JP2954638B2 - Synthetic resin composition for sliding members - Google Patents
Synthetic resin composition for sliding membersInfo
- Publication number
- JP2954638B2 JP2954638B2 JP2065153A JP6515390A JP2954638B2 JP 2954638 B2 JP2954638 B2 JP 2954638B2 JP 2065153 A JP2065153 A JP 2065153A JP 6515390 A JP6515390 A JP 6515390A JP 2954638 B2 JP2954638 B2 JP 2954638B2
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- Prior art keywords
- resin
- phosphate
- powder
- synthetic resin
- weight
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- Sliding-Contact Bearings (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
【発明の詳細な説明】 (産業上の利用分野) 本発明は、軸受、カム、歯車、すべり板、可撓軸用ラ
イナーチューブ、ガイド部材等に用いられて好適な摺動
部材用合成樹脂組成物に関するものである。The present invention relates to a synthetic resin composition for a sliding member suitable for use in bearings, cams, gears, sliding plates, liner tubes for flexible shafts, guide members and the like. It is about things.
(従来の技術) 一般に軸受等の摺動用途に用いられる合成樹脂に自己
潤滑性、耐摩耗性などの摺動特性を向上させる目的で、
また強度等、機械的性質を向上させる目的で、ポリ四フ
ッ化エチレン樹脂(以下PTFEという)および/またはガ
ラス繊維、炭素繊維等を配合することはよく知られてお
り、例えば、特開昭55−227号、特開昭58−179262号、
特開昭61−190553号、特開昭61−162549号、特開昭62−
185747号、特開昭62−223262号、特開昭63−278968号、
特開平1−127306号、特開平1−259059号等において種
々提案されている。(Prior art) Synthetic resins generally used for sliding applications such as bearings have the purpose of improving sliding characteristics such as self-lubrication and wear resistance.
It is well known to blend polytetrafluoroethylene resin (hereinafter referred to as PTFE) and / or glass fiber, carbon fiber and the like for the purpose of improving mechanical properties such as strength. -227, JP-A-58-179262,
JP-A-61-190553, JP-A-61-162549, JP-A-62
No. 185747, JP-A-62-223262, JP-A-63-278968,
Various proposals have been made in JP-A-1-127306 and JP-A-1-259059.
これら従来技術に開示された摺動部材は、ベース樹脂
に対し一定割合のPTFEを配合することにより摺動特性を
向上させ、一定割合のガラス繊維、炭素繊維などを配合
することにより耐摩耗性、機械的性質を向上させるもの
で、いずれも摺動面に潤滑油を供給することなく乾燥摩
耗条件下での使用を可能とするものである。The sliding members disclosed in these prior arts have improved sliding characteristics by blending a certain ratio of PTFE with a base resin, and have abrasion resistance by blending a certain ratio of glass fiber and carbon fiber. All of them improve mechanical properties, and can be used under dry wear conditions without supplying lubricating oil to the sliding surface.
(発明が解決しようとする問題点) しかしながら、乾燥摩擦条件下において使用される摺
動部材においては、相手材、例えば軸などの表面(摺動
面)への潤滑被膜形成の巧拙がその性能を大きく左右す
る。(Problems to be Solved by the Invention) However, in a sliding member used under dry friction conditions, the ability of forming a lubricating film on a surface (sliding surface) of a mating material, for example, a shaft, may deteriorate the performance. It depends greatly.
しかるに、上述した従来技術に開示された摺動部材に
おいては、相手材表面への潤滑被膜の形成が必ずしも良
好とは言い難く、結果として断続運転による再起動時の
摩擦係数が高く、動摩擦係数が不安定であるという問題
を生ずる。However, in the sliding member disclosed in the related art described above, it is difficult to say that the formation of the lubricating film on the surface of the mating material is not always good, and as a result, the coefficient of friction at the time of restarting by intermittent operation is high, and the dynamic friction coefficient is low. The problem of instability arises.
また、ガラス繊維、炭素繊維等を配合して、摺動部材
の耐摩耗性および機械的性質を向上させる試みは種々行
なわれているが、これらの繊維はそれ自体硬質であるこ
とから、配合割合には特に注意が必要である。強度等の
向上を目的として多量に配合すると相手材を損傷させた
り、相手材表面に形成された潤滑被膜を掻き取ったりす
る欠点があり、これらの欠点に起因してアブレッシブ摩
耗に発展するという問題を生ずる。Various attempts have been made to improve the wear resistance and mechanical properties of sliding members by blending glass fibers, carbon fibers, and the like. Requires special attention. When a large amount is blended for the purpose of improving the strength, etc., there is a defect that the mating material is damaged or a lubricating coating formed on the surface of the mating material is scraped off, and these defects lead to abrasive wear. Is generated.
本発明は、上述した問題を解決するべくなされたもの
で、相手材表面への潤滑被膜の形成能に優れ、摺動特性
ならびに機械的性質に優れた摺動部材用合成樹脂組成物
を得ることを目的とするものである。The present invention has been made in order to solve the above-described problems, and provides a synthetic resin composition for a sliding member that has excellent forming ability of a lubricating film on the surface of a mating member, and has excellent sliding characteristics and mechanical properties. It is intended for.
(問題点を解決するための手段) 上述した目的を達成するべく、本発明はつぎの技術的
手段(構成)を採る。すなわち、合成樹脂に、a)ポリ
四フッ化エチレン樹脂3〜40重量%、b)リン酸塩0.5
〜15重量%、c)ガラス繊維、ガラス粉末、炭素繊維、
無定形炭素粉末から選択される補強充填材1〜30重量%
を均一に混合してなる摺動部材用合成樹脂組成物であ
る。(Means for Solving the Problems) In order to achieve the above object, the present invention employs the following technical means (configuration). That is, a) 3 to 40% by weight of a polytetrafluoroethylene resin, b) phosphate 0.5
~ 15% by weight, c) glass fiber, glass powder, carbon fiber,
Reinforcement filler selected from amorphous carbon powder 1-30% by weight
Are uniformly mixed with each other.
本発明に使用される合成樹脂は、摺動部材に要求され
る機械的性質、化学的性質を備えていればよく、加うる
に耐摩耗性や自己潤滑性を具有しているものであれば一
層好ましい。また、用途によっては振動などを吸収し得
る弾性を有するものであってもよい。The synthetic resin used in the present invention may have the mechanical properties and chemical properties required for the sliding member, as long as it has abrasion resistance and self-lubricating properties. More preferred. Further, depending on the application, the material may have elasticity capable of absorbing vibration and the like.
具体的には、ポリアセタール樹脂、ポリアミド樹脂、
ABS樹脂、ポリアミドイミド樹脂、ポリイミド樹脂、ポ
リエーテルイミド樹脂、ポリエチレン樹脂、ポリプロピ
レン樹脂、ポリエチレンテレフタレート樹脂、ポリブチ
レンテレフタレート樹脂、ポリアリレート樹脂、ポリフ
ェニレンサルファイド樹脂、ポリエーテルサルフォン樹
脂、ポリエーテルエーテルケトン樹脂、ポリカーボネー
ト樹脂、ポリエーテルエステル樹脂、ポリウレタン樹
脂、エポキシ樹脂、フェノール樹脂から選択される。Specifically, polyacetal resin, polyamide resin,
ABS resin, polyamide imide resin, polyimide resin, polyether imide resin, polyethylene resin, polypropylene resin, polyethylene terephthalate resin, polybutylene terephthalate resin, polyarylate resin, polyphenylene sulfide resin, polyether sulfone resin, polyether ether ketone resin, It is selected from polycarbonate resin, polyetherester resin, polyurethane resin, epoxy resin, and phenol resin.
主成分をなす上記ベース樹脂に配合されるPTFEは、ベ
ース樹脂の自己潤滑性、低摩擦性に寄与するもので、本
発明において好適なPTFEとしては、例えば三井デュポン
フロロケミカル社製の商品名「テフロン7J」、「テフロ
ン7AJ」、ダイキン工業社製の商品名「ルブロンL−
2」、「ルブロンL−5」、「ルブロンLD−1」、喜多
村社製の商品名「KTL−610」等が挙げられる。The PTFE compounded in the base resin as a main component contributes to the self-lubricating property and low friction property of the base resin, and as the PTFE suitable in the present invention, for example, a product name `` Mitsui DuPont Fluorochemical Co., Ltd. "Teflon 7J", "Teflon 7AJ", product name "LUBRON L-
2, "Rublon L-5", "Rublon LD-1", and the brand name "KTL-610" manufactured by Kitamura Corporation.
このPTFEの配合割合は3〜40重量%、就中10〜25重量
%が好ましい。3重量%未満の配合割合ではベース樹脂
の自己潤滑性、低摩擦性に効果が現われず、また40重量
%を超えて配合すると、成形性の悪化、機械的強度の低
下をきたすことになる。The compounding ratio of the PTFE is preferably 3 to 40% by weight, more preferably 10 to 25% by weight. If the amount is less than 3% by weight, no effect is exerted on the self-lubricating properties and low frictional properties of the base resin. If the amount exceeds 40% by weight, the moldability deteriorates and the mechanical strength decreases.
リン酸塩は、それ自体は何ら潤滑性を示さないが、主
成分をなす合成樹脂に対し前述したPTFEとともに配合さ
れることにより、摺動の際、相手材表面(摺動面)への
PTFEの潤滑被膜の形成を助長し、且つ該被膜の相手材へ
の保持性を高め、被膜の耐久性を高めるという効果を発
揮する。Phosphate does not show any lubricity per se, but is mixed with the synthetic resin, which is the main component, together with the above-mentioned PTFE, so that it can adhere to the surface of the mating material (sliding surface) during sliding.
It has the effect of promoting the formation of a lubricating coating of PTFE, increasing the retention of the coating on the mating material, and increasing the durability of the coating.
リン酸塩としては、アルカリ金属、アルカリ土類金属
などの金属の第三リン酸塩、第二リン酸塩、ピロリン酸
塩、亜リン酸塩、メタリン酸塩およびそれらの混合物が
挙げられる。中でも、第三リン酸塩、第二リン酸塩及び
ピロリン酸塩が上述した潤滑被膜の形成の点で好まし
い。Phosphates include tertiary phosphates, secondary phosphates, pyrophosphates, phosphites, metaphosphates, and mixtures thereof, of metals such as alkali metals and alkaline earth metals. Among them, tertiary phosphate, second phosphate and pyrophosphate are preferred in terms of forming the above-mentioned lubricating coating.
具体的には、リン酸三リチウム、リン酸水素二リチウ
ム、ピロリン酸リチウム、リン酸三カルシウム、リン酸
水素カルシウム、ピロリン酸カルシウム、リン酸三マグ
ネシウム、リン酸水素マグネシウム、ピロリン酸マグネ
シウム、リン酸三バリウム、リン酸水素バリウム、ピロ
リン酸バリウムが好ましい。Specifically, trilithium phosphate, dilithium hydrogen phosphate, lithium pyrophosphate, tricalcium phosphate, calcium hydrogenphosphate, calcium pyrophosphate, trimagnesium phosphate, magnesium hydrogenphosphate, magnesium pyrophosphate, triphosphate Barium, barium hydrogen phosphate and barium pyrophosphate are preferred.
リン酸塩の配合割合は0.5〜15重量%、就中3〜10重
量%が好ましい。0.5重量%未満の配合割合では相手材
表面へのPTFEの潤滑被膜の形成、該被膜の保持性、耐久
性に効果が発揮されず、また15重量%を超えて配合する
と、相手材表面へのPTFEの潤滑被膜の形成量が多くなり
すぎ、却って摺動特性を悪化させるという欠点が現われ
る。The proportion of the phosphate is preferably 0.5 to 15% by weight, more preferably 3 to 10% by weight. If the compounding ratio is less than 0.5% by weight, the formation of a PTFE lubricating film on the surface of the mating material and the effect on the retention and durability of the film are not exerted. There is a disadvantage that the amount of the PTFE lubricating film formed is too large, and the sliding characteristics are rather deteriorated.
補強充填材としてのガラス繊維、ガラス粉末、炭素繊
維、無定形炭素粉末は主成分としての合成樹脂に配合さ
れて、特に摺動部材としての機械的強度を向上させる役
割と摺動部材の摺動面の表面硬度を高めて耐摩耗性を向
上させる役割を果たす。Glass fiber, glass powder, carbon fiber, and amorphous carbon powder as reinforcing fillers are mixed with synthetic resin as a main component to improve mechanical strength, especially as a sliding member, and to slide the sliding member. It plays the role of increasing the surface hardness of the surface and improving the wear resistance.
これら補強充填材の配合割合は1〜30重量%、就中5
〜20重量%が好ましい。The compounding ratio of these reinforcing fillers is 1 to 30% by weight, especially 5
~ 20% by weight is preferred.
一般に、補強充填材の多量の配合は、相手材との摺動
において相手材を損傷させ、発生た摩耗粉の介在に起因
してアブレッシブ摩耗を引き起こすなどの理由から避け
るべきであるが、本発明においては、上述したリン酸塩
の効果により、相手材表面へのPTFEの潤滑被膜の形成が
助長されるとともに、該被膜の保持性、耐久性が高めら
れるために、補強充填材と相手材との直接接触を防ぐこ
とから30重量%という多量の配合が可能となる。In general, a large amount of the reinforcing filler should be avoided for reasons such as damaging the mating material in sliding with the mating material and causing abrasive wear due to the presence of generated wear powder. In the above, the effect of the phosphate described above promotes the formation of a lubricating coating of PTFE on the surface of the mating material, and the retention and durability of the film are enhanced. As a result, a large amount of 30% by weight can be blended.
補強充填材として使用されるガラス繊維は、従来から
当該技術分野において通常使用されているガラス繊維、
即ち非晶質性のケイ酸塩ガラス、ホウ酸塩ガラス等に加
えて、ウォラストナイト、チタン酸カリウムウィスカ等
も使用することができる。Glass fibers used as reinforcing fillers are glass fibers conventionally used in the art,
That is, wollastonite, potassium titanate whisker, and the like can be used in addition to amorphous silicate glass, borate glass, and the like.
炭素繊維としては、ポリアクリロニトリル、レーヨ
ン、ポリビニルアルコール、フェノール、ピッチ等を出
発原料とする炭素繊維が使用される。As the carbon fiber, a carbon fiber starting from polyacrylonitrile, rayon, polyvinyl alcohol, phenol, pitch or the like is used.
これらの繊維はその径が1〜20μm、就中5〜15μm
のもので、長さは20〜6000μm、就中50〜300μmのも
のが好適である。These fibers have a diameter of 1-20 μm, especially 5-15 μm
Preferably, the length is 20 to 6000 μm, especially 50 to 300 μm.
ガラス粉末としては、上述した非晶質性のケイ酸塩ガ
ラス、ホウ酸塩ガラス等からなる粉末が使用される。As the glass powder, a powder made of the above-mentioned amorphous silicate glass, borate glass, or the like is used.
無定形炭素粉末としてはコークス粉末、無煙炭粉末、
カーボンブラック粉末、木炭粉末などの無定形炭素粉末
あるいはフェノール樹脂粉末等の高分子化合物粉末を不
活性雰囲気中550℃を超える温度で熱処理してなる粉末
(鐘紡社製の商品名「ベルパール」)などが使用され
る。Coke powder, anthracite powder, and amorphous carbon powder
Powder obtained by heat-treating amorphous carbon powder such as carbon black powder or charcoal powder, or polymer compound powder such as phenol resin powder in an inert atmosphere at a temperature exceeding 550 ° C (“Bell Pearl” manufactured by Kanebo) Is used.
これらの粉末の粒径は100μm以下、就中1〜40μm
のものが使用される。The particle size of these powders is 100 μm or less, especially 1 to 40 μm
Is used.
本発明の摺動部材用合成樹脂組成物は、上述した成分
組成からなるものであるが、これら成分組成に加えて、
成形性、耐摩耗性、耐荷重性の一層の向上を計るべく、
例えば二硫化モリブデン、グラファイトなどの固体潤滑
剤、鉛などの軟質金属などを5重量%以下の割合で配合
することができる。Although the synthetic resin composition for a sliding member of the present invention is composed of the above-described component compositions, in addition to these component compositions,
In order to further improve moldability, wear resistance, and load resistance,
For example, a solid lubricant such as molybdenum disulfide or graphite, a soft metal such as lead, or the like can be blended at a ratio of 5% by weight or less.
(実施例) 以下、本発明の実施例について説明する。(Example) Hereinafter, an example of the present invention will be described.
<実施例1〜3および比較例1> ポリアミド樹脂(以下PAという:東レ社製、商品名
「ナイロン66CM3001N」)粉末に、PTFE(ダイキン工業
社製、商品名「ルブロンL−5」)粉末とガラス繊維
(以下GFという)、無定形炭素粉末(以下CPという)も
しくは炭素繊維(以下CFという)およびリン酸塩粉末を
混合して得た混合粉末を成形材料とし、これをスクリュ
ウインライン型射出成形機によって、成形温度250〜290
℃および射出成形圧力700kg/cm2の条件で成形し、一片
が30mm、厚さ5mmの方形状試験片を得た。<Examples 1 to 3 and Comparative Example 1> Polyamide resin (hereinafter referred to as PA: manufactured by Toray Industries, trade name "Nylon 66CM3001N") powder was mixed with PTFE (manufactured by Daikin Industries, trade name "Rublon L-5") powder. Glass fiber (hereafter GF), amorphous carbon powder (hereafter CP) or mixed powder obtained by mixing carbon fiber (hereafter CF) and phosphate powder is used as molding material, which is screw-in-line injection molding Depending on the machine, molding temperature 250-290
Molding was performed under the conditions of ° C. and an injection molding pressure of 700 kg / cm 2 to obtain a square test piece having a thickness of 30 mm and a thickness of 5 mm.
<実施例4〜6および比較例2> ポリフェニレンサルファイド樹脂(以下PPSという:
トープレン社製、商品名「T−4」)粉末に前記PTFE粉
末とGF、CFもしくはCPおよびリン酸塩粉末を混合して得
た混合粉末を成形材料とし、これをスクリュウインライ
ン型種出成形機によって、成形温度270〜300℃および射
出成形圧力800kg/cm2の条件で成形し、一片が30mm、厚
さ5mmの方形状試験片を得た。<Examples 4 to 6 and Comparative Example 2> Polyphenylene sulfide resin (hereinafter referred to as PPS:
A mixed-in powder obtained by mixing the PTFE powder, GF, CF or CP and phosphate powder with powder (trade name “T-4” manufactured by Topren Co., Ltd.) is used as a molding material, and this is used as a screw-in-line type seed molding machine. The molding was performed under the conditions of a molding temperature of 270 to 300 ° C. and an injection molding pressure of 800 kg / cm 2 to obtain a square test piece having a thickness of 30 mm and a thickness of 5 mm.
<実施例7、8> ポリカーボネート樹脂(以下PCという:三菱瓦斯化学
社製、商品名「ユーピロンS2000」)粉末に、前記PTFE
粉末とGFもしくはCPおよびリン酸塩粉末をそれぞれ混合
して得た混合粉末を成形材料とし、これをスクリュウイ
ンライン型射出成形機によって、成形温度250〜300℃お
よび射出成形圧力1000kg/cm2の条件で成形し、一片が30
mm、厚さ5mmの方形状試験片を得た。<Examples 7 and 8> Polycarbonate resin (hereinafter, referred to as PC: manufactured by Mitsubishi Gas Chemical Company, trade name “Iupilon S2000”) was mixed with powder of PTFE.
The mixed powder obtained by mixing the powder with GF or CP and the phosphate powder is used as a molding material, and is subjected to a screw-in-line type injection molding machine at a molding temperature of 250 to 300 ° C. and an injection molding pressure of 1000 kg / cm 2 . Molded with 30 pieces
A square test specimen having a thickness of 5 mm and a thickness of 5 mm was obtained.
<実施例9、10および比較例3> フェノール樹脂(以下PHという:昭和ユニオン合成社
製、商品名「BRP−520」)粉末に、前記PTFE粉末とCFも
しくはCPおよびリン酸塩粉末とを混合して得た混合粉末
を成形材料とし、これを圧縮成形機によって、成形温度
160℃、成形圧力200kg/cm2の条件で成形し、一片が30m
m、厚さ5mmの方形状試験片を得た。<Examples 9 and 10 and Comparative Example 3> The PTFE powder, CF or CP and a phosphate powder were mixed with a phenol resin (hereinafter referred to as PH: Showa Union Gosei Co., Ltd. product name "BRP-520") powder. The obtained mixed powder is used as a molding material, and this is molded at a molding temperature by a compression molding machine.
160 ° C., and molded under the conditions of molding pressure 200 kg / cm 2, a piece is 30m
A rectangular test piece having a thickness of 5 mm and a thickness of 5 mm was obtained.
上記各実施例、比較例で得られた成形物について以下
の条件にてスラスト試験を行った結果を表に示す。The results of a thrust test performed on the molded products obtained in the above Examples and Comparative Examples under the following conditions are shown in the table.
<試験条件> すべり速度:20m/min 荷 重:10kg/cm2 相 手 材:SUS304(外径25.5mm、内径20.0mm) #800エメリー仕上げ 潤 滑:無潤滑 時 間:24時間 表中、aはPTFE、bはリン酸塩、cは補強充填材であ
る。また、摩擦係数は試験開始後1時間以降の変動幅を
示す。<Test conditions> Sliding speed: 20m / min Load: 10kg / cm 2- phase Hand material: SUS304 (outer diameter 25.5mm, inner diameter 20.0mm) # 800 emery finish Lubrication: no lubrication Time: 24 hours Is PTFE, b is phosphate, and c is reinforcing filler. Further, the coefficient of friction indicates a fluctuation range after one hour from the start of the test.
上述した試験結果から、本実施例の合成樹脂組成物は
比較例に比べて試験時間中を通じて安定した低い摩擦係
数を示し、摩耗量も極めて小さい値を示していることが
判る。実施例1乃至10においては、試験後の相手材表面
にPTFEの潤滑被膜が強固に形成されているのが観察され
た。 From the test results described above, it can be seen that the synthetic resin composition of this example shows a stable low coefficient of friction throughout the test time and a very small value of the wear amount as compared with the comparative example. In Examples 1 to 10, it was observed that a lubricating coating of PTFE was firmly formed on the surface of the mating member after the test.
(発明の効果) 本発明の摺動部材用合成樹脂組成物は、相手材表面へ
の潤滑被膜の形成能に優れ、摺動特性ならびに機械的性
質に優れている。その結果として、再起動時の摩擦係数
が低くかつ動摩擦係数が安定しており、すべり速度に関
係なく耐摩耗性に優れる。(Effect of the Invention) The synthetic resin composition for a sliding member of the present invention is excellent in the ability to form a lubricating film on the surface of a mating material, and is excellent in sliding properties and mechanical properties. As a result, the coefficient of friction at the time of restart is low, the coefficient of dynamic friction is stable, and the wear resistance is excellent regardless of the sliding speed.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI C08K 7/14 C08K 7/14 F16C 33/20 F16C 33/20 A //(C08L 101/00 27:18) (56)参考文献 特開 平1−79259(JP,A) 特開 昭62−104871(JP,A) 特公 昭38−20715(JP,B1) (58)調査した分野(Int.Cl.6,DB名) C08L 27/18 C08L 101/00 C08K 3/32 C08K 3/04 C08K 3/40 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 6 Identification code FI C08K 7/14 C08K 7/14 F16C 33/20 F16C 33/20 A // (C08L 101/00 27:18) (56) Reference Document JP-A-1-79259 (JP, A) JP-A-62-104871 (JP, A) JP-B-38-20715 (JP, B1) (58) Fields investigated (Int. Cl. 6 , DB name) C08L 27/18 C08L 101/00 C08K 3/32 C08K 3/04 C08K 3/40
Claims (3)
S樹脂、ポリアミドイミド樹脂、ポリイミド樹脂、ポリ
エーテルイミド樹脂、ポリエチレン樹脂、ポリプロピレ
ン樹脂、ポリエチレンテレフタレート樹脂、ポリブチレ
ンテレフタレート樹脂、ポリアリレート樹脂、ポリフェ
ニレンサルファイド樹脂、ポリエーテルサルフォン樹
脂、ポリエーテルエーテルケトン樹脂、ポリカーボネー
ト樹脂、ポリエーテルエステル樹脂、ポリウレタン樹
脂、エポキシ樹脂、フェノール樹脂から選択される合成
樹脂を主成分とし、該合成樹脂に、 a)ポリ四フッ化エチレン樹脂3〜40重量%、 b)リン酸塩0.5〜15重量%、 c)ガラス繊維、ガラス粉末、炭素繊維、無定形炭素粉
末から選択される補強充填材1〜30重量% を均一に混合してなる摺動部材用合成樹脂組成物。1. Polyacetal resin, polyamide resin, AB
S resin, polyamide imide resin, polyimide resin, polyether imide resin, polyethylene resin, polypropylene resin, polyethylene terephthalate resin, polybutylene terephthalate resin, polyarylate resin, polyphenylene sulfide resin, polyether sulfone resin, polyether ether ketone resin, A synthetic resin selected from a polycarbonate resin, a polyetherester resin, a polyurethane resin, an epoxy resin, and a phenol resin as a main component, wherein the synthetic resin includes: a) 3 to 40% by weight of a polytetrafluoroethylene resin, b) phosphoric acid 0.5 to 15% by weight of a salt, c) A synthetic resin composition for a sliding member, which is obtained by uniformly mixing 1 to 30% by weight of a reinforcing filler selected from glass fiber, glass powder, carbon fiber and amorphous carbon powder.
ルカリ土類金属のリン酸塩である請求項1に記載の摺動
部材用合成樹脂組成物。2. The synthetic resin composition for a sliding member according to claim 1, wherein the phosphate is a phosphate of an alkali metal or an alkaline earth metal.
酸水素二リチウム、ピロリン酸リチウム、リン酸三カル
シウム、リン酸水素カルシウム、ピロリン酸カルシウ
ム、リン酸三マグネシウム、リン酸水素マグネシウム、
ピロリン酸マグネシウム、リン酸三バリウム、リン酸水
素バリウム、ピロリン酸バリウムのうちの少なくとも1
種以上である請求項2に記載の摺動部材用合成樹脂組成
物。3. The method according to claim 1, wherein the phosphate is trilithium phosphate, dilithium hydrogen phosphate, lithium pyrophosphate, tricalcium phosphate, calcium hydrogenphosphate, calcium pyrophosphate, trimagnesium phosphate, magnesium hydrogenphosphate.
At least one of magnesium pyrophosphate, tribarium phosphate, barium hydrogen phosphate, barium pyrophosphate
The synthetic resin composition for a sliding member according to claim 2, which is at least one kind.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2065153A JP2954638B2 (en) | 1990-03-15 | 1990-03-15 | Synthetic resin composition for sliding members |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2065153A JP2954638B2 (en) | 1990-03-15 | 1990-03-15 | Synthetic resin composition for sliding members |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH03265646A JPH03265646A (en) | 1991-11-26 |
| JP2954638B2 true JP2954638B2 (en) | 1999-09-27 |
Family
ID=13278653
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2065153A Expired - Lifetime JP2954638B2 (en) | 1990-03-15 | 1990-03-15 | Synthetic resin composition for sliding members |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2954638B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2022059344A1 (en) | 2020-09-16 | 2022-03-24 | オイレス工業株式会社 | Resin composition for sliding member, and sliding member |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2608195B2 (en) * | 1991-06-24 | 1997-05-07 | セントラル硝子株式会社 | Thermoplastic urethane resin composition |
| JPH07145248A (en) * | 1993-11-24 | 1995-06-06 | Daido Metal Co Ltd | Sliding member for vibration absorption |
| DE19606948A1 (en) * | 1996-02-23 | 1997-08-28 | Hoechst Ag | Plastic molding compounds with less wear |
| JP2000074136A (en) * | 1998-08-28 | 2000-03-07 | Oiles Ind Co Ltd | Sliding structure combining two sliding members and slide bearing device using the same |
| JP4209974B2 (en) * | 1998-09-17 | 2009-01-14 | 株式会社クレハ | Sliding member for transfer device |
| JP4554742B2 (en) * | 1998-09-29 | 2010-09-29 | オイレス工業株式会社 | Resin composition for sliding member and slide bearing |
| JP4668375B2 (en) * | 1999-08-19 | 2011-04-13 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | Low melt viscosity polytetrafluoroethylene composition |
| JP2001323115A (en) * | 2000-05-17 | 2001-11-20 | Oiles Ind Co Ltd | Resin composition for sliding member, and sliding member |
| JP2001323116A (en) * | 2000-05-17 | 2001-11-20 | Oiles Ind Co Ltd | Resin composition for sliding member and sliding member |
| JP2002105306A (en) * | 2000-10-04 | 2002-04-10 | Sumitomo Bakelite Co Ltd | Polyether aromatic ketone resin composition and film and sheet |
| JP4825365B2 (en) * | 2001-05-29 | 2011-11-30 | オイレス工業株式会社 | Seismic isolation device for lightweight structures |
| JP6139338B2 (en) * | 2013-09-02 | 2017-05-31 | 三菱エンジニアリングプラスチックス株式会社 | Sliding polycarbonate resin composition and molded product |
| JP7704603B2 (en) * | 2021-07-20 | 2025-07-08 | 帝人株式会社 | Polybutylene naphthalate resin composition and molded article using same |
-
1990
- 1990-03-15 JP JP2065153A patent/JP2954638B2/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2022059344A1 (en) | 2020-09-16 | 2022-03-24 | オイレス工業株式会社 | Resin composition for sliding member, and sliding member |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH03265646A (en) | 1991-11-26 |
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