JPH0744111B2 - Substrate material for thin film magnetic head - Google Patents
Substrate material for thin film magnetic headInfo
- Publication number
- JPH0744111B2 JPH0744111B2 JP1018910A JP1891089A JPH0744111B2 JP H0744111 B2 JPH0744111 B2 JP H0744111B2 JP 1018910 A JP1018910 A JP 1018910A JP 1891089 A JP1891089 A JP 1891089A JP H0744111 B2 JPH0744111 B2 JP H0744111B2
- Authority
- JP
- Japan
- Prior art keywords
- substrate material
- thin film
- magnetic head
- aln
- film magnetic
- 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 - Fee Related
Links
Landscapes
- Ceramic Products (AREA)
- Magnetic Heads (AREA)
- Thin Magnetic Films (AREA)
Description
【発明の詳細な説明】 <産業上の利用分野> 本発明はコンピューターの周辺装置であるフロッピーデ
ィスク装置やハードディスク装置に組み込まれる磁気ヘ
ッドの基板材料に関し、特に薄膜磁気ヘッド用非磁性基
板材料に関するものである。The present invention relates to a substrate material of a magnetic head incorporated in a floppy disk device or a hard disk device which is a peripheral device of a computer, and more particularly to a non-magnetic substrate material for a thin film magnetic head. Is.
<従来の技術> 高密度記録用磁気ヘッドとして従来のフェライトを使用
したヘッドに変り、最近では薄膜ヘッドが注目されて来
ている。<Prior Art> Instead of a conventional head using ferrite as a magnetic head for high-density recording, a thin film head has recently been drawing attention.
ここで薄膜ヘッド用基板材料としてはAl2O3−TiCが用い
られている。その理由としては、他材料に比較し高硬度
かつ高強度なため高密度磁気記録用として使われる金属
系の記録媒体との接触起動停止に対し高い耐久性を示す
事があげられる。Here, Al 2 O 3 —TiC is used as the substrate material for the thin film head. The reason is that it has high hardness and strength compared to other materials, and therefore exhibits high durability against contact start / stop with a metal-based recording medium used for high-density magnetic recording.
<発明が解決しようとする課題> しかしながらAl2O3−TiCセラミックスよりなる薄膜磁気
ヘッド用基板材料は燃結性が悪いために、基板材料と
して必要な緻密なものを得るためには焼結温度を1850〜
1900℃の高温としなければならない事、機械加工性が
悪いために小型化の要求に対応できない事等の欠点があ
げられる。<Problems to be Solved by the Invention> However, since the substrate material for a thin-film magnetic head made of Al 2 O 3 —TiC ceramics has poor flammability, the sintering temperature is required to obtain a dense substrate material. From 1850
There are drawbacks such as the need to use a high temperature of 1900 ° C and the inability to meet the demand for miniaturization due to poor machinability.
本発明に斯る欠点を除去するため行われたもので、その
技術的課題は焼結性及び機械加工性に優れた薄膜磁気ヘ
ッド用基板材料を提供する事にある。The present invention has been carried out in order to eliminate such drawbacks, and its technical problem is to provide a substrate material for a thin film magnetic head which is excellent in sinterability and machinability.
<課題を解決するための手段> 本発明は前述の欠点を改善する様構成したもので薄膜磁
気ヘッド用基板材料であるAl2O3−15〜60wt%TiCセラミ
ックスにおいて周期律表IV a,V a,VI a族金属Ti,Zr,Nb,
Ta,Cr,Mo,W等の珪化物を0.1〜1wt%、AlNとCaOとをそれ
ぞれ0.1〜1wt%添加してなり、その焼結性、及び加工性
を改良したものである。<Means for Solving the Problems> The present invention is configured to improve the above-mentioned drawbacks, and in the Al 2 O 3 -15 to 60 wt% TiC ceramics which is a substrate material for a thin film magnetic head, the periodic table IVa, V a, VI Group a metal Ti, Zr, Nb,
It is made by adding 0.1 to 1 wt% of silicides such as Ta, Cr, Mo and W, and 0.1 to 1 wt% of AlN and CaO, respectively, and improving its sinterability and workability.
即ち,本発明によれば,主成分と,添加物とからなるセ
ラミックスであって,前記主成分は,15〜60wt%のTiCと
残部が実質的にAl2O3からなり,前記添加物は,前記セ
ラミックスの総重量に対して,0.1〜1wt%含有されたAlN
と,0.1〜1wt%含有されたCaOと,総量で0.1〜1wt%含有
されたTi,Zr,Nb,Ta,Cr,Mo,Wの夫々の珪化物からなる群
から選択された少なくとも一種の金属珪化物とからなる
ことを特徴とする薄膜磁気ヘッド用基板材料が得られ
る。That is, according to the present invention, a ceramic comprising a main component and an additive, wherein the main component comprises 15 to 60 wt% TiC and the balance substantially Al 2 O 3 , and the additive is , 0.1 to 1 wt% of AlN contained in the total weight of the ceramics
And at least one metal selected from the group consisting of 0.1 to 1 wt% of CaO and 0.1 to 1 wt% of each of Ti, Zr, Nb, Ta, Cr, Mo and W silicides. A substrate material for a thin film magnetic head, which is characterized by comprising a silicide, is obtained.
つまり本発明において金属珪化物の添加量を制御するこ
とにより焼結性を改善したもので、特に0.1〜1wt%の添
加量の時、焼結体の密度最大となる。この時金属珪化物
は主成分の粒成長を抑えながら緻密化を進行させるため
相対密度が高いにもかかわらず得られた焼結体は機械加
工性に優れたものとなる。この様な効果は添加量が0.1w
t%未満では得られず、また1wt%を超えると焼結時に粒
界層における液相の生成が著しくなり焼結性は向上する
ものの粒径は大きくなりまた同時に粒界強度も低下し材
料の機械強度は劣化する。That is, in the present invention, the sinterability is improved by controlling the addition amount of the metal silicide, and particularly when the addition amount is 0.1 to 1 wt%, the density of the sintered body becomes maximum. At this time, since the metal silicide promotes the densification while suppressing the grain growth of the main component, the sintered body obtained is excellent in machinability even though the relative density is high. This kind of effect is 0.1w
If it is less than t%, it cannot be obtained, and if it exceeds 1 wt%, the liquid phase is remarkably generated in the grain boundary layer during sintering and the sinterability is improved, but the grain size is increased and at the same time the grain boundary strength is decreased and Mechanical strength deteriorates.
一方AlNとCaOの添加についても焼結性の改善と、これと
同時に機械加工性の向上が観察されAlN,CaOそれぞれの
添加量が0.1〜1wt%の時最大となる。AlNとCaOは液相を
生成する事が知られておりAlNとCaOとの同時添加により
液相焼結が進行するものと考えられる。またAlNは高硬
度、高強度であるにもかかわらず比較的機械加工性に優
れているため得られた焼結体は高強度でかつ機械加工性
に優れたものとなる。この様な効果はAlNとCaOとを同時
に添加した場合しか得られずまたそれぞれの添加量が0.
1wt%未満では効果が不十分であり一方1wt%を超えると
AlNの難焼結性がが顕著になり焼結性の低下を引起す。On the other hand, with regard to the addition of AlN and CaO, improvement in sinterability and, at the same time, improvement in machinability are observed, and the maximum is obtained when the addition amounts of AlN and CaO are each 0.1 to 1 wt%. It is known that AlN and CaO form a liquid phase, and it is considered that liquid phase sintering proceeds by simultaneous addition of AlN and CaO. Further, since AlN has a relatively high machinability and a relatively high machinability despite its high hardness, the obtained sintered body has a high strength and an excellent machinability. Such an effect can be obtained only when AlN and CaO are added at the same time.
If it is less than 1 wt%, the effect is insufficient, while if it exceeds 1 wt%,
AlN becomes difficult to sinter, which causes a decrease in sinterability.
さらに主成分に関してはTiCとAl2O3の合計に対するTiC
量が15wt%未満ではHvが2000kg/mm2以下となり、また60
wt%を超えると焼結性が著しく低下するため主成分のTi
C量は15〜60wt%が望ましい。Furthermore, regarding the main component, TiC relative to the total of TiC and Al 2 O 3
If the amount is less than 15 wt%, Hv will be 2000 kg / mm 2 or less.
If the content exceeds wt%, the sinterability will decrease significantly, so the main component Ti
The amount of C is preferably 15-60 wt%.
以下本発明を実施例に従い詳細に説明する。Hereinafter, the present invention will be described in detail according to examples.
<実施例> 平均粒径0.1〜0.5μm、純度99%以上のAl2O3,TiC,TiSi
2,ZrSi2,NbSi2,TaSi2,CrSi2,MoSi2,WSi2,AlN,CaCO3の各
粉末原料を第1表に示す組成比となる様に秤量しNo.1〜
10の各試料とした。表中の主成分TiC及びAl2O3は主成分
の組成比(wt%)を示し、添加物の量は主成分の総量に
対する重量比(wt%)で示している。なおCaCO3につい
てはCaOに換算した値である。<Example> Al 2 O 3 , TiC, TiSi having an average particle size of 0.1 to 0.5 μm and a purity of 99% or more
2, ZrSi 2, NbSi 2, TaSi 2, CrSi 2, MoSi 2, WSi 2, AlN, were weighed so as to be the composition ratios shown each powder raw material of CaCO 3 in Table 1 No.1~
There were 10 samples. In the table, the main components TiC and Al 2 O 3 indicate the composition ratio (wt%) of the main components, and the amounts of additives are indicated by the weight ratio (wt%) to the total amount of the main components. Note that CaCO 3 is a value converted to CaO.
試料No.1〜5が本発明の適用例であり、No.6〜10は比較
のためのものである。Sample Nos. 1 to 5 are application examples of the present invention, and Nos. 6 to 10 are for comparison.
No.1〜10の各試料をそれぞれ前述の様に秤量後エタノー
ルを溶媒としボールミルにて20〜40時間混合した。次に
濾過、乾燥後、有機系バインダーを添加し30×30×10mm
のブロックに加圧成型した。次にこのブロックを1750
℃、Ar気流中にて2時間焼結した後Arガスを圧力媒体と
して用い、圧力1000kg/cm2温度1650℃2時間保持の条件
で熱間静水圧プレス(HIP)処理を施した。Each sample of Nos. 1 to 10 was weighed as described above and mixed with ethanol as a solvent in a ball mill for 20 to 40 hours. Next, after filtering and drying, add an organic binder and add 30 x 30 x 10 mm.
Was molded into blocks. Then this block 1750
After sintering at ℃ for 2 hours in Ar flow, Ar gas was used as a pressure medium, and hot isostatic pressing (HIP) treatment was performed under the conditions of pressure 1000 kg / cm 2 temperature 1650 ℃ 2 hours holding.
以上の工程より得られた試料の材料特性の評価として相
対密度ビッカース硬度Hv、抗折強度F、の測定を行っ
た。また各試料より5×5×20mmの角柱を切り出した後
この角柱の隣接する5×20mmの2面を鏡面加工し陵部に
生じた2×2μm以上のチッピング数を1000倍の倍率を
有する光学顕微鏡を用いてカウントして1cm当りの発生
率に換算し加工性の評価とした。さらに組織観察を行い
平均粒径を求めた。The relative density Vickers hardness Hv and the bending strength F were measured to evaluate the material properties of the samples obtained through the above steps. Also, after cutting out a 5 × 5 × 20 mm prism from each sample, two adjacent 5 × 20 mm surfaces of this prism are mirror-polished and the chipping number of 2 × 2 μm or more generated at the ridge has a magnification of 1000 times. It was counted using a microscope and converted into an occurrence rate per cm to evaluate workability. Further, the structure was observed to determine the average particle size.
以上の結果を第1表に組成の値とともに記載した。The above results are shown in Table 1 together with the composition values.
この表から、試料No.6の無添加例に比較し、No.1〜5の
TiSi2,ZrSi2,NbSi2,TaSi2,CrSi2,MoSi2,WSi2の少なくと
も一種を0.1〜1wt%、AlNとCaOのそれぞれを0.1〜1wt%
添加した試料では平均粒径1.1〜1.2μmの小粒径組織で
あるにもかかわらず相対密度は99.96〜99.98%と高く、
かつHv,F,チッピング発生率ともに向上している。From this table, in comparison with the additive-free example of sample No. 6,
TiSi 2, ZrSi 2, NbSi 2 , TaSi 2, CrSi 2, MoSi 2, at least one of 0.1 to 1 wt% of WSi 2, 0.1 to 1 wt% each of AlN and CaO
In the added sample, the relative density is as high as 99.96 to 99.98% despite the fact that the average particle size is 1.1 to 1.2 μm and the particle size is small.
Moreover, the Hv, F, and chipping occurrence rates are all improved.
また金属珪化物のみの添加(No.7)の場合、無添加剤
(No.6)に比較し密度、組成、機械強度及び加工性いず
れも改善されているが、金属珪化物の添加に加えさらに
AlNとCaOとを同時に添加した本発明例(No.1〜5)より
はF,チッピング発生率ともに多少劣っている。In addition, in the case of adding only metal silicide (No.7), the density, composition, mechanical strength and workability are all improved compared to the additive-free additive (No.6). further
Both the F and chipping occurrence rates are somewhat inferior to those of the present invention examples (Nos. 1 to 5) in which AlN and CaO were added simultaneously.
試料No.8についてはAlN,CaOのみの添加であり、無添加
例に比較し焼結性は向上しているものの相対密度は95%
程度と低い。Sample No. 8 has only AlN and CaO added, and has better sinterability than the non-added example, but the relative density is 95%.
The degree is low.
金属珪化物の添加量が1wt%を超えると(No.9)焼結性
は向上するものの粒成長が顕著になり、かつHv,Fの低
下、チッピング発生率の増加が観察される。When the amount of metal silicide added exceeds 1 wt% (No.9), sinterability is improved, but grain growth becomes remarkable, and Hv, F decrease and chipping incidence increase.
一方AlNの添加量が1wt%を超えると(No.10)、AlNの持
つ難焼結性が現れ焼結性の低下をきたす。On the other hand, if the amount of AlN added exceeds 1 wt% (No. 10), the sinterability of AlN appears and the sinterability decreases.
<発明の効果> 以上述べた如く本発明によれば、焼結性に優れ小粒径組
織かつ緻密で機械加工性に優れた薄膜磁気ヘッド用高密
度Al2O3−TiCセラミックス基板材料の提供が可能となっ
た。 <Effects of the Invention> As described above, according to the present invention, there is provided a high-density Al 2 O 3 —TiC ceramics substrate material for a thin film magnetic head, which is excellent in sinterability, has a small grain size structure, is dense, and is excellent in machinability. Became possible.
Claims (1)
であって,前記主成分は,15〜60wt%のTiCと残部が実質
的にAl2O3からなり, 前記添加物は,前記セラミックスの総重量に対して, 0.1〜1wt%含有されたAlNと,0.1〜1wt%含有されたCaO
と, 総量で0.1〜1wt%含有されたTi,Zr,Nb,Ta,Cr,Mo,Wの夫
々の珪化物からなる群から選択された少なくとも一種の
金属珪化物とからなることを特徴とする薄膜磁気ヘッド
用基板材料。1. A ceramic comprising a main component and an additive, wherein the main component comprises 15 to 60 wt% TiC and the balance substantially Al 2 O 3 , and the additive is the ceramic. 0.1 to 1 wt% of AlN and 0.1 to 1 wt% of CaO based on the total weight of
And at least one metal silicide selected from the group consisting of respective silicides of Ti, Zr, Nb, Ta, Cr, Mo, and W contained in a total amount of 0.1 to 1 wt%. Substrate material for thin film magnetic heads.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1018910A JPH0744111B2 (en) | 1989-01-28 | 1989-01-28 | Substrate material for thin film magnetic head |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1018910A JPH0744111B2 (en) | 1989-01-28 | 1989-01-28 | Substrate material for thin film magnetic head |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH02199808A JPH02199808A (en) | 1990-08-08 |
| JPH0744111B2 true JPH0744111B2 (en) | 1995-05-15 |
Family
ID=11984761
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1018910A Expired - Fee Related JPH0744111B2 (en) | 1989-01-28 | 1989-01-28 | Substrate material for thin film magnetic head |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0744111B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007153653A (en) | 2005-12-02 | 2007-06-21 | Tdk Corp | Sintered compact for magnetic head slider, its producing method and magnetic head slider |
| JP2009026405A (en) * | 2007-07-20 | 2009-02-05 | Tdk Corp | Material for magnetic head slider, magnetic head slider, hard disk device, and manufacturing method of material for magnetic head slider |
-
1989
- 1989-01-28 JP JP1018910A patent/JPH0744111B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH02199808A (en) | 1990-08-08 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPH0622053B2 (en) | Substrate material | |
| JPS6323643B2 (en) | ||
| JPH062615B2 (en) | Magnetic head slider material | |
| US4902651A (en) | Material for magnetic head substrate member | |
| JP2003342058A (en) | Ceramic substrate material for thin film magnetic head | |
| JPS6354664B2 (en) | ||
| JPH0744111B2 (en) | Substrate material for thin film magnetic head | |
| JPS5918157A (en) | Aluminum oxide ceramic for cutting tool | |
| JPH0670925B2 (en) | Substrate material for thin film magnetic head | |
| JPS59190274A (en) | Silicon nitride sintered body and manufacture | |
| JPS5945969A (en) | High hardness high tenacity zirconium oxide ceramic and manufacture | |
| JPS59232971A (en) | Abrasion resistant sialon base ceramics | |
| JPH0531514B2 (en) | ||
| JP2571070B2 (en) | Method of manufacturing substrate material for thin film magnetic head | |
| JPS59199578A (en) | silicon nitride sintered body | |
| JP2858965B2 (en) | Aluminum oxide sintered body | |
| JPS6339115A (en) | Substrate material for thin film magnetic head | |
| JPH07315916A (en) | Substrate material for thin film head | |
| JPH07220238A (en) | Substrate material for magnetic head | |
| JPS6323641B2 (en) | ||
| JPS63100054A (en) | Material for magnetic head substrate | |
| JPS63134559A (en) | Non-magnetic ceramics for magnetic head | |
| US20090068498A1 (en) | Material of ceramic substrate for thin-film magnetic head | |
| JPS6323642B2 (en) | ||
| JPS6335587B2 (en) |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |