JPS5829973B2 - wear resistant paint - Google Patents
wear resistant paintInfo
- Publication number
- JPS5829973B2 JPS5829973B2 JP8442378A JP8442378A JPS5829973B2 JP S5829973 B2 JPS5829973 B2 JP S5829973B2 JP 8442378 A JP8442378 A JP 8442378A JP 8442378 A JP8442378 A JP 8442378A JP S5829973 B2 JPS5829973 B2 JP S5829973B2
- Authority
- JP
- Japan
- Prior art keywords
- parts
- wear
- resistant paint
- coating film
- resin powder
- 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
- 239000003973 paint Substances 0.000 title claims description 17
- 229920005989 resin Polymers 0.000 claims description 16
- 239000011347 resin Substances 0.000 claims description 16
- 238000002156 mixing Methods 0.000 claims description 13
- 239000000843 powder Substances 0.000 claims description 11
- 239000003960 organic solvent Substances 0.000 claims description 8
- 239000004642 Polyimide Substances 0.000 claims description 7
- 229920001721 polyimide Polymers 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 6
- 239000006185 dispersion Substances 0.000 claims description 5
- 229920001774 Perfluoroether Polymers 0.000 claims description 4
- 150000001408 amides Chemical class 0.000 claims description 3
- 238000000576 coating method Methods 0.000 description 18
- 239000011248 coating agent Substances 0.000 description 17
- 239000010408 film Substances 0.000 description 15
- 239000004033 plastic Substances 0.000 description 11
- 229920003023 plastic Polymers 0.000 description 11
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical group CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 238000005299 abrasion Methods 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 229910052782 aluminium Inorganic materials 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- -1 polyacecool Polymers 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000004734 Polyphenylene sulfide Substances 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 229920006026 co-polymeric resin Polymers 0.000 description 2
- 210000003298 dental enamel Anatomy 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 229920000069 polyphenylene sulfide Polymers 0.000 description 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 2
- 239000004810 polytetrafluoroethylene Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229920006361 Polyflon Polymers 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium peroxydisulfate Substances [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 1
- VAZSKTXWXKYQJF-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)OOS([O-])=O VAZSKTXWXKYQJF-UHFFFAOYSA-N 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000006223 plastic coating Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Paints Or Removers (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Description
【発明の詳細な説明】 本発明は耐摩耗性塗料に関する。[Detailed description of the invention] The present invention relates to wear-resistant paints.
近年、無潤滑すべり軸受材料として四フッ化エチレン樹
脂、ナイロン、ポリカーボネート、ポリアセクール、ポ
リイミド、ポリフェニレンサルファイド樹脂などが、単
独でまたは助剤を添加した複合組成で、益々利用されて
いる。In recent years, tetrafluoroethylene resin, nylon, polycarbonate, polyacecool, polyimide, polyphenylene sulfide resin, and the like have been increasingly used as lubricant-free sliding bearing materials alone or in composite compositions with the addition of auxiliary agents.
これらは全てプラスチックスのすべり特性が良好である
ことを利用したものであるか、プラスチックスの耐摩耗
性は金属に比し一般に劣っているので、プラスチックス
軸受は金属軸受に比し寿命が短かく、また使用可能f、
K P V値の範囲が非常に狭いという欠点がある。All of these are based on the good sliding properties of plastics, or the wear resistance of plastics is generally inferior to that of metals, so plastic bearings have a shorter lifespan than metal bearings. Thus, it can also be used f,
It has the disadvantage that the range of KPV values is very narrow.
すなわち、耐摩耗性の大小によって軸受の寿命が定まる
ため、耐摩耗性が優れかつすべり特性の優れたプラスチ
ックスが切望されている。That is, since the life of a bearing is determined by its wear resistance, there is a strong desire for plastics that have excellent wear resistance and sliding properties.
また、プラスチックス軸受はプラスチックス成形品と金
属素材のプラスチックス塗装品とに大別されるが、プラ
スチックス成形品は、金属軸受に比し耐荷重性が劣り摩
擦熱の放散が悪く、またプラスチックス塗装品に比し原
料使用量が多くなるために原価が高くなるという欠点が
あるので、金属素材のプラスチックス塗装品が所望され
ている。In addition, plastic bearings are broadly classified into plastic molded products and plastic coated metal products, but plastic molded products have inferior load bearing capacity and poor dissipation of frictional heat compared to metal bearings. Plastic-coated products made of metal are desired because they have the disadvantage of higher cost because they require more raw materials than plastic-coated products.
しかし、プラスチックス塗装品はプラスチックス塗膜は
塗膜厚が薄いので助剤添加量が制限されるため、未だ満
足すべきものが製造されておらず、優れた耐摩耗性を有
する塗料が切望されている。However, since plastic coatings have a thin film thickness and the amount of additives added is limited, no satisfactory product has been manufactured yet, and there is a strong need for coatings with excellent abrasion resistance. ing.
本発明はプラスチック軸受材料として特に好適な、顕著
に優れた耐摩耗性と良好なすべり性とを有する耐摩耗性
塗料を提供することを目的とする。An object of the present invention is to provide a wear-resistant coating material that is particularly suitable as a plastic bearing material and has significantly superior wear resistance and good slip properties.
しかして、本発明の耐摩耗性塗料はパーフロロアルコキ
シ(以下、PFAと称する。Therefore, the wear-resistant paint of the present invention is made of perfluoroalkoxy (hereinafter referred to as PFA).
)樹脂粉末を有機溶剤に分散した分散液に、ポリイミド
(以下、PIと称する。) Polyimide (hereinafter referred to as PI) is added to a dispersion of resin powder dispersed in an organic solvent.
)またはポリイミドアミド(以下、PIAと称する。) or polyimide amide (hereinafter referred to as PIA).
)を有機溶剤に溶解した溶液を、PFA樹脂粉末100
重量部に対しPIまたはPIA50重量部より下であっ
て400重量部以下の割合で添加混合して得た混合物を
塗膜構成の主成分とするものである。) in an organic solvent, PFA resin powder 100%
The main component of the coating film is a mixture obtained by adding and mixing less than 50 parts by weight and 400 parts by weight of PI or PIA to parts by weight.
PFA樹脂はポリテトラフルオロエチレンF (’j−)+ F の主鎖の所所にパーフルオロアルコキシ基−Rf が結合し構造式 ftl で示される構造を有するものと考えられる。PFA resin is polytetrafluoroethylene F (’j-)+ F Perfluoroalkoxy group -Rf in the main chain of is combined with the structural formula ftl It is thought to have the structure shown below.
PFA樹脂の一種であるテトラフルオロエチレン−パー
フルオロビニルエーテル共重合体樹脂ハチドラフルオロ
エチレン
CF2−CF2
とパーフルオロビニルエーテル
CF3・CF2・CF2・0−CF−CF2とを重合さ
せると得られる。It is obtained by polymerizing a tetrafluoroethylene-perfluorovinyl ether copolymer resin, a type of PFA resin, hydrofluoroethylene CF2-CF2 and perfluorovinyl ether CF3.CF2.CF2.0-CF-CF2.
重合はパーフルオロカーボンあるいは0(J!3F 、
CI(CJ?F2のようなフロン類を溶剤とする溶液
重合、あるいは水またはフロンを添加した水中での乳化
重合、懸濁重合などによって行われる。Polymerization is perfluorocarbon or 0 (J!3F,
This is carried out by solution polymerization using fluorocarbons such as CI (CJ?F2) as a solvent, or by emulsion polymerization or suspension polymerization in water or water to which fluorocarbons are added.
開始剤にはフロン可溶の有機過酸化物、または過硫酸ア
ンモニウムのような水溶性過酸化物を用いる。As an initiator, a Freon-soluble organic peroxide or a water-soluble peroxide such as ammonium persulfate is used.
PFA樹脂粉末を有機溶剤に分散して得た分散液に、P
IまたはPIAを有機溶剤に溶解して得た溶液を添加混
合するが、有機溶剤としては例えばジメチルホルムアミ
ド、トルエン、キシレン、またはこれらの混合物などが
好ましい。A dispersion obtained by dispersing PFA resin powder in an organic solvent is
A solution obtained by dissolving I or PIA in an organic solvent is added and mixed, and the organic solvent is preferably dimethylformamide, toluene, xylene, or a mixture thereof.
なお、PFA樹脂粉末とPIまたはPIAとの混合物に
有機溶剤を添概混合した場合には得られる塗膜の性質は
不良である。Incidentally, when an organic solvent is roughly mixed into a mixture of PFA resin powder and PI or PIA, the properties of the resulting coating film are poor.
PFA樹脂粉末の分散液にPIまたはPIAの溶液を添
加混合する方法は例えば攪拌混合法、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、石臼混合法など倒れの方法で
もよい。Examples of methods for adding and mixing a PI or PIA solution to a dispersion of PFA resin powder include stirring mixing method, tumbler mixing method, shaking mixing method, ultrasonic mixing method, ball mill mixing method, roller mill mixing method, and stone mill mixing method. It is also possible to use a method of collapsing.
なお、PFA樹脂粉末として球形状のものを使用する際
はPFA樹脂粉末の球形形状が維持されるような方法で
混合することが好ましい。In addition, when using a spherical PFA resin powder, it is preferable to mix it in such a way that the spherical shape of the PFA resin powder is maintained.
本発明の耐摩耗性塗料には所望により顔料、充填剤など
を添加してもよい。Pigments, fillers, etc. may be added to the wear-resistant paint of the present invention, if desired.
また、本発明の耐摩耗性塗料を塗装する素材としては例
えば、鉄、鋼、ステンレス鋼、アルミニウム、アルミニ
ウム被覆鋼などの如き金属、ガラス、陶磁器類などがあ
る。Examples of materials to be coated with the wear-resistant paint of the present invention include metals such as iron, steel, stainless steel, aluminum, and aluminum-coated steel, glass, and ceramics.
本発明の耐摩耗性塗料は通常の方法で塗布、乾燥、焼付
けて塗装することができる。The wear-resistant paint of the present invention can be coated, dried, and baked by a conventional method.
本発明の耐摩耗性塗料より得た塗膜は耐摩耗性が顕著に
優れ、かつすべり性も良好であり、しかも被塗物に対す
る接着性、耐食性なども優れ、また−回の塗装で100
〜150μの厚さの塗膜を得ることができるなど幾多の
利点がある。The coating film obtained from the abrasion-resistant paint of the present invention has outstanding abrasion resistance and good slip properties, as well as excellent adhesion to the object to be coated and corrosion resistance.
It has many advantages such as being able to obtain a coating film with a thickness of ~150μ.
次に、本発明を実施例、参考例および比較例によって説
明する。Next, the present invention will be explained using Examples, Reference Examples, and Comparative Examples.
部は重量部を示す。実施例1〜2、参考例1〜8および
比較例1〜2塗料の調整
PFA樹脂粉末(三井フロロケミカル株式会社製(MP
−10、テトラフルオロエチレン−パーフルオロビニル
エーテル共重合体樹脂粉末、平均粒径35μ、球形度1
.05)100部を、ジメチルホルムアミドとトルエン
との4:6重量比況合液40部に分散して得た分散液を
A液とする。Parts indicate parts by weight. Examples 1-2, Reference Examples 1-8 and Comparative Examples 1-2 Preparation of paint PFA resin powder (manufactured by Mitsui Fluorochemical Co., Ltd. (MP
-10, tetrafluoroethylene-perfluorovinyl ether copolymer resin powder, average particle size 35μ, sphericity 1
.. 05) A dispersion obtained by dispersing 100 parts in 40 parts of a 4:6 weight ratio mixture of dimethylformamide and toluene is referred to as Solution A.
次に、PIA(日立化成株式会社製HI−600)30
部にカーボンブラック3部、ベンガラ8部を混合し、ジ
メチルホルムアミド28部、トルエン42部、非イオン
界面活性剤0.1部を添加混合して得た溶液をB液とす
る。Next, PIA (Hitachi Chemical Co., Ltd. HI-600) 30
A solution obtained by mixing 3 parts of carbon black and 8 parts of red iron oxide, and adding and mixing 28 parts of dimethylformamide, 42 parts of toluene, and 0.1 part of a nonionic surfactant is designated as Solution B.
使用時に上記A液とB液とを所要量添加混合して塗料を
得る。At the time of use, the above-mentioned liquids A and B are added and mixed in required amounts to obtain a paint.
混合には攪拌混合機を用いた。塗膜の形成
ブラスト法で表面を粗面化した清浄f、に90myn×
60mmX1mmのアルミ板に塗料を100μの塗膜厚
が得られるように吹付塗装しso’cで乾燥後350°
Cで20分間焼付けし、次いで室温で放冷した。A stirring mixer was used for mixing. Formation of coating film: 90min×
Spray paint on a 60mm x 1mm aluminum plate to a coating thickness of 100μ and dry at 350° in SO'C.
C. for 20 minutes and then allowed to cool at room temperature.
実施例t〜2、参考例1〜8および比較例1〜2の性質
を下記の塗膜の性質衣に示す。The properties of Examples t to 2, Reference Examples 1 to 8, and Comparative Examples 1 to 2 are shown in the coating film properties below.
比摩耗量はスラスト型摩耗試験機を用い次記条件におい
て測定した。The specific wear amount was measured using a thrust type wear tester under the following conditions.
相手材 5us304(+500研摩紙仕上げ)
面圧 5.1%
すべり速度 30m/min
剥離強度は塗膜に幅5間の被塗物に達する切目を入れ、
その塗膜の一端をひきはがし直角方向に引っ張った時の
剥離強度gで示す。Compatible material: 5us304 (+500 abrasive paper finish) Surface pressure: 5.1% Sliding speed: 30m/min Peel strength is determined by making a cut in the coating film that reaches the object to be coated with a width of 5 mm.
It is expressed as the peel strength (g) when one end of the coating film is peeled off and pulled in the perpendicular direction.
下記表より、本発明の耐摩耗性塗料より得た塗膜は耐摩
耗性が顕著に優れており、また被塗物に対する接着性も
顕著に優れていることがわかる。From the table below, it can be seen that the coating film obtained from the abrasion-resistant paint of the present invention has significantly excellent abrasion resistance and also has significantly excellent adhesion to the object to be coated.
また、参考例6の塗膜の動摩擦係数をスラスト型摩耗試
験機を用いて次記条件において測定したところ、0.2
25なる値を得た。In addition, when the dynamic friction coefficient of the coating film of Reference Example 6 was measured using a thrust type abrasion tester under the following conditions, it was found to be 0.2.
A value of 25 was obtained.
面圧 5.1%
すべり速度 30m/min
相手材 5US304(−#=500研摩紙仕上げ
)
無潤滑
上記動摩擦係数より本発明の耐摩耗性塗料はすべり性も
良好であることがわかる。Surface pressure: 5.1% Sliding speed: 30 m/min Compatible material: 5US304 (-#=500 abrasive paper finish) From the above dynamic friction coefficient without lubrication, it can be seen that the wear-resistant paint of the present invention has good sliding properties.
四フッ化エチレン樹脂塗料として、ダイキン工業KK製
EK−1883GBポリフロンプライマーをブラスト処
理を施した90間X60mmX1m扉のアルミ板に吹付
塗装し800Cで乾燥後380°Cで20分間焼付し室
温で放冷後、ポリフロントツブエナメルEK−4183
GB塗料を吹付塗装し、プライマーと同様に乾燥焼付し
た。As a polytetrafluoroethylene resin paint, EK-1883GB Polyflon Primer manufactured by Daikin Industries KK was spray-painted on a blasted 90mm x 60mm x 1m door aluminum plate, dried at 800C, baked at 380C for 20 minutes, and left at room temperature. After cooling, polyfront tube enamel EK-4183
GB paint was spray painted and dried and baked in the same way as the primer.
トップエナメルの塗装、乾燥、焼付を5回くり返して1
00μ以上の膜厚を得た。Repeat painting, drying, and baking the top enamel 5 times.
A film thickness of 00μ or more was obtained.
このようにして得た塗膜の比摩耗量を実施例1〜2およ
び参考例1〜8と同様の方法で測定した値を上記塗膜の
性質表に示す。The specific wear amount of the coating film thus obtained was measured in the same manner as in Examples 1 to 2 and Reference Examples 1 to 8, and the values are shown in the above coating film property table.
比較例 4
ポリフェニレンサルファイド樹脂塗料としてアメリカ合
衆国ウィツトフォード社製ザイラン8610塗料をブラ
スト処理を施した9 0mmX 60gX l mmの
アルミ板に吹付塗装し80℃で乾燥後、380℃で30
分間焼付し、50μの塗膜厚を得た。Comparative Example 4 Polyphenylene sulfide resin paint, Zylan 8610 paint made by Whitsford Co., USA, was spray-painted on a blast-treated 90 mm x 60 g x 1 mm aluminum plate, dried at 80°C, and then heated at 380°C for 30 minutes.
Baking was carried out for 5 minutes to obtain a coating thickness of 50μ.
このようにして得た塗膜の比摩耗量を実施例1〜2およ
び参考例1〜8と同様の方法で測定した値を上記塗膜の
性質表に示す。The specific wear amount of the coating film thus obtained was measured in the same manner as in Examples 1 to 2 and Reference Examples 1 to 8, and the values are shown in the above coating film property table.
Claims (1)
、ポリイミドまたはポリイミドアミドの有機溶剤溶液を
、パーフロロアルコキシ樹脂粉末100重量部に対しポ
リイミドまたはポリイミドアミド50重量部より大であ
って400重量部以下の割合で、添加混合して得た混合
物を主成分とすることを特徴とする耐摩耗性塗料。1. An organic solvent solution of polyimide or polyimide amide is added to an organic solvent dispersion of perfluoroalkoxy resin powder in an amount of more than 50 parts by weight and less than 400 parts by weight of polyimide or polyimide amide per 100 parts by weight of perfluoroalkoxy resin powder. A wear-resistant paint characterized by having as its main component a mixture obtained by adding and mixing the same proportions.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8442378A JPS5829973B2 (en) | 1978-07-11 | 1978-07-11 | wear resistant paint |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8442378A JPS5829973B2 (en) | 1978-07-11 | 1978-07-11 | wear resistant paint |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5512135A JPS5512135A (en) | 1980-01-28 |
| JPS5829973B2 true JPS5829973B2 (en) | 1983-06-25 |
Family
ID=13830168
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP8442378A Expired JPS5829973B2 (en) | 1978-07-11 | 1978-07-11 | wear resistant paint |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5829973B2 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS587861B2 (en) * | 1980-04-14 | 1983-02-12 | 東京シリコ−ン株式会社 | piston |
| EP0604799A1 (en) * | 1992-12-29 | 1994-07-06 | International Business Machines Corporation | Coated filler and use thereof |
| US9029452B2 (en) * | 2010-05-27 | 2015-05-12 | E I Du Pont De Nemours And Company | Fluoropolymer additive for coatings |
| US9290596B2 (en) * | 2010-05-27 | 2016-03-22 | The Chemours Company Fc, Llc | Solvent-based fluoropolymer additives and their use in coating compositions |
-
1978
- 1978-07-11 JP JP8442378A patent/JPS5829973B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5512135A (en) | 1980-01-28 |
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