JPS59203771A - Non-magnetic ceramic composition for magnetic head - Google Patents

Non-magnetic ceramic composition for magnetic head

Info

Publication number
JPS59203771A
JPS59203771A JP58075245A JP7524583A JPS59203771A JP S59203771 A JPS59203771 A JP S59203771A JP 58075245 A JP58075245 A JP 58075245A JP 7524583 A JP7524583 A JP 7524583A JP S59203771 A JPS59203771 A JP S59203771A
Authority
JP
Japan
Prior art keywords
magnetic
porcelain
ceramic composition
thermal expansion
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.)
Granted
Application number
JP58075245A
Other languages
Japanese (ja)
Other versions
JPS6158428B2 (en
Inventor
光男 田村
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.)
Tokin Corp
Original Assignee
Tohoku Metal Industries Ltd
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 Tohoku Metal Industries Ltd filed Critical Tohoku Metal Industries Ltd
Priority to JP58075245A priority Critical patent/JPS59203771A/en
Publication of JPS59203771A publication Critical patent/JPS59203771A/en
Publication of JPS6158428B2 publication Critical patent/JPS6158428B2/ja
Granted legal-status Critical Current

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

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本発明は、各種磁気ヘッド特にフロッピーディスクヘッ
ドを構成する非磁性構造材料に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to non-magnetic structural materials constituting various magnetic heads, particularly floppy disk heads.

従来よシ磁気ヘッド用非磁性構造材料としてはアルミナ
、フォルステライト、ステアタイト磁器等が用いられて
いた。しかしながらこれらの欠点は、磁性材料のフェラ
イトの組成が磁気ヘンドの仕様の違いにより多少異なる
ため、それに応じて熱膨張係数が変り、フェライトと非
磁性材料の熱膨張係数が一致せず、ガラスボンディング
工程でいずれかに割れが生じ歩留りを低下させることで
あった。
Conventionally, alumina, forsterite, steatite porcelain, etc. have been used as nonmagnetic structural materials for magnetic heads. However, these drawbacks are that the composition of the magnetic material ferrite differs slightly depending on the specifications of the magnetic hand, so the coefficient of thermal expansion changes accordingly, and the coefficient of thermal expansion of the ferrite and non-magnetic material do not match, resulting in a problem in the glass bonding process. Cracks occurred in one of the parts, reducing the yield.

この磁気ヘッド用の非磁性材料は、常にフェライトと同
時に高速でフロッピーディスク面を摺動し々がら移動す
る。従って、その耐摩耗性がフェライトと同程度でない
場合、フェライト部と非磁性材料との間にすき間を生じ
、磁気ヘッドの機能を低下させる。壕だ材質の表面に3
0μ以上のrイドがある場合、ボイド部から微少なカケ
を生じて磁気記憶媒体の表面にキズをつける原因に々る
This non-magnetic material for the magnetic head always slides on the floppy disk surface at high speed simultaneously with the ferrite. Therefore, if its wear resistance is not on the same level as ferrite, a gap will be created between the ferrite portion and the nonmagnetic material, reducing the functionality of the magnetic head. 3 on the surface of the trench material
If there is an r-id of 0μ or more, this may cause minute chips to occur from the void portion and cause scratches on the surface of the magnetic storage medium.

さらに、これらの構成部品は、精密々加工工程を経て磁
気ヘッドに加工するので2機械加工に際して適度の加工
性の良さを要求される。
Furthermore, since these components are processed into the magnetic head through precision machining processes, appropriate workability is required during two-machining processes.

アルミナ、フォルステライト、ステアタイト等はこれら
の要求に対して満足できるものでなく。
Alumina, forsterite, steatite, etc. cannot satisfy these requirements.

最近になり、Nトznフェライトを用いるヘッドに対し
ては、マイクロ波誘電体材料として既知の材料であるB
a0−TiO2−ZrO2系の磁器が用いられるのが一
般的になっている。これは+ BaO’r+02−Zr
O2系磁器が適度の加工性と耐摩耗性を備え、かつ組成
比の調整により機械的性質を損うことなく90〜100
X 10−7/℃の範囲で熱膨張係数を自由に変えるこ
とができるととが見い出されたことによる。
Recently, for heads using N-zn ferrite, B, a material known as a microwave dielectric material, has been used.
It has become common to use a0-TiO2-ZrO2-based porcelain. This is +BaO'r+02-Zr
O2-based porcelain has appropriate workability and wear resistance, and by adjusting the composition ratio, it can be improved to 90 to 100 without impairing mechanical properties.
This is based on the discovery that the coefficient of thermal expansion can be freely changed within the range of X 10-7/°C.

しかしながら、近年フロッピーディスク装置の高性能化
がはかられるにつれて、磁気ヘッド材料に対する要求も
次第に厳しくなり、研摩面のがイドに対する要求値も5
μ以下が標準となりつつある。この要求に対してBa0
−TtC)2ZrO2系磁器は通常の製法では対応でき
なくなり、ホットプレスや熱間静水圧プレス(HIP 
)が用いられている。これらの高密度化の手法により研
摩面のボイドは一応要求性能を満足できるようになった
が価格が高く巾広い普及がはげ腫れている。
However, as the performance of floppy disk devices has improved in recent years, the requirements for magnetic head materials have become increasingly strict, and the required value for the polished surface has increased to 5.
Below μ is becoming the standard. Ba0 for this request
-TtC)2ZrO2-based porcelain can no longer be manufactured using normal manufacturing methods, and hot press or hot isostatic press (HIP)
) is used. These high-density techniques have made it possible to reduce the voids on the polished surface to a certain extent to meet the required performance, but the high price has prevented widespread use.

本発明の目的は9通常の焼結手法ながら研摩面のボイド
が5μ以下で、熱膨張係数が90〜100×l0−7/
℃のBaOT r 02−Z ro2系の磁気ヘッド用
非磁性磁器組成物を掃供するものである。
The purpose of the present invention is to reduce the voids on the polished surface to 5μ or less despite the normal sintering method, and to have a coefficient of thermal expansion of 90 to 100×l0-7/
℃ BaOT r 02-Z ro2 type non-magnetic ceramic composition for magnetic heads.

本発明は、 TiO280〜91.0mot%、 Ba
O6〜] 6.Omob%、ZrO20,5〜3.0m
ot% 、k120..0.05〜1.Omot%。
The present invention includes TiO280-91.0 mot%, Ba
O6~] 6. Omob%, ZrO20.5~3.0m
ot%, k120. .. 0.05-1. Omot%.

Y2O30,05〜1. Omot%の成分範囲よりな
り合計が1、OOmot%になる組成で熱膨張係数が9
0X10−’ン℃〜100×10−7/℃の範囲となる
ことを特徴とする磁気ヘッド用非磁性磁器組成物である
Y2O30,05~1. The total is 1 from the component range of Omot%, and the thermal expansion coefficient is 9 with a composition of OOmot%.
This is a non-magnetic ceramic composition for a magnetic head, characterized in that the temperature is in the range of 0x10-'°C to 100x10-7/°C.

Ba0−TiO系においてT IO2のmat比が80
モル%以上の組成域ではBaT Oの結晶相とT IO
2の2つの  9 結晶相から成ることが通常の相平衡状態図から予想でき
るが、マイクロ波誘電体に関する詳細な研究から第3の
結晶相としてB a 2 T l 9020が存在する
ことが確認され、さらにこの結晶相が含まれる量が多い
程磁器としての強度が向上することが知られている。仮
焼条件、焼結条件によりとのBa2TI 9020の結
晶相の生成量は異なるが、添加物としてZ(イ)2゜S
nO2,を含むと、Ba2Ti902oの結晶相の生成
を促進できることが認められ、捷たこれにより誘電特性
が向上することから、BaOTlO2ZrO2系磁器が
マイクロ波の誘電体として用いられていた。
In the Ba0-TiO system, the mat ratio of TIO2 is 80
In the composition range of mol% or more, the crystal phase of BaT O and T IO
Although it can be predicted from the usual phase equilibrium diagram that B a 2 T l 9020 consists of two crystal phases of 2, detailed research on microwave dielectrics confirmed the existence of B a 2 T l 9020 as a third crystal phase. Furthermore, it is known that the greater the amount of this crystalline phase contained, the greater the strength of the porcelain. Although the amount of Ba2TI 9020 crystal phase produced differs depending on the calcination and sintering conditions, Z(a)2゜S as an additive
It has been recognized that inclusion of nO2 can promote the formation of the Ba2Ti902o crystal phase, and this improves dielectric properties, so BaOTlO2ZrO2 ceramics have been used as dielectric materials for microwaves.

磁気ヘッドの構造材用磁器としてB ao−T i 0
2−Z ro2系の磁器をみた場合、Ba2TI、02
oの生成によシ機械的強度が増したことは応用上好都合
である。またBaOとT + ’02の比率を変えるこ
とによりB a 2T I q O20の結晶相とTi
O2の結晶相の比率をコントロールでき、双方の体積比
で熱膨張係数をコントロールできるという長所がある。
Bao-T i 0 as a structural material for magnetic heads
When looking at 2-Z ro2 type porcelain, Ba2TI, 02
The increase in mechanical strength due to the formation of o is advantageous for applications. In addition, by changing the ratio of BaO and T + '02, the crystal phase of Ba 2T I q O20 and Ti
It has the advantage that the ratio of the O2 crystal phase can be controlled and the coefficient of thermal expansion can be controlled by the volume ratio of both.

これらのことから。from these things.

B ao T iO2−Z r O2系の磁器が磁気ヘ
ッド用の構造材料として一般的に用いられるように々っ
た。
Bao TiO2-ZrO2-based porcelain has come to be commonly used as a structural material for magnetic heads.

本発明におけるT r 02及びBaOの配合比率は熱
膨張係数を90X]O/℃から100xl−0/℃の間
でコントロールするために必須のものである。
The blending ratio of T r 02 and BaO in the present invention is essential for controlling the thermal expansion coefficient between 90X]O/°C and 100xl-0/°C.

Z ro 2は、上記説明のようにBa2T I 90
20の結晶相の生成を促進させるだめのものである。Z
 rO2の量が+ 0.5mot%未満では、この効果
が認められず。
Z ro 2 is Ba2T I 90 as explained above
This is a substance that promotes the formation of 20 crystal phases. Z
This effect was not observed when the amount of rO2 was less than +0.5 mot%.

3 mot%を越えると焼結過程で焼結体の内部が還元
しやすくなる。
If it exceeds 3 mot%, the inside of the sintered body is likely to be reduced during the sintering process.

焼結体の研磨面のボイドの大きさ及び量は仮焼粉の粉砕
後の粒径に反比例する。即ち粉砕が進行するにつれて、
焼結密度は向上し、研磨面のボイドは小さくなりかつ数
量も減る。ボイドの小さい焼結体を得るためには、いか
に効率の良い仮焼後の粉砕を行うかがポイントである。
The size and amount of voids on the polished surface of the sintered body are inversely proportional to the particle size of the calcined powder after pulverization. That is, as the crushing progresses,
The sintered density is improved and the voids on the polished surface are smaller and less numerous. In order to obtain a sintered body with small voids, the key is how efficiently the pulverization after calcination can be carried out.

一つの対策としては、々るべく仮焼温度を下げて軟い粉
末にして粉砕すれば良いが、あまり低い温度で仮焼した
場合、原料の炭酸バリウム(BaC03)が充分分解し
ないことがあり、焼結体の内部に見学するガス(CO2
)のため巨大ボイドが生じて逆効果となる。
One countermeasure is to reduce the calcination temperature as much as possible and grind it into a soft powder, but if calcination is performed at too low a temperature, the raw material barium carbonate (BaC03) may not be sufficiently decomposed. Gas (CO2) to be observed inside the sintered body
), a huge void is generated and has the opposite effect.

発明者はBaO’r+02 ZrO2系に種々の添加物
を試みた結果、 A/=、、03.Y2O3の添加が仮
焼時の反応を抑制し、BaCOxが充分分解する仮焼条
件下でも軟い仮焼粉が得られることを見い出した。さら
に、これを湿式再粉砕して得た粉末を成形、焼結して得
られた磁器の研磨面のボイドは、従来のB ao T 
r 02− ZrO2系で同一仮焼、粉砕、焼結して得
られた磁器に比して、著しく小さくかつ数が減少するこ
とを見い出した。
As a result of trying various additives to the BaO'r+02 ZrO2 system, the inventor found that A/=,,03. It has been found that the addition of Y2O3 suppresses the reaction during calcination, and a soft calcined powder can be obtained even under calcination conditions in which BaCOx is sufficiently decomposed. Furthermore, the voids in the polished surface of the porcelain obtained by molding and sintering the powder obtained by wet re-grinding are removed by conventional Bao T
It has been found that the size and number of particles are significantly smaller than that of porcelain obtained by the same calcining, crushing, and sintering process using the r 02-ZrO2 system.

fi、t203. Y2O3の添加量を、いずれも00
5から1.0に限定した理由は、添加量をこれ以下にし
たら効果が失われること、またこれ以上にすると磁器の
内部が焼結過程で環元しやすくなることまた材質が硬く
なり加工性が劣化することが認められたからである。
fi, t203. The amount of Y2O3 added is 00 in both cases.
The reason for limiting the amount from 5 to 1.0 is that if the amount added is less than this, the effect will be lost, and if it is more than this, the inside of the porcelain will easily form rings during the sintering process, and the material will become hard and difficult to work with. This is because it has been recognized that the deterioration of

以下実施例をもって本発明の詳細な説明する。The present invention will be explained in detail below with reference to Examples.

T +021 BaCO3,Z r02は純度99係以
上の試薬を用い。
For T +021 BaCO3 and Z r02, use reagents with a purity level of 99 or higher.

寸だ、添加物としてのAt203及びY2O3も純度9
9%以上の試薬を用いた。表の組成になるように原料を
配合し、が−ルミルで湿式混合した。乾燥後粉砕し、 
1100℃から1200℃の間で3時間仮焼した。
The purity of At203 and Y2O3 as additives is 9.
9% or more of reagent was used. The raw materials were blended so as to have the composition shown in the table, and wet-mixed using a galmill. After drying, crush
Calcining was performed for 3 hours between 1100°C and 1200°C.

仮焼粉は樹脂製のボールミルを用いて20時間以上粉砕
した。次に乾燥後、バインダーを混合し。
The calcined powder was pulverized for 20 hours or more using a resin ball mill. Next, after drying, mix the binder.

10〜2.Ot/cJの圧力で成形した。焼結は128
0℃〜1360℃の間で大気中で行った。得られた試料
の密度及び熱膨張係数を測定し更に研磨面のボイドを金
属顕微鏡を用いて観察した。その結果を表に示す。
10-2. It was molded at a pressure of Ot/cJ. Sintering is 128
The test was carried out in the atmosphere between 0°C and 1360°C. The density and coefficient of thermal expansion of the obtained sample were measured, and voids on the polished surface were observed using a metallurgical microscope. The results are shown in the table.

以下余白 (7) 実験試刺扁1〜27はそれぞれTlO2とBa0O比が
一定の配合に対してZnO2,At203.Y2O3の
配合量が異なる試料群である。
Blank space below (7) Experimental test strips 1 to 27 are ZnO2, At203. These are sample groups with different amounts of Y2O3.

熱膨張係数はほぼTlO2とBaOの比率で決る。The coefficient of thermal expansion is determined approximately by the ratio of TlO2 and BaO.

NlZnフェライトを用いる磁気ヘッド用非磁性磁器と
しては熱膨張係数が90〜100×10−7/℃の値が
要求される。これを満足できる試料は&1〜25で、こ
れらのTlO2とBaOの配合比はそれぞれ80〜9]
、、Omo1%、 6〜16.0mo7%であることが
わかる。
Nonmagnetic ceramics for magnetic heads using NlZn ferrite are required to have a coefficient of thermal expansion of 90 to 100 x 10-7/°C. Samples that can satisfy this are &1 to 25, and the blending ratios of TlO2 and BaO are 80 to 9, respectively]
,, Omo1%, 6-16.0mo7%.

ZrO2の効果は磁器の焼結性を改善し1機械的強度が
改善される。また還元を防止する効果があり。
The effect of ZrO2 improves the sinterability of porcelain, and the mechanical strength is improved. It also has the effect of preventing reduction.

少くとも0.5mot%まではこの効果が認められた。This effect was observed up to at least 0.5 mot%.

またZ n O2の量が3 mo1%を越えると逆に還
元しゃす〈々りまだ研磨面のボイドが大きくなる。試料
扁1.11,16.21はZ r O2が過剰のため磁
器の機械的強度が弱く寸だ研磨面のボイドが大きく好1
しくなり、5,10,15,20.25はZ r O2
を含丑ない場合であり焼結体の内部が部分的に還元し、
灰色となり実用上好しくない。
On the other hand, if the amount of ZnO2 exceeds 3 mol %, the reduction will occur and the voids on the polished surface will become larger. Sample planes 1.11 and 16.21 have excessive Z r O2, so the mechanical strength of the porcelain is weak and the voids on the polished surface are large.
5, 10, 15, 20.25 are Z r O2
In this case, the inside of the sintered body is partially reduced,
The color turns gray, which is not practical.

At203は焼結時の粒の成長を阻止し緻密な焼結体を
得るために有効である。その効果は0.05moA%以
上で認められた。が+ 1.0 mo7%を越えると磁
器が硬くまたもろくなり加工性が劣る。またBaOとT
 r 02の比によっては還元しゃすぐ々る。
At203 is effective in preventing grain growth during sintering and obtaining a dense sintered body. The effect was observed at 0.05 moA% or more. If it exceeds +1.0 mo7%, the porcelain becomes hard and brittle and has poor workability. Also BaO and T
Depending on the ratio of r02, reduction may be possible.

Y2O3は仮焼時の反応を抑制し仮焼粉の粉砕を容易に
し焼結体のボイドを細くする効果がある。その効果は0
.05mo/:%以上で認められた。一方Y2O3の含
有量が増大して1.、Omot%を越えると、At2o
3と同様に材質を硬くし加工性を劣化させる。4゜9.
14,19.24 はAt203.Y2O3のいずれか
が過剰になった例で加工性の劣るものである。
Y2O3 has the effect of suppressing reactions during calcination, facilitating pulverization of calcined powder, and narrowing voids in the sintered body. Its effect is 0
.. 05mo/:% or more. On the other hand, the content of Y2O3 increases and 1. , when Omot% is exceeded, At2o
Similar to 3, it hardens the material and deteriorates workability. 4゜9.
14, 19.24 is At203. This is an example in which either Y2O3 is in excess, and the workability is poor.

上記実施例の説明から明らかなように1本発明によれば
、熱膨張係数が、90〜100×10−7/℃の範囲に
あり、ディトが少なく2機械的強度の大きな非磁性磁器
組成物を得ることができ、これは、磁気ヘッドの非磁性
構造材料として適している。
As is clear from the description of the above examples, 1. According to the present invention, a non-magnetic porcelain composition having a thermal expansion coefficient in the range of 90 to 100 x 10-7/°C, and 2. can be obtained, which is suitable as a non-magnetic structural material for magnetic heads.

Claims (1)

【特許請求の範囲】[Claims] 1.TiO280〜91.0mol%、BaO6〜16
.0mol%、ZrO20.5〜3.0mol%、Al
2O30.05〜1.0mol%、Y2O30.05〜
1.0 mot%、の成分範囲よりなシ合計が100m
o1%に力る組成物からなることを特徴とする磁気ヘッ
ド用非磁性磁器組成物。
1. TiO280-91.0mol%, BaO6-16
.. 0 mol%, ZrO20.5-3.0 mol%, Al
2O30.05~1.0mol%, Y2O30.05~
The total amount from the component range of 1.0 mot% is 100m
1. A non-magnetic ceramic composition for a magnetic head, characterized in that the composition is made of a composition having a concentration of 0.1%.
JP58075245A 1983-04-28 1983-04-28 Non-magnetic ceramic composition for magnetic head Granted JPS59203771A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58075245A JPS59203771A (en) 1983-04-28 1983-04-28 Non-magnetic ceramic composition for magnetic head

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58075245A JPS59203771A (en) 1983-04-28 1983-04-28 Non-magnetic ceramic composition for magnetic head

Publications (2)

Publication Number Publication Date
JPS59203771A true JPS59203771A (en) 1984-11-17
JPS6158428B2 JPS6158428B2 (en) 1986-12-11

Family

ID=13570642

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58075245A Granted JPS59203771A (en) 1983-04-28 1983-04-28 Non-magnetic ceramic composition for magnetic head

Country Status (1)

Country Link
JP (1) JPS59203771A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH09257287A (en) * 1996-03-19 1997-09-30 Seibu Electric Ind Co Ltd Air purifier at inlet port

Also Published As

Publication number Publication date
JPS6158428B2 (en) 1986-12-11

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