨張率、硬度とも磁性膜構造体とほぼ同等の特性を得る
ことができる。
EFFECTS OF THE INVENTION As described above, (1) the non-magnetic substrate having the composition of the present invention can obtain substantially the same thermal expansion coefficient and hardness as the magnetic film structure.

このため、磁性膜構造体の剥離やクラックの発生を著し
く防止できる。
Therefore, the peeling of the magnetic film structure and the occurrence of cracks can be significantly prevented.

(2)さらに、硬度を高めることにより磁気ヘッドの短
寿命化や非磁性基板の変形、割れ等を抑えることがで
き、ヘッドの耐摩耗性、耐久性に特にすぐれている利点
がある。
(2) Further, by increasing the hardness, it is possible to shorten the life of the magnetic head and suppress the deformation and cracking of the non-magnetic substrate, and there is an advantage that the wear resistance and durability of the head are particularly excellent.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】CoxNi2-xO2(ただし0.2≦x≦1.8)を基本
組成として、該組成物100wt%に対し1〜5wt%のSiO2
添加したことを特徴とする磁気ヘッド用非磁性基板。
1. A magnetic head characterized in that Co x Ni 2-x O 2 (where 0.2 ≦ x ≦ 1.8) is used as a basic composition, and 1 to 5 wt% of SiO 2 is added to 100 wt% of the composition. Non-magnetic substrate.
JP1214206A 1989-08-22 1989-08-22 Non-magnetic substrate for magnetic head Expired - Lifetime JPH0782616B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1214206A JPH0782616B2 (en) 1989-08-22 1989-08-22 Non-magnetic substrate for magnetic head

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1214206A JPH0782616B2 (en) 1989-08-22 1989-08-22 Non-magnetic substrate for magnetic head

Publications (2)

Publication Number Publication Date
JPH0380411A JPH0380411A (en) 1991-04-05
JPH0782616B2 true JPH0782616B2 (en) 1995-09-06

Family

ID=16651993

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1214206A Expired - Lifetime JPH0782616B2 (en) 1989-08-22 1989-08-22 Non-magnetic substrate for magnetic head

Country Status (1)

Country Link
JP (1) JPH0782616B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009198532A (en) * 2008-02-19 2009-09-03 Aoyama Gankyo Kk Attaching/detaching mechanism for decorating member for spectacle frame

Also Published As

Publication number Publication date
JPH0380411A (en) 1991-04-05

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