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JPH04285693A - Sliding member - Google Patents

Sliding member

Info

Publication number
JPH04285693A
JPH04285693A JP4949291A JP4949291A JPH04285693A JP H04285693 A JPH04285693 A JP H04285693A JP 4949291 A JP4949291 A JP 4949291A JP 4949291 A JP4949291 A JP 4949291A JP H04285693 A JPH04285693 A JP H04285693A
Authority
JP
Japan
Prior art keywords
fine particles
sliding member
coated
dispersed
composite plating
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.)
Withdrawn
Application number
JP4949291A
Other languages
Japanese (ja)
Inventor
Masahito Shimomura
下村 雅人
Katsuhiro Hashizume
克浩 橋爪
Akihiko Matsui
昭彦 松井
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.)
Mitsubishi Heavy Industries Ltd
Original Assignee
Mitsubishi Heavy Industries 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 Mitsubishi Heavy Industries Ltd filed Critical Mitsubishi Heavy Industries Ltd
Priority to JP4949291A priority Critical patent/JPH04285693A/en
Publication of JPH04285693A publication Critical patent/JPH04285693A/en
Withdrawn legal-status Critical Current

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  • Sliding-Contact Bearings (AREA)
  • Lubricants (AREA)

Abstract

PURPOSE:To provide a sliding member excellent in selflubricating ability and abrasion resistance and readily producible. CONSTITUTION:A sliding member composed of a metal matrix composite plating layer produced by dispersing rigid fine particles covered with a water-insoluble organic polymer substance and codepositing them.

Description

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

【0001】0001

【産業上の利用分野】本発明は乾燥摩擦条件下および油
潤滑条件下で、潤滑性および耐摩耗性を有する摺動部材
に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a sliding member having lubricity and wear resistance under dry friction conditions and oil lubrication conditions.

【0002】0002

【従来の技術】分散複合めっきは自己潤滑性や耐摩耗性
などの機能を求めて、種々の金属マトリックスと微粒子
の組合せが検討されている。
BACKGROUND OF THE INVENTION Various combinations of metal matrices and fine particles have been studied for dispersion composite plating in order to provide functions such as self-lubricating properties and wear resistance.

【0003】表面技術VoL.30,No.11,P.
442(1985)では硬質微粒子あるいは自己潤滑性
を有する微粒子の一方のみを共析させる分散複合めっき
が紹介されており、硬質微粒子を分散させたものは耐摩
耗性に優れ、耐摩耗材あるいは油潤滑条件下での摺動部
材として使用されるが、乾燥摩擦条件下での使用が困難
であるのに対して、自己潤滑性を有する微粒子を分散さ
せたものは潤滑性に優れるが、耐摩耗性に乏しいという
性質が知られている。
[0003] Surface technology Vol. 30, No. 11, P.
442 (1985) introduces dispersion composite plating in which either hard fine particles or self-lubricating fine particles are eutectoid.Those with hard fine particles dispersed have excellent wear resistance and are suitable for wear-resistant materials or oil lubrication conditions. Although it is used as a sliding member under dry friction conditions, it is difficult to use it under dry friction conditions, whereas those with self-lubricating fine particles dispersed have excellent lubricity but have poor wear resistance. It is known for its scarcity properties.

【0004】一方、特開平01−21096号公報では
硬質微粒子および自己潤滑性を有する微粒子を同時に、
均一に分散共析させた複合めっき層で形成された摺動部
材が提案されており、耐摩耗性があり、かつ自己潤滑性
に優れた摺動部材が実現している。
On the other hand, in Japanese Unexamined Patent Publication No. 01-21096, hard fine particles and self-lubricating fine particles are simultaneously
A sliding member formed of a composite plating layer that is uniformly dispersed and eutectoid has been proposed, and a sliding member that is wear resistant and has excellent self-lubricating properties has been realized.

【0005】[0005]

【発明が解決しようとする課題】前記の従来の分散複合
めっきのうち、硬質微粒子と自己潤滑性を有する微粒子
を同時に均一に分散させたものは優れた自己潤滑性と耐
摩耗性を兼備している点で、無給油化も含めて各種機械
摺動部の要求に十分対応しうる画期的な摺動部材である
が、性質の異なる2種類の微粒子を同時に均一に分散さ
せるためのめっきプロセスの制御が必ずしも容易ではな
いことから、優れた自己潤滑性と耐摩耗性を兼備し、か
つ作製の容易な摺動部材の実現が要望されていた。
[Problems to be Solved by the Invention] Among the conventional dispersion composite platings described above, those in which hard fine particles and self-lubricating fine particles are uniformly dispersed at the same time have both excellent self-lubricating properties and wear resistance. It is an innovative sliding member that can fully meet the requirements of various mechanical sliding parts, including the need for no lubrication, but it requires a plating process to uniformly disperse two types of fine particles with different properties at the same time. Since it is not always easy to control the sliding member, there has been a demand for a sliding member that has both excellent self-lubricating properties and wear resistance, and is easy to manufacture.

【0006】本発明は上記要望に応じうる摺動部材を提
供しようとするものである。
[0006] The present invention seeks to provide a sliding member that can meet the above requirements.

【0007】[0007]

【課題を解決するための手段】本発明は水に不溶な有機
高分子物質で被覆した硬質微粒子を分散共析させた金属
マトリックス複合めっき層で形成されてなることを特徴
とする摺動部材である。
[Means for Solving the Problems] The present invention provides a sliding member formed of a metal matrix composite plating layer in which hard fine particles coated with a water-insoluble organic polymer substance are dispersed and eutectoid. be.

【0008】本発明の摺動部材を構成する有機高分子物
質は、めっき工程でのめっき浴への溶解を避けるために
、水に不溶という条件を満たす必要があり、フルオロア
ルキルアクリレートやフルオロアルキルメタクリレート
の重合体、フッ化エチレン樹脂(三フッ化エチレン樹脂
、四フッ化エチレン樹脂など)、ポリエチレン、ポリプ
ロピレン、ポリスチレンなどが使用される。これらの高
分子物質による硬質微粒子の被覆状態としては、硬質微
粒子が有機高分子物質で物理的に被覆されたマイクロカ
プセルであってもよいし、硬質微粒子表面と有機高分子
鎖とが化学的に結合(共有結合)したものであってもよ
い。
The organic polymeric substance constituting the sliding member of the present invention must satisfy the condition of being insoluble in water in order to avoid dissolution in the plating bath during the plating process. polymers, fluorinated ethylene resins (trifluorinated ethylene resins, tetrafluorinated ethylene resins, etc.), polyethylene, polypropylene, polystyrene, etc. are used. The coating state of the hard fine particles with these polymeric substances may be microcapsules in which the hard fine particles are physically coated with an organic polymeric substance, or microcapsules in which the hard fine particles are physically coated with an organic polymeric substance, or chemically coated hard fine particles with organic polymer chains. It may be a bond (covalent bond).

【0009】一方、本発明の摺動部材を構成する硬質微
粒子の材料としては、アルミナの他、酸化物系、窒化物
系または炭化物系セラミックスなどが使用される。
On the other hand, as the material of the hard particles constituting the sliding member of the present invention, in addition to alumina, oxide-based, nitride-based or carbide-based ceramics, etc. are used.

【0010】また、本発明の摺動部材を構成する金属マ
トリックスとしては、銅、コバルト、ニッケルなどが使
用される。
[0010] Copper, cobalt, nickel, etc. are used as the metal matrix constituting the sliding member of the present invention.

【0011】[0011]

【作用】マトリックス金属中に分散した微粒子は有機高
分子物質で被覆された硬質微粒子であって、有機高分子
物質が自己潤滑性を有することから潤滑性を高め、硬質
微粒子が摩耗を防ぐため、本発明の摺動部材は優れた摩
擦摩耗特性を示す。
[Function] The fine particles dispersed in the matrix metal are hard fine particles coated with an organic polymeric substance.The organic polymeric substance has self-lubricating properties, which increases lubricity, and the hard fine particles prevent wear. The sliding member of the present invention exhibits excellent friction and wear characteristics.

【0012】また、従来の、硬質微粒子と自己潤滑性を
有する微粒子を同時に、均一分散させた摺動部材が難度
の高いめっきプロセス、すなわち性質の異なる2種類の
微粒子の分散を制御する工程を経て作製されるのに対し
て、本発明の摺動部材は、マトリックス金属に含まれる
微粒子が1種類のみであるため、極めて容易に作製する
ことができる。
[0012] In addition, the conventional sliding member in which hard fine particles and self-lubricating fine particles are uniformly dispersed at the same time has undergone a highly difficult plating process, that is, a process that controls the dispersion of two types of fine particles with different properties. In contrast, the sliding member of the present invention can be manufactured extremely easily since the matrix metal contains only one type of fine particles.

【0013】[0013]

【実施例】分散性の点から硬質微粒子の粒子径0.5〜
2.0μmとし、有機高分子物質の被覆量を該硬質微粒
子に対する重量比で0.03〜0.3として、有機高分
子物質で被覆した硬質微粒子を分散させた金属マトリッ
クス複合めっき層を形成させる試験を行った結果、複合
めっき層中に有機高分子物質で被覆した硬質微粒子を2
〜40vol.%の範囲内で分散させたものが優れた自
己潤滑性と耐摩耗性を兼備することを確認した。次に、
その代表例を示す。
[Example] From the viewpoint of dispersibility, the particle size of hard fine particles is 0.5~
2.0 μm, and the coating amount of the organic polymer substance is set to 0.03 to 0.3 in weight ratio to the hard fine particles, and a metal matrix composite plating layer is formed in which hard fine particles coated with an organic polymer substance are dispersed. As a result of the test, two hard particles coated with an organic polymer substance were added to the composite plating layer.
~40vol. It was confirmed that those dispersed within this range had both excellent self-lubricity and wear resistance. next,
A typical example is shown below.

【0014】(例1)回転式攪拌翼を備えた反応容器内
で平均粒子径2.0μmのアルミナ微粒子100g、水
500ml、2,2,3,3−テトラフルオロプロピル
メタクリレート100gを混合し、65℃に保った後、
過硫酸カリウム(重合開始剤)1.5gを水100ml
に溶解させて前記混合物に加え、回転数700rpm 
で攪拌しながら重合を開始した。3時間後、反応器内容
物を氷冷し、ジエチルエーテルで未反応の2,2,3,
3−テトラフルオロプロピルメタクリレートを抽出して
重合を停止し、遠心分離により、2,2,3,3−テト
ラフルオロプロピルメタクリレートの重合体で被覆され
たアルミナ微粒子(以下、被覆微粒子Aと略記、被覆量
はアルミナ微粒子に対する重量比で0.28)を得た。
(Example 1) In a reaction vessel equipped with a rotary stirring blade, 100 g of alumina fine particles with an average particle diameter of 2.0 μm, 500 ml of water, and 100 g of 2,2,3,3-tetrafluoropropyl methacrylate were mixed. After keeping at ℃,
1.5 g of potassium persulfate (polymerization initiator) in 100 ml of water
and added to the above mixture, and the rotation speed was 700 rpm.
Polymerization was started while stirring. After 3 hours, the contents of the reactor were cooled with ice, and unreacted 2,2,3,
3-tetrafluoropropyl methacrylate is extracted to stop the polymerization, and centrifugation is performed to obtain alumina fine particles coated with a polymer of 2,2,3,3-tetrafluoropropyl methacrylate (hereinafter abbreviated as coated fine particles A). The weight ratio to the alumina fine particles was 0.28).

【0015】硫酸銅浴(硫酸銅CuSO4 ・5H2 
O  200g/l、硫酸H2 SO4 60g/l)
に被覆微粒子A(10〜200g/l)を分散させため
っき浴中で、炭素銅(S45C)製の円筒型摺動試験片
上に被覆微粒子Aを分散させた銅マトリックス複合めっ
き層を50〜100μm電析させた。なお、めっき浴の
温度は25℃、pHは0.5、電流密度は3.5A/d
m2 とした。
Copper sulfate bath (copper sulfate CuSO4 ・5H2
O 200g/l, sulfuric acid H2 SO4 60g/l)
In a plating bath in which coated fine particles A (10 to 200 g/l) were dispersed, a copper matrix composite plating layer with coated fine particles A dispersed therein was deposited to a thickness of 50 to 100 μm on a cylindrical sliding specimen made of carbon copper (S45C). Electrodeposited. The temperature of the plating bath was 25°C, the pH was 0.5, and the current density was 3.5A/d.
m2.

【0016】上記のようにして分散複合めっきを施した
円筒型試験片を固定片とし、表面を高周波焼入れした軸
受綱を回転片とした二円筒端面試験機を用いて、すべり
速度0.2m/sec 、面圧4.9Kgf /cm2
 、室温大気中で乾燥摩擦試験を行った。
Using a two-cylindrical end face testing machine with the cylindrical test piece coated with dispersion composite plating as described above as a fixed piece and the bearing cable whose surface was induction hardened as a rotating piece, a sliding speed of 0.2 m/ sec, surface pressure 4.9Kgf/cm2
, a dry friction test was conducted in the air at room temperature.

【0017】また、比較材として金属系自己潤滑材の代
表である銅に黒鉛を分散させた複合焼結材を用い、該比
較材を固定片として上記と同じ乾燥摩擦の比較試験を行
った。
Furthermore, a composite sintered material in which graphite is dispersed in copper, which is a typical metal-based self-lubricating material, was used as a comparative material, and the same dry friction comparison test as above was conducted using the comparative material as a fixed piece.

【0018】以上の結果を分散複合めっき層の被覆微粒
子Aの含有量とともに表1に示す。
The above results are shown in Table 1 together with the content of coated fine particles A in the dispersed composite plating layer.

【表1】[Table 1]

【0019】表1から明らかなように、被覆微粒子Aを
分散させた銅マトリックス複合めっき層からなる本発明
の摺動部材の摩擦係数は金属系自己潤滑材の代表である
銅と黒鉛の複合焼結材と同程度もしくはそれより小さく
、潤滑性に優れ、また、耐摩耗性は上記の複合焼結材よ
りも優れる結果を得た。
As is clear from Table 1, the friction coefficient of the sliding member of the present invention comprising a copper matrix composite plating layer in which coated fine particles A are dispersed is as follows. The size is the same as or smaller than the sintered material, has excellent lubricity, and has better wear resistance than the composite sintered material described above.

【0020】(例2)回転式攪拌翼を備えた反応器内で
平均粒子径0.5μmの炭化ケイ素微粒子100gとビ
ニルトリメトキシシラン500mlとを混合し、回転数
700rpm で攪拌しながら110℃で3時間反応さ
せた後、遠心分離により、反応器内容物から炭化ケイ素
微粒子を単離した。次いで、この、ビニルトリメトキシ
シランで処理した、炭化ケイ素100g、スチレン50
0ml、2,2′−アゾビスイソブチロニトリル(重合
開始剤)0.5gを回転式攪拌翼を備えた反応器内で混
合し、回転数700rpm で攪拌しながら、70℃で
24時間の重合を行った。重合後、反応器内容物をトル
エンで希釈し、遠心分離でトルエン相を除去した後にメ
タノール中に投じ、さらに遠心分離を行うことにより、
表面にポリスチレンが共有結合した炭化ケイ素微粒子(
被覆微粒子Bと略記、被覆量は炭化ケイ素微粒子に対す
る重量比で0.03)を得た。
(Example 2) 100 g of silicon carbide fine particles with an average particle size of 0.5 μm and 500 ml of vinyltrimethoxysilane were mixed in a reactor equipped with a rotary stirring blade, and the mixture was heated at 110° C. while stirring at a rotation speed of 700 rpm. After reacting for 3 hours, silicon carbide fine particles were isolated from the reactor contents by centrifugation. Next, 100 g of this vinyltrimethoxysilane-treated silicon carbide and 50 g of styrene were added.
0 ml and 0.5 g of 2,2'-azobisisobutyronitrile (polymerization initiator) were mixed in a reactor equipped with a rotary stirring blade, and stirred at 700 rpm for 24 hours at 70°C. Polymerization was performed. After polymerization, the contents of the reactor are diluted with toluene, the toluene phase is removed by centrifugation, and then poured into methanol, followed by further centrifugation.
Silicon carbide fine particles with polystyrene covalently bonded to the surface (
Abbreviated as coated fine particles B, the coating amount was 0.03 as a weight ratio to the silicon carbide fine particles.

【0021】硫酸銅浴(硫酸銅CuSO4 ・5H2 
O  200g/l、硫酸H2 SO4 60g/l)
に被覆微粒子B(10〜200g/l)を分散させため
っき浴中で、炭素銅(S45C)製の円筒型摺動試験片
上に被覆微粒子Bを分散させた銅マトリックス複合めっ
き層を50〜100μm電析させた。なお、めっき浴の
温度は25℃、pHは0.5、電流密度は3.5A/d
m2 とした。上記のようにして分散複合めっきを施し
た円筒型試験片を固定片とし、表面を高周波焼入れした
軸受綱を回転片とした二円筒端面試験機を用いて、すべ
り速度0.2m/sec 、面圧4.9Kgf /cm
2 、室温大気中で乾燥摩擦試験を行った。
Copper sulfate bath (copper sulfate CuSO4 ・5H2
O 200g/l, sulfuric acid H2 SO4 60g/l)
In a plating bath in which coated fine particles B (10 to 200 g/l) were dispersed, a copper matrix composite plating layer with coated fine particles B dispersed therein was deposited on a cylindrical sliding test piece made of carbon copper (S45C) to a thickness of 50 to 100 μm. Electrodeposited. The temperature of the plating bath was 25°C, the pH was 0.5, and the current density was 3.5A/d.
m2. Using a two-cylindrical end face testing machine with the cylindrical test piece coated with dispersion composite plating as described above as a fixed piece and the bearing rope whose surface was induction hardened as a rotating piece, the surface was tested at a sliding speed of 0.2 m/sec. Pressure 4.9Kgf/cm
2. A dry friction test was conducted in the air at room temperature.

【0022】また、比較材として銅に黒鉛を分散させた
例1と同じ焼結材を用い、例1と同じ比較試験を行った
Furthermore, the same comparative test as in Example 1 was conducted using the same sintered material as in Example 1, in which graphite was dispersed in copper, as a comparative material.

【0023】以上の結果を分散複合めっき層の被覆微粒
子Bの含有量とともに表2に示す。
The above results are shown in Table 2 together with the content of coated fine particles B in the dispersed composite plating layer.

【表2】[Table 2]

【0024】表2から明らかなように、被覆微粒子Bを
分散させた銅マトリックス複合めっき層からなる本発明
の摺動部材の摩擦係数は金属系自己潤滑材の代表である
銅と黒鉛の複合焼結材と同程度であり、潤滑性に優れ、
また、耐摩耗性は上記の複合焼結材よりも優れる結果を
得た。
As is clear from Table 2, the coefficient of friction of the sliding member of the present invention comprising a copper matrix composite plating layer in which coated fine particles B are dispersed is as follows. It has the same level of lubricity as binder, and has excellent lubricity.
Furthermore, the wear resistance was superior to that of the above-mentioned composite sintered material.

【0025】表1および表2で明らかなように、有機高
分子物質の被覆量を硬質微粒子に対する重量比で0.0
3〜0.3とし、有機高分子物質で被覆した硬質微粒子
を2vol.%以上含有させれば優れた自己潤滑性と耐
摩耗性を兼備するが、多量に含有させてもその効果は顕
著ではなく、40vol.%以下が実用範囲であること
がわかる。
As is clear from Tables 1 and 2, the amount of organic polymer material coated is 0.0 in terms of weight ratio to the hard fine particles.
3 to 0.3 and coated with an organic polymer substance in 2 vol. % or more provides both excellent self-lubricity and wear resistance, but even if it is contained in a large amount, the effect is not significant, and 40 vol. % or less is a practical range.

【0026】[0026]

【発明の効果】本発明の摺動部材は、有機高分子で被覆
した硬質微粒子を分散させた複合めっき層を有するため
、潤滑性と耐摩耗性の双方に優れたものである。また、
この複合めっき層を有する本発明の摺動部材は、金属系
自己潤滑材の代表である銅と黒鉛の複合焼結材よりも潤
滑性と耐摩耗性の双方に優れ、乾燥摩擦条件下の摺動部
材として適用できる。例えば、グリース給油している印
刷機の軸受に本発明の摺動部材を適用し無給油化すれば
、グリースによる紙の汚れ防止、メンテナンスフリー、
低コストなどの利点がある。
[Effects of the Invention] The sliding member of the present invention has a composite plating layer in which hard fine particles coated with an organic polymer are dispersed, so that it has excellent both lubricity and wear resistance. Also,
The sliding member of the present invention having this composite plating layer has better lubricity and wear resistance than a composite sintered material of copper and graphite, which is a typical metal-based self-lubricating material, and has excellent sliding properties under dry friction conditions. Can be applied as a moving member. For example, if the sliding member of the present invention is applied to the bearings of a printing press that is currently lubricated with grease, and the bearings of a printing press are lubricated, the paper can be prevented from becoming stained by grease, and maintenance is free.
It has advantages such as low cost.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】  水に不溶な有機高分子物質で被覆した
硬質微粒子を分散共析させた金属マトリックス複合めっ
き層で形成されてなることを特徴とする摺動部材。
1. A sliding member comprising a metal matrix composite plating layer in which hard fine particles coated with a water-insoluble organic polymer substance are dispersed and co-deposited.
JP4949291A 1991-03-14 1991-03-14 Sliding member Withdrawn JPH04285693A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4949291A JPH04285693A (en) 1991-03-14 1991-03-14 Sliding member

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4949291A JPH04285693A (en) 1991-03-14 1991-03-14 Sliding member

Publications (1)

Publication Number Publication Date
JPH04285693A true JPH04285693A (en) 1992-10-09

Family

ID=12832648

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4949291A Withdrawn JPH04285693A (en) 1991-03-14 1991-03-14 Sliding member

Country Status (1)

Country Link
JP (1) JPH04285693A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013522820A (en) * 2010-03-11 2013-06-13 エルジー ケム. エルティーディ. Organic polymer-silicon composite particles, method for producing the same, negative electrode including the same, and lithium secondary battery

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013522820A (en) * 2010-03-11 2013-06-13 エルジー ケム. エルティーディ. Organic polymer-silicon composite particles, method for producing the same, negative electrode including the same, and lithium secondary battery
US9142859B2 (en) 2010-03-11 2015-09-22 Lg Chem, Ltd. Polymer-silicon composite particles, method of making the same, and anode and lithium secondary battery including the same

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