JPS60199045A - Fluororesin composition - Google Patents

Fluororesin composition

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Publication number
JPS60199045A
JPS60199045A JP5495384A JP5495384A JPS60199045A JP S60199045 A JPS60199045 A JP S60199045A JP 5495384 A JP5495384 A JP 5495384A JP 5495384 A JP5495384 A JP 5495384A JP S60199045 A JPS60199045 A JP S60199045A
Authority
JP
Japan
Prior art keywords
fluororesin
polyolefin resin
weight
particle size
composition
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
JP5495384A
Other languages
Japanese (ja)
Other versions
JPH0471942B2 (en
Inventor
Nobukazu Atsumi
渥美 信和
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.)
JNC Corp
Original Assignee
Chisso Corp
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 Chisso Corp filed Critical Chisso Corp
Priority to JP5495384A priority Critical patent/JPS60199045A/en
Publication of JPS60199045A publication Critical patent/JPS60199045A/en
Publication of JPH0471942B2 publication Critical patent/JPH0471942B2/ja
Granted legal-status Critical Current

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Abstract

PURPOSE:To obtain a composition of significantly improved moldability while retaining the excellent characteristics inherent in fluororesin, also causing no corrosion of the molding machine, by kneading, under a molten state, a fluororesin of specific particle size and polyolefin resin. CONSTITUTION:The objective composition can be obtained by kneading, under a molten state, (A) 90-60wt% of a fluororesin of an average particle size 2-20mu and (B) 10-40wt% of a polyolefin resin, alternatively, another composition comprising (1) 85-50wt% of said fluororesin, (2) 5-10wt% of graphite or molybdenum disulfide, (3) 10-40wt% of said polyolefin resin will have higher resistance to wear. Said fluororesin should be polytetrafluoroethylene, whereas the polyolefin resin either polyethylene or polypropylene one.

Description

【発明の詳細な説明】 本発明はふっ素樹脂組成物に関する。さらに詳しくは平
均粒径が2〜20μのふっ素樹脂にポリオレフィン樹脂
を混合しまたは該ふっ素樹脂にポリオレフィン樹脂とグ
ラファイトまたは2硫化モリブデンを混合し、それぞれ
溶融混線せしめてなるふっ素樹脂組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to fluororesin compositions. More specifically, the present invention relates to a fluororesin composition prepared by mixing a fluororesin with an average particle size of 2 to 20 μm with a polyolefin resin, or mixing the fluororesin with a polyolefin resin and graphite or molybdenum disulfide, and melting and intermixing the mixture.

ふっ素樹脂特にボリテ)′yフルオロエチレン(以下P
TFBという。)は耐熱性、耐薬品性、電気絶縁性、低
摩擦係数、低摩耗性、非粘着性など種々の特徴を有して
いるため、その応用分野も化学、機械、電気・電子の工
業用分野から家庭用品の分野まで巾広く広がっている。
Fluororesin (especially volite)'y fluoroethylene (hereinafter P
It's called TFB. ) has various characteristics such as heat resistance, chemical resistance, electrical insulation, low coefficient of friction, low abrasion, and non-adhesion, so its application fields are chemical, mechanical, electrical and electronic industrial fields. It has spread widely to the field of household goods.

しかしながら、融点が327℃、溶融粘度が10”−1
0t*ボイズと極めて高く、融点を越えても流動しない
ため、一般のプラスチックに適用される溶融加工成形法
は適用出来ない。従つて成形方法として圧縮成形、ラム
押出成形などの特殊な成形方法が必要となる。このよう
な成形性を改良するため融点および溶融粘度を低下させ
たふっ素樹脂、例えば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(PFA)、テ
トラフルオロエチレン−ヘキサフルオロプロピレン共重
合体(FBP) 、ポリクロロトリフルオロエチレン(
PCTFE)、fドラフルオロエチレン−エチレン共重
合体(ETFE )始め数種類のふっ素樹脂が熱溶融タ
イプのふっ素樹脂として開発され、市販されている。し
かしながら、一般の熱可塑性樹脂と同様の成形が出来る
前記熱溶融タイプのふっ素樹脂が数多く開発された現在
においても成形性に問題があるといわれるFTFBがそ
の優れた耐熱性、耐薬品性、電気絶縁性、非粘着性、低
摩擦係数などの性質のため全ふっ素樹脂出荷量の70−
以上の量使用されている。
However, the melting point is 327°C and the melt viscosity is 10"-1
Since it has an extremely high 0t* void and does not flow even if it exceeds its melting point, melt processing and molding methods applied to general plastics cannot be applied. Therefore, a special molding method such as compression molding or ram extrusion molding is required. In order to improve such moldability, fluororesins with lowered melting points and melt viscosity, such as tetrafluoroethylene-perfluoroalkyl vinyl ether copolymers (PFA), tetrafluoroethylene-hexafluoropropylene copolymers (FBP), Polychlorotrifluoroethylene (
Several types of fluororesins, including PCTFE) and f-fluoroethylene-ethylene copolymer (ETFE), have been developed as heat-melting type fluororesins and are commercially available. However, even though many heat-melting type fluororesins have been developed that can be molded in the same way as general thermoplastic resins, FTFB, which is said to have moldability problems, has excellent heat resistance, chemical resistance, and electrical insulation. Due to its properties such as flexibility, non-adhesiveness, and low coefficient of friction, 70% of total fluoropolymer resins are shipped.
are used in greater amounts.

また、融点および溶融粘度を低下させ、一般の熱可塑性
樹脂と同様な押出成形、射出成形が可能であるといわれ
る熱溶融タイプのふっ素樹脂でも成形機の腐食の問題が
あシ、また射出成形ではスプル、ランナ、ゲートを太く
、短かくするなどの必要があるなど溶融流動性が一般ポ
リオレフイン樹脂より劣り、ポリオレフィン樹脂とまっ
たく同様の成形をするのには難点がある。
In addition, even heat-melting type fluororesin, which has a lower melting point and melt viscosity and is said to be able to be extruded and injection molded in the same way as general thermoplastic resins, has problems with molding machine corrosion, and injection molding Its melt fluidity is inferior to general polyolefin resins, such as the need to make sprues, runners, and gates thicker and shorter, making it difficult to mold in exactly the same way as polyolefin resins.

本発明者は、ふっ素樹脂のかかる問題点を改善するべく
鋭意研究した。その結果、ふっ素樹脂特にFTFBにポ
リオレフィン樹脂を10〜40重量%添加することによ
シ、ふっ素樹脂としての諸性能(優れた耐熱性、耐薬品
性、電気絶縁性、低摩擦係数、低摩耗性など)を保持し
、かつポリオレフィン樹脂とまったく同様の成形性を有
し、腐蝕の問題のないふっ素樹脂が得られることを見い
出し、本発明を完成した。
The present inventor has conducted extensive research in order to improve these problems with fluororesins. As a result, by adding 10 to 40% by weight of polyolefin resin to fluororesin, especially FTFB, various properties as fluororesin (excellent heat resistance, chemical resistance, electrical insulation, low coefficient of friction, low abrasion) can be improved. The present invention has been completed based on the discovery that it is possible to obtain a fluororesin that has the same properties as polyolefin resins, has exactly the same moldability as polyolefin resins, and is free from corrosion problems.

以上の記述から明らか力ように本発明の目的はふっ素樹
脂の諸性能を保持しながら、ポリオレフィン樹脂と同等
の成形が可能で、腐食の問題のないふっ素樹脂組成物を
提供することである。
As is clear from the above description, an object of the present invention is to provide a fluororesin composition that can be molded to the same level as polyolefin resins and is free from corrosion problems, while maintaining the various properties of fluororesins.

本発明は下記の構成を有する。The present invention has the following configuration.

(1)平均粒径が2〜20μのふっ素樹脂90〜60重
量%とポリオレフィン樹脂10〜40重量−を混合、溶
融混線せしめて表るふっ素樹脂組成物。
(1) A fluororesin composition obtained by mixing 90 to 60% by weight of a fluororesin with an average particle size of 2 to 20 μm and 10 to 40% by weight of a polyolefin resin, and then melting and cross-mixing the mixture.

(2)平均粒径が2〜20μのふっ素樹脂85〜50重
量%、グラファイトまたは2硫化モリブデン5〜10チ
、ポリオレフィン樹脂10〜40重量−を混合、溶融せ
しめてなるふっ素樹脂組成物。
(2) A fluororesin composition prepared by mixing and melting 85-50% by weight of a fluororesin having an average particle size of 2-20μ, 5-10% by weight of graphite or molybdenum disulfide, and 10-40% by weight of a polyolefin resin.

本発明で用いられるふっ素樹脂としては、耐熱性、電気
絶縁性、低摩擦係数、低摩耗性など種々の諸性能に優れ
ている粒径2〜20μのPTFBが好ましい。特に粒径
が2〜10μのPTPEが好ましい。
As the fluororesin used in the present invention, PTFB having a particle size of 2 to 20 μm is preferable because it is excellent in various properties such as heat resistance, electrical insulation, low coefficient of friction, and low abrasion. Particularly preferred is PTPE having a particle size of 2 to 10 microns.

粒径が2μ未満であるとポリオレフィン樹脂との混合時
に2次凝集を起こし易くなり分散性を悪ろくする。また
粒径が20μを超えるとポリオレフィン樹脂とUP T
 F B樹脂との混合時の見かけの分散は良くなるが、
成形品としだときの材質中での該ポリオレフィン樹脂相
と該FTFB樹脂相の分散は逆に悪ろくなり充分な性能
が発揮され々くなるので好ましくない。
When the particle size is less than 2 μm, secondary aggregation tends to occur during mixing with the polyolefin resin, resulting in poor dispersibility. Also, if the particle size exceeds 20μ, polyolefin resin and UPT
Although the apparent dispersion improves when mixed with F B resin,
This is not preferable because the dispersion of the polyolefin resin phase and the FTFB resin phase in the material used to form the molded product becomes worse, and sufficient performance is not exhibited.

またポリオレフィン樹脂としてはエチレン、プロビレ/
、ブテン等のα−オレフィンの単独重合体、該α−オレ
フィンと他のα−オレフィンとのランダム共重合体、ブ
ロック共重合体およびこれらの二以上の混合物が用いら
れる。ポリオレフィン樹脂の添加量は10〜40重量%
の範囲が好ましい。特に好ましくは10〜30重量%の
範囲である。10重量%未満では良好な成形性が得られ
ず、ポリオレフィン樹脂と同様な成形が困難となる。ま
た40重量%を超えるとふっ素樹脂の有する諸性能特に
耐摩耗性、低摩擦係数といった特性が低下してしまい好
ましくない。
In addition, as polyolefin resins, ethylene,
, homopolymers of α-olefins such as butene, random copolymers of the α-olefins and other α-olefins, block copolymers, and mixtures of two or more of these are used. The amount of polyolefin resin added is 10 to 40% by weight.
A range of is preferred. A particularly preferable range is 10 to 30% by weight. If the amount is less than 10% by weight, good moldability cannot be obtained, and molding similar to that of polyolefin resins becomes difficult. Moreover, if it exceeds 40% by weight, various properties of the fluororesin, particularly properties such as wear resistance and low coefficient of friction, deteriorate, which is not preferable.

またポリオレフィン樹脂の添加量が50重量−以上にな
るとふっ素樹脂としての諸性能特に耐摩耗性、低摩擦係
数といった特性が1オ一ダー以上悪るくなり、もはやふ
っ素樹脂としての用途には適用が困難と寿る。この点が
本発明に係る組成物と、ふっ素樹脂を50−以下含有す
るポリオレフィン樹脂組成物と異なる点である。
Furthermore, if the amount of polyolefin resin added exceeds 50% by weight, the various properties of the fluororesin, especially its wear resistance and low friction coefficient, deteriorate by an order of magnitude or more, making it no longer suitable for use as a fluororesin. Live with hardship. This point is different from the composition according to the present invention and a polyolefin resin composition containing 50 or less fluororesin.

また該組成物の機械的性質特に耐摩耗性をさらに改食す
るために必要に応じてグラファイトまたは2硫化モリブ
デンを5〜10重量%添加事ることが出来る。5重量%
未溝の添加ではその改良効果が顕著でなく、また10重
量%を超えて添加するとその効果の向上の割に成形性の
低下が大きく好ましくない。
Furthermore, in order to further improve the mechanical properties, particularly the wear resistance, of the composition, 5 to 10% by weight of graphite or molybdenum disulfide may be added as necessary. 5% by weight
When added without grooves, the improvement effect is not significant, and when added in an amount exceeding 10% by weight, the moldability is greatly reduced in spite of the improvement in the effect, which is not preferable.

また本発明にあっては通常ポリオレフィンに添加される
添加剤例えば酸化防止剤、帯電防止剤、高級脂肪酸の金
属塩類、顔料、無機質充填剤、ガラス繊維などを併用す
ることが出来る。
Further, in the present invention, additives which are usually added to polyolefins, such as antioxidants, antistatic agents, metal salts of higher fatty acids, pigments, inorganic fillers, glass fibers, etc., can be used in combination.

本組成物は所定量のふっ素樹脂、ポリオレフィン樹脂、
必要に応じてグラフアイ)または2硫化モリブデンなど
を混合し、2軸の押出機で溶融混練することにより得ら
れる。
This composition contains a predetermined amount of fluororesin, polyolefin resin,
It is obtained by mixing molybdenum disulfide or the like as required, and melting and kneading the mixture in a twin-screw extruder.

混合装置としてはヘンセルミキサー(商品名)、スーパ
ーミキサーなどの高速撹拌機付混合機、パンパリミキサ
ー、リボングレンダーなどの混合装置を使用すれば良い
。溶融混線は通常の2軸押出機が用いられる。溶融混線
温度は200℃〜300℃、好ましくは220℃〜28
0℃である。
As a mixing device, a mixing device such as a Hensel mixer (trade name), a mixer with a high-speed stirrer such as a super mixer, a Panpari mixer, a ribbon grinder, etc. may be used. A normal twin-screw extruder is used for melt mixing. The melt crosstalk temperature is 200°C to 300°C, preferably 220°C to 28°C.
It is 0°C.

かくして得られたふっ素樹脂組成物のペレットから各種
試験片の作成を兼ねて射出成形機による成形性を調べた
。当然のようにふっ素樹脂100重量%のものは通常の
射出成形条件では成形物が得られなかった。これに引き
替え、本発明になるふっ素樹脂組成物は通常のポリオレ
フィン樹脂とまったく同様の成形条件での成形が可能で
あることが確認され、試験片が成形出来た。これらの試
験片を用いて機械的特性である摩耗性および動的、静的
摩擦係数の測定を実施した。摩耗性の測定はJIS K
 7204に準拠(C817輪、1 kg荷重、23℃
、1000回転)し、動的、静的摩擦係数の測定はA8
TMT) 1894に準拠(長さ65m5巾65龍、厚
さ2+111の平板、耐研き鋼)して行なった。
Various test pieces were prepared from the pellets of the fluororesin composition thus obtained, and their moldability using an injection molding machine was examined. Naturally, a molded article of 100% by weight fluororesin could not be obtained under normal injection molding conditions. In contrast, it was confirmed that the fluororesin composition of the present invention could be molded under exactly the same molding conditions as ordinary polyolefin resins, and test pieces could be molded. Mechanical properties such as abrasion resistance and dynamic and static friction coefficients were measured using these test pieces. Measurement of abrasion resistance is based on JIS K
7204 (C817 wheels, 1 kg load, 23℃
, 1000 rotations), and the dynamic and static friction coefficients were measured using A8.
TMT) 1894 (length: 65 m, width: 65 mm, thickness: 2+111 flat plate, sharpening-resistant steel).

また比較対照品としては、ふっ素樹脂の成形が不可能で
あったため、市販品を入手して比較試験した。
In addition, as a comparative product, since it was impossible to mold fluororesin, a commercially available product was obtained and a comparative test was conducted.

その結果、本発明に係るふっ素樹脂組成物はふっ素樹脂
の特性の1つである低摩耗性、低摩擦係数を満足し、か
つ通常のポリオレフィン樹脂どまったく同様の成形法で
成形が可能な組成物であることが確認された。
As a result, the fluororesin composition of the present invention satisfies low abrasion and low friction coefficient, which are one of the characteristics of fluororesins, and can be molded using the same molding method as ordinary polyolefin resins. It was confirmed that

PTFI!を樹脂は常温においてはいわゆる工/ジニア
リ/グ樹脂のような機械的強度(引張強度)を持ってい
るのでは々く、ポリオレフィン樹脂とほぼ同等の機械的
強度を示すにすぎないが低温または高温になると一般の
プラスチックに比較して極めて優れた機械的強度を示す
PTFI! At room temperature, the resin has mechanical strength (tensile strength) similar to that of so-called engineering/engineering resins, but it only exhibits mechanical strength roughly equivalent to that of polyolefin resins, but at low or high temperatures. It exhibits extremely superior mechanical strength compared to general plastics.

本発明に係わる組成物もFTFB樹脂そのものよシは高
温時の機械的強度(引張強度)は若干劣るものの一般の
プラスチックにくらべて、はるかに大きい高温時引張強
度を有しており、充分ふっ素樹脂としての使用に耐える
ものである本発明に係る組成物はその成形性の良好さと
相まって低摩耗性、低摩擦性を利用した摺動材の用途を
始めとして自動車部品、電機製品部品その他一般工業用
部品の分野へ利用出来る。
Although the composition according to the present invention has a much higher tensile strength at high temperatures than general plastics, although its mechanical strength (tensile strength) at high temperatures is slightly inferior to that of the FTFB resin itself, it has sufficient tensile strength at high temperatures. The composition of the present invention is suitable for use as a sliding material that takes advantage of its good moldability and low abrasion and friction properties, as well as automobile parts, electrical appliance parts, and other general industrial applications. It can be used in the field of parts.

以下実施例および対照例で本発明を具体的に示すO 実施例1、対照例1 5μの粒径を有するポリテトラフルオロエチレン70重
量%とポリオレフィン樹脂としてメルトフローレートが
8.0r710分(温度230℃における荷重2.16
 kgを加えた場合の10分間のWI融樹脂の吐出量)
のポリプロピレン単独重合体またはメルトフローレート
が4.(1710分のプロピレンエチレン共重合体30
重量%とをヘンセルミキサーで混合し、口径45非の2
軸押出機で250℃の溶融混線温度で溶融混練しペレタ
イズし九〇 これらのベレットを通常のポリオレフィン用の射出成形
機にかけ、射出圧40〜14 okgt/crlG(4
!!圧−1次圧)、射出速度4011I/秒、樹脂温度
250℃、金型温度50℃の成形条件によシその成形性
を観察するとともに長さZoom、巾10011%厚さ
21111の平板を成形した。
The present invention will be concretely illustrated in the following examples and comparative examples.O Example 1, comparative example 1 70% by weight of polytetrafluoroethylene having a particle size of 5μ and a polyolefin resin have a melt flow rate of 8.0 r 710 minutes (temperature 230 Load at °C 2.16
Discharge amount of WI melt resin for 10 minutes when adding kg)
Polypropylene homopolymer or melt flow rate of 4. (1710 min propylene ethylene copolymer 30
% by weight in a Hensel mixer, and
Melt-knead and pelletize using a shaft extruder at a melt mixing temperature of 250°C.90 These pellets are put into an ordinary injection molding machine for polyolefins, and the injection pressure is 40 to 14 okgt/crlG (4
! ! The moldability was observed under the following molding conditions: injection speed 4011 I/sec, resin temperature 250°C, mold temperature 50°C, and a flat plate with length Zoom, width 10011% and thickness 21111 was molded. did.

また対照例1として、ポリテトラフルオロエチレンの市
販の成形品を使用した。
Furthermore, as Control Example 1, a commercially available molded product of polytetrafluoroethylene was used.

以上の如き試験片を用いて、摩耗性、動的、静的¥擦係
数を測定した。
Using the above test pieces, abrasion properties, dynamic and static friction coefficients were measured.

実施例2 5μの粒径を有するポリテトラフルオロエチレン70重
量−とポリオレフィン樹脂としてメルトインデックスが
s、or/lo分(温度190℃における荷重2.15
kgを加えた場合の10分間の溶融樹脂の吐出量)のポ
リエチレン単独重合体30重量−とを実施例1と同様の
方法でペレタイズし、実施例1と同様の方法、条件で射
出成形し、成形性の観察ならびに摩耗性、動的、静的摩
擦係数を測定した。
Example 2 70% by weight of polytetrafluoroethylene with a particle size of 5μ and a polyolefin resin with a melt index of s, or/lo min (load of 2.15 at a temperature of 190°C)
A polyethylene homopolymer (30 weight) of molten resin (discharge amount of molten resin in 10 minutes when adding kg) was pelletized in the same manner as in Example 1, injection molded in the same manner and under the same conditions as in Example 1, Formability was observed, and abrasion properties, dynamic and static friction coefficients were measured.

実施例3、対照例2 5μの粒径を有するポリテトラフルオロエチレン70重
量%とポリオレフィン樹脂としてメルトフローレートが
8.0f/10分のポリプロピレン単独重合体またはメ
ルトフローレートが4.0F710分のプロピレンエチ
レン共重合体20重量%およびグラファイト10重量%
とをヘンセルミキサーで混合後、実施例1と同様の方法
でその成形性ならびに摩耗性、動的、静的摩擦係数を測
定した。
Example 3, Control Example 2 70% by weight of polytetrafluoroethylene having a particle size of 5μ and polypropylene homopolymer with a melt flow rate of 8.0 f/10 min as a polyolefin resin or propylene with a melt flow rate of 4.0 f/10 min 20% by weight of ethylene copolymer and 10% by weight of graphite
After mixing with a Hensel mixer, the moldability, abrasion properties, and dynamic and static friction coefficients were measured in the same manner as in Example 1.

対照例2としてグラファイト入りのポリテトラフルオロ
エチレンの市販成形品を使用した。
As Control Example 2, a commercially available molded product of polytetrafluoroethylene containing graphite was used.

実施例4、対照例3 5μの粒径を有するポリテトラフルオロエチレン70重
量%とポリオレフィン樹脂としてメルト70−レートが
8.0f/1G分のポリプロピレン単独重合体、または
メルト70−レートカ4、 Ot / lo分のプロピ
レンエチレン共重合体20重量%および2硫化モリブデ
ン10重量%とをへンセルミキサーで混合後、実施例1
と同様の方法でその成形性ならびに摩耗性、動的、静的
摩擦係数を測定した。
Example 4, Control Example 3 A polypropylene homopolymer with a melt 70-rate of 8.0 f/1G as a polyolefin resin and 70% by weight of polytetrafluoroethylene having a particle size of 5μ, or a melt 70-rate of 4, Ot/ After mixing 20% by weight of propylene ethylene copolymer and 10% by weight of molybdenum disulfide in a Hensel mixer, Example 1
Its formability, abrasion resistance, and dynamic and static friction coefficients were measured using the same method as above.

また対照例3として2硫化モリブデン入りのポリテトラ
フルオロエチレンの市販成形品を使用した。
Further, as a control example 3, a commercially available molded product of polytetrafluoroethylene containing molybdenum disulfide was used.

これらの結果を第1表にまとめて示す。These results are summarized in Table 1.

第 1 表 第1表から判るように本発明に係るふっ素樹脂組成物は
通常のポリオレフィンとまったく同様の方法および条件
で成形することが出来、しかもふっ素樹脂のもつ優れた
諸性能を保持していることが確認された。
Table 1 As can be seen from Table 1, the fluororesin composition according to the present invention can be molded in exactly the same manner and under the same conditions as ordinary polyolefins, and yet maintains the excellent performance of fluororesins. This was confirmed.

本発明に係る組成物はその成形性の良好さとともに、低
摩耗性、低摩擦性を利用した摺動材の用途を始め各種自
動車部品、電機製品部品、一般工業用部品などの分野へ
巾広く利用出来ることが判明した。
The composition according to the present invention has good moldability, and is widely used in fields such as sliding materials that take advantage of its low abrasion and low friction properties, as well as various automobile parts, electrical appliance parts, and general industrial parts. It turned out that it can be used.

以上 手 続 補 正 書 唱和59年i月2tH L 事FFO表示 昭和59年特許願@54953号 & 発明の名称 ふっ素樹脂組成瞼 & 補正をする看 事件との関係 q#杵出出願 人阪府大阪市北区中之島三丁目6番32号(〒530)
(20))チッソ株式会社 代表者野木貞雄 本代理人 東京都新宿区新宿2丁目8番1号(〒160)a 補正
により増加する発明O数 な し 嘔 補正の対象 明細書「発明の詳細な説明」の欄 a 補正oP3e 明細書落8頁1行目「リボングレンダー」を「リボンズ
レンダー」に訂正する。
Amendment of the above procedure Written in April 1983 2tH L Matter of FFO Indication 1982 Patent Application @ 54953 & Title of invention Fluororesin composition & Relationship to the case making the amendment q # Applicant Osaka, Osaka Prefecture 3-6-32 Nakanoshima, Ichikita-ku (530)
(20)) Chisso Co., Ltd. Representative Sadao Nogi Principal Agent 2-8-1 Shinjuku, Shinjuku-ku, Tokyo (160)a No number of inventions will increase as a result of the amendment. "Explanation" column a Correction oP3e Correct "Ribbon Grender" in the first line of page 8 of the specification to "Ribbons Lender."

以上that's all

Claims (4)

【特許請求の範囲】[Claims] (1)平均粒径が2〜20μのふっ素樹脂90〜60重
量%とポリオレフィン樹脂10〜40重量−を混合、溶
融混線せしめてなるふっ素樹脂組成物。
(1) A fluororesin composition prepared by mixing 90 to 60% by weight of a fluororesin with an average particle size of 2 to 20 μm and 10 to 40% by weight of a polyolefin resin, and then melting and cross-mixing the mixture.
(2)平均粒径が2〜20μのふっ素樹脂85〜50重
量−、グラファイトまたは2硫化モリブデン5〜10重
量−、ポリオレフィン樹脂10〜40重量−を混合、溶
融混線せしめてなるふっ素樹脂組成物。
(2) A fluororesin composition prepared by mixing 85 to 50 weight of a fluororesin with an average particle size of 2 to 20 μm, 5 to 10 weight of graphite or molybdenum disulfide, and 10 to 40 weight of a polyolefin resin, and melting and cross-mixing them.
(3)平均粒径が2〜20μのふっ素樹脂がポリテトラ
フルオロエチレンであり、ポリオレフィン樹脂がポリエ
チレン樹脂またはポリプロピレン樹脂である特許請求の
範囲第1項記載の組成物。
(3) The composition according to claim 1, wherein the fluororesin having an average particle size of 2 to 20 μm is polytetrafluoroethylene, and the polyolefin resin is polyethylene resin or polypropylene resin.
(4)平均粒径が2〜20μのふっ素樹脂がポリテトラ
フルオロエチレンであり、ポリオレフィン樹脂がポリエ
チレン樹脂またはポリプロビレ/樹脂である特許請求の
範囲第2項記載の組成物。
(4) The composition according to claim 2, wherein the fluororesin having an average particle size of 2 to 20 μm is polytetrafluoroethylene, and the polyolefin resin is polyethylene resin or polypropylene/resin.
JP5495384A 1984-03-22 1984-03-22 Fluororesin composition Granted JPS60199045A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5495384A JPS60199045A (en) 1984-03-22 1984-03-22 Fluororesin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5495384A JPS60199045A (en) 1984-03-22 1984-03-22 Fluororesin composition

Publications (2)

Publication Number Publication Date
JPS60199045A true JPS60199045A (en) 1985-10-08
JPH0471942B2 JPH0471942B2 (en) 1992-11-17

Family

ID=12985030

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5495384A Granted JPS60199045A (en) 1984-03-22 1984-03-22 Fluororesin composition

Country Status (1)

Country Link
JP (1) JPS60199045A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0228777A2 (en) * 1985-12-19 1987-07-15 E.I. Du Pont De Nemours And Company Melt extrudable composition of perfluorocarbon polymers
US5393819A (en) * 1994-02-25 1995-02-28 Alphaflex Industries Asphalt modifier
US5418270A (en) * 1994-04-12 1995-05-23 Alphaflex Industries, Inc. Modified thermoplastic elastomeric compositions
US5645603A (en) * 1995-07-25 1997-07-08 Peters; William E. Method of enhancing physical properties of non-elastomeric thermoplastic materials and resulting compositions
WO2002042372A1 (en) * 2000-11-20 2002-05-30 3M Innovative Properties Company Conductive fluoropolymers
GB2444543A (en) * 1987-06-25 2008-06-11 Dassault Electronique Ultrahigh frequency transparent polymeric coating material and shaped products thereof

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4893862A (en) * 1972-03-16 1973-12-04

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4893862A (en) * 1972-03-16 1973-12-04

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0228777A2 (en) * 1985-12-19 1987-07-15 E.I. Du Pont De Nemours And Company Melt extrudable composition of perfluorocarbon polymers
EP0228777A3 (en) * 1985-12-19 1988-11-02 E.I. Du Pont De Nemours And Company Melt extrudable composition of perfluorocarbon polymers
GB2444543A (en) * 1987-06-25 2008-06-11 Dassault Electronique Ultrahigh frequency transparent polymeric coating material and shaped products thereof
GB2444543B (en) * 1987-06-25 2008-11-12 Dassault Electronique Ultrahigh frequency transparent polymeric coating material and shaped products thereof
US5393819A (en) * 1994-02-25 1995-02-28 Alphaflex Industries Asphalt modifier
US5418270A (en) * 1994-04-12 1995-05-23 Alphaflex Industries, Inc. Modified thermoplastic elastomeric compositions
US5645603A (en) * 1995-07-25 1997-07-08 Peters; William E. Method of enhancing physical properties of non-elastomeric thermoplastic materials and resulting compositions
WO2002042372A1 (en) * 2000-11-20 2002-05-30 3M Innovative Properties Company Conductive fluoropolymers
US6533955B1 (en) 2000-11-20 2003-03-18 3M Innovative Properties Company Conductive fluoropolymers
JP2004514757A (en) * 2000-11-20 2004-05-20 スリーエム イノベイティブ プロパティズ カンパニー Conductive fluoropolymer
US6827881B2 (en) 2000-11-20 2004-12-07 3M Innovative Properties Company Conductive fluoropolymers
US7387750B2 (en) 2000-11-20 2008-06-17 3M Innovative Properties Company Conductive fluoropolymers

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