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JPH0459264B2 - - Google Patents

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Publication number
JPH0459264B2
JPH0459264B2 JP59059932A JP5993284A JPH0459264B2 JP H0459264 B2 JPH0459264 B2 JP H0459264B2 JP 59059932 A JP59059932 A JP 59059932A JP 5993284 A JP5993284 A JP 5993284A JP H0459264 B2 JPH0459264 B2 JP H0459264B2
Authority
JP
Japan
Prior art keywords
weight
magnetic
thermal expansion
thin film
coefficient
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
JP59059932A
Other languages
Japanese (ja)
Other versions
JPS60204669A (en
Inventor
Akio Koyama
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 JP59059932A priority Critical patent/JPS60204669A/en
Publication of JPS60204669A publication Critical patent/JPS60204669A/en
Publication of JPH0459264B2 publication Critical patent/JPH0459264B2/ja
Granted legal-status Critical Current

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  • Compositions Of Oxide Ceramics (AREA)
  • Thin Magnetic Films (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

〔産業上の利用分野〕 本発明は磁気ヘツドの構成に用いられる非磁性
セラミツク材料に係り、特に金属磁性薄膜を蒸着
あるいはスパツタリング等をするための薄膜磁気
ヘツド用の非磁性セラミツク基板材料に関するも
のである。 〔従来技術〕 磁気ヘツドはVTR(Video Tape Recorder)、
コンピユータ、オーデイオ機器の心臓部品として
近年需要が急拡大している。 VTRやコンピユータ等の高密度記録が一段と
進むにつれ、次世代の磁気ヘツドとして薄膜で構
成する薄膜磁気ヘツドの研究が最近活発に行なわ
れている。 薄膜ヘツドは記録、再生機能をパーマロイ
(Fe−Ni)、センダスト(Fe−Al−Si)等の金属
磁性薄膜に持たせ、耐摩耗性等の摺動性能を非磁
性基板に持たせる複合ヘツドであり、基板自体に
も重要な特性が要求される。 従来、この種の非磁性セラミツク基板としては
チタン酸バリウムBaTiO3、チタン酸カルシウム
CaTiO3、アルミナ・炭化チタンAl2O3・T・C
等のセラミツク材料が提案されていた。 〔発明が解決しようとする問題点〕 ところがこのような材料で構成されたセラミツ
ク基板には次の如き問題があつた。 すなわち、金属磁性薄膜の特性を引き出すため
の蒸着、スパツタリング等の膜形成の際、および
その後の熱処理や、ギヤツプ部のガラスボンデイ
ング時に後述するように基板との熱膨張率の相異
から薄膜が剥離するという難点があつた。 また従来提案されていた前記セラミツク基板は
その熱膨張係数が高々10×10-6/℃程度と小さ
く、又熱膨張率が金属磁性薄膜と一致するガラス
の場合には硬度が低く、磁気テープとの摺動時の
摩耗が大きい欠点があつた。 このためパーマロイ等の金属磁性薄膜の熱膨張
率12〜15×10-6/℃にほぼ合致し、フエライト並
みの耐摩耗性を有する非磁性基板の出現が強く要
望されていた。 〔問題を解決するための手段〕 本発明者はかかる点に鑑み鋭意研究を進め、特
定組成のTiO2−NiO−CaO−MgO複合酸化物が
かかる目的に合致することを見出したが、さらに
改良を進めた結果、Al2O3,ZrO2又はCr2O3の少
なくとも1種を添加することによりさらに好まし
い耐摩耗性を付与することを見出し、本発明をな
すに至つた。 本発明の薄膜ヘツド用セラミツク基板材料で形
成された非磁性基板の特徴は、TiO220〜60重量
%、NiO20〜60重量%、CaO又はMgOの少なく
とも1種が10〜40重量%で、Al2O3,ZrO2又は
Cr2O3の少なくとも1種が2.5〜10重量%を含むこ
とにあり、これにより熱膨張率が11〜14×10-6
℃と金属磁性薄膜にほぼ合致しフエライト以上の
耐摩耗性を有するものを提供する点にある。 前記範囲において、TiO2は20重量%以下では
耐摩耗性が悪く、60重量%以上では熱膨張率が小
さくなる。NiOは熱膨張率を高めるものであるが
20重量%以下では熱膨張率が小さく、60重量%以
上では耐摩耗性が悪くなる。CaO又はMgOの少
なくとも1種が10重量%以下では熱膨張率が小さ
く、40重量%以上では耐摩耗性が低下する。そし
てAl2O3,ZrO2又はCr2O3の少なくとも1種の量
は2.5〜10重量%である必要があり、これ以上で
は熱膨張率が小さくなる。 〔実施例〕 本発明の磁気ヘツド用非磁性セラミツク材料に
よりセラミツク基板を製造する方法について1例
を示す。 所定量の酸化チタン、酸化ニツケル、酸化カル
シウム、酸化マグネシウムあるいは焼成によりこ
れらの酸化物に変換しうる化合物をボールミル等
の混合機を用いて充分混合したのち、この混合物
を800〜1200℃の温度で仮焼する。 次にこの仮焼粉末にAl2O3,ZrO2,Cr2O3粉末
を加え、ボールミル等の混合機を用いて再混合粉
砕し、乾燥後プレスバインダーを混ぜて成形し、
1250〜1400℃の温度範囲で大気中又は窒素中で焼
成する。この場合、各原料を独立粉末として用い
てもよいし、任意の組合せの仮焼粉末を用いても
よい。さらに共沈法やコロイド添加法等の公知の
手段によつて調整した複合酸化物、複合酸化物粉
末として用いてもよい。成形後の焼成においては
常圧焼結法以外にホツトプレス法などの高密度化
焼成法を使用してもよい。 次に具体的な実施例により、本発明をさらに詳
しく説明する。 なお熱膨張率はJIS法に準じ室温より500℃にお
ける平均線膨張より求めた。又耐摩耗性はピン−
円板式摩耗試験機を使用し、荷重50Kg/cm2、周速
150cm/secの条件で100時間運転し、試験片の長
さの変化より求めた。なおピンにサンプル、円板
には鉄を用いた。 実施例 酸化チタン、酸化ニツケル、酸化マグネシウム
及び炭酸カルシウムの比率を変え、ボールミルで
24時間湿式混合し、乾燥後大気中で1000℃で焼成
し、各種仮焼粉末を作成した。次に得られた各種
粉末にAl2O3,ZrO2,Cr2O3各粉末を各種比率で
加え、ボールミルで24時間湿式混合し、乾燥後プ
レスバインダーとして得られた粉末に対して
PVA(ポリビニルアルコール)1重量%を加え、
2ton/cm2で成形し、1300℃1時間大気中焼成して
表1に示すサンプル1〜20を作成した。
[Industrial Application Field] The present invention relates to a non-magnetic ceramic material used in the construction of a magnetic head, and in particular to a non-magnetic ceramic substrate material for a thin-film magnetic head for depositing or sputtering a metal magnetic thin film. be. [Prior art] The magnetic head is a VTR (Video Tape Recorder),
Demand has been rapidly increasing in recent years as a core component of computers and audio equipment. As high-density recording in VTRs, computers, etc. continues to advance, research into thin-film magnetic heads made of thin films has recently been actively conducted as the next generation magnetic head. Thin film heads are composite heads in which recording and reproducing functions are provided by a metal magnetic thin film such as Permalloy (Fe-Ni) or Sendust (Fe-Al-Si), and a non-magnetic substrate is provided with sliding performance such as wear resistance. The substrate itself also requires important characteristics. Conventionally, barium titanate BaTiO 3 and calcium titanate have been used as non-magnetic ceramic substrates of this type.
CaTiO 3 , alumina/titanium carbide Al 2 O 3・T・C
Ceramic materials such as [Problems to be Solved by the Invention] However, ceramic substrates made of such materials have the following problems. In other words, during film formation such as evaporation and sputtering to bring out the characteristics of the metal magnetic thin film, and during subsequent heat treatment and glass bonding at the gap part, the thin film may peel off due to the difference in thermal expansion coefficient with the substrate as described later. There was a problem with that. Furthermore, the previously proposed ceramic substrates have a small thermal expansion coefficient of about 10×10 -6 /°C, and glass, whose thermal expansion coefficient matches that of a metal magnetic thin film, has low hardness and is not suitable for magnetic tapes. The disadvantage was that there was a large amount of wear during sliding. For this reason, there has been a strong demand for a non-magnetic substrate that has a thermal expansion coefficient of 12 to 15×10 -6 /° C. of a metal magnetic thin film such as permalloy, and has wear resistance comparable to that of ferrite. [Means for Solving the Problem] In view of the above, the present inventor has conducted extensive research and found that a TiO 2 -NiO-CaO-MgO composite oxide with a specific composition meets the above objective. As a result of further research, it was discovered that more preferable wear resistance can be imparted by adding at least one of Al 2 O 3 , ZrO 2 or Cr 2 O 3 , and the present invention has been completed. The non-magnetic substrate made of the ceramic substrate material for thin film heads of the present invention is characterized by 20-60% by weight of TiO2 , 20-60% by weight of NiO, 10-40% by weight of at least one of CaO or MgO, and 10-40% by weight of at least one of CaO or MgO. 2 O 3 , ZrO 2 or
At least one of Cr 2 O 3 is contained in an amount of 2.5 to 10% by weight, which increases the thermal expansion coefficient to 11 to 14×10 -6 /
The object of the present invention is to provide a material that has a wear resistance that almost matches that of a metal magnetic thin film in terms of temperature and has a wear resistance that is higher than that of ferrite. In the above range, if TiO 2 is less than 20% by weight, the wear resistance will be poor, and if it is more than 60% by weight, the coefficient of thermal expansion will be small. Although NiO increases the coefficient of thermal expansion,
If it is less than 20% by weight, the coefficient of thermal expansion will be small, and if it is more than 60% by weight, the abrasion resistance will be poor. If the content of at least one of CaO or MgO is less than 10% by weight, the coefficient of thermal expansion will be small, and if it is more than 40% by weight, the wear resistance will decrease. The amount of at least one of Al 2 O 3 , ZrO 2 or Cr 2 O 3 needs to be 2.5 to 10% by weight, and if it is more than this, the coefficient of thermal expansion will be small. [Example] An example of a method for manufacturing a ceramic substrate using the nonmagnetic ceramic material for a magnetic head of the present invention will be described. After thoroughly mixing a predetermined amount of titanium oxide, nickel oxide, calcium oxide, magnesium oxide, or a compound that can be converted into these oxides by firing using a mixer such as a ball mill, this mixture is heated at a temperature of 800 to 1200℃. Calculate. Next, Al 2 O 3 , ZrO 2 , and Cr 2 O 3 powders are added to this calcined powder, mixed and ground again using a mixer such as a ball mill, and after drying, a press binder is mixed and molded.
Calcinate in air or nitrogen at a temperature range of 1250-1400°C. In this case, each raw material may be used as an independent powder, or any combination of calcined powders may be used. Furthermore, it may be used as a composite oxide or composite oxide powder prepared by known means such as a coprecipitation method or a colloid addition method. In the firing after molding, a high-density firing method such as a hot press method may be used in addition to the pressureless sintering method. Next, the present invention will be explained in more detail with reference to specific examples. The coefficient of thermal expansion was determined from the average linear expansion from room temperature to 500°C according to the JIS method. In addition, the wear resistance is
Using a disc type abrasion tester, load 50Kg/cm 2 , circumferential speed
The test piece was operated for 100 hours at a speed of 150 cm/sec, and the change in length of the test piece was determined. The sample was used as the pin, and iron was used as the disk. Example: Varying the ratio of titanium oxide, nickel oxide, magnesium oxide and calcium carbonate, using a ball mill.
The mixture was wet mixed for 24 hours, dried, and then fired at 1000°C in the air to produce various calcined powders. Next, Al 2 O 3 , ZrO 2 , and Cr 2 O 3 powders were added in various ratios to the various powders obtained, wet mixed in a ball mill for 24 hours, and after drying, the powders obtained as a press binder were mixed.
Add 1% by weight of PVA (polyvinyl alcohol),
Samples 1 to 20 shown in Table 1 were prepared by molding at 2 tons/cm 2 and firing in the air at 1300° C. for 1 hour.

【表】【table】

〔効果〕〔effect〕

本発明によれば、その熱膨張率が金属磁性薄膜
にほぼ合致し、しかも摩耗量が小さい、非磁性の
薄膜ヘツド用セラミツク基板として好適なものを
得ることができる。 なお、本発明のセラミツク材料は前記薄膜ヘツ
ド用として限定されるものではなく、かかる性能
が適用しうる他の磁気ヘツド用非磁性セラミツク
材料として当然に使用し得るものである。
According to the present invention, it is possible to obtain a non-magnetic ceramic substrate suitable for a thin film head, which has a coefficient of thermal expansion that almost matches that of a metal magnetic thin film and has a small amount of wear. It should be noted that the ceramic material of the present invention is not limited to the thin film head described above, but can naturally be used as a non-magnetic ceramic material for other magnetic heads to which such performance can be applied.

Claims (1)

【特許請求の範囲】 1 TiO220〜60重量%、NiO20〜60重量%、
CaO又はMgOの少なくとも1種が10〜40重量%
及びAl2O3,ZrO2又はCr2O3の少なくとも1種が
2.5〜10重量%よりなることを特徴とする磁気ヘ
ツド用非磁性セラミツク材料。 2 熱膨張率が11〜14×10-6/℃を有することを
特徴とする特許請求の範囲第1項記載の磁気ヘツ
ド用セラミツク材料。
[Claims] 1 TiO 2 20 to 60% by weight, NiO 20 to 60% by weight,
At least one of CaO or MgO is 10 to 40% by weight
and at least one of Al 2 O 3 , ZrO 2 or Cr 2 O 3
A non-magnetic ceramic material for a magnetic head, characterized by comprising 2.5 to 10% by weight. 2. The ceramic material for a magnetic head according to claim 1, which has a coefficient of thermal expansion of 11 to 14×10 -6 /°C.
JP59059932A 1984-03-28 1984-03-28 Non-magnetic ceramic material for magnetic head Granted JPS60204669A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59059932A JPS60204669A (en) 1984-03-28 1984-03-28 Non-magnetic ceramic material for magnetic head

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59059932A JPS60204669A (en) 1984-03-28 1984-03-28 Non-magnetic ceramic material for magnetic head

Publications (2)

Publication Number Publication Date
JPS60204669A JPS60204669A (en) 1985-10-16
JPH0459264B2 true JPH0459264B2 (en) 1992-09-21

Family

ID=13127390

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59059932A Granted JPS60204669A (en) 1984-03-28 1984-03-28 Non-magnetic ceramic material for magnetic head

Country Status (1)

Country Link
JP (1) JPS60204669A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62143857A (en) * 1985-12-17 1987-06-27 株式会社トーキン Non-magnetic material for magnetic head
JPH04141810A (en) * 1990-10-01 1992-05-15 Nec Corp Magnetic head

Also Published As

Publication number Publication date
JPS60204669A (en) 1985-10-16

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