JPH06305823A - Sliding member material - Google Patents

Sliding member material

Info

Publication number
JPH06305823A
JPH06305823A JP5101337A JP10133793A JPH06305823A JP H06305823 A JPH06305823 A JP H06305823A JP 5101337 A JP5101337 A JP 5101337A JP 10133793 A JP10133793 A JP 10133793A JP H06305823 A JPH06305823 A JP H06305823A
Authority
JP
Japan
Prior art keywords
cao
sliding member
sliding
member material
fe2o3
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.)
Pending
Application number
JP5101337A
Other languages
Japanese (ja)
Inventor
Tsunehiko Nakamura
恒彦 中村
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.)
Kyocera Corp
Original Assignee
Kyocera 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 Kyocera Corp filed Critical Kyocera Corp
Priority to JP5101337A priority Critical patent/JPH06305823A/en
Publication of JPH06305823A publication Critical patent/JPH06305823A/en
Pending legal-status Critical Current

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  • Compositions Of Oxide Ceramics (AREA)
  • Powder Metallurgy (AREA)

Abstract

PURPOSE:To provide a sliding member material small in pore sizes, enhanced in surface smoothness and improved in sliding characteristics so as not to give defects, abrasion, etc., to the sliding member material by specifying a CaO/Fe2O3 ratio and surface roughness in a calcium ferrite. CONSTITUTION:The characteristic of this sliding member material comprises containing CaO and Fe2O3 as main components in a CaO/Fe2O3 molar ratio of 45/55 to 67/33 and having a surface roughness Ra of <=300Angstrom . The sliding member material has a composition represented by the composition formula of Ca2Fe2-xAlxO5 wherein 0<x<=1.2, and has a surface roughness Ra of <=300Angstrom . When the CaO/Fe2O3 molar ratio is smaller than the lower limit, the lowering of the sintering property of the sliding member material, the easy generation of pores and the deterioration of sliding characteristics are caused. When the CaO/Fe2O3 molar ratio is larger than the upper limit, the generation of a small amount of a CaO phase in the material, the enlargement of the sizes of the pores, and the remarkable deterioration of the sintering property are caused. When (x) exceeds the upper limit in the composition formula of Ca2Fe2-xAlxO5, the deterioration of the sintering property, the easy generation of the pores and the deterioration of the sliding characteristics are caused.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、例えば、磁気テープガ
イド等の帯材摺動部材、繊維用糸道等の線材摺動部材に
用いられる摺動部材料に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a sliding portion material used for a strip sliding member such as a magnetic tape guide or a wire sliding member such as a fiber yarn path.

【0002】[0002]

【従来技術】従来、磁気テープガイド等の帯材摺動部
材、繊維用糸道等の線材摺動部材等に用いられる摺動部
材料としては、チタニア,チタン酸バリウム,チタン酸
カルシウム,ルチル,アルミナ,ジルコニア等を主成分
とする焼結体が用いられている。
2. Description of the Related Art Conventionally, as sliding part materials used for band material sliding members such as magnetic tape guides and wire rod sliding members such as fiber yarn paths, titania, barium titanate, calcium titanate, rutile, A sintered body containing alumina, zirconia or the like as a main component is used.

【0003】[0003]

【発明が解決しようとする問題点】しかしながら、摺動
部材料として使用されるチタニア,アルミナ,ジルコニ
ア等を主成分とする焼結体は、その内部に生じるポア径
が大きく、また、焼結性が悪いという問題があった。こ
れにより、表面粗さRaも0.05μm程度で大きいと
いう問題があった。
However, a sintered body containing titania, alumina, zirconia or the like as a main component, which is used as a material for the sliding portion, has a large pore diameter generated therein and has a high sinterability. There was a problem that was bad. As a result, there is a problem that the surface roughness Ra is as large as about 0.05 μm.

【0004】即ち、摺動部材料として、チタニア,アル
ミナ,ジルコニア等を主成分とする焼結体を使用した場
合、例えば、磁気テープガイドでは磁性粉体の摩耗によ
る記憶内容の消失が問題となったり、また、繊維用糸道
の場合には白粉の発生や糸切れ等が発生するという問題
がある。即ち、磁気テープガイドの場合、磁気媒体を破
壊したり、データの破壊やヘッドの破損を生じ、磁気記
録装置の信頼性を著しく低下させるという問題があっ
た。特に近年では磁気テープが薄くなり、僅かな摺動性
の不調でも信頼性が低下するようになったため、ポアサ
イズの小さな磁気テープガイドが要求されるようになっ
ている。また、同時に磁気媒体と磁気テープガイドの摩
擦係数が大きいと磁気媒体へのダメージが大きく媒体を
傷つける要因となることが分かっている。これらの問題
を解決するため、近年では磁気テープ等の帯材や繊維等
の線材を摩耗させず、またキズを生じさせることがな
く、しかも、摩擦係数の小さい材料が要求されるように
なっている。
That is, when a sintered body containing titania, alumina, zirconia or the like as a main component is used as the material for the sliding portion, for example, in a magnetic tape guide, the loss of stored contents due to wear of the magnetic powder becomes a problem. In addition, in the case of a fiber yarn path, there is a problem that white powder is generated or yarn breakage occurs. That is, in the case of the magnetic tape guide, there is a problem that the magnetic medium is destroyed, the data is destroyed, and the head is destroyed, so that the reliability of the magnetic recording device is significantly lowered. Particularly in recent years, magnetic tapes have become thinner, and reliability has deteriorated even with slight slippage, so that magnetic tape guides having a small pore size are required. At the same time, it is known that if the friction coefficient between the magnetic medium and the magnetic tape guide is large, the damage to the magnetic medium is large and the medium is damaged. In order to solve these problems, in recent years, there has been a demand for a material that does not cause wear on a band material such as a magnetic tape or a wire material such as a fiber and does not cause scratches, and that has a small friction coefficient. There is.

【0005】[0005]

【問題点を解決するための手段】本発明者は、焼結体表
面に生じるポア径を小さくするとともに、焼結性を向上
すべく、種々の検討を重ねた結果、カルシウムフェライ
トにおいて酸化カルシウムと酸化鉄のモル比率を所定値
に特定し、表面粗さを所定値以下に限定することによ
り、摺動特性に優れた摺動部材を得ることができること
を突き止めた。
[Means for Solving the Problems] The inventors of the present invention have conducted various studies to reduce the pore diameter generated on the surface of the sintered body and to improve the sinterability. It has been found that a sliding member having excellent sliding characteristics can be obtained by specifying the molar ratio of iron oxide to a predetermined value and limiting the surface roughness to a predetermined value or less.

【0006】また、本発明者は、カルシウムフェライト
において鉄の一部をアルミニウムで置換した固溶体にお
いて鉄とアルミニウムのモル比率を所定値に設定し、表
面粗さを所定値以下に限定することにより、摺動特性に
優れた摺動部材を得ることができることを突き止めた。
Further, the present inventors set a molar ratio of iron and aluminum to a predetermined value in a solid solution in which a part of iron is replaced with aluminum in calcium ferrite, and limit the surface roughness to a predetermined value or less. It has been found that a sliding member having excellent sliding characteristics can be obtained.

【0007】即ち、本発明の摺動部材料は、CaOとF
2 3 を主成分として含有するとともに、CaO/F
2 3 で示されるモル比が45/55〜67/33で
あり、表面粗さRaが300Å以下であるものである。
また、Ca2 Fe2-X AlX5 で表される組成式にお
いて、0<X≦1.2であり、表面粗さRaが300Å
以下であるものである。
That is, the material of the sliding portion of the present invention is CaO and F.
with mainly containing e 2 O 3, CaO / F
The molar ratio represented by e 2 O 3 is 45/55 to 67/33 and the surface roughness Ra is 300 Å or less.
Further, in the composition formula represented by Ca 2 Fe 2 -X Al X O 5 , 0 <X ≦ 1.2 and the surface roughness Ra is 300Å
It is the following.

【0008】ここで、CaO/Fe2 3 で示されるモ
ル比を45/55〜67/33としたのは、モル比が4
5/55よりも小さいと(Fe2 3 が過剰)、焼結性
が低下し、ポアが発生し易くなり、摺動特性が劣化する
からである。一方、モル比が67/33よりも大きくな
ると(CaOが過剰)、材料中に微量のCaO相が生じ
ポアサイズが大きくなり、焼結性が著しく悪くなるから
である。CaOおよびFe2 3 の最も好ましい比率
は、CaO/Fe2 3 のモル比50/50〜66/3
4である。
The molar ratio represented by CaO / Fe 2 O 3 is 45/55 to 67/33 because the molar ratio is 4
If it is less than 5/55 (Fe 2 O 3 is excessive), the sinterability is lowered, pores are easily generated, and the sliding characteristics are deteriorated. On the other hand, when the molar ratio is larger than 67/33 (excessive amount of CaO), a small amount of CaO phase is generated in the material, the pore size is increased, and the sinterability is significantly deteriorated. The most preferable ratio of CaO and Fe 2 O 3 is the CaO / Fe 2 O 3 molar ratio of 50/50 to 66/3.
It is 4.

【0009】また、Ca2 Fe2-X AlX 5 で表され
る組成式において、0<X≦1.2としたのは、Xが
1.2を越えると焼結性が低下し、ポアが発生し易くな
り、摺動特性が劣化するようになるからである。
In the composition formula represented by Ca 2 Fe 2 -X Al X O 5 , 0 <X ≦ 1.2 means that when X exceeds 1.2, the sinterability decreases. This is because pores are likely to occur and sliding characteristics are deteriorated.

【0010】また、請求項1記載の磁器中に、Zr
2 ,TiO2 ,MgO,Al2 3 のうちの少なくと
も一種を合計で2重量%以下含有し、請求項2記載の磁
器中に、ZrO2 ,TiO2 ,MgOのうちの少なくと
も一種を合計で2重量%以下含有することが、焼結性向
上のため好ましい。即ち、ZrO2 ,TiO2 ,Mg
O,Al2 3 のうちの少なくとも一種が、合計で2重
量%よりも多く含有されている場合には、焼結性が悪く
なり、ポアサイズも大きくなる傾向にあるからである。
これらの酸化物は焼結助剤として別途添加する他、Ca
OやFe2 3 等の原料中や粉砕,混合等のボールの摩
耗により混入する場合もある。
Further, in the porcelain according to claim 1, Zr
The total content of at least one of O 2 , TiO 2 , MgO, and Al 2 O 3 is 2% by weight or less, and the porcelain according to claim 2 contains at least one of ZrO 2 , TiO 2 , and MgO. In order to improve the sinterability, it is preferable to contain 2% by weight or less. That is, ZrO 2 , TiO 2 , Mg
This is because if at least one of O and Al 2 O 3 is contained in a total amount of more than 2% by weight, the sinterability tends to deteriorate and the pore size tends to increase.
These oxides are added separately as a sintering aid, and Ca
It may be mixed in raw materials such as O and Fe 2 O 3 or by abrasion of balls such as crushing and mixing.

【0011】本発明の摺動部材料は、例えば、純度99
%以上のFe2 3 (不純物としてNb2 5 ,Ba
O,SiO2 ,SrO等を含む)を使い、CaO源とし
てCaCl2 ,CaCO3 およびAl2 3 等を使用
し、これらを所定量秤量し、この後ボールミル等を用い
て湿式混合し、これを乾燥し、乾燥後の原料を酸化性雰
囲気(大気中)において800〜1200℃で2〜10
時間仮焼し、仮焼後の原料を平均粒径が所定以下となる
ように微粉砕する。そして、これにバインダーを加えて
造粒を行った後、所定圧力でプレス成形し焼成すること
により得られる。焼成方法としては酸化性雰囲気(大気
中)において1100〜1350℃の常圧で焼成する。
この焼結体のポア径を小さくするため、さらに焼結体を
Ar雰囲気またはN2 雰囲気中において1000〜13
00℃でHIP処理しても良い。
The sliding portion material of the present invention has, for example, a purity of 99.
% Fe 2 O 3 (Nb 2 O 5 , Ba as impurities
(Including O, SiO 2 , SrO, etc.) and CaCl 2 , CaCO 3, Al 2 O 3, etc. as CaO sources, weighed a predetermined amount of them, and then wet-mixed them with a ball mill or the like. And the raw material after drying is heated at 800 to 1200 ° C. for 2 to 10 in an oxidizing atmosphere (in the air).
The material is calcined for a period of time, and the raw material after calcination is finely pulverized so that the average particle diameter becomes a predetermined value or less. Then, it is obtained by adding a binder to this, granulating, press-molding at a predetermined pressure and firing. As a firing method, firing is performed at a normal pressure of 1100 to 1350 ° C. in an oxidizing atmosphere (in the air).
In order to reduce the pore diameter of this sintered body, the sintered body was further heated to 1000 to 13 in an Ar atmosphere or an N 2 atmosphere.
You may perform HIP processing at 00 degreeC.

【0012】[0012]

【作用】本発明の摺動部材料では、ポアサイズが小さ
く、表面の平滑性に優れ、摺動材へのキズや摩耗等のダ
メージを与えることがなく、摺動特性を向上することが
可能となる。
With the sliding material of the present invention, the pore size is small, the surface is smooth, and the sliding characteristics can be improved without damaging the sliding material such as scratches and abrasion. Become.

【0013】[0013]

【実施例】【Example】

(実施例1)市販されている純度99%以上のFe2
3 (不純物としてNb2 5 ,BaO,SiO2 ,Sr
O等を1重量%以下含む)を使い、CaO源としてCa
Cl2 ,CaCO3 等を使用し、表1に示すような組成
比となるように秤量し、ボールミルを用いて湿式混合し
た。これを乾燥し、乾燥後の原料を酸化性雰囲気(大気
中)において1000℃で6時間仮焼を行った。
(Example 1) Commercially available Fe 2 O having a purity of 99% or more
3 (Nb 2 O 5 , BaO, SiO 2 , Sr as impurities
(Including O and the like in an amount of 1% by weight or less) as a CaO source
Cl 2 , CaCO 3, etc. were used, weighed so as to have the composition ratio shown in Table 1, and wet-mixed using a ball mill. This was dried, and the raw material after drying was calcined at 1000 ° C. for 6 hours in an oxidizing atmosphere (in the air).

【0014】仮焼後の原料をアルミナボールまたはジル
コニアボール,メノーボール等を用い平均粒径が2μm
以下となるように微粉砕した。尚、この粉砕によりジル
コニアまたはアルミナ,シリカ等が1重量%以下混入す
ることがある。これにバインダーを加えて造粒を行った
後、0.8〜2.0ton/cm2 の圧力でプレス成形した。
その後、酸化性雰囲気(大気中)において表1の温度で
焼成し、ガス種Arにより1100℃の温度で2000
気圧の熱間静水圧処理を行い、各試料を得た。
Alumina balls, zirconia balls, meno balls, etc. are used as the raw material after calcination and the average particle size is 2 μm.
Finely pulverized to the following. Incidentally, zirconia, alumina, silica or the like may be mixed in an amount of 1% by weight or less by this pulverization. After adding a binder to this and granulating, it was press-molded at a pressure of 0.8 to 2.0 ton / cm 2 .
Then, it is fired at a temperature shown in Table 1 in an oxidizing atmosphere (in the air), and 2000 at a temperature of 1100 ° C. by a gas species Ar.
Each sample was obtained by performing hot isostatic treatment at atmospheric pressure.

【0015】得られた試料について熱膨張係数,ポア
率,焼結性について調べ、表1に結果を記した。
The thermal expansion coefficient, the porosity, and the sinterability of the obtained sample were investigated, and the results are shown in Table 1.

【0016】[0016]

【表1】 [Table 1]

【0017】ここで、熱膨張係数は熱膨張係数測定装置
により求め、ポア率は1μmのダイヤモンド砥粒による
最終ラップ面に生じるポア径を測定することにより評価
した。ポア率はポア平均径が5μm以上を×,2〜5μ
mを△,1〜2μmを○,1μm以下を□で示した。焼
結性は吸水率2%以上を×,1〜2%を△,0.5〜1
%を○,0.5%以下を□で示した。
Here, the thermal expansion coefficient was determined by a thermal expansion coefficient measuring device, and the pore ratio was evaluated by measuring the pore diameter generated on the final lap surface by the diamond abrasive grains of 1 μm. Pore ratio is x when the average pore diameter is 5 μm or more, 2 to 5 μm
m is represented by Δ, 1 to 2 μm is represented by ◯, and 1 μm or less is represented by □. Sinterability is x for water absorption of 2% or more, △ for 1-2%, 0.5-1
% Is indicated by ◯, and 0.5% or less is indicated by □.

【0018】また、表1の試料No.1〜13について、
砥粒径0.25μmのダイヤモンド砥粒を用いて2本の
レールを有する磁気ヘッドのスライダー形状に加工し、
取付金具を介してディスク上にセットした。そして、デ
ィスクの最大回転数を3600rpmとして回転と停止
(CSS)を繰り返した。即ち、最大回転数に達するま
での時間を5秒とし最大回転数を5秒間保持した。ま
た、最大回転数から停止までの時間を4秒、停止時間を
5秒として停止状態から回転し停止するまでの19秒サ
イクルをCSS回数1回とした。CSS回数の5000
回毎にディスクと試料の傷の有無及び回転開始時の最大
摩擦係数,表面粗さRaを調べ、この結果を表2に記載
した。
For samples Nos. 1 to 13 in Table 1,
Using a diamond abrasive grain with an abrasive grain size of 0.25 μm, it is processed into a slider shape of a magnetic head having two rails.
It was set on the disc through the mounting bracket. Then, the maximum rotation number of the disk was set to 3600 rpm, and rotation and stop (CSS) were repeated. That is, the time required to reach the maximum rotation speed was 5 seconds and the maximum rotation speed was held for 5 seconds. Further, the time from the maximum rotation speed to the stop was 4 seconds, the stop time was 5 seconds, and the 19-second cycle from the stopped state to the rotation and stop was set to one CSS number. 5000 times of CSS
The presence or absence of scratches on the disk and the sample, the maximum friction coefficient at the start of rotation, and the surface roughness Ra were examined every time, and the results are shown in Table 2.

【0019】[0019]

【表2】 [Table 2]

【0020】表1,2の結果において、試料No.2〜
6は本発明の範囲内の摺動部材料であり、ポア率および
焼結性は良好であった。これに対し、試料No.1はC
aOが若干多いため、焼結性が劣っている。また、試料
No.7およびNo.8は酸化鉄が多く、焼結性が劣っ
ている。一方、試料No.2〜6については、表2の結
果より優れた摺動特性を有することが判る。
In the results of Tables 1 and 2, sample No. 2 to
No. 6 was a sliding part material within the range of the present invention, and the porosity and sinterability were good. On the other hand, the sample No. 1 is C
Since the amount of aO is slightly large, the sinterability is poor. In addition, the sample No. 7 and No. No. 8 had a large amount of iron oxide and was inferior in sinterability. On the other hand, sample No. As for 2 to 6, it is understood from the results in Table 2 that the sliding characteristics are superior.

【0021】尚、試料No.9〜11は、純度99.9
%のFe2 3 を使用した場合であり、試料No.9,
10については本発明の範囲内の摺動部材料で、ポア率
および焼結性は良好である。これに対し、試料No.1
1はFe2 3 が多く、ポア率,焼結性が劣っている。
Sample No. 9 to 11 have a purity of 99.9.
% Fe 2 O 3 was used, and sample No. 9,
No. 10 is a sliding part material within the scope of the present invention, and has a good porosity and sinterability. On the other hand, the sample No. 1
No. 1 has a large amount of Fe 2 O 3 and is inferior in porosity and sinterability.

【0022】さらに、表1における試料No.2,3,
9,10の組成に対して、ZrO2 ,TiO2 ,Mg
O,Al2 3 を表3に示したような組成となるように
秤量混合し、成形した後、表3の温度で焼成し、ガス種
Arにより1100℃の温度で2000気圧の熱間静水
圧処理を行い、この磁器を上記と同様の方法により、熱
膨張係数,ポア率,焼結性を調べ、その結果を表3に記
載した。
Further, the samples No. 2, 3, and 3 in Table 1
For compositions of 9 and 10, ZrO 2 , TiO 2 , Mg
O, Al 2 O 3 were weighed and mixed so as to have the composition shown in Table 3, molded, and then fired at the temperature shown in Table 3, and hot static at 2000 atm at a temperature of 1100 ° C. with a gas species Ar. Hydrothermal treatment was carried out, and the porcelain was examined for thermal expansion coefficient, porosity and sinterability by the same method as described above, and the results are shown in Table 3.

【0023】[0023]

【表3】 [Table 3]

【0024】この表3により、ZrO2 ,MgO,Ti
2 ,Al2 3 を2重量%以下添加することにより、
無添加のNo.2,3,9,10に比較して焼結性が良く
なることが判る。
According to Table 3, ZrO 2 , MgO, Ti
By adding 2% by weight or less of O 2 and Al 2 O 3 ,
It can be seen that the sinterability is improved as compared with No. 2, 3, 9, and 10 without addition.

【0025】(実施例2)市販されている純度99%以
上のFe2 3 (不純物としてNb2 5 ,BaO,S
iO2 ,SrO等を1重量%以下含む)を使い、CaO
源としてCaCl2 ,CaCO3 、およびAl2 3
使用し、ボールミルを用いて湿式混合した。これを乾燥
し、乾燥後の原料を酸化性雰囲気(大気中)において1
000℃で6時間仮焼を行った。
Example 2 Commercially available Fe 2 O 3 having a purity of 99% or more (Nb 2 O 5 , BaO, S as impurities)
(including 1% by weight or less of iO 2 , SrO, etc.)
CaCl 2 , CaCO 3 , and Al 2 O 3 were used as sources, and wet mixed using a ball mill. This is dried, and the raw material after drying is subjected to 1 in an oxidizing atmosphere (in the air).
Calcination was performed at 000 ° C. for 6 hours.

【0026】仮焼後の原料をアルミナボールまたはジル
コニアボール,メノーボール等を用い平均粒径が1μm
以下となるように微粉砕した。尚、この粉砕によりジル
コニアまたはアルミナ,シリカ等が1重量%以下混入す
ることがある。これにバインダーを加えて造粒を行った
後、0.8〜2.0ton/cm2 の圧力でプレス成形した。
その後、酸化性雰囲気(大気中)において表4の温度で
焼成し、引き続きガス種Arにより1100℃で200
0気圧で熱間静水圧処理(HIP処理)を行い、Ca2
Fe2-X AlX 5 で表わすと表4に示すようなXの値
を採る焼結体を得た。得られた試料について実施例1と
同様にして熱膨張係数,ポア率,焼結性について調べ、
表4に結果を記した。尚、得られた試料の結晶をX線回
折装置により調べた結果、斜方晶を主体としていること
を確認した。
Alumina balls, zirconia balls, meno balls, etc. are used as the raw material after calcination and the average particle size is 1 μm.
Finely pulverized to the following. Incidentally, zirconia, alumina, silica or the like may be mixed in an amount of 1% by weight or less by this pulverization. After adding a binder to this and granulating, it was press-molded at a pressure of 0.8 to 2.0 ton / cm 2 .
Then, it is fired at a temperature shown in Table 4 in an oxidizing atmosphere (in the air), and then at 200 ° C. at 1100 ° C. with a gas species Ar.
Hot isostatic pressure treatment (HIP treatment) was performed at 0 atm, and Ca 2
When expressed by Fe 2−x Al x O 5 , a sintered body having a value of X as shown in Table 4 was obtained. The obtained sample was examined for the coefficient of thermal expansion, the porosity, and the sinterability in the same manner as in Example 1,
The results are shown in Table 4. As a result of examining the crystals of the obtained sample with an X-ray diffractometer, it was confirmed that the crystals were mainly orthorhombic.

【0027】[0027]

【表4】 [Table 4]

【0028】この表4より、試料No.18〜22は本発
明の範囲内のものであり、ポア率及び焼結性が良好であ
る。これに対して試料No.23及び24はアルミニウム
が多くポアサイズが試料No.18〜22よりも大きい。
From Table 4, Sample Nos. 18 to 22 are within the scope of the present invention, and have good porosity and sinterability. On the other hand, Samples Nos. 23 and 24 contained a large amount of aluminum and had a larger pore size than Samples Nos. 18-22.

【0029】そして、本発明者は、これらの試料を、2
本のレールを有する磁気ヘッドのスライダー形状に加工
し、取付金具を介してディスク上にセットし、実施例1
と同様にしてディスクと試料の傷の有無および表面粗さ
Raを調べ、この結果を表5に記載した。
The present inventor then applied these samples to
A magnetic head having two rails was processed into a slider shape, and the magnetic head was set on a disk through a mounting bracket.
The presence or absence of scratches on the disk and the sample and the surface roughness Ra were examined in the same manner as in, and the results are shown in Table 5.

【0030】[0030]

【表5】 [Table 5]

【0031】表5から本発明の材料ではディスクに傷が
入り難く、摺動特性が優れていることが判る。
From Table 5, it can be seen that the material of the present invention hardly scratches the disk and has excellent sliding characteristics.

【0032】(実施例3)市販されている純度99%以
上の酸化鉄(不純物としてNb2 5 ,BaO,SiO
2 ,SrO等を1重量%以下含む)を使い、酸化カルシ
ウム(CaO)源として塩化カルシウム(CaC
2 ),炭酸カルシウム(CaCO3 )、および酸化ア
ルミニウム(Al2 3 )を使い、さらに焼結体中にお
けるZrO2 ,MgO,TiO2 の含有量が表6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
合した。後は上記実施例2と同様にして成形,焼成,H
IP処理を行い、各試料を得た。得られた試料について
実施例1と同様に熱膨張係数,ポア率,焼結性について
調べ、表6に記した。
Example 3 Commercially available iron oxide with a purity of 99% or more (Nb 2 O 5 , BaO, SiO as impurities)
2 , containing 1% by weight or less of SrO, etc., and calcium chloride (CaC) as a source of calcium oxide (CaO).
l 2 ), calcium carbonate (CaCO 3 ), and aluminum oxide (Al 2 O 3 ) are used, and the content of ZrO 2 , MgO, and TiO 2 in the sintered body is adjusted so that the composition ratio shown in Table 6 is obtained. Weighed and wet mixed using a ball mill. Thereafter, molding, firing, and H are performed in the same manner as in Example 2 above.
IP treatment was performed to obtain each sample. The thermal expansion coefficient, the porosity, and the sinterability of the obtained sample were examined in the same manner as in Example 1 and shown in Table 6.

【0033】[0033]

【表6】 [Table 6]

【0034】表6により、ZrO2 ,MgO,TiO2
を2重量%以下含有することにより焼結性が良くなるこ
とが判る。
According to Table 6, ZrO 2 , MgO, TiO 2
It can be seen that the sinterability is improved by containing 2% by weight or less.

【0035】[0035]

【発明の効果】以上詳述した通り、本発明の摺動部材料
では、ポアサイズが小さく、表面の平滑性に優れ、摺動
材へのキズや摩耗等のダメージを与えることがなく、摺
動特性を大幅に向上することができる。これにより、例
えば、本発明の摺動部材料を磁気テープガイドに適用し
た場合には、このガイドによる磁性粉体の摩耗が殆ど生
じることがなく、記憶内容が消失する等の問題が生じる
ことがなく、また、繊維用糸道ガイドに本発明の材料を
適用した場合には白粉の発生や糸切れ等が発生すること
を確実に防止することができる。
As described in detail above, in the sliding part material of the present invention, the pore size is small, the surface is excellent in smoothness, and the sliding member is free from damage such as scratches and abrasion. The characteristics can be greatly improved. As a result, for example, when the sliding portion material of the present invention is applied to a magnetic tape guide, wear of the magnetic powder due to this guide hardly occurs, and problems such as loss of stored contents may occur. Moreover, when the material of the present invention is applied to the fiber yarn path guide, it is possible to reliably prevent generation of white powder, yarn breakage, and the like.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】CaOとFe2 3 を主成分として含有す
るとともに、CaO/Fe2 3 で示されるモル比が4
5/55〜67/33であり、表面粗さRaが300Å
以下であることを特徴とする摺動部材料。
1. A composition containing CaO and Fe 2 O 3 as main components and having a molar ratio of CaO / Fe 2 O 3 of 4
5/55 to 67/33 and surface roughness Ra of 300Å
The following is a sliding part material characterized by the following.
【請求項2】Ca2 Fe2-X AlX 5 で表される組成
式において、0<X≦1.2であり、表面粗さRaが3
00Å以下であることを特徴とする摺動部材料。
2. In the composition formula represented by Ca 2 Fe 2 -X Al X O 5 , 0 <X ≦ 1.2 and the surface roughness Ra is 3
Sliding part material characterized by being less than 00Å.
JP5101337A 1993-04-27 1993-04-27 Sliding member material Pending JPH06305823A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5101337A JPH06305823A (en) 1993-04-27 1993-04-27 Sliding member material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5101337A JPH06305823A (en) 1993-04-27 1993-04-27 Sliding member material

Publications (1)

Publication Number Publication Date
JPH06305823A true JPH06305823A (en) 1994-11-01

Family

ID=14298030

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5101337A Pending JPH06305823A (en) 1993-04-27 1993-04-27 Sliding member material

Country Status (1)

Country Link
JP (1) JPH06305823A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007039331A (en) * 2006-09-25 2007-02-15 Toshiba Corp Method of manufacturing silicon nitride sintered compact, method of manufacturing chemical resistant member using the same and method of manufacturing bearing member

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007039331A (en) * 2006-09-25 2007-02-15 Toshiba Corp Method of manufacturing silicon nitride sintered compact, method of manufacturing chemical resistant member using the same and method of manufacturing bearing member

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