Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JPH0682448B2 - Oxide substrate and magnetic head using the same - Google Patents
[go: Go Back, main page]

JPH0682448B2 - Oxide substrate and magnetic head using the same - Google Patents

Oxide substrate and magnetic head using the same

Info

Publication number
JPH0682448B2
JPH0682448B2 JP23364085A JP23364085A JPH0682448B2 JP H0682448 B2 JPH0682448 B2 JP H0682448B2 JP 23364085 A JP23364085 A JP 23364085A JP 23364085 A JP23364085 A JP 23364085A JP H0682448 B2 JPH0682448 B2 JP H0682448B2
Authority
JP
Japan
Prior art keywords
mol
mgo
nio
substrate
tio
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
JP23364085A
Other languages
Japanese (ja)
Other versions
JPS6292206A (en
Inventor
修 井上
健 廣田
三男 里見
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial 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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP23364085A priority Critical patent/JPH0682448B2/en
Priority to DE8686103255T priority patent/DE3681806D1/en
Priority to EP86103255A priority patent/EP0194650B1/en
Publication of JPS6292206A publication Critical patent/JPS6292206A/en
Priority to US07/235,717 priority patent/US5034285A/en
Publication of JPH0682448B2 publication Critical patent/JPH0682448B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Magnetic Heads (AREA)

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、磁気ヘッド等に用いられる酸化物基板および
これを用いて構成した磁気ヘッドに関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an oxide substrate used for a magnetic head and the like, and a magnetic head configured using the oxide substrate.

従来の技術 従来、磁気ヘッドの構成として、磁気コア材料軟磁性の
パーマロイ・センダスト・アモルファス合金・Mn−Zn−
フェライト等を使用し、これを基板に接合又は接着する
が、基板上に蒸着・スパッタ・CVD・メッキ等の方法で
薄膜として形成したものが知られている。
Conventional technology Conventionally, magnetic head materials are composed of soft magnetic materials such as permalloy, sendust, amorphous alloy, Mn-Zn-
Ferrite or the like is used, and this is bonded or adhered to the substrate, and it is known that it is formed as a thin film on the substrate by a method such as vapor deposition, sputtering, CVD or plating.

このような構成の磁気ヘッドでは、軟磁性材料と基板材
料の熱膨脹係数が等しいか又はその差が極めて小さくな
ければ、温度変化によって両材料の界面に応力が生じ、
亀裂発生の原因となったり、あるいは磁歪効果によって
軟磁性体の磁気特性が悪化する。このため使用する軟磁
性材料の種類・組成による熱膨脹係数に対応して、自由
に熱膨脹係数を変える事の出来る基板材料が必要とな
り、結晶化ガラス、CaO−SrO−TiO2系セラミック基板
(特開昭52−57218号公報)、NiMnO2系セラミック基板
(特開昭53−16399号公報)、MgO−TiO2系セラミック基
板(特開昭58−139322号公報)などが提案されている。
これらの基板材料は、その組成を調整する事により、広
い範囲で熱膨脹係数を選択できるものである。
In the magnetic head having such a structure, unless the thermal expansion coefficient of the soft magnetic material and the substrate material are equal to each other or the difference between them is extremely small, stress is generated at the interface between the two materials due to temperature change,
This may cause cracking or deteriorate the magnetic characteristics of the soft magnetic material due to the magnetostrictive effect. For this reason, a substrate material that can freely change the coefficient of thermal expansion is required in accordance with the coefficient of thermal expansion depending on the type and composition of the soft magnetic material used, and crystallized glass, CaO-SrO-TiO 2 -based ceramic substrate (JP No. 52-57218), a NiMnO 2 -based ceramic substrate (JP-A-53-16399), an MgO-TiO 2 -based ceramic substrate (JP-A-58-139322), and the like have been proposed.
By adjusting the composition of these substrate materials, the thermal expansion coefficient can be selected in a wide range.

発明が解決しようとする問題点 しかしながら、結晶化ガラスやCaO−SrO−TiO2系セラミ
ック基板では、成分としてアルカリ金属あるいはCaを含
むために化学的に不安定であり、これらの基板を用いて
磁気ヘッドを構成した場合、磁気テープ等を実際に走行
させると、基板表面に磁性粉が付着する現象を生じ、磁
気ヘッド特性が低下する。NiMnO2系セラミック基板で
は、このような磁気テープからの付着現象は生じない
が、MnOが空気中で加熱されると酸化されてMn2O3になり
やすいために、焼成時の雰囲気を非酸化性としなければ
ならず、製造コストが高くなり、又、使用形状に加工す
る時の研削加工性が悪く、加工能率が低いなどの欠点が
あった。
Problems to be Solved by the Invention However, crystallized glass and CaO-SrO-TiO 2 -based ceramic substrates are chemically unstable because they contain an alkali metal or Ca as a component. When the head is configured, when a magnetic tape or the like is actually run, a phenomenon in which magnetic powder adheres to the substrate surface occurs, and the magnetic head characteristics deteriorate. With NiMnO 2 ceramic substrates, such adhesion phenomenon from the magnetic tape does not occur, but when MnO is heated in air, it easily oxidizes to Mn 2 O 3 , so the atmosphere during firing is non-oxidized. However, there are drawbacks such as high manufacturing cost, poor grindability when working into a used shape, and low working efficiency.

一方、MgO−TiO2系セラミック基板では、上記のような
問題点は生じないが、熱膨脹係数が95×10-7/℃(25〜4
00℃)を越えるような組成のものでは、MgOとTiO2のモ
ル比が2:1を越えるために、焼結体中に遊離のMgOを含
み、これが高湿度条件下で潮解現象を起こすという欠点
があった。
On the other hand, with the MgO-TiO 2 -based ceramic substrate, the above problems do not occur, but the coefficient of thermal expansion is 95 × 10 -7 / ℃ (25 ~ 4
With a composition exceeding 00 ° C), the molar ratio of MgO and TiO 2 exceeds 2: 1, so free MgO is contained in the sintered body, which causes deliquescent phenomenon under high humidity conditions. There was a flaw.

問題点を解決するための手段 MgOを2〜96モル%、NiOを2〜96モル%、残分TiO2より
なり、MgOとNiOの合量が50〜98モル%であり、酸化物複
合焼結体を主成分として基板を構成する。
Means for solving the problem MgO is 2 to 96 mol%, NiO is 2 to 96 mol%, the balance is TiO 2 , and the total amount of MgO and NiO is 50 to 98 mol%. A substrate is formed by using a bonded body as a main component.

作用 発明者等は、MgO−NiO−TiO2系セラミックスが、組成比
により、熱膨脹係数を85〜130×10-7/℃(25℃〜400
℃)の範囲内で調整可能な事、又、基板表面に磁気テー
プを走行させても磁性粉が付着しない事、研削加工が容
易である事、潮解性を生じない事等を見い出した。
Action The inventors have found that MgO-NiO-TiO 2 ceramics has a thermal expansion coefficient of 85 to 130 × 10 -7 / ° C (25 ° C to 400 ° C) depending on the composition ratio.
It has been found that the temperature can be adjusted within the range of (° C.), that magnetic powder does not adhere even when a magnetic tape is run on the substrate surface, that grinding is easy, and that deliquescent does not occur.

MgOとNiOの合量を50〜98モル%にするすなわち、TiO2
を2モル%以上にすれば、良好な研削加工性を得ること
ができ、又、基板表面上に蒸着・スパッター・CVD・メ
ッキ等の方法で形成される金属磁性薄膜の熱膨脹係数95
〜125×10-7/℃(25〜400℃)と同等の熱膨脹係数が得
られる。MgO量を2〜96モル%に限定する理由はMgO量が
少量でありすぎると研削加工性が低下し、MgO量が96モ
ル%を越えると潮解性を生じるめである。また逆に、Ni
O量を2〜96モル%に限定した理由は、NiO量が少量であ
りすぎると潮解性を生じ、NiO量が96モル%を越えると
研削加工性が低下するためである。
If the total amount of MgO and NiO is 50 to 98 mol%, that is, if the amount of TiO 2 is 2 mol% or more, good grindability can be obtained, and vapor deposition / sputtering / CVD on the substrate surface is possible.・ The coefficient of thermal expansion of metal magnetic thin film formed by plating 95
A coefficient of thermal expansion equivalent to ~ 125 × 10 -7 / ℃ (25 ~ 400 ℃) can be obtained. The reason for limiting the amount of MgO to 2 to 96 mol% is that if the amount of MgO is too small, the grindability deteriorates, and if the amount of MgO exceeds 96 mol%, deliquescent occurs. Conversely, Ni
The reason for limiting the O amount to 2 to 96 mol% is that if the NiO amount is too small, deliquescent occurs, and if the NiO amount exceeds 96 mol%, the grindability deteriorates.

このMgO−NiO−TiO2系セラミック基板は熱膨脹係数が調
節可能で、製造が容易で、かつ優れた耐候性・研削加工
性を持つ。
The MgO-NiO-TiO 2 based ceramic substrate is adjustable thermal expansion coefficient, easy to manufacture, and has excellent weather resistance and grinding processability.

実施例 以下実施例をしめす。Examples Examples are shown below.

試薬特級のMgO,NiO,TiO2をそれぞれ秤量し、アルコール
を分散媒としたボールミルにて16時間混合した後、150
℃で乾燥して各種組成の混合粉末を得た。これらの混合
粉末を900℃で空気中仮焼した後、再度ボールミルにて1
6時間粉砕し、150℃で乾燥した。この仮焼粉末に5wt%
のポリビニールアルコール水溶液を10wt%加えて造粒
し、1000kg/cm2の圧力で加圧成形した。成形体は、その
組成に応じて、1200〜1350℃の間の温度で加圧(300kg/
cm2)焼結した。得られた焼結体に対して、アルキメデ
ス法による密度速度を行った結果、いずれの組成におい
ても焼結体密度は真密度の99.5%以上であった。そこで
この焼結体より試料を切り出し、熱膨脹率計による25℃
〜400℃間の熱膨脹係数測定を行った。また、通常の研
削切断加工機と人造ダイア150番・直径100mm・厚さ0.5m
mの研削砥石を用い、砥石回転速度3000rpm・送り速度10
mm/min・研削深さ3mmの条件で湿式研削切断加工を行
い、主軸モーターの消費電力の変化と比削材の重量減少
より、比研削エネルギーを求めた。さらに、試料を鏡面
研摩し、表面粗さRmax<100Åとしたのち水中に投入
し、24時間後に再度表面粗さを測定することによりその
耐水性を評価した。比較のため、結晶化ガラス、および
NiMnO2系セラミック基板に対しても同様の測定を行っ
た。その結果を第1表に示す。
Special grades of MgO, NiO, and TiO 2 were weighed and mixed for 16 hours in a ball mill using alcohol as a dispersion medium.
It was dried at ℃, to obtain a mixed powder of various compositions. After calcining these mixed powders in air at 900 ° C, 1 again with a ball mill.
It was crushed for 6 hours and dried at 150 ° C. 5wt% to this calcinated powder
10 wt% of the polyvinyl alcohol aqueous solution was added for granulation, and pressure molding was performed at a pressure of 1000 kg / cm 2 . The molded body is pressed at a temperature between 1200 and 1350 ° C (300 kg / 300 kg /
cm 2 ) Sintered. The density of the obtained sintered body was measured by the Archimedes method. As a result, the density of the sintered body was 99.5% or more of the true density in any composition. Therefore, a sample was cut out from this sintered body and the temperature was measured at 25 ° C using a thermal expansion coefficient meter.
The coefficient of thermal expansion between ~ 400 ° C was measured. Also, with a normal grinding and cutting machine and artificial diamond No. 150, diameter 100 mm, thickness 0.5 m
Grinding wheel rotation speed 3000 rpm, feed speed 10 using m grinding wheel
Wet grinding and cutting was performed under the conditions of mm / min and grinding depth of 3 mm, and the specific grinding energy was calculated from the change in power consumption of the spindle motor and the weight reduction of the specific cutting material. Further, the sample was mirror-polished to have a surface roughness Rmax <100 Å, then put into water, and after 24 hours, the surface roughness was measured again to evaluate its water resistance. For comparison, crystallized glass, and
The same measurement was performed on the NiMnO 2 ceramic substrate. The results are shown in Table 1.

表1より、熱膨張係数はMgOとNiOとの合量が増えるに従
って増加することがわかる。熱膨張係数を95×10-7/℃
以上とするためには、MgOとNiOとの合量を50モル%以上
とする必要がある。一方、比研削エネルギーも同様の傾
向を示すが、NiO量が96モル%以下で、MgOが2モル%以
上の組成範囲内では結晶化ガラスやNiMnO2系セラミック
基板よりも充分に小さく、最大でもその1/2程度であっ
た。次に、耐水性については、NiO量が2モル%未満の
物ではRmax≒2000Å程度の面荒れが生じたが、NiO量2
モル%以上の物ではRmax<300Åであった。このよう
に、耐水性についてはNiO量が2モル%以上であれば充
分である。従って、高い熱膨張係数・低い比研削エネル
ギー・高い耐水性を同時に満たす組成範囲として、MgO
を2〜96モル%、NiOを2〜96モル%、MgOとNiOの合量
が50〜98モル%で、TiO2が2〜50モル%とする必要があ
る。
It can be seen from Table 1 that the coefficient of thermal expansion increases as the total amount of MgO and NiO increases. Coefficient of thermal expansion 95 × 10 -7 / ℃
To achieve the above, the total amount of MgO and NiO must be 50 mol% or more. On the other hand, the specific grinding energy also shows the same tendency, but it is sufficiently smaller than the crystallized glass or NiMnO 2 -based ceramic substrate in the composition range where the NiO content is 96 mol% or less and the MgO content is 2 mol% or more. It was about half that. Regarding the water resistance, when the NiO content was less than 2 mol%, surface roughness of Rmax ≈ 2000Å occurred, but the NiO content was 2
The Rmax <300Å was obtained for the substances with mol% or more. As described above, it is sufficient for the water resistance that the NiO content is 2 mol% or more. Therefore, as a composition range that simultaneously satisfies high thermal expansion coefficient, low specific grinding energy, and high water resistance, MgO
Is 2 to 96 mol%, NiO is 2 to 96 mol%, the total amount of MgO and NiO is 50 to 98 mol%, and TiO 2 is 2 to 50 mol%.

そこで次に、熱膨脹係数が114×10-7/℃であるMgO=75
モル%,NiO=13モル%,TiO212モル%の基板を選び、そ
の表面にCo−Zr系アモルファス磁性金属薄膜をスパッタ
リングにより形成し、磁気ヘッドを作成した。比較のた
め、結晶化ガラス、NiMnO2系セラミック、MgO−TiO2
セラミックを用いてそれぞれ同様の方法で磁気ヘッドを
作成した。これらの磁気ヘッドに対して各種環境下で金
属磁気テープを実走行させて、ヘッドの出力変化・耐磨
耗性・耐環境性をテストした。その結果、測定開始後数
時間の場合、環境条件が温度20℃・湿度50%では基板の
種類による特性差は特に見られなかったが、温度20℃・
湿度10%では結晶化ガラスを基板とした磁気ヘッドで
は、基板表面上に磁気テープの金属粉が付着し、ヘッド
出力が数dB低下した。また、温度40℃・湿度80%ではMg
O−TiO2系セラミック基板を用いて磁気ヘッドでは、遊
離のMgOの溶解により、基板に粒径に対応した段差が生
じ、ヘッド出力が2〜3dB低下した。測定開始後約100時
間の場合、MgO−TiO2系セラミック基板を用いた磁気ヘ
ッドでは、温度20℃・湿度80%おいても前述した遊離の
MgOの溶解が生じ、ヘッド出力が数dB低下した。また、N
iMnO2系セラミック基板を用いた磁気ヘッドにおいて
も、100時間後には基板とアモルファス軟磁性体との磨
耗性に差があるため、ヘッド表面に段差を生じ、ヘッド
出力が低下した。しかるに本発明のMgO−NiO−TiO2基板
を用いた磁気ヘッドでは、あらゆる環境条件下において
も付着・溶解等を起こすことがなく、またアモルファス
軟磁性体との磨耗性のマッチングも良く、長時間使用し
てもヘッド出力の変化は1dB以内であった。
Therefore, next, MgO = 75, which has a coefficient of thermal expansion of 114 × 10 -7 / ° C.
A magnetic head was prepared by selecting a substrate of mol%, NiO = 13 mol% and TiO 2 12 mol% and forming a Co—Zr system amorphous magnetic metal thin film on the surface by sputtering. For comparison, magnetic heads were made in the same manner using crystallized glass, NiMnO 2 system ceramics, and MgO—TiO 2 system ceramics. Metal magnetic tapes were actually run on these magnetic heads under various environments, and the head output change, abrasion resistance, and environmental resistance were tested. As a result, in the case of several hours after the start of measurement, there was no particular difference in the characteristics depending on the type of substrate when the environmental conditions were temperature 20 ° C and humidity 50%.
At a humidity of 10%, in a magnetic head using crystallized glass as a substrate, the metal powder of the magnetic tape adhered to the substrate surface, and the head output dropped by a few dB. Also, at a temperature of 40 ° C and a humidity of 80%, Mg
In the magnetic head using the O-TiO 2 ceramic substrate, the free MgO was dissolved, and a step corresponding to the grain size was generated on the substrate, and the head output was reduced by 2-3 dB. In the case of about 100 hours after the start of measurement, the magnetic head using the MgO-TiO 2 -based ceramic substrate had the above-mentioned free emission even at a temperature of 20 ° C and a humidity of 80%.
Dissolution of MgO occurred and the head output decreased by several dB. Also, N
Even in the magnetic head using the iMnO 2 ceramic substrate, there was a difference in abradability between the substrate and the amorphous soft magnetic material after 100 hours, so that a step was generated on the head surface and the head output was reduced. However, in the magnetic head using the MgO-NiO-TiO 2 substrate of the present invention, adhesion and dissolution do not occur even under all environmental conditions, and the abrasion resistance with the amorphous soft magnetic material is also good, and it can be used for a long time. Even when used, the change in head output was within 1 dB.

以上の実施例においては、熱膨脹係数が114×10-7/℃の
Co−Zr系アモルファス軟磁性薄膜を用いる場合を示した
が、軟磁性材料としてはこれに限らず、他の組成のアモ
ルファス材料、パーマロイ・センダスト等の合金材料、
あるいはMn−Znフェライトなど、どのような磁気コア材
料にたいしても、その熱膨脹係数に応じて、MgO,NiO,Ti
O2の含有量を変えることにより、最適の基板を提供出来
るものである。
In the above examples, the coefficient of thermal expansion is 114 × 10 -7 / ° C.
Although the case of using a Co-Zr type amorphous soft magnetic thin film is shown, the soft magnetic material is not limited to this, an amorphous material of other composition, an alloy material such as Permalloy-Sendust,
Or, for any magnetic core material such as Mn-Zn ferrite, depending on its thermal expansion coefficient, MgO, NiO, Ti
The optimum substrate can be provided by changing the O 2 content.

また、本発明で用いる基板材料はMgO,NiO,TiO2を主成分
とし、機械加工性を改善するためや焼結性を改善するた
め、少量のZrO2,SiO2等を添加したり、原料中に含まれ
少量の不純物が含まれたりしても、なんら問題を生じる
ものではない。
Further, the substrate material used in the present invention is MgO, NiO, TiO 2 as a main component, to improve the machinability and sinterability, to add a small amount of ZrO 2 , SiO 2, etc. Even if it is contained in the glass and contains a small amount of impurities, it does not cause any problem.

発明の効果 本発明の酸化物基板は、MgOを2〜96モル%、NiOを2〜
96モル%、残分TiO2の3成分よりなり、MgOとNiOの合量
が50〜98モル%である、酸化物複合焼結体を主成分とす
る基板であり、磁気ヘッド用の基板として用いた場合磁
気記録媒体による接触走行に対して、カルシウムやアル
カリ金属を含まないため安定で、また、軟磁性材料との
耐磨耗性のマッチングも良い。さらに、製造および加工
が容易である。
The oxide substrate of the present invention contains MgO in an amount of 2 to 96 mol% and NiO in an amount of 2 to 96 mol%.
A substrate mainly composed of an oxide composite sintered body, which comprises 96 mol% and a balance of TiO 2 and has a total content of MgO and NiO of 50 to 98 mol%, and is used as a substrate for a magnetic head. When used, it is stable against contact running with a magnetic recording medium because it does not contain calcium or alkali metal, and has good wear resistance matching with a soft magnetic material. Moreover, it is easy to manufacture and process.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】MgOを2〜96モル%、NiOを2〜96モル%、
残分TiO2よりなり、MgOとNiOの合量が50〜98モル%であ
る酸化物複合焼結体を主成分とする酸化物基板。
1. MgO of 2 to 96 mol%, NiO of 2 to 96 mol%,
An oxide substrate mainly composed of an oxide composite sintered body composed of the balance TiO 2 and having a total content of MgO and NiO of 50 to 98 mol%.
【請求項2】MgOを2〜96モル%、NiOを2〜96モル%、
残分TiO2よりなり、MgOとNiOの合量が50〜98モル%であ
る酸化物複合焼結体を主成分とする酸化物基板を用い、
この基板に磁気コアとして軟磁性材料を形成したことを
特徴とする磁気ヘッド。
2. MgO of 2 to 96 mol%, NiO of 2 to 96 mol%,
An oxide substrate mainly composed of an oxide composite sintered body, which is composed of the balance TiO 2 and has a total amount of MgO and NiO of 50 to 98 mol%,
A magnetic head characterized in that a soft magnetic material is formed as a magnetic core on this substrate.
JP23364085A 1985-03-13 1985-10-18 Oxide substrate and magnetic head using the same Expired - Lifetime JPH0682448B2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP23364085A JPH0682448B2 (en) 1985-10-18 1985-10-18 Oxide substrate and magnetic head using the same
DE8686103255T DE3681806D1 (en) 1985-03-13 1986-03-11 MAGNETIC HEAD.
EP86103255A EP0194650B1 (en) 1985-03-13 1986-03-11 Magnetic head
US07/235,717 US5034285A (en) 1985-03-13 1988-08-22 Magnetic head

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP23364085A JPH0682448B2 (en) 1985-10-18 1985-10-18 Oxide substrate and magnetic head using the same

Publications (2)

Publication Number Publication Date
JPS6292206A JPS6292206A (en) 1987-04-27
JPH0682448B2 true JPH0682448B2 (en) 1994-10-19

Family

ID=16958207

Family Applications (1)

Application Number Title Priority Date Filing Date
JP23364085A Expired - Lifetime JPH0682448B2 (en) 1985-03-13 1985-10-18 Oxide substrate and magnetic head using the same

Country Status (1)

Country Link
JP (1) JPH0682448B2 (en)

Also Published As

Publication number Publication date
JPS6292206A (en) 1987-04-27

Similar Documents

Publication Publication Date Title
JP4100847B2 (en) Piezoelectric ceramic composition
EP0153141B1 (en) Thin film magnetic heads
JPH05290347A (en) Nonmagnetic substrate material and magnetic head
JPH0682448B2 (en) Oxide substrate and magnetic head using the same
EP0194650B1 (en) Magnetic head
JPS6222411A (en) Nonmagnetic substrate material and magnetic head
JPH08259316A (en) Production of manganese-zinc-based ferrite
JP2880044B2 (en) Non-magnetic substrate material for magnetic head
JPH0120523B2 (en)
JPS6295810A (en) Oxide substrate and magnetic head using the same
JPH0580045B2 (en)
JPH02180754A (en) Slider of magnetic head
JPH0335258B2 (en)
JPH0345024B2 (en)
JPH05254938A (en) Ceramic sintered compact
JPH0580044B2 (en)
JPH06316459A (en) Structural nonmagnetic ceramics material
JPH06290409A (en) Non-magnetic substrate material for magnetic head
JPH068203B2 (en) Oxide substrate material
JPS63170262A (en) Method for manufacturing ZrO↓2-TiC-SiC sintered body
JPS63134559A (en) Non-magnetic ceramics for magnetic head
JPH02243562A (en) Nonmagnetic ceramic material for magnetic head
JPH0449604A (en) Nonmagnetic oxide substrate and magnetic head using it
JPS6359984B2 (en)
JPS6296356A (en) Oxide substrate material

Legal Events

Date Code Title Description
EXPY Cancellation because of completion of term