JPS6243459A - Electrically conductive sliding material composition - Google Patents

Electrically conductive sliding material composition

Info

Publication number
JPS6243459A
JPS6243459A JP18446785A JP18446785A JPS6243459A JP S6243459 A JPS6243459 A JP S6243459A JP 18446785 A JP18446785 A JP 18446785A JP 18446785 A JP18446785 A JP 18446785A JP S6243459 A JPS6243459 A JP S6243459A
Authority
JP
Japan
Prior art keywords
coated
nickel
component
resin
wollastonite
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.)
Granted
Application number
JP18446785A
Other languages
Japanese (ja)
Other versions
JPH0561306B2 (en
Inventor
Masaki Egami
正樹 江上
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.)
YOUBEA LE-RON KOGYO KK
Original Assignee
YOUBEA LE-RON 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 YOUBEA LE-RON KOGYO KK filed Critical YOUBEA LE-RON KOGYO KK
Priority to JP18446785A priority Critical patent/JPS6243459A/en
Publication of JPS6243459A publication Critical patent/JPS6243459A/en
Publication of JPH0561306B2 publication Critical patent/JPH0561306B2/ja
Granted legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K9/00Use of pretreated ingredients
    • C08K9/02Ingredients treated with inorganic substances

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Character Spaces And Line Spaces In Printers (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Conductive Materials (AREA)

Abstract

PURPOSE:An electrically conductive sliding material composition, obtained by adding an Ni-coated solid lubricant, carbon fibers, Ni-coated wollastonite, polytetrafluoroethylene resin and molybdenum disulfide to polyphenylene sulfide resin and having improved sliding characteristics and electric conductivity at the same time. CONSTITUTION:An electrically conductive sliding material composition obtained by adding (A) 15-30wt%, based on the total composition, solid lubricant, e.g. mica or graphite, having the surface coated with Ni by the electric or chemical plating, (B) 8-18wt%, based on the total composition, carbon fibers, (C) 5-25wt% based on the total composition, crystals of wollastonite or potassium titanate having the surface coated with Ni, (D) 2-15wt%, based on the total composition, powdery or fine powdery polytetrafluoroethylene resin and (E) 2-7wt% fine powdery molybdenum disulfide to polyphenylene sulfide resin. Preferred amounts of the components are as follows, 15-25wt% component (A), 8-13wt% component (B), 8-15wt% component (C), 5-12wt% component (D) and 3-6wt% component (E).

Description

【発明の詳細な説明】 〔産業上の利用分野〕 この発明はポリフェニレンサルファイド樹脂を主成分と
した導電性摺動材組成物に関するものである。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] This invention relates to a conductive sliding material composition containing polyphenylene sulfide resin as a main component.

〔従来の技術〕[Conventional technology]

近年、合成樹脂滑り軸受の用途分野が拡大するにつれて
軸受の使用条件、特に高温雰囲気下において良好な摩擦
摩耗特性を発揮する耐熱性のある合成樹脂製軸受が強く
要望されるようになり、また、事務の機械化の急速な進
展に伴って、摺動特性のほかに導電性も兼備することが
要求されている。
In recent years, as the field of application for synthetic resin sliding bearings has expanded, there has been a strong demand for heat-resistant synthetic resin bearings that exhibit good friction and wear characteristics under bearing usage conditions, especially in high-temperature environments. With the rapid progress in mechanization of office work, it is required to have not only sliding properties but also electrical conductivity.

従来、耐熱性が良く機械的強度の優れた熱可塑性合成樹
脂としてポリフェニレンサルファイド(PPSと略称す
る)樹脂が用いられていることはよく知られている。し
かし、このPPS樹脂はそれ自体の自己潤滑性が乏しい
ため、潤滑性を必要とする部分の材料として使用するに
際しては、潤滑剤などを添加して別途潤滑性を付与しな
ければならず、たとえば黒鉛、ポリテトラフルオロエチ
レン樹脂、潤滑油、金属酸化物、芳香族ポリアミド樹脂
等を用いた複合材料が開発されてはいるものの、このよ
うな複合材料も高温、高負荷条件のもとて良好な摩擦摩
耗特性を発揮させるうえで充分であるとは言えない。
It is well known that polyphenylene sulfide (abbreviated as PPS) resin has been used as a thermoplastic synthetic resin with good heat resistance and mechanical strength. However, this PPS resin itself has poor self-lubricating properties, so when using it as a material for parts that require lubricity, it is necessary to add a lubricant or the like to provide lubricity, for example. Although composite materials using graphite, polytetrafluoroethylene resin, lubricating oil, metal oxides, aromatic polyamide resin, etc. have been developed, these composite materials also have very poor performance under high temperature and high load conditions. It cannot be said that this is sufficient to exhibit friction and wear characteristics.

一方、PPS樹脂自体に導電性を付与するためにルイス
酸、硫酸ハロゲン等電子受容性化合物を塗布または混合
する技術が既に開示されているが、未だ実用化には至っ
ていない。また、導電性カーボン等の添加によって導電
性を付与したものがあるが、良好な摺動特性とともに良
好な導電性を得ようとする場合、摺動特性が損われない
と体積抵抗率が大きくなったり、逆に体積抵抗率が小さ
いと摺動特性が損われたりまたは機械的性質が極端に劣
ったりして、高温において摺動特性と導電性とを兼ね備
えた材料は得られていない。
On the other hand, a technique of applying or mixing an electron-accepting compound such as a Lewis acid or a halogen sulfate in order to impart conductivity to the PPS resin itself has already been disclosed, but it has not yet been put to practical use. In addition, there are products that have been given conductivity by adding conductive carbon, etc., but if you are trying to obtain good conductivity as well as good sliding properties, the volume resistivity will increase unless the sliding properties are impaired. On the other hand, if the volume resistivity is low, the sliding properties will be impaired or the mechanical properties will be extremely poor, so that a material that has both sliding properties and electrical conductivity at high temperatures has not been obtained.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

このように、従来の技術においては摺動特性と導電性と
の両方を兼ね備えた材料がなく世間の要望に対処し得な
いという問題点があった。
As described above, the conventional technology has had the problem of not being able to meet the needs of the public because there is no material that has both sliding properties and electrical conductivity.

〔問題点を解決するための手段〕[Means for solving problems]

上記の問題点を解決するために、この発明はPPS樹脂
を主成分とし、これにニッケルで表面を被覆した固体潤
滑剤15〜30%(%は組成物全量に対する重量%、以
下同じ)、炭素繊維8〜18%、ニッケルでL面を被覆
したウオラストナイトもしくはチタン酸カリウムの結晶
5〜25%、ポリテトラフルオロエチレン樹脂2〜15
%、二硫化モリブデン2〜7%を添加するという手段を
採用したものである。以下その詳細を述へる。
In order to solve the above-mentioned problems, this invention is a solid lubricant whose main component is PPS resin and whose surface is coated with nickel. 8-18% fiber, 5-25% wollastonite or potassium titanate crystals coated on the L side with nickel, 2-15% polytetrafluoroethylene resin
%, and 2 to 7% of molybdenum disulfide is added. The details will be described below.

まず、この発明におけるPPS樹脂は、一般式%式%) で示される合成樹脂である。ここで、式中−ph−は9
m であり、QはF、CI、BrのハロゲンもしくはC)I
3テアリ、mは1〜4の整数を示す。これらのうち、特
に典型的なものは で示されるものであり、米°国フィリップス・ペトロー
リアム社から「ライドン」の商標で市販され、その製造
方法は米国特許第3,354,129号(対応特許特公
昭45−3368号)に開示されている。それによると
、ライドンはN−メチルピロリドン溶媒中、160〜2
50℃、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って製造され、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
とによって自由に製造することができるので、目的の溶
媒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。
First, the PPS resin in this invention is a synthetic resin represented by the general formula %. Here, -ph- in the formula is 9
m, and Q is a halogen of F, CI, Br or C)I
3, m represents an integer of 1 to 4. Among these, a particularly typical one is commercially available from Phillips Petroleum Company of the United States under the trademark "Rydon," and its manufacturing method is described in U.S. Pat. No. 3,354,129 (corresponding patent It is disclosed in Japanese Patent Publication No. 45-3368). According to it, Lydon is 160-2 in N-methylpyrrolidone solvent.
It is produced by reacting P-dichlorobenzene and sodium disulfide under pressure at 50°C, and the resin has various degrees of polymerization, ranging from no cross-linking to partial cross-linking. Since the solvent can be freely manufactured by subjecting it to a post-heat treatment process, it is possible to arbitrarily select and use a solvent having appropriate melt viscosity characteristics for the desired solvent blend.

つぎに、この発明におけるニッケルで表面を被覆した固
体潤滑剤C以下これをニッケル被覆潤滑剤と呼ぶ)は、
たとえば雲母、黒鉛、芳香族ポリアミド繊維その他の固
体潤滑剤の表面に電気的または化学的なメッキによって
ニッケルを被覆したものであって、導電性が付与された
ものであれば固体潤滑剤の種類を特に限定するものでは
ない。
Next, the solid lubricant C whose surface is coated with nickel in this invention (hereinafter referred to as nickel-coated lubricant) is:
For example, if the surface of mica, graphite, aromatic polyamide fiber, or other solid lubricant is coated with nickel by electrical or chemical plating, and it is made conductive, the type of solid lubricant is determined. It is not particularly limited.

また、この発明における炭素繊維は、通常の炭素繊維は
勿論のことニッケル等の金属を被覆したものであっても
よく、東し社製:トレヵM L D −300、呉羽化
学工業社製:クレハカーボンファイバ−M2O2S、東
邦ヘスロン社製: HTCF/Ni  などを例示する
ことができる。
Further, the carbon fiber in the present invention may be not only a normal carbon fiber but also one coated with a metal such as nickel. Examples include carbon fiber M2O2S, manufactured by Toho Heslon Co., Ltd.: HTCF/Ni.

また、この発明におけるニッケルで表面を被覆したウオ
ラストナイトもしくはチタン酸カリウムの結晶はウオラ
ストナイトもしくはチタン酸カリウムの結晶表面に、た
とえば電気的メッキまたは無電解(化学)メッキによっ
てニッケル層を設は導電性を付与したものであり、導電
性があればウオラストナイトまたはチタン酸カリウムの
結晶の種類を特に限定するものではない。ここでウオラ
ストナイトはケイ(珪)灰石とも呼ばれ、カルシウム、
鉄、マンカ゛ンのシクロケイ酸塩で、板状、柱状晶、繊
維状もしくは塊状集合体の天然鉱物であり、またチタン
酸カリウムは針状(ホイスカー)もしくは板状晶の合成
物質である。
Further, in the wollastonite or potassium titanate crystal whose surface is coated with nickel in this invention, a nickel layer is provided on the surface of the wollastonite or potassium titanate crystal by, for example, electroplating or electroless (chemical) plating. The type of wollastonite or potassium titanate crystal is not particularly limited as long as it has conductivity. Here, wollastonite is also called wollastonite, and contains calcium,
It is a cyclosilicate of iron and manganese, and is a natural mineral with plate-like, columnar, fibrous, or block-like aggregates, and potassium titanate is a synthetic substance with whisker or plate-like crystals.

マタ、この発明におけるポリテトラフルオロエチレン樹
脂は、四フッ化エチレンの重合体であり、成形用の粉末
であっても、またいわゆる固体、フ滑剤用の微粉末のい
ずれであってもよく、たとえば三井デュポンフロロケミ
カル社製:テフロン7JTLP−10、旭硝子社製ニア
フロンG163、ダイキン工業社製:ポリフロンM15
、ルブロンし5などを例示することができる。
The polytetrafluoroethylene resin in this invention is a polymer of tetrafluoroethylene, and may be a powder for molding, a so-called solid, or a fine powder for use as a lubricant, for example. Mitsui DuPont Fluorochemical Co., Ltd.: Teflon 7JTLP-10, Asahi Glass Co., Ltd. Nearflon G163, Daikin Industries, Ltd.: Polyflon M15
, LeBlon Shi5, etc. can be exemplified.

また、この発明における二硫化モリブデンは固体潤滑剤
として通常使用されている微粉末状のものでよく、たと
えばダウコーニング社製:モリコーLトZなどを例示す
ることができる。
The molybdenum disulfide used in the present invention may be in the form of a fine powder that is commonly used as a solid lubricant, such as Molycoor L and Z manufactured by Dow Corning.

以上のニッケル被覆潤滑剤、炭素繊維、ニッケル被覆ウ
オラストナイトもしくはチタン酸カリウムの結晶、ポリ
テトラフルオロエチレン樹脂、二硫化モリブデン等それ
ぞれの添加量を前記のように限定する理由は、それぞれ
の下限未満の少量または上限を越える多量ではいずれも
摺動特性と導電性との両立が困難となって好ましくない
からである。すなわち、ニッケル被覆固体潤滑剤が15
%未満では導電性が劣り、ほかの添加物との組合わせに
よっては摩耗特性が悪く、また30%を越える多量にす
ればほかの添加物の添加ができなくなり摩耗特性が著し
く悪化するからであり、実質・ 的には15〜25%が
好ましい。また炭素繊維は8%未満の少量では摺動特性
が悪くなり、18%を越える多量では摩擦係数が大きく
なるので、実質的には8〜13%が好ましい。またニッ
ケル被覆のウオラストナイトまたはチタン酸カリウム結
晶の添加量が5%未満のときは導電性が充分でなく、2
5%を越える多量では導電性は良好であっても摩耗特性
が悪化してしまうからであって、好ましくは8〜15%
である。またポリテトラフルオロエチレン樹脂が2%未
満の少量では摺動特性が悪く、15%を越える多量では
ほかの添加物の添加量が制約されて導電性の向上が不可
能になるので好ましくは5〜12%であり、二硫化モリ
ブデンは2%未満では摺動特性が悪く、7%を越える多
量になると脆くなって使用に耐えなくなるので実質的に
は3〜6%が好ましい。
The reason why the amounts of each of the above nickel-coated lubricants, carbon fibers, nickel-coated wollastonite or potassium titanate crystals, polytetrafluoroethylene resin, molybdenum disulfide, etc. are limited as above is that they are less than the respective lower limits. This is because a small amount or a large amount exceeding the upper limit is undesirable because it becomes difficult to achieve both sliding properties and conductivity. That is, the nickel-coated solid lubricant is 15
If the amount is less than 30%, the conductivity will be poor, and depending on the combination with other additives, the wear characteristics will be poor, and if the amount exceeds 30%, it will become impossible to add other additives, and the wear characteristics will deteriorate significantly. , 15 to 25% is preferable in practice. Furthermore, if the amount of carbon fiber is less than 8%, the sliding properties will deteriorate, and if the amount is more than 18%, the coefficient of friction will become large. In addition, when the amount of nickel-coated wollastonite or potassium titanate crystal added is less than 5%, conductivity is insufficient and 2
If the amount exceeds 5%, the wear characteristics will deteriorate even if the conductivity is good, so it is preferably 8 to 15%.
It is. In addition, if the polytetrafluoroethylene resin is contained in a small amount (less than 2%), the sliding properties will be poor, and if the amount exceeds 15%, the amount of other additives added will be restricted, making it impossible to improve the conductivity. If molybdenum disulfide is less than 2%, the sliding properties will be poor, and if it exceeds 7%, it will become brittle and unusable, so 3 to 6% is practically preferable.

ここで、配合割合の決まった各添加物を混合する方法は
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、たとえば主成分となる樹脂、その他の諸原料をそれ
ぞれ個別に、またはヘンシェルミキサー、ボールミル、
タンブラ−ミキサー等の混合機によって適宜乾式混合し
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−1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
形するにあたっても、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、これをジェットミル、
冷凍粉砕機等によって粉砕し、所望の粒径に分級するが
、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
Here, the method of mixing each additive with a fixed blending ratio is not particularly limited, and any commonly used method may be used, such as mixing the main component resin and other raw materials individually, or using a Henschel mixer. , ball mill,
After dry mixing as appropriate using a mixer such as a tumbler mixer, the mixture is supplied to an injection molding machine or melt extrusion molding machine with good melt mixing properties, or it is melted in advance using a heated roll, kneader, Banbury mixer 1 melt extruder, etc. A method such as mixing may be used. In addition, the method for molding the composition of the present invention is not particularly limited, and conventional methods such as compression molding, extrusion molding, injection molding, etc.
Or after melt-mixing the composition, use a jet mill,
The powder is pulverized by a freezing pulverizer or the like and classified to a desired particle size, or it is also possible to perform fluidized dip coating, electrostatic powder coating, etc. using the obtained powder without classifying it.

〔作用〕 以上述べたこの発明の組成物の成形体表面を研磨して摺
動面を形成すると、この面にはPPS樹脂、ニッケル被
覆を構成している金属ニッケル、ニッケルに被覆された
固体潤滑剤、炭素繊維、ニッケルに被覆されたウオラス
トナイトもしくはチタン酸カリウムの結晶、ポリテトラ
フルオロエチレン樹脂および二硫化モリブデンの7種類
の相が露出し、これらのうち金属ニッケルおよび炭素繊
維の二つの相は、それぞれもしくは互に密に接し合って
電路を形成し導電性の増大に貢献すると同時に、この炭
素繊維およびその他四つの相(固体潤滑剤、ウオラスト
ナイトもしくはチタン酸カリウム、ポリテトラフルオロ
エチレン樹脂、および二硫化モリブデンの各相)がPP
S樹脂に対する潤滑性付与に大きく寄与するのである。
[Operation] When the surface of the molded product of the composition of the present invention described above is polished to form a sliding surface, this surface is coated with PPS resin, metal nickel constituting the nickel coating, and solid lubricant coated with nickel. Seven types of phases are exposed: metallic nickel, carbon fiber, wollastonite or potassium titanate crystals coated with nickel, polytetrafluoroethylene resin, and molybdenum disulfide, and two of these phases, metallic nickel and carbon fiber, are exposed. At the same time, these carbon fibers and the other four phases (solid lubricant, wollastonite or potassium titanate, polytetrafluoroethylene resin) , and molybdenum disulfide phases) are PP
It greatly contributes to imparting lubricity to the S resin.

〔実施例〕〔Example〕

実施例および比較例に使用するため、っぎの原材料を準
備した。
Raw materials were prepared for use in Examples and Comparative Examples.

■PPSm脂(米国フィリップス・ベトローリ7ムl、
[:ライトンp−4パウター)、■ニッケル被覆雲母(
平均粒径22μmのレプコ社製:S−250の金雲母に
無電解法によって、ニッケル被覆雲母の重量に占めるニ
ッケルの重量割合が約40%となるようにニッケルメツ
キ層を設けたもの)、 ■炭素繊維(呉羽化学工業社製:クレハカーボンファイ
バーM2O7S)、 ■ニッケル被覆ウオラストナイト(平均繊維長25μm
1平均繊維径3μmの丸印バイオケミカル社製:ケモリ
ットに無電解法によって、ニッケル被覆ウオラストナイ
ト全量に対するニッケルメッキ層の重量割合が約60%
となるようにニッケルメッキ層を形成したもの)、 ■ニッケル被覆チタン酸カリウム(平均繊維長20〜3
0μm、平均繊維径0.2〜0.3μmの大球化学社製
:テイスモD101に無電解法によって、ニッケル被覆
チタン酸カリウムホイスカーに対して重量割合が約65
%となるようにニッケルメッキ層を形成したもの)、 ■ポリテトラフルオロエチレン樹脂(三井デュポンフロ
ロケミカル社製;ふっ素樹脂潤滑粉TLP−10) ■二硫化モリブデン(ダウ・コーニング社製:モ リ 
コ − ト Z ) ■チタン酸カリウムホイスカー(大球化学社製:テイス
モ0101) ■ケッチェンブラック(ライオン社製:ケッチェンブラ
ックEC) [相]芳香族ポリアミド繊維(米国デュポン社製:ケブ
ラー49、繊維長1 mm ) 実施例1〜3 上記の原材料を第1表に示す割合(重量%)で配合した
。組成物の調製にあたっては、まず原材料をヘンシェル
ミキサーで充分混合し、二軸溶融押出機に供給し、シリ
ンダ一温度300°C1回転数毎分100回転の溶融混
合条件で押出して造粒し、得られたペレットを樹脂温度
310℃、射出圧力800 kg/cm  、金型温度
130℃の射出成形条件で内径20 mm、外径25 
mm、長さB mmの円筒状試験片を成形した。この試
験片を軟鋼545Cで試験片とのはめ合いすきまを9.
5 mm とした円筒状の軸にはめ、ラジアル方向に1
0kgの荷重をかけて190°Cまで加熱した。軸を毎
分69回転の速度で回転し、回転開始時、15時間後、
第  1  表 第  2  表 44時間後のそれぞれの回転トルクを測定した。
■PPSm fat (Philips Vetroli, USA 7 ml,
[: Ryton p-4 powder), ■Nickel-coated mica (
A nickel plating layer is provided on S-250 phlogopite with an average particle size of 22 μm by an electroless method so that the weight ratio of nickel to the weight of the nickel-coated mica is approximately 40%), Carbon fiber (manufactured by Kureha Chemical Industry Co., Ltd.: Kureha Carbon Fiber M2O7S), ■Nickel-coated wollastonite (average fiber length 25 μm)
1 Average fiber diameter of 3 μm, manufactured by Maruji Biochemical Co., Ltd.: The weight ratio of the nickel plating layer to the total amount of nickel-coated wollastonite is approximately 60% using the electroless method on Chemolite.
Nickel-coated potassium titanate (average fiber length 20-3
0 μm, average fiber diameter 0.2 to 0.3 μm manufactured by Daikyu Kagaku Co., Ltd.: Teismo D101 by electroless method, the weight ratio is about 65 to the nickel-coated potassium titanate whisker.
%), ■Polytetrafluoroethylene resin (manufactured by Mitsui DuPont Fluorochemical Co., Ltd.; fluororesin lubricating powder TLP-10) ■Molybdenum disulfide (manufactured by Dow Corning Company: Molybdenum)
Coat Z) ■Potassium titanate whisker (manufactured by Daikyu Kagaku Co., Ltd.: Teismo 0101) ■Ketjen Black (manufactured by Lion Corporation: Ketjen Black EC) [Phase] Aromatic polyamide fiber (manufactured by DuPont, USA: Kevlar 49, Fiber length: 1 mm) Examples 1 to 3 The above raw materials were blended in the proportions (wt%) shown in Table 1. To prepare the composition, first, the raw materials are thoroughly mixed in a Henschel mixer, then fed to a twin-screw melt extruder, and extruded and granulated at a cylinder temperature of 300°C and a rotation speed of 100 revolutions per minute. The resulting pellets were injection molded at a resin temperature of 310°C, an injection pressure of 800 kg/cm, and a mold temperature of 130°C to an inner diameter of 20 mm and an outer diameter of 25 mm.
A cylindrical test piece with a length of B mm and a length of B mm was molded. This test piece was made of mild steel 545C with a fitting clearance of 9.
Fit it into a cylindrical shaft with a diameter of 5 mm, and 1 in the radial direction.
It was heated to 190°C with a load of 0 kg applied. Rotate the shaft at a speed of 69 revolutions per minute, at the start of rotation, after 15 hours,
Table 1 Table 2 The respective rotational torques were measured after 44 hours.

また、44時間後における重量減をも測定し、これをも
って摩耗量とした。また運転時の音の発生の有無も調べ
、円筒状試験片の両端面間を電極に挾んで電気抵抗を測
定し、これらの結果を第2表にまとめた。
In addition, the weight loss after 44 hours was also measured, and this was taken as the amount of wear. The presence or absence of sound during operation was also investigated, and the electrical resistance was measured by sandwiching the end surfaces of the cylindrical test piece between electrodes, and the results are summarized in Table 2.

第2表から明らかなように、比較例1〜3は実施例1〜
3とは異なって電気抵抗が小さくても回転トルクが不安
定で摩耗量も(比較例2および3のように)大きいか、
トルクおよび摩耗の結果が良好でも(比較例1のように
)電気抵抗が大きくて、電気抵抗が小さく、回転トルフ
カr安定して小さく、しかも摩耗量が少ないというよう
な組成物は得られなかった。
As is clear from Table 2, Comparative Examples 1 to 3 are Examples 1 to 3.
Unlike 3, even if the electrical resistance is small, the rotational torque is unstable and the amount of wear is large (as in Comparative Examples 2 and 3).
Even if the torque and wear results were good (as in Comparative Example 1), a composition with high electrical resistance, low electrical resistance, stable low rotational torque, and low wear amount could not be obtained. .

〔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、高温下で小さい運転トルクを示し、優れた耐摩耗
性を保持しながら導電性が付与されティるので、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
とえば複写機のアースもしくは通電ベアリング、OA機
器類のキャリツヂベアリング、自動車のステアリングコ
ラム部通電ベアリング、各種コンピュータ機器のアース
ボタンなどの素材として格好のものであるといえる。
As described above, the molded product obtained from the composition of the present invention exhibits low operating torque at high temperatures and is imparted with electrical conductivity while maintaining excellent wear resistance. It is suitable as a material for applications where dual functions are required at the same time, such as grounding or current-carrying bearings in copying machines, carriage bearings in office automation equipment, current-carrying bearings in steering columns of automobiles, and grounding buttons in various computer equipment. It can be said that it belongs to

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。
In addition, since injection molding is possible and molding is easy, it can be said that the significance of this invention is extremely large.

特許出願人   洋ベア・ルーロン工業株式会社同代理
人 鎌 1)文 二
Patent applicant: Western Bear Rulon Industrial Co., Ltd. Agent: Kama 1) Text 2

Claims (1)

【特許請求の範囲】[Claims] ポリフェニレンサルファイド樹脂を主成分とし、これに
ニッケルで表面を被覆した固体潤滑剤15〜30%(%
は組成物全量に対する重量%、以下同じ)、炭素繊維8
〜18%、ニッケルで表面を被覆したウオラストナイト
もしくはチタン酸カリウムの結晶5〜25%、ポリテト
ラフルオロエチレン樹脂2〜15%、二硫化モリブデン
2〜7%を添加したことを特徴とする導電性摺動材組成
物。
A solid lubricant whose main component is polyphenylene sulfide resin and whose surface is coated with nickel (15-30%).
(% by weight based on the total composition, the same applies hereinafter), carbon fiber 8
~18%, nickel-coated wollastonite or potassium titanate crystals 5-25%, polytetrafluoroethylene resin 2-15%, and molybdenum disulfide 2-7%. Sliding material composition.
JP18446785A 1985-08-20 1985-08-20 Electrically conductive sliding material composition Granted JPS6243459A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP18446785A JPS6243459A (en) 1985-08-20 1985-08-20 Electrically conductive sliding material composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP18446785A JPS6243459A (en) 1985-08-20 1985-08-20 Electrically conductive sliding material composition

Publications (2)

Publication Number Publication Date
JPS6243459A true JPS6243459A (en) 1987-02-25
JPH0561306B2 JPH0561306B2 (en) 1993-09-06

Family

ID=16153663

Family Applications (1)

Application Number Title Priority Date Filing Date
JP18446785A Granted JPS6243459A (en) 1985-08-20 1985-08-20 Electrically conductive sliding material composition

Country Status (1)

Country Link
JP (1) JPS6243459A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
EP0427858A1 (en) * 1989-02-28 1991-05-22 Kanebo Ltd. Antibacterial or conductive composition and applications thereof
US6818706B2 (en) 2001-02-21 2004-11-16 Nexans Polymer mixture
CN110746777A (en) * 2019-11-12 2020-02-04 张家港大塚化学有限公司 Preparation method of polyphenylene sulfide and high-temperature nylon composite material
KR20200110457A (en) * 2018-03-16 2020-09-23 가부시키가이샤 씽크. 라보라토리 Current collector member and plating device for cylinder body plating device

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
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
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
EP0427858A1 (en) * 1989-02-28 1991-05-22 Kanebo Ltd. Antibacterial or conductive composition and applications thereof
EP0427858A4 (en) * 1989-02-28 1993-03-10 Kanebo Ltd. Antibacterial or conductive composition and applications thereof
US6818706B2 (en) 2001-02-21 2004-11-16 Nexans Polymer mixture
KR20200110457A (en) * 2018-03-16 2020-09-23 가부시키가이샤 씽크. 라보라토리 Current collector member and plating device for cylinder body plating device
CN110746777A (en) * 2019-11-12 2020-02-04 张家港大塚化学有限公司 Preparation method of polyphenylene sulfide and high-temperature nylon composite material

Also Published As

Publication number Publication date
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