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JP2912034B2 - Multi-layer sliding member - Google Patents

Multi-layer sliding member

Info

Publication number
JP2912034B2
JP2912034B2 JP1677391A JP1677391A JP2912034B2 JP 2912034 B2 JP2912034 B2 JP 2912034B2 JP 1677391 A JP1677391 A JP 1677391A JP 1677391 A JP1677391 A JP 1677391A JP 2912034 B2 JP2912034 B2 JP 2912034B2
Authority
JP
Japan
Prior art keywords
weight
sliding member
phosphate
lubricating composition
powder
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP1677391A
Other languages
Japanese (ja)
Other versions
JPH04236299A (en
Inventor
隆 中丸
憲司 山田
忠 渡井
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.)
Oiresu Kogyo KK
Original Assignee
Oiresu Kogyo KK
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 Oiresu Kogyo KK filed Critical Oiresu Kogyo KK
Priority to JP1677391A priority Critical patent/JP2912034B2/en
Priority to US07/693,243 priority patent/US5300366A/en
Priority to DE69122299T priority patent/DE69122299T2/en
Priority to KR1019910007425A priority patent/KR0169707B1/en
Priority to EP91304125A priority patent/EP0456471B1/en
Publication of JPH04236299A publication Critical patent/JPH04236299A/en
Application granted granted Critical
Publication of JP2912034B2 publication Critical patent/JP2912034B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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

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、摺動面にポリテトラフ
ルオロエチレン(以下「PTFE」という。)樹脂を主
成分とする潤滑組成物を備えた複層摺動部材に関するも
のである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a multi-layer sliding member provided with a lubricating composition mainly composed of polytetrafluoroethylene (hereinafter referred to as "PTFE") resin on a sliding surface.

【0002】[0002]

【従来の技術】従来より、PTFE樹脂は自己潤滑性に
優れ、摩擦係数が低く、更には優れた耐薬品性および耐
熱性を具備することから、軸受等の摺動部材として広く
使用されている。
2. Description of the Related Art Conventionally, PTFE resins have been widely used as sliding members such as bearings because of their excellent self-lubricating properties, low coefficient of friction, and excellent chemical and heat resistance. .

【0003】しかしながら、一方ではこのPTFE樹脂
のみからなる摺動部材は耐摩耗性や耐クリープ性に劣る
ため、摺動部材の用途に応じて、例えば(1)黒鉛、二硫
化モリブデン、ガラス繊維などの充填材を配合したり、
(2) 薄鋼板上に一体に被着形成された多孔質焼結合金層
に含浸被覆したり、して上記欠点を解決している。上記
(2) の態様からなる摺動部材としては、例えば特公平1
−22486号公報や特開平2−107818号公報等
に開示されている摺動部材が提案されている。
However, on the other hand, sliding members made of only PTFE resin are inferior in abrasion resistance and creep resistance. Therefore, depending on the use of the sliding member, for example, (1) graphite, molybdenum disulfide, glass fiber, etc. Blending fillers,
(2) The above disadvantage is solved by impregnating and coating a porous sintered alloy layer integrally formed on a thin steel plate. the above
As the sliding member having the mode (2), for example,
A sliding member disclosed in, for example, Japanese Patent Application Laid-Open No. 22486 and Japanese Patent Application Laid-Open No. 2-107818 has been proposed.

【0004】[0004]

【発明が解決しようとする課題】上記従来技術の摺動部
材は、優れた摩擦特性や耐摩耗性等の摺動特性を発揮す
るものであったが、摺動部材の使用用途(例えばOA機
器の摺動部等)によっては導電性が要求される。しかし
ながら、前記従来技術の摺動部材ではこれらの要求に対
して十分に対応することができない、という新たな問題
が提起された。一般に、合成樹脂に導電性を付与する方
法として、炭素繊維やカーボンブラック等の導電性物質
を添加しているが、PTFE樹脂にこれら物質を添加す
ると、導電性は向上するが、摺動特性が低下し、特に炭
素繊維を添加した場合、相手軸を傷つけるという問題が
あった。
The sliding members of the prior art described above exhibited sliding characteristics such as excellent friction characteristics and abrasion resistance. However, the sliding members are used for applications (for example, OA equipment). In some cases, conductivity is required. However, there has been a new problem that the sliding member of the prior art cannot sufficiently meet these requirements. In general, as a method for imparting conductivity to a synthetic resin, a conductive material such as carbon fiber or carbon black is added. When these materials are added to a PTFE resin, the conductivity is improved, but the sliding characteristics are reduced. In particular, when carbon fibers are added, there is a problem that the mating shaft is damaged.

【0005】本発明は、優れた摺動特性を発揮するとと
もに、導電性をも有する複層摺動部材を得ることを目的
とするものである。
An object of the present invention is to provide a multilayer sliding member exhibiting excellent sliding characteristics and also having conductivity.

【0006】[0006]

【課題を解決するための手段】上述の課題を解決するべ
く、本発明はつぎの技術的手段を提供するものである。
すなわち、本発明は、鋼裏金上に形成された多孔質焼結
金属層にPTFE樹脂を主成分としこれに充填材として
炭素繊維5〜30重量%およびリン酸塩0.1〜15重
量%あるいはこれらにさらに導電性物質0.1〜10重
量%を含有する潤滑組成物が含浸被覆されていることを
特徴とする複層摺動部材を提供するものである。
In order to solve the above-mentioned problems, the present invention provides the following technical means.
That is, according to the present invention, the porous sintered metal layer formed on the steel back metal contains PTFE resin as a main component and 5 to 30% by weight of carbon fiber and 0.1 to 15% by weight of phosphate as a filler. An object of the present invention is to provide a multilayer sliding member characterized in that these are further impregnated and coated with a lubricating composition containing 0.1 to 10% by weight of a conductive substance.

【0007】上述した構成において、裏金は金属薄板か
らなり、一般には構造用圧延鋼薄板が使用されるが、摺
動部材の用途によっては、他の鋼薄板あるいは鋼以外の
金属薄板でも良く、これらの金属薄板に銅メッキ等を施
して耐蝕性を向上させたものであってもよい。該裏金上
に一体的に形成される多孔質焼結金属層は青銅、鉛青
銅、リン青銅など摩擦摩耗特性に優れた銅合金で形成さ
れるが、目的、用途に応じて銅合金以外、例えばアルミ
ニウム合金、鉄等から形成してもよい。これら合金粉末
の粒子形態は、塊状もしくは不規則形状のものが好まし
い。
In the above-described construction, the back metal is made of a metal sheet, and a rolled steel sheet for a structure is generally used. However, depending on the use of the sliding member, another steel sheet or a metal sheet other than steel may be used. The metal thin plate may be plated with copper or the like to improve corrosion resistance. The porous sintered metal layer integrally formed on the back metal is formed of a copper alloy having excellent friction and wear properties such as bronze, lead bronze, and phosphor bronze. It may be formed from an aluminum alloy, iron, or the like. The particle form of these alloy powders is preferably a lump or irregular.

【0008】潤滑組成物の主成分をなすPTFE樹脂と
しては、ファインパウダー(例えば三井デュポンフロロ
ケミカル社製の「テフロン6CJ(商品名)」、ダイキ
ン工業社製の「ポリフロンF201(商品名)」、旭硝
子社製の「フルオンCD−076、CD−126、CD
−4(商品名)」)が用いられる。
Examples of the PTFE resin as a main component of the lubricating composition include fine powders (for example, “Teflon 6CJ (trade name)” manufactured by DuPont Mitsui Fluorochemicals, “Polyflon F201 (trade name)” manufactured by Daikin Industries, "Fluon CD-076, CD-126, CD" manufactured by Asahi Glass Co., Ltd.
-4 (product name) ”).

【0009】該PTFE樹脂への充填材として、本発明
では炭素繊維、リン酸塩、場合によって更に導電性物質
の粉末が使用される。炭素繊維(以下「CF」とい
う。)は潤滑組成物に導電性を付与する物質としての役
割とPTFE樹脂の耐摩耗性および耐クリープ性に劣る
欠点を補う役割を担うものである。CFとしては低温
(約1000〜1500℃)処理したピッチ系、PAN
(ポリアクリルニトリル)系およびフェノール系CF並
びに高温(約2000〜2500℃)処理したピッチ
系、PAN系およびフェノール系CFが使用されるが、
潤滑組成物に高い導電性を付与する観点からは後者のC
F、耐摩耗性や耐クリープ性を補う観点からは前者のC
Fを使用することが好ましい。ピッチ系CFの具体例と
しては日東紡績社製の「ザイラス(商品名)」、PAN
系炭素繊維の具体例としては三菱レーヨン社製の「パイ
ロフイル(商品名)」、フェノール系CFの具体例とし
ては日本カイノール社製の「カイノールCF16BT
(商品名)」を挙げることができる。CFの大きさ、す
なわち直径と長さについては、直径が1〜20μm、長
さが30μm〜3mmが好ましく、とくに潤滑組成物の
製造上の問題を加味すると直径が約10μm前後で長さ
が100μm前後のものが好ましい。そして、潤滑組成
物に対してのCFの配合割合は5〜30重量%である。
5重量%以下の配合では潤滑組成物に導電性を付与しが
たく、また30重量%を越えて配合しても導電性のそれ
以上の向上は期待できず、また、摺動部材としての摩擦
摩耗特性を却って低下させる。
In the present invention, as a filler for the PTFE resin, carbon fibers, phosphates, and, in some cases, a powder of a conductive substance are used. Carbon fiber (hereinafter, referred to as “CF”) plays a role as a substance for imparting conductivity to the lubricating composition and a role to compensate for a defect of the PTFE resin inferior in wear resistance and creep resistance. As a CF, pitch system treated at low temperature (about 1000 to 1500 ° C), PAN
(Polyacrylonitrile) -based and phenol-based CF and pitch-based, PAN-based and phenol-based CF treated at high temperature (about 2000 to 2500 ° C.) are used.
From the viewpoint of imparting high conductivity to the lubricating composition, the latter C
F, from the viewpoint of compensating wear resistance and creep resistance, the former C
It is preferred to use F. Specific examples of pitch-based CF include “Zyrath (trade name)” manufactured by Nitto Boseki Co., Ltd., and PAN.
As a specific example of the carbon fiber, "Pyrofil (trade name)" manufactured by Mitsubishi Rayon Co., Ltd., and as a specific example of the phenolic CF, "Kynol CF16BT" manufactured by Nihon Kainol Co., Ltd.
(Product name) ". Regarding the size of the CF, that is, the diameter and the length, the diameter is preferably 1 to 20 μm and the length is preferably 30 to 3 mm. In consideration of the problem in the production of the lubricating composition, the diameter is about 10 μm and the length is 100 μm. The one before and after is preferred. And the compounding ratio of CF with respect to the lubricating composition is 5 to 30% by weight.
When the content is less than 5% by weight, it is difficult to impart conductivity to the lubricating composition, and when the content exceeds 30% by weight, further improvement in conductivity cannot be expected. Instead, it degrades the wear characteristics.

【0010】リン酸塩はそれ自体、例えば黒鉛、二硫化
モリブデンのような潤滑性を示す物質ではないが、PT
FE樹脂に配合されることにより相手材との摺動におい
て、相手材表面(摺動面)へのPTFE樹脂の潤滑被膜
の造膜性を助長する効果を発揮する。このリン酸塩によ
る効果は、該PTFE樹脂に配合される硬質のCFと相
手材との直接の接触(摺動)を防ぎ、CFの相手材を損
傷させ摺動部材の耐摩耗性を低下させるという欠点を抑
制するもので、乾燥摩擦潤滑下で使用される摺動部材に
必要とされる重要な要件である。本発明において使用さ
れるリン酸塩としては、第三リン酸塩、第二リン酸塩、
ピロリン酸、亜リン酸、メタリン酸などの金属塩および
それらの混合物が挙げられる。この中でも、第三リン酸
塩、第二リン酸塩およびピロリン酸塩が好ましい。金属
としてはアルカリ金属、アルカリ土類金属および遷移金
属が使用され、中でもアルカリ金属およびアルカリ土類
金属が好ましく、とくにリチウム、カルシウム、マグネ
シウムおよびバリウムが好ましい。具体的には、リン酸
リチウム、リン酸水素リチウム、ピロリン酸リチウム、
リン酸三カルシウム、ピロリン酸カルシウムおよびリン
酸水素カルシウムが最も好ましいものである。また、ハ
イドロキシアパタイトも好ましく使用することができ
る。このリン酸塩は上述したPTFE樹脂およびCFと
均一に混合されるもので、その粒度は平均20μm以下
のものが好ましい。リン酸塩は、潤滑組成物に対して少
量の配合割合、例えば0.1重量%の配合で前述した潤
滑被膜の造膜性を助長する効果が現れはじめ、15重量
%の配合割合まで造膜性の効果は維持される。しかし、
15重量%を越えて配合すると、相手材表面への潤滑被
膜の造膜量が多くなりすぎ、却って耐摩耗性を低下させ
る。したがって、リン酸塩の配合割合は0.1〜15重
量%、就中3〜10重量%が好ましい。
[0010] Phosphate itself is not a lubricating substance such as, for example, graphite or molybdenum disulfide.
When blended with the FE resin, it has an effect of promoting the film forming property of the lubricating coating of the PTFE resin on the surface (sliding surface) of the partner material in sliding with the partner material. The effect of the phosphate prevents direct contact (sliding) between the hard CF compounded in the PTFE resin and the mating material, damaging the mating material of the CF and reducing the wear resistance of the sliding member. This is an important requirement required for sliding members used under dry friction lubrication. As the phosphate used in the present invention, tertiary phosphate, secondary phosphate,
Metal salts such as pyrophosphoric acid, phosphorous acid, and metaphosphoric acid, and mixtures thereof. Among them, tertiary phosphate, secondary phosphate and pyrophosphate are preferred. As the metal, an alkali metal, an alkaline earth metal and a transition metal are used. Among them, an alkali metal and an alkaline earth metal are preferable, and lithium, calcium, magnesium and barium are particularly preferable. Specifically, lithium phosphate, lithium hydrogen phosphate, lithium pyrophosphate,
Tricalcium phosphate, calcium pyrophosphate and calcium hydrogen phosphate are most preferred. Also, hydroxyapatite can be preferably used. This phosphate is uniformly mixed with the above-mentioned PTFE resin and CF, and preferably has an average particle size of 20 μm or less. Phosphate starts to show the effect of promoting the film-forming property of the lubricating film in a small proportion of the lubricating composition, for example, in a proportion of 0.1% by weight, and forms a film to 15% by weight. The sexual effect is maintained. But,
If the amount exceeds 15% by weight, the amount of the lubricating film formed on the surface of the mating member becomes too large, and the wear resistance is rather lowered. Therefore, the mixing ratio of the phosphate is preferably 0.1 to 15% by weight, more preferably 3 to 10% by weight.

【0011】上述したPTFE樹脂、CFおよびリン酸
塩からなる潤滑組成物に対し、さらに摩擦摩耗特性を低
下させることなく一定割合の導電性物質の粉末を配合す
ることができ、該導電性物質の配合により潤滑組成物に
より高い導電性を付与することができる。本発明におい
て使用される導電性物質としては、コークス、無煙炭、
カーボンブラックおよび木炭などの無定形炭素粉末、天
然黒鉛、人造黒鉛およびキッシュ黒鉛などの黒鉛質炭素
粉末、銅粉末、ニッケル粉末、並びに鉛、錫及びインジ
ウム等の軟質金属粉末が挙げられる。これらの導電性物
質はそのほとんどが摩擦摩耗特性の向上に寄与しない物
質であるため、その配合割合についてはとくに注意を要
する。本発明では、上述した潤滑組成物に対し0.1〜
10重量%の範囲内であれば、摩擦摩耗特性を低下させ
ることなく潤滑組成物により高い導電性を付与すること
ができることを確認した。
A certain percentage of powder of a conductive substance can be blended with the lubricating composition comprising the above-mentioned PTFE resin, CF and phosphate without further lowering the friction and wear characteristics. By blending, a higher conductivity can be imparted to the lubricating composition. As the conductive substance used in the present invention, coke, anthracite,
Examples include amorphous carbon powder such as carbon black and charcoal, graphitic carbon powder such as natural graphite, artificial graphite and quiche graphite, copper powder, nickel powder, and soft metal powder such as lead, tin and indium. Since most of these conductive substances do not contribute to the improvement of the friction and wear characteristics, attention should be paid especially to the mixing ratio. In the present invention, 0.1 to 0.1
It was confirmed that within the range of 10% by weight, the lubricating composition could be provided with higher conductivity without lowering the friction and wear characteristics.

【0012】つぎに、摺動部材の製造方法について説明
する。 (潤滑組成物の調製)PTFE樹脂粉末に対し、5〜3
0重量%のCFおよび0.1〜10重量%のリン酸塩、
場合によって0.1〜10重量%の導電性物質の粉末を
PTFE樹脂の室温転移点(19℃)以下の温度で粉砕
しながら混合し、この混合物を19℃以下の温度に保持
しながら潤滑組成物100重量部に対し、石油系溶剤1
5〜20重量部を加えて攪拌混合して湿潤潤滑組成物を
得る。ここで、石油系溶剤としてはナフサ、トルエン、
キシレン、脂肪族系溶剤、脂肪族、ナフテン系混合溶剤
が使用される。潤滑組成物への石油系溶剤の配合割合が
15重量部以下では後述する多孔質焼結金属層への含浸
被覆工程における潤滑組成物の展延性が悪く、焼結層へ
の含浸被覆にムラを生じやすくなる。また、25重量部
を越える配合では含浸被覆作業がやりにくくなるばかり
でなく、被覆厚さの均一性が損なわれたり、潤滑組成物
と焼結層との密着強度が悪くなる。この混合をPTFE
樹脂の室温転移点以下の温度で行なうことにより、該P
TFE樹脂の繊維化が妨げられ、均一な混合物を得るこ
とができる。
Next, a method of manufacturing the sliding member will be described. (Preparation of lubricating composition) 5 to 3 parts of PTFE resin powder
0% by weight of CF and 0.1-10% by weight of phosphate,
In some cases, 0.1 to 10% by weight of a conductive substance powder is mixed while being pulverized at a temperature lower than the room temperature transition point (19 ° C.) of the PTFE resin, and the lubricating composition is maintained while maintaining the mixture at a temperature lower than 19 ° C. Petroleum solvent 1
5-20 parts by weight are added and mixed with stirring to obtain a wet lubricating composition. Here, naphtha, toluene,
Xylene, aliphatic solvents, aliphatic and naphthenic mixed solvents are used. If the blending ratio of the petroleum solvent to the lubricating composition is 15 parts by weight or less, the spreadability of the lubricating composition in the impregnating coating step on the porous sintered metal layer described below is poor, and the impregnating coating on the sintered layer may be uneven. It is easy to occur. If the amount exceeds 25 parts by weight, not only does the impregnation coating work become difficult, but also the uniformity of the coating thickness is impaired, and the adhesion strength between the lubricating composition and the sintered layer is deteriorated. This mixture is PTFE
By carrying out at a temperature below the room temperature transition point of the resin,
Fiberization of the TFE resin is prevented, and a uniform mixture can be obtained.

【0013】(摺動部材の製造)(a) 湿潤性が与え
られた潤滑組成物を裏金上に形成された多孔質焼結金属
層上に散布供給し、ローラで圧延して焼結層に潤滑組成
物を含浸するとともに該焼結層の表面に一様な潤滑組成
物の被覆層を形成する。この工程では潤滑組成物が最終
製品に必要とされる樹脂被覆厚さの2〜2.5倍の厚さ
に被覆される。多孔質焼結金属層の空隙中への樹脂の充
填はこの工程でその大部分が進行する。 (b) つぎに、多孔質焼結金属層に潤滑組成物が含浸
被覆された裏金を200〜250℃の温度に加熱された
乾燥炉内に数分間保持することにより、石油系溶剤を逸
散除去し、その後、乾燥した潤滑組成物層をローラによ
って所定の厚さになるように概ね300〜600kg/
cm2 の加圧力によって加圧する。 (c) ついで、ローラで加圧した乾燥潤滑組成物層を
備えた裏金を加熱炉に導入して360〜380℃の温度
で数分ないし10数分加熱して焼成を行なった後、これ
を炉から取り出し、再びローラを通して寸法のバラツキ
を調整する。 (d) 寸法調整後、摺動面層が形成された裏金を冷却
し、ついで必要に応じて裏金のうねりなどを矯正するた
めの矯正ローラに通して所望の複層摺動部材とする。 この複層摺動部材を適宜の大きさに切断したのち、平板
の状態ですべり板として使用することができ、また、丸
曲げして円筒状の巻きブッシュとして使用することがで
きる。
(Manufacture of sliding member) (a) A lubricating composition provided with wettability is sprayed and supplied onto a porous sintered metal layer formed on a backing metal, and rolled by a roller to form a sintered layer. The lubricating composition is impregnated and a uniform coating layer of the lubricating composition is formed on the surface of the sintered layer. In this step, the lubricating composition is coated to a thickness of 2 to 2.5 times the resin coating thickness required for the final product. Most of the filling of the resin into the voids of the porous sintered metal layer proceeds in this step. (B) Next, the back metal, in which the porous sintered metal layer is impregnated with the lubricating composition, is kept in a drying furnace heated to a temperature of 200 to 250 ° C. for several minutes to dissipate the petroleum-based solvent. Removed, and then the dried lubricating composition layer is roughly 300 to 600 kg /
It is pressurized by a pressure of cm 2 . (C) Next, the back metal provided with the dry lubricating composition layer pressed by a roller is introduced into a heating furnace, heated at a temperature of 360 to 380 ° C. for several minutes to several tens of minutes, and baked. Take it out of the furnace and pass it through the rollers again to adjust the dimensional variation. (D) After adjusting the dimensions, the back metal on which the sliding surface layer is formed is cooled, and then, if necessary, passed through a straightening roller for correcting undulations of the back metal to obtain a desired multilayer sliding member. After the multilayer sliding member is cut into an appropriate size, it can be used as a slide plate in a flat state, or can be round-bent and used as a cylindrical wound bush.

【0014】[0014]

【実施例】以下、本発明を実施例により詳細に説明す
る。 〔実施例1〕PTFE樹脂粉末として平均粒径80μm
以下の三井デュポンフロロケミカル社の「テフロン6C
J」を使用し、このPTFE樹脂粉末に、直径12μ
m、長さ100μmのCF(日東紡績社の「ザイラスG
PMF100JL」)5〜30重量%およびリン酸塩と
して350メッシュを通過するピロリン酸カルシウム
(関東化学社製)5重量%をヘンシェルミキサー内に投
入して粉砕混合し、該混合粉末100重量部に対し、石
油系溶剤として脂肪族・ナフテン系混合溶剤(エクソン
化学社の「エクソール」)20重量部を配合し、該PT
FE樹脂の室温転移点以下の温度で混合して湿潤潤滑組
成物を得た。該湿潤潤滑組成物を金属薄板からなる鋼裏
金上に形成された多孔質焼結金属層上に供給し、ローラ
で圧延して厚さ1.20mmになるように被覆して複層
板とし、該複層板を200℃の温度に加温した熱風乾燥
炉中に5分間保持して溶剤を飛散除去した後、乾燥潤滑
組成物層をローラによって加圧力400kg/ cm2
て加圧し厚さ1.05mmとした。次に、加圧された該
複層板を加熱炉内に導入して370℃の温度で10分加
熱焼成した後、再びローラにより加圧し、寸法調整なら
びに板のうねり等の矯正を行なった後切断し、辺30m
m×30mm×厚さ1.05mmの板状摺動部材試験片
を得た。この〔実施例1〕からなる摺動部材を構成する
潤滑組成物の成分組成を表1に示す。
DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described below in detail with reference to embodiments. [Example 1] PTFE resin powder having an average particle size of 80 µm
The following “Teflon 6C” of Mitsui DuPont Fluorochemicals
J ”and add 12 μm in diameter to this PTFE resin powder.
m, CF with a length of 100 μm (Zyras G
PMF100JL ") 5 to 30% by weight and 5% by weight of calcium pyrophosphate (manufactured by Kanto Chemical Co., Ltd.) passing through a 350 mesh as a phosphate are charged into a Henschel mixer and pulverized and mixed. As a petroleum-based solvent, 20 parts by weight of an aliphatic / naphthene-based mixed solvent (“EXSOL” of Exxon Chemical Co., Ltd.) was blended, and the PT
The wet lubricating composition was obtained by mixing at a temperature below the room temperature transition point of the FE resin. The wet lubricating composition is supplied onto a porous sintered metal layer formed on a steel backing made of a thin metal plate, and is rolled by a roller to coat so as to have a thickness of 1.20 mm to form a multilayer plate. After holding the multilayer plate in a hot-air drying furnace heated to a temperature of 200 ° C. for 5 minutes to remove the solvent by scattering, the dried lubricating composition layer was pressed by a roller at a pressing force of 400 kg / cm 2 to obtain a thickness. 1.05 mm. Next, the pressed multi-layer plate is introduced into a heating furnace and baked for 10 minutes at a temperature of 370 ° C., and then pressurized again by a roller to adjust the dimensions and correct the undulation of the plate. Cut, side 30m
A plate-like sliding member test piece of mx 30 mm x thickness 1.05 mm was obtained. Table 1 shows the component composition of the lubricating composition constituting the sliding member according to [Example 1].

【0015】〔実施例2〕PTFE樹脂粉末として平均
粒径80μm以下の三井デュポンフロロケミカル社の
「テフロン6CJ」を使用し、このPTFE樹脂粉末
に、直径12μm、長さ100μmのCF15重量%お
よびリン酸塩として350メッシュを通過するピロリン
酸リチウム(米山化学工業社製)3〜10重量%をヘン
シェルミキサー内に投入して粉砕混合し、該混合粉末1
00重量部に対し、石油系溶剤として脂肪族・ナフテン
系混合溶剤(エクソン化学社の「エクソール」)20重
量部を配合し、該PTFE樹脂の室温転移点以下の温度
で混合して湿潤潤滑組成物を得た。以下、製造工程は前
記〔実施例1〕と同一にして製造し、辺30mm×30
mm×厚さ1.05mmの板状摺動部材試験片を得た。
この〔実施例2〕からなる摺動部材を構成する潤滑組成
物の成分組成を表1に示す。
Example 2 As a PTFE resin powder, "Teflon 6CJ" manufactured by DuPont-Mitsui Fluorochemicals Co., Ltd. having an average particle diameter of 80 μm or less was used, and 15% by weight of CF having a diameter of 12 μm and a length of 100 μm was added to this PTFE resin powder. 3 to 10% by weight of lithium pyrophosphate (Yoneyama Chemical Industry Co., Ltd.) passing through a 350 mesh as an acid salt is charged into a Henschel mixer, pulverized and mixed.
20 parts by weight of a petroleum-based solvent of an aliphatic / naphthene-based mixed solvent (“EXSOL” manufactured by Exxon Chemical Co., Ltd.) and mixed at a temperature lower than the room temperature transition point of the PTFE resin. I got something. Hereinafter, the manufacturing process was performed in the same manner as in [Example 1], and the side was 30 mm × 30 mm.
A plate-like sliding member test piece having a size of 1.0 mm × 1.05 mm was obtained.
Table 1 shows the component composition of the lubricating composition constituting the sliding member made of [Example 2].

【0016】〔実施例3〕PTFE樹脂粉末として平均
粒径80μm以下の三井デュポンフロロケミカル社の
「テフロン6CJ」を使用し、このPTFE樹脂粉末
に、直径12μm、長さ100μmのCF5〜20重量
%、リン酸塩として350メッシュを通過するピロリン
酸カルシウム(関東化学社製)5重量%および導電性物
質としてカーボンブラック(三菱化成工業社製:CB3
750、以下「CB」という。)2重量%をヘンシェル
ミキサー内に投入して粉砕混合し、該混合粉末100重
量部に対し、石油系溶剤として脂肪族・ナフテン系混合
溶剤(エクソン化学社の「エクソール」)20重量部を
配合し、該PTFE樹脂の室温転移点以下の温度で混合
して湿潤潤滑組成物を得た。以下、製造工程は前記〔実
施例1〕と同一にして製造し、辺30mm×30mm×
厚さ1.05mmの板状摺動部材試験片を得た。この
〔実施例3〕からなる摺動部材を構成する潤滑組成物の
成分組成を表1に示す。
[Example 3] Teflon 6CJ of Mitsui DuPont Fluorochemicals having an average particle size of 80 µm or less was used as PTFE resin powder, and 5 to 20% by weight of CF having a diameter of 12 µm and a length of 100 µm was added to the PTFE resin powder. 5% by weight of calcium pyrophosphate (manufactured by Kanto Kagaku) passing through 350 mesh as a phosphate and carbon black (manufactured by Mitsubishi Kasei Kogyo KK: CB3)
750, hereinafter referred to as “CB”. ) 2% by weight was put into a Henschel mixer and pulverized and mixed, and 100 parts by weight of the mixed powder was mixed with 20 parts by weight of an aliphatic / naphthene-based mixed solvent ("EXSOL" of Exxon Chemical Company) as a petroleum-based solvent. Then, the PTFE resin was mixed at a temperature lower than the room temperature transition point to obtain a wet lubricating composition. Hereinafter, the manufacturing process is performed in the same manner as in [Example 1], and the side is 30 mm × 30 mm ×
A plate-shaped sliding member test piece having a thickness of 1.05 mm was obtained. Table 1 shows the component composition of the lubricating composition constituting the sliding member made of [Example 3].

【0017】〔比較例〕PTFE樹脂粉末として平均粒
径80μm以下の三井デュポンフロロケミカル社の「テ
フロン6CJ」を使用し、このPTFE樹脂粉末に、
(1)直径12μm、長さ100μmのCF30重量
%、(2)直径12μm、長さ100μmのCF40重
量%およびピロリン酸カルシウム5重量%(3)直径1
2μm、長さ100μmのCF40重量%、ピロリン酸
カルシウム5重量%および導電性物質としてCB2重量
%、(4)直径12μm、長さ100μmのCF15重
量%および導電性物質としてCB2重量%、をヘンシェ
ルミキサー内に投入して粉砕混合し、該混合粉末100
重量部に対し、石油系溶剤として脂肪族・ナフテン系混
合溶剤(エクソン化学社の「エクソール」)20重量部
を配合し、該PTFE樹脂の室温転移点以下の温度で混
合して湿潤潤滑組成物を得た。以下、製造工程は前記
〔実施例1〕と同一にして製造し、辺30mm×30m
m×厚さ1.05mmの板状摺動部材試験片を得た。こ
の〔比較例〕からなる摺動部材を構成する潤滑組成物の
成分組成を表1に示す。
[Comparative Example] As the PTFE resin powder, “Teflon 6CJ” manufactured by Mitsui DuPont Fluorochemicals Co., Ltd. having an average particle size of 80 μm or less was used.
(1) 30% by weight of CF having a diameter of 12 μm and a length of 100 μm; (2) 40% by weight of CF having a diameter of 12 μm and a length of 100 μm; and 5% by weight of calcium pyrophosphate.
2 μm, 40% by weight of CF having a length of 100 μm, 5% by weight of calcium pyrophosphate and 2% by weight of CB as a conductive substance, (4) 15% by weight of CF having a diameter of 12 μm and 100 μm in length and 2% by weight of CB as a conductive substance in a Henschel mixer And pulverized and mixed, and the mixed powder 100
A wet lubricating composition is prepared by mixing 20 parts by weight of an aliphatic / naphthene-based mixed solvent (“EXSOL” of Exxon Chemical Co., Ltd.) as a petroleum-based solvent with respect to parts by weight and mixing at a temperature below the room temperature transition point of the PTFE resin. I got Hereinafter, the manufacturing process is performed in the same manner as in [Example 1], and the side is 30 mm × 30 m.
A plate-shaped sliding member test piece of mx 1.05 mm in thickness was obtained. Table 1 shows the component composition of the lubricating composition constituting the sliding member made of this [Comparative Example].

【0018】次に、上述した実施例および比較例で得た
摺動部材の摩擦摩耗特性および体積抵抗率(Ω・cm)
について試験した結果を述べる。 〔摩擦摩耗特性〕摩擦摩耗特性については、下記に示す
摺動条件で行った。 (摺動条件) すべり速度 11m/min 荷重 100kgf/cm2 試験時間 8時間 潤滑 無潤滑 相手材 機械構造用炭素鋼(S45C) 摩擦係数については試験開始後1時間以後の摩擦係数の
変動値を示し、また摩耗量については試験時間8時間後
の摩耗量を測定した。 〔体積抵抗率〕体積抵抗率については、各摺動部材表面
に垂直な方向の体積抵抗率を四探針抵抗率測定法により
三菱油化社の抵抗率計(Lolester APMcp
−T400)を用いて測定した。各摺動部材の摩擦摩耗
特性および体積抵抗率を表1に示す。
Next, the friction and wear characteristics and the volume resistivity (Ω · cm) of the sliding members obtained in the above Examples and Comparative Examples are described.
The results of the tests for are described below. [Friction and wear characteristics] The friction and wear characteristics were measured under the following sliding conditions. (Sliding conditions) Sliding speed 11 m / min Load 100 kgf / cm 2 Test time 8 hours Lubrication Unlubricated partner Material Carbon steel for machine structure (S45C) The friction coefficient indicates the fluctuation value of the friction coefficient 1 hour after the start of the test. As for the amount of wear, the amount of wear after 8 hours of the test time was measured. [Volume resistivity] The volume resistivity in the direction perpendicular to the surface of each sliding member was measured by a four-probe resistivity measurement method using a resistivity meter (Lolster APMcp) manufactured by Mitsubishi Yuka Co., Ltd.
-T400). Table 1 shows the friction and wear characteristics and the volume resistivity of each sliding member.

【0019】[0019]

【表1】 [Table 1]

【0020】試験結果から、実施例1乃至実施例3から
なる摺動部材は試験時間を通して低い摩擦係数で安定し
た性能を示し、試験後の摺動部材の摩耗量も極めて小さ
いものであった。実施例1−6からなる摺動部材はCF
を30重量%含有しているにもかかわらず、試験後の相
手材表面は何らの損傷も認められなかった。また、体積
抵抗率は108 〜10-1の値を示した。一般に、OA機
器の摺動部に要求される導電性は体積抵抗率108 以下
であることを考えると十分満足のいく性能である。
From the test results, it was found that the sliding members of Examples 1 to 3 exhibited stable performance with a low coefficient of friction throughout the test time, and the amount of wear of the sliding members after the test was extremely small. The sliding member of Example 1-6 is CF
Despite containing 30% by weight, no damage was observed on the surface of the mating material after the test. The volume resistivity showed a value of 10 8 to 10 −1 . Generally, the conductivity required for the sliding portion of the OA equipment is a satisfactory performance considering that the volume resistivity is 10 8 or less.

【0021】一方、比較例からなる摺動部材は、導電性
の観点からは非常に優れた材料であるが、摩擦摩耗特性
については摩擦係数が高く、摩耗量も多く、また、相手
材表面に細い筋状の損傷が多数認められた。
On the other hand, the sliding member according to the comparative example is a very excellent material from the viewpoint of conductivity, but has a high coefficient of friction and a large amount of wear in terms of friction and wear characteristics. Numerous fine streak-like injuries were observed.

【0022】[0022]

【発明の効果】本発明は上述した構成からなるもので、
以下の特有の効果を有する。 (1)裏金上に形成された多孔質焼結金属層に含浸被覆
された潤滑組成物は、相手材との摺動において相手材を
何ら損傷させることなく低い摩擦係数で安定した性能を
発揮する。 (2)裏金上に形成された多孔質焼結金属層に含浸被覆
された潤滑組成物は、導電性を有するため、帯電防止効
果が要求される各種OA機器の摺動部へも使用でき、使
用用途範囲が大幅に拡大される。
The present invention has the above-mentioned structure,
It has the following unique effects. (1) The lubricating composition impregnated and coated on the porous sintered metal layer formed on the back metal exerts stable performance with a low friction coefficient without damaging the mating material in sliding with the mating material. . (2) Since the lubricating composition impregnated and coated on the porous sintered metal layer formed on the back metal has conductivity, it can be used for sliding parts of various OA equipments that require an antistatic effect, The range of use is greatly expanded.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI F16C 33/18 F16C 33/18 33/20 33/20 Z // C10N 10:02 10:04 10:16 20:06 30:06 40:02 (58)調査した分野(Int.Cl.6,DB名) C10M 169/04 C10M 107/38 C10M 125/02 C10M 125/24 C10N 40:02 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 6 Identification code FI F16C 33/18 F16C 33/18 33/20 33/20 Z // C10N 10:02 10:04 10:16 20:06 30: 06 40:02 (58) Field surveyed (Int.Cl. 6 , DB name) C10M 169/04 C10M 107/38 C10M 125/02 C10M 125/24 C10N 40:02

Claims (5)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 鋼裏金上に形成された多孔質焼結金属層
にポリテトラフルオロエチレン樹脂を主成分としこれに
充填材として炭素繊維5〜30重量%およびリン酸塩
0.1〜15重量%を含有する潤滑組成物が含浸被覆さ
れていることを特徴とする複層摺動部材。
1. A porous sintered metal layer formed on a steel backing metal containing polytetrafluoroethylene resin as a main component, 5 to 30% by weight of carbon fiber and 0.1 to 15% by weight of phosphate as a filler. %, Which is impregnated with a lubricating composition containing 0.1% by weight.
【請求項2】 潤滑組成物が更に導電性物質を0.1〜
10重量%含有する請求項1記載の複層摺動部材。
2. The lubricating composition further comprises a conductive substance of 0.1 to
The multilayer sliding member according to claim 1, which contains 10% by weight.
【請求項3】 導電性物質は、無定形炭素粉末、黒鉛質
炭素粉末、銅粉末、ニッケル粉末及び軟質金属粉末の1
種又は2種以上から選択される請求項2記載の複層摺動
部材。
3. The conductive substance is one of amorphous carbon powder, graphitic carbon powder, copper powder, nickel powder and soft metal powder.
3. The multi-layer sliding member according to claim 2, wherein the member is selected from a kind or two or more kinds.
【請求項4】 リン酸塩は、第三リン酸、第二リン酸、
ピロリン酸、亜リン酸及びメタリン酸の一種又は二種以
上から選択される金属塩である請求項1乃至3のいずれ
か一項に記載の複層摺動部材。
4. The phosphate is a tertiary phosphoric acid, a secondary phosphoric acid,
The multilayer sliding member according to any one of claims 1 to 3, wherein the sliding member is a metal salt selected from one or more of pyrophosphoric acid, phosphorous acid, and metaphosphoric acid.
【請求項5】 リン酸塩は、リン酸リチウム、リン酸水
素リチウム、ピロリン酸リチウム、リン酸三カルシウ
ム、ピロリン酸カルシウム、リン酸水素カルシウム及び
ハイドロキシアパタイトの1種又は2種以上から選択さ
れる請求項1乃至4のいずれか一項に記載の複層摺動部
材。
5. The phosphate is selected from one or more of lithium phosphate, lithium hydrogen phosphate, lithium pyrophosphate, tricalcium phosphate, calcium pyrophosphate, calcium hydrogenphosphate and hydroxyapatite. Item 5. The multilayer sliding member according to any one of Items 1 to 4.
JP1677391A 1990-05-09 1991-01-18 Multi-layer sliding member Expired - Lifetime JP2912034B2 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP1677391A JP2912034B2 (en) 1991-01-18 1991-01-18 Multi-layer sliding member
US07/693,243 US5300366A (en) 1990-05-09 1991-04-29 Fluororesin composition for a sliding member and a sliding member
DE69122299T DE69122299T2 (en) 1990-05-09 1991-05-08 Fluororesin composition for use in a sliding material and sliding material
KR1019910007425A KR0169707B1 (en) 1990-05-09 1991-05-08 A fluororesin composition suitable for use in a sliding member and a sliding member
EP91304125A EP0456471B1 (en) 1990-05-09 1991-05-08 A fluororesin composition suitable for use in a sliding member and a sliding member

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1677391A JP2912034B2 (en) 1991-01-18 1991-01-18 Multi-layer sliding member

Publications (2)

Publication Number Publication Date
JPH04236299A JPH04236299A (en) 1992-08-25
JP2912034B2 true JP2912034B2 (en) 1999-06-28

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001132756A (en) * 1999-11-08 2001-05-18 Ndc Co Ltd Sliding member coated with resin and method of manufacturing the same
JP4736867B2 (en) * 2006-03-07 2011-07-27 オイレス工業株式会社 Cylindrical cylindrical bearing bush, manufacturing method thereof, and hinge structure using the cylindrical cylindrical bushing
JP4737077B2 (en) * 2006-12-27 2011-07-27 オイレス工業株式会社 Multi-layer sliding member and hinge structure using the multi-layer sliding member
KR101066789B1 (en) * 2010-11-29 2011-09-21 주식회사 넥스텍 Sintered bearing and its manufacturing method
JP6198042B2 (en) * 2013-06-03 2017-09-20 株式会社ジェイテクト Steering device
JP2019168106A (en) * 2018-03-26 2019-10-03 オイレス工業株式会社 Multi-layer sliding member

Also Published As

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