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Coatings fluorinated polymer

Glass fibre woven fabric Fluorine polymer coating... [Pg.42]

Ltd., UK) fluorinated polymer coating giving contact angles of pure water on such a surface on the order of ITO", with hysteresis <2°. [Pg.468]

Fluorinated polymer coatings. Fluorinated ethylene propylene (FEP) provides the best release. Perfluoro alkoxy alkane (PFA) gives release and wear resistance. PTFE provides best low friction. Ensure that the grade chosen is approved for food use. [Pg.201]

SiHcone resins provide coatings having outstanding heat resistance and exterior durabiHty. The cost is relatively high but for specialized appHcations these resins are important binders (64). Silicone-modified acryHc and polyester resins provide binders having intermediate durabiHty properties and cost. Fluorinated polymers also exhibit outstanding durabiHty properties. High cost, however, limits appHcabiHty. [Pg.341]

Chlorinated polyether used in temperatures up to 120°C in forms of coatings, extruded pipe and sheet linings is an intermediate between the low-cost commodity polymers such as PVC and polyethylene, and fluorinated polymers [61 ]. [Pg.117]

Modification of alkyd resins with high proportions of silicones considerably reduces rates of attack, but the most spectacular extension of life is shown by fluorinated polymers such as polyvinylidene fluoride where erosion rates can be reduced to 0 -1 /tm/year. If this level of durability can be achieved an initial coating, if firmly adherent and free from any breaks, may often be expected to maintain protection over a metal substrate for the likely life of the structure. The considerably increased first cost, as compared with more conventional coatings, has to be balanced against the probable saving in maintenance costs or consequences of failure. [Pg.619]

Micelle formation in standard organic solvents such as toluene or THF is very useful, since fluorinated polymers are usually not soluble in standard solvents micelle formation therefore enables processing of fluorinated products with classical technologies, e.g., for coating applications. [Pg.156]

This chapter examines the deposition of fluorinated polymers using plasma-assisted physical vapor deposition. Ultrathin coatings, between 20 and 5000 nm have been produced, using RF magnetron sputtering. The method of coating, fabrication, and deposition conditions are described. [Pg.313]

Conference Papers Fluorine in Coatings, Salford, September 28-30, 1994 Banks, R.E., Ed. Chemical and Polymer, Chemservc Ltd. and Paint Research Association Teddington. 1994. [Pg.85]

Much attention has been paid to the synthesis of fluorine-containing condensation polymers because of their unique properties (43) and different classes of polymers including polyethers, polyesters, polycarbonates, polyamides, polyurethanes, polyimides, polybenzimidazoles, and epoxy prepolymers containing pendent or backbone-incorporated bis-trifluoromethyl groups have been developed. These polymers exhibit promise as film formers, gas separation membranes, seals, soluble polymers, coatings, adhesives, and in other high temperature applications (103,104). Such polymers show increased solubility, glass-transition temperature, flame resistance, thermal stability, oxidation and environmental stability, decreased color, crystallinity, dielectric constant, and water absorption. [Pg.539]

If solid polymer objects are fluorinated or polymer particles much larger than 100 mesh are used, only surface conversion to fluorocarbon results. Penetration of fluorine and conversion of the hydrocarbon to fluorocarbon to depths of at least 0.1 mm is a result routinely obtained and this assures nearly complete conversion of finely powdered polymers. These fluorocarbon coatings appear to have a number of potentially useful applications ranging from increasing the thermal stability of the surface and increasing the resistance of polymer surfaces to solvents and corrosive chemicals, to improving friction and wear properties of polymer surfaces. It is also possible to fluorinate polymers and polymer surfaces partially to produce a number of unusual surface effects. The fluorination process can be used for the fluorination of natural rubber and other elastomeric surfaces to improve frictional characteristics and increase resistance to chemical attack. [Pg.177]

The great value of the unique characteristics of fluorinated polymers in the development of modern industries has ensured an increasing technological interest since the discovery of the first fluoropolymer, poly(chlorotrifluoro-ethylene) in 1934. Hence, their fields of applications are numerous paints and coatings [10] (for metals [11], wood and leather [12], stone and optical fibers [13, 14]), textile finishings [15], novel elastomers [5, 6, 8], high performance resins, membranes [16, 17], functional materials (for photoresists and optical fibers), biomaterials [18], and thermostable polymers for aerospace. [Pg.168]

The formation of coagulum is observed in all types of emulsion polymers (i) synthetic rubber latexes such as butadiene-styrene, acrylonitrile-butadiene, and butadiene-styrene-vinyl pyridine copolymers as well as polybutadiene, polychloroprene, and polyisoprene (ii) coatings latexes such as styrene-butadiene, acrylate ester, vinyl acetate, vinyl chloride, and ethylene copolymers (iii) plastisol resins such as polyvinyl chloride (iv) specialty latexes such as polyethylene, polytetrafluoroethylene, and other fluorinated polymers (v) inverse latexes of polyacrylamide and other water-soluble polymers prepared by inverse emulsion polymerization. There are no major latex classes produced by emulsion polymerization that are completely free of coagulum formation during or after polymerization. [Pg.201]

Benzyl alcohol is incompatible with methylcellulose and is only slowly sorbed by closures composed of natural rubber, neoprene, and butyl rubber closures, the resistance of which can be enhanced by coating with fluorinated polymers. ... [Pg.70]


See other pages where Coatings fluorinated polymer is mentioned: [Pg.484]    [Pg.45]    [Pg.484]    [Pg.45]    [Pg.299]    [Pg.462]    [Pg.364]    [Pg.872]    [Pg.226]    [Pg.112]    [Pg.313]    [Pg.389]    [Pg.112]    [Pg.313]    [Pg.402]    [Pg.473]    [Pg.154]    [Pg.59]    [Pg.232]    [Pg.150]    [Pg.161]    [Pg.30]    [Pg.28]    [Pg.155]    [Pg.12]    [Pg.593]    [Pg.353]    [Pg.286]    [Pg.232]    [Pg.233]    [Pg.262]    [Pg.283]   
See also in sourсe #XX -- [ Pg.117 ]




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