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JPH0561305B2 - - Google Patents

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Publication number
JPH0561305B2
JPH0561305B2 JP16635785A JP16635785A JPH0561305B2 JP H0561305 B2 JPH0561305 B2 JP H0561305B2 JP 16635785 A JP16635785 A JP 16635785A JP 16635785 A JP16635785 A JP 16635785A JP H0561305 B2 JPH0561305 B2 JP H0561305B2
Authority
JP
Japan
Prior art keywords
nickel
volume
conductivity
parts
carbon fiber
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
JP16635785A
Other languages
Japanese (ja)
Other versions
JPS6227458A (en
Inventor
Masaki Egami
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.)
NTN Corp
Original Assignee
NTN Toyo Bearing Co 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 NTN Toyo Bearing Co Ltd filed Critical NTN Toyo Bearing Co Ltd
Priority to JP16635785A priority Critical patent/JPS6227458A/en
Publication of JPS6227458A publication Critical patent/JPS6227458A/en
Publication of JPH0561305B2 publication Critical patent/JPH0561305B2/ja
Granted legal-status Critical Current

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  • Conductive Materials (AREA)

Description

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

〔産業上の利用分野〕 この発明は、摩擦係数が小さく、耐摩耗性が優
れ、同時に体積抵抗率が小さいことを目的とする
導電性摺動材組成物に関するものである。 〔従来の技術〕 近年、電子機器、電気機器の小型化または軽量
化に伴つて、それらの部品に合成樹脂が盛んに利
用されるようになつて来た。そして、特に摺動特
性と導電性とを兼備した摺動材料のプラスチツク
化が強く要望されるようになり、合成樹脂を基材
とし、これに耐摩耗性の向上と導電性の付与とを
目的として、黒鉛、導電性カーボン、金属粉、金
属繊維などの充填材を添加した材料が開発され
た。しかし、黒鉛、導電性カーボンを添加した材
料では体積抵抗率は101〜102Ω・cm程度得られる
が、ポリフエニレンサルフアイド等に添加したと
きは耐摩耗性が著しく悪い。また、金属粉を添加
するときは、金、銀、銅、アルミニウム、ニツケ
ル等の粉末が用いられるが、金および銀は化学的
に安定でしかも高導電性のものではあるがきわめ
て高価であり、したがつて、これらの代替品とし
て使用される銅、アルミニウムは成形加工する際
に酸化されやすく、得られる製品の導電性は不安
定となつて導電性付与材には適しない。さらにニ
ツケル粉は化学的にも比較的安定で、合成樹脂に
添加して得られる製品の導電性および安定性は共
に良好ではあるものの、耐摩耗性は著しく悪い。
また、金属繊維には黄銅フアイバー、アルミニウ
ムフアイバーなどがあるが、これらはいずれも前
記の粉末状のものと同様に酸化されやすく、通常
の市販品の多くは径60μm、長さ3mmと寸法が大
きく、摺動材料用の充填材にこのような大型繊維
を使用したときは、材料面より端が突出して相手
材表面を損傷することもあることから、決して望
ましいものとは言えない。その結果、この発明者
は、潤滑性のある材料を金属で被覆し、これを合
成樹脂に可能な限り多量に充填し、その特性の確
認を試みたが、期待される導電性のものは得られ
ず、またポリオレフインまたは射出成形可能なフ
ツ素樹脂にニツケル粉末もしくはイツケル被覆材
と炭素繊維とを組み合わせて添加した組成物を開
発し(たとえば特願昭60−11361号、同−11360
号)が、これら組成物は優れた摺動特性と良好な
導電性を有してはいるものの、射出成形可能なフ
ツ素樹脂は生産価格が高く事務機器などに使用す
るには経済的不利を免れず、またポリオレフイン
は安価であつても耐熱温度が低く使用環境が限ら
れることから、いずれも市場の要求に充分適応出
来るものとは言えない。 〔発明が解決しようとする問題点〕 このように従来の導電性摺導材組成物には摩擦
係数が小さく、耐摩耗性および導電性が共に優れ
ていて、しかも耐用範囲が広く安価であるという
諸条件を満足するものがないと言う解決すべき問
題点があつた。 〔問題点を解決するための手段〕 上記の問題点を解決するために、この発明はポ
リフエニレンサルフアイド100容量部に対して、
ニツケル被覆雲母と炭素繊維とを両者の容量比が
15:80から80:20の範囲で総量が30〜140容量部
となるように添加した組成物とする手段を採用し
たものである。以下その詳細を述べる。 まず、この発明におけるポリフエニレンサルフ
アイド(以下PPSと略記する)は、つぎの一般式 で示される合成樹脂であり、米国フイリツプス・
ペトローリアム社から「ライトン」の商標で市販
されている。その製造方法は米国特許第3354129
号(対応特許特公昭45−3368号)に開示されてい
て、それによるとライトンはN−メチルピロリド
ン溶媒中、160〜250℃、加圧条件下にp−ジクロ
ルベンゼンと二硫化ソーダとを反応させることに
よつて製造され、樹脂中に交叉結合が全くないも
のから部分的交叉結合を有するものに至るまで各
種重合度のものを後熱処理工程にかけることによ
つて自由に製造することができるので、目的の溶
融ブレンドに適正な溶融粘度特性を有するものを
任意に選択使用することが可能である。 また、この発明におけるニツケル被覆雲母は、
固体潤滑剤として知られている金雲母などの雲母
(マイカ)粉末の表面を電気的もしくは化学的に
ニツケルめつきして、表面に導電性を付与したも
のである。 さらに、この発明における炭素繊維は耐摩耗
性、耐クリープ性を向上させるという役割を果す
が、ニツケル被覆雲母を分散させたとき、これら
が相互に接触して全体の導電性を満遍なく高めよ
うとする目的に使用されるものであるから、炭素
繊維自身に良好な導電性が必要であることは勿論
である。したがつて、より高度の導電性が要求さ
れるようなときは、たとえばニツケルなどの金属
を被覆した炭素繊維(たとえば東邦ベスロン社
製:HTCF/Ni)などを使用すればよい。いず
れにしても、このような炭素繊維はこの発明の組
成物の混合、成形等の容易さおよび成形面からの
突出等の点から、径は20μm以下、好ましくは6
〜15μm、長さは6mm以下、好ましくは0.02〜3.0
mmのものが望ましく、一般的には東レ社製:トレ
カMLDまたは呉羽化学工業社製:クレハカーボ
ンフアイバーなどの市販品を例示することができ
る。 この発明において、ニツケル被覆雲母と炭素繊
維との混合割合を容量比で15:80から80:20の範
囲内に限定する理由はニツケル被覆雲母の量を前
記下限値よりも少なくしたのでは導電性が期待で
きず、また逆に上限値よりも多くすると導電性は
あつても摺動性が得られなくなるからであつて、
好ましくは40:60から70:30の範囲にするとよ
い。そして、このようなニツケル被覆雲母と炭素
繊維との混合物すなわちこれらの総量を、合成樹
脂100容量部に対して30〜140容量部添加する理由
は、30容量部より少ないときは期待する導電性が
得られず、140容量部よりも多いときは摺動特性
が悪化するか、または成形が困難になつたり、成
形できたとしても成形品の機械的強度(たとえば
衝撃強度)が低下して好ましくないからであつ
て、望ましくは50〜100容量部にするとよい。 ここで、この発明において配合割合をすべて容
量比で示す理由は、通常の炭素繊維と金属被覆炭
素繊維とでは比重が著しく異なり、重量比ではこ
の発明の構成範囲を客観的に示し得ないからであ
り、各原料についてそれぞれ重量と真比重とを測
定し、その重量を真比重で除した値を容積(体
積)とする方法を用いた。そして配合量の決まつ
た各原料を混合する方法は特に限定するものでは
なく、通常広く用いられている方法、たとえば
PPS樹脂、ニツケル被覆雲母、炭素繊維などをそ
れぞれ個別に、またはヘンシエルミキサー、ボー
ルミル、タンブラーミキサー等の混合機によつて
適宜乾式混合した後、溶融混合性のよい射出成形
機もしくは溶融押出成形機に供給するか、または
予め熱ロール、ニーダ、バンバリーミキサー、溶
融押出機などで溶融混合するなどの方法を利用す
ればよい。また、この発明の組成物を成形するに
あたつても、特にその方法を限定するものではな
く、圧縮成形、押出成形、射出成形等の通常の方
法、または組成物を溶融混合した後、これをジエ
ツトミル、冷凍粉砕機等によつて粉砕し、所望の
粒径に分級するかまたは分級しないままで、得ら
れた粉末を用いた流動浸漬塗装、静電粉体塗装な
どを行なうことも可能である。なお、この発明の
組成物は、潤滑性をより向上させるために、ポリ
四フツ化エチレン、黒鉛、二硫化モリブデン、オ
イル等の潤滑剤を添加しても構わない。 〔作用〕 以上述べたことの発明の組成物の成形体表面を
研磨して摺動面とした面には、PPSの相、ニツケ
ル被覆の相のほかに、ニツケル被覆雲母に内蔵さ
れている固体潤滑剤としての雲母と炭素繊維とは
潤滑性の向上に、ニツケル被覆層は互にまたは炭
素繊維と密に接して電路を形成し導電性の増大に
寄与するのである。 〔実施例〕 実施例および比較例に用いた諸原料はつぎのと
おりである。すなわち、 ポリフエニレンサルフアイド(米国フイリツ
プス・ペトローリアム社製:ライトンP4)、 四フツ化エチレン樹脂(三井デユポンフロロ
ケミカル社製:テフロン7J)、 ニツケル被覆雲母(平均粒径12μmの金雲母
に無電解法によつて平均膜厚0.1μmのニツケル
めつきを形成したもの)、 ニツケル被覆炭素繊維(東邦ベスロン社製:
HTCF/Ni、繊維径7.5μm、繊維長300μm、平
均ニツケル膜厚0.25μm)、 ニツケル粉末(米国インコ社製:ニツケルパ
ウダー255、平均粒径3μm)、 炭素繊維(東レ社製:トレカMLD−300、繊
維径7μm、繊維長300μm)である。 そして、実施例1〜4における各原料の配合割
合はポリフエニレンサルフアイド100容量部に対
し、また比較例1〜4における各原料の配合割合
も同じくポリフエニレンサルフアイド100容量部
に対するそれぞれの容量部の値で示し、これらを
一括して表にまとめた。これら諸原料はヘンシエ
ルミキサーで充分混合した後、二軸溶融押出機に
供給し、シリンダー温度300℃、回転数100rpmの
溶融混合条件で押出して造粒した。得られたペレ
ツトを樹脂温度310℃、射出圧力800Kg/cm2、金型
温度130℃の射出成形条件で外径23mm、内径14mm、
長さ13mmのリング状試験片および幅12.7mm、長さ
63mm、厚さ3mmの板状試験片を成形し、リング状
試験片を用いて体積抵抗率の測定および摩擦摩耗
試験を行ない、一方板状試験片はASTM−D790
に準拠して曲げ強さを測定した。ここで、摩擦係
数は滑り速度を毎分100m、荷重1Kg/cm2の条件
でスラスト型摩擦試験機を用いて測定し、摩耗係
数は滑り速度毎分128m、荷重1.6Kg/cm2の条件で
スラスト型摩耗試験機を用いて求めいずれも相手
材には軸受鋼SUJ−2(焼入れ、研削仕上げ)を
使用した。得られた結果をすべてまとめて表に併
記した。この表から明らかなように、比較例1〜
4においては体積抵抗率が低い値を示しても摩耗
係数が著しく大きいか、または逆に摩耗係
[Industrial Application Field] The present invention relates to a conductive sliding material composition which aims to have a small coefficient of friction, excellent wear resistance, and at the same time a low volume resistivity. [Prior Art] In recent years, as electronic devices and electrical devices have become smaller and lighter, synthetic resins have come to be widely used for their parts. In particular, there was a strong demand for plastic sliding materials that had both sliding properties and electrical conductivity, and the aim was to use synthetic resin as a base material to improve wear resistance and impart electrical conductivity. As a result, materials containing fillers such as graphite, conductive carbon, metal powder, and metal fibers have been developed. However, when graphite or conductive carbon is added to a material, a volume resistivity of about 10 1 to 10 2 Ω·cm can be obtained, but when added to polyphenylene sulfide or the like, wear resistance is extremely poor. Furthermore, when adding metal powder, powders of gold, silver, copper, aluminum, nickel, etc. are used, but although gold and silver are chemically stable and highly conductive, they are extremely expensive. Therefore, copper and aluminum used as substitutes for these materials are easily oxidized during molding, and the resulting products have unstable conductivity, making them unsuitable as conductivity imparting materials. Further, nickel powder is chemically relatively stable, and although products obtained by adding it to synthetic resins have good conductivity and stability, their wear resistance is extremely poor.
In addition, metal fibers include brass fibers and aluminum fibers, but these are all easily oxidized like the powdered ones mentioned above, and most commercially available products are large, with a diameter of 60 μm and a length of 3 mm. When such large fibers are used as fillers for sliding materials, their ends may protrude beyond the surface of the material and damage the surface of the mating material, which is by no means desirable. As a result, the inventor tried to confirm the properties of a lubricating material by coating it with metal and filling it into a synthetic resin as much as possible, but he was unable to find the expected electrical conductivity. In addition, a composition was developed in which a combination of nickel powder or a coating material of nickel and carbon fiber was added to a polyolefin or an injection moldable fluororesin (for example, Japanese Patent Application No. 11361/1982, Japanese Patent Application No. 11360/1983).
Although these compositions have excellent sliding properties and good conductivity, injection moldable fluororesins are expensive to produce and are economically disadvantageous for use in office equipment. Moreover, even though polyolefins are inexpensive, their heat resistance is low and the environment in which they can be used is limited. Therefore, it cannot be said that any of them can be fully adapted to the demands of the market. [Problems to be solved by the invention] As described above, conventional conductive sliding material compositions have a small coefficient of friction, excellent wear resistance and conductivity, and have a wide range of service life and are inexpensive. There was a problem that needed to be solved: there was nothing that satisfied the various conditions. [Means for Solving the Problems] In order to solve the above problems, the present invention provides that, for 100 parts by volume of polyphenylene sulfide,
The capacity ratio of nickel-coated mica and carbon fiber is
A method is adopted in which the composition is added in a ratio of 15:80 to 80:20 in a total amount of 30 to 140 parts by volume. The details will be described below. First, polyphenylene sulfide (hereinafter abbreviated as PPS) in this invention has the following general formula: It is a synthetic resin shown by
It is marketed by Petroleum Corporation under the trademark "Ryton." The manufacturing method is US Patent No. 3354129
No. 45-3368 (corresponding patent No. 45-3368), according to which Ryton prepared p-dichlorobenzene and sodium disulfide in an N-methylpyrrolidone solvent at 160 to 250°C under pressure. It is produced by a reaction, and can be freely produced by subjecting the resin to various degrees of polymerization, from those with no cross-linking to those with partial cross-linking, by subjecting it to a post-heat treatment process. Therefore, it is possible to arbitrarily select and use those having melt viscosity characteristics suitable for the desired melt blend. Further, the nickel-coated mica in this invention is
The surface of mica powder such as phlogopite, which is known as a solid lubricant, is electrically or chemically plated with nickel to give it electrical conductivity. Furthermore, the carbon fibers in this invention play the role of improving wear resistance and creep resistance, but when the nickel-coated mica is dispersed, they come into contact with each other and try to uniformly increase the overall conductivity. Since the carbon fiber is used for this purpose, it goes without saying that the carbon fiber itself must have good electrical conductivity. Therefore, when a higher degree of conductivity is required, carbon fiber coated with a metal such as nickel (for example, HTCF/Ni manufactured by Toho Bethlon Co., Ltd.) may be used. In any case, such carbon fibers have a diameter of 20 μm or less, preferably 6 μm or less, from the viewpoint of ease of mixing and molding the composition of the present invention and protrusion from the molding surface.
~15μm, length less than 6mm, preferably 0.02~3.0
mm is preferable, and commercially available products such as Torayca MLD (manufactured by Toray Industries, Inc.) and Kureha Carbon Fiber (manufactured by Kureha Chemical Industry Co., Ltd.) can generally be used. In this invention, the reason why the mixing ratio of nickel-coated mica and carbon fiber is limited to a range of 15:80 to 80:20 by volume is that if the amount of nickel-coated mica is less than the lower limit, the conductivity cannot be expected, and conversely, if the amount exceeds the upper limit, even if conductivity is achieved, sliding properties cannot be obtained.
Preferably it is in the range of 40:60 to 70:30. The reason why such a mixture of nickel-coated mica and carbon fiber, that is, the total amount thereof, is added in 30 to 140 parts by volume to 100 parts by volume of synthetic resin is that if it is less than 30 parts by volume, the expected conductivity will not be achieved. If the amount is more than 140 parts by volume, the sliding properties may deteriorate, or it may become difficult to mold, or even if it can be molded, the mechanical strength (for example, impact strength) of the molded product will decrease, which is undesirable. The amount is preferably from 50 to 100 parts by volume. The reason why all compounding ratios in this invention are expressed as volume ratios is that normal carbon fibers and metal-coated carbon fibers have significantly different specific gravity, and weight ratios cannot objectively indicate the range of composition of this invention. A method was used in which the weight and true specific gravity of each raw material were measured, and the volume was determined by dividing the weight by the true specific gravity. The method of mixing each raw material in a fixed amount is not particularly limited, and may be any commonly used method, such as
PPS resin, nickel-coated mica, carbon fiber, etc. are mixed individually or appropriately using a mixer such as a Henschel mixer, a ball mill, or a tumbler mixer, and then mixed in an injection molding machine or melt extrusion molding machine with good melt mixing properties. Alternatively, a method such as melt mixing in advance using a hot roll, kneader, Banbury mixer, melt extruder, etc. may be used. Furthermore, the method for molding the composition of the present invention is not particularly limited, and may be performed by a conventional method such as compression molding, extrusion molding, or injection molding, or by melt-mixing the composition. It is also possible to pulverize the powder using a jet mill, frozen pulverizer, etc. and classify it to the desired particle size, or to perform fluidized dip coating, electrostatic powder coating, etc. using the resulting powder without classifying it. be. In order to further improve the lubricity of the composition of the present invention, a lubricant such as polytetrafluoroethylene, graphite, molybdenum disulfide, or oil may be added. [Operation] In addition to the PPS phase and the nickel-coated phase, the surface of the molded product of the composition of the invention described above is polished and made into a sliding surface, and the solid contained in the nickel-coated mica Mica and carbon fibers serve as lubricants to improve lubricity, and the nickel coating layer forms an electrical path in close contact with each other or with carbon fibers, contributing to increased conductivity. [Example] The raw materials used in the Examples and Comparative Examples are as follows. Namely, polyphenylene sulfide (manufactured by Philips Petroleum Co., USA: Ryton P4), tetrafluoroethylene resin (manufactured by Mitsui Dupont Fluorochemical Co., Ltd.: Teflon 7J), nickel-coated mica (electroless phlogopite with an average particle size of 12 μm) nickel plating with an average thickness of 0.1 μm), nickel-coated carbon fiber (manufactured by Toho Veslon Co., Ltd.)
HTCF/Ni, fiber diameter 7.5 μm, fiber length 300 μm, average nickel film thickness 0.25 μm), nickel powder (manufactured by Inco, USA: Nickel Powder 255, average particle size 3 μm), carbon fiber (manufactured by Toray Industries, Inc.: Torayca MLD-300) , fiber diameter 7 μm, fiber length 300 μm). The blending ratio of each raw material in Examples 1 to 4 is based on 100 parts by volume of polyphenylene sulfide, and the blending ratio of each raw material in Comparative Examples 1 to 4 is also based on 100 parts by volume of polyphenylene sulfide. The values are expressed in terms of volumetric parts and are summarized in a table. These raw materials were thoroughly mixed in a Henschel mixer, then supplied to a twin-screw melt extruder, and extruded and granulated under melt mixing conditions of a cylinder temperature of 300° C. and a rotation speed of 100 rpm. The obtained pellets were injection molded under the following injection molding conditions: resin temperature 310℃, injection pressure 800Kg/cm 2 , mold temperature 130℃, outer diameter 23mm, inner diameter 14mm,
Ring-shaped specimen with a length of 13 mm and a width of 12.7 mm, length
A plate-shaped test piece of 63 mm and 3 mm thickness was formed, and the ring-shaped test piece was used to measure the volume resistivity and perform a friction and wear test.
The bending strength was measured according to the following. Here, the friction coefficient is measured using a thrust type friction tester at a sliding speed of 100 m/min and a load of 1 kg/ cm2 , and the wear coefficient is measured at a sliding speed of 128 m/min and a load of 1.6 kg/ cm2 . The test results were determined using a thrust-type wear tester, and bearing steel SUJ-2 (quenched and ground) was used as the mating material in both cases. All the obtained results are summarized and listed in the table. As is clear from this table, Comparative Examples 1 to
4, even if the volume resistivity shows a low value, the wear coefficient is extremely large, or conversely, the wear coefficient is low.

【表】【table】

〔効果〕〔effect〕

以上述べたように、この発明の組成物から得ら
れる成形体は、低摩擦係数を有し、そのうえニツ
ケル被覆雲母および炭素繊維の添加により優れた
耐摩耗性を保持しながら導電性が付与されている
ので、耐摩耗性と導電性との二つの機能が同時に
要求される用途、たとえばフロツピデイスクドラ
イブ部のアースボタン、自動車のステアリングコ
ラム部通電ベアリング、OA機器類のキヤリツヂ
ベアリング、複写機のアースもしくは通電ベアリ
ングなどヒートロール軸受、滑り軸受基材に格好
のものであると言える。また射出成形も可能であ
るため成形も容易であることからこの発明の意義
はきわめて大きいということができる。
As described above, the molded article obtained from the composition of the present invention has a low coefficient of friction, and furthermore, the addition of nickel-coated mica and carbon fiber imparts electrical conductivity while maintaining excellent wear resistance. Therefore, it is suitable for applications that require both wear resistance and conductivity at the same time, such as ground buttons in floppy disk drives, current-carrying bearings in steering columns of automobiles, carriage bearings in OA equipment, and photocopying. It can be said that it is suitable as a base material for heat roll bearings and sliding bearings, such as machine grounding or current-carrying bearings. In addition, since injection molding is possible and molding is easy, it can be said that the significance of this invention is extremely large.

Claims (1)

【特許請求の範囲】[Claims] 1 ポリフエニレンサルフアイド100容量部に対
して、ニツケル被覆雲母と炭素繊維とを両者の容
量比が15:80から80:20の範囲で総量が30〜140
容量部となるように添加したことを特徴とする導
電性摺動材組成物。
1. For 100 parts by volume of polyphenylene sulfide, add nickel-coated mica and carbon fiber at a volume ratio of 15:80 to 80:20 and a total amount of 30 to 140 parts.
A conductive sliding material composition, characterized in that it is added in a capacitive part.
JP16635785A 1985-07-26 1985-07-26 Electrically conductive sliding material composition Granted JPS6227458A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16635785A JPS6227458A (en) 1985-07-26 1985-07-26 Electrically conductive sliding material composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP16635785A JPS6227458A (en) 1985-07-26 1985-07-26 Electrically conductive sliding material composition

Publications (2)

Publication Number Publication Date
JPS6227458A JPS6227458A (en) 1987-02-05
JPH0561305B2 true JPH0561305B2 (en) 1993-09-06

Family

ID=15829885

Family Applications (1)

Application Number Title Priority Date Filing Date
JP16635785A Granted JPS6227458A (en) 1985-07-26 1985-07-26 Electrically conductive sliding material composition

Country Status (1)

Country Link
JP (1) JPS6227458A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5283133A (en) * 1988-07-27 1994-02-01 Mitsubishi Denki Kabushiki Kaisha Magneto-optical disk
US8299159B2 (en) * 2009-08-17 2012-10-30 Laird Technologies, Inc. Highly thermally-conductive moldable thermoplastic composites and compositions
JP6996351B2 (en) * 2017-03-31 2022-01-17 東レ株式会社 Fiber-reinforced thermoplastic resin composition, fiber-reinforced thermoplastic resin molding material, and molded products made of the same.

Also Published As

Publication number Publication date
JPS6227458A (en) 1987-02-05

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