Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Epoxy polymer coatings

Towns, J.K. Bao, J. Regnier, FB. Synthesis and evaluation of epoxy polymer coatings for the analysis of proteins by capillary zone electrophoresis. J. Chromatogr. 1992,599,721. [Pg.2175]

The sparing solubility of these multifunctional inhibitor compounds lend themselves more readily to incorporation into paints as slow-release corrosion protection. To avoid possible interference of rare earths elements with epoxy polymer coating systems, as has been observed, an encapsulation mechanism may be considered to successfully incorporate rare earth organic inhibitors into paint formulations. This would limit any detrimental interaction, while still allowing the release of an inhibitor as required. [Pg.133]

Kayaks are often made of a high-strength polymer coated with epoxy resin., --- ... [Pg.673]

The presence of redox catalysts in the electrode coatings is not essential in the c s cited alx)ve because the entrapped redox species are of sufficient quantity to provide redox conductivity. However, the presence of an additional redox catalyst may be useful to support redox conductivity or when specific chemical redox catalysis is used. An excellent example of the latter is an analytical electrode for the low level detection of alkylating agents using a vitamin 8,2 epoxy polymer on basal plane pyrolytic graphite The preconcentration step involves irreversible oxidative addition of R-X to the Co complex (see Scheme 8, Sect. 4.4). The detection by reductive voltammetry, in a two electron step, releases R that can be protonated in the medium. Simultaneously the original Co complex is restored and the electrode can be re-used. Reproducible relations between preconcentration times as well as R-X concentrations in the test solutions and voltammetric peak currents were established. The detection limit for methyl iodide is in the submicromolar range. [Pg.76]

Loss of Tin. The preparation and characterization of organ-otin-epoxy polymers have been reported earlier (3). In an effort to determine the loss of tin from these controlled release formulations, 0.5-mm thick coatings were kept immersed in 4% sodium chloride solution under conditions approximating Figure 2a. The concentration of TBTC1 in the aqueous phase was maintained low by continuously extracting it into hexane. Analysis of the coating at the end of 16 months revealed that not more than 2% tin was lost in any of the four cases studied. [Pg.177]

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]

Oligophenylethoxysiloxanes are used as modifiers for various polymers to improve their weather resistance and other technical characteristics, as well as to increase the heat resistance of coatings. E.g., PES-50 is used to modify polyethers, aciylic and epoxy polymers PES-80 is used to modify alkyd and urea-formaldehyde resins. Besides, PES-80 is used as an additive in paints and enamels (to improve their flow properties, gloss and colour), as well as in concrete mixes (to improve the water resistance and durability of concrete works). [Pg.214]

Many studies have used these methods for processing of both thermosetting and thermoplastic polymers. Y. Liao (53) dissolved epoxy in a well-dispersed, ultra-sonicated CNT suspension. The solvent was evaporated, and the epoxy was subsequently cured to form a nanocomposite in which the good CNT dispersion was achieved. Jin et al. (54) produced various types of polymer-coated and polymer-grafted MWNT solutions, in some cases evaporating the solvent and subsequently melt-mixing with another polymer. Yudasaka et al. (55) used a mixture of SWNTs and PMMA in monochlorobenzene (MCB) for dispersion, purification and subsequent spin-casting of the material. [Pg.398]

Epoxy seal coating was first applied as test patches in industrial plants in 1953. In 1957 epoxy polymer concrete was first used as a wearing course in the repair of popouts and spalled areas on the surfaces of various bridge decks in California (ACI, 1993). [Pg.60]

Epoxy polymers (including epoxy novolacs) have been designed to meet most of these requirements and are almost universally used in such encap-sulant applications. Epoxy polymers exhibit superior adhesion that in many cases eliminates the need for a barrier or junction coating. They have a low coefScient of thermal expansion low shrinkage and low injection velocity, which means that low transfer or injection pressures can be used. These polymers also possess excellent mechanical properties coupled with low moisture and gas permeability. Above all, they are cheap and readily available. Other transfer-molding materials used to a limited extent include silicones, phenolic materials, and even polyesters. Most molding formulations are highly filled (70-75%) with materials such as quartz, fused silica, short... [Pg.18]

Considering that x = 3.5-5 cm (Eq. [6.6]), the thickness of the epoxy-rubber coating 8 = 12-16 cm. This means that the sum of the thickness of the polymer coating layer and the height of the compressed concrete zone is 17-20 cm, which is approximately equal to the total height of the beam (20 cm). [Pg.206]

Tests show that the epoxy-rubber coating strength of reinforced concrete beams reduces deformability of the reinforced concrete beams in bending, especially before crack formation in concrete the most favorable results are obtained for beams with a polymer concrete layer on three sides. [Pg.214]

Many studies have appeared dealing with the properties of crosslinked polymer systems. These include adhesion of epoxy-acrylates onto tin-plate, adhesion of isocyanate and epoxy-resin coatings, adhesion of butadiene-acrylate rubbers onto metals, glass, and ceramics, adhesion of acrylic, thiol, and polyester resins to aluminium bodies, and the mechanical and physical properties of photo-crosslinkable poly(vinyl cinnamate), vinyl-divinyl copolymers,polythiols, acrylates, epoxies, and thiols,epoxy resins, polyesters on wood, ... [Pg.518]

Thicker epoxy-based coatings, highly flexibllized with amine-reactive nitrile liquid polymer, have been described by Mendelsohn (50) in which the flexibilizing hardener is comprised of an admixture of ATBN, fatty polyamide and boron trifluoride/amine complex. This coating ages well at 100°C and has excellent toughness/ flex with good abrasion and vibration absorption properties. [Pg.10]

The formation of a cross-linked polymer is exemplified by the reaction of epoxy polymers, which have been used traditionally as adhesives and coatings and, more recently, as the most common matrix in aerospace composite materials. Epoxies exist at ordinary temperatures as low-molecular-weight viscous liquids or prepolymers. The most widely used prepolymer is diglycidyl ether of bisphenol A (DGEBA), as shown below (15) ... [Pg.21]


See other pages where Epoxy polymer coatings is mentioned: [Pg.424]    [Pg.424]    [Pg.358]    [Pg.45]    [Pg.364]    [Pg.236]    [Pg.192]    [Pg.186]    [Pg.146]    [Pg.199]    [Pg.507]    [Pg.57]    [Pg.58]    [Pg.59]    [Pg.51]    [Pg.61]    [Pg.45]    [Pg.485]    [Pg.252]    [Pg.11]    [Pg.141]    [Pg.475]    [Pg.234]    [Pg.535]    [Pg.64]    [Pg.45]    [Pg.187]    [Pg.520]    [Pg.273]   
See also in sourсe #XX -- [ Pg.69 , Pg.73 ]




SEARCH



Coatings epoxy

Epoxy polymers

Epoxy-based polymer coatings

Polymer coatings

© 2024 chempedia.info