JPS59131567A - Abrasion resistant sliding material - Google Patents
Abrasion resistant sliding materialInfo
- Publication number
- JPS59131567A JPS59131567A JP58004963A JP496383A JPS59131567A JP S59131567 A JPS59131567 A JP S59131567A JP 58004963 A JP58004963 A JP 58004963A JP 496383 A JP496383 A JP 496383A JP S59131567 A JPS59131567 A JP S59131567A
- Authority
- JP
- Japan
- Prior art keywords
- graphite
- wear
- sliding
- sliding material
- temperature
- 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
Links
- 239000000463 material Substances 0.000 title claims description 37
- 238000005299 abrasion Methods 0.000 title claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 21
- 229910002804 graphite Inorganic materials 0.000 claims description 19
- 239000010439 graphite Substances 0.000 claims description 19
- 239000000314 lubricant Substances 0.000 claims description 6
- 239000007787 solid Substances 0.000 claims description 5
- 239000003610 charcoal Substances 0.000 claims 1
- 239000003575 carbonaceous material Substances 0.000 description 17
- 229910021397 glassy carbon Inorganic materials 0.000 description 13
- 239000002184 metal Substances 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 238000005260 corrosion Methods 0.000 description 5
- 230000007797 corrosion Effects 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 239000007833 carbon precursor Substances 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 238000005087 graphitization Methods 0.000 description 4
- 239000011261 inert gas Substances 0.000 description 4
- 238000005461 lubrication Methods 0.000 description 4
- 238000003763 carbonization Methods 0.000 description 3
- 230000001186 cumulative effect Effects 0.000 description 3
- 238000010304 firing Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 230000003746 surface roughness Effects 0.000 description 3
- 229910000906 Bronze Inorganic materials 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 239000003570 air Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000010974 bronze Substances 0.000 description 2
- 238000010000 carbonizing Methods 0.000 description 2
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229910021382 natural graphite Inorganic materials 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000011295 pitch Substances 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000012080 ambient air Substances 0.000 description 1
- 239000011305 binder pitch Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 238000005255 carburizing Methods 0.000 description 1
- 238000005056 compaction Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000007849 furan resin Substances 0.000 description 1
- 239000007770 graphite material Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 230000013011 mating Effects 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000005272 metallurgy Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 1
- 229910052982 molybdenum disulfide Inorganic materials 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000006253 pitch coke Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
Landscapes
- Ceramic Products (AREA)
- Sliding-Contact Bearings (AREA)
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μ4jする。更に詳しく
は、無給油でも高湿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 provides a wear-resistant sliding material. More specifically, the present invention relates to a wear-resistant sliding material that can be used even at high humidity without lubrication.
無給油で高湿迄仲用可能な摺η11利刺としては、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、耐蘂品性にすぐれかつ自己潤滑性
があるため、角4給帽]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1/する。Graphite bearings have conventionally been used as sliding bearings that can be used in high humidity conditions without lubrication, and have been used as sliding bearings. Graphite bearings have excellent wear resistance and self-lubricating properties, so they can be used up to high temperatures.However, their large porosity and therefore poor mechanical strength is a major drawback. do.
そこで・この機械的強度を補強する意味など力)ら、気
孔部に熱硬化性樹脂や比較的イ氏融1点の金属を含浸さ
せることが行われている。し力)しな力(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
が異なることカニ原因となって、ブリスタリング現象(
火ぶくわ、現象)が起る。捷だ、金属を含浸した場合に
け、而を薬、5古性、耐食性が悪くなり、また摺動特性
もイ氏下し、焼付現象が発生するようにt「る。Therefore, in order to reinforce this mechanical strength, the pores are impregnated with a thermosetting resin or a metal with a relatively high melting point. When impregnated with resin or metal, it expands, decomposes, melts, and leaches under high temperature and pressure. Due to decomposition, heat resistance and humidity are below 200℃, and the difference in thermal expansion coefficient between graphite and resin causes blistering phenomenon (
fire, phenomenon) occurs. However, if it is impregnated with metal, it will deteriorate its durability, corrosion resistance, and its sliding properties will deteriorate, causing a seizure phenomenon.
更に、青銅系、鉄系の金、邑fll t4中(・こ粉i
z冶金法によって黒鉛、二硫化モリブデンなどをJ/J
−Gころ)赦させた固体澤滑剤分散型煙結金g軸受など
もJ目いられており、これは黒鉛軸受G−比べ、機械的
り主席は改善され、しかも無給油て高ンへA迄494用
できるが、素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。In addition, bronze-based and iron-based gold
J/J of graphite, molybdenum disulfide, etc. using Z metallurgy method
-G roller) The solid lubricant dispersion type smoky metal g bearing is also popular, and compared to the graphite bearing G, the mechanical stability is improved, and it is possible to achieve high A without lubrication. Although it can be used up to 494, since the base material is metal, it has poor chemical resistance and corrosion resistance, and it not only has poor wear resistance at high temperatures, but also causes the inner diameter of the bearing to shrink due to oxidation expansion, affecting the bearing clearance. There are some shortcomings.
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1d
含浸された潤滑油の寿命などを考慮した使11ノ@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i1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、耐熱温度が約250℃と高いばが
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、面圧が大きくなっ
たり、高温になる程クリープが大きく、変Jし、流れ出
しなどの障害が起る。更に、熱膨張係数が10 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, plastic bearings and sintered oil-impregnated bearings are also used, but these are based on the heat resistance temperature of the material itself or
Considering the service life of the impregnated lubricating oil, etc., the operating temperature is approximately 80 to 120℃, excluding fluororesin bearings.
Alternatively, it is actually used at a temperature of 11 or lower. In addition, fluororesin bearings do not only have a high heat resistance temperature of approximately 250°C, but also have characteristics such as a low coefficient of friction and excellent chemical resistance, but on the other hand, they are soft and prone to creep. It has its drawbacks. In particular, the greater the surface pressure or the higher the temperature, the greater the creep, deformation, and problems such as flow. Furthermore, the coefficient of thermal expansion is on the order of 10, which is an 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
摺動材料を提供するものであり、ガラス状炭素材料およ
び固体潤滑剤黒鉛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、また不活性ガ
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 made of a glassy carbon material and a solid lubricant graphite can be Self-lubricating properties are maintained up to about 450°C in the atmosphere and up to about 2500°C in an inert 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(H/C)を調
整したピッチから誘導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 derived from a pitch with an adjusted hydrogen/carbon atomic ratio (H/C) 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2000〜3ooo℃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材料であり、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、この黒鉛化にょって、潤滑性に乏しいガラス状炭素
材料が金M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 300° C. using a graphitization furnace. However, the glassy carbon material is a non-graphitizable material, and even if such high-temperature heat treatment is performed, graphitization will progress only slightly, but this graphitization will cause the glassy carbon material to have poor lubricity. When a carbon material causes contact between gold and M, developing a graphite structure improves lubricity, although the hardness slightly decreases.
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 2500℃ and an extremely high specific strength, and is mainly used in crucibles, boats,
It has been traditionally used for heaters, electrodes, etc.
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
の黒鉛は、六方晶系の結晶構造を有し、層に平行な方向
にせん断が起り易いなどのために自己潤清作JIJがあ
り、かつ廉価な材料である。黒鉛は、ガラス状炭素材料
との配合物巾約20〜70重粘%の配合割合で用いられ
る。これより少ない使用割合では、潤滑性に欠けるため
摩擦係数が高くなり、一方これより多い割合で用いられ
ると、摺動材料トしての機械的強度が不足するようにな
る。Graphite as a solid lubricant blended into such a glassy carbon material has a hexagonal crystal structure and tends to be sheared in a direction parallel to the layers, so it has self-lubricating JIJ and It is an inexpensive material. Graphite is used in a blending ratio of about 20 to 70% by weight of the glassy carbon material. If the proportion is less than this, the coefficient of friction will increase due to lack of lubricity, while if the proportion is greater than this, the mechanical strength of the sliding material will be insufficient.
摺動材料の製造は、ガラス状炭素材料形成材料と黒鉛と
の均一混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、黒鉛との
配合物単独からは厚さ3圓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膜させた形で用いられる。The sliding material is manufactured by forming a homogeneous mixture of a glassy carbon material forming material and graphite into a predetermined shape, and then carbonizing this at the firing temperature of the glassy carbon material forming material. When using a cured resin molded product, since a sliding material with a thickness of only about 3 mm can be produced from a mixture with graphite alone, a carbon material such as graphite or a carbon precursor containing an oxygen functional group is 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.
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。また
、酸素官能基含有炭素前駆体物質がガラス状炭素材別形
成拐料として用いられる場合には、黒鉛との均一配合粉
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、そこに炭素繊維、黒鉛繊組などを配
合し、カーボン−カーボン複合材料とすることもできる
。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. In addition, when the oxygen-functional group-containing carbon precursor substance is used as a material for forming a glassy carbon material, after powder-forming a uniformly blended powder with graphite into a predetermined shape with an arbitrary thickness under pressure at room temperature, 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, It is also possible to form a carbon-carbon composite material 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大きく、
シかも耐熱性のあるガラス状炭素材料を素地材料とし、
これに固体潤滑剤としての黒鉛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℃の高温迄潤滑性を保持
している。更に、耐薬品性、耐食性にすぐれ、高温造化
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、フッ素樹脂軸受にみ
られるようなりリープし易いという現象もなく、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 base material is a heat-resistant glassy carbon material.
Since it contains graphite as a solid lubricant, it has excellent wear resistance and maintains its lubricity up to high temperatures of about 450°C in the air and about 2500°C in an inert gas atmosphere. Furthermore, it has excellent chemical resistance and corrosion resistance, and is stable even in high-temperature forming chemicals, so it does not have the drawbacks of poor chemical resistance and corrosion resistance or oxidation that were found in conventional metal-impregnated graphite bearings and graphite-dispersed sintered metal bearings. There is no such phenomenon as expansion. Furthermore, even at high temperatures, it does not tend to leap as seen in fluororesin 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1
粒径10μ以下のピッチコークスおよびバインダーピッ
チの重量比7:3の粉末混合物を、常温下に成形圧力3
000 rで、直径5Qmm、厚さ1011171の円
板状に粉末成形した。Example 1 A powder mixture of pitch coke with a particle size of 10μ or less and binder pitch in a weight ratio of 7:3 was heated at room temperature under a compacting pressure of 3.
The powder was molded into a disk shape with a diameter of 5 Qmm and a thickness of 1011171 mm at 000 r.
一方、液状のフラン系樹脂50重量部中に天然黒鉛(粒
径10〜20μ)50重量部を均一に分散させ、この分
散液を上記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℃/hrの昇温速度で1000℃迄
昇温し、焼成、炭化を行なった。On the other hand, 50 parts by weight of natural graphite (particle size 10 to 20 μm) was uniformly dispersed in 50 parts by weight of liquid furan-based resin, and this dispersion was applied several times to the surface of the disc-shaped powder compact with a brush. Each time, curing was repeated to form a film there. Then, the coating surface was polished to make it flat, and the temperature was raised to 1000° C. at a rate of 10° C./hr in an inert gas atmosphere to perform firing and carbonization.
円板体の表面には、約1闇の厚さの被膜が形成され、そ
れは50重量%の黒鉛を含有する、非常に硬質のガラス
状炭素材料から形成されていた。A coating approximately 1 mm thick was formed on the surface of the disk and was made of a very hard glassy carbon material containing 50% by weight graphite.
これについて、銘木式摩擦摩耗試験機(スラストタイプ
試験機)を用いて、廐擦摩耗特性を調べた。摩擦摩耗試
験は、この円板体試験片(表面粗さ3s)の上に、内径
20羽、外径25.671111の円柱状相手材(54
5a浸炭焼入、硬度HRC51〜54、表面粗さISX
摺動面積27)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。Regarding this, the frontal friction and wear characteristics were investigated using a precious wood type friction and wear tester (thrust type tester). In the friction and wear test, a cylindrical mating material (54 mm) with an inner diameter of 20 blades and an outer diameter of 25.671111 mm was placed on this disc test piece (surface roughness: 3 s).
5a carburizing and quenching, hardness HRC51-54, surface roughness ISX
The test piece was mounted so that the sliding area 27) was fixed, and the test piece was rotated under the following conditions.
給油 :なし
回転速度゛40mA上一定(回転数559 rpm )
面圧 :0.5.3.0.5.5、S、O〜(累積負
荷)運転時間;各面圧に8時間保持(合計32時間)界
囲気温度;常濡
比較例1
ピッチから誘導された酸素官能基含有炭素前駆体物質の
みの粉末成形体の焼成、炭化を、20℃/hrの昇温速
度で1000 ℃迄昇温して行ない、それ(表面粗さ3
S)についての摩擦摩耗特性を同様に調べた。Lubrication: None Rotation speed: Constant above 40mA (Rotation speed: 559 rpm)
Surface pressure: 0.5.3.0.5.5, S, O ~ (cumulative load) Operating time: Maintained at each surface pressure for 8 hours (32 hours in total) Ambient air temperature: Normally wet Comparative example 1 Induction from pitch The powder compact containing only the oxygen-functional group-containing carbon precursor material was fired and carbonized by increasing the temperature to 1000 °C at a temperature increase rate of 20 °C/hr.
The friction and wear characteristics of S) were similarly investigated.
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拐料(比較例2)3よび黒鉛材料
(比較例3)についても、同様にM擦摩耗特性を調べた
。Furthermore, for comparison, the M abrasion characteristics were similarly investigated for a graphite-dispersed bronze-based sintered metal bearing material (Comparative Example 2) 3 and a graphite material (Comparative Example 3), both of which had a surface roughness of 38. Ta.
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」二昇温度の値は、いずれも第1図のグラフに示
される。また、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測定した結果は、次の表
1に示される。The values of the friction coefficient and the temperature rise with respect to the cumulative load (and its converted PV value) are both shown in the graph of FIG. Further, 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 1 below.
表1
実施例1’ 0.002 0.4比較例1
0.−017 3.51/ 2 0
.029 2・6// 3 0.012
2.3第1図および表1の結果から、本発明に係
る摺動材料は、他の材料と比べて、摩擦係数、上昇温度
および摩耗量がいずれも小さく、摺動材料として十分使
用できることが分る。Table 1 Example 1' 0.002 0.4 Comparative Example 1
0. -017 3.51/ 2 0
.. 029 2・6// 3 0.012
2.3 From the results shown in Figure 1 and Table 1, the sliding material according to the present invention has a smaller coefficient of friction, lower temperature rise, and lower wear amount than other materials, and can be used satisfactorily as a sliding material. I understand.
実施例2
比較例1において、天然黒鉛(粒径1o〜20μ)50
重量%を含有する円板体の粉末成形およびそれの焼成、
炭化が同様に行われた。Example 2 In Comparative Example 1, natural graphite (particle size 1o~20μ) 50
Powder compaction of a disc body containing % by weight and sintering thereof,
Carbonization was carried out similarly.
これを高周波加熱装置付きの銘木式摩擦摩耗試験機(ス
ラストタイプ試験機)で300℃に加熱して、′i′f
、擦摩耗試験を行なった。試験条件は、回転速度を5
m1分、面圧を8〜、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。This was heated to 300℃ using a precious wood type friction and wear tester (thrust type tester) equipped with a high-frequency heating device, and 'i'f
, an abrasion test was conducted. The test conditions were a rotation speed of 5
The procedure was the same as in Example 1, except that the pressure was changed to m1 minute, the surface pressure was changed to 8 to 100 hours, and the operating time was changed to 100 hours.
な:13、前5己各比岐例の材イS1についても、同様
の試験が行われた。A similar test was conducted on material S1 of each of the ratios of Na:13 and Mae 5.
1ニアH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
2に、それぞれ示される。The amount of 1 near H wear is shown in the graph in Figure 2, and 100
The friction coefficients of each test piece immediately before the end of the time run are shown in Table 2 below.
表2
実施例2 0.19
比較例1033
tt 20.36
〃3 0.28
第2図および表2の結果から、300℃という高湿度条
件下においても、本発明に係る摺動利得は、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1れ、凹凸が
激しくなっていたが、本発明の摺動材料はその括;動面
が滑らかであり、良好なIス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 2 Example 2 0.19 Comparative Example 1033 tt 20.36 〃3 0.28 From the results in Figure 2 and Table 2, even under the high humidity condition of 300°C, the sliding gain according to the present invention is It can be seen that the amount of wear is significantly lower than that of the material, and the coefficient of friction is also small and stable. In addition, when observing the sliding surface after the friction and wear test, other materials had clear sliding marks and severe unevenness, but the sliding material of the present invention has a smooth sliding surface. This confirms that a good I-scan condition was maintained during sliding.
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 IB 俊 夫
第1図
0 100 、 200
300 4oo p1
4(Q/l−1ψ)第2図
番転蛸Rtl (時間)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. Further, 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 IB Toshio Figure 1 0 100, 200
300 4oo p1
4 (Q/l-1ψ) 2nd figure number change Rtl (time)
Claims (1)
なる耐摩耗性摺動材料。 2 黒鉛が約20〜70重那゛%含有される特8′IM
求の範囲第1項記載の耐摩耗性摺動材ネ′1゜3 すべ
り軸受として成形される特許jj;j求のモ+1間第1
項または第2項記載の耐摩耗性摺動材’p’FQ4 す
べり軸受の摺動面として軸受試料に被a子される特許f
tl’7求の範jl−r(第、1項咬たは第2頂記1騰
)耐摩tC性摺動拐料。[Claims] 1. Glassy charcoal=? A wear-resistant sliding material made of a lubricant and a solid lubricant. 2 Special 8'IM containing about 20 to 70% graphite
Abrasion-resistant sliding material N'1゜3 described in item 1 of the scope of interest Patent jj;
Wear-resistant sliding material 'p'FQ4 described in item or item 2 Patent f applied to a bearing sample as a sliding surface of a sliding bearing
tl'7 desired range jl-r (1st, 1st term or 2nd term, 1st term) Wear-resistant tC sliding material.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58004963A JPS59131567A (en) | 1983-01-14 | 1983-01-14 | Abrasion resistant sliding material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58004963A JPS59131567A (en) | 1983-01-14 | 1983-01-14 | Abrasion resistant sliding material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59131567A true JPS59131567A (en) | 1984-07-28 |
JPS6132273B2 JPS6132273B2 (en) | 1986-07-25 |
Family
ID=11598239
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58004963A Granted JPS59131567A (en) | 1983-01-14 | 1983-01-14 | Abrasion resistant sliding material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59131567A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1988005874A1 (en) * | 1987-02-09 | 1988-08-11 | Kabushiki Kaisha Sankyo Seiki Seisakusho | Bearing material and plastic bearing |
JPS63195417A (en) * | 1987-02-09 | 1988-08-12 | Sankyo Seiki Mfg Co Ltd | Resin bearing |
JPS63199924A (en) * | 1987-02-10 | 1988-08-18 | Sankyo Seiki Mfg Co Ltd | Plastic bearing |
JPS6449714A (en) * | 1987-08-20 | 1989-02-27 | Sankyo Seiki Seisakusho Kk | Resin bearing |
FR2684370A1 (en) * | 1991-11-29 | 1993-06-04 | Mitsubishi Pencil Co | CARBONACEOUS MATERIAL FOR ELECTRODES AND PROCESS FOR ITS PREPARATION. |
US5236784A (en) * | 1987-02-09 | 1993-08-17 | Kabushiki Kaisha Sankyo Seiki Seisakusho | Bearing material and plastic bearing |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS52117891A (en) * | 1976-03-31 | 1977-10-03 | Showa Denko Kk | Production of carbonageous molded product |
-
1983
- 1983-01-14 JP JP58004963A patent/JPS59131567A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS52117891A (en) * | 1976-03-31 | 1977-10-03 | Showa Denko Kk | Production of carbonageous molded product |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1988005874A1 (en) * | 1987-02-09 | 1988-08-11 | Kabushiki Kaisha Sankyo Seiki Seisakusho | Bearing material and plastic bearing |
JPS63195417A (en) * | 1987-02-09 | 1988-08-12 | Sankyo Seiki Mfg Co Ltd | Resin bearing |
US5236784A (en) * | 1987-02-09 | 1993-08-17 | Kabushiki Kaisha Sankyo Seiki Seisakusho | Bearing material and plastic bearing |
JPS63199924A (en) * | 1987-02-10 | 1988-08-18 | Sankyo Seiki Mfg Co Ltd | Plastic bearing |
JPS6449714A (en) * | 1987-08-20 | 1989-02-27 | Sankyo Seiki Seisakusho Kk | Resin bearing |
FR2684370A1 (en) * | 1991-11-29 | 1993-06-04 | Mitsubishi Pencil Co | CARBONACEOUS MATERIAL FOR ELECTRODES AND PROCESS FOR ITS PREPARATION. |
US5391433A (en) * | 1991-11-29 | 1995-02-21 | Mitsubishi Pencil Kabushiki Kaisha | Carbon material for electrodes and process for preparing it |
Also Published As
Publication number | Publication date |
---|---|
JPS6132273B2 (en) | 1986-07-25 |
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