JPS59131575A - Abrasion resistant sliding material - Google Patents

Abrasion resistant sliding material

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Publication number
JPS59131575A
JPS59131575A JP58004962A JP496283A JPS59131575A JP S59131575 A JPS59131575 A JP S59131575A JP 58004962 A JP58004962 A JP 58004962A JP 496283 A JP496283 A JP 496283A JP S59131575 A JPS59131575 A JP S59131575A
Authority
JP
Japan
Prior art keywords
wear
sliding
friction
sliding material
graphite
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.)
Granted
Application number
JP58004962A
Other languages
Japanese (ja)
Other versions
JPS6127351B2 (en
Inventor
佐々木 卓男
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.)
Nok Corp
Original Assignee
Nippon Oil Seal Industry 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 Nippon Oil Seal Industry Co Ltd filed Critical Nippon Oil Seal Industry Co Ltd
Priority to JP58004962A priority Critical patent/JPS59131575A/en
Publication of JPS59131575A publication Critical patent/JPS59131575A/en
Publication of JPS6127351B2 publication Critical patent/JPS6127351B2/ja
Granted legal-status Critical Current

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Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本発明は、耐摩耗性摺動材料に関する。更に詳しくは、
無給油でも高温迄使用可能な耐摩耗性摺動材料に関する
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to wear-resistant sliding materials. For more details,
This invention relates to wear-resistant sliding materials that can be used up to high temperatures even without lubrication.

無給油で高温迄使用可能な摺動材料としては、従来から
黒鉛軸受があり、これがすべり軸受として用いられてい
る。黒鉛軸受は、耐薬品性にすぐれかつ自己潤滑性があ
るため、無給油で高温迄使用できるものの、気孔率が大
きく、そのため機械的強度に劣るのが大きな欠点となっ
ている。
As a sliding material that can be used up to high temperatures without lubrication, graphite bearings have been used as sliding bearings. Graphite bearings have excellent chemical resistance and self-lubricating properties, so they can be used up to high temperatures without lubrication, but a major drawback is that they have a large porosity and therefore poor mechanical strength.

そこで、この機械的強度を補強する意味などから、気孔
部に熱硬化性樹脂や比吹的低融点の金属を含浸させるこ
とが行わ汎ている。しかしながら、含浸物質たる樹脂ま
たは金属は、高温高圧下では膨張、分解、溶融、浸出な
どがひき起される。その結果、樹脂を含浸した場合には
、樹脂の変質、分解があるため、耐熱湿度は200℃以
下となり、また黒鉛と樹脂との熱膨張係数が異なること
が原因となって、ブリスタリング現象(火ぶくれ現象)
が起る。また、金属を含浸した場合には、耐薬品性、耐
食性が悪くなり、また摺動特性も低下し、焼付現象が発
生するようになる。
Therefore, for the purpose of reinforcing this mechanical strength, it is common practice to impregnate the pores with a thermosetting resin or a metal with a relatively low melting point. However, the impregnating material, resin or metal, expands, decomposes, melts, leaches, etc. under high temperature and high pressure. As a result, when impregnated with resin, the heat and humidity resistance is lower than 200°C due to deterioration and decomposition of the resin, and the difference in thermal expansion coefficient between graphite and resin causes the blistering phenomenon ( blistering phenomenon)
happens. Furthermore, when impregnated with metal, chemical resistance and corrosion resistance deteriorate, sliding properties also deteriorate, and seizure phenomenon occurs.

更に、青銅系、鉄系の金属母材中に粉末冶金法によって
黒鉛、二硫化モリブデンなどを均一に分散させた固体潤
滑剤分散型焼結金属軸受なども用いられており、これは
黒鉛軸受に比べ、機械的強度は改善され、しかも無給油
で高潟迄使用できるが、累地が金属であるので、耐薬品
性、耐食性に劣り・かつ高温では耐摩耗性に劣るばかり
ではなく、酸化膨張のため軸受内径が収縮し、軸受隙間
に影響を与えるなどの欠点がみられる。
Furthermore, solid lubricant-dispersed sintered metal bearings are also used, in which graphite, molybdenum disulfide, etc. are uniformly dispersed in a bronze-based or iron-based metal base material using a powder metallurgy method. Compared to this, the mechanical strength is improved and it can be used up to Takagata without lubrication, but since the base is made of metal, it has poor chemical resistance and corrosion resistance, and is not only inferior in wear resistance at high temperatures, but also suffers from oxidation expansion. Therefore, there are drawbacks such as the inner diameter of the bearing shrinking and affecting the bearing clearance.

この他に、プラスチック軸受、焼結含油軸受も用いられ
ているが、これらは材料そのものの耐熱温度あるいは含
浸された潤滑油の寿命などを考慮した使用限界温度から
、フッ素樹脂軸受を除いては、約80〜120℃あるい
はそれ以下の温度で実際には使用される。また、フッ素
樹脂軸受は、耐熱湿度が約250℃と高いばかりではな
く、摩擦係数が低く、耐薬品性にもすぐれているなどの
特性を有しているが、反面柔かく、クリープし易いとい
う欠点を有している。特に、血圧が大きくなったり、高
温になる程クリープが大きく、変形、流れ出しなどの障
害が起る。更に、熱膨張係数が10−5のオーダーで金
属より一桁大きく、このような熱膨張係数やクリープの
ため、実用的には200℃以下で使用されることが多い
In addition to these, plastic bearings and sintered oil-impregnated bearings are also used, but with the exception of fluororesin bearings, these have a limited operating temperature that takes into consideration the heat resistance temperature of the material itself or the lifespan of the lubricating oil impregnated with it. In practice, it is used at temperatures of about 80-120°C or lower. In addition, fluororesin bearings not only have high heat and humidity resistance of about 250°C, but also have characteristics such as a low coefficient of friction and excellent chemical resistance, but on the other hand, they have the disadvantage of being soft and prone to creep. have. In particular, the higher the blood pressure or the higher the temperature, the greater the creep, causing problems such as deformation and outflow. Furthermore, the coefficient of thermal expansion is on the order of 10-5, which is one order of magnitude larger than that of metals, and because of such coefficient of thermal expansion and creep, it is often used practically at temperatures below 200°C.

本発明は、このような欠点をいずれも示さない耐摩耗性
jjす動材料を提供するものであり、ガラス状炭素材料
および固体潤滑剤窒化ホウ素よりなる本発明の耐摩擦性
摺動材料は、無給油のまま大気中では約450℃迄、ま
た不活・准ガス雰囲気中では約2500℃の高温迄自己
潤滑性が保持されている。
The present invention provides a wear-resistant sliding material that does not exhibit any of these drawbacks, and the friction-resistant sliding material of the present invention, which is made of a glassy carbon material and a solid lubricant boron nitride, Self-lubricating properties are maintained up to about 450°C in the air without oil, and up to about 2500°C in an inert/semi-gas atmosphere.

ガラス状炭素材料は、フラン系樹脂、フェノール系樹脂
またはこれらの混合樹脂の硬化成形体を高温、一般には
約1000℃以上の温度の不活性雰囲気中で焼成して炭
化させ、必要に応じてこれを更に黒鉛化することによっ
て得られる。また、水素/炭素原子比(Hlo )を調
整したピッチから誘匈プされた酸素官能基を有する炭素
前駆体物質を粉末成形後、同様に焼成して炭化し、必要
に応じてこれを更に黒鉛化することによって得られる。
Glassy carbon materials are produced by carbonizing a cured molded product of furan resin, phenol resin, or a mixture thereof in an inert atmosphere at a high temperature, generally at a temperature of about 1000°C or higher, and if necessary. It can be obtained by further graphitizing. In addition, a carbon precursor material having an oxygen functional group induced from a pitch with an adjusted hydrogen/carbon atomic ratio (Hlo) is powder-molded, then similarly fired and carbonized, and if necessary, this is further added to graphite. It can be obtained by converting

必要に応じて行われる黒鉛化処理は、一旦焼成させたも
のを黒鉛化炉を用いて約2000〜3000℃で長時間
高温処理す−ることによって行われる。ただし、ガラス
状炭素材料は難黒鉛化性利料であり、このような高温熱
処理を行なっても、黒鉛化はわずかに進行する程度であ
るが、この黒鉛化によって、潤滑性に乏しいガラス状炭
素材料が金属間接触を発生させた場合などに、黒鉛構造
を発達させることにより、硬度は若干低下するものの、
潤滑性をより良好とさせる。
Graphitization treatment, which is performed as necessary, is performed by subjecting the fired material to high temperature treatment for a long time at about 2000 to 3000° C. using a graphitization furnace. However, glassy carbon materials are difficult to graphitize, and graphitization only slightly progresses even with such high-temperature heat treatment. Although the hardness decreases slightly due to the development of a graphite structure when the material causes metal-to-metal contact,
Improves lubricity.

これらのガラス状炭素材料は、黒鉛などと同様に比重が
軽いが、非常に硬質で強度も大きく、耐薬品性、耐食性
にすぐれ、耐熱性も大気中で約450℃、また不活性ガ
ス雰囲気中で約2500℃と高く、更に比強度のきわめ
て高い新炭素材料であり、主としてルツボ、ボート、ヒ
ーター、電極などの用途に従来から用いられている。
These glassy carbon materials have a light specific gravity like graphite, but are very hard and strong, have excellent chemical resistance and corrosion resistance, and have a heat resistance of about 450°C in the air and in an inert gas atmosphere. It is a new carbon material with a high temperature of about 2,500°C and an extremely high specific strength, and has traditionally been used mainly for applications such as crucibles, boats, heaters, and electrodes.

かかるガラス状炭素材料に配合される固体潤滑剤として
の窒化ホウ素は、その結晶構造が黒鉛のそれと類似する
六角網面の積み重なりを持つため・潤滑性の点で非常に
すぐれている。しかも、それの分解温度は約3000℃
と高く、従って空気中では約゛700〜900℃、また
不活性ガス雰囲気中では約2800℃迄の高温で使用す
ることができる。
Boron nitride, which is used as a solid lubricant to be blended into such a glassy carbon material, has extremely good lubricity because its crystal structure has a stack of hexagonal mesh planes similar to that of graphite. Moreover, its decomposition temperature is approximately 3000℃.
Therefore, it can be used at high temperatures of about 700 to 900°C in air and up to about 2800°C in an inert gas atmosphere.

窒化ホウ素は、ガラス状炭素材料との配合物中約5〜5
0重量%の配合割合で用いられる。これより少ない使用
割合では、得られる摺動材料が潤滑性に欠け、摩擦係数
も高く、耐摩耗性にも劣るようになる。一方、これより
多い割合で用いられると、硬度が低くなり、曲げ強度、
圧縮強度などの機械的強度が不足するばかりではなく、
後述するように、摺動材料を製造するための硬化あるい
は粉末成形体の製作を困難とする。
Boron nitride is present in the blend with the glassy carbon material at about 5 to 5
It is used at a blending ratio of 0% by weight. If the usage rate is less than this, the resulting sliding material will lack lubricity, have a high coefficient of friction, and have poor wear resistance. On the other hand, if it is used in a higher proportion than this, the hardness will decrease and the bending strength will decrease.
Not only does it lack mechanical strength such as compressive strength,
As will be described later, this makes it difficult to harden or produce powder compacts for producing sliding materials.

摺動材料の製造は、ガラス状炭素材料形成材料と窒化ホ
ウ素との均一配合物を所定形状に成形した後、これをガ
ラス状炭素材料形成材料の焼成温度で炭化させることに
より行われる。樹脂の硬化成形体を用いる場合には、窒
化ホウ素との配合物単独からは厚さ3711111程度
の摺動材料しか製造し得ないので、一般には黒鉛などの
炭素材料あるいは酸素官能基含有炭素前駆体物質の焼成
品から形成される、基材としての成形体上に被覆させた
形で用いられる。この場合、樹脂が炭素材料などの基材
成形体の気孔部に含浸されるので、被膜が成形体に強固
に接着されると同時に、成形体自体の強度もそれによっ
て向上する。1だ、酸素官能基含有炭素前駆体物質がガ
ラス状炭素材料形成材料として用いられる場合には、窒
イ1=ホウ素との均一配合粉末を常温加圧下に任意の厚
さで所定形状に粉末成形した後、焼成、炭化が行われる
。なお、このようにして製造される摺動材料は、ガラス
状炭素材料を素地としているため、十分な機械的強度を
有しているが、それを更に向上させるためには、そこに
炭素線維、黒鉛線−維などを配合し、カーボン−カーボ
ン複合材料とすることもできる。
The sliding material is manufactured by forming a uniform mixture of a glassy carbon material forming material and boron nitride into a predetermined shape, and then carbonizing the mixture at the firing temperature of the glassy carbon material forming material. When using a cured molded resin, a sliding material with a thickness of about 3711111 can only be produced from a compound with boron nitride alone, so carbon materials such as graphite or carbon precursors containing oxygen functional groups are generally used. It is used in the form of a coating on a molded body as a base material, which is formed from a fired product of the substance. In this case, since the resin is impregnated into the pores of the molded body made of a base material such as a carbon material, the coating is firmly adhered to the molded body, and at the same time, the strength of the molded body itself is improved thereby. 1. When an oxygen functional group-containing carbon precursor substance is used as a material for forming a glassy carbon material, a uniformly mixed powder of nitrogen and boron is powder-molded into a predetermined shape with an arbitrary thickness under pressure at room temperature. After that, firing and carbonization are performed. The sliding material manufactured in this way has sufficient mechanical strength because it is made of glassy carbon material, but in order to further improve it, it is necessary to add carbon fiber, A carbon-carbon composite material can also be obtained by blending graphite fibers or the like.

本発明に係る摺動材料は、非常に硬質で強度が犬きく、
シかも耐熱性のあるガラス状炭素材料を素地月利とし、
これに固体潤滑剤としての窒化ホウ素を含有せしめてい
るため、耐摩耗性にすぐれ、大気中では約450℃、ま
た不活性ガス雰囲気中では約2500℃の高湿迄潤滑性
を保持し・ている。更に、耐薬品性、耐食性にすぐれ、
高温進化学的にも安定であるので、従来の金属含浸黒鉛
軸受や黒鉛分散型焼結金属軸受にみられた耐薬品性、耐
食性に劣るという欠点あるいは酸化膨張などという現象
は、いずれも存在しない。また、高温でも、フッ素樹月
旨軸受にみられるようなりリーブし易し)と依Aう現象
もなく、熱膨張係数も鉄より若干低い程度であり、軸受
隙間のコントロールなども容易である。
The sliding material according to the present invention is extremely hard and has high strength.
The substrate is made of heat-resistant glassy carbon material,
Because it contains boron nitride as a solid lubricant, it has excellent wear resistance and maintains lubricity up to approximately 450°C in the atmosphere and at high humidity of approximately 2500°C in an inert gas atmosphere. There is. Furthermore, it has excellent chemical resistance and corrosion resistance,
Since it is stable even at high temperatures, it does not suffer from the disadvantages of poor chemical resistance and corrosion resistance, or oxidation expansion, which were observed in conventional metal-impregnated graphite bearings and graphite-dispersed sintered metal bearings. . In addition, even at high temperatures, it does not suffer from the phenomenon of reeving seen in fluorine wood bearings, and its coefficient of thermal expansion is slightly lower than that of iron, making it easy to control the bearing clearance.

次に、実施例について本発明を説明する。Next, the present invention will be explained with reference to examples.

実施例]− ピッチから誘導された酸素官能基含有炭素前駆体物質(
粒径10μ以下)80重量部および窒化ホウ外(粒径5
 It以下)20重位部の均一配合粉末を、常温下に成
形圧力3000 rで、直径60詣、厚さ10閲の円板
状に粉末成形し、不活性界’dM気中30℃/hrの昇
温速度で1000℃迄昇湿させ、炭素前駆体物質の炭化
を行なった。
Examples] - Oxygen functional group-containing carbon precursor material derived from pitch (
80 parts by weight (particle size 10μ or less) and 80 parts by weight (particle size 5
20 weight parts of uniformly mixed powder was powder-molded into a disc shape with a diameter of 60 cm and a thickness of 10 cm at room temperature at a molding pressure of 3000 r, and then heated at 30°C/hr in an inert atmosphere 'dM. The carbon precursor material was carbonized by raising the temperature to 1000° C. at a heating rate of .

比較例1 実施例1において、窒化ホウ素を用いずに円板体の粉末
成形およびそれの炭化を行なった。
Comparative Example 1 In Example 1, a disk was powder-molded and carbonized without using boron nitride.

実施例1および比較例1で焼成された円板体(表面粗さ
3s)の北特性値を測定し、その結果を次の表1に示し
た。
The north characteristic values of the disk bodies (surface roughness 3s) fired in Example 1 and Comparative Example 1 were measured, and the results are shown in Table 1 below.

表1 項  目       実施例1   比較例1かさ密
度 (りA11)   1.72 、   1.59開
気孔率 (容量%)   5.4    4.3ショア
硬度   (HS)    119     128曲
げ強度  (〜)   820   910圧縮強度 
 (η)   4400   4900また、これらの
焼成円板体を試験片に用い、鈴木式摩擦間耗試験機(ス
ラストタイプ試験機)を用いて、摩擦摩耗特性を調べた
。摩擦M耗試験は、この試験片の上に、内径2Qfl1
71.外径25.6 mmの円柱状相手材(5450浸
炭焼入、硬度HRC51〜54、表面粗さ1s、摺動面
積2i)を固定させるようにして載せ、下記条件下で試
験片の方を回転させることにより行われた。
Table 1 Item Example 1 Comparative Example 1 Bulk density (A11) 1.72, 1.59 Open porosity (volume %) 5.4 4.3 Shore hardness (HS) 119 128 Bending strength (~) 820 910 compressive strength
(η) 4400 4900 Furthermore, using these fired disk bodies as test pieces, the friction and wear characteristics were examined using a Suzuki type friction and wear tester (thrust type tester). In the friction wear test, an inner diameter of 2Qfl1 was placed on this test piece.
71. A cylindrical mating material with an outer diameter of 25.6 mm (5450 carburized and quenched, hardness HRC 51 to 54, surface roughness 1s, sliding area 2i) was placed in a fixed manner, and the test piece was rotated under the following conditions. It was done by letting

給油  :なし 回転速度:40m/分一定(回転数: 559 rpm
 )面圧  :0.5.3,0.5.5.8.0〜(累
積負荷)運転時間:各面圧に8時間保持(合計32時間
)雰囲気温度:常湿 更に比較のために、いずれも表面粗さが38の黒鉛分散
型青銅系焼結金属軸受材料(比較例2)、炭素繊維充填
フッ素樹脂材料(比較例3)および黒鉛材料(比較例4
)についても、同様に摩擦摩耗特性を調べた。
Lubrication: None Rotation speed: Constant 40m/min (Rotation speed: 559 rpm
) Surface pressure: 0.5.3, 0.5.5.8.0 ~ (cumulative load) Operating time: Maintained at each surface pressure for 8 hours (32 hours in total) Atmosphere temperature: Normal humidity Furthermore, for comparison, Graphite-dispersed bronze-based sintered metal bearing material (Comparative Example 2), carbon fiber-filled fluororesin material (Comparative Example 3), and graphite material (Comparative Example 4) all have a surface roughness of 38.
), the friction and wear characteristics were similarly investigated.

累積倉荷(およびそれのう業算pv値)に対する摩擦係
数および上昇湿度の値は、いずれも第1図のグラフに示
される。すだ、32時間運転終了時における各試験片お
よびそれらの相手材の摩耗量を瀞1宝した結果は、次の
表2に示される。
The values of the coefficient of friction and the increased humidity for the cumulative cargo (and its calculated pv value) are both shown in the graph of FIG. The results of measuring the amount of wear of each test piece and its counterpart material at the end of 32 hours of operation are shown in Table 2 below.

表2 実施例1    0.002    0.8比軟例10
゜017    3.5 //  2   0.029   2.6//  3 
  0.005    0.9//  4   .0.
012   2.3第1図および表2の結果から、本発
明に係る摺動材利け、常温において炭素繊維充填フッ素
樹脂材料よりも摩擦係数、上昇温度共低く、また摩耗量
も少ないので、摺動材料として十分に使用できることか
分る。
Table 2 Example 1 0.002 0.8 ratio soft example 10
゜017 3.5 // 2 0.029 2.6 // 3
0.005 0.9// 4. 0.
012 2.3 From the results shown in Fig. 1 and Table 2, the sliding material according to the present invention has a lower coefficient of friction and lower temperature rise than the carbon fiber-filled fluororesin material at room temperature, and also has less wear. It can be seen that it can be used sufficiently as a dynamic material.

実施例2 液状のフラン系樹脂70重量部中に窒化ホウ素(粒径5
μ以下)30重量部を均一に分散させ、この分散液を比
較例1の円板状粉末成形体の表面に数回刷毛で塗布し、
そのたび毎に硬化をくり返し、そこに被膜を形成させた
。そして、被膜面を平面を出すために研磨し、不活性ガ
ス雰囲気中、10 IC/hrの昇温速度で1500℃
迄昇温し、焼成、炭化を行なった。
Example 2 Boron nitride (particle size 5
μ or less) was uniformly dispersed, and this dispersion was applied several times to the surface of the disc-shaped powder compact of Comparative Example 1 with a brush.
Each time, curing was repeated to form a film there. Then, the coating surface was polished to make it flat, and heated to 1500°C at a heating rate of 10 IC/hr in an inert gas atmosphere.
The temperature was raised to 100%, followed by calcination and carbonization.

円板体の表面に、約17・露の厚ざの被膜が形成され、
それは30重量%の窒化ホウ素を含有する、非常に硬質
のガラス状炭繁材料から形成されていた。これを、高周
波加熱装置付きの結水式摩擦摩耗試験機(スラストタイ
プ試験機)で300℃に加熱して、摩擦摩耗試験を行な
った。試験条件は、回転速度を5m/分、血圧を8し、
運転時間を100時間と変更した以外は、実施例1の場
合と同じである。なお、前記各比較例の材料についても
、同様の試験が行われた。
A film about 17 mm thick is formed on the surface of the disk,
It was formed from a very hard glassy carbonaceous material containing 30% by weight boron nitride. This was heated to 300° C. using a water condensation type friction and wear tester (thrust type tester) equipped with a high-frequency heating device, and a friction and wear test was conducted. The test conditions were a rotation speed of 5 m/min, blood pressure of 8,
The procedure was the same as in Example 1 except that the operating time was changed to 100 hours. Note that similar tests were conducted on the materials of each of the comparative examples.

摩耗量については第2図のグラフに、また100時間運
転終了直前における各試験片の摩擦係数は次の表3に、
それぞれ示される。
The amount of wear is shown in the graph in Figure 2, and the friction coefficient of each test piece just before the end of 100 hours of operation is shown in Table 3 below.
shown respectively.

表3 例     摩擦係数 実施例2     0.22 比較例1     0.33 1/  2     0.36 “ 3     0.32 //  4     0.28 第2図および表3の結果から、300℃という高温度条
件下においても、本発明に係る摺動材料は、他の材料よ
りも摩耗量が大幅に少なく、かつ摩擦係数も小さく安定
していることが分る。また、摩擦摩耗試験後の摺動面を
観察すると、他の材料は摺動痕が明瞭に刻まれ、凹凸が
激しくなっていたが、本発明の摺動材料はその摺動面が
滑らかであり、良好な摩擦状態が摺動時に維持されてい
たことを裏付けている。
Table 3 Example Friction coefficient Example 2 0.22 Comparative example 1 0.33 1/2 0.36 “ 3 0.32 // 4 0.28 From the results in Figure 2 and Table 3, the high temperature condition of 300°C It can be seen from the figure below that the sliding material according to the present invention has significantly less wear than other materials, and has a small and stable friction coefficient.Also, the sliding surface after the friction and wear test is When observed, other materials had clear sliding marks and severe unevenness, but the sliding material of the present invention had a smooth sliding surface and maintained a good frictional state during sliding. This confirms that

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は、摩擦摩耗試験における累積負荷(およびそれ
の換算PV値)に対する摩擦係数および上昇温度の値を
示したグラフである。また、第2図は、摩擦摩耗試験に
おける運転時間に対する摩耗量の値を示したグラフであ
る。 代理人 弁理士  吉 1)俊 夫 計2図 運転時開(時閉)
FIG. 1 is a graph showing the values of the friction coefficient and temperature rise with respect to the cumulative load (and its converted PV value) in the friction and wear test. Moreover, FIG. 2 is a graph showing the value of the amount of wear against the operating time in the friction and wear test. Representative Patent Attorney Yoshi 1) Toshio Total of 2 diagrams Open when driving (closed when driving)

Claims (1)

【特許請求の範囲】 1、ガラス状炭素材料および固体潤滑剤窒化ポウ素より
なる耐摩耗性摺動材料。 2 g化ホウ素が約5〜50重M%含有される特許請求
の範囲第1項記載の耐摩耗性摺動材料。 3、ずぺり軸受として成形される特許請求の範囲第1項
または第2項記載の耐摩耗性摺動材料。 4 すベリ軸受の摺動面として軸受暴利に被樟される特
許請求の範囲第1項または第2項記載の耐摩耗性摺動材
料。
[Claims] 1. A wear-resistant sliding material comprising a glassy carbon material and a solid lubricant boron nitride. 2. The wear-resistant sliding material according to claim 1, which contains about 5 to 50% by weight of boron. 3. The wear-resistant sliding material according to claim 1 or 2, which is formed as a double bearing. 4. The wear-resistant sliding material according to claim 1 or 2, which is used as a sliding surface of a sliding bearing and is subject to bearing profiteering.
JP58004962A 1983-01-14 1983-01-14 Abrasion resistant sliding material Granted JPS59131575A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58004962A JPS59131575A (en) 1983-01-14 1983-01-14 Abrasion resistant sliding material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58004962A JPS59131575A (en) 1983-01-14 1983-01-14 Abrasion resistant sliding material

Publications (2)

Publication Number Publication Date
JPS59131575A true JPS59131575A (en) 1984-07-28
JPS6127351B2 JPS6127351B2 (en) 1986-06-25

Family

ID=11598208

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58004962A Granted JPS59131575A (en) 1983-01-14 1983-01-14 Abrasion resistant sliding material

Country Status (1)

Country Link
JP (1) JPS59131575A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006240555A (en) * 2005-03-07 2006-09-14 Jtekt Corp Locking device

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006240555A (en) * 2005-03-07 2006-09-14 Jtekt Corp Locking device
JP4736477B2 (en) * 2005-03-07 2011-07-27 株式会社ジェイテクト Locking device

Also Published As

Publication number Publication date
JPS6127351B2 (en) 1986-06-25

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