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JPS58160347A - Resin composition - Google Patents

Resin composition

Info

Publication number
JPS58160347A
JPS58160347A JP4424082A JP4424082A JPS58160347A JP S58160347 A JPS58160347 A JP S58160347A JP 4424082 A JP4424082 A JP 4424082A JP 4424082 A JP4424082 A JP 4424082A JP S58160347 A JPS58160347 A JP S58160347A
Authority
JP
Japan
Prior art keywords
weight
wear
fluorocarbon polymer
oxybenzoyl polyester
value
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
JP4424082A
Other languages
Japanese (ja)
Other versions
JPH0339110B2 (en
Inventor
Teruo Tsumato
照夫 妻藤
Kuniaki Asai
浅井 邦明
Isamu Nakagawa
勇 中川
Hiroshi Ishida
博士 石田
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical 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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP4424082A priority Critical patent/JPS58160347A/en
Publication of JPS58160347A publication Critical patent/JPS58160347A/en
Publication of JPH0339110B2 publication Critical patent/JPH0339110B2/ja
Granted legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To provide a resin compsn. suitable for use as a sliding material for oilless bearing, gear, cam, etc., by blending an arom. polyether ketone resin, a fluorocarbon polymer and an oxybenzoyl polyester in a specified ratio. CONSTITUTION:95-30wt% arom. polyether ketone resin having an intrinsic viscosity of pref. 0.7-2.6, 2.5-60wt% fluorocarbon polymer such as lubricant grade polytetrafluoroethylene having an average particle size of 20mu or below, and 2.5-60wt% oxybenzoyl polyester such as Ekonol E-101 (a product of Sumitomo Kagaku Kogyo K. K.) are blended together.

Description

【発明の詳細な説明】 本発明は芳香族ポリエーテルケトンにフルオロカーボン
重合体壜よびオキシベンゾイルポリエステルを配合する
ことによって摺動特性のすぐれた成形品を与える樹脂組
成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a resin composition that provides a molded article with excellent sliding properties by blending an aromatic polyetherketone with a fluorocarbon polymer bottle and an oxybenzoyl polyester.

更に詳しくは、耐摩耗、潤滑特性のすぐれた無給油軸受
を与える樹脂組成物に関する。
More specifically, the present invention relates to a resin composition that provides an oil-free bearing with excellent wear resistance and lubrication properties.

芳香族ポリエーテルケトン樹脂は、特開昭54−902
96などの記載にみられるごとく、高い耐熱性、耐燃性
、機械的、電気的性質、耐薬品性を有することが知られ
ている。これらのす(1) ぐれた諸性質を生かして、特に電線やケーブルの絶縁被
覆としての利用が示唆されているが、電線やケーブルの
被覆に留まらず、各種導電体の絶縁被覆や耐食性の付与
などにより、その利用範囲が拡大することで、電気、機
械など各種産業の発展が期待される。また芳香族ポリエ
ーテルケトンにフルオロカーボン重合体、好ましくはポ
リテトラフルオロエチレンを含有してなる組成物は、上
記特性に加えて、自己潤滑特性が付与されるため摺動を
伴なう種々の用途への展開が期待される。
Aromatic polyetherketone resin is disclosed in Japanese Patent Application Laid-open No. 54-902.
It is known to have high heat resistance, flame resistance, mechanical, electrical properties, and chemical resistance, as described in 96 et al. (1) Taking advantage of their excellent properties, it has been suggested that they can be used as insulating coatings for electric wires and cables, but they are also used not only for coating electric wires and cables, but also for providing insulation coatings and corrosion resistance for various conductors. By expanding the scope of its use, development of various industries such as electrical and mechanical industries is expected. In addition, compositions containing aromatic polyetherketone and a fluorocarbon polymer, preferably polytetrafluoroethylene, have self-lubricating properties in addition to the above properties, making them suitable for various applications involving sliding. is expected to develop.

しかしながら、芳香族ポリエーテルケトン樹脂にフルオ
ロカーボン重合体を含有してなる組成物を無給油軸受な
どに使用するには、摺動特性が不充分である。
However, the sliding properties of a composition comprising an aromatic polyetherketone resin and a fluorocarbon polymer are insufficient for use in oil-free bearings and the like.

一般にプラスチックを軸受などの摺動材として使用する
ためには、摩擦係数が低く安定していることに加えて、
限界PV値が高いことおよび耐摩耗特性を表わす摩耗係
数が低いことなどの特性が要求される。
In general, in order to use plastics as sliding materials such as bearings, in addition to having a low and stable coefficient of friction,
Properties such as a high limit PV value and a low wear coefficient representing wear resistance are required.

(2) pv値とは、軸受にかかる圧力Pと摺動速度■との積で
限界pv値とは軸受などの接触端面における摩擦熱の発
生により温度が著しく上昇し、プラスチックの軟化、溶
融、化学的分解などが起り、正常な摩擦運動が続けられ
なくなる限界のpv値である。しかしながら限界pv値
内での使用条件下でも、必ず少しずつ摩耗は進行するの
で寿命を考慮しなければならない。
(2) The pv value is the product of the pressure P applied to the bearing and the sliding speed. This is the limit pv value at which chemical decomposition occurs and normal frictional motion cannot continue. However, even under usage conditions within the limit pv value, wear always progresses little by little, so the life span must be taken into consideration.

このために軸受設計の資料としては、限界PV値より摩
耗係数の方が重要であり、限界PV値は軸受などの使用
限界の1つの目安として使われている。
For this reason, as a material for bearing design, the wear coefficient is more important than the limit PV value, and the limit PV value is used as a guideline for the usage limit of bearings, etc.

ところで摩耗係数には一般的に次式で表わされる。By the way, the wear coefficient is generally expressed by the following formula.

K=W/PVT 〔W:摩耗11 (mm) 、 P :圧力(K117
0m” ) 、 V :速度(m/min ) 、 T
 :時間(hr)、:]このKの値は限界pv値と同様
に、使用するpv値が同じでもPおよびVの値によって
変化するものである。すなわち、同じpv値でも高圧、
(3) 低速の条件と低圧、高速の条件によって変動するもので
ある。しかし一般的には圧力と走行距離(速度と時間の
積)に比例するのでKの単位り軸受の場合、この値がl
Xl0’  以下であれば、無給油の状態で、寿命の因
子を考慮しても問題なく使用可能であるとされている。
K=W/PVT [W: Wear 11 (mm), P: Pressure (K117
0m”), V: Speed (m/min), T
:Time (hr), :] Similar to the limit pv value, the value of K changes depending on the values of P and V even if the pv value used is the same. In other words, even at the same pv value, high pressure,
(3) It varies depending on low speed conditions, low pressure, and high speed conditions. However, in general, it is proportional to pressure and traveling distance (product of speed and time), so in the case of a K unit bearing, this value is l
It is said that if it is below Xl0', it can be used without any lubrication without any problem even considering the life factor.

ところが、芳香族ポリエーテルケトン樹脂にフルオロカ
ーボン重合体を含有してなる組成物から得た軸受を無給
油の状態で限界pv値内(約400 Kg/cm2・m
/min )  テ使用した場合、K値は5X10 ’
〜5X10 ”  の範囲であり、要求される値より1
桁以上大きいため、軸受寿命は非常に短かい。このため
、該組成物に更にガラス繊維、炭素繊維などの繊維状補
強材を充填させることによりに値は若干低下するものの
、相手材金属を損傷するという問題を生ずる。特に相手
材金属が、アルミニウム、SUSなどの軟質金属である
場合、この現象は著しく、一旦金属摩耗粉が生ずると、
これがプラスチック側に(4) ざらつき摩耗的に働き、摩擦係数が不安定になるととも
に、プラスチック側の摩耗も促進される。また該組成物
に更に黒鉛などの固体潤滑剤を含有させることにより、
潤滑性が更に向上し、熱伝導性も付与されるため、K値
は若干改良されるが、充分なものとはならない。
However, a bearing obtained from a composition containing a fluorocarbon polymer in an aromatic polyetherketone resin was found to be within the limit pv value (approximately 400 Kg/cm2・m2) without lubrication.
/min) When using Te, the K value is 5X10'
~5X10'', 1 less than the required value
Since it is an order of magnitude larger, the bearing life is extremely short. Therefore, if the composition is further filled with a fibrous reinforcing material such as glass fiber or carbon fiber, the value may be slightly reduced, but this poses a problem of damaging the mating metal. This phenomenon is particularly noticeable when the mating metal is a soft metal such as aluminum or SUS, and once metal wear particles are generated,
This acts as a rough and abrasive effect on the plastic side (4), making the coefficient of friction unstable and accelerating wear on the plastic side. In addition, by further containing a solid lubricant such as graphite in the composition,
Since the lubricity is further improved and thermal conductivity is imparted, the K value is slightly improved, but it is not sufficient.

本発明者らは、上記問題点を改良するため、鋭意検討し
た結果、芳香族ポリエーテルケトン樹脂にフルオロカー
ボン重合体を含有してなる組成物に更にオキシベンゾイ
ルポリエステルを含有せしめることによって、摩耗係数
にの値が軸受として使用した場合、寿命因子を考慮して
も問題なく使用でき、また相手材の損傷もないことがわ
かり本発明に至ったのである。
In order to improve the above-mentioned problems, the present inventors have made extensive studies and found that by further containing oxybenzoyl polyester in a composition comprising an aromatic polyetherketone resin and a fluorocarbon polymer, the wear coefficient can be improved. It was found that when used as a bearing with a value of , it can be used without problems even considering the life factor, and there is no damage to the mating material, leading to the present invention.

すなわち、芳香族ポリエーテルケトン樹脂95〜30重
量%、フルオロカーボン重合体2.5〜60重量%およ
びオキシベンゾイルポリエステル2.5〜60重Iq6
の組成物にすることにより上記問題点を解決できること
がわかり本発明に(5) 至ったのである。
That is, 95-30% by weight of aromatic polyetherketone resin, 2.5-60% by weight of fluorocarbon polymer, and 2.5-60% by weight of oxybenzoyl polyester.
It was found that the above-mentioned problems could be solved by creating a composition of the following, leading to the present invention (5).

本発明に使用される芳香族ポリエーテルケトンは反復単
位 −Q−O−Q−CO+〇−を単独で、または他の反復単
位と一緒に含み、かつ固有粘度が0.7ないし2゜6以
下、好ましくは0.8ないし1.8のものである。他の
反復単位としては、 (yco÷〇− 00÷502÷〇− −JC>SO2÷〇− などを25重量%未満含み得るが、25重量−以上含有
した重合体は、該ポリエーテルケトン本来の特性が失な
われ好ましくない。また固有粘度は溶液100Ci”当
り重合体0.12を含む密度1.84 L!I/ctm
3  の濃硫酸中の重合体溶液について測定した固有粘
度のことである。
The aromatic polyetherketone used in the present invention contains the repeating unit -Q-O-Q-CO+〇- alone or together with other repeating units, and has an intrinsic viscosity of 0.7 to 2.6 or less. , preferably from 0.8 to 1.8. Other repeating units may include less than 25% by weight of (yco÷〇- 00÷502÷〇- -JC>SO2÷〇-), but polymers containing 25% by weight or more are properties are lost, which is undesirable.In addition, the intrinsic viscosity is 1.84 L!I/ctm containing 0.12 polymer per 100 Ci of solution.
3 is the intrinsic viscosity measured for a polymer solution in concentrated sulfuric acid.

固有粘度の測定には溶媒流出時間が約2分であ(6) る粘度計を用いて行なった。この固有粘度は重合体の分
子量と一義的に対応する値である。
The intrinsic viscosity was measured using a viscometer with a solvent flow time of approximately 2 minutes (6). This intrinsic viscosity is a value that uniquely corresponds to the molecular weight of the polymer.

また該ポリエーテルケトンの固有粘度が0.7よりも低
い重合体は、耐熱性が低く成形品が得られても非常に脆
い。一方2.6を越えると溶融粘度が高すぎて加工性が
悪く一般には使用できない。
Further, the polyetherketone having an intrinsic viscosity lower than 0.7 has low heat resistance and is extremely brittle even if a molded article is obtained. On the other hand, if it exceeds 2.6, the melt viscosity is too high and the processability is poor, making it generally unusable.

本発明に使用し得るフルオロカーボン重合体は、ポリテ
トラフルオロエチレン、ポリテトラフルオロエチレン−
へキサフルオロプロピレン共重合体、ポリトリクロロフ
ルオロエチレン、テトラフルオロエチレン−パーフルオ
ロアルキルビニルエーテル共重合体などを含むが、特に
ポリテトラフルオロエチレン(以下PTFE と略す)
が好ましい。また、PTFE  の中でも平均粒径20
μ未満の滑剤級 PTFE粉末が好ま□しく、市販され
ているものの例としては、堺ルオン■169 、 L 
170 、 L 171 (ICI壬礫製)、ルブロン
■L−2,L−5,LD−1(ダイキン工業社製)テフ
ロン■TLP −IQ 、 TLP −(7) 10F−1(デュポン社製)などがある。
Fluorocarbon polymers that can be used in the present invention include polytetrafluoroethylene, polytetrafluoroethylene-
It includes hexafluoropropylene copolymer, polytrichlorofluoroethylene, tetrafluoroethylene-perfluoroalkyl vinyl ether copolymer, etc., but especially polytetrafluoroethylene (hereinafter abbreviated as PTFE).
is preferred. Also, among PTFE, the average particle size is 20
Lubricant grade PTFE powder of less than μ is preferred, and commercially available examples include Sakai Luon 169, L
170, L 171 (manufactured by ICI Miki), LeBron ■L-2, L-5, LD-1 (manufactured by Daikin Industries), Teflon ■TLP-IQ, TLP-(7) 10F-1 (manufactured by DuPont), etc. There is.

本発明に使用し得るオキシベンゾイルポリエステルは、
一般に次式σV)の反復単位を有するものであり、 400℃以下の温度では、はとんど軟化することなく耐
摩耗性、耐圧縮クリープ特性、耐薬品性において非常に
すぐれたものである。また結晶構造が黒鉛や二硫化モリ
ブデンのような固体潤滑剤に類似し7た板状結晶を有し
ているため、自己潤滑性にすぐれており、特に PTF
Eの耐摩耗性改良材として使用されているものである。
The oxybenzoyl polyester that can be used in the present invention is
Generally, it has a repeating unit of the following formula σV), and it hardly softens at temperatures below 400°C and has excellent wear resistance, compression creep resistance, and chemical resistance. In addition, its crystal structure is similar to solid lubricants such as graphite and molybdenum disulfide, and it has plate-shaped crystals, so it has excellent self-lubricating properties.
It is used as a wear resistance improving material for E.

たとえばP T F E にオキシベンゾイルポリエス
テルを20重量%含有せしめると、摩耗量は、PTFE
の約1/1000以下となり摩擦係数もPTFE  の
低い値を維持するだけでなく、安定でかつ相手材を損傷
しないという特性を有したすぐれた摺動材となる。
For example, when PTFE contains 20% by weight of oxybenzoyl polyester, the amount of wear is lower than that of PTFE.
The coefficient of friction is approximately 1/1000 or less of that of PTFE, which not only maintains the low value of PTFE, but also provides an excellent sliding material that is stable and does not damage the mating material.

(8) このオキシベンゾイルポリエステルの合成法としては、
特公昭46−6796、特公昭47−47870  で
用いられているような高沸点溶剤を重合媒体として用い
る方法や特開昭54−46287、特開昭54−462
91 に見られるような重合系に実質的に溶剤を用いな
い塊状重合法があり、このものはエコノール■E 10
1 (住友化学工業製)という商品名で市販されている
(8) The method for synthesizing this oxybenzoyl polyester is as follows:
A method using a high boiling point solvent as a polymerization medium as used in Japanese Patent Publication No. 46-6796 and Japanese Patent Publication No. 47-47870, Japanese Patent Publication No. 54-46287, and Japanese Patent Publication No. 54-462
There is a bulk polymerization method that does not substantially use a solvent in the polymerization system, as shown in 91.
1 (manufactured by Sumitomo Chemical Industries).

配合量としては、芳香族ポリエーテルケトン95〜30
重量%、フルオロカーボン重合体2.5〜60重量%、
オキシベンゾイルポリエステル2.5〜60重量%(フ
ルオロカーボン重合体とオキシベンゾイルポリエステル
の合計量としては全樹脂組成物の5〜70重量%)配合
したものが有効である。
The blending amount is aromatic polyetherketone 95-30
% by weight, fluorocarbon polymer 2.5-60% by weight,
A blend of 2.5 to 60% by weight of oxybenzoyl polyester (the total amount of fluorocarbon polymer and oxybenzoyl polyester is 5 to 70% by weight of the total resin composition) is effective.

すなわち、フルオロカーボン重合体とオキシベンゾイル
ポリエステルの合計量が樹脂組成物の70重量%を越え
、芳香族ポリエーテルケトンの量が30重量−未満の時
は、樹脂組成物の流動性が失なわれ、たとえ射出成形に
より成形(9) 品を得ることができても、機械的強度において非常に低
くもろいものとなる。また、フルオロカーボン重合体と
オキシベンゾイルポリエステルの合計量が5重量%未満
の時は、十分な摺動特性が得られない。
That is, when the total amount of the fluorocarbon polymer and oxybenzoyl polyester exceeds 70% by weight of the resin composition and the amount of the aromatic polyetherketone is less than 30% by weight, the resin composition loses its fluidity. Even if a molded article (9) could be obtained by injection molding, it would have very low mechanical strength and be brittle. Furthermore, when the total amount of the fluorocarbon polymer and oxybenzoyl polyester is less than 5% by weight, sufficient sliding properties cannot be obtained.

また、フルオロカーボン重合体とオキシベンゾイルポリ
エステルの合計量が5〜70重量%であっても、フルオ
ロカーボンの量か2.5重量%未満であれば、潤滑性が
不十分で、60重量%を越えると、分散性、相溶性が低
下し、均一な組成物が得られにくい。一方、オキシベン
ゾイルポリエステルの量は2.5重量%未満では、耐摩
耗性において不充分で、量がふえるに従って耐摩耗性の
向上は顕著となるが、60重量%を越えると組成物の流
動性の著しい低下と、得られた成形品の強度低下が顕著
になる。
Furthermore, even if the total amount of fluorocarbon polymer and oxybenzoyl polyester is 5 to 70% by weight, if the amount of fluorocarbon is less than 2.5% by weight, the lubricity will be insufficient, and if it exceeds 60% by weight, the lubricity will be insufficient. , dispersibility and compatibility deteriorate, making it difficult to obtain a uniform composition. On the other hand, if the amount of oxybenzoyl polyester is less than 2.5% by weight, the abrasion resistance is insufficient, and as the amount increases, the improvement in abrasion resistance becomes more remarkable, but if it exceeds 60% by weight, the fluidity of the composition There is a significant decrease in the strength of the resulting molded product.

本発明の樹脂組成物には、更に潤滑性を向上させるため
に、黒鉛、二硫化モリブデンなどの°゛固体潤滑剤を加
えることも可能である。
It is also possible to add a solid lubricant such as graphite or molybdenum disulfide to the resin composition of the present invention in order to further improve the lubricity.

本発明の樹脂組成物を得るための混合方法と(10) しては、芳香族ボリエ・−チルケトンとフルオロカーボ
ン重合体およびオキシベンゾイルポリエステルヲ、タト
えばヘンシェルミキサー、スーパーミキサーなどの混合
機でトライブレンドした後、−軸または多軸の押出機で
溶融混練し、ストランドを押出し、カッターにてペレッ
ト化する方法が一般的であるが特にこれに限定されるも
のではない。また本発明の組成物から軸受などの成形品
を得るには射出成形を適用するのが一般的である。
The mixing method (10) for obtaining the resin composition of the present invention includes tri-blending aromatic borie-thylketone, fluorocarbon polymer, and oxybenzoyl polyester using a mixer such as a Henschel mixer or a super mixer. After that, a common method is to melt-knead the mixture using a -screw or multi-screw extruder, extrude the strands, and pelletize them using a cutter, but the method is not particularly limited thereto. Furthermore, injection molding is generally applied to obtain molded products such as bearings from the composition of the present invention.

本発明にかかる樹脂組成物はすぐれた摺動特性を有し、
軸受設計の上での一つの資料となる摩耗係数が芳香族ポ
リエーテルケトンとフルオロカーボン重合体とからなる
組成物のそれにくらべ、1桁以上低い値 (IX□。−5〜IOX□。−5二/夏)を有す6えめ
、Km  Cm2 無給油軸受として好適な成形材料である。
The resin composition according to the present invention has excellent sliding properties,
The wear coefficient, which is one of the data for bearing design, is more than an order of magnitude lower than that of the composition consisting of aromatic polyetherketone and fluorocarbon polymer (IX□.-5 to IOX□.-52). /summer), Km Cm2 It is a molding material suitable for use as an oil-free bearing.

本発明は、以下の実施例によって説明するが、これらは
好適な態様の例示であって本発明の範囲を限定するもの
ではない。
The present invention will be explained by the following examples, but these are illustrative of preferred embodiments and are not intended to limit the scope of the present invention.

実施例1〜6 −Q−O÷COテyO−なる基本構造単位を有し、固有
粘度が1゜4の芳香族ポリエーテルケトンとPTFE 
(フルオン■L 196 。
Examples 1 to 6 Aromatic polyetherketone and PTFE having the basic structural unit -Q-O÷COTYO- and having an intrinsic viscosity of 1°4
(Fluon L 196.

ICI社製)および平均粒径約20μを有するオキシベ
ンゾイルポリエステル(エコノール■E 101 、住
友化学工業社製)を第1表の組成比となるようにヘンシ
ェルミキサーで混合し、二軸タイプの押出機(他見鉄工
製 PCM−30)でシリンダー中央部温度を340〜
360℃に設定し、押出し造粒を行ないペレットを得た
。これらを10Z射出成形機(住友重機械製ネオマット
47/28 )  を用いてシリンダー中央部温度を3
60〜380℃に設定し、JIS  1号ダンベルおよ
び摩耗リング(外径25・6 mm、内径20 mm、
高さ15mm)を成形した。JIS  1号ダンベルか
らは引張特性を測定し、摩耗リングからは銘木式摩耗試
験機を用いて圧力P−10Kf/cm2、速度20m/
minの条件下相手材をSUS 3Q4とし、2時間の
ならし運転を行なった後、20時間の摺動を行ない、摩
擦係数、摩耗係数、相手材の摩耗量ポリエステルの添加
量とともに、引張強度、伸びは幾分低下するものの、耐
摩耗性を表わす摩耗係数にの値の低下は顕著となり、い
す下で摩擦係数も低く安定で、相手材であるSUS 3
04の摩耗もほとんどみられなかった。
ICI) and oxybenzoyl polyester (Econol ■E 101, manufactured by Sumitomo Chemical Industries, Ltd.) having an average particle size of about 20μ were mixed in a Henschel mixer at the composition ratio shown in Table 1, and then mixed in a twin-screw extruder. (PCM-30 made by Tamami Tekko) to set the temperature at the center of the cylinder to 340~
The temperature was set at 360°C, and extrusion granulation was performed to obtain pellets. Using a 10Z injection molding machine (Neomat 47/28 manufactured by Sumitomo Heavy Industries), the temperature at the center of the cylinder was adjusted to 3.
Set the temperature to 60 to 380°C, and use JIS No. 1 dumbbells and wear rings (outer diameter 25.6 mm, inner diameter 20 mm,
15 mm in height). The tensile properties of JIS No. 1 dumbbells were measured, and the wear rings were measured using a precious wood type abrasion tester at a pressure of P-10 Kf/cm2 and a speed of 20 m/cm.
The mating material was SUS 3Q4 under the minimum condition, and after 2 hours of break-in operation, 20 hours of sliding was performed to determine the friction coefficient, wear coefficient, wear amount of the mating material, amount of polyester added, tensile strength, Although the elongation decreased somewhat, the decrease in the wear coefficient, which indicates wear resistance, was significant, and the friction coefficient was low and stable under the chair, compared to the mating material SUS 3.
Almost no wear was observed on 04.

(13) また、実施例3.5の組成物につき、射出成形にて外径
15mm、内径6□m、長さ10rnmの軸受を成形し
、小型軸受試験機を用いてP11″ =10Kg/cn”、速度20m/min  (y)条
件s相手材である軸をSUS 304として初期の2時
間、50時間、100時間、300時間の摺動を行ない
その摩耗量から摩耗係数を求めた。これらの結果を第2
表に示す。
(13) Also, using the composition of Example 3.5, a bearing with an outer diameter of 15 mm, an inner diameter of 6 □m, and a length of 10 rnm was molded by injection molding, and P11'' = 10 Kg/cn using a small bearing testing machine. '', speed 20 m/min (y) Conditions S SUS 304 was used as the mating shaft, and sliding was performed for an initial period of 2 hours, 50 hours, 100 hours, and 300 hours, and the wear coefficient was determined from the amount of wear. These results are the second
Shown in the table.

表から明らかなように、2つの組成ともに、初期の2h
r の摩耗係数は若干高いが時間とともに摩耗係数は低
下し、aoo hr テストを行なっても異常はまった
くみられなかった。
As is clear from the table, for both compositions, the initial 2h
Although the wear coefficient of r was slightly high, the wear coefficient decreased with time, and no abnormality was observed even when an aoo hr test was performed.

(14) 比較例1〜4 実施例1〜7とまったく同じ芳香族ポリエーテルケトン
、フルオロカーボン重合体、オキシベンゾイルポリエス
テルを用いて、これらの組成を有効な範囲以外の各種配
合比について同様の検討を行なった結果を第3表に示す
(14) Comparative Examples 1 to 4 Using exactly the same aromatic polyether ketone, fluorocarbon polymer, and oxybenzoyl polyester as in Examples 1 to 7, similar studies were conducted on various blending ratios outside the effective range of these compositions. The results are shown in Table 3.

オキシベンゾイルポリエステルがまったく含まれていな
い系(比較例1)および2.5重量%より少ない系(比
較例2)はいずれも耐摩耗性において不充分で、フルオ
ロカーボン重合体の量が2.5重量%より少ない系(比
較例3)は摩擦係数、摩耗係数とも高い。またフルオロ
カーボン重合体とオキシベンゾイルポリエステルの総量
が70重量%を越える系(比較例4)は、流動性が不足
のため射出成形困難であった。
Both the system containing no oxybenzoyl polyester (Comparative Example 1) and the system containing less than 2.5% by weight (Comparative Example 2) have insufficient abrasion resistance, and the amount of fluorocarbon polymer is 2.5% by weight. % (Comparative Example 3) has a high coefficient of friction and a high coefficient of wear. Furthermore, a system in which the total amount of fluorocarbon polymer and oxybenzoyl polyester exceeded 70% by weight (Comparative Example 4) was difficult to injection mold due to insufficient fluidity.

Claims (1)

【特許請求の範囲】[Claims] 芳香族ポリエーテルケトン95〜30重量%、フルオロ
カーボン重合体2.5〜60重量%およびオキシベンゾ
イルポリエステル2.5〜60重量%を含有してなる摺
動特性のすぐれた樹脂組成物。
A resin composition with excellent sliding properties containing 95-30% by weight of aromatic polyetherketone, 2.5-60% by weight of fluorocarbon polymer and 2.5-60% by weight of oxybenzoyl polyester.
JP4424082A 1982-03-18 1982-03-18 Resin composition Granted JPS58160347A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4424082A JPS58160347A (en) 1982-03-18 1982-03-18 Resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4424082A JPS58160347A (en) 1982-03-18 1982-03-18 Resin composition

Publications (2)

Publication Number Publication Date
JPS58160347A true JPS58160347A (en) 1983-09-22
JPH0339110B2 JPH0339110B2 (en) 1991-06-12

Family

ID=12686003

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4424082A Granted JPS58160347A (en) 1982-03-18 1982-03-18 Resin composition

Country Status (1)

Country Link
JP (1) JPS58160347A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59223755A (en) * 1982-10-14 1984-12-15 ソシエテ・シミツク・デ・シヤルボナ−ジユ Thermoplastic composite material and manufacture
JPS61192764A (en) * 1985-02-21 1986-08-27 Idemitsu Kosan Co Ltd Lubricating resin composition
JPS62257828A (en) * 1986-05-01 1987-11-10 Toray Ind Inc Sliding member of clip chain for oven
JPS6366256A (en) * 1986-09-05 1988-03-24 Yobea Rulon Kogyo Kk Aromatic polyether ketone resin composition
US4777214A (en) * 1986-01-03 1988-10-11 Raychem Corporation Blends of poly(arylene ether ketones) and tetrafluoroethylene copolymers
US5115077A (en) * 1988-12-14 1992-05-19 Idemitsu Kosan Company Limited Polyetheric copolymers, process for preparing the same compositions containing the same, their molded products, and their use

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59223755A (en) * 1982-10-14 1984-12-15 ソシエテ・シミツク・デ・シヤルボナ−ジユ Thermoplastic composite material and manufacture
JPS61192764A (en) * 1985-02-21 1986-08-27 Idemitsu Kosan Co Ltd Lubricating resin composition
US4777214A (en) * 1986-01-03 1988-10-11 Raychem Corporation Blends of poly(arylene ether ketones) and tetrafluoroethylene copolymers
JPS62257828A (en) * 1986-05-01 1987-11-10 Toray Ind Inc Sliding member of clip chain for oven
JPH0464296B2 (en) * 1986-05-01 1992-10-14 Toray Industries
JPS6366256A (en) * 1986-09-05 1988-03-24 Yobea Rulon Kogyo Kk Aromatic polyether ketone resin composition
US5115077A (en) * 1988-12-14 1992-05-19 Idemitsu Kosan Company Limited Polyetheric copolymers, process for preparing the same compositions containing the same, their molded products, and their use

Also Published As

Publication number Publication date
JPH0339110B2 (en) 1991-06-12

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