JPS60228558A - Polyphenylene sulfide resin composition - Google Patents
Polyphenylene sulfide resin compositionInfo
- Publication number
- JPS60228558A JPS60228558A JP8387084A JP8387084A JPS60228558A JP S60228558 A JPS60228558 A JP S60228558A JP 8387084 A JP8387084 A JP 8387084A JP 8387084 A JP8387084 A JP 8387084A JP S60228558 A JPS60228558 A JP S60228558A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- sliding
- resin composition
- inorganic filler
- polyphenylene sulfide
- 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.)
- Pending
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- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
本発明はポリフェニレンサルファイド樹脂(以下22日
樹脂という)にポリテトラフルオロエチレン樹脂(以下
pTIPm Ia4脂という)、二値化モリブテン、ヘ
キ開性を有する無機充填剤および線維状充填剤を一定割
合で含有せしめた摺動性能が良好で、耐熱性、耐摩耗性
、成形性などに優れた摺動部材として高度に応用が可能
な成形用組成物に関する4のである。DETAILED DESCRIPTION OF THE INVENTION The present invention consists of polyphenylene sulfide resin (hereinafter referred to as 22-day resin), polytetrafluoroethylene resin (hereinafter referred to as pTIPm Ia4 resin), binary molybdenum, an inorganic filler having hexagonal property, and a fibrous Item 4 relates to a molding composition that contains a filler in a certain proportion and has good sliding performance and can be highly applied as a sliding member with excellent heat resistance, abrasion resistance, moldability, etc.
近年、軸受なとの摺動部材に、軽量、易加工性などの点
で合成樹脂の使用が拡大している。In recent years, synthetic resins have been increasingly used for sliding members such as bearings due to their light weight and ease of processing.
合成樹脂の中で、ポリエチレン樹脂、ポリプロピレン樹
脂、ポリアセタール樹脂、ポリアミド樹脂などの熱可塑
性樹脂は成形性、耐摩耗性など忙優れていることから摺
動部材としての実用化が進んでいる。かかる合成樹脂の
自己潤滑性はゴムに比較して富むもののFTFFi樹脂
などのフッ素系樹脂に比べると著るしく劣っていて、摺
動性を向上せしめるにFia滑剤の配合が必要とされて
いる。かかる熱可塑性樹脂において、ポリエチレン樹脂
、ポリプロピレン樹脂に潤滑剤の配合された摺動材料か
らなる成形品は、ポリエチレン樹脂、ポリプロピレン樹
脂そのものの熱変形温度が低いことから、使用時の温度
上昇によって変形するという欠点があり、ポリアセター
ル樹脂に潤滑剤が配合された材料からなる成形品も摺動
性は優れているが耐熱性に劣り、しかも成形収縮率が大
きく精密成形品には適さないという欠点がある。また、
潤滑性を有するFTFFi樹脂は温度上昇に伴なって軟
化し相手部材の摺動面に付着し易くなり、その結果とし
て摩耗が急速に進行することから使用分野が制限される
という問題がある。更に、比較的耐熱性のあるポリアミ
ド樹脂は吸水性を有するため成形品の寸法安定性に難点
がある。Among synthetic resins, thermoplastic resins such as polyethylene resins, polypropylene resins, polyacetal resins, and polyamide resins have excellent moldability and abrasion resistance, and are therefore being put into practical use as sliding members. Although the self-lubricating properties of such synthetic resins are higher than that of rubber, they are significantly inferior to fluororesins such as FTFFi resins, and it is necessary to incorporate Fia lubricant to improve sliding properties. Among such thermoplastic resins, molded products made of sliding materials containing polyethylene resin or polypropylene resin with a lubricant will deform when the temperature rises during use, since the heat distortion temperature of the polyethylene resin or polypropylene resin itself is low. Molded products made of polyacetal resin mixed with a lubricant also have excellent sliding properties, but have poor heat resistance, and have a large mold shrinkage rate that makes them unsuitable for precision molded products. . Also,
FTFFi resin, which has lubricating properties, softens as the temperature rises and tends to adhere to the sliding surface of a mating member.As a result, wear progresses rapidly, which limits the field of use. Furthermore, polyamide resins, which are relatively heat resistant, have water absorption properties, which poses a problem in the dimensional stability of molded products.
かかる状況において、最近、急速にオフィスオートメー
ション化が進展し、それに関連して用いられる、いわゆ
る0ム機器に使用される摺動部材に耐熱性が高く、高度
な寸法安定性と精密成形が可能な成形用組成物が強くめ
られている。Under these circumstances, office automation has recently progressed rapidly, and sliding members used in so-called zero-meter equipment used in connection with this have high heat resistance, a high degree of dimensional stability, and are capable of precision molding. Molding compositions are strongly recommended.
耐熱性が高く、機械的強度の優れた熱・可塑性樹脂と−
してPPl3樹脂はエンジニアリングプラスチックの分
野において実用化が進んでいる。Thermoplastic resin with high heat resistance and excellent mechanical strength
PPl3 resin is now being put to practical use in the field of engineering plastics.
かかるpps樹脂は熱可塑性樹脂であシながら、加熱な
どにより架橋し得る熱硬化性樹脂のような性質を有して
いて、耐熱性、機械的強度はもとより、成形性、耐薬品
性にも優れているという特徴を有するが、pps樹脂単
独では伸びが少なく脆弱であるので成形材料とし、ての
形態は通常、強化材や補強剤が配合され強化がけがられ
ている。また、pps樹脂自体は前記の熱可塑性樹脂と
同様に自己潤滑性に乏しいため、摺動部材としての使用
形態においては潤滑剤などの配合により摺動性を付与す
ることが必要となる。Although such pps resin is a thermoplastic resin, it has properties similar to a thermosetting resin that can be crosslinked by heating, etc., and it has excellent moldability and chemical resistance as well as heat resistance and mechanical strength. However, pps resin alone has low elongation and is brittle, so it is used as a molding material, and the form of pps resin is usually reinforced by adding reinforcing materials or reinforcing agents. Further, since the pps resin itself has poor self-lubricating properties like the above-mentioned thermoplastic resins, when used as a sliding member, it is necessary to impart sliding properties by adding a lubricant or the like.
一般に、合成樹脂の摺動性を向上せしめるための手段と
して#1PTFI樹脂、黒鉛、二硫化モリブテン、窒化
ホウ素などの微粉末状固体潤滑剤を配合したり、常温で
液状のシリコン油、フッ素化油などの合成油、鉱油など
を添加する方法が採られている。Generally, as a means to improve the sliding properties of synthetic resins, finely powdered solid lubricants such as #1 PTFI resin, graphite, molybdenum disulfide, and boron nitride are blended, and silicone oils and fluorinated oils that are liquid at room temperature are mixed. Methods of adding synthetic oils such as mineral oils, etc., have been adopted.
而して、pps樹脂に、摺動性を付与する種々の試みに
おいて、特開昭52−129761号公報にけPP8樹
脂に黒鉛、FT、F’E樹脂を添加した要滑部材が提案
され、また、特公昭57−13586号公報にけPP8
樹脂、二硫化モリブデン、および炭素pa、taを含有
するPP8樹脂組成物が開示されている。しかしながら
、前者の要滑部材においてけ黒鉛やp T F Km脂
の含有量が多いため部材の摩耗量が増大し、しかも補強
材が含有されないことから機械的強度は低く、使用分野
が限定されるという問題があり、また後者の組成物から
なる摺動部材も二硫化モリブテンや炭素繊維の含有量が
多いことから部材の摩耗量が大きく、しかも摺動時の限
界pv値が低いことから加重に対する抵抗力およびスピ
ードに対する抵抗力が弱いという欠点を有している。In various attempts to impart sliding properties to pps resin, a sliding member made by adding graphite, FT, and F'E resin to PP8 resin was proposed in Japanese Patent Application Laid-open No. 52-129761. Also, in Japanese Patent Publication No. 57-13586, PP8
A PP8 resin composition containing a resin, molybdenum disulfide, and carbon pa, ta is disclosed. However, the former sliding members have a high content of graphite and p T F Km fat, which increases the amount of wear of the members, and because they do not contain reinforcing materials, their mechanical strength is low, limiting the field of use. Furthermore, since sliding members made of the latter composition have a high content of molybdenum disulfide and carbon fiber, the amount of wear on the member is large, and the limit pv value during sliding is low, so it is difficult to withstand loads. It has the disadvantage of low resistance to resistance and speed.
本発明者は上記問題点に鑑みて、耐熱性が高く、機械的
強度に優れたPP8樹脂に低摩擦性を付与せしめ、耐摩
耗性および限界pv値を高める手段を種々検討、研究し
た。その結果、耐摩耗性に影響を及ばずのは、黒鉛、F
TFB樹脂、二硫化モリブテンなどの低摩擦性付与剤が
多量に含有されることくよる本のであり、これらを減量
することによって耐摩耗性は改良されるが、摩擦係数は
増大する。他方、低摩擦性付与剤を多量に含有せしめ、
耐摩性を改良する目的でガラスファイバー、ガラスピー
ズ、シリカなどの含有は相手方部材を損傷せしめること
が判明した。これらのことから、相手方部材を損傷させ
ることなく、低摩擦性、耐摩耗性などの摺動性能を向上
せしめるKJd低摩擦性付与剤の含有量を特定範囲内に
制限し、かつ、へき開性を有する無機充填剤を特定範囲
の量で含有せしめることが極めて効果のあることを見い
出し本発明を完成するに至った4のである。In view of the above-mentioned problems, the present inventors have studied and researched various means to impart low friction properties to PP8 resin, which has high heat resistance and excellent mechanical strength, and to increase wear resistance and critical pv value. As a result, graphite, F
This is because low-friction imparting agents such as TFB resin and molybdenum disulfide are contained in large amounts, and reducing the amount of these agents improves wear resistance, but increases the coefficient of friction. On the other hand, it contains a large amount of a low friction agent,
It has been found that the inclusion of glass fiber, glass beads, silica, etc. for the purpose of improving wear resistance damages the mating member. For these reasons, the content of the KJd low-friction imparting agent, which improves sliding performance such as low friction and wear resistance, without damaging the mating member, is limited within a specific range, and the cleavage property is The present invention was completed based on the discovery that it is extremely effective to contain the inorganic filler in an amount within a specific range.
本発明ハボリフエニレンサルファイド樹脂30〜70重
量係、ポリテトラフルオロエチレン樹脂粉末5〜15重
量係、二硫化モリブデン1〜5重i%、ヘキ開性を有す
る無機充填剤10〜25重景%お重量繊維状強化材10
〜25重景係を重量するポリフェニレンサルファイド樹
脂組成物である。The polyphenylene sulfide resin of the present invention is 30 to 70% by weight, polytetrafluoroethylene resin powder is 5 to 15% by weight, molybdenum disulfide is 1 to 5% by weight, and an inorganic filler with cleavage property is 10 to 25% by weight. Heavy fibrous reinforcement 10
It is a polyphenylene sulfide resin composition weighing ~25 kg.
本発明の組成物において使用されるpps樹脂樹脂一般
式(0S)で表わされる繰返し単位からなる重合体であ
って、前記一般式の繰返し単位を90モルチ以上含むも
のが特性上から好ましい。その号が90モル係未満であ
ると特有の性質を有する組成物を得輯い傾向がある。Polymers consisting of repeating units represented by the pps resin general formula (0S) used in the composition of the present invention, and containing 90 mol or more of repeating units of the general formula, are preferred from the viewpoint of properties. If the number is less than 90 moles, there is a tendency to obtain a composition with specific properties.
この重合体を得る方法としての重合方法は公知の種々の
方法を採用し得るが、硫化す) IJウムとP−ジクロ
ルベンゼンとをNメチルピロリドン、ジメチルアセトア
ミドなどのアミノ系溶媒やスルホランなどのスルホン系
溶媒中で反応させるのが好適である。共重合成分として
10モルチ未満であって、重合体の結晶性に影響を与ス
ルフィド結合< (欠s−)などの共重合成分一
を含んでいてもよい。PP8樹脂は粉末状であって、そ
の粒径が大きくなると成形時にガスが発生して、初動部
材にクラックやボイドの発生が多くなり、また微粒すぎ
るとpps樹脂粒子の脱落傾向がある。かかるpps樹
脂において、米国フィリッブスペトロリアム社より市販
されている1ライドンPPS F−4、またはPR−0
6’(商品名)が好適に用いられる。PP8樹脂は組成
物中30〜70重量%含有されるのが精密成形性、ある
いけ成形された摺動部材の耐熱性、摺動性、耐摩耗性、
その他の特性に好適である。Various known methods can be used for the polymerization method to obtain this polymer. It is preferable to carry out the reaction in a sulfonic solvent. The copolymerization component may contain less than 10 molti of copolymerization components such as sulfide bonds < (missing s-), which affect the crystallinity of the polymer. PP8 resin is in powder form, and if the particle size becomes large, gas will be generated during molding, which will increase the occurrence of cracks and voids in the initial moving member, and if the particles are too fine, the pps resin particles will tend to fall off. Among such pps resins, 1Rydon PPS F-4 or PR-0, which is commercially available from Phillips Petroleum Company of the United States, is used.
6' (trade name) is preferably used. PP8 resin containing 30 to 70% by weight in the composition improves precision moldability, heat resistance, sliding properties, and abrasion resistance of molded sliding members.
Suitable for other properties.
本発明の組成物には樹脂成分としてPPS樹脂々共にP
TFE樹脂が含有される。FTFI樹脂は耐熱性に優れ
ていて、pps樹脂に添加されることによって成形され
た摺動部材の摩擦係数の低下に寄与するが、多量の添加
は摺動部材の摩耗を起こすので、必要且つ充分な召であ
るのが好ましく、その舞としては組成物中5〜15¥X
、骨チが適当である。15重重量%越える添加は上記の
摺動部材の摩耗の他に成形時の樹脂組成物の流動性は低
下して精密な摺動部材の成形には適さなくなり、また5
重量%より少ないと摩擦係数の低下に寄与することなく
、摺動性は劣ったものとなる。FTFFi樹脂は通常の
成形用に使用される粉末状のものであれば充分であるが
、微粒子であるものが好ましい。The composition of the present invention includes both PPS resin and PPS resin as resin components.
Contains TFE resin. FTFI resin has excellent heat resistance, and when added to pps resin, it contributes to lowering the coefficient of friction of molded sliding members, but adding a large amount will cause wear of the sliding members, so it is necessary and sufficient. It is preferable that the composition is 5 to 15 yen
, bone chi is appropriate. If the addition exceeds 15% by weight, in addition to the above-mentioned abrasion of the sliding member, the fluidity of the resin composition during molding will decrease, making it unsuitable for molding precision sliding members.
If it is less than % by weight, it will not contribute to lowering the coefficient of friction and the sliding properties will be poor. It is sufficient that the FTFFi resin is in the form of a powder that is used for ordinary molding, but it is preferable that it be in the form of fine particles.
二硫化モリブテンは、本発明の樹脂組成物におけるpp
s樹脂、FTFI樹脂、あるいは繊維状強化材などに対
し優れた親和性を示す。二硫化モルブテンの使用形nは
微粒子粉末状のものが好ましく、樹脂組成物中の含有量
はヘキ開性を有する無機充填剤の含有量と共に成形され
た摺動部材の摺動性に影禅を及はすが、1〜5重量重量
あるの蕨魂当である。5重量%を越える素の添加は、成
形された摺動部材が脆弱となり、摩耗量が増大して耐摩
耗性は劣ったものとなる。Molybdenum disulfide is pp in the resin composition of the present invention.
Shows excellent affinity for S resin, FTFI resin, fibrous reinforcement, etc. The molybutene disulfide used is preferably in the form of fine particles, and its content in the resin composition, together with the content of the cleavable inorganic filler, affects the sliding properties of the molded sliding member. However, it is a warabi ton that weighs between 1 and 5 pounds. If more than 5% by weight of the element is added, the molded sliding member becomes brittle, the amount of wear increases, and the wear resistance becomes poor.
本発明の樹脂組成において含有されるヘキ開性を有する
無機充凋剤1、摺動部材としてめら力る次のような基本
的糸外を満足するのに極めで有用なものである。The cleavable inorganic filler 1 contained in the resin composition of the present invention is extremely useful for satisfying the following basic requirements as a sliding member.
(1) 摺動性に関し、摩擦係数が小さいこと(2)相
手方部材を摩耗しないこと
(3) 長期的耐久性から自己の摩耗量が少ないこと
本発明の樹脂組成物の特徴はヘキ開性を有する無機充填
剤が含有されてなることにある。ヘキ開性とけ通常、結
晶や岩石が機械的な打撃によって、それらの内部構造に
おいて相対的に結合の弱い方向があると、こね、に直角
な面に平行に割れたり、はがれた抄する性質として知ら
れていて、このように平行に割れたり、はがれたすした
面はヘキ開面と呼ばれている。ヘキ開性。(1) In terms of sliding properties, the coefficient of friction is small (2) It does not wear out the mating member (3) It has a small amount of wear on itself due to long-term durability The characteristics of the resin composition of the present invention are that it has a high cleavage property. The reason is that it contains an inorganic filler that has Normally, crystals and rocks are mechanically struck, and if there is a direction in which the bonds in their internal structure are relatively weak, they will crack parallel to the plane perpendicular to the kneading, or they will peel off. This type of parallel cracked or peeled surface is called a cleavage surface. Hexapatency.
を有する無機充填剤鉱、本発明の樹脂組成物に含有され
て摺動部材として成形されると摺動作動中に削られた場
合であっても、あたかもヘキ開面から一枚づつl!11
り取られるが如き状態で摩耗するので、相手部材に変化
を及ぼすことがない。かかるヘキ開性を有する無機充填
剤として好適に使用し得るものけタルク、マイカ、クレ
ー、黒鉛などである。これらは1種に限定されることな
く2種以上を併用してもよい。また、これらの粒径は0
.1〜50μ、好ましくけα5〜10μのものである。When the resin composition of the present invention contains an inorganic filler ore having an inorganic filler ore and is molded into a sliding member, even if it is scraped during the sliding operation, it will be removed one by one from the hexagonal surface! 11
Since it wears out as if it were being removed, there is no change in the mating member. Mononoke talc, mica, clay, graphite, etc., which can be suitably used as the inorganic filler having such cleavability, include monomer talc, mica, clay, and graphite. These are not limited to one type, and two or more types may be used in combination. Also, these particle sizes are 0
.. 1 to 50μ, preferably α5 to 10μ.
樹脂組成物中の含有量としては10〜25重−Illで
あるのが適当であって、この範囲を越える含有は摺動部
材の成形時に流動性の低下を招くので精密部品の成形な
どKは適当でない。また、この範囲より少ない埠合は成
形された摺動部材の耐摩耗性は劣ったものとなり麿耗量
が増大する。ヘキ開性を有する無機充填剤を含有せしめ
ることけ、摺動部材に多竜に含有されると好オしくない
PTFE樹脂や二硫化モリブデンの含有量を減量せしめ
ることを可能とし、その結果、摺動部材における基本的
条件としての前記(1)〜(3)を満足せしめることと
なる。The appropriate content in the resin composition is 10 to 25 F-Ill, and if the content exceeds this range, the fluidity will decrease during molding of sliding members, so K is not suitable for molding precision parts. It's not appropriate. Further, if the amount of contact is less than this range, the wear resistance of the molded sliding member will be poor and the amount of wear will increase. By containing an inorganic filler with cleavage properties, it is possible to reduce the content of PTFE resin and molybdenum disulfide, which are undesirable when contained in sliding members, and as a result, the sliding member The basic conditions (1) to (3) for moving members are satisfied.
本発明の樹脂組成物によって成形された摺動部材の機械
的強度を向上せしめる目的で繊維状強化材が含有される
。PP8樹脂に対する繊維状強化材としては通常、ガラ
ス締、維が用いられるが、摺動部材においてガラス繊維
の含有は相手部材に傷を生ぜしめ、摩耗を促進するので
好ましくない。本発明の樹脂組成物に含有される繊維状
強化材として好適に用い得るものは炭素繊維、チタン酸
カリウム繊維であり、また、これら繊維の併用である。A fibrous reinforcing material is contained for the purpose of improving the mechanical strength of the sliding member molded from the resin composition of the present invention. Glass fibers are usually used as a fibrous reinforcing material for PP8 resin, but the inclusion of glass fibers in sliding members is not preferable because it causes damage to the mating member and accelerates wear. Carbon fibers, potassium titanate fibers, and combinations of these fibers can be suitably used as the fibrous reinforcing material contained in the resin composition of the present invention.
かかる錯雑状強化材は一般に市販されている長さ6fi
程度のチョツプドファイバーが用いられる。樹脂組成物
中に含有される量は10〜25重景係が重量であり、こ
の範囲を鱗える量を含有すると成形時に流れ性が低下し
、しかも所要量以上を含有せしめても機械的強度の向上
は望めない。また上記範囲に及ばない少量の含有でI/
i機械的強度は低いものとなるので適当ではない。Such complex reinforcements are generally commercially available in length 6fi.
A certain amount of chopped fiber is used. The amount contained in the resin composition is 10 to 25 parts by weight, and if it is contained in an amount within this range, the flowability during molding will be reduced, and even if it is contained in an amount exceeding the required amount, the mechanical strength will be decreased. cannot be expected to improve. In addition, if the content is in a small amount that does not fall within the above range, I/
i Mechanical strength is low, so it is not suitable.
本発明の樹脂組成物において、PP8樹脂、PTFE樹
脂、二硫化モリブテン、ヘキ開性を有する無機充填剤及
び繊維状強化材を配合し混線する方法は特に限定される
と七なく、通常、粉状物の混合用に用いられる混合機、
例えばヘンシェルミキサー、タンブラ−ミキサー、V形
ミキサーなどによって機械的に均一混合させる方法を採
ることができる。次にその混合物をスクリュ一式の単@
オたけ2軸の混練押出成形機に投入し、300〜400
℃の高温加熱下に溶融混練してストランド状に押出した
後、冷却し、ペレタイザーによってペレット状の成形材
料とすることができる。In the resin composition of the present invention, there are no particular limitations on the method of blending and mixing the PP8 resin, PTFE resin, molybdenum disulfide, cleavable inorganic filler, and fibrous reinforcing material, and the method is usually in the form of a powder. A mixer used for mixing things,
For example, a method of uniformly mixing mechanically using a Henschel mixer, a tumbler mixer, a V-type mixer, etc. can be used. Next, pour the mixture into a set of screws.
Put it into a kneading extrusion molding machine with two screws, and
After melt-kneading and extruding into a strand while heating at a high temperature of .degree. C., it can be cooled and made into a pellet-like molding material using a pelletizer.
このようにして得られたベレットは通常広く用いられて
いる熱可塑性樹脂の成形機、例えば射出成形機、圧縮成
形機あるいは押出成形機によって所望の形状に成形する
ことができる。かかる成形方法における成形条件は特に
限定されることなく通常の成形条件で行なわれる。The pellet thus obtained can be molded into a desired shape using a commonly used thermoplastic resin molding machine, such as an injection molding machine, a compression molding machine, or an extrusion molding machine. The molding conditions in this molding method are not particularly limited and may be carried out under normal molding conditions.
本発明の樹脂組成物は成形時の流動性に優れていること
から、寸法精度をめられる精密部材の成形に好適であり
、しかも成形された摺動部材岐耐熱性、機械的強度にも
優れていて、摺動作動中における形状変化がなく、庵擦
に対する摺動性能を長期に亘って維持することができる
。庵擦に対する摺動性能を摩擦係数μで示すとα2以下
であって、他の潤滑性付与剤などを使用することなく、
機械類の摺動部材となり得るものであね、特にOA機器
の摺動部材として好適に使用し得るものである。更に相
手部材、例えば摺動軸を損傷せしめるようなことはなく
、従来高価な材料が使用さねでいた摺動軸の頻繁な交換
も不要となるなどコストダウンに資するという利点を有
している。Since the resin composition of the present invention has excellent fluidity during molding, it is suitable for molding precision parts that require dimensional accuracy, and also has excellent heat resistance and mechanical strength for molded sliding parts. Therefore, there is no change in shape during sliding operation, and sliding performance against abrasion can be maintained over a long period of time. The sliding performance against friction is expressed by the friction coefficient μ, which is less than α2, and without using any other lubricity imparting agent.
It can be used as a sliding member of machinery, and is particularly suitable for use as a sliding member of OA equipment. Furthermore, it does not damage the mating parts, such as the sliding shaft, and has the advantage of contributing to cost reductions, such as eliminating the need for frequent replacement of the sliding shaft, which conventionally required expensive materials. .
以下に本発明を実施例九より具体的に説明するが、本発
明はこれら実施例のみに限定される4のでないことは勿
論である。面、実施例において摺動性能の評価方法は次
の条件にて行なった。The present invention will be explained in more detail below using Example 9, but it goes without saying that the present invention is not limited only to these Examples. In the Examples, the sliding performance was evaluated under the following conditions.
摩擦係数及び摩耗係数:荷重4.2 kg7cm”、摩
擦速度60 m / Win s相手部材 8450ハ
ードクロムメッキ仕上げ。Friction coefficient and wear coefficient: load 4.2 kg 7 cm", friction speed 60 m / Wins mating part 8450 hard chrome plated finish.
限界pv値:帛擦速度60yq/min、相手部材84
5Cハードクロムメッキ仕上げ、荷重は可変。Limit pv value: cloth rubbing speed 60yq/min, mating member 84
5C hard chrome plating finish, load is variable.
実施例1
PP日樹脂1ライドンPP8″ (商品名:P−4グレ
ード、米国フィリッブスペトローリアム社製品)45部
(重量部、以下同じ) 、PTFFi樹脂(L−169
、旭フロロポリマー社製品)12部、二値化モリブテン
(粉末グレード、住鉱潤滑剤製品)3部、ヘキ開性を有
する無機充填剤としてメルク(P−2、松材産業製品)
20部及び締維状補強材として150℃で5時間乾燥し
た炭素繊維(M−102、呉羽化学社製品)20部をV
型ミキサーにて5分間混合した。得られ光混合物を40
−φ単軸押出機のホッパ K投入し、シリンダ一温度を
310℃に設定して混練した後、押出してペレットを成
形した。このようにして得られたペレットを120℃で
12時間乾燥した後、シリンダ一温度が320℃に設定
された1オンス射出成形機にて金型温度125℃に保持
された金製内に射出し、内径2α口慎、外径25.6m
m、長さ15−の円筒形の摺動性能評価用試験片を成形
した。この試験片を用いて、摩擦係数、摩耗係数、限界
pv値及び相手部材の損傷の有無などの摺動性能を測定
した。それらの結果を第1表に示した。Example 1 PP Nippon Resin 1 Rydon PP8'' (trade name: P-4 grade, product of Phillips Petroleum, USA) 45 parts (parts by weight, same hereinafter), PTFFi resin (L-169)
, Asahi Fluoropolymer Co., Ltd. product) 12 parts, binarized molybdenum (powder grade, Sumiko lubricant product) 3 parts, Merck as an inorganic filler with cleavage property (P-2, Matsuzai Sangyo product)
20 parts and 20 parts of carbon fiber (M-102, Kureha Kagaku Co., Ltd. product) dried at 150°C for 5 hours as a fibrous reinforcement material.
Mixed for 5 minutes using a mold mixer. The resulting light mixture is 40
The mixture was put into the hopper K of a -φ single-screw extruder, and the cylinder temperature was set at 310° C. for kneading, followed by extrusion to form pellets. After drying the pellets thus obtained at 120°C for 12 hours, they were injected into a metal mold with a mold temperature of 125°C in a 1-ounce injection molding machine with a cylinder temperature of 320°C. , inner diameter 2α diameter, outer diameter 25.6m
A cylindrical test piece for evaluating sliding performance with a length of 15 m and a length of 15 mm was molded. Using this test piece, sliding performance such as friction coefficient, wear coefficient, limit pv value, and presence or absence of damage to the mating member was measured. The results are shown in Table 1.
第1表に示されるように優れた摩耗特性をもつものが得
られることを確認した。As shown in Table 1, it was confirmed that products with excellent wear characteristics could be obtained.
実施例2〜4
実施例1におけるヘキ開性を有する無機充填剤のタルク
をマイカ(パウダー、上屋カオリン製品)、黒鉛(F−
3、日本黒鉛工業社製品)、及びクレー(KNカオリン
、上屋カオリン製品)のそれぞれに変えた他は、実施例
1と同様に混合、混練してペレットを得た。得られたペ
レットを射出成形機によって槽動性能評価用試験片を成
形した。この試験片について摺動性能を測定し第1表に
示す結果を得た。第1表に示されるように優れた摩耗特
性をもつものが得られることを確認した。Examples 2 to 4 Talc, the inorganic filler with cleavage properties in Example 1, was mixed with mica (powder, Kagaya Kaolin product) and graphite (F-
3. Nippon Graphite Industries Co., Ltd. product) and clay (KN Kaolin, Ueya Kaolin product) were mixed and kneaded in the same manner as in Example 1 to obtain pellets. The obtained pellets were molded into test pieces for evaluating tank dynamic performance using an injection molding machine. The sliding performance of this test piece was measured and the results shown in Table 1 were obtained. As shown in Table 1, it was confirmed that products with excellent wear characteristics could be obtained.
比較例1〜2
実施例1に訃けるヘキ開性を有する無機充填剤のタルク
をヘキ開性を有しない無機充填剤としてシリカ1イムシ
ルA−10H’(商品名:たつちり社製品)あるいはガ
ラスピース(粒径平均値17μ、東芝パロテイー二社製
品)K変えた他社実施例1と同様に混合、混練してペレ
ット化し光。得られたペレットを射出成形して摺動性能
評価用試験片を成形して、その摺動性能を測定した。測
定結果を第1表に示したが、摩耗特性は劣ったものであ
ることが確認された。Comparative Examples 1 to 2 Talc, an inorganic filler with cleavage property that is inferior to Example 1, was replaced with silica 1-Imucil A-10H' (trade name: Tatsuchiri Co., Ltd. product) or glass as an inorganic filler without cleavage property. Pieces (average particle size 17μ, manufactured by Toshiba Parotech 2) were mixed, kneaded, and pelletized in the same manner as in Example 1, except for K. The obtained pellets were injection molded to form test pieces for evaluating sliding performance, and the sliding performance was measured. The measurement results are shown in Table 1, and it was confirmed that the wear characteristics were poor.
実施例5〜6.比較例3
実施例1における繊維状補強材としての炭素繊維をチタ
ン酸カリウム繊維”テイヌモD”(大塚薬品製品)、炭
素繊維とチタン酸カリウム繊維(1:1)の併用、ある
いはガラス繊維(O8−03−MA497、旭ファイバ
ーグラス社製品)に変えた他は実施例1と同様に混合、
混練してペレット化した。得られたペレットを射出成形
して摺動性能評価用試験片を成形して、その摺動性能を
測定した。測定結果を第2表に示した。Examples 5-6. Comparative Example 3 Carbon fiber as the fibrous reinforcing material in Example 1 was replaced with potassium titanate fiber "Teinumo D" (Otsuka Pharmaceutical Products), a combination of carbon fiber and potassium titanate fiber (1:1), or glass fiber (O8 -03-MA497, a product of Asahi Fiberglass Co., Ltd.) was mixed in the same manner as in Example 1.
The mixture was kneaded and pelletized. The obtained pellets were injection molded to form test pieces for evaluating sliding performance, and the sliding performance was measured. The measurement results are shown in Table 2.
実施例7〜8.比較例4
実施例1におけるPTFE樹脂及び二硫化モリブテンの
含有量を第2表に示すような量に変更した他社実施例1
と同様に混合、混練してペレット化した。得られたペレ
ットを射出成形して摺動性能評価用試験片を成形して、
その摺動性能を測定した。測定結果を第2表に示した。Examples 7-8. Comparative Example 4 Example 1 of another company in which the contents of PTFE resin and molybdenum disulfide in Example 1 were changed to the amounts shown in Table 2.
The mixture was mixed and kneaded in the same manner as above to form pellets. The obtained pellets were injection molded to form test pieces for evaluating sliding performance.
Its sliding performance was measured. The measurement results are shown in Table 2.
比較例4は相手方部材を損傷することはないが、耐摩耗
性および限界pv値の劣ったものであることが認めらね
る。Comparative Example 4 does not damage the mating member, but it cannot be recognized that the wear resistance and limit pv value are inferior.
Claims (1)
0重%1ポリテトラフルオロエチレン樹脂粉末5〜15
重!#係、二値化モリブテン1〜5重?&%、ヘキ開性
を有する無機充填剤10〜25重量係お重量錯雑状強化
材10〜25@舞%を含有するポリフェニレンサルファ
イド樹脂組成物。 2 ヘキ開性を有する無機充填剤がタルク、マイカ、ク
レー、黒鉛の少なくとも1種からなる特許請求の範囲第
1項記載のポリフェニレンサルファイド樹脂組成物。 五 繊維状強化材が炭素*、維またはチタン酸カリウム
繊維あるいけそれらの併用繊維からなる特許請求の範囲
第1項記載のポリフェニレンサルファイド樹脂組成物。[Claims] 1. y't! I) Phenylene sulfide resin 30-7
0% by weight 1 polytetrafluoroethylene resin powder 5-15
Heavy! Person #, binarized molybdenum 1 to 5 layers? A polyphenylene sulfide resin composition containing 10 to 25% by weight of an inorganic filler having cleavability and 10 to 25% by weight of a complex reinforcing material. 2. The polyphenylene sulfide resin composition according to claim 1, wherein the cleavable inorganic filler comprises at least one of talc, mica, clay, and graphite. (5) The polyphenylene sulfide resin composition according to claim 1, wherein the fibrous reinforcing material is carbon*, fiber, potassium titanate fiber, or a combination thereof.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8387084A JPS60228558A (en) | 1984-04-27 | 1984-04-27 | Polyphenylene sulfide resin composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8387084A JPS60228558A (en) | 1984-04-27 | 1984-04-27 | Polyphenylene sulfide resin composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS60228558A true JPS60228558A (en) | 1985-11-13 |
Family
ID=13814695
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP8387084A Pending JPS60228558A (en) | 1984-04-27 | 1984-04-27 | Polyphenylene sulfide resin composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60228558A (en) |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6140357A (en) * | 1984-07-31 | 1986-02-26 | Otsuka Chem Co Ltd | Polyphenylene sulfide resin composition |
| JPS62232457A (en) * | 1986-04-03 | 1987-10-12 | Dainippon Ink & Chem Inc | Polyphenylene sulfide resin composition |
| WO1988009356A1 (en) * | 1987-05-29 | 1988-12-01 | Otsuka Kagaku Kabushiki Kaisha | Resin composition for scroll type compressor members and process for manufacturing scroll type compressor parts |
| JPS63301259A (en) * | 1987-05-29 | 1988-12-08 | Otsuka Chem Co Ltd | Resin composition for slidable mechanical part |
| JPS63306265A (en) * | 1987-06-05 | 1988-12-14 | Asahi Glass Co Ltd | Sliding valve for carburetor |
| JPH08253679A (en) * | 1996-01-17 | 1996-10-01 | Dainippon Ink & Chem Inc | Polyphenylene sulfide resin composition |
| JP4755828B2 (en) * | 2002-12-18 | 2011-08-24 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | Low friction coefficient thermoplastic composition containing filler |
| CN111574833A (en) * | 2020-05-17 | 2020-08-25 | 上海交通大学 | High-wear-resistance polyphenylene sulfide/regenerated carbon fiber composite material and preparation thereof |
| CN111819244A (en) * | 2018-08-17 | 2020-10-23 | 株式会社Lg化学 | Low friction resin composite |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS52129761A (en) * | 1976-04-26 | 1977-10-31 | Oiles Industry Co Ltd | Lubricationnrequired part of polyphenylene sulfide resin having high lubricating properties |
| JPS5713586A (en) * | 1980-06-27 | 1982-01-23 | Canon Inc | Printing device |
-
1984
- 1984-04-27 JP JP8387084A patent/JPS60228558A/en active Pending
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS52129761A (en) * | 1976-04-26 | 1977-10-31 | Oiles Industry Co Ltd | Lubricationnrequired part of polyphenylene sulfide resin having high lubricating properties |
| JPS5713586A (en) * | 1980-06-27 | 1982-01-23 | Canon Inc | Printing device |
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6140357A (en) * | 1984-07-31 | 1986-02-26 | Otsuka Chem Co Ltd | Polyphenylene sulfide resin composition |
| JPS62232457A (en) * | 1986-04-03 | 1987-10-12 | Dainippon Ink & Chem Inc | Polyphenylene sulfide resin composition |
| US5131827A (en) * | 1987-05-29 | 1992-07-21 | Otsuka Kagaku Kabushiki Kaisha | Fiber- and whisker-reinforced injection moldable resin composition for scroll compressor parts and method of manufacturing scroll compressor parts |
| JPS63301259A (en) * | 1987-05-29 | 1988-12-08 | Otsuka Chem Co Ltd | Resin composition for slidable mechanical part |
| JPS63301258A (en) * | 1987-05-29 | 1988-12-08 | Otsuka Chem Co Ltd | Resin composition for scroll type compressor member and production of scroll type compressor member |
| WO1988009356A1 (en) * | 1987-05-29 | 1988-12-01 | Otsuka Kagaku Kabushiki Kaisha | Resin composition for scroll type compressor members and process for manufacturing scroll type compressor parts |
| JPS63306265A (en) * | 1987-06-05 | 1988-12-14 | Asahi Glass Co Ltd | Sliding valve for carburetor |
| JPH08253679A (en) * | 1996-01-17 | 1996-10-01 | Dainippon Ink & Chem Inc | Polyphenylene sulfide resin composition |
| JP4755828B2 (en) * | 2002-12-18 | 2011-08-24 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | Low friction coefficient thermoplastic composition containing filler |
| CN111819244A (en) * | 2018-08-17 | 2020-10-23 | 株式会社Lg化学 | Low friction resin composite |
| US11905371B2 (en) | 2018-08-17 | 2024-02-20 | Lg Chem, Ltd. | Low friction resin composites |
| CN111574833A (en) * | 2020-05-17 | 2020-08-25 | 上海交通大学 | High-wear-resistance polyphenylene sulfide/regenerated carbon fiber composite material and preparation thereof |
| CN111574833B (en) * | 2020-05-17 | 2022-03-11 | 上海交通大学 | High-wear-resistance polyphenylene sulfide/regenerated carbon fiber composite material and preparation thereof |
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