JP2003026883A - Abrasion-resistant fluororesin composition and member for sliding - Google Patents

Abrasion-resistant fluororesin composition and member for sliding

Info

Publication number
JP2003026883A
JP2003026883A JP2001216280A JP2001216280A JP2003026883A JP 2003026883 A JP2003026883 A JP 2003026883A JP 2001216280 A JP2001216280 A JP 2001216280A JP 2001216280 A JP2001216280 A JP 2001216280A JP 2003026883 A JP2003026883 A JP 2003026883A
Authority
JP
Japan
Prior art keywords
fluororesin
radiation
sliding
composition
irradiated
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
Application number
JP2001216280A
Other languages
Japanese (ja)
Inventor
Masahiro Hirose
昌宏 廣瀬
Akira Setogawa
晃 瀬戸川
Yasuaki Yamamoto
康彰 山本
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.)
Hitachi Cable Ltd
Original Assignee
Hitachi Cable 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 Hitachi Cable Ltd filed Critical Hitachi Cable Ltd
Priority to JP2001216280A priority Critical patent/JP2003026883A/en
Publication of JP2003026883A publication Critical patent/JP2003026883A/en
Pending legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To provide a fluororesin composition exhibiting excellent abrasion resistance under sliding with an another resin having a rough surface and a member for sliding composed of the composition. SOLUTION: This composition is composed of a first fluororesin unexposed to radiation, a second fluororesin exposed to radiation at 1-10 kGy under <=100 Torr of oxygen pressure and a filler.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明の属する技術分野】本発明は、耐摩耗性弗素樹脂
組成物および摺動用部材に関し、特に、表面の粗い相手
方との摺動下において優れた耐摩耗性を示す弗素樹脂組
成物と、この組成物より構成された摺動用部材に関す
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a wear-resistant fluororesin composition and a sliding member, and more particularly to a fluororesin composition exhibiting excellent wear resistance under sliding with an opponent having a rough surface, and The present invention relates to a sliding member composed of a composition.

【0002】[0002]

【従来の技術】弗素樹脂は、表面潤滑性、耐熱性、耐薬
品性あるいは電気的特性等に優れていることから、パッ
キン、ガスケット、絶縁材あるいは半導体製造用容器な
どとして広く利用されている。しかし、弗素樹脂は、耐
摩耗性と耐クリープ性に劣るため、摺動環境下あるいは
高温圧縮環境下等で使用される用途には、適用が難しい
ものとされている。
2. Description of the Related Art Fluorine resins are widely used as packings, gaskets, insulating materials, containers for semiconductor production, etc. because of their excellent surface lubricity, heat resistance, chemical resistance, electrical characteristics and the like. However, since the fluororesin is inferior in wear resistance and creep resistance, it is difficult to apply it to applications where it is used in a sliding environment or a high temperature compression environment.

【0003】これらの特性を向上させるための対処策と
して、弗素樹脂に放射線を照射することによって分子間
を架橋化する方法が知られており、この方法は、たとえ
ば、摺動用部材等への弗素樹脂の適用を可能にする有効
手段として活用されている。
As a countermeasure for improving these characteristics, there is known a method of cross-linking the molecules by irradiating a fluorine resin with radiation, and this method is, for example, fluorine for a sliding member or the like. It is used as an effective means to enable the application of resins.

【0004】[0004]

【発明が解決しようとする課題】しかし、従来の照射弗
素樹脂に基づく摺動用部材によると、摺動の相手方の表
面粗さが一定以上に大きくなったとき、耐摩耗性が急激
に低下する欠点があり、このため、適用範囲が制約され
るという問題を有している。
However, according to the conventional sliding member based on the irradiated fluorine resin, when the surface roughness of the other party of sliding becomes larger than a certain level, the wear resistance sharply decreases. Therefore, there is a problem that the application range is restricted.

【0005】従って、本発明の目的は、表面の粗い相手
方との摺動下において優れた耐摩耗性を示す弗素樹脂組
成物と、この組成物より構成された摺動用部材を提供す
ることにある。
Accordingly, it is an object of the present invention to provide a fluororesin composition which exhibits excellent wear resistance under sliding with a counterpart having a rough surface, and a sliding member composed of this composition. .

【0006】[0006]

【課題を解決するための手段】本発明は、上記の目的を
達成するため、放射線を照射されていない第1の弗素樹
脂と、100torr以下の酸素濃度のもとで1〜10
MGyの放射線を照射された第2の弗素樹脂と、充填剤
より成ることを特徴とする耐摩耗性弗素樹脂組成物を提
供するものである。
In order to achieve the above object, the present invention provides a first fluororesin which is not irradiated with radiation and an oxygen concentration of 1 to 10 under an oxygen concentration of 100 torr or less.
A wear-resistant fluororesin composition comprising a second fluororesin irradiated with MGy radiation and a filler.

【0007】また、本発明は、上記の目的を達成するた
め、接触する相手方との間で摺動を行う成型体より構成
される摺動用部材において、前記成型体は、放射線を照
射されていない第1の弗素樹脂と、100torr以下
の酸素濃度のもとで1〜10MGyの放射線を照射され
た第2の弗素樹脂と、充填剤の混和物より構成されるこ
とを特徴とする摺動用部材を提供するものである。
Further, in order to achieve the above object, the present invention provides a sliding member composed of a molded body that slides with a contacting partner, wherein the molded body is not irradiated with radiation. A sliding member comprising a mixture of a first fluororesin, a second fluororesin irradiated with radiation of 1 to 10 MGy under an oxygen concentration of 100 torr or less, and a filler. It is provided.

【0008】上記した第1の弗素樹脂としては、テトラ
フルオロエチレン重合体(以下PTFEという)、テト
ラフルオロエチレンーパーフルオロ(アルキルビニルエ
ーテル)系共重合体(以下、PFAという)、あるいは
テトラフルオロエチレンーヘキサフルオロプロピレン系
共重合体(以下、FEPという)等が使用される。
Examples of the above-mentioned first fluororesin include tetrafluoroethylene polymer (hereinafter referred to as PTFE), tetrafluoroethylene-perfluoro (alkyl vinyl ether) copolymer (hereinafter referred to as PFA), or tetrafluoroethylene- A hexafluoropropylene-based copolymer (hereinafter referred to as FEP) or the like is used.

【0009】また、たとえば、PTFEにパーフルオロ
(アルキルビニルエーテル)、ヘキサフルオロプロピレ
ン、(パーフルオロアルキル)エチレンあるいはクロロ
トリフルオロエチレン等の重合単位を1モル%以下共重
合させたもの、さらには、以上の重合体あるいは共重合
体に少量の第3成分を共重合させたものなども使用可能
であり、なかでもPTFEの使用が特に好適といえる。
Further, for example, PTFE obtained by copolymerizing 1 mol% or less of a polymer unit such as perfluoro (alkyl vinyl ether), hexafluoropropylene, (perfluoroalkyl) ethylene or chlorotrifluoroethylene, further, It is also possible to use a polymer or copolymer obtained by copolymerizing a small amount of the third component, and it is particularly preferable to use PTFE.

【0010】以上に列挙した具体例は、第2の弗素樹脂
の場合も同じであり、同様の重合体あるいは共重合体が
適用される。充填剤としては、カーボン繊維の使用が特
に好ましく、これ以外の他の好適な充填剤としては、ガ
ラス繊維、金属繊維等を挙げることができる。
The specific examples listed above are the same in the case of the second fluororesin, and the same polymer or copolymer is applied. It is particularly preferable to use carbon fiber as the filler, and other suitable fillers include glass fiber, metal fiber and the like.

【0011】本発明において、第2の弗素樹脂への放射
線照射時の酸素濃度を100torr以下に限定する理
由は、酸素濃度がこれを超えると、材料の酸化劣化が発
生して良好な耐摩耗性が得られなくなるためであり、ま
た、放射線の照射量を1〜10MGyに限定する理由
は、照射量が1kGyを下廻ると、耐摩耗性の向上効果
に充分なものが得られず、逆に、10MGyを超過する
と、伸び等が著しく低下するためである。なお、より好
ましい酸素濃度としては、10torr以下に設定する
ことができ、その場合、不活性ガスの雰囲気下であるこ
とが好ましい。
In the present invention, the reason why the oxygen concentration at the time of irradiating the second fluororesin with radiation is limited to 100 torr or less is that when the oxygen concentration exceeds this, oxidative deterioration of the material occurs and good wear resistance is obtained. The reason why the irradiation dose of radiation is limited to 1 to 10 MGy is that when the irradiation dose is less than 1 kGy, a sufficient effect of improving wear resistance cannot be obtained. This is because if it exceeds 10 MGy, the elongation and the like are significantly reduced. A more preferable oxygen concentration can be set to 10 torr or less, and in that case, it is preferable that the atmosphere is an inert gas atmosphere.

【0012】なお、第2の弗素樹脂に照射される放射線
としては、多くの場合、電子線、γ線、X線、中性子線
あるいは高エネルギーイオン等の電離性放射線が使用さ
れる。また、その照射は、弗素樹脂の結晶融点以上に加
熱して行うことが好ましく、具体的には、弗素樹脂がP
TFEの場合で327℃以上、PFAの場合で310℃
以上、FEPの場合で275℃以上に加熱することが好
適な条件となる。
In many cases, ionizing radiation such as electron beam, γ ray, X ray, neutron ray or high energy ion is used as the radiation applied to the second fluororesin. The irradiation is preferably carried out by heating above the crystalline melting point of the fluororesin.
327 ℃ or higher for TFE and 310 ℃ for PFA
As described above, in the case of FEP, heating to 275 ° C. or higher is a preferable condition.

【0013】以上に述べた照射に際しての加熱は、弗素
樹脂を構成する主鎖の分子運動を活発化させるように作
用するため、効率のよい架橋作業の遂行を可能にする。
但し、過剰な加熱は、分子主鎖の切断と分解を招くこと
になるので、その温度は、結晶融点の10〜30℃高い
範囲内に設定されるべきである。
The heating at the time of irradiation as described above acts to activate the molecular motion of the main chain constituting the fluororesin, so that efficient crosslinking work can be performed.
However, since excessive heating causes breakage and decomposition of the molecular main chain, its temperature should be set within a range 10 to 30 ° C. higher than the crystal melting point.

【0014】[0014]

【発明の実施の形態】次に、本発明による耐摩耗性弗素
樹脂組成物および摺動用部材の実施の形態を説明する。
BEST MODE FOR CARRYING OUT THE INVENTION Next, embodiments of the wear resistant fluororesin composition and the sliding member according to the present invention will be described.

【実施例1】PTFEのモールディングパウダー(旭硝
子社製、G−163)を空気中において380℃に30
分間加熱することによって焼成した後、酸素濃度0.1
torrの真空中および340℃の加熱下において電子
線を100kGyの線量となるように照射し、さらに、
これをジェットミルで粉砕することによって平均粒径が
20μmの第2の弗素樹脂としての改質PTFE粉末を
得た。
[Example 1] A molding powder of PTFE (G-163, manufactured by Asahi Glass Co., Ltd.) was heated to 380 ° C for 30 times in the air.
After firing by heating for 1 minute, oxygen concentration 0.1
Irradiation with an electron beam at a dose of 100 kGy in a vacuum of torr and under heating at 340 ° C.,
By pulverizing this with a jet mill, a modified PTFE powder as a second fluororesin having an average particle diameter of 20 μm was obtained.

【0015】次に、この改質PTFE粉末10重量部、
放射線照射をされていない第1の弗素樹脂としての未照
射PTFE粉末(三井デュポン社製、TFM−170
0)85重量部、およびカーボン繊維(呉羽化学社製、
M−201S)5重量部を20℃以下に冷却しながらヘ
ンシルミキサーによって混合し、得られた混合粉を室温
および圧力50MPaのもとで圧縮成型した後、ピーク
温度350℃および2時間の条件下で焼結することによ
り直径40mm×長さ60mmのロッドを成型し、最後
に、これを旋盤でスライスすることにより厚さが0.5
mmのシートを製作した。
Next, 10 parts by weight of this modified PTFE powder,
Non-irradiated PTFE powder (TFM-170 manufactured by Mitsui DuPont Co., Ltd.) as the first fluororesin which has not been irradiated.
0) 85 parts by weight, and carbon fiber (Kureha Chemical Co.,
(M-201S) 5 parts by weight are mixed with a Hensyl mixer while being cooled to 20 ° C. or lower, and the obtained mixed powder is compression molded at room temperature and a pressure of 50 MPa, and then the peak temperature is 350 ° C. and the conditions are 2 hours. A rod having a diameter of 40 mm and a length of 60 mm is formed by sintering below, and finally, the rod is sliced by a lathe to have a thickness of 0.5.
mm sheet was produced.

【0016】[0016]

【実施例2】実施例1において、改質PTFE粉末の混
合量を10重量部、未照射PTFE粉末の混合量を80
重量部、およびカーボン繊維の混合量を10重量部に設
定するとともに、他を同一条件に設定することによって
厚さが0.5mmのシートを製作した。
Example 2 In Example 1, the modified PTFE powder was mixed in an amount of 10 parts by weight, and the unirradiated PTFE powder was mixed in an amount of 80 parts by weight.
A sheet having a thickness of 0.5 mm was manufactured by setting the weight part and the mixing amount of the carbon fiber to 10 parts by weight and setting the other conditions to the same conditions.

【0017】[0017]

【実施例3】実施例1において、改質PTFE粉末の混
合量を10重量部、未照射PTFE粉末の混合量を70
重量部、およびカーボン繊維の混合量を20重量部に設
定するとともに、他を同一条件に設定することによって
厚さが0.5mmのシートを製作した。
[Example 3] In Example 1, the modified PTFE powder was mixed in an amount of 10 parts by weight and the unirradiated PTFE powder was mixed in an amount of 70 parts by weight.
A sheet having a thickness of 0.5 mm was manufactured by setting the weight part and the mixing amount of the carbon fibers to 20 parts by weight and setting the other conditions to the same conditions.

【0018】[0018]

【比較例1】実施例1の未照射PTFE粉末を温度35
0℃および圧力50MPaのもとで1時間圧縮成型し、
引き続き、50MPaの圧力を維持したまま常温まで冷
却することにより直径40mm×長さ60mmのロッド
を成型した後、これを旋盤でスライスすることにより厚
さが0.5mmのシートを製作した。
Comparative Example 1 The unirradiated PTFE powder of Example 1 was heated to a temperature of 35.
Compression molding for 1 hour at 0 ° C. and a pressure of 50 MPa,
Subsequently, a rod having a diameter of 40 mm and a length of 60 mm was molded by cooling to room temperature while maintaining a pressure of 50 MPa, and then a rod having a thickness of 0.5 mm was manufactured by slicing the rod.

【0019】[0019]

【比較例2】実施例1の改質PTFE粉末20重量部と
未照射PTFE粉末80重量部を20℃以下に冷却しな
がらヘンシルミキサーによって混合し、得られた混合粉
を室温および圧力50MPaのもとで圧縮成型した後、
ピーク温度350℃および2時間の条件下で焼結するこ
とにより直径40mm×長さ60mmのロッドを成型
し、最後に、これを旋盤でスライスすることにより厚さ
が0.5mmのシートを製作した。
Comparative Example 2 20 parts by weight of the modified PTFE powder of Example 1 and 80 parts by weight of unirradiated PTFE powder were mixed with a Hensyl mixer while cooling to 20 ° C. or lower, and the resulting mixed powder was heated at room temperature and a pressure of 50 MPa. After compression molding under the original
A rod having a diameter of 40 mm and a length of 60 mm was molded by sintering at a peak temperature of 350 ° C. for 2 hours, and finally, a rod having a thickness of 0.5 mm was manufactured by slicing the rod with a lathe. .

【0020】[0020]

【比較例3】実施例1の改質PTFE粉末50重量部と
未照射PTFE粉末50重量部を20℃以下に冷却しな
がらヘンシルミキサーによって混合した後、得られた混
合粉を温度350℃および圧力50MPaのもとで1時
間圧縮成型し、引き続き、50MPaの圧力を維持した
まま常温まで冷却することにより直径40mm×長さ6
0mmのロッドを成型し、最後に、これを旋盤でスライ
スすることにより厚さが0.5mmのシートを製作し
た。
Comparative Example 3 50 parts by weight of the modified PTFE powder of Example 1 and 50 parts by weight of unirradiated PTFE powder were mixed with a Hensyl mixer while cooling to 20 ° C. or lower, and the resulting mixed powder was heated at a temperature of 350 ° C. It is compression-molded under a pressure of 50 MPa for 1 hour, and subsequently cooled to room temperature while maintaining a pressure of 50 MPa, so that a diameter of 40 mm and a length of 6
A 0 mm rod was molded, and finally, this was sliced by a lathe to manufacture a sheet having a thickness of 0.5 mm.

【0021】表1は、以上の実施例および比較例におけ
る弗素樹脂組成物の組成内容と、これらより得られたシ
ートサンプルの特性試験結果をまとめたものである。な
お、主な特性の試験内容は以下による。
Table 1 summarizes the compositional contents of the fluororesin compositions in the above Examples and Comparative Examples and the characteristic test results of the sheet samples obtained from them. The test contents of the main characteristics are as follows.

【0022】・比摩耗量:スラスト型摩擦摩耗試験装置
を使用し、JIS K 7218に準じてSUS304製
の円筒状リング(外径25.6mm×内径20.6m
m)に試験片(外径25.6mm×内径20.6mm×
厚さ0.5mm)を貼り合わせ、圧力0.4MPaおよ
び速度125mm/分の条件下で試験を実施したときの
50時間経過後の摩耗量を示す。
Specific wear amount: Using a thrust type friction wear tester, a cylindrical ring made of SUS304 (outer diameter 25.6 mm × inner diameter 20.6 m) according to JIS K 7218.
m) test piece (outer diameter 25.6 mm × inner diameter 20.6 mm ×
The amount of wear after 50 hours has elapsed when the test was carried out under the conditions of a pressure of 0.4 MPa and a speed of 125 mm / min after bonding (0.5 mm in thickness).

【0023】・クリープ:ASTMD621−64に準
拠し、200℃で圧縮したときのクリープ性を測定。 ・永久変形:7MPaの圧力荷重を連続して24時間加
えた後に荷重を解放し、荷重解放後24時間を経過した
ときの変形率を示す。 ・引張試験(伸び、引張強さ):JIS K 6891に
準じ、引張速度200mm/分にて実施。
Creep: According to ASTM D621-64, the creep property when compressed at 200 ° C. is measured. -Permanent deformation: The deformation rate is shown when a pressure load of 7 MPa is continuously applied for 24 hours, the load is released, and 24 hours after the load is released. -Tensile test (elongation, tensile strength): According to JIS K 6891, a tensile speed of 200 mm / min.

【0024】[0024]

【表1】 [Table 1]

【0025】表1によれば、実施例1〜3が、比摩耗量
において低い水準にとどまっているのに比べ、比較例1
および2の場合には、著しく高い比摩耗量を示してい
る。これは、比較例1が改質弗素樹脂およびカーボン繊
維の双方を含んでおらず、一方、比較例2がカーボン繊
維を含んでいないことが影響しているもので、これらの
違いが比摩耗量の差となって現れたものである。
According to Table 1, in comparison with Examples 1 to 3 where the specific wear amount remains at a low level, Comparative Example 1
In the cases of 1 and 2, a remarkably high specific wear amount is shown. This is because Comparative Example 1 does not include both the modified fluororesin and the carbon fiber, while Comparative Example 2 does not include the carbon fiber, and the difference between them is the specific wear amount. It appears as the difference between.

【0026】なお、比較例3の比摩耗量が試験Aのケー
スにおいて実施例1〜3より優れた結果を示している
が、これは、摺動相手の表面粗さが細かいためであり、
粗さの大きな試験Bの場合には、実施例1〜3より格段
に高い比摩耗量を示している。耐摩耗性の良否は、表面
の粗い相手方との摺動のときに明確に現れるものであ
り、従って、実施例が備える優れた耐摩耗性は、この比
較例3と対比するとき、特に顕著となる。
In the case of the test A, the specific wear amount of Comparative Example 3 is superior to that of Examples 1 to 3, but this is because the surface roughness of the sliding partner is fine.
In the case of the test B having a large roughness, the specific wear amount is remarkably higher than those of Examples 1 to 3. The good or bad wear resistance is clearly shown when sliding with a counterpart having a rough surface, and therefore, the excellent wear resistance provided in the example is particularly remarkable when compared with this comparative example 3. Become.

【0027】表1は、本発明による耐摩耗性弗素樹脂組
成物、およびこれを使用して構成される摺動用部材の特
異性と有用性を明白に示しており、本発明による弗素樹
脂の応用性向上の効果は大であるといえる。
Table 1 clearly shows the specificity and usefulness of the abrasion-resistant fluororesin composition according to the present invention and the sliding member formed by using the composition, and the application of the fluororesin according to the present invention. It can be said that the effect of improving the sex is great.

【0028】[0028]

【発明の効果】以上説明したように、本発明によれば、
放射線を照射されていない第1の弗素樹脂、100to
rr以下の酸素濃度のもとで1〜10MGyの放射線を
照射された第2の弗素樹脂、および充填剤による組成構
成としているため、表面の粗い相手方との摺動において
優れた耐摩耗性を有する弗素樹脂組成物を提供すること
ができ、さらに、これを使用した高耐摩耗性の摺動用部
材を提供することができる。
As described above, according to the present invention,
1st fluorine resin not irradiated with radiation, 100to
The composition is composed of the second fluororesin irradiated with 1 to 10 MGy of radiation under the oxygen concentration of rr or less, and the filler, so that it has excellent wear resistance in sliding with the counterpart with a rough surface. A fluororesin composition can be provided, and further, a highly wear-resistant sliding member using the same can be provided.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 山本 康彰 茨城県日立市日高町5丁目1番1号 日立 電線株式会社総合技術研究所内 Fターム(参考) 4J002 BD15W BD15X BD16W BD16X BE04W BE04X DA016 FA046 GM04 GM05    ─────────────────────────────────────────────────── ─── Continued front page    (72) Inventor Yasuaki Yamamoto             Hitachi, 1-1 Hidaka-cho, Hitachi City, Ibaraki Prefecture             Electric Cable Co., Ltd. F term (reference) 4J002 BD15W BD15X BD16W BD16X                       BE04W BE04X DA016 FA046                       GM04 GM05

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】放射線を照射されていない第1の弗素樹脂
と、100torr以下の酸素濃度のもとで1〜10M
Gyの放射線を照射された第2の弗素樹脂と、充填剤よ
り成ることを特徴とする耐摩耗性弗素樹脂組成物。
1. A first fluororesin that has not been irradiated with radiation and 1 to 10 M under an oxygen concentration of 100 torr or less.
A wear-resistant fluororesin composition comprising a second fluororesin irradiated with Gy radiation and a filler.
【請求項2】前記第1および第2の弗素樹脂は、テトラ
フルオロエチレン系重合体であることを特徴とする請求
項1項記載の耐摩耗性弗素樹脂組成物。
2. The abrasion-resistant fluororesin composition according to claim 1, wherein the first and second fluororesins are tetrafluoroethylene-based polymers.
【請求項3】前記充填剤は、カーボン繊維であることを
特徴とする請求項1項記載の耐摩耗性弗素樹脂組成物。
3. The wear-resistant fluororesin composition according to claim 1, wherein the filler is carbon fiber.
【請求項4】接触する相手方との間で摺動を行う成型体
より構成される摺動用部材において、前記成型体は、第
1の弗素樹脂と、100torr以下の酸素濃度のもと
で1〜10MGyの放射線を照射された第2の弗素樹脂
と、充填剤の混和物より構成されることを特徴とする摺
動用部材。
4. A sliding member formed of a molded body that slides with a contacting partner, wherein the molded body has a first fluororesin and an oxygen concentration of 1 to 100 torr or less. A sliding member comprising a mixture of a second fluororesin irradiated with 10 MGy of radiation and a filler.
JP2001216280A 2001-07-17 2001-07-17 Abrasion-resistant fluororesin composition and member for sliding Pending JP2003026883A (en)

Priority Applications (1)

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Publication Number Publication Date
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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004346265A (en) * 2003-05-26 2004-12-09 Hitachi Industrial Equipment Systems Co Ltd Sliding material and oil-free scroll compressor
WO2006120882A1 (en) * 2005-05-02 2006-11-16 Daikin Industries, Ltd. Crosslinkable polytetrafluoroethylene composition, cross- linked polytetrafluoroethylene powder, polytetrafluoro- ethylene moldings, resin blend compositions, and resin blend moldings
JP2007332208A (en) * 2006-06-13 2007-12-27 Hitachi Cable Ltd Modified fluororesin composition and molded product thereof
JP2011016956A (en) * 2009-07-10 2011-01-27 Daikin Industries Ltd Crosslinking polytetrafluoroethylene (ptfe) composition and molding of the same

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004346265A (en) * 2003-05-26 2004-12-09 Hitachi Industrial Equipment Systems Co Ltd Sliding material and oil-free scroll compressor
WO2006120882A1 (en) * 2005-05-02 2006-11-16 Daikin Industries, Ltd. Crosslinkable polytetrafluoroethylene composition, cross- linked polytetrafluoroethylene powder, polytetrafluoro- ethylene moldings, resin blend compositions, and resin blend moldings
JPWO2006120882A1 (en) * 2005-05-02 2008-12-18 ダイキン工業株式会社 Crosslinkable polytetrafluoroethylene composition, crosslinked polytetrafluoroethylene powder, polytetrafluoroethylene molded article, resin blend composition, and resin blend molded article
JP5029359B2 (en) * 2005-05-02 2012-09-19 ダイキン工業株式会社 Crosslinkable polytetrafluoroethylene composition, crosslinked polytetrafluoroethylene powder, polytetrafluoroethylene molded article, resin blend composition, and resin blend molded article
JP2007332208A (en) * 2006-06-13 2007-12-27 Hitachi Cable Ltd Modified fluororesin composition and molded product thereof
JP2011016956A (en) * 2009-07-10 2011-01-27 Daikin Industries Ltd Crosslinking polytetrafluoroethylene (ptfe) composition and molding of the same

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