JPS59190264A - Ceramic composition for magnetic head - Google Patents

Ceramic composition for magnetic head

Info

Publication number
JPS59190264A
JPS59190264A JP58065087A JP6508783A JPS59190264A JP S59190264 A JPS59190264 A JP S59190264A JP 58065087 A JP58065087 A JP 58065087A JP 6508783 A JP6508783 A JP 6508783A JP S59190264 A JPS59190264 A JP S59190264A
Authority
JP
Japan
Prior art keywords
thermal expansion
magnetic
magnetic head
composition
ceramic composition
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
JP58065087A
Other languages
Japanese (ja)
Other versions
JPS6224387B2 (en
Inventor
治 山下
有坂 仁史
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.)
Proterial Ltd
Original Assignee
Sumitomo Special Metals Co 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 Sumitomo Special Metals Co Ltd filed Critical Sumitomo Special Metals Co Ltd
Priority to JP58065087A priority Critical patent/JPS59190264A/en
Publication of JPS59190264A publication Critical patent/JPS59190264A/en
Publication of JPS6224387B2 publication Critical patent/JPS6224387B2/ja
Granted legal-status Critical Current

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  • Compositions Of Oxide Ceramics (AREA)
  • Adjustment Of The Magnetic Head Position Track Following On Tapes (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】 この発明は、磁気ヘッドの構造部品に用いる非1丑付イ
4 J’lに係り、」ンビュータ等の各g8磁気ヘッド
、1カにフロッピーディスク用フエライl−磁気ヘッI
・の(111成に不可欠のスライダーあるいはスペーリ
ーに使用する磁気ヘッド用磁器組成物に閏する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a magnetic head for use as a structural part of a magnetic head. I
・This applies to porcelain compositions for magnetic heads used for sliders or spacers, which are essential for 111 construction.

一般に磁気l\ラッド、lln −ZTIフェライト、
NL−Zηノエライ[〜の磁性材料からなるコアと非磁
性材料からなるII′1+ja部品とをガラス溶名して
組立てられでおり、特にデジタル用磁気ヘッドには磁性
材わ1どし−C2,高周波特性及び耐rg耗性のJ−ぐ
れたN。
Generally magnetic l\rad, lln -ZTI ferrite,
The core made of magnetic material of NL-Zη Noelai [~] and the II'1+ja parts made of non-magnetic material are assembled by glass melting, and especially for digital magnetic heads, magnetic material 1-C2, J-Gutta N with high frequency characteristics and rg wear resistance.

−Zη)上ライ1〜に変えて高透磁率のMn  Znフ
エライ+−が使用され、非磁性構造部品手Δ料には熱膨
張係数が同等の1iO2BaO系磁器が使用されている
-Zη) High magnetic permeability Mn Zn ferrite+- is used in place of the upper layer 1~, and 1iO2BaO based porcelain having the same coefficient of thermal expansion is used for the non-magnetic structural component material Δ.

すなわち、コア材と、非磁性((″4構造品との熱膨張
係数が異なると、これらをガラス溶着する際に、歪を生
じ、磁気特性の劣化が起こるだ(ブでなく、ひび、剥離
専を生じ−C1a気l\ツドの組立上人込な問題となっ
ている。
In other words, if the thermal expansion coefficients of the core material and the non-magnetic (4) structural product are different, distortion will occur when glass welding them together, resulting in deterioration of magnetic properties. This has caused a huge problem in the assembly of C1a.

ざらに、この非磁性構造部品材料に気孔が多く存在する
と、磁気ヘッドと記録媒体どの接触走行時に、記録媒体
にコーチインクされた磁性粉が」ニ記気孔に何名したり
、デツピングを生じて磁気ヘッドや記録媒体を損傷する
ため、気孔率の低い高密度化された非磁性磁器組成物が
切望されている。
In general, if there are many pores in this non-magnetic structural component material, when the magnetic head and the recording medium come into contact with each other, the magnetic powder coated on the recording medium may enter the pores or cause depping. To prevent damage to magnetic heads and recording media, a highly densified non-magnetic ceramic composition with low porosity is desired.

従来のTL 02  Ba O系磁器組成物は、BaO
の早ととも(こ熱膨張係数か直線的に大きくなることが
知られており、上述したコア4AのMn −Zηフェラ
イトの熱膨張係数は要求される電磁気特性によって定ま
る組成により固定されるが、   105・−115×
10−7/℃であるため、非磁性構造部品材層の熱膨張
係数をフェライトの方に合せる必要があり、熱膨張係数
の差を2xlO−7/°C以下に抑えるべく、TL02
 50・” 75wt%、BaO25〜50wt%の組
成からなる磁器組成物が使用されていた1゜一方、磁器
組成物の気孔を低減する方法として、−1−記組成の優
妾器組成物に、 #203 、5LO2,MgO。
The conventional TL 02 Ba O based porcelain composition is based on BaO
It is known that the coefficient of thermal expansion increases linearly as the temperature increases, and the coefficient of thermal expansion of the Mn-Zη ferrite of the core 4A mentioned above is fixed by the composition determined by the required electromagnetic properties. 105・-115×
10-7/°C, it is necessary to match the thermal expansion coefficient of the non-magnetic structural component material layer to that of ferrite, and in order to suppress the difference in thermal expansion coefficient to 2xlO-7/°C or less, TL02
A porcelain composition having a composition of 50.'' 75 wt% and 25 to 50 wt% of BaO was used.On the other hand, as a method for reducing the porosity of a porcelain composition, a porcelain composition having the composition as described in -1- #203, 5LO2, MgO.

SrO、CclO、ZrO2等の焼結補助々Δを少なく
とも1種以」−で4wt%以−ド添加し、焼結密度を改
善する方法が知られているが、大気中焼結では1〜3%
の気孔が残存し、とくにZr 02の添加量が2wt%
以下の場合は、成形体の寸法が40mm X 20mm
 X 20mmと人さ″くなると通常の焼結法では焼結
体の内部が還元され−C黒色化する問題があった。
A method is known in which the sintering density is improved by adding at least one kind of sintering aid Δ such as SrO, CClO, ZrO2 at 4 wt% or more. %
pores remain, especially when the added amount of Zr02 is 2wt%
In the following cases, the dimensions of the molded object are 40mm x 20mm
When the size of the sintered body becomes 20 mm, the normal sintering method has a problem in that the inside of the sintered body is reduced and becomes -C black.

また、気孔率を低減づる方法とし−C1熱間静水圧プレ
ス処理が知られており、極めて有効ではあるが、この処
理が通常アルゴン雰囲気中で行なわれるため、彼処理拐
表面が還元されて黒色化する問題かあり、酸素雰囲気中
で再び熱処理を施しても、完全に脱色ツることが困難で
材料内部まで均一に回復させることができなかった。
In addition, C1 hot isostatic pressing is a known method for reducing porosity, and although it is extremely effective, since this treatment is usually carried out in an argon atmosphere, the treated surface is reduced and becomes black. Even if heat treatment was performed again in an oxygen atmosphere, it was difficult to completely decolorize the color, and it was not possible to uniformly restore the color to the inside of the material.

この発明は、上述の問題点に鑑み、Mn −Zηフ工プ
ライ1〜同等の熱膨張係数を有し、結晶組織が非常に緻
密であり、熱間静水圧プレス処理を施づ−ことなく、通
常の焼結処理で熱間静水圧プレス処理と同等の、0.2
%以下の気孔ヰ′をイ)リ−るTL 02  Ba O
系磁器組成物を提案するものである。
In view of the above-mentioned problems, this invention has a coefficient of thermal expansion equivalent to Mn-Zη fiber ply 1, has a very dense crystal structure, and does not require hot isostatic pressing. 0.2, which is equivalent to hot isostatic pressing with normal sintering.
TL 02 Ba O
This paper proposes a ceramic composition based on the ceramic composition.

すなわち、この発明は、T、02 !〕0”□ 75w
t%、BaO25〜50wt%からなり、 TL 02
 、 Ba Oの合計を100として、Zy 0210
・” 15wt%を含有し、Ba TL4 、 TL 
O2゜Zy Tj 04の3相からなり、気孔率0.2
%以下に高密度化したことを要旨どづ−る磁気ヘッド用
磁器組成物である。
That is, this invention is T,02! ]0”□ 75w
t%, BaO25-50wt%, TL 02
, Zy 0210, taking the total of BaO as 100
・Contains 15wt% of Ba TL4, TL
It consists of three phases: O2゜Zy Tj 04, and has a porosity of 0.2
This is a ceramic composition for a magnetic head that has a high density of less than 1.

この発明による磁器組成物は、Ba T1.40B 、
 TL 02 。
The porcelain composition according to the present invention includes Ba T1.40B,
TL 02.

Zr TL 04の3相からなることを特徴どし、熱間
静水圧プレス処理材料の気孔率と同程1哀に高密度化で
きるとともに、熱膨張係数を105−115x io 
−7/°Cの範囲に精度よく調整することがてパき、Z
r 02の含有により従来の焼結温度J、り低温で焼結
できるため、緻密で孔が少なく欠陥のない月利で耐厚耗
性が良く、結晶粒径も十分に小ざく加工性も良い。
It is characterized by being composed of three phases of Zr TL 04, and can be made denser to the same level as the porosity of hot isostatically pressed materials, and has a thermal expansion coefficient of 105-115x io.
It is possible to accurately adjust the temperature within the range of -7/°C.
Because it contains r02, it can be sintered at a lower temperature than the conventional sintering temperature J, so it is dense, has few pores, has no defects, has good wear resistance, and has a sufficiently small crystal grain size and good workability. .

この発明による磁器組成物にお(jるZy TL 0&
相を、X綜マイクa )yプライリ“−により観察する
と、Zr Ti Ot相はほと/Vど粒界に生成されて
おり、同相が増加Jるど結晶中にZy TL O4相を
通じて02の流入か可能になると思われ、焼結体内部の
黒色化防止にイ」効どなる。
The porcelain composition according to the invention (jruZy TL 0&
When the phase is observed using an It is thought that this will allow for the inflow of the sintered body, which will be very effective in preventing blackening inside the sintered body.

この発明による(6器組成物の成分を限定した理由は以
下のどJ3りて゛ある。
The reasons for limiting the components of the six-piece composition according to this invention are as follows.

丁Lo、BaO系において熱膨張係数はTL 025 
(hv t%に−(届大伯11!iX 10−’ /°
Cに達づ′るので、TLO850wL%未h)1の含有
ては、熱膨張係数が  115×10−7/°C以下に
なるが、抗折ηフが著しく低下し、T* 02が75)
v1%を超える含有であると、熱膨張係数か  つ05
x 10−’ / ”C未ン筒となり、Mn −Znn
フシイ1〜とのカラス清福の相手月利として不適である
ため、TL0□50□〜75wt%の含有とする。
In Ding Lo, BaO system, the thermal expansion coefficient is TL 025
(hv t% - (notification Daihaku 11! iX 10-' /°
Therefore, if TLO850 wL% (h)1 is contained, the thermal expansion coefficient will be less than 115 x 10-7/°C, but the transverse refraction η will be significantly lowered and T*02 will be 75 )
If the content exceeds v1%, the thermal expansion coefficient and 05
x 10-' / "C becomes a cylinder, Mn -Znn
Since it is unsuitable as a partner for Karasu Seifuku with Fushii 1~, the content is set at TL0□50□~75wt%.

BaOはTL 02尾どの関連におい−U、[3aOが
50wt%を超える含有では、熱膨張係数が115X1
0−7/℃以下になるが、抗折シJが茗しく低下し、B
aOが25wt%未渦の含有であると、熱膨張係数が 
105xlO−7/’C未)闇どなり、l”In  Z
nnフシイ1〜どのガラス溶看の相手相別として不)尚
であるため、Ba025〜50wt%の含有とする。
BaO has a TL 02 tail related odor - U, [If the content of 3aO exceeds 50 wt%, the thermal expansion coefficient is 115X1
0-7/℃ or less, but the bending shear J decreases sharply and B
When the aO content is 25 wt% unvortexed, the coefficient of thermal expansion is
105xlO-7/'C) Dark roar, l"In Z
Since it is not compatible with any glass melting device, Ba025 to 50 wt% is contained.

Zy 02はTL 02  Ba O系の気孔率を改j
へ一す−るために添加するものであるが、その含有がT
j 02 、 Ba Oの合計を100として、10w
t%未渦では磁器組成物焼結体の気孔率が1.0%以上
になり、組織がBa TL40g 。
Zy 02 changes the porosity of TL 02 Ba O system
It is added to stabilize the temperature, but its content is T
j 02 , the total of Ba O is 100, 10w
When t% is not swirled, the porosity of the sintered ceramic composition is 1.0% or more, and the structure is BaTL40g.

TiO2,ZrO2の3相となり、焼結体内部は還元さ
れやすくなり黒色化するため好Jニジ<ない。、また1
5wt%を超える含有では焼結体の気孔率が0.2%以
上となり、加工性も悪化づ−るためソフトフエライ1へ
の相手月利として不適と4するため、10−15wt%
の添加とする。
There are three phases of TiO2 and ZrO2, and the inside of the sintered body is easily reduced and becomes black, so there is no good J color. , also 1
If the content exceeds 5 wt%, the porosity of the sintered body will be 0.2% or more, and the workability will deteriorate, so it is considered unsuitable as a counterpart to Soft Ferrite 1. Therefore, 10-15 wt%
The addition of

以下に、この発明を実施例に基づいて説明覆る。The present invention will be explained below based on examples.

市販されているTLO2、BaCO3、ZyOaを用い
て、第1表に示す如く、焼結後の組成がこの発明による
組成比(N:1.1− 6)ならびにこの発明の′;&
囲外の組成比(トわ7〜9)となるよう秤Q”i Ll
、ボールミルで混合し、乾燥した後、空気中で900 
’C12時間の仮焼を行った。さらに仮焼した原料を再
びボールミル−C宇均粒度1.3加(こなるまで、微粉
砕し、次に結合剤とし℃ポリビニルアルコールを1.5
1Vt%加え”C造粒した。造粒後に、2oookツ4
の成形J」]で40X 20X 2Ontmの刈払に成
形し、空気中で1200″C121+、冒j1;の焼結
を行った。
Using commercially available TLO2, BaCO3, and ZyOa, as shown in Table 1, the composition after sintering was the composition ratio according to the present invention (N: 1.1-6) and the composition ratio according to the present invention;
The balance Q"i Ll is adjusted so that the composition ratio outside the range (7 to 9) is obtained.
, mixed in a ball mill and dried in air for 900 min.
Calcination was performed for 12 hours. Further, the calcined raw material was again pulverized in a ball mill until the average particle size was 1.3°C, and then polyvinyl alcohol was added as a binder to 1.5°C.
Added 1Vt% and granulated it. After granulation, 2oook 4
The molded material was molded into a 40×20×2 Ontm brush cutter with a 1200″ C121+ sintering process in air.

(”)られた磁器について、密度、熱膨張係数、ヒラカ
ース砂層等の特性を調べ、第2表に測定結果を示してい
る。また、表中の加工付は、同一の加工機を使用しての
主軸モーフの電力増加量をワラ1へ単位で表わし評価し
ている。
Properties such as density, coefficient of thermal expansion, and hirakasu sand layer were investigated for the processed porcelain, and the measurement results are shown in Table 2. The power increase of the main axis morph is expressed in units of 1 and evaluated.

第1表、第2表から明らかな如く、試別No、 7・〜
9の比較例はだの熱膨張係数が比−Zηフ〕−ライ1−
の熱t15う張係数 105・〜11!ix 10−7
/ ”Cに合致りるが気孔棹′が恕いのに対し、この発
明の実施例(試オ’1lNo1・−〇)は、熱膨張係数
を 105〜115x10−7/”Cの間にコン1ヘロ
ールすることがてぎ、機械的強度、加二[性等ちりぐれ
た特性を示しており、特に、熱間静水圧プレス処理した
vJ斜と同等に緻密化され、結晶粒径が小さくイ玄り、
孔が少なく加工性の良好なる磁器が得られているため、
耐厚耗性にすぐれ、記録媒体が摺動−リ−る磁気ヘッド
構造部品用イオオ′31に最適であることがわかる。。
As is clear from Tables 1 and 2, trial No. 7.
9 Comparative Example The coefficient of thermal expansion of the bare body is the ratio -Zη plane] -Lye 1-
Heat t15 bulge coefficient 105・~11! ix 10-7
/ ``C, but the pore size is poor, whereas the embodiment of this invention (sample No. 1 -〇) has a thermal expansion coefficient of 105 to 115 x 10-7/''C. It exhibits outstanding properties such as mechanical strength and hardness, and is especially densified to the same degree as VJ slope treated with hot isostatic pressing, and has a small crystal grain size. Gentleness,
Because the porcelain has few holes and has good workability,
It can be seen that it has excellent wear resistance and is most suitable for magnetic head structural parts on which the recording medium slides. .

第1図 以下余白Figure 1 Below margin

Claims (1)

【特許請求の範囲】[Claims] 1  TLo+! 50.〜75wt%、BaO25−
50wt%がらなり、丁j 02  、 Ba Oの合
h1を100として、Zr 0210−15wt%を金
石し、気孔率0.2%以下に高密度化したことを特徴ど
する磁気ヘッド用磁器組成物。
1 TLo+! 50. ~75wt%, BaO25-
A ceramic composition for a magnetic head, characterized in that the composition consists of 50wt% of Zr0210-15wt%, with the sum of h1 of Zr02 and BaO being 100, and the porosity is increased to 0.2% or less. .
JP58065087A 1983-04-12 1983-04-12 Ceramic composition for magnetic head Granted JPS59190264A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58065087A JPS59190264A (en) 1983-04-12 1983-04-12 Ceramic composition for magnetic head

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58065087A JPS59190264A (en) 1983-04-12 1983-04-12 Ceramic composition for magnetic head

Publications (2)

Publication Number Publication Date
JPS59190264A true JPS59190264A (en) 1984-10-29
JPS6224387B2 JPS6224387B2 (en) 1987-05-28

Family

ID=13276799

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58065087A Granted JPS59190264A (en) 1983-04-12 1983-04-12 Ceramic composition for magnetic head

Country Status (1)

Country Link
JP (1) JPS59190264A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0625491A1 (en) * 1993-05-21 1994-11-23 Murata Manufacturing Co., Ltd. Dielectric ceramic composition for use in high frequency

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
MAT. RES. BULL.=1977 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0625491A1 (en) * 1993-05-21 1994-11-23 Murata Manufacturing Co., Ltd. Dielectric ceramic composition for use in high frequency

Also Published As

Publication number Publication date
JPS6224387B2 (en) 1987-05-28

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