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JPH0818861B2 - Ceramic material and magnetic head manufacturing method - Google Patents
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JPH0818861B2 - Ceramic material and magnetic head manufacturing method - Google Patents

Ceramic material and magnetic head manufacturing method

Info

Publication number
JPH0818861B2
JPH0818861B2 JP61282259A JP28225986A JPH0818861B2 JP H0818861 B2 JPH0818861 B2 JP H0818861B2 JP 61282259 A JP61282259 A JP 61282259A JP 28225986 A JP28225986 A JP 28225986A JP H0818861 B2 JPH0818861 B2 JP H0818861B2
Authority
JP
Japan
Prior art keywords
magnetic head
titanium carbide
powder
slider
ceramic material
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
JP61282259A
Other languages
Japanese (ja)
Other versions
JPS63139046A (en
Inventor
行雄 川口
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.)
TDK Corp
Original Assignee
TDK 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 TDK Corp filed Critical TDK Corp
Priority to JP61282259A priority Critical patent/JPH0818861B2/en
Publication of JPS63139046A publication Critical patent/JPS63139046A/en
Publication of JPH0818861B2 publication Critical patent/JPH0818861B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/01Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
    • C04B35/46Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on titanium oxides or titanates
    • C04B35/462Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on titanium oxides or titanates based on titanates
    • C04B35/465Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on titanium oxides or titanates based on titanates based on alkaline earth metal titanates

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  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Ceramic Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Oxide Ceramics (AREA)

Description

【発明の詳細な説明】 I.発明の背景 技術分野 本発明は、セラミック材料と磁気ヘッドとの製造方法
に関するものである。
Description: BACKGROUND OF THE INVENTION 1. Technical Field The present invention relates to a method of manufacturing a ceramic material and a magnetic head.

従来技術とその問題点 従来、セラミック材料、特に磁気ヘッドのスライダ材
料としては、例えばチタン酸カルシウム、チタン酸バリ
ウム、チタン酸カリウム、チタン酸ストロンチウム、ア
ルミナ、結晶化ガラスなどのセラミック材料が一般に用
いられている。
2. Description of the Related Art Conventional technology and its problems Conventionally, as a ceramic material, particularly as a slider material for a magnetic head, for example, a ceramic material such as calcium titanate, barium titanate, potassium titanate, strontium titanate, alumina, or crystallized glass is generally used. ing.

しかしながら、センダスト系のコアを有する磁気ヘッ
ドのスライダ材料として上記のセラミックを用いた場合
には、次のような不都合を生じる。
However, when the above ceramic is used as a slider material of a magnetic head having a sendust-based core, the following inconvenience occurs.

すなわち、センダスト系のコア材質の熱膨張係数が13
0×10-7deg-1程度であるのに対し、上記のセラミック材
料は10×10-7〜70×10-7deg-1程度であり、両者の差は
約2〜13倍である。
That is, the coefficient of thermal expansion of the sendust-based core material is 13
To 0 × 10 -7 in the range of about deg -1, said ceramic material is 10 × 10 -7 ~70 × 10 -7 deg about -1, the difference between them is about 2 to 13. times.

このため、センダスト系のコア材料と上記のセラミッ
ク材料を熱硬化性もしくは反応性等の接着剤や無機接着
剤を介して設けた場合には接着剤硬化や融着の際の加熱
によって、また上記のセラミック基板上に、センダスト
をスパッタ等により薄膜として設けた場合には、基板の
温度上昇によって、これらいずれの場合にもセラミック
の熱的スポーリングが発生しやすい。
For this reason, when the sendust-based core material and the above ceramic material are provided via a thermosetting or reactive adhesive or an inorganic adhesive, by heating during adhesive curing and fusion, When sendust is provided as a thin film on the ceramic substrate by sputtering or the like, thermal spalling of the ceramic is likely to occur in any of these cases due to the temperature rise of the substrate.

また、このような磁気ヘッドスライダ材料としてのセ
ラミック材料は二次加工性が悪く、チッピング等が発生
しやすい。
Further, such a ceramic material as a magnetic head slider material has poor secondary workability and is apt to cause chipping or the like.

また、研削、研磨の際の加工性も悪い。 In addition, workability during grinding and polishing is also poor.

そこでこのような不都合を解消し、生産性の良好なセ
ラミック材料が要望されている。
Therefore, there is a demand for a ceramic material that eliminates such inconvenience and has good productivity.

II.発明の目的 本発明の目的は、磁気ヘッド作製時に発生するスライ
ダの熱的スポーリングを防ぎしかも二次加工性に優れた
セラミック材料およびこの材料を用いた特にセンダスト
系の磁気ヘッドの製造方法を提供することにある。
II. Objects of the Invention An object of the present invention is to prevent thermal spalling of the slider that occurs during the manufacture of a magnetic head and to provide a ceramic material excellent in secondary workability, and a method of manufacturing a sendust-based magnetic head using this material. To provide.

III.発明の開示 このような目的は、下記の本発明によって達成され
る。
III. Disclosure of the Invention Such an object is achieved by the present invention described below.

すなわち第1の発明は、炭化チタンがチタン酸カルシ
ウムと炭化チタンとの総和に対し5〜20wt%となるよう
に、チタン酸カルシウム粉末と炭化チタン粉末とを混合
し、これを焼結するセラミック材料の製造方法である。
That is, the first invention is a ceramic material in which calcium titanate powder and titanium carbide powder are mixed and sintered so that titanium carbide is 5 to 20 wt% with respect to the total of calcium titanate and titanium carbide. Is a manufacturing method.

また第2の発明は、スライダとコアとを有し、 スライダがチタン酸カルシウムと炭化チタンを含有す
る磁気ヘッドを製造するに際し、 炭化チタンの含有量がチタン酸カルシウムと炭化チタ
ンとの総和に対し5〜20wt%となるように、チタン酸カ
ルシウム粉末と炭化チタン粉末を混合し、焼結してスラ
イダを得、さらにコアを形成する磁気ヘッドの製造方法
である。
The second invention has a slider and a core, and when the slider manufactures a magnetic head containing calcium titanate and titanium carbide, the content of titanium carbide is relative to the sum of calcium titanate and titanium carbide. This is a method of manufacturing a magnetic head in which calcium titanate powder and titanium carbide powder are mixed so as to be 5 to 20 wt% and sintered to obtain a slider, and further a core is formed.

IV.発明の具体的構成 以下、本発明の具体的構成について詳細に説明する。IV. Specific Structure of the Invention Hereinafter, the specific structure of the present invention will be described in detail.

本発明のセラミック材料、特に磁気ヘッドスライダ材
料としては、チタン酸カルシウム−炭化チタン焼結体を
用いる。すなわち、チタン酸カルシウム(CaTiO3)の粉
末と炭化チタン(TiC)の粉末との混合物を通常の焼結
体製造方法によって製作するものである。
A calcium titanate-titanium carbide sintered body is used as the ceramic material of the present invention, particularly the magnetic head slider material. That is, a mixture of calcium titanate (CaTiO 3 ) powder and titanium carbide (TiC) powder is manufactured by an ordinary sintered body manufacturing method.

用いるCaTiO3の粉末は微粉化することが好ましく、平
均粒子径が0.1〜3.0μm、特に0.5〜1.0μmであること
が好ましい。
The CaTiO 3 powder used is preferably finely divided and has an average particle diameter of 0.1 to 3.0 μm, particularly 0.5 to 1.0 μm.

原料としては、CaOとTiO2を用いることもできるが、
予め仮焼したCaTiO3粉末を用いないと、焼結時の収縮率
が大きく、また焼結に際し、CaOの針状粉が粒成長しや
すく、鏡面加工時に粒脱落を生じ、しかも良好な鏡面加
工精度、すなわち良好な平滑度が得られない。またCaO
粉末は吸水性が大きく、使用しにくい。
Although CaO and TiO 2 can be used as raw materials,
If the pre-calcined CaTiO 3 powder is not used, the shrinkage rate during sintering will be large, and during sintering, CaO needle-shaped powder will easily grow into grains, and grains will fall off during mirror finishing, and good mirror finishing is achieved. Accuracy, that is, good smoothness cannot be obtained. Also CaO
The powder has high water absorption and is difficult to use.

また、TiC粉末もCaTiO3と同様に微粉化することが好
ましく、平均粒子径が0.1〜3.0μm、特に0.5〜1.5μm
であることが好ましい。
Also, it is preferable that the TiC powder is also pulverized similarly to CaTiO 3, and the average particle size is 0.1 to 3.0 μm, particularly 0.5 to 1.5 μm.
It is preferred that

CaTiO3とTiCとの混合比率は、CaTiO3とTiCの総和に対
してTiCが5〜20wt%である。
Mixing ratio of CaTiO 3 and TiC is, TiC is 5 to 20 wt% with respect to the total sum of the CaTiO 3 and TiC.

TiCが5wt%未満となるとCaTiO3の粒成長のコントロー
ルが困難となり、切断加工や鏡面加工時のチッピングや
粒脱落等が発生する。また20wt%をこえると、熱膨張係
数が低下し、切断加工速度が低下する。そして、熱スポ
ーリングが生じ易くなり、鏡面加工性も低下する。
When TiC is less than 5 wt%, it becomes difficult to control the grain growth of CaTiO 3 , and chipping or grain shedding during cutting or mirror finishing occurs. On the other hand, if it exceeds 20 wt%, the coefficient of thermal expansion decreases, and the cutting speed decreases. Then, heat spalling is likely to occur, and the mirror surface workability also deteriorates.

また、通常、本発明の焼結体は、CaTiO3とTiCのみで
構成されるが、その他の添加物として、BaCO3、CeO2、T
iO2、NiO2、CaOを全体の0.1〜10wt%添加されていても
よい。
Further, usually, the sintered body of the present invention is composed only of CaTiO 3 and TiC, but as other additives, BaCO 3 , CeO 2 , T
0.1 to 10 wt% of iO 2 , NiO 2 and CaO may be added to the whole.

なお、CaTiO3およびTiCは、通常、その化学量論組成
近傍のものとされる。
Note that CaTiO 3 and TiC are usually near their stoichiometric composition.

CaTiO3−TiC焼結体は、通常これらの粉末を所定量混
合した後、成形体とし、非酸化性雰囲気中でのホットプ
レス焼結法により、この成形体を焼結し、放冷して得ら
れる。
A CaTiO 3 -TiC sintered body is usually formed by mixing a predetermined amount of these powders into a molded body, sintering the molded body by a hot press sintering method in a non-oxidizing atmosphere, and allowing it to cool. can get.

この場合の焼結温度は600〜1500℃、特に800〜1200℃
が好ましい。
The sintering temperature in this case is 600-1500 ℃, especially 800-1200 ℃
Is preferred.

温度が600℃より低いと、緻密な焼結体が得られず、1
500℃より高いと、CaTiO3の昇華が増し、表面層と内部
が異構造になるからである。
If the temperature is lower than 600 ° C, a dense sintered body cannot be obtained.
This is because if the temperature is higher than 500 ° C, the sublimation of CaTiO 3 increases and the surface layer and the inside have a different structure.

また、プレス圧力は200〜300Kg/cm2程度である。The pressing pressure is about 200 to 300 Kg / cm 2 .

非酸化性雰囲気としては、N2、Ar、He等の不活性ガ
ス、H2、CO、各種炭化水素等、あるいはこれらの混合雰
囲気、さらには真空等種々のものであってもよい。
The non-oxidizing atmosphere may be an inert gas such as N 2 , Ar, or He, H 2 , CO, various hydrocarbons, a mixed atmosphere thereof, or a vacuum.

非酸化性雰囲気にするのは、TiCの酸化を防止するた
めである。
The non-oxidizing atmosphere is used to prevent the oxidation of TiC.

焼結時間は、一般に1〜3時間である。 The sintering time is generally 1 to 3 hours.

なお、焼結に際しては、原料粉末の成形体を非酸化性
雰囲気中(例えば400℃まで真空中、その後はAr雰囲気
中等が好ましい。)で予備焼結し、次いでHIP炉内でこ
の予備焼結体を焼結する熱間等方等圧加圧(HIP)法を
用いてもよい。予備焼結の温度は600〜1500℃、その時
間は1〜3時間とするのがよい。また、HIP法における
温度は400〜1350℃、焼結時間は1〜5時間、圧力は100
0〜1500Kg/cm2であり、そしてAr等の不活性雰囲気中で
行うことが望ましい。
In addition, at the time of sintering, the raw powder compact is pre-sintered in a non-oxidizing atmosphere (for example, it is preferable to vacuum up to 400 ° C. and then Ar atmosphere), and then this pre-sintering in a HIP furnace. The hot isostatic pressing (HIP) method of sintering the body may be used. The presintering temperature is preferably 600 to 1500 ° C. and the time is preferably 1 to 3 hours. In the HIP method, the temperature is 400 to 1350 ° C, the sintering time is 1 to 5 hours, and the pressure is 100.
It is 0 to 1500 Kg / cm 2 , and it is desirable to carry out in an inert atmosphere such as Ar.

この場合、室温でArガス等を300〜400Kg/cm2まで加圧
し、その後、上記のように加熱により圧力をかける。
In this case, Ar gas or the like is pressurized to 300 to 400 Kg / cm 2 at room temperature, and then pressure is applied by heating as described above.

なお、このように形成された焼結体のうち、TiCの一
部はTiO2に変化していてもよい。
Incidentally, in the sintered body thus formed, part of TiC may be changed to TiO 2 .

このようにして得られたCaTiO3−TiC焼結体は、その
物性値として100×10-7〜130×10-7deg-1の熱膨張係数
を有し、しかもTiCの添加量を変化させることによっ
て、この値はある程度、任意に設定することができる。
The CaTiO 3 -TiC sintered body thus obtained has a thermal expansion coefficient of 100 × 10 −7 to 130 × 10 −7 deg −1 as its physical property value, and the amount of TiC added is changed. Therefore, this value can be arbitrarily set to some extent.

そしてこの値は、センダスト系のコア材質とほぼ同程
度の値の熱膨張係数となるので、本発明のCaTiO3−TiC
焼結体をセンダスト磁気ヘッドのスライダ材料として用
いれば、前述したように従来発生していた熱スポーリン
グの発生はほぼ完全に防止できる。
And since this value is a coefficient of thermal expansion of about the same value as the sendust-based core material, the CaTiO 3 -TiC of the present invention.
If the sintered body is used as the slider material of the sendust magnetic head, the generation of thermal spalling, which has conventionally occurred as described above, can be almost completely prevented.

また本発明のセラミック材料は、高硬度を有し、耐摩
耗性に優れ、しかも二次加工性にも優れるため加工速度
を大きくしてもチッピング、粒脱落などはきわめて発生
しにくい。鏡面加工後の平滑度も良好である。上述した
ように、本発明のセラミック材料は各種用途に用いるこ
とができるが磁気ヘッドスライダとして、特にセンダス
ト系の磁気ヘッドに用いた場合には、特に優れた効果を
発揮する。
Further, the ceramic material of the present invention has high hardness, excellent wear resistance, and excellent secondary workability, so that chipping and grain detachment are extremely unlikely to occur even when the working speed is increased. The smoothness after mirror finishing is also good. As described above, the ceramic material of the present invention can be used for various purposes, but when it is used as a magnetic head slider, particularly in a sendust-based magnetic head, it exhibits a particularly excellent effect.

このような磁気ヘッドスライダを用いたセンダスト系
の磁気ヘッドは、公知の種々のセンダスト材料からなる
ヘッドコア、巻線等を有し構成される。
A sendust type magnetic head using such a magnetic head slider has a head core made of various known sendust materials, a winding, and the like.

ヘッドコアを形成するセンダストは、公知の種々の組
成のものであってよい。
The sendust forming the head core may have various known compositions.

なお、センダスト系のコアの熱膨張係数は通常90×10
-7〜130×10-7deg-1程度である。
The thermal expansion coefficient of the sendust core is usually 90 × 10
It is about -7 to 130 × 10 -7 deg -1 .

このようなセンダストからなるヘッドコアと本発明の
組成材料からなるスライダとを、熱硬化性もしくは反応
性の接着剤やガラスを介して設層した場合、あるいはス
ライダを基板とし、センダストをスパッタ等により薄膜
として設置した場合等いずれの場合であってもこれらの
熱膨張係数がほぼ同一であるためスライダの熱的スポー
リングはほとんど発生しない。
When a head core made of such sendust and a slider made of the composition material of the present invention are layered via a thermosetting or reactive adhesive or glass, or the slider is used as a substrate and sendust is formed into a thin film by sputtering or the like. In any case, the thermal expansion coefficient of these sliders is almost the same, and thermal spalling of the slider hardly occurs.

V.発明の具体的作用効果 本発明によれば、高い硬度をもち、加工性にすぐれ、
しかも熱膨張率がセンダスト材料のそれと同程度の値を
有するセラミック材料が得られる。
V. Specific Action and Effect of the Invention According to the present invention, it has high hardness and excellent workability,
Moreover, a ceramic material having a thermal expansion coefficient similar to that of the sendust material can be obtained.

従って、本発明のセラミック材料をセンダスト系の磁
気ヘッドのスライダとして用いた場合、従来製造工程中
で発生していたスライダの熱スポーリングの発生を防ぐ
ことができ、しかもこのスライダ材料は二次加工性にも
優れたものとなる。
Therefore, when the ceramic material of the present invention is used as a slider of a sendust-based magnetic head, it is possible to prevent the thermal spalling of the slider which has occurred during the conventional manufacturing process, and this slider material is subjected to secondary processing. It also has excellent properties.

VI.発明の具体的実施例 以下、本発明の具体的実施例を示し、本発明の効果を
さらに詳細に説明する、 実施例 平均粒径0.5μmのCaTiO3(純度99.9%)粉末と平均
粒径0.5μmのTiC(純度99%、炭素含有量19%以上でそ
の1%以下は遊離コクエンである。)とを表1に示すよ
うな割合で添加し、ボールミルにより40時間湿式混合を
行った。
VI. Specific Examples of the Invention Hereinafter, specific examples of the present invention will be shown to explain the effect of the present invention in more detail. Examples CaTiO 3 (purity 99.9%) powder having an average particle size of 0.5 μm and average particles TiC having a diameter of 0.5 μm (purity 99%, carbon content 19% or more and 1% or less thereof is free coquence) was added at a ratio shown in Table 1, and wet mixing was performed for 40 hours by a ball mill. .

混合したスラリーを#35フルイパスした後、乾燥造粒
し、内径77mmの黒鉛型に充填した。
The mixed slurry was passed through # 35 sieve, dried and granulated, and then filled in a graphite mold having an inner diameter of 77 mm.

これを真空雰囲気中で1時間、焼結温度600〜1500
℃、プレス圧力200〜300Kg/cm2でホットプレス焼結を行
った。
This for 1 hour in a vacuum atmosphere, sintering temperature 600 ~ 1500
Hot press sintering was carried out at a temperature of ℃ and a pressing pressure of 200 to 300 Kg / cm 2 .

冷却後、それぞれの焼結体を型から取り出し、#200
ダイヤモンド砥石にて加工し、φ3インチ、4mm厚の試
料(表1)を作製した。
After cooling, remove each sintered body from the mold and # 200
The sample was processed with a diamond grindstone to prepare a sample (Table 1) having a diameter of 3 inches and a thickness of 4 mm.

また、TiCを混入しない試料301も上と同様に作製し
た。さらに、ともに平均粒径0.5μmのTiO2粉末とCaO粉
末とを用いた試料401を作製した。
A sample 301 containing no TiC was also prepared in the same manner as above. Further, a sample 401 using both TiO 2 powder and CaO powder having an average particle size of 0.5 μm was prepared.

上記試料101〜105、201〜202および301、401につい
て、特性を表1に示す。
Table 1 shows the characteristics of the above samples 101 to 105, 201 to 202 and 301 and 401.

特性の評価は下記のとおりである。 The evaluation of the characteristics is as follows.

(1)熱スポーリング センダストをスパッタ等により基板上に薄膜化した試
料を切断加工した後、切断面を研削研摩した時のセンダ
ストと基板の密着性を顕微鏡観察した。
(1) Heat spalling After the sample in which sendust was thinned on the substrate by sputtering or the like was cut and processed, the adhesion between the sendust and the substrate when the cut surface was ground and polished was observed under a microscope.

(2)切断加工性 (a)切断性(定圧切断実験) 1軸スラストベアリングの上にガラスを接着し、その
上に試料(幅30mm、厚さ4mm)を接着し、この試料を500
gおよび1000gのおもりで引っぱり、ダイヤモンド切断砥
石で切断加工したときの切断速度を測定した。
(2) Cutting workability (a) Cutting performance (constant pressure cutting experiment) Glass was bonded onto a uniaxial thrust bearing, and a sample (width 30 mm, thickness 4 mm) was bonded onto it, and this sample was applied to 500
The cutting speed at the time of pulling with a weight of 1000 g and 1000 g and cutting with a diamond cutting whetstone was measured.

(b)チッピング発生(定速切断実験) 定速送り(25mm/min)により、ダイヤモンド切断砥石
で切断加工したとき、切断面から10μm以上の深さのチ
ッピングの発生率(幅30mm、厚さ4mmの試料について30m
mあたりの発生率)を顕微鏡(200倍)で調べた。
(B) Chipping occurrence (constant speed cutting experiment) When cutting with a diamond cutting grindstone by constant speed feed (25 mm / min), the occurrence rate of chipping at a depth of 10 μm or more from the cutting surface (width 30 mm, thickness 4 mm) About the sample of 30m
Incidence rate per m) was examined with a microscope (200 times).

5個以内を○、5〜10個を△、それ以上を×で表わ
す。
Five or less are indicated by O, 5-10 by Δ, and more are indicated by X.

(3)熱膨張係数 40℃〜300℃における熱膨張係数を石英標準試料(3
×3×20L)と比較し測定した。
(3) Coefficient of thermal expansion The coefficient of thermal expansion at 40 ℃ ~ 300 ℃
X 3 x 20 L ) and measured.

試料は、3×3×20Lに加工した。The sample was processed into 3 × 3 × 20 L.

(4)鏡面加工性 各試料をグリーンカーバイド(GC)砥粒でラップ加工
した後、ダイヤモンド砥粒でポリシング加工し、2次電
子像の回析および表面あらさ計により粒脱落の有無を調
べた。
(4) Mirror Surface Machinability Each sample was lapped with green carbide (GC) abrasive grains, and then polished with diamond abrasive grains, and the presence or absence of grain omission was examined by diffraction of a secondary electron image and a surface roughness meter.

また、この際の平滑度を測定し、Rmax30nm未満を◎、30
〜80nmを○、80nm超を×とした。
In addition, the smoothness at this time is measured, and if Rmax is less than 30 nm, ◎, 30
-80 nm was marked with ◯, and more than 80 nm was marked with x.

表1の結果より本発明の効果は明らかである。 From the results in Table 1, the effect of the present invention is clear.

すなわち、TiC5wt%未満ではチッピングが多発し、粒
脱落が多発する。またTiC20wt%超では、熱膨張係数が
低下し、この結果熱スポーリングが増加し、また切断加
工速度や鏡面加工性が低下し、粒脱落や面粗さも増大し
ている。また、CaTiO3仮焼粉を用いないときには、鏡面
加工性が低下し、粒脱落や面粗さが増大している。
That is, if the TiC content is less than 5 wt%, chipping frequently occurs and grain dropout frequently occurs. On the other hand, if the content of TiC exceeds 20 wt%, the coefficient of thermal expansion decreases, resulting in an increase in thermal spalling, a decrease in cutting processing speed and mirror surface workability, and an increase in grain loss and surface roughness. Further, when the CaTiO 3 calcined powder is not used, the mirror surface workability is deteriorated and the grains are dropped and the surface roughness is increased.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】炭化チタンがチタン酸カルシウムと炭化チ
タンとの総和に対し5〜20wt%となるように、チタン酸
カルシウム粉末と炭化チタン粉末とを混合し、これを焼
結するセラミック材料の製造方法。
1. A method for producing a ceramic material, which comprises mixing calcium titanate powder and titanium carbide powder and sintering the mixture so that titanium carbide is contained in an amount of 5 to 20 wt% with respect to the sum of calcium titanate and titanium carbide. Method.
【請求項2】スライダとコアとを有し、 スライダがチタン酸カルシウムと炭化チタンを含有する
磁気ヘッドを製造するに際し、 炭化チタンの含有量がチタン酸カルシウムと炭化チタン
との総和に対し5〜20wt%となるように、チタン酸カル
シウム粉末と炭化チタン粉末を混合し、焼結してスライ
ダを得、さらにコアを形成する磁気ヘッドの製造方法。
2. When manufacturing a magnetic head having a slider and a core, wherein the slider contains calcium titanate and titanium carbide, the content of titanium carbide is 5 to the total amount of calcium titanate and titanium carbide. A method of manufacturing a magnetic head, wherein calcium titanate powder and titanium carbide powder are mixed so as to be 20 wt% and sintered to obtain a slider, and further a core is formed.
【請求項3】コアがセンダスト系材料である特許請求の
範囲第2項の磁気ヘッドの製造方法。
3. The method of manufacturing a magnetic head according to claim 2, wherein the core is a sendust material.
JP61282259A 1986-11-27 1986-11-27 Ceramic material and magnetic head manufacturing method Expired - Lifetime JPH0818861B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61282259A JPH0818861B2 (en) 1986-11-27 1986-11-27 Ceramic material and magnetic head manufacturing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61282259A JPH0818861B2 (en) 1986-11-27 1986-11-27 Ceramic material and magnetic head manufacturing method

Publications (2)

Publication Number Publication Date
JPS63139046A JPS63139046A (en) 1988-06-10
JPH0818861B2 true JPH0818861B2 (en) 1996-02-28

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Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JPH0818861B2 (en)

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6048470A (en) * 1983-08-26 1985-03-16 株式会社東芝 Refrigerator
JPS61222958A (en) * 1985-03-29 1986-10-03 住友電気工業株式会社 Porcelain composition for thin film magnetic head

Also Published As

Publication number Publication date
JPS63139046A (en) 1988-06-10

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