JPH047376A - Coating composition for sliding part - Google Patents

Coating composition for sliding part

Info

Publication number
JPH047376A
JPH047376A JP11128790A JP11128790A JPH047376A JP H047376 A JPH047376 A JP H047376A JP 11128790 A JP11128790 A JP 11128790A JP 11128790 A JP11128790 A JP 11128790A JP H047376 A JPH047376 A JP H047376A
Authority
JP
Japan
Prior art keywords
parts
weight
less
tetrafluoroethylene
coating 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.)
Pending
Application number
JP11128790A
Other languages
Japanese (ja)
Inventor
Yoshiro Oki
芳郎 沖
Yoshibumi Terayama
寺山 義文
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.)
Chukoh Chemical Industries Ltd
NTN Engineering Plastics Corp
Original Assignee
Chukoh Chemical Industries Ltd
NTN Engineering Plastics 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 Chukoh Chemical Industries Ltd, NTN Engineering Plastics Corp filed Critical Chukoh Chemical Industries Ltd
Priority to JP11128790A priority Critical patent/JPH047376A/en
Publication of JPH047376A publication Critical patent/JPH047376A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Paints Or Removers (AREA)

Abstract

PURPOSE:To obtain a coating composition for a sliding part which is improved in low frictional properties and abrasion resistance by compounding a polyphenylene sulfide resin, a polyether sulfone resin, a fluorocarbon polymer and lead fluoride. CONSTITUTION:100 parts, by weight, low molecular weight polyphenylene sulfide resin with an average particle size of 5mum or less is compound with 20-100 parts, by weight, polyether sulfone resin with an average particle size of 10mum or less, 10 to 100 parts, by weight, fluorocarbon polymer with an average particle size of 20mum or less and an average molecular weight of 50,000 or less (e.g. a tetrafluoroethylene-ethylene copolymer) and 20-50 parts, by weight, lead fluoride with an average particle size of 10mum or less.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 この発明は産業機器の摺動部用塗料に用いる摺動部用塗
料組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] This invention relates to a coating composition for sliding parts used as a coating for sliding parts of industrial equipment.

〔従来の技術] 一般に、機械・化学・電気・食品・宇宙・航空産業等の
各産業機器における滑り面、滑り軸受などの摺動部には
、無給油状態でも良好な低摩擦特性、耐摩耗性、耐熱性
を保つように滑り性の良好な摺動部用塗料が用いられて
いる。
[Conventional technology] In general, sliding parts such as sliding surfaces and sliding bearings in industrial equipment in the mechanical, chemical, electrical, food, space, and aviation industries have good low-friction properties and wear resistance even in the unlubricated state. Paints for sliding parts with good slip properties are used to maintain durability and heat resistance.

このような摺動部用塗料には、大別して2つのタイプが
ある。第1のタイプとしては、テトラフルオロエチレン
樹脂(以下、PTFEと略称する)、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
(以下、PFAと略称する)、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(以下、FEPと
略称する)その他のフッ素系重合体をバインダー樹脂と
共に有機溶媒に分散したものである。上記バインダー樹
脂としては、エポキシ樹脂、フェノール樹脂、ポリアミ
ドイミド樹脂またはポリイミド樹脂等がある。このよう
なバインダー樹脂を含んだ第1のタイプは、焼成時にバ
インダー樹脂が表面工ぶルギーの差によって下地側に片
寄るため密着性が良く、また、フッ素系重合体は表層側
に移動してその非粘着性が表層に現れる。このタイプは
、焼成時にフッ素系重合体を溶融する必要がなく、焼成
温度は前記したバインダー樹脂の溶融・硬化温度(18
0〜250°C程度)とすればよいため、加工が容易で
ある。
There are two types of paints for sliding parts. The first type includes tetrafluoroethylene resin (hereinafter abbreviated as PTFE), tetrafluoroethylene/perfluoroalkyl vinyl ether copolymer (hereinafter abbreviated as PFA), and tetrafluoroethylene/hexafluoropropylene copolymer. Another fluoropolymer (hereinafter abbreviated as FEP) is dispersed in an organic solvent together with a binder resin. Examples of the binder resin include epoxy resin, phenol resin, polyamideimide resin, and polyimide resin. The first type, which contains such a binder resin, has good adhesion because the binder resin is biased toward the substrate due to the difference in surface roughness during firing, and the fluoropolymer moves toward the surface layer and is bonded to the substrate. Non-stick properties appear on the surface layer. This type does not require melting of the fluoropolymer during firing, and the firing temperature is the above-mentioned melting/hardening temperature of the binder resin (18
(about 0 to 250°C), processing is easy.

しかし、この第1のタイプの摩擦特性および耐摩耗性は
、たとえば事務用機器などにおける2〜3 kgf/c
4程度の低荷重下での使用には充分耐え得るが、自動車
用摺動部材などにおける10kgf/(−4以上の高荷
重の使用条件では充分とはいえない。また、表層にはバ
インダー樹脂も混在するため、フッ素樹脂本来の優れた
非粘着性は得られなかった。
However, this first type of friction property and wear resistance is limited to 2 to 3 kgf/c in office equipment, etc.
Although it can withstand use under a low load of about 4, it cannot be said to be sufficient for use under a high load of 10 kgf/(-4 or more, such as in sliding parts for automobiles. Also, there is no binder resin on the surface layer. Because of the mixture, the excellent non-stick properties inherent to fluororesins could not be obtained.

このような欠点に対処するものとして、非粘着性に優れ
たポリフェニレンサルファイド樹脂(以下、PPSと略
称する)を用いたものも公知であり(特開昭57−90
043号、特開昭57−90044号)、PTFEと配
合したものも知られている。
To address these drawbacks, a method using polyphenylene sulfide resin (hereinafter abbreviated as PPS), which has excellent non-adhesive properties, is also known (Japanese Patent Laid-Open No. 57-90
No. 043, JP-A No. 57-90044), and those blended with PTFE are also known.

しかし、PPSは、ガラス転移点が約100’Cであり
、耐熱性に劣るものであった。また、PPSとガラス転
移点230°Cのポリエーテルサルファイド樹脂(以下
、PESと略称する)を配合したものも知られているが
、耐熱性は満足し得るものではない。
However, PPS had a glass transition point of about 100'C and was inferior in heat resistance. Also, a mixture of PPS and a polyether sulfide resin (hereinafter abbreviated as PES) having a glass transition point of 230°C is known, but the heat resistance is not satisfactory.

第2のタイプとして、PTFE、PFA、FEPまたは
テトラフルオロエチレン・エチレン共重合体(以下、E
TFEと略称する)を単独または充填剤と共に、前記し
たフッ素系重合体に配合したものがある。この摺動部用
塗料は、下地材である摺動部に密着させるため所定のプ
ライマーを塗布し、フッ素系重合体の溶融を利用して熱
融着して用いる。使用例としては、フライパン、鍋、包
丁またははさみなどのシルバーストーン(デュポン社製
)が揚げられる。
The second type is PTFE, PFA, FEP or tetrafluoroethylene-ethylene copolymer (hereinafter referred to as E
There are products in which TFE (abbreviated as TFE) is blended alone or with a filler into the above-mentioned fluoropolymer. This paint for sliding parts is used by applying a predetermined primer and heat-sealing it using the melting of the fluoropolymer in order to make it adhere to the underlying sliding part. Examples of use include frying pans, pots, knives, or scissors such as Silverstone (manufactured by DuPont).

上記した第2のタイプは、表層でフッ素系重合体がフィ
ルム化するので非粘着性に優れている。
The above-mentioned second type has excellent non-adhesiveness because the fluoropolymer forms a film on the surface layer.

しかし、前記した第1のタイプ以上に耐摩耗性に劣り、
破れ、剥れ等の問題を起こすことから工業用摺動材料と
して用いることができなかった。
However, it is inferior to the above-mentioned first type in wear resistance,
It could not be used as an industrial sliding material because it caused problems such as tearing and peeling.

〔発明が解決しようとする課題〕[Problem to be solved by the invention]

以上のように、フッ素系重合体本来の良好な非粘着性を
表層に有しながら低摩擦性、耐摩耗性に優れた摺動部用
塗料組成物は得られていないという問題点があり、これ
を解決することが課題となっていた。
As mentioned above, there is a problem in that a coating composition for sliding parts that has excellent low friction and wear resistance while having the good non-adhesive properties inherent to fluoropolymer in the surface layer has not been obtained. The challenge was to solve this problem.

〔課題を解決するための手段〕[Means to solve the problem]

上記の課題を解決するために、この発明はポリフェニレ
ンサルファイド樹脂100重量部、ポリエーテルサルフ
ォン樹脂20〜100重量部と、フッ素系重合体10〜
100重量部およびフン他船20〜50重量部を必須成
分とする摺動部用塗料組成物を採用したものである。
In order to solve the above problems, the present invention consists of 100 parts by weight of polyphenylene sulfide resin, 20 to 100 parts by weight of polyether sulfone resin, and 10 to 100 parts by weight of fluoropolymer.
A coating composition for sliding parts containing 100 parts by weight and 20 to 50 parts by weight as essential components is employed.

また、上記のフッ素系重合体はテトラフルオロエチレン
・エチレン共重合体、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、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および
テトラフルオロエチレン重合体からなる群から選ばれる
IN以上の重合体であればよく、上記ポリエーテルサル
フォン樹脂、フッ素系重合体およびフン他船が平均粒径
1101r以下の微粒子であればよい。以下、その詳細
を述べる。
Furthermore, the above fluorine-based polymer is selected from the group consisting of tetrafluoroethylene/ethylene copolymer, tetrafluoroethylene/perfluoroalkyl vinyl ether copolymer, tetrafluoroethylene/hexafluoropropylene copolymer, and tetrafluoroethylene polymer. It is sufficient that the selected polymer has an IN or more, and the polyether sulfone resin, fluoropolymer, and fluoropolymer are fine particles having an average particle diameter of 1101r or less. The details will be described below.

この発明におけるPPSは、特に限定されるものではな
く、主要構造単位として、−数式で示される繰り返し単
位からなるポリマーである。
PPS in this invention is not particularly limited, and is a polymer consisting of a repeating unit represented by the formula - as a main structural unit.

PPSは、吹き付は塗装に際して有機溶剤あるいは水に
均一に分散させて用いるため、平均粒径5n以下の低分
子量のものが好ましい。このような条件を満たす市販の
PPSとしては、米国フィリップスペトロリアム社製ラ
イドンシー1あるいは米国特許第4046749号記載
のPPSオリゴマーが望ましい、しかし、塗装方法とし
て、流動浸漬等のパウダーコーティング法を採用するな
らば直鎖状pps (たとえば呉羽化学工業社製:KS
P)、架橋型PPS (たとえばトーブレン社製:T−
4)も使用し得る。
Since PPS is used after being uniformly dispersed in an organic solvent or water during spray painting, it is preferable to use a low molecular weight one with an average particle size of 5 nm or less. As a commercially available PPS that satisfies these conditions, it is desirable to use Rydon Sea 1 manufactured by Phillips Petroleum in the United States or the PPS oligomer described in U.S. Patent No. 4,046,749. Linear pps (for example, manufactured by Kureha Chemical Industry Co., Ltd.: KS
P), cross-linked PPS (for example, T-
4) may also be used.

また、この発明におけるポリエーテルサルフォン樹yJ
Fj(以下、PESと略称する)は、特に限定されるも
のではなく、主要構造単位とじてで示される繰り返し単
位からなる非品性熱可塑性樹脂である。このようなPE
Sは、平均粒径10趨以下のものが好ましく、冷凍粉砕
などの手法で微粒子化したものを採用し得る。また、そ
の配合割合をP P S 100重量部に対して20〜
100重量部とする理由は、20重量部未満の少量では
形成された塗膜に充分な耐摩耗性が得られず、100重
量部を越える多量では、摺動部下地材との密着強度が弱
まり、耐摩耗性に劣るからである。
Moreover, the polyether sulfone tree yJ in this invention
Fj (hereinafter abbreviated as PES) is not particularly limited, and is a non-grade thermoplastic resin consisting of repeating units shown as main structural units. Such PE
S preferably has an average particle size of 10 or less, and may be made into fine particles by a method such as freezing and pulverization. In addition, the blending ratio is 20 to 100 parts by weight of PPS.
The reason why it is set at 100 parts by weight is that if the amount is less than 20 parts by weight, the formed coating film will not have sufficient wear resistance, and if the amount is more than 100 parts by weight, the adhesion strength with the sliding base material will be weakened. This is because the wear resistance is inferior.

また、この発明におけるフッ素系重合体は、PTFE、
PFA、ETFE、FEPからなる群から選ばれる1種
以上の重合体であればよい。フッ素系重合体は、配合時
の分散性を考慮して、平均分子量5oooo以下が好ま
しく、5000〜30000が特に好ましい。同様に、
平均粒径では、20−以下が好ましく、5〜10−が特
に好ましい。このような条件を満たす市販のフッ素系重
合体としては、次のものが挙げられる。すなわち、PT
FEとして旭硝子社製ルーブリカントL169、ヘキス
ト社製TF9502、セントラル硝子社製セフラルルー
ブ、ETFEとして旭硝子社製アフロンCOP、PFA
として三井デュポン・フロロケミカル社製MPIOなど
である。
Further, the fluoropolymer in this invention includes PTFE,
Any one or more polymers selected from the group consisting of PFA, ETFE, and FEP may be used. The average molecular weight of the fluoropolymer is preferably 5000 or less, particularly preferably 5,000 to 30,000, in consideration of dispersibility during blending. Similarly,
The average particle diameter is preferably 20 or less, particularly preferably 5 to 10. Commercially available fluoropolymers that meet these conditions include the following. That is, P.T.
As FE, Lubricant L169 manufactured by Asahi Glass, TF9502 manufactured by Hoechst, Cepral Lube manufactured by Central Glass, and Aflon COP manufactured by Asahi Glass, PFA as ETFE.
Examples include MPIO manufactured by DuPont Mitsui Fluorochemical Company.

素糸重合体が10重量部未満の少量では充分な非粘着性
および摺動特性が得られず、100重量部を越える多量
では、摺動部下地材との密着強度が弱まり耐摩耗性に劣
るからである。フッ素系重合体の併用例としては、ET
FEとPTFEまたはPFAとPTFEなどが挙げられ
る。
If the amount of thread polymer is less than 10 parts by weight, sufficient non-adhesion and sliding properties cannot be obtained, and if it is more than 100 parts by weight, the adhesion strength with the sliding base material will be weakened and the abrasion resistance will be poor. It is from. Examples of combined use of fluoropolymer include ET
Examples include FE and PTFE or PFA and PTFE.

この発明におけるフッ化鉛は、形成される塗膜表面の平
滑性を保つため、平均粒径Ion以下の一般工業用のも
のを使用し得る。その配合割合は、PP5100重量部
に対して20〜50重量部としている。なぜなら20重
量部未満の少量では塗膜に充分な摺動特性が得られず、
50重蓋部を越える多量では、摺動部下地材との密着強
度が弱まり耐摩耗性に劣るからである。
The lead fluoride used in this invention may be a general industrial type having an average particle size of Ion or less in order to maintain the smoothness of the surface of the coating film formed. The blending ratio is 20 to 50 parts by weight based on 5100 parts by weight of PP. This is because if the amount is less than 20 parts by weight, the coating film will not have sufficient sliding properties.
This is because if the amount exceeds 50 layers, the adhesion strength with the sliding base material will be weakened and the wear resistance will be poor.

なお、この発明の目的を損なわない範囲で、樹脂組成物
に汎用される添加剤類を配合してもよい。
Additionally, commonly used additives may be added to the resin composition within a range that does not impair the purpose of the present invention.

添加剤類の適当な配合割合は、それぞれ比重が異なるた
め体積部でこれを示せば、P P S 100体積部に
対して5〜50体積部が好ましく、15〜35体積部が
特に好ましい0代表的な添加剤類を以下に列挙する。
Since each additive has a different specific gravity, the appropriate blending ratio of the additives is preferably 5 to 50 parts by volume, particularly preferably 15 to 35 parts by volume, based on 100 parts by volume of PPS. Typical additives are listed below.

潤滑剤:グラファイト、二硫化モリブデン、補強剤ニガ
ラス繊維、カーボン繊維、ボロン繊維、炭化ケイ素繊維
、カーボンウィス カー、アスベスト、金属繊維、ロック ウールなど、 難燃剤:酸化アンチモン、炭酸マグネシウム、炭酸カル
シウムなど、 電気特性向上剤:クレー、マイカなど、熱伝導度向上剤
二鉄、亜鉛、アルミニウム、銅その他の金属化合物 その他の充填材ニガラスビーズ、ガラス球、アルミナ、
タルク、ケイソウ土、 水和アルミナ、シラスバルー ン、酸化亜鉛、酸化チタン、 その他金属酸化物で500°C以 上で安定な天然若しくは合成 の化合物、 以上の材料を配合した組成物を製造するには、水または
有機溶剤へ分散させ、磁性ボール等によって粉砕し、均
質に混合する。このようにして得られた摺動部用塗料組
成物は、スプレー塗装、流動浸漬、静!塗装等によって
塗装する。
Lubricant: graphite, molybdenum disulfide, reinforcing agent Niglass fiber, carbon fiber, boron fiber, silicon carbide fiber, carbon whisker, asbestos, metal fiber, rock wool, etc. Flame retardant: antimony oxide, magnesium carbonate, calcium carbonate, etc., electricity Characteristic improvers: clay, mica, etc., thermal conductivity improvers, diiron, zinc, aluminum, copper and other metal compounds, other fillers, glass beads, glass spheres, alumina,
To produce a composition containing talc, diatomaceous earth, hydrated alumina, shirasu balloon, zinc oxide, titanium oxide, and other metal oxides, natural or synthetic compounds that are stable at temperatures above 500°C, Disperse in water or organic solvent, pulverize with a magnetic ball, etc., and mix homogeneously. The thus obtained coating composition for sliding parts can be used for spray coating, fluid dipping, and static coating. Paint by painting, etc.

〔作用〕[Effect]

以上述べたように、この発明の摺動部用塗料組成物は、
必須成分としてPPS、PES、フッ素系重合体および
フッ化鉛をそれぞれ所定の割合で併用することにより、
フッ素系重合体の非粘着性を表層に有して低摩擦性であ
り、かつ耐摩耗性に優れた塗膜を形成する。
As described above, the coating composition for sliding parts of the present invention is
By using PPS, PES, fluoropolymer, and lead fluoride as essential components in the prescribed proportions,
The surface layer has the non-adhesive properties of a fluoropolymer to form a coating film with low friction and excellent abrasion resistance.

〔実施例] 実施例および比較例1〜4に用いた諸原料を一括して示
すと以下の通りである。
[Example] The raw materials used in Examples and Comparative Examples 1 to 4 are listed below.

■PPS (米国フィリップス社製1−1)■ETFE
 (旭硝子社製ニアフロンcop )■PFA(三井・
デュポンフロロケミカル社製:テフロンPF^門P−1
0) ■FEP (三井・デュポンフロロケミカル社製:テフ
ロン100) ■PTFE (ヘキスト社製: TF9205)■ポリ
エーテルサルフォン樹脂(IC1社製:vICTREX
5003P )  (P E S )■フッ化鉛(一般
試薬) ■グラファイト(日本黒鉛社製:ACP)■界面活性剤
(ローム&ハス社製ニドライドンX100)[相]プロ
ピレングリコール(一般試薬)実施例1〜4: 前記した有機粉体、無機充填側、界面活性剤および溶剤
を第1表に示す組成で一括して仕込み、第 表 塗料化した。すなわち、PPSを250gとして、各実
施例の組成の全量を1.5リツトルの容器に入れ、多数
の磁性ポール(直径205m+または25ma+のもの
をそれぞれ0.54 kgずつ)を混在させて、回転数
8Orpmで80時間、この磁性ボールを回転して組成
物を粉砕、混合した。
■PPS (1-1 manufactured by Philips, USA) ■ETFE
(Near Floon cop manufactured by Asahi Glass Co., Ltd.) ■PFA (Mitsui,
Manufactured by DuPont Fluorochemical Company: Teflon PF^mon P-1
0) ■FEP (manufactured by Mitsui DuPont Fluorochemical Company: Teflon 100) ■PTFE (manufactured by Hoechst Company: TF9205) ■Polyether sulfone resin (manufactured by IC1 Company: vICTREX)
5003P ) (P E S ) ■Lead fluoride (general reagent) ■Graphite (manufactured by Nippon Graphite Co., Ltd.: ACP) ■Surfactant (manufactured by Rohm & Hass Co., Ltd.: Nidrydon X100) [Phase] Propylene glycol (general reagent) Example 1 ~4: The above-mentioned organic powder, inorganic filler, surfactant, and solvent were added together in the composition shown in Table 1 to form a paint shown in Table 1. That is, assuming that PPS is 250 g, the entire amount of the composition of each example is placed in a 1.5 liter container, a large number of magnetic poles (205 m+ diameter or 25 ma+ diameter, 0.54 kg each) are mixed, and the rotation speed is adjusted. The composition was ground and mixed by rotating the magnetic ball at 8 rpm for 80 hours.

なお、第1表中の組成比は、PP5100重量部に対す
る重量部で示した。
The composition ratios in Table 1 are expressed in parts by weight based on 5100 parts by weight of PP.

得られた塗料をスプレーガンでリング状の外径33閣、
内径6m、長さ6mの5UJ2プレートに吹き付け、3
70°Cで45分間焼付けて平滑な塗膜を得た。この塗
膜に対して*S摩耗特性、密着性、表面硬度、非粘着性
および耐熱性を以下の方法で調べ、得られた結果を第2
表にまとめて示した。
Spray the resulting paint into a ring shape with an outer diameter of 33 mm.
Spray on a 5UJ2 plate with an inner diameter of 6m and a length of 6m, 3
A smooth coating was obtained by baking at 70°C for 45 minutes. The *S wear characteristics, adhesion, surface hardness, non-adhesiveness, and heat resistance of this coating film were investigated using the following methods, and the obtained results were used in the second test.
They are summarized in the table.

(1)摩擦試験 相手材として5UJ2の内径17■、外径21+m+、
長さ10■のリング試片を採用し、滑り速度12.0m
/分、面圧5.Okgf/cdの条件でスラスト型開S
試験機を用い動摩擦係数を測定した。
(1) Friction test partner material: 5UJ2 inner diameter 17cm, outer diameter 21+m+,
A ring specimen with a length of 10cm is used, and the sliding speed is 12.0m.
/min, surface pressure 5. Thrust type open S under Okgf/cd conditions
The coefficient of dynamic friction was measured using a testing machine.

(2)摩耗試験 相手材として5UJ2の内径17m、外径21aw、長
さ10mnのリング試片を採用し、滑り速度1.0m/
分、面圧30.okgf/cdの条件でスラスト型摩擦
試験機を用い50時間後の摩耗量(■)を測定した。
(2) A 5UJ2 ring specimen with an inner diameter of 17 m, an outer diameter of 21 aw, and a length of 10 mm was used as the wear test partner material, and the sliding speed was 1.0 m/
min, surface pressure 30. The amount of wear (■) after 50 hours was measured using a thrust type friction tester under the condition of okgf/cd.

(3)密着性試験 塗膜に1m11角の基盤目状のクロスカットを10列I
O行形成し、感圧接着テープを用いて剥がれ強度試験を
行なった。その評価は、たとえばクロスカットの100
目中a目剥がれた場合、(100−a)/100と表示
して評価した。
(3) Adhesion test Make 10 rows of 1m11 square cross-cuts on the coating film.
A peel strength test was conducted using a pressure-sensitive adhesive tape. For example, the evaluation is 100 for crosscut.
When the a-eye peeled off, it was evaluated by displaying it as (100-a)/100.

(4)−表面硬度試験 鉛筆硬度試験機を用いて、荷重500gでの塗膜引っか
き痕の発生を鉛筆硬度で評価した。
(4) - Surface hardness test Using a pencil hardness tester, the occurrence of paint film scratch marks at a load of 500 g was evaluated by pencil hardness.

(5)非粘着性試験 塗膜表面に水を滴下した際、両者の境界の接触角を接触
角測定器で測定した。
(5) Non-adhesion test When water was dropped onto the surface of the coating film, the contact angle at the boundary between the two was measured using a contact angle measuring device.

比較例1〜4: 前記した有機粉体、無機充填側、界面活性剤および溶剤
を第1表に示す組成で一括して仕込み、実施例1〜4と
全く同様の手法で塗料および塗膜を得た。さらに、実施
例と比較するため、前記した試験(1)〜(6)を行な
い、この結果を第2表中に併記した。
Comparative Examples 1 to 4: The above-mentioned organic powder, inorganic filler, surfactant, and solvent were charged at once in the composition shown in Table 1, and paints and coatings were formed in exactly the same manner as in Examples 1 to 4. Obtained. Furthermore, for comparison with Examples, the above-mentioned tests (1) to (6) were conducted, and the results are also listed in Table 2.

比較例5: PTFE系熱融着熱融着タイプA社製プライマーaをス
プレーガンで外径33mm、内径6IfiI11、長さ
6rImのSUJ 2プレートに吹き付け、100°C
で10分間乾燥し、その上に同社製のプライマーbを別
途同様に吹き付け、100℃で10分間乾燥した。さら
にトップコートとしてPTFE系ディスバージョンを吹
き付け、370°Cで45分間焼付けた。
Comparative Example 5: PTFE heat fusion heat fusion type Primer a manufactured by Company A was sprayed onto a SUJ 2 plate with an outer diameter of 33 mm, an inner diameter of 6 IfiI11, and a length of 6 rIm at 100°C.
Primer b manufactured by the same company was separately sprayed thereon in the same manner, and dried at 100° C. for 10 minutes. Furthermore, a PTFE dispersion was sprayed as a top coat and baked at 370°C for 45 minutes.

比較例6: PFA系熱融熱融着タイプ販B社製プライマーをスプレ
ーガンで外径33s1内径6IIIIl11長さ6wn
のSUJ 2プレートに吹き付け、100°Cで10分
間乾燥し、その上にトップコートとしてPFA系ディス
バージョンを吹き付け、350″Cで30分間焼付けた
Comparative Example 6: Using a spray gun, use a spray gun to apply a PFA-based thermal fusion type primer manufactured by Sales Company B with an outer diameter of 33s1 an inner diameter of 6IIIl11 and a length of 6wn.
It was sprayed onto a SUJ 2 plate, dried at 100°C for 10 minutes, and then a PFA-based dispersion was sprayed on top as a top coat, and baked at 350″C for 30 minutes.

比較例7: ポリアミドイミドとPTFEとからなるエナメルタイプ
の市販C社製塗料をスプレーガンで外径33諭、内径6
m、長さ6WのSUJ 2に吹き付け、100°Cで1
0分間乾燥し、さらに230°Cで45分間焼付けた。
Comparative Example 7: An enamel-type commercially available paint manufactured by Company C made of polyamideimide and PTFE was sprayed with an outer diameter of 33 mm and an inner diameter of 6 mm.
m, length 6W, sprayed on SUJ 2, 1 at 100°C.
It was dried for 0 minutes and then baked at 230°C for 45 minutes.

比較例5〜7で得られた塗膜に対して、前記試験(1)
〜(6)を行ない、得られた結果を第2表中に併記した
The above test (1) was applied to the coating films obtained in Comparative Examples 5 to 7.
- (6) were carried out, and the obtained results are also listed in Table 2.

第2表からも明らかなように、PPS、PES、フッ素
系重合体およびフッ化鉛からなる実施例1〜4は、動摩
擦係数が0.150〜0.180と低く、また、接触角
は110度と大きく、フッ素重合体本来の非粘着性が表
層に充分現われると共に、摩耗量も0.7■以下となり
、耐摩耗性にもきわめて優れた性質を示した。このよう
な特性は、PTEFとETFEを併用した実施例2で特
に顕著であった。
As is clear from Table 2, Examples 1 to 4 made of PPS, PES, fluoropolymer, and lead fluoride had a low dynamic friction coefficient of 0.150 to 0.180, and a contact angle of 110. The non-adhesive nature of the fluoropolymer was sufficiently exhibited on the surface layer, and the amount of wear was less than 0.7 cm, showing extremely excellent abrasion resistance. Such characteristics were particularly remarkable in Example 2 in which PTEF and ETFE were used together.

しかし、PPSにPESのみを40重量部配合した比較
例1.PTEFを30重量部配合した比較例2、PTE
Fを30重量部とフッ化鉛30重量部とを配合した比較
例3およびPTEFを30重量部とPESを40重量部
とを配合した比較例4は、実施例1〜4に比較して耐摩
耗性に劣っており、とくに、比較例1は、非粘着性にも
劣るものであった。また、PTFE系の熱融着タイプで
ある比較例5およびPFA系タイプである比較例6は、
非粘着性に優れるが、いずれも耐摩耗性および表面硬度
に劣り、摩耗量試験開始後、約1時間で下地が露出した
。バインダー樹脂とPTFE混合のエナメルタイプであ
る比較例7は、摩擦係数が高く、耐摩耗性および非粘着
性に劣るものであった。
However, Comparative Example 1 in which only 40 parts by weight of PES was blended with PPS. Comparative example 2 containing 30 parts by weight of PTEF, PTE
Comparative Example 3, which blended 30 parts by weight of F and 30 parts by weight of lead fluoride, and Comparative Example 4, which blended 30 parts by weight of PTEF and 40 parts by weight of PES, had better durability than Examples 1 to 4. The abrasion properties were poor, and in particular, Comparative Example 1 was also poor in non-adhesion properties. In addition, Comparative Example 5, which is a PTFE-based heat-sealing type, and Comparative Example 6, which is a PFA-based type,
Although they were excellent in non-adhesion, they were both inferior in abrasion resistance and surface hardness, and the base was exposed about 1 hour after the start of the abrasion loss test. Comparative Example 7, which was an enamel type in which binder resin and PTFE were mixed, had a high friction coefficient and was inferior in abrasion resistance and non-adhesion.

〔効果〕〔effect〕

この発明の摺動部用塗料組成物は、以上説明したように
、フッ素系重合体本来の非粘着性を表層に有すると共に
、低摩擦性でありかつ耐摩耗性に優れる塗膜を得ること
ができ、従来の塗料組成物に比べてはるかに優れた特性
を示すものであって、工業用摺動部用塗料として好適な
ものである。したがって、この発明の意義は、きわめて
大きいといえる。
As explained above, the coating composition for sliding parts of the present invention has the non-adhesive property inherent to the fluoropolymer in the surface layer, and is capable of producing a coating film that has low friction and excellent wear resistance. It exhibits far superior properties compared to conventional coating compositions, and is suitable as a coating for industrial sliding parts. Therefore, it can be said that the significance of this invention is extremely large.

Claims (3)

【特許請求の範囲】[Claims] (1)ポリフェニレンサルファイド樹脂100重量部、
ポリエーテルサルフォン樹脂20〜100重量部と、フ
ッ素系重合体10〜100重量部およびフッ化鉛20〜
50重量部を必須成分とする摺動部用塗料組成物。
(1) 100 parts by weight of polyphenylene sulfide resin,
20 to 100 parts by weight of polyether sulfone resin, 10 to 100 parts by weight of fluoropolymer, and 20 to 100 parts by weight of lead fluoride
A coating composition for sliding parts containing 50 parts by weight as an essential component.
(2)フッ素系重合体がテトラフルオロエチレン・エチ
レン共重合体、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、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およびテトラ
フルオロエチレン重合体からなる群から選ばれる1種以
上の重合体である請求項1記載の摺動部用塗料組成物。
(2) The fluoropolymer is selected from the group consisting of tetrafluoroethylene/ethylene copolymer, tetrafluoroethylene/perfluoroalkyl vinyl ether copolymer, tetrafluoroethylene/hexafluoropropylene copolymer, and tetrafluoroethylene polymer The coating composition for sliding parts according to claim 1, which is one or more kinds of polymers.
(3)ポリエーテルサルフォン樹脂、フッ素系重合体お
よびフッ化鉛が平均粒径10μm以下の微粒子である請
求項1記載の摺動部用塗料組成物。
(3) The coating composition for sliding parts according to claim 1, wherein the polyether sulfone resin, the fluorine-based polymer, and the lead fluoride are fine particles with an average particle size of 10 μm or less.
JP11128790A 1990-04-25 1990-04-25 Coating composition for sliding part Pending JPH047376A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11128790A JPH047376A (en) 1990-04-25 1990-04-25 Coating composition for sliding part

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11128790A JPH047376A (en) 1990-04-25 1990-04-25 Coating composition for sliding part

Publications (1)

Publication Number Publication Date
JPH047376A true JPH047376A (en) 1992-01-10

Family

ID=14557403

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11128790A Pending JPH047376A (en) 1990-04-25 1990-04-25 Coating composition for sliding part

Country Status (1)

Country Link
JP (1) JPH047376A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4961660A (en) * 1987-12-28 1990-10-09 Sharp Kabushiki Kaisha Method for correcting mistypes in an electric typewriter
JP2000081081A (en) * 1998-06-26 2000-03-21 Bridgestone Corp Slider
JP2001055478A (en) * 1999-08-19 2001-02-27 E I Du Pont De Nemours & Co Polytetrafluoroethylene composition having low melt viscosity
JP2002322432A (en) * 2001-02-26 2002-11-08 Daikin Ind Ltd Non-sticky abrasion-resistant coating composition and non-sticky abrasion-resistant coated article
WO2020241121A1 (en) * 2019-05-31 2020-12-03 ダイキン工業株式会社 Primer for ethylene/tetrafluoroethylene copolymer coating materials

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4961660A (en) * 1987-12-28 1990-10-09 Sharp Kabushiki Kaisha Method for correcting mistypes in an electric typewriter
JP2000081081A (en) * 1998-06-26 2000-03-21 Bridgestone Corp Slider
JP2001055478A (en) * 1999-08-19 2001-02-27 E I Du Pont De Nemours & Co Polytetrafluoroethylene composition having low melt viscosity
JP2002322432A (en) * 2001-02-26 2002-11-08 Daikin Ind Ltd Non-sticky abrasion-resistant coating composition and non-sticky abrasion-resistant coated article
WO2020241121A1 (en) * 2019-05-31 2020-12-03 ダイキン工業株式会社 Primer for ethylene/tetrafluoroethylene copolymer coating materials
JP2020196865A (en) * 2019-05-31 2020-12-10 ダイキン工業株式会社 Primer for ethylene/tetrafluoroethylene copolymer coating
CN113891766A (en) * 2019-05-31 2022-01-04 大金工业株式会社 Primer for ethylene/tetrafluoroethylene copolymer coating
CN113891766B (en) * 2019-05-31 2022-12-06 大金工业株式会社 Primer for ethylene/tetrafluoroethylene copolymer paint

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