JPS6252172A - Ceramic composition for magnetic head - Google Patents
Ceramic composition for magnetic headInfo
- Publication number
- JPS6252172A JPS6252172A JP19289185A JP19289185A JPS6252172A JP S6252172 A JPS6252172 A JP S6252172A JP 19289185 A JP19289185 A JP 19289185A JP 19289185 A JP19289185 A JP 19289185A JP S6252172 A JPS6252172 A JP S6252172A
- Authority
- JP
- Japan
- Prior art keywords
- composition
- thermal expansion
- ferrite
- phase
- 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
Links
Landscapes
- Compositions Of Oxide Ceramics (AREA)
- Adjustment Of The Magnetic Head Position Track Following On Tapes (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】
(産業上の利用分野)
本発明はフロッピーディスク等の磁気ヘッドに使用され
る磁極片(フェライトコア)を支持する磁気ヘッド用磁
器(以下磁器ヘッド用スライダと称す)の磁器組成物に
関するものであり、さらに詳しくはMn −Zn 7エ
ライトに適した磁器ヘッド用スライダの磁器組成物に関
する。Detailed Description of the Invention (Field of Industrial Application) The present invention relates to a magnetic head porcelain (hereinafter referred to as a porcelain head slider) that supports a magnetic pole piece (ferrite core) used in a magnetic head such as a floppy disk. The present invention relates to a porcelain composition, and more particularly to a porcelain composition for a slider for a porcelain head suitable for Mn-Zn 7 elite.
(背景技術)
゛ 図に示す如く前記スライダ1は一般に7エフイトコ
ア2を接着ガラス3を介して熱処理により接着され磁気
ヘッドを信成している。したがって、これらスライダ及
びフェライトコアの各々に太きな熱膨張差があると熱処
理時の熱履歴によシ、これら材料に亀裂や残留歪が生じ
組付は工程中にガフスハガレ等を生じる。そのためスラ
イダはその磁器組成及び組成比を選択してフェライトコ
アの熱膨張係数に一致させなければならない。(Background Art) As shown in the figure, the slider 1 generally has a seven-effect core 2 bonded to it by heat treatment via an adhesive glass 3 to form a magnetic head. Therefore, if there is a large difference in thermal expansion between each of the slider and the ferrite core, the thermal history during heat treatment will cause cracks and residual strain in these materials, resulting in guff peeling and the like during the assembly process. Therefore, the porcelain composition and composition ratio of the slider must be selected to match the coefficient of thermal expansion of the ferrite core.
また、フェライトコアにはその用途に応じ各種のグレー
ドが存在し、熱膨張係数もこのグレードにより105〜
125×10/℃の広い範囲に適用される必要がある。In addition, there are various grades of ferrite core depending on its use, and the coefficient of thermal expansion varies from 105 to 105 depending on the grade.
It needs to be applied over a wide range of 125×10/°C.
そのためスライダもその組成比を変化させることにより
105〜125 X 10 /℃の広い範囲の熱膨張
係数を容易に選択されることが望まれている。Therefore, it is desired that the coefficient of thermal expansion of the slider can be easily selected from a wide range of 105 to 125 x 10 /°C by changing its composition ratio.
また、このスライダはその磁器焼結体にボアが出来るだ
け少ないことが要求される。フロッピーディスクに接触
する焼結体表面にボアが多く存在すると、該ディスク表
面にコーティングされた磁性粉末がボア内に付着し易く
なシ、付着した磁性体
粉の存Vによυ記録・再生時の磁気特性に障害をも九ら
す。Further, this slider is required to have as few bores as possible in its sintered porcelain body. If there are many bores on the surface of the sintered body that comes into contact with the floppy disk, the magnetic powder coated on the disk surface will not easily adhere to the inside of the bore, and the presence of the attached magnetic powder will cause problems during recording and playback. It also impairs the magnetic properties of
また、このスライダはその磁器が充分に焼結し緻密化し
ていなければならない。焼結が不充分で強度や靭性が劣
っていると磁器にチッピングやクヲククカ生じ、フロッ
ピーディスクへ走行させた場合ディスク自体を損傷させ
るという重大な欠陥をまねく。Furthermore, the porcelain of this slider must be sufficiently sintered and densified. If the porcelain is insufficiently sintered and its strength and toughness are poor, chipping and cracking will occur in the porcelain, leading to serious defects such as damage to the disk itself when it is run on a floppy disk.
一方、磁気ヘッドのコアとしては従来からNi−Znフ
ェライトが使用されていたが70ツビーデイスク用フエ
ライトコアとしては現在Ni −ZnよυもMn −Z
n 7エフイトの方が磁性特性、特に抗磁力が優れてい
ることから、Mn −Znフェライトに移行しつつある
。On the other hand, Ni-Zn ferrite has traditionally been used as the core of magnetic heads, but currently Ni-Zn, Mn-Z
Since n7 eft has better magnetic properties, especially coercive force, it is being replaced by Mn-Zn ferrite.
(従来技術の説明)
従来、Ni、 −Znフェライトに適用されるスライダ
組成物としてはこの熱膨張係数90〜98 X 10/
℃とほぼ同程度の7オルステライトやチタン酸バリウム
が知られている。しかしながら、Mn−Znフェライト
にこれら磁器を適用する場合、Mn−Zn7エライトの
熱膨張係数が105〜125X10/℃であシ熱膨張差
が大きすぎこれら磁器を適用することは困難である。(Description of Prior Art) Conventionally, a slider composition applied to Ni, -Zn ferrite has a thermal expansion coefficient of 90 to 98 x 10/
7-orsterite and barium titanate, which have a temperature almost the same as ℃, are known. However, when applying these porcelains to Mn-Zn ferrite, it is difficult to apply these porcelains because the coefficient of thermal expansion of Mn-Zn7 ferrite is 105 to 125X10/°C, and the difference in thermal expansion is too large.
一方、Mn −Znフェライトに適用するスフイタ組成
物としては従来からチタン酸塩系化合物を主体とする例
えばチタン酸カルシウム、チタン酸マグネシウム及びチ
タン酸ストロンチウム等がMn−Znフェライトの熱膨
張係数とほぼ同程度であることが知られている。しかし
ながら、Mn −Znフェライトは要求特性に応じて1
05〜125 X 10 /℃の広い範囲で多種多様
のグレードが存在するが、従来からこの広い範囲の熱膨
張係数を組成比を変更するのみで直線的に変化させ各種
グレードの熱膨張係数に容易に一致させる磁気ヘッド用
スライダ組成物が見出されていない。On the other hand, Sphyta compositions applied to Mn-Zn ferrite have traditionally been based on titanate-based compounds, such as calcium titanate, magnesium titanate, and strontium titanate, which have a coefficient of thermal expansion almost the same as that of Mn-Zn ferrite. It is known that the degree of However, Mn-Zn ferrite is
There are a wide variety of grades in the wide range of 05 to 125 x 10 /℃, but conventionally the thermal expansion coefficient in this wide range can be changed linearly by simply changing the composition ratio, making it easy to create the thermal expansion coefficient of various grades. A slider composition for a magnetic head that matches the above has not been found.
一方、前記チタン酸塩化合物を主体とする組成において
は例えばアルゴンガス中で焼成した場合にT1イオンが
還元堰れるため極端に磁器の色調が変化する。この場合
変化した磁器の色を元に戻す処理が必要となる。On the other hand, in the case of a composition mainly composed of the titanate compound, when fired in argon gas, for example, T1 ions are reduced and the color tone of the porcelain changes drastically. In this case, a process is required to restore the changed color of the porcelain.
さらに、前記チタン酸塩イへを主体とする焼結体は鏡面
加工時に結晶粒の脱離が問題となることから、脱粒及び
選択研摩(軟1弱な粒が選択的に研摩されること)のな
い加工性に優れた磁気へラドスライダの組成物が望まれ
ている。Furthermore, since the sintered body mainly composed of the titanate Ihe has a problem of detachment of crystal grains during mirror finishing, grain removal and selective polishing (soft grains are selectively polished) There is a desire for a composition for a magnetic herad slider that has excellent workability and is free of .
(本発明が解決しようとする問題点)
本発明者は上記現状に鑑み鋭意研究の結果、 Mn−Z
nyエフイトの熱膨張係数に近いCaO−5lot系化
合物の主成分に対し、特定量のTiO2を添加したこと
により、5102成分をガフス相以外のケイ酸カルシウ
ム(CaSi、Os )化合物トチタン酸力/I/Vウ
ム(CaTj−03)との均一仮焼物からなる安定な結
晶とし、且つこれらの混合比を調整することにより、M
n−Zn 7エライトの熱膨張係数105〜125Xl
o/℃の広い範囲に適用することができ、しかも焼結性
が良好でボアの発生が少なく、還元雰囲気処理による色
むらの発生を防止できると共に鏡面加工性が優れた磁気
ヘッド用スライダ組成物が得られることを知見した。(Problems to be Solved by the Present Invention) In view of the above-mentioned current situation, the present inventor has conducted extensive research and found that Mn-Z
By adding a specific amount of TiO2 to the main component of the CaO-5lot compound, which has a thermal expansion coefficient close to that of nyefite, the 5102 component was converted into a calcium silicate (CaSi, Os) compound totitanium acidity/I other than the Gaffs phase. M
Thermal expansion coefficient of n-Zn 7 elite 105-125Xl
A slider composition for a magnetic head that can be applied to a wide range of o/℃, has good sinterability, reduces the occurrence of bores, prevents the occurrence of color unevenness due to reducing atmosphere treatment, and has excellent mirror finish properties. We found that it is possible to obtain
(発明の目的) したがって、本発明はケイ酸カルシウム(Ca。(Purpose of the invention) Therefore, the present invention provides calcium silicate (Ca).
51os )化合物とflX”/酸力A/シ17 A
(CaTi03)とからなるガラス成分の少ない緻密質
の焼結体でh ’) 、且ツMn −Znフェライトの
熱膨張係aの広い範囲に適用でき、焼結性が良好でボア
の発生が少なく、さらに還元雰囲気処理による色むらの
発生を防止できると共に、鏡面仕上性に優れた磁気ヘッ
ド用スフイダ組成物を提供することを目的とする。51os) compound and flX”/acidity A/shi17 A
It is a dense sintered body with a small glass component consisting of (CaTi03) h'), and can be applied to a wide range of thermal expansion coefficients a of Mn-Zn ferrite, and has good sinterability and less occurrence of bores. Another object of the present invention is to provide a magnetic head sifter composition that can prevent the occurrence of color unevenness due to treatment in a reducing atmosphere and has an excellent mirror finish.
(問題を解決するための手段)
本発明によればSi、Ozを22〜50モル%と、Ti
O2を2〜30−1ニア9%と、OaOを45〜47
モ/L’%とから成る磁気ヘッド用磁器組成物が提供さ
れる。(Means for solving the problem) According to the present invention, 22 to 50 mol% of Si and Oz and Ti
O2 2-30-1 near 9% and OaO 45-47
There is provided a ceramic composition for a magnetic head comprising: %Mo/L'%.
上記組成範囲から成る磁器組成物はその適正焼成温度に
おいては主としてCa5103相又はCa 35izO
フ相の1種以上とCaTiO3相から成る@細な均一混
在組織を有し、従来のフォルステライト等のMgo −
810z系磁器よシも焼結性が向上し、緻密質の焼結体
が得られる。A porcelain composition having the above composition range mainly consists of Ca5103 phase or Ca35izO phase at the proper firing temperature.
It has a fine uniform mixed structure consisting of one or more types of F phases and CaTiO3 phase, and is different from conventional Mgo − such as forsterite.
The sinterability of 810z-based porcelain also improves, and a dense sintered body can be obtained.
さらに、上記組成範囲から成る磁器組成物においてはC
a510s相又はCa5SizOv相とCaTiOs
)7fJ (7)均一混在組織が主体となシ、ガラス成
分が少ないため、粒界に存在するガラス成分が原因で生
じる鏡面加工時の脱粒及び選択研摩が少なくなる。また
、Ca5l−03相やCaxSi、20y相の存在によ
り従来のチタン酸系スライダ材質よりも硬度がよりMn
−Znフェライトに近づき、ガラス溶着後のヘッド保証
面(フロッピーディスクへ接触する側の面)の平坦度を
維持し易くなる。また、CaSi、03とCaTiOs
との均一仮焼物からなる安定な結晶相を有するので、熱
膨張係数105〜125 X 10 /’Cの広い範
囲において組成比を変化させることにより熱膨張係数を
直接的に変化させることができ、所望の熱膨張率を有す
るスライダを得ることができる。Furthermore, in a porcelain composition having the above composition range, C
a510s phase or Ca5SizOv phase and CaTiOs
)7fJ (7) Since the homogeneous mixed structure is the main component and the glass component is small, grain shedding and selective polishing during mirror finishing caused by the glass component present in the grain boundaries are reduced. In addition, due to the presence of Ca5l-03 phase, CaxSi, and 20y phase, the hardness is higher than that of conventional titanate-based slider materials.
- Zn is close to ferrite, making it easier to maintain the flatness of the head guarantee surface (the surface that contacts the floppy disk) after glass welding. Also, CaSi, 03 and CaTiOs
Since it has a stable crystal phase consisting of a uniform calcined product of A slider having a desired coefficient of thermal expansion can be obtained.
5iOzが22モル%未満ではCaO添加量の多い側で
焼結体の緻密化が阻害され、 TiO2lO2添加−側
で焼結体の緻密化は良好であるが還元による色調変化・
色むらが発生し易くなる。 5lo2が50モル%を超
えるとSi、Ozが単独で存在しガラス相が形成され易
くなるのでボアが発生して充分な緻密化が果し得ない。When 5iOz is less than 22 mol%, densification of the sintered body is inhibited on the side where the amount of CaO added is large, and densification of the sintered body is good on the side where TiO2lO2 is added, but the color tone changes due to reduction.
Color unevenness is more likely to occur. When 5lo2 exceeds 50 mol%, Si and Oz exist alone and a glass phase tends to be formed, resulting in the formation of bores and insufficient densification.
Tl−0sが2モル%未満ではCaSiO3及びCas
Si 20 tの焼結を充分促進させ得ないため、ボ
アの発生を充分抑制することができない。T1.02が
30モル%を超えると、CaOFA加の多い側でca’
rIQs相の生成が増加するため、還元雰囲気下での影
響が顕著になシ、色むらが発生し易<すυ、 5lo2
VIA加の多い側で CaTi、5iOs相(熱膨張係
数は65 X 1o−7℃)が生成するため熱膨張係数
が極端に低くなる。CaOが45モル%未満では510
2添加の多い側でSiO!を主成分とするガラス相が生
成し易くなシ焼結体の緻密性が悪化し、TiO2添加が
多い側で前記熱膨張係数の低い0aTis1os相が生
成する領域となυ、極端に熱膨張係数が低下する。Ca
Oが57モル%を超えると、CaOが未反応状態で存在
し易くなり、水和性を有し耐水性が悪くなり一般的に磁
気ヘッド用スライダとして不適切なものとなる。When Tl-0s is less than 2 mol%, CaSiO3 and Cas
Since the sintering of Si 20 t cannot be sufficiently promoted, the generation of bores cannot be sufficiently suppressed. When T1.02 exceeds 30 mol%, ca'
Since the formation of the rIQs phase increases, the effect under a reducing atmosphere becomes more pronounced, and color unevenness is more likely to occur.5lo2
Since CaTi and 5iOs phases (thermal expansion coefficient: 65×1o-7° C.) are formed on the side where the VIA addition is large, the thermal expansion coefficient becomes extremely low. 510 when CaO is less than 45 mol%
2 SiO on the side with more addition! The compactness of the sintered body is deteriorated, in which a glass phase mainly composed of decreases. Ca
If O exceeds 57 mol %, CaO tends to exist in an unreacted state, resulting in hydration and poor water resistance, making the slider generally unsuitable for use in magnetic heads.
CaSi、03及びCa1Si、zOt相は純粋組成比
(CaO:5102=5〇二50モル%及び60 :
40モル%)からの調合では緻密な焼結体を得るのが困
難である負
が、TiO2の添加により髄5iO3及びCa3Si、
・20y 相の形成に助剤効果を果し、両相が従来のT
j−Ch −CaO系よυも比較的低温の仮焼温度、即
ち従来1000〜1150℃程度であったものが約90
0〜1100℃程度で結晶形成が進行し、本焼成時に均
一な結晶成長がおこり、異常粒成長を抑制することがで
きる。The CaSi, 03 and Ca1Si, zOt phases have pure composition ratios (CaO:5102=50250 mol% and 60:
However, by adding TiO2, it is difficult to obtain a dense sintered body from 5iO3 and Ca3Si,
・Has an auxiliary effect on the formation of the 20y phase, and both phases are similar to the conventional T
Compared to the j-Ch -CaO system, the calcination temperature is relatively low, that is, the conventional calcination temperature of about 1,000 to 1,150°C has been reduced to about 90°C.
Crystal formation progresses at about 0 to 1100°C, uniform crystal growth occurs during main firing, and abnormal grain growth can be suppressed.
以下、実施例により本発明の詳細な説明する。Hereinafter, the present invention will be explained in detail with reference to Examples.
本発明において磁気ヘッド用スライダを製作する方法は
、所定の組成比に原料を秤量し、混合粉砕後仮焼し、次
いでこの仮焼物を@粉砕し、有機バインダを添加して造
粒し、所定形状に成形後焼成する通常の方法が採用され
る。In the method of manufacturing a magnetic head slider in the present invention, raw materials are weighed to a predetermined composition ratio, mixed and pulverized, and then calcined.The calcined product is then pulverized, an organic binder is added and granulated, and a predetermined composition ratio is obtained. The usual method of shaping and firing is used.
(実施例)
市販の工業原料(純度98%以上)で、シリカ源として
シリカ(Si、Ch)、チタニア源として酸化チタン(
Ti0z ) 、力〜シア源として炭酸カルシ’7 ム
(CaCO3)又は水酸化力AsVつ: (Ca(OF
()z)などを選び、それぞれ第1表に示す組成比とな
るように秤量し、ボールミルを用いて湿式混合し、乾燥
後900〜1100℃で1〜2時間仮焼を行なった。仮
焼後不純物の混入を抑えて微粉砕し、有機バインダ等を
添加して造粒後1.0〜2.Ot / dで加圧成形を
した。その後、1250〜1380℃で大気中で焼成し
第1表に示す試料&1〜15を得た。(Example) Commercially available industrial raw materials (purity 98% or higher) were used, including silica (Si, Ch) as a silica source and titanium oxide (as a titania source).
Ti0z), calcium carbonate (CaCO3) or hydroxylation power AsV as a shear source: (Ca(OF
()z), etc., were weighed so as to have the composition ratios shown in Table 1, wet mixed using a ball mill, dried, and then calcined at 900 to 1100°C for 1 to 2 hours. After calcination, it is finely pulverized to suppress the contamination of impurities, and an organic binder etc. are added, and after granulation it is 1.0 to 2. Pressure molding was performed at Ot/d. Thereafter, it was fired in the air at 1250 to 1380°C to obtain samples &1 to 15 shown in Table 1.
得られた焼結体の結晶相はX線回折法によって同定した
。生成量比の判定はビしり比で行ない、同時に画像解析
装置により試料鏡面をXMA装置を用いて各結晶相によ
る光の反射率の違いから面積比を測定して体積比率に換
算して評価した。なおこの値はX線回折法によって求め
た量比とほぼ一致した。硬度は荷重1 kg (E(V
(1,o )で示す)のビッカース硬度で示した。測
定算出はJ工5Z2244に準拠し、単位はkg/−で
示した。焼結体の緻密性は吸水率2%を超えるものをX
印で、0%のものを○印で、その中間をΔ印で示した。The crystalline phase of the obtained sintered body was identified by X-ray diffraction. The production amount ratio was determined by the beat ratio, and at the same time, the area ratio was measured from the difference in light reflectance of each crystal phase using an XMA device on the mirror surface of the sample using an image analysis device, and evaluated by converting it into a volume ratio. . Note that this value almost coincided with the quantitative ratio determined by X-ray diffraction method. The hardness is determined by the load of 1 kg (E(V
The Vickers hardness is expressed as (1,o). The measurement calculation was based on J Engineering 5Z2244, and the unit was expressed in kg/-. The density of the sintered body is X if the water absorption rate exceeds 2%.
0% is indicated by ○, and the middle is indicated by Δ.
色むらは還元雰囲気処理後の焼結体の内部を観察し、表
面との色の差異があるかどうかで評価した。Color unevenness was evaluated by observing the inside of the sintered body after treatment in a reducing atmosphere and determining whether there was a difference in color from the surface.
第1表から理解される様に、試料&t、s、9,10.
11及び13は本発明の組成範囲外のものであシ、試料
五1及び8はTiO2量が少ないため焼結が充分促進さ
れていない。試料悪9及びlOはSi、Oz量が少ない
糸であり、CaO量の多い側(試料五9)では焼結体の
緻密化が阻害され、TiO2量の多い側(試料iFx
10 )では色むらが発生している。試料zffill
はTiOz量が多い系であり、5iOz添加が比較的多
い側で熱膨張係数の低いCaTi5iOs相が生成され
ておす熱膨張係数が65×10−77℃と極端に低いこ
とが分かる。試料A13は5i02 iが若干多くなっ
ているため5i02が単独で存在しガラス相を形成され
ておシボアの発生のため充分に緻密化していない。試料
A14は従来のT10 t−ca。As understood from Table 1, samples &t, s, 9, 10.
Samples Nos. 11 and 13 are outside the composition range of the present invention, and Samples 51 and 8 have a small amount of TiO2, so sintering is not promoted sufficiently. Samples 9 and 1O are yarns with a small amount of Si and Oz, and the side with a large amount of CaO (sample 59) inhibits the densification of the sintered body, and the side with a large amount of TiO2 (sample iFx)
10), color unevenness occurs. samplezffill
is a system with a large amount of TiOz, and it can be seen that a CaTi5iOs phase with a low coefficient of thermal expansion is generated on the side where the addition of 5iOz is relatively large, and the coefficient of thermal expansion is extremely low at 65 x 10-77°C. Sample A13 has a slightly large amount of 5i02i, so 5i02 exists alone, forming a glass phase, and is not sufficiently densified due to the occurrence of grains. Sample A14 is a conventional T10 t-ca.
系組成物でCaTiO2相及びTi−0x相の2相から
構成される典型的例であり、色むらを生じ硬度がMn
−かフェライトの硬度的650 kg /−よυ相当大
きくなシ!1!面加工時にMn −Znフェライト側が
選択研摩され易くなる。試料15は従来のフオ〃ステラ
イト磁器であシ、熱膨張係数が小さく、且つ硬度が大き
過ぎMn −Znフェライト用のスフイダとして適用す
ることができない。This is a typical example of a system composition consisting of two phases, CaTiO2 phase and Ti-0x phase, which causes color unevenness and hardness of Mn.
-The hardness of ferrite is 650 kg/-, which is quite large! 1! During surface processing, the Mn-Zn ferrite side is more likely to be selectively polished. Sample 15 is a conventional phostellite porcelain, which has a small coefficient of thermal expansion and is too hard to be applied as a spherite for Mn--Zn ferrite.
これに対し試料&2〜7及び12は本発明の範囲内のも
のであり、熱膨張係数がMn −Znフェライトに適用
できる105〜125 X 10 /℃の範囲内で選
択されておシ、磁器の硬度及び焼結性が良好で緻密質な
焼結体が得られていると共に、色むらの発生がない。On the other hand, Samples &2 to 7 and 12 are within the scope of the present invention, and their thermal expansion coefficients are selected within the range of 105 to 125 x 10 /°C, which is applicable to Mn-Zn ferrite. A dense sintered body with good hardness and sinterability was obtained, and no color unevenness occurred.
さらに試料点14と本発明の範囲内である各試料A2〜
7の仮焼温度を比較してみると従来のTiO2−CaO
糸より比較的低温であることが理解される。Further, sample point 14 and each sample A2 to within the scope of the present invention
Comparing the calcination temperature of No. 7, the conventional TiO2-CaO
It is understood that the temperature is relatively lower than that of yarn.
上述の如く本発明は5j−Oz −Ti、02− Ca
O系としてこれらを特定の組成比とすることによりMn
−Znフェライトの熱膨張係数の広い範囲に適用でき
、焼結体の緻密化が充分でボアの発生が少なく、さらに
還元雰囲気処理による色むらの発生を防止できると共に
、鏡面化工性に優れた磁気ヘッド用スフイダ組成物が得
られる。As mentioned above, the present invention uses 5j-Oz-Ti, 02-Ca
By setting these as O-based in a specific composition ratio, Mn
- It can be applied to a wide range of thermal expansion coefficients of Zn ferrite, the sintered body is sufficiently densified, there are few bores, and it is possible to prevent color unevenness due to reducing atmosphere treatment, and it has excellent mirror finishing properties. A Sufida composition for heads is obtained.
図面ハフロッピーディスクに使用される磁気ヘッドの斜
視図である。FIG. 1 is a perspective view of a magnetic head used in a floppy disk.
Claims (1)
2〜30モル%と、CaOを45〜57モル%とからな
る磁気ヘッド用磁器組成物。(1) A ceramic composition for a magnetic head comprising 22 to 50 mol% of SiO_2, 2 to 30 mol% of TiO_2, and 45 to 57 mol% of CaO.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19289185A JPH0633168B2 (en) | 1985-08-30 | 1985-08-30 | Porcelain composition for magnetic head |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19289185A JPH0633168B2 (en) | 1985-08-30 | 1985-08-30 | Porcelain composition for magnetic head |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6252172A true JPS6252172A (en) | 1987-03-06 |
JPH0633168B2 JPH0633168B2 (en) | 1994-05-02 |
Family
ID=16298694
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP19289185A Expired - Lifetime JPH0633168B2 (en) | 1985-08-30 | 1985-08-30 | Porcelain composition for magnetic head |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0633168B2 (en) |
-
1985
- 1985-08-30 JP JP19289185A patent/JPH0633168B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH0633168B2 (en) | 1994-05-02 |
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