JPS5830343B2 - abrasion resistant paint - Google Patents
abrasion resistant paintInfo
- Publication number
- JPS5830343B2 JPS5830343B2 JP14833379A JP14833379A JPS5830343B2 JP S5830343 B2 JPS5830343 B2 JP S5830343B2 JP 14833379 A JP14833379 A JP 14833379A JP 14833379 A JP14833379 A JP 14833379A JP S5830343 B2 JPS5830343 B2 JP S5830343B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- weight
- abrasion
- mixed
- thermosetting
- 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.)
- Expired
Links
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- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
- Lubricants (AREA)
Description
【発明の詳細な説明】
本発明は耐熱性で溶融性のあるパーフルオロアルコキシ
基を有するポリテトラフルオロエチレン樹脂(以下P、
F、A、と称する)、或はP、F、A、にポリテトラフ
ルオロエチレン樹脂(以下
P、T、F、E、と相する)を混入した樹脂に固体潤滑
剤と耐熱性及び付着性を有する熱硬化性樹脂を混合し、
金属またはセラミックス及び一般に固体のすべり面周の
耐磨耗性塗料に関する。Detailed Description of the Invention The present invention relates to heat-resistant and meltable polytetrafluoroethylene resin (hereinafter referred to as P) having a perfluoroalkoxy group.
(hereinafter referred to as F, A), or P, F, A mixed with polytetrafluoroethylene resin (hereinafter referred to as P, T, F, E), solid lubricant, heat resistance and adhesion. Mix a thermosetting resin with
Concerning abrasion-resistant coatings around sliding surfaces of metals or ceramics and generally solids.
固体の摺動部分のすべり面では摩擦損失が少なく、さら
に磨耗量が少ないことが要求される。The sliding surfaces of solid sliding parts are required to have low friction loss and low wear.
このため従来から各種の潤滑材料が用いられている。For this reason, various lubricating materials have conventionally been used.
これらの潤滑材料は大別すると次のように分類される。These lubricating materials can be broadly classified as follows.
(1) (a) 石油原油、シエール油及び石炭の
低温乾溜タールから精製される砿物油
(b) 動物油あるいは植物油などの脂肪油(e)
上記(a)と(b)との合成油としてグリースなどの
混合油
(2)低温用としてのシリコーン油、耐熱性、耐薬品性
のよいふっ素泊
(3J MoS2、石墨、金属酸化物を水又は油、グ
リースに分散させた固体潤滑剤
(4)鍍金、溶射、蒸着などによる表面硬化処理(5)
プラスチック製品化
(6)プラスチックコーティング
上記の分類を簡単に説明する。(1) (a) Crude oil refined from petroleum crude oil, sierre oil, and low-temperature dry-distilled tar of coal (b) Fatty oils such as animal or vegetable oils (e)
Mixed oil such as grease as a synthetic oil of the above (a) and (b) (2) Silicone oil for low temperature use, fluorine oxide with good heat resistance and chemical resistance (3J MoS2, graphite, metal oxides, etc.) in water or Solid lubricant dispersed in oil or grease (4) Surface hardening treatment by plating, thermal spraying, vapor deposition, etc. (5)
Plastic products (6) Plastic coatings The above classifications will be briefly explained.
(1)は耐食性、耐熱性、耐寒性に難点があるとともに
焼付などを発生し、従って一定のすべり面を保つことが
困難である。(1) has disadvantages in corrosion resistance, heat resistance, and cold resistance, and also causes seizure, making it difficult to maintain a constant sliding surface.
(2)のシリコーン油は油性、ふっ素泊は粘度特性が劣
る。The silicone oil (2) is oily, and the fluorine oil has poor viscosity characteristics.
(37は耐熱性は良いが高温で粉末となり、飛散する。(Although 37 has good heat resistance, it turns into powder at high temperatures and scatters.
(1)、(2)、(3)のいずれもすべり面の環境汚染
が大きい。All of (1), (2), and (3) cause significant environmental pollution on the sliding surface.
(4)の処理を受けた部分の耐磨耗性は向上するが、相
手材料の磨耗やきすの発生が多(、嵌合精度が悪くなり
易く、かつこの処理のみでは摩擦抵抗が大きいの貰1)
又は(2)の併用が必要となる。Although the abrasion resistance of the part treated in (4) improves, the mating material often wears out and scratches occur (and the fitting accuracy tends to deteriorate, and this treatment alone causes high frictional resistance). 1)
Or, combination of (2) is required.
(5)の方法は汎用部品に多く採用されて来ているが、
金属製に比較しては機械的強度、寸法安定性が劣り、か
つ熱の放散が悪いので、精度の高い機械部品や苛酷な環
境下の使用はできない。Method (5) has been widely adopted for general-purpose parts, but
Compared to metal, it has inferior mechanical strength and dimensional stability, and has poor heat dissipation, so it cannot be used as highly precise mechanical parts or in harsh environments.
(6)の方法は金属やセラミックス、一般に固体の表面
に加工するので、機械的強度や寸法安定性の信頼度が高
(、加えて熱の放散は(5)よりもはるかによ(、また
加工材料も少量ですむ。Since method (6) processes the surface of metals, ceramics, and generally solids, it has high reliability in mechanical strength and dimensional stability (and, in addition, heat dissipation is much better than (5)). Only a small amount of processing material is required.
ことに(1)、(2)、(3)、(4)ではいづれも給
油機構を設けねばならず、その給油機構の保守管理は容
易でなく、また使用する潤滑剤の飛散による環境汚染、
すなわち機器各部の汚染、さらには公害問題が発生する
。In particular, (1), (2), (3), and (4) all require a lubricating mechanism, which is difficult to maintain and manage, and the lubricant used may scatter, causing environmental pollution.
In other words, contamination of various parts of the equipment and further pollution problems occur.
また(5)には前記のように機械的強度や寸法精度に難
点がある。Furthermore, as mentioned above, (5) has drawbacks in mechanical strength and dimensional accuracy.
しかるに(6)の方法では無給油潤滑であるので前記の
諸問題の発生もなく、また機械的強度や寸法精度は保持
出来るので従来から各種の材料で検討され、P、T、F
、E、は最も優れているとされて来ていた。However, since method (6) uses oil-free lubrication, the above-mentioned problems do not occur, and mechanical strength and dimensional accuracy can be maintained, so it has been studied for various materials, and P, T, F
, E, has been considered to be the best.
しかしP、T、F、E、の塗料は加工性が悪く、更に機
械的強度が劣り、気孔の発生と傷が入りやすく、また耐
磨耗性が低い欠点があった。However, the P, T, F, and E paints had disadvantages such as poor workability, poor mechanical strength, easy formation of pores and scratches, and low abrasion resistance.
本発明は前記の(3Jと(6)との組合せを考え、付着
性の良い熱硬化性樹脂に固体潤滑剤を分散させ、これに
塗膜形成材としてP、F、 A、或はP、F、A、にP
、T、F、E、を加えて、耐熱性を持ち、かつ低磨耗性
のすべり面周耐磨耗塗料である。The present invention considers the combination of (3J and (6)) above, and disperses a solid lubricant in a thermosetting resin with good adhesion, and adds P, F, A, or P as a coating film forming material to this. F, A, niP
, T, F, and E, it is a heat-resistant and low-wear coating around the sliding surface.
P、T、F、E、の構造式は で示される。The structural formulas of P, T, F, and E are It is indicated by.
但Cは炭素、Fはふっ素、nは個数を示す。However, C is carbon, F is fluorine, and n is the number.
この主鎖の一つにパーフルオロアルコキシ基が結合した
ものがP、F、A、であり、その構で示される。Those in which a perfluoroalkoxy group is bonded to one of the main chains are P, F, and A, and are represented by the structure.
但Rfはフルオロアルキル基で、0−Rfはパーフルオ
ロアルコキシ基である。However, Rf is a fluoroalkyl group, and 0-Rf is a perfluoroalkoxy group.
P、F、A、は溶融加工ができるP、T、F、E、とよ
ばれ非粘着性で、融点は302℃内至310℃、引張り
強さは100℃にて238 kg/crrxであり、し
かも連続使用温度260℃にて変化しないことが公知技
術として知られている。P, F, and A are called P, T, F, and E, which can be melt-processed and are non-adhesive, with a melting point of 302°C to 310°C and a tensile strength of 238 kg/crrx at 100°C. Moreover, it is known as a known technique that it does not change at a continuous use temperature of 260°C.
またP、F、A。は化学的に安定で、通常の酸、アルカ
リ、酸化環元剤、ハロゲンや溶剤によってほとんど変化
せず、また耐熱性がすぐれていることも公知技術である
。Also P, F, A. It is a well-known technology that it is chemically stable, almost unaltered by ordinary acids, alkalis, oxidized ring-forming agents, halogens and solvents, and has excellent heat resistance.
しかるにP、F、Aは前記の通り非粘着性であるため被
塗装物への接着性が悪い欠点を持っている。However, since P, F, and A are non-adhesive as described above, they have the disadvantage of poor adhesion to objects to be coated.
本発明は前記の欠点を除去するために、耐磨耗性は劣る
が付着性にすぐれている熱硬化性樹脂を混合し、更に固
体潤滑剤を前記熱硬化性樹脂に予め分散して置くことに
よって得られる混合塗料を塗布し、焼付加工して焼付塗
膜を得ることによって、摩擦係数は少さく、耐熱性、耐
薬品性にすぐれたP、F、A、並びに分散内蔵している
固体潤滑剤を接着性のよい熱硬化性樹脂の三次元構造に
より被塗装物に密着させるものである。In order to eliminate the above-mentioned drawbacks, the present invention mixes a thermosetting resin with poor abrasion resistance but excellent adhesion, and further disperses a solid lubricant in the thermosetting resin in advance. By applying the mixed paint obtained by and baking to obtain a baked coating film, P, F, A, which has a low coefficient of friction and excellent heat resistance and chemical resistance, as well as solid lubricant with built-in dispersion. The adhesive is brought into close contact with the object to be coated using the three-dimensional structure of thermosetting resin with good adhesive properties.
すなわち本発明の塗膜は熱硬化性樹脂を混合したために
P、F、A、単体の塗膜よりは幾分劣るが、機械的強度
が劣り、傷の発生し易い欠点を有するP、 T、 F、
E、や他の潤滑剤に比べて耐磨耗性能はいちぢるしく
向上し、加えて相手摺動面に傷や損傷を与えないという
使用に際して有利、重要な特徴を有するもみでなく、密
着性のよい特徴を有するものである。That is, since the coating film of the present invention is mixed with a thermosetting resin, it is somewhat inferior to P, F, A, and P, T, which have the drawbacks of poor mechanical strength and being easily scratched. F,
Compared to E and other lubricants, its wear resistance is significantly improved, and it also has the advantageous and important feature of not causing scratches or damage to the mating sliding surface. It has good sexual characteristics.
塗膜の形成には(1)P、F、A、を有機分散剤又は水
に溶解あるいは分散させる。To form a coating film, (1) P, F, and A are dissolved or dispersed in an organic dispersant or water.
(2)熱硬化性樹脂の溶液又は粉末のみ又は更に固体潤
滑剤の粉末を別の有機分散剤又は水に溶解あるいは分散
させる。(2) Dissolving or dispersing only the thermosetting resin solution or powder or the solid lubricant powder in another organic dispersant or water.
(1)と(2)を適当な割合で混合すれば塗膜原料が得
られる。A coating film raw material can be obtained by mixing (1) and (2) in an appropriate ratio.
P、F、A、 と熱硬化性樹脂及び固体潤滑剤がいづれ
も粉末の場合にはトライブレンド法により混合物を得て
塗膜原料とする。When P, F, A, the thermosetting resin, and the solid lubricant are all powders, a mixture is obtained by the triblend method and used as a raw material for the coating film.
混合には攪拌混合法、タンブラ混合法、シェーキング混
合法、超音波混合法、ボールミル混合法、ローラーミル
混合法のいづれを使用してもよいがP、F、A、の粒形
を傷つげないようにする。Any of the stirring mixing method, tumbler mixing method, shaking mixing method, ultrasonic mixing method, ball mill mixing method, and roller mill mixing method may be used for mixing, but the particle shape of P, F, and A may be damaged. Make sure not to.
また使用する溶剤、分散剤は熱硬化性樹脂の種類により
主として決定するが分散性、塗装性、皮膜形成能から最
終的決定をする。The solvent and dispersant to be used are mainly determined by the type of thermosetting resin, but the final decision is made based on dispersibility, coating properties, and film-forming ability.
被塗装物は焼付温度附近で劣化しないものであれば各種
金属、ガラス、陶磁器を含むセラミックス類、耐熱性プ
ラスチックスのように固体であれば形状、寸法にかかわ
らず塗装可能である。As long as the object to be painted does not deteriorate near the baking temperature, it can be painted regardless of its shape or size, as long as it is solid such as various metals, glass, ceramics including ceramics, and heat-resistant plastics.
ただ被塗装材の表面は塗装前に十分に洗浄しなげればな
らない。However, the surface of the material to be painted must be thoroughly cleaned before painting.
洗浄には溶剤、酸、アルカリ、洗剤を用いた浸漬、シャ
ワー、バブリング、超音波洗浄、その他一般の洗浄法で
行なう。Cleaning is performed by dipping, showering, bubbling, ultrasonic cleaning, and other general cleaning methods using solvents, acids, alkalis, and detergents.
その後更に塗膜と被塗装物との接着性を高めるために次
の処理をすることもある。After that, the following treatment may be performed to further improve the adhesion between the coating film and the object to be coated.
すなわち、サンドブラスト、ショツトブラスト、グリッ
ドブラスト、ホーニング、ペーパースクラッチ、ワイヤ
ースクラッチ、ヘアーライン処理、金属又はセラミック
スの溶射、アルマイト処理、ベーマスト処理、クラック
メッキ処理、化学エツチング、化成皮膜処理を加える。That is, sandblasting, shotblasting, gridblasting, honing, paper scratching, wire scratching, hairline treatment, thermal spraying of metal or ceramics, alumite treatment, bee mast treatment, crack plating treatment, chemical etching, and chemical conversion coating treatment are added.
塗装方法としては次の2種が主なるものである。There are two main types of coating methods:
溶解又は分散させた場合には刷毛塗り、浸漬、エヤース
プレー、静電スプレー、ヘラ塗り、ローラーコTト、カ
ーテンコート、遠心力を利用したスピンコード、電気泳
動塗装を塗装方法とし、又P、F、A、 と熱硬化性
樹脂及び固体潤滑剤のそれぞれの粉末混合の場合には粉
末スプレー、静電スプレー、流動浸漬、静電流動浸漬、
プロバック、加圧成形を塗装方法とする。When dissolved or dispersed, coating methods include brush coating, dipping, air spraying, electrostatic spraying, spatula coating, roller coating, curtain coating, spin cord using centrifugal force, electrophoresis coating, and P, F , A, and a thermosetting resin and a solid lubricant, respectively, by powder spraying, electrostatic spraying, fluidized dipping, electrostatic dynamic dipping,
The coating method is Provac and pressure molding.
上記のように塗装した後、乾燥すればP、F、A。After painting as above and drying, it becomes P, F, A.
と熱硬化性樹脂及び固体潤滑剤の固形分のみかのこる。and the solid content of thermosetting resin and solid lubricant.
この段階で更に重ね塗りをして必要な膜厚とすることも
できる。At this stage, additional coatings may be applied to obtain the required film thickness.
本発明では一度塗りで150μmまでの塗膜形成が可能
である特徴を有する。The present invention has a feature that it is possible to form a coating film of up to 150 μm in one coat.
乾燥温度は溶剤の種類によって決定されるが粉末塗装の
場合には塗装後直ちに焼付処理が可能である。The drying temperature is determined by the type of solvent, but in the case of powder coating, baking treatment can be performed immediately after coating.
焼付温度はP、F、A、の融点近くで320℃内至38
0℃が適当しており、これより高温にて行なうと耐磨耗
性が低下する。The baking temperature is close to the melting point of P, F, A, within 320℃ to 38℃.
A temperature of 0°C is suitable; if the temperature is higher than this, the abrasion resistance will decrease.
焼付処理後放冷し、そのまま使用するか、または研磨、
切削加工、プレス処理を行なって、寸法精度や表面荒ら
さを所定のものとする。After baking, let it cool and use it as is, or polish it,
Cutting and pressing are performed to achieve the specified dimensional accuracy and surface roughness.
耐磨耗試験は銘木松原式磨耗試験法を用い、無給油状態
でのスライド磨耗係数を下記の条件にて測定した。The abrasion resistance test was carried out using the Matsubara type abrasion test method, and the slide abrasion coefficient without oil was measured under the following conditions.
試験片は40mmX 40imX 2mmのアルミニウ
ム板を用い、負荷−10kgycrA、すべり速度−3
0m/winの条件で、相手材はステンレスのSUS
304を使用し、試験片の表面をトリクロールエチレン
にて脱脂し、表面に各種類の塗膜を形成したものを試験
した。The test piece was a 40 mm x 40 im x 2 mm aluminum plate, with a load of -10 kgycrA and a sliding speed of -3.
Under the condition of 0m/win, the mating material is stainless steel SUS
304, the surface of the test piece was degreased with trichlorethylene, and various types of coating films were formed on the surface.
以下図面の中の数値は上記の耐磨耗試験による耐磨耗係
数である。The numerical values in the drawings below are the abrasion resistance coefficients determined by the above abrasion resistance test.
上記摺動条件にて従来は磨耗係数がlOO×100−1
OcrlA・m以下であれば摺動材料として使用可能と
され、現在市販されている有機高分子系摺動材料の磨耗
係数は100 X 10−10cnv’に9−m前後の
ものが多く最もすぐれているとされている上記(6)の
プラスチックコーテングの場合でも40〜70 X 1
0−10i/kg、 mのものがあるのみである。Under the above sliding conditions, the conventional wear coefficient was lOO x 100-1
If it is less than OcrlA・m, it can be used as a sliding material, and the wear coefficient of the organic polymer sliding materials currently on the market is 100 x 10-10 cnv', which is often around 9-m. Even in the case of the plastic coating mentioned in (6) above, which is said to be 40 to 70 x 1
There are only 0-10i/kg and m.
本発明の塗膜はIX 10XI 0−10cr/l/k
g−mの好結果を示している。The coating film of the present invention is IX 10XI 0-10cr/l/k
It shows good results for g-m.
熱硬化性樹脂には現在十数種類あるが、いづれも耐熱性
にとみ、三次元網状構造を持ち、硬化して永久に不融、
不溶性となる特性を持ち、その構造から接着性が犬で塗
料並びに塗料基材として用いられている。There are currently more than a dozen types of thermosetting resins, but all of them are heat resistant, have a three-dimensional network structure, and are permanently infusible after curing.
It has the property of being insoluble, and because of its structure, it has adhesive properties and is used as a paint and paint base material.
ポリアミドイミド樹脂(以下P、A、I、 と称する)
、ポリイミド樹脂(以下P、1.と称する)、エポキシ
樹脂、ウレタン樹脂、シリコーン樹脂はいづれも熱硬化
性樹脂0一つであり、それぞれ特質を有している。Polyamideimide resin (hereinafter referred to as P, A, I)
, polyimide resin (hereinafter referred to as P, 1.), epoxy resin, urethane resin, and silicone resin are all thermosetting resins, and each has its own characteristics.
P、A、1.の構造式は、Rをアルキル基として、で表
わされ、アミド結合とイミド結合が交叉している構造を
持つ樹脂で、適度の吸湿性を有するアミド結合を有する
のでたわみ性を持ち、電気絶縁1本材料として使用され
る。P, A, 1. The structural formula is represented by, where R is an alkyl group.It is a resin with a structure in which an amide bond and an imide bond are crossed.It has flexibility as it has an amide bond with moderate hygroscopicity, and is an electrical insulator. Used as a single material.
P、I、の構造式は
で表わされ、近年開発されたもので軟化点は700℃、
熱分解重量減はヘリウム中400℃で連続15時間でも
1.5%以下の微量であり、電気材料として使用される
。The structural formula of P and I is expressed by, and it has been developed in recent years and has a softening point of 700°C.
The weight loss due to thermal decomposition is very small, less than 1.5% even in helium at 400°C for 15 hours continuously, and it is used as an electrical material.
エポキシ樹脂は分子内に2個以上のエチレンオ :キシ
ド結合(OH−CH2)、すなわちエポキシ基\1
0 ※※を有する
鎖状縮合体、およびそれをアミン、無水化物などによっ
て硬化した樹脂で、広く接着剤や塗料として使用され、
接着性はよい。Epoxy resin is a chain condensate having two or more ethylene oxide bonds (OH-CH2), that is, epoxy groups\10** in the molecule, and resins that are cured with amines, anhydrides, etc., and are widely used. Used as an adhesive or paint
Good adhesion.
その構造式は で表わされ、R1とR2は置換基である。Its structural formula is It is represented by R1 and R2 are substituents.
この他に のものも使用できる。In addition to this You can also use.
RはHl CH3など。R is Hl CH3 etc.
*
* ウレタン樹脂はブロックイソシアネートを用いた一
成分性の熱硬化型が好ましく、その構造式は一例として
、
を示す。* * The urethane resin is preferably a one-component thermosetting type using blocked isocyanate, and its structural formula is shown as an example.
接着力は最も大きく耐水性もよいので塗料として用いら
れるが耐候性に劣る。It has the highest adhesive strength and good water resistance, so it is used as a paint, but its weather resistance is poor.
シリコーン樹脂で使用されるのはSiO2、CH35i
n3/!、(CH3) 2S io、(CH3) 3S
i 03Aの構造単位の共重合体であるメチルシリコ
ーンワニス、又は構造単位がCH35iO3/2、(C
H3) 2 S i O,C6H5S io3/2、(
C6H5) (CH3) 5iO1(C,H5)2Si
Oであるフェニルメチルシリコーンワニス及びこれらの
アルキド、フェノール、メラミン、エポキシ、ポリエス
テル、アクリル、ウレタン変性シリコーンワニスをも用
いる。Silicone resins used are SiO2 and CH35i
n3/! , (CH3) 2S io, (CH3) 3S
Methyl silicone varnish which is a copolymer of the structural unit of i03A, or whose structural unit is CH35iO3/2, (C
H3) 2 S i O, C6H5S io3/2, (
C6H5) (CH3) 5iO1(C,H5)2Si
Also used are phenylmethyl silicone varnishes, which are O, and alkyd, phenol, melamine, epoxy, polyester, acrylic, and urethane-modified silicone varnishes thereof.
耐熱性、耐寒性、耐油性でしかも発水性を持ち、電気絶
縁材として用いられる。It is heat resistant, cold resistant, oil resistant, and water repellent, and is used as an electrical insulation material.
固体潤滑剤としては前記(3Jのもの以外に顔料といわ
れる鉱物質、さらに有機質が金属と化合したレーキ顔料
を含み、一般に粉体として使用されるが、特定用途以外
では従来は粉体のため飛散し、環境汚染を発生する欠点
がある。Solid lubricants include, in addition to those mentioned above (3J), mineral substances called pigments, and lake pigments in which organic substances are combined with metals, and are generally used in powder form, but except for specific uses, they have traditionally been dispersed in powder form. However, it has the disadvantage of causing environmental pollution.
P、T、F、E、は摺動性に富むのですべり面塗群の基
材として用いられて来たが、前述の通りP、T、F、E
、の塗膜は気孔やきすを発生しやすく、従って機械的強
度が劣るため塗膜形成性が低く、塗膜性能が不安定でか
つ耐磨耗性も悪い。P, T, F, and E have been used as base materials for sliding surface coatings because they have excellent sliding properties.As mentioned above, P, T, F, and E
The coating film of , is prone to generate pores and scratches, and therefore has poor mechanical strength, resulting in poor film formation, unstable coating performance, and poor abrasion resistance.
しかしP、F、A、には良く混合するので、P、F、A
、 の溶融性をP、T、F、E、に加えたものはすべり
面周耐磨耗塗料として特徴ある塗料が得られる。However, since P, F, and A mix well, P, F, and A
By adding the meltability of , to P, T, F, and E, a coating with characteristics as a wear-resistant coating around the sliding surface can be obtained.
以下実測例を示す。An actual measurement example is shown below.
第1図は平均粒径35μnのP、F、A、を75重量%
、P、A、1.固形分を25重量%(但このP、A、1
.固形分中にM。Figure 1 shows 75% by weight of P, F, and A with an average particle size of 35 μn.
,P,A,1. 25% by weight of solids (however, this P, A, 1
.. M in solid content.
S2をP、A、I、単体の5重量%含有する)を混合し
た塗膜の顕微鏡写真の線図である。It is a diagram of a micrograph of a coating film mixed with S2 (P, A, I, containing 5% by weight of the simple substance).
aは断面図で斜線部分は被塗装材料である。A is a cross-sectional view, and the shaded area is the material to be coated.
bは塗膜の表面の平面図である。いづれも焼付前の状態
である。b is a plan view of the surface of the coating film. All are in the state before baking.
a′はaの、b′はbの焼付後の状態で、焼付前では白
い円1、焼付後では連続した白い部分1′がP、F、A
。a' is the state of a, and b' is the state of b after baking. Before baking, the white circle 1 is, and after baking, the continuous white part 1' is P, F, A.
.
であり、黒い部分の焼付前2と焼付後2′がM。The black part before baking 2 and after baking 2' is M.
S2を含有するP、A、I、である。These are P, A, and I containing S2.
a′で被塗装材料の面3′にP、A、I、が密着してい
るのが2′で示されている。2' indicates that P, A, and I are in close contact with the surface 3' of the material to be coated at a'.
耐磨耗性の試験は銘木、松原式磨耗試験機を使用し、無
給油状態でのスラスト磨耗を測定して磨耗係数を得た。The abrasion resistance test used precious wood and a Matsubara type abrasion tester, and the thrust abrasion was measured without lubrication to obtain the abrasion coefficient.
試片として40m1X 40mmX 2朋のアルミニウ
ム板をトリクロールエチレンにて脱脂後、以下記述する
各種の塗膜を形成して用いた。As test specimens, aluminum plates measuring 40 m x 40 mm x 2 were degreased with trichlorethylene, and various coating films described below were formed thereon and used.
試験条件は、(1)荷重は1 okg/ci、(2)す
べり速度は30m/M(3J相手材料はSUS’304
ステンレス材である。The test conditions were: (1) load was 1 kg/ci, (2) sliding speed was 30 m/M (3J mating material was SUS'304).
It is made of stainless steel.
上記条件で金属面が露出するまで試験し、露出した時の
定常磨耗量から磨耗係数(c11t/kg0m)を算出
1.f、−8第2図は平均粒径35μmの球状のP、F
:A、)にP、A、1.固形分(但し、この中にはP、
A、1.単体の5重量%の後記(7)lffi体潤滑体
上滑剤する)の添加重量%を横軸に、磨耗係数(X 1
0−10cril/kg 、 m )を縦軸に取った関
係を示す。Test under the above conditions until the metal surface is exposed, and calculate the wear coefficient (c11t/kg0m) from the steady wear amount when exposed.1. f, -8 Figure 2 shows spherical P, F with an average particle size of 35 μm.
:A,) to P, A, 1. Solid content (However, this includes P,
A.1. The wear coefficient (X 1
0-10 cril/kg, m) is shown on the vertical axis.
−×−で示す折線イは固体潤滑剤を無添加の場合で、す
なわちP、A、1.のみの場合を示す。The broken line A indicated by -×- is the case when no solid lubricant is added, that is, P, A, 1. Indicates the case of only
これにベンガラ(酸化第二鉄)を加えたものを一ム−で
示す折線口、カーボンを加えたものを−△−で示す折線
へグラファイトを加えたものを−・−で示す折線二、M
oS2を加えたものを一〇−で示す折線ホでそれぞれ示
しである。The fold line where red iron oxide (ferric oxide) is added is shown as 1, the line where carbon is added is shown as -△-, and the line where graphite is added is shown as -.
The values obtained by adding oS2 are shown by the broken lines ``10-'' and ``e''.
これらの折線群からいづれの場合でもP、A、I。From these polyline groups, P, A, and I in any case.
が25添加重量%前後が最も小さい磨耗係数を与え、す
なわち最もよい耐磨耗性を示すことがわかる。It can be seen that addition of around 25% by weight gives the smallest abrasion coefficient, that is, the best abrasion resistance.
また固体潤滑剤を加えない折線イの25重量%の値が約
45 X l O−10cal/kg 、 mであるの
に対し、固体潤滑剤を添加したものは約2内至18倍耐
磨耗性が良く、一般のコーテング材料よりも100倍近
く良くなることがわかる。In addition, the value of 25% by weight of the broken line A without solid lubricant is approximately 45 X l O-10cal/kg, m, whereas the value with solid lubricant added is approximately 2 to 18 times more resistant to wear. It can be seen that the coating properties are good and are nearly 100 times better than general coating materials.
最も耐磨耗性のすぐれたものは一〇−で示す折線ホのM
。The one with the best abrasion resistance is M with the broken line E indicated by 10-.
.
S2添加のもので2.5 x 10−10crtl/k
g −mの値が得られる。2.5 x 10-10crtl/k with S2 addition
The value of g −m is obtained.
MoS2の添加量はP、A、1.05重量%である。The amount of MoS2 added was 1.05% by weight of P and A.
第3図にその他の熱硬化性樹脂にMoS2をP、A、1
.の場合と同じく5重量%含有したときの熱硬化性樹脂
添加重量%と磨耗係数との関係を示しである。Figure 3 shows MoS2 P, A, 1 in other thermosetting resins.
.. The graph shows the relationship between the weight percent of the thermosetting resin added and the wear coefficient when the thermosetting resin is contained at 5 weight percent as in the case of .
図中−△−で示す折線ハはフェニル・メチル・シリコー
ン樹脂、−〇−で示す折線イはエポキシ樹脂とメラミン
樹脂との混合樹脂、・−で示す折線口はウレタン樹脂、
−ム−で示す折線二はウレタン樹脂をP、F、A、に加
えたときである。In the figure, the fold line C indicated by -△- is phenyl methyl silicone resin, the fold line A indicated by -〇- is a mixed resin of epoxy resin and melamine resin, and the fold line opening indicated by - is urethane resin.
The second broken line indicated by -mu is when the urethane resin is added to P, F, and A.
この四本の折線の内、折線二を除くフェニル・メチル・
シリコーン樹脂、エポキシ樹脂とメラミン樹脂との混合
樹脂、ウレタン樹脂を添加したものは広い添加範囲で低
い磨耗係数を示す特徴を有する。Of these four fold lines, except for fold line 2, phenyl, methyl,
Silicone resins, mixed resins of epoxy resins and melamine resins, and those to which urethane resins are added have the characteristic of exhibiting a low coefficient of wear over a wide range of additives.
また第2図の折線ハに就いて、P、A、I、固形分の添
加が25重量%のものについてP、F、A。Also, regarding the broken line C in Fig. 2, P, A, I, and P, F, A for the case where the solid content is 25% by weight.
の平均粒径と磨耗係数との関係を求めたのが第4図であ
る。Figure 4 shows the relationship between the average particle size and the wear coefficient.
第4図から平均粒径が小さいもの程低い磨耗係数を示し
ている。FIG. 4 shows that the smaller the average particle diameter, the lower the wear coefficient.
第5図はP、A、1.単体の5重量%のカーボンを含む
P、A、1.固形分を全量の25重量%とし、残りの7
5重量%をP、F、A、とP、T、F、E、としたとき
のP、F、A、 に対するP、T、F、E、の添加量
と磨耗係数との関係を求めたものである。Figure 5 shows P, A, 1. P, A, 1. containing 5% by weight of elemental carbon. The solid content is 25% by weight of the total amount, and the remaining 7
When 5% by weight is P, F, A and P, T, F, E, the relationship between the amount of P, T, F, E added to P, F, A, and the wear coefficient was determined. It is something.
第5図からP、F、A、の70重量%までP、T、F、
E。From Figure 5, P, T, F, up to 70% by weight of P, F, A,
E.
を置換しても磨耗係数は余り変化がないことがわかり、
これから特別に機械的強度を必要としないときにはP、
T、F、E、をP、F、A、 の70重量%まで置換し
ても使用可能なことが示される。It was found that the wear coefficient did not change much even if the
If no special mechanical strength is required from now on, P,
It is shown that it can be used even if T, F, E, is substituted up to 70% by weight of P, F, A.
70重量%を超すと急激に耐磨耗性が減少する。If it exceeds 70% by weight, the abrasion resistance decreases rapidly.
他の固体潤滑剤についても同じである。The same applies to other solid lubricants.
第6図は第5図のカーボンの代りにMoS2を各熱硬化
性樹脂の5重量%づつを各熱硬化性樹脂に加えたものを
25重量%とし、残りの75重量%をP、F、A、とP
、T、F、E、とした場合にP、F、A、粉末に対して
P、T、F、E、粉末の混合重量%を変化したときの磨
耗係数とP、F、A、に対するP、T、F、E、混合重
量%との関係を示す。In Figure 6, instead of carbon in Figure 5, 5% by weight of MoS2 is added to each thermosetting resin to make 25% by weight, and the remaining 75% by weight is P, F, A, and P
, T, F, E, P, F, A, P, T, F, E, abrasion coefficient when changing the mixed weight percentage of powder and P, F, A, , T, F, E, and the relationship with the mixing weight %.
−〇−で示す折線イはP、1.、−・−で示す折線口は
エポキシ樹脂とメラミン樹脂との混合樹脂、−×−で示
す折線/\はウレタン樹脂、−△−で示す折線二はフェ
ニルメチルシリコーン樹脂の熱硬化性樹脂を加えた場合
である。The broken line A indicated by -〇- is P, 1. The fold line indicated by -・- is a mixed resin of epoxy resin and melamine resin, the fold line indicated by -×-/\ is urethane resin, and the second fold line indicated by -△- is a thermosetting resin of phenylmethyl silicone resin. This is the case.
第6図からP、1.とウレタン樹脂では70重量%、フ
ェニル・メチル・シリコーン樹脂テハ60重量%、エポ
キシ樹脂とメラミン樹脂との混合樹脂では80重量%以
上、P、F、A、にP、T、F、E。From Figure 6, P, 1. 70% by weight for urethane resin, 60% by weight for phenyl methyl silicone resin, 80% by weight or more for mixed resin of epoxy resin and melamine resin, P, F, A, P, T, F, E.
を添加すると耐磨耗性が低下することがわかる。It can be seen that the addition of 20% reduces the abrasion resistance.
次に実施例1〜11に就いて具体的に説明する。Next, Examples 1 to 11 will be specifically described.
実施例 1
平均粒径35μmの球状P、F、A、をジメチル・ホル
ムアミドとトルテンの混合液中に分散させ、次に市販の
P、A、1. ワニス中にM。Example 1 Spherical P, F, A with an average particle size of 35 μm were dispersed in a mixture of dimethyl formamide and tolten, and then commercially available P, A, 1. M in varnish.
S2をP、A、1.単体に列して5重量%になるように
添加し、ボールミルにて混練り後、上記p、F、A。S2 as P, A, 1. The above p, F, and A were added in a single unit so as to have a concentration of 5% by weight, and kneaded in a ball mill.
分散液中に添加し、攪拌混合した。It was added to the dispersion liquid and stirred and mixed.
このときP、A、1. とMoS2との混合固形分は
P、F、A。At this time, P, A, 1. The mixed solid content of and MoS2 is P, F, and A.
に対して25重量%になるようにした。The amount was adjusted to 25% by weight.
本塗料を5PHC製ビデオデスク集光レンズホルダーの
内径11朋、長さ10朋の一端を閉じた状態にして、他
端から流し込み、ホルダー内に本塗料が満たされたどき
下端から流出させてホルダー内面を塗装した後、80℃
〜150℃にて25分間乾燥して、次に330℃で30
分間焼付処理をした。Close one end of the 5PHC video desk condensing lens holder (inner diameter 11 mm, length 10 mm) and pour the paint from the other end. When the holder is filled with the paint, let it flow out from the bottom of the holder. After painting the inner surface, 80℃
Dry at ~150°C for 25 minutes, then at 330°C for 30 minutes.
I baked it for a minute.
この内面を更に切削加工して30μmの皮膜を残して使
用に供した処、製品はステックスリップ現象を示さず円
滑な摺動が得られ、その結果耐磨耗性が向上し、500
0時間以上の使用でも良好に作動している。When this inner surface was further machined to leave a 30 μm film and used for use, the product showed no stick-slip phenomenon and smooth sliding was obtained, resulting in improved wear resistance and a 500 μm coating.
It is working well even after 0 hours of use.
実施例 2
平均粒径70μmのp、F、A、樹脂粉末に対し、平均
ね径50μm以下のP、1.粉末を25重量%になるよ
うに混合した。Example 2 P, F, A, and resin powders with an average particle size of 70 μm were compared to P, 1. The powders were mixed at 25% by weight.
このP、 1.粉末はあらかじめP、I、単体に対し5
重量%のカーボンを含有している。This P, 1. Powder is prepared in advance by 5 for P, I, and simple substance.
% carbon by weight.
この混合粉末を350℃に加熱して、400朋X100
O朋X31ixmの鉄板に粉末吹付は塗装し、更に35
0℃にて30分間焼付をして約150μmの皮膜を得た
。This mixed powder was heated to 350°C, and
Powder spraying was applied to the iron plate of Oho X31ixm, and 35
Baking was carried out at 0° C. for 30 minutes to obtain a film of about 150 μm.
この板をリハビリテーション用ルームランニング装置の
ガラス繊維強化ナイロン製ランニングベルトとの摺動向
に使用した処、従来の硬質クロムメッキ板よりよい円滑
なすべり性が得られ、従って寿命も倍加し、塗膜の耐磨
耗性も良好であった。When this board was used for sliding movement with the glass fiber reinforced nylon running belt of a room running device for rehabilitation, it achieved smoother sliding properties than conventional hard chrome plated boards, thus doubling the lifespan and improving the paint film. Abrasion resistance was also good.
実施例 3
平均粒径20μ扉のP、F、A、樹脂粉末をキジロール
とブタノールの混合溶剤中に分散させた分散液にエポキ
シ樹脂とメラミン樹脂との混合溶液中に添加して、固形
分比にてP、F、A、75重量%対エポキシ樹脂とメラ
ミン樹脂25重量%の混合塗料を作成した。Example 3 P, F, A, resin powders with an average particle size of 20μ were added to a dispersion of a mixed solvent of pheasant roll and butanol, and added to a mixed solution of an epoxy resin and a melamine resin to determine the solid content ratio. A mixed paint containing 75% by weight of P, F, and A to 25% by weight of epoxy resin and melamine resin was prepared.
なおこのエポキシ樹脂とメラミン樹脂との混合溶液には
あらかじめこの混合溶液の固形分の5重量%のM。Note that this mixed solution of epoxy resin and melamine resin is preliminarily mixed with M in an amount of 5% by weight based on the solid content of this mixed solution.
S2が混入しである。前記混合塗料をアルミニウム製家
庭用ガスコック閉子にはけ塗りをし、80℃で乾燥後、
350℃にて30分間焼付処理して約70μm厚さの皮
膜を得た。S2 is mixed in. The mixed paint was brushed onto an aluminum household gas cock closer, and after drying at 80°C,
Baking treatment was performed at 350° C. for 30 minutes to obtain a film with a thickness of about 70 μm.
これをバイト切削をして厚さ40μmの皮膜として、無
給油状態で使用し、2万回以上の開閉をしたがガスもれ
もなく良好なすべり性が得られた。This was cut with a cutting tool to form a film with a thickness of 40 μm, which was used without lubrication and was opened and closed more than 20,000 times, but no gas leaked and good sliding properties were obtained.
実施例 4
平均粒径20μmのP、F、A、粉末をエポキシ樹脂と
尿素樹脂との混合焼付塗料の中に添加混合°し、P、
F、A、を70重量%に対し、前記混合焼付塗料を30
重量%の割合の塗料を作った。Example 4 P, F, A powders with an average particle size of 20 μm were added and mixed into a mixed baking paint of epoxy resin and urea resin.
70% by weight of F and A, 30% of the mixed baking paint
Paints were made in the proportions of % by weight.
なおエポキシ樹脂と尿素樹脂の混合焼付塗料固形分の5
重量%のM。In addition, the solid content of mixed baking paint of epoxy resin and urea resin is 5
M in weight %.
S2があらかじめ混入しである。このP、F、A、 と
エポキシ樹脂と尿素樹脂及びMoS2の混合塗料をジョ
ークプラスト処理をした直径4.651m1X長さ11
5關のセラミック製プランジャーに吹付塗装をし、80
℃で指触乾燥後、350℃にて20分間焼付処理を行い
、約50μmの厚さの皮膜を得た。S2 is mixed in advance. This P, F, A, and mixed paint of epoxy resin, urea resin, and MoS2 were treated with Joke Plast.
Spray paint the 5-piece ceramic plunger, and
After drying to the touch at .degree. C., baking treatment was performed at 350.degree. C. for 20 minutes to obtain a film with a thickness of about 50 .mu.m.
これをセンターレス研磨により30〜40μmの厚さと
し、薬液制御用プシンジャーとして使用した結果、耐薬
品性、すべり性、シール性ともに満足な結果が得られた
。This was polished to a thickness of 30 to 40 μm by centerless polishing and used as a pusher for controlling chemical liquids, and as a result, satisfactory results were obtained in terms of chemical resistance, slipperiness, and sealability.
実施例 5
平均粒径20μmのP、 F、 A、樹脂を市販の熱硬
化性ウレタン塗料のキシレン溶液中に非イオン性界面活
性剤にて湿潤させて添加し、攪拌混合して粘稠塗料を作
成する。Example 5 P, F, A, and resins with an average particle size of 20 μm were added to a xylene solution of a commercially available thermosetting urethane paint, moistened with a nonionic surfactant, and stirred and mixed to form a viscous paint. create.
この粘稠塗料にはP、F、A、樹脂の固形分の15重量
%がウレタン樹脂の固形分となっている。In this viscous paint, 15% by weight of the solid content of P, F, A, and resin is the solid content of urethane resin.
またウレタン塗料ニはあらかじめウレタン塗料の固形分
の5重量%のMoS2が混入しである。Further, the urethane paint (2) was mixed with MoS2 in an amount of 5% by weight of the solid content of the urethane paint.
この混合した粘稠塗料を直径46n×長さ18Uの鉄製
ピストンの外周面にこのピストンを回転させなからへら
塗装をして80℃にて10分間乾燥した後に、330℃
にて15分間焼付をして、焼付皮膜の厚さ130μmを
得た。This mixed viscous paint was applied to the outer circumferential surface of an iron piston with a diameter of 46 nm and a length of 18 U using a spatula while the piston was not rotating. After drying at 80°C for 10 minutes, the mixture was heated to 330°C.
Baking was carried out for 15 minutes in a vacuum cleaner to obtain a baked film with a thickness of 130 μm.
この焼付処理後バイト切削にて厚さを50μmまで切削
し、浄化槽用コンプレッサーピストンとして使用した処
、従来のピストンリング使用に比べ性能が3倍以上向上
し、軽量でコンパクトにすることが可能となった。After this baking treatment, the material was cut to a thickness of 50 μm using a cutting tool and used as a compressor piston for a septic tank. Compared to conventional piston rings, the performance was improved by more than three times, and it was possible to make it lighter and more compact. Ta.
実施例 6
平均粒径20μmのP、F、A、樹脂粉末をフェニル・
メチル・シリコーン樹脂のキシレン溶液中に添加混合し
、シリコーン樹脂固形分に対し70重量%のP、F、A
、樹脂を作成した。Example 6 P, F, A, resin powder with an average particle size of 20 μm was mixed with phenyl.
Add and mix into a xylene solution of methyl silicone resin, and add 70% by weight of P, F, and A based on the solid content of the silicone resin.
, created a resin.
なおこのフェニル・メチル・シリコーン樹脂には固形分
の5重量%のM。Note that this phenyl methyl silicone resin contains M with a solid content of 5% by weight.
S2をあらかじめ混入しである。この混合塗料をオート
バイ用鉄製クラッチ部品にスプレー塗装し、45μmの
厚さの焼付皮膜を得た。S2 is mixed in advance. This mixed paint was spray-painted on a steel clutch part for a motorcycle to obtain a baked film with a thickness of 45 μm.
これは80℃にて10分間乾燥後、330℃で15分間
焼付処理をした。This was dried at 80°C for 10 minutes and then baked at 330°C for 15 minutes.
このクラッチ部品はグリースの使用なくして円滑な摺動
性を示し、耐食性もよく、従来の給油方式に比し、無給
油でありながらクラッチ作動がスムースになった。This clutch component slides smoothly without the use of grease, has good corrosion resistance, and compared to conventional lubrication systems, clutch operation is smoother without lubrication.
実施例 7
平均粒径20μmのP、F、A、粉末と平均粒径10μ
m以下のP、T、F、E、粉末を3ニアの重量割合でト
ルエンとノルマルメチル・ピロリドンとの混合液に分散
させた分散液を市販のP、A、I。Example 7 P, F, A powder with an average particle size of 20 μm and an average particle size of 10 μm
Commercially available dispersions of P, T, F, E, and powders of m or less are dispersed in a mixture of toluene and normal methyl pyrrolidone at a weight ratio of 3 nia.
ワニスのノルマルメチル・ビロリドントトルエンとの混
合液に添加混合し、P、F、A、樹脂とP、T、F、E
・、′樹脂の混合粉末の固形分に対し25重量%のP、
A、I、樹脂の固形分になるように調整した。P, F, A, resin and P, T, F, E
・,'25% by weight of P based on the solid content of the resin mixed powder,
A, I, the solid content of the resin was adjusted.
なおP、A、1.ワニスのノルマルメチル・ピロリドン
混合液にはP、A、1.の固形分の5重量%のMoS2
があらかじめ混入しである。Note that P, A, 1. The normal methyl pyrrolidone mixture for varnish contains P, A, 1. 5% by weight of solid content of MoS2
is pre-mixed.
この調整した塗料を酸化アルミニウム粒にてプラスト処
理した直径30m1X長さ80皿のADC−12製の冷
凍機用コンプレッサーピストンにノズル口径1.2朋の
スプレーガンにて吹圧2 kg/cyifでスプレー塗
装し、90μmの厚さの焼付皮膜を得た。This prepared paint was sprayed with a spray gun with a nozzle diameter of 1.2 mm at a blowing pressure of 2 kg/cyif onto an ADC-12 refrigerator compressor piston with a diameter of 30 m and a length of 80 plates, which had been treated with aluminum oxide particles. A baked film with a thickness of 90 μm was obtained by painting.
乾燥は150℃で10分間、焼付は350℃で30分間
行った。Drying was performed at 150°C for 10 minutes, and baking was performed at 350°C for 30 minutes.
皮膜はバイト切削で40μm厚さとして使用した処、完
全に無給油状態で使用しても音は静かで、従来のピスト
ンリング使用の給油式に比べ、小型化、軽量化更にコス
トダウンが可能になり、かつメンテナンスの手間が無く
なるなど著しい利点と効果があった。The coating is 40μm thick when cutting with a cutting tool, and it is quiet even when used completely without oil, making it possible to be smaller, lighter, and lower in cost than the conventional oil-lubricated type that uses piston rings. It has significant advantages and effects, such as eliminating the need for maintenance.
実施例 8
平均粒径70μmのP、 F、A、樹脂50.10μm
以下のP、T、 F、 E、樹脂50.5Qltm以下
のP、I、樹脂30の各重量での割合の混合粉末を作る
。Example 8 P, F, A, resin with average particle size of 70 μm, 50.10 μm
A mixed powder is prepared in the following proportions by weight of P, T, F, E, resin 50.5 Qltm or less, P, I, and resin 30.
P、I、樹脂にはその固形分の5重量%のMoS2があ
らかじめ混入されている。The P, I, and resins were premixed with 5% by weight of MoS2 based on their solid content.
この混合粉末を350℃に加熱したステンレス製エスカ
レータの手すりゴムベルトの支持金具に粉末吹付塗装し
、更に350℃で40分間焼付して厚さ70〜100μ
mの皮膜を形成した。This mixed powder was powder spray coated on the supporting metal of the handrail rubber belt of a stainless steel escalator heated to 350°C, and then baked at 350°C for 40 minutes to a thickness of 70 to 100 μm.
A film of m was formed.
この支持金具を連らねてエスカレータの手すりベルトの
支持具として使用した処、ベルトのステンクスリップが
なくなり、摩擦音も著しく低減し好結果を得た。When these support fittings were connected in series and used as a support for an escalator handrail belt, good results were obtained, with no belt slippage and a significant reduction in frictional noise.
実施例 9
平均粒径20μmのP、F”、A、樹脂と10μm以下
のP、 T、F、 E、樹脂を5:5の重量割合で含む
キシレン分散液中にエポキシ樹脂と尿素樹脂との混合型
焼付塗料を添加混合して、P、F、A、樹脂とP、T、
F、E、樹脂の全固形分に対してエポキシ樹脂と尿素樹
脂との混合樹脂固形分が35重量%になるように調整し
た、エポキシ樹脂と尿素樹脂との固形分の5重量%のカ
ーボンをあらかじめエポキシ樹脂と尿素樹脂との混合物
に混入しである。Example 9 An epoxy resin and a urea resin were mixed in a xylene dispersion containing P, F'', A, resin with an average particle size of 20 μm and P, T, F, E, resin with an average particle size of 10 μm or less in a weight ratio of 5:5. By adding and mixing the mixed baking paint, P, F, A, resin and P, T,
F, E, carbon with a solid content of epoxy resin and urea resin of 5% by weight, adjusted so that the solid content of the mixed resin of epoxy resin and urea resin is 35% by weight based on the total solid content of the resin. It is mixed in advance into a mixture of epoxy resin and urea resin.
この調整した混合塗料を直径35關×長さ140mmの
鉄製ギヤシフト部品に吹付塗装し、60〜80℃で10
分間乾燥後、350℃で40分間焼付し、厚さ約40μ
mの皮膜を得た。This adjusted mixed paint was spray-coated on a steel gear shift part with a diameter of 35 mm and a length of 140 mm.
After drying for 40 minutes at 350℃, the thickness is approximately 40μ.
A film of m was obtained.
この部品を使用した結果ギヤ作動時に発生する衝撃音が
著しく少なくなり、無給油にて円滑なギヤ作動が確保さ
れた。As a result of using this part, the impact noise generated during gear operation was significantly reduced, and smooth gear operation was ensured without lubrication.
実施例 10
平均粒径20μmのP、 F、 A、樹脂と10μm以
下のP、T、F、E、を4=6の重量割合で含むキシレ
ン分散液に熱硬化型ウレタン塗料を添加攪拌混合し、P
、 F、 A、樹脂とP、T、F、E、樹脂の全固形分
に対し、ウレタン樹脂固形分が30重量%になるように
調整した塗料を作った。Example 10 A thermosetting urethane paint was added to a xylene dispersion containing P, F, A, resin with an average particle size of 20 μm and P, T, F, E with a weight ratio of 10 μm or less in a weight ratio of 4=6. , P
, F, A, resin and P, T, F, E, A paint was prepared in which the solid content of the urethane resin was adjusted to 30% by weight based on the total solid content of the resin.
ウレタン樹脂にはその固形分の5重量%のM。The urethane resin contains 5% M by weight of its solid content.
S2があらかじめ混入している。S2 is mixed in advance.
巾250imX長さ500關の鉄製エスカレータ用側壁
パネルをショツトブラストし、次にニッケル、アルミニ
ウム混合金属粉末をフレーム溶射処理し、その上に前記
塗料をスプレー塗装した。A steel escalator side wall panel measuring 250 mm wide x 500 mm long was shot blasted, then flame sprayed with nickel and aluminum mixed metal powder, and the paint was spray-painted thereon.
乾燥は80℃で10分間赤外線乾燥を行い、320℃で
30分間焼付して厚さ50μmの皮膜を得た。For drying, infrared drying was performed at 80°C for 10 minutes, followed by baking at 320°C for 30 minutes to obtain a film with a thickness of 50 μm.
この塗装をしたパネルを連ねてエスカレータ側壁に設置
した処、くっとのすべり性がよくなり、耐磨耗性がよく
傷付きがほとんど認められない。When panels coated with this coating are installed in a row on the side wall of an escalator, they have good sliding properties and are highly abrasion resistant, with almost no scratches being observed.
また従来の金属板使用のときに発生した足の巻き込み事
故の防止も可能で極めて重要である。It is also possible to prevent foot-injury accidents that occur when using conventional metal plates, which is extremely important.
実施例 11
平均粒径20μmのP、F、A、樹脂30重量%に幻し
、10μ771以下のP、T、F、E、樹脂70重量%
を混合した粉末をキシレン溶液中に分散させ、この分散
液に市販のエポキシ変性シリコーン樹脂を添加混合し、
P、F、A、樹脂とP、T、F、E、樹脂の全固形分7
0重量%に幻してエポキシ樹脂変性シリコーン樹脂の固
形分30重量%になる塗料を作成した。Example 11 P, F, A, resin with an average particle size of 20 μm, 30% by weight, P, T, F, E, resin with an average particle size of 10μ771 or less, 70% by weight
Disperse the mixed powder in a xylene solution, add and mix a commercially available epoxy-modified silicone resin to this dispersion,
P, F, A, resin and P, T, F, E, total solid content of resin 7
A paint was prepared in which the solid content of the epoxy resin-modified silicone resin was 30% by weight, instead of 0% by weight.
なおこのエポキシ樹脂変性シリコーン樹脂にはその5重
量%のM。Note that this epoxy resin-modified silicone resin contains 5% by weight of M.
S2があらかじめ混入されている。S2 is mixed in advance.
この塗料を直径80imX長さ115間の鉄製電算機プ
リンタロールに浸漬塗装し、80℃にて10分間乾燥後
320 ’Cにて20分間焼付して約60μmの塗膜を
得た。This paint was dip-coated onto a steel computer printer roll measuring 80 mm in diameter and 115 mm in length, dried at 80° C. for 10 minutes, and then baked at 320° C. for 20 minutes to obtain a coating film of about 60 μm.
この塗膜をセンターレス研磨に−て40〜50μmの厚
さとして使用した。This coating film was used for centerless polishing to a thickness of 40 to 50 μm.
従来P、F、A、樹脂を混入せぬP、T、F、E、樹脂
のみの場合に比べて著しく耐磨耗性が向上した。The abrasion resistance was significantly improved compared to the conventional case of using only P, T, F, E, and resin without mixing P, F, A, and resin.
以上述べたように本発明は耐熱性と非粘着性及び溶解性
にすぐれたP、F、A、に、固体潤滑剤が分散している
熱硬化性樹脂を加え、熱硬化性樹脂のすぐれた付着性に
より、被塗装材料に焼付加工にて密着させ、耐熱性を持
ち、かつ低磨耗性で相手摺動面に傷や損傷を与えない特
徴を有するすべり面周耐磨耗性塗料を提供し、更にまた
摺動性ではP、F、A、よりすぐれてはいるが、気孔の
発生や傷が入りやすく機械的強度が劣るP、T、F、E
。As described above, the present invention adds a thermosetting resin in which a solid lubricant is dispersed to P, F, and A, which have excellent heat resistance, non-adhesiveness, and solubility. We provide abrasion-resistant paint around sliding surfaces that adheres closely to the material to be coated through baking processing due to its adhesion properties, has heat resistance, and has low abrasion properties that do not cause scratches or damage to mating sliding surfaces. Furthermore, P, T, F, and E are superior in sliding properties to P, F, and A, but are prone to pores and scratches and have inferior mechanical strength.
.
にP、F、A、を加え、P、F、A、の溶解性により上
記欠点を補完し、上記と同様に固体潤滑剤が分散してい
る熱硬化性樹脂を加えて摺動性に特徴を有する耐熱性、
低磨耗性のすべり面周耐磨耗性塗料を提供するものであ
る。By adding P, F, and A, the solubility of P, F, and A compensates for the above drawbacks, and by adding a thermosetting resin in which a solid lubricant is dispersed in the same way as above, the sliding property is improved. Heat resistance, with
The present invention provides a coating material with low abrasion properties and abrasion resistance around the sliding surface.
第1図は塗膜の焼付前後の顕微鏡写真線図、第2図は磨
耗係数とP、A、I、固形分重量%、第3図は磨耗係数
と熱硬化性樹脂重量%、第4図は磨耗係数とP、F、A
、平均粒径(μm)、第5図は磨耗係数とP、T、F、
E、固形分重量%(但しカーボン)、第6図は磨耗係数
とP、T、F、E、固形分重量%(但しM。
S2)である。1.1′・・・・・・P、F、A、粉末
、2,2’、γ・・・・・・熱硬化性樹脂、3 、3’
・・・・・・すべり面。Figure 1 is a micrograph diagram of the coating film before and after baking, Figure 2 is the abrasion coefficient and P, A, I, solid content weight %, Figure 3 is the abrasion coefficient and thermosetting resin weight %, and Figure 4 is is the wear coefficient and P, F, A
, average particle diameter (μm), Figure 5 shows wear coefficient and P, T, F,
E, solid content weight % (however, carbon); FIG. 6 shows the wear coefficient and P, T, F, E, solid content weight % (however, M. S2). 1.1'...P, F, A, powder, 2,2', γ...thermosetting resin, 3,3'
...Slip surface.
Claims (1)
オロエチレン樹脂と固体潤滑剤と熱硬化性樹脂とからな
るすべり面周耐磨耗性塗料。 2 熱硬化性樹脂としてポリアミドイミド樹脂を用いた
特許請求の範囲第1項記載の耐磨耗性塗料。 3 熱硬化性樹脂としてポリイミド樹脂を用いた特許請
求の範囲第1項記載の耐磨耗性塗料。 4 熱硬化性樹脂としてエポキシ樹脂を用いた特許請求
の範囲第1項記載の耐磨耗性塗料。 5 熱硬化性樹脂としてウレタン樹脂を用いた特許請求
の範囲第1項記載の耐磨耗性塗料。 6 熱硬化性樹脂としてシリコーン樹脂を用いた特許請
求の範囲第1項記載の耐磨耗性塗料。 7 パーフルオロアルコキシ基を有するポリテトラフル
オロエチレン樹脂とポリテトラフルオロエチレン樹脂と
固体潤滑剤と熱硬化性樹脂とからなるすべり面周耐磨耗
性塗料。 8 熱硬化性樹脂としてポリアミドイミド樹脂を用いた
特許請求の範囲第7項記載の耐磨耗性塗料。 9 熱硬化性樹脂としてポリイミド樹脂を用いた特許請
求の範囲第1項記載の耐磨耗性塗料。 10 熱硬化性塗料としてエポキシ樹脂を用いた特許
請求の範囲第7項記載の耐磨耗性塗料。 11 熱硬化性塗料としてウレタン樹脂を用いた特許
請求の範囲第7項記載の耐磨耗性塗料。 12 熱硬化性樹脂としてシリコーン樹脂を用いた特
許請求の範囲第7項記載の耐磨耗性塗料。[Scope of Claims] 1. A sliding surface abrasion-resistant coating comprising a polytetrafluoroethylene resin having a perfluoroalkoxy group, a solid lubricant, and a thermosetting resin. 2. The abrasion-resistant paint according to claim 1, which uses polyamideimide resin as the thermosetting resin. 3. The abrasion-resistant paint according to claim 1, which uses polyimide resin as the thermosetting resin. 4. The abrasion-resistant paint according to claim 1, which uses an epoxy resin as the thermosetting resin. 5. The abrasion-resistant paint according to claim 1, which uses urethane resin as the thermosetting resin. 6. The abrasion-resistant paint according to claim 1, which uses a silicone resin as the thermosetting resin. 7. A sliding surface abrasion-resistant coating comprising a polytetrafluoroethylene resin having a perfluoroalkoxy group, a polytetrafluoroethylene resin, a solid lubricant, and a thermosetting resin. 8. The abrasion-resistant paint according to claim 7, which uses polyamideimide resin as the thermosetting resin. 9. The abrasion-resistant paint according to claim 1, which uses polyimide resin as the thermosetting resin. 10. The abrasion-resistant paint according to claim 7, which uses an epoxy resin as the thermosetting paint. 11. The abrasion-resistant paint according to claim 7, which uses a urethane resin as the thermosetting paint. 12. The abrasion-resistant paint according to claim 7, which uses a silicone resin as the thermosetting resin.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14833379A JPS5830343B2 (en) | 1979-11-17 | 1979-11-17 | abrasion resistant paint |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14833379A JPS5830343B2 (en) | 1979-11-17 | 1979-11-17 | abrasion resistant paint |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5672058A JPS5672058A (en) | 1981-06-16 |
JPS5830343B2 true JPS5830343B2 (en) | 1983-06-28 |
Family
ID=15450418
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP14833379A Expired JPS5830343B2 (en) | 1979-11-17 | 1979-11-17 | abrasion resistant paint |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5830343B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59147335U (en) * | 1983-03-23 | 1984-10-02 | クラリオン株式会社 | parts fixing device |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4404276A (en) * | 1982-06-14 | 1983-09-13 | Eastman Kodak Company | Polymer compositions containing crosslinked silicone polycarbinol and having a low coefficient of friction |
JPS6381173A (en) * | 1986-09-22 | 1988-04-12 | Nitto Electric Ind Co Ltd | Insulating coating compound of self-lubricating polyamide-imide |
EP0539585A4 (en) * | 1991-04-22 | 1993-09-01 | Takata Corporation | Surface-coated member |
KR20010002974A (en) * | 1999-06-18 | 2001-01-15 | 김영 | Membrance coating method for improving adhesive strength and prevent corrosion of iron reinforce |
CN203557820U (en) * | 2013-02-20 | 2014-04-23 | 皇冠包装技术公司 | Container decoration machine equipment |
CN104263120A (en) * | 2014-09-19 | 2015-01-07 | 山东瑞特新材料有限公司 | Polytetrafluoroethylene coating and preparation method thereof |
-
1979
- 1979-11-17 JP JP14833379A patent/JPS5830343B2/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59147335U (en) * | 1983-03-23 | 1984-10-02 | クラリオン株式会社 | parts fixing device |
Also Published As
Publication number | Publication date |
---|---|
JPS5672058A (en) | 1981-06-16 |
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