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Epoxy number

Let us consider the elastic properties of epoxy polymer thin films on substrates with various surface energies. The elasticity of the boundary layers and its contribution to the elasticity of the film on the substrate were assessed by the dependence of the modulus of elasticity on the thickness of the polymeric coating formed on high-energy (aluminum) and low-energy (polyethylene terephthalate) surfaces. ED-20 epoxy resin (molecular weight 420, epoxy number 21.6) was selected... [Pg.18]

Epoxy number n. The number of gram-equivalents of epoxy groups per 100 g of polymer, equal to 1/100 of the reciprocal of the epoxides equivalent. [Pg.364]

A large number of polycyclic aromatic hydrocarbons are known Many have been synthesized m the laboratory and several of the others are products of com bustion Benzo[a]pyrene for example is present m tobacco smoke contaminates food cooked on barbecue grills and collects m the soot of chimneys Benzo[a]pyrene is a carcinogen (a cancer causing substance) It is converted m the liver to an epoxy diol that can induce mutations leading to the uncontrolled growth of certain cells... [Pg.435]

Because of the special stabiHty of the hexafluoroarsenate ion, there are a number of appHcations of hexafluoroarsenates. For example, onium hexafluoroarsenates (33) have been described as photoinitiators in the hardening of epoxy resins (qv). Lithium hexafluoroarsenate [29935-35-1] has been used as an electrolyte in lithium batteries (qv). Hexafluoroarsenates, especially alkaH and alkaline-earth metal salts or substituted ammonium salts, have been reported (34) to be effective as herbicides (qv). Potassium hexafluoroarsenate [17029-22-0] has been reported (35) to be particularly effective against prickly pear. However, environmental and regulatory concerns have severely limited these appHcations. [Pg.153]

Miscellaneous. Flame-resistant cross-linked polyethylene can be made with a number of fluoroborates and antimony oxide. This self-extinguishing material may contain the fluoroborates of NH, Na", K", Ca ", Mg ", Sr ", or Ba " in amounts of 4—20% (76). Magnesium fluoroborate cataly2es the epoxy treatment of cotton fabrics for permanent-press finishes (77) (see Textiles). [Pg.167]

Beckman Elutriation Method. The Beckman elutriation method uses a chamber designed so that the centrifugal effect of the radial inward fluid flow is constant (Fig. 3). The separation chambers are made of transparent epoxy resin which faciUtates observation of the movements of the cell boundary in strobe light illumination. This enables detection of the radius at which the cells are separating. When a mixture of cells, eg, mononuclear white cells, enters the chamber, separation can be achieved by fine tuning centrifuge speed and inward fluid flow to the specific cell group. This is a laboratory method suitable for relatively small numbers of cells. Chambers are available in sizes to handle 2-3 x 10 , 1 2 x 10 , and 1 x 10 ° cells. The Beckman chambers can be appHed to collect mononuclear cells from bone marrow aspirates. [Pg.522]

Cost bilizers. The variety of known costabiHzers for the mixed metal stabilizers is a very long listing. There are, however, a relatively small number of commercially used costabiHzers. Some of these additives can also be added by the PVC compounder or processor ia addition to the stabilizer package to further enhance the desired performance characteristics. The epoxy compounds and phenoHc antioxidants are among the most commonly used costabiHzers with the mixed metal stabilizers. [Pg.550]

The rate of stripping or the stripabiUty on cataly2ed urethane and epoxy resin finishes can be increased by adding formic acid, acetic acid, and phenol. Sodium hydroxide, potassium hydroxide, and trisodium phosphate [10101-89-0] may be added to the formula to increase the stripabiUty on enamel and latex paints. Other activators include oleic acid [112-80-17, trichloroacetic acid [76-85-9], ammonia, triethanolamine [102-71-6], and monoethyl amine. Methylene chloride-type removers are unique in their abiUty to accept cosolvents and activators that allow the solution to be neutral, alkaline, or acidic. This abihty gready expands the number of coatings that can be removed with methylene chloride removers. [Pg.551]

Benzene, toluene, and xylene are made mosdy from catalytic reforming of naphthas with units similar to those already discussed. As a gross mixture, these aromatics are the backbone of gasoline blending for high octane numbers. However, there are many chemicals derived from these same aromatics thus many aromatic petrochemicals have their beginning by selective extraction from naphtha or gas—oil reformate. Benzene and cyclohexane are responsible for products such as nylon and polyester fibers, polystyrene, epoxy resins (qv), phenolic resins (qv), and polyurethanes (see Fibers Styrene plastics Urethane POLYiffiRs). [Pg.216]

The number of ethylene oxide units added to the phenoxide depends on the apphcation of the ethoxylate. This chemistry is closely related to the reaction between an alkylphenol and epichlorohyddn which is used ia epoxy resias (qv). [Pg.60]

Wet chemical methods determining titratable amine ate reported for products entering urethane (amine number as meq/g) or epoxy (AHEW = amine hydrogen equivalent weight) trade appHcations. For secondary amines /V-nitrosamine contaminants are reportable down to ppb using Thermoelectron Corporation thermal energy analy2er techniques. [Pg.212]

A large number of fibers ate cut to length, and potted in epoxy resin at each end (see Embedding). The fiber bundle is shrouded in a cylinder which aids in permeate collection, reduces airborne contarnination, and allows back pressing of the membrane. HoUow-fiber membranes (qv) have also found use in ultrafilttation. [Pg.303]

Tertiary bismuthines appear to have a number of uses in synthetic organic chemistry (32), eg, they promote the formation of 1,1,2-trisubstituted cyclopropanes by the iateraction of electron-deficient olefins and dialkyl dibromomalonates (100). They have also been employed for the preparation of thin films (qv) of superconducting bismuth strontium calcium copper oxide (101), as cocatalysts for the polymerization of alkynes (102), as inhibitors of the flammabihty of epoxy resins (103), and for a number of other industrial purposes. [Pg.131]

The energy required to initiate an explosion and the maximum explosive pressure developed by a number of polyester—epoxy powder coatings has been studied in some detail (89). The variables studied included composition, level and type of pigmentation, particle size, and concentration in air. The lowest MEG for unfilled and unpigmented powders was 33—35 g/m. ... [Pg.326]

Fig. 5. Interlaminar fracture toughness, for a number of thermosetting and thermoplastic composites (36,37). Open white bars represent glass-fiber composites shaded bars are for carbon fibers. The materials are A, polyester (unidirectional) B, vinyl ester (CSM = chopped strand mat) C, epoxy (R/BR1424) D, epoxy (T300/914) E, PPS F, PES and G, PEEK. To convert J/m to fdbf/in. multiply by 2100. Fig. 5. Interlaminar fracture toughness, for a number of thermosetting and thermoplastic composites (36,37). Open white bars represent glass-fiber composites shaded bars are for carbon fibers. The materials are A, polyester (unidirectional) B, vinyl ester (CSM = chopped strand mat) C, epoxy (R/BR1424) D, epoxy (T300/914) E, PPS F, PES and G, PEEK. To convert J/m to fdbf/in. multiply by 2100.
A number of amorphous thermoplastics are presently employed as matrices in long fiber composites, including polyethersulfone (PES), polysulfone (PSU), and polyetherimide (PEI). AH offer superior resistance to impact loading and higher interlaminar fracture toughnesses than do most epoxies. However, the amorphous nature of such polymers results in a lower solvent resistance, clearly a limitation if composites based on such polymers are to be used in aggressive environments. [Pg.8]

A number of polymeric coatings, primarily polyimides, epoxies, and sHicones, are used as adhesives and ia other aspects of packagiag, as well as for final eacapsulatioa and protection of the iategrated circuit. [Pg.126]

Gel-permeation chromatography studies of epoxy resins prepared by the taffy process shown n values = 0, 1, 2, 3, etc, whereas only even-numbered repeat units are observed for resins prepared by the advancement process. This is a consequence of adding a difunctional phenol to a diglycidyl ether derivative of a difunctional phenol in the polymer-forming step. [Pg.367]

A number of cement materials are used with brick. Standard are phenolic and furan resins, polyesters, sulfur, silicate, and epoxy-based materials. Carbon-filled polyesters and furanes are good against nonoxidizing acids, salts, and solvents. Silica-filled resins should not be used against hydrofluoric or fluosihcic acids. Sulfur-based cements are limited to 93°C (200°F), while resins can be used to about 180°C (350°F). The sodium silicate-based cements are good against acids to 400°C (750°F). [Pg.2453]

Unless great care is taken in control of phenol/acetone ratios, reaction conditions and the use of catalysts, a number of undesirable by-products may be obtained such as the o-,p- and o-,o- isomers of bis-phenol A and certain chroman-type structures. Although tolerable when the bis-phenol A is used in epoxy resins, these have adverse effects on both physical properties and the colour of polycarbonate resins. [Pg.558]

The number of epoxy groups per molecule will vary but for modified soya bean oils there are an average of about four whereas there are about six for epoxidised linseed oils. [Pg.767]

Using a method suggested by Saint-Flour and Papirer [100], Schultz and Lavielle obtained A// -values for the interaction of several vapors of differing donor numbers and acceptor numbers with various treated and untreated carbon fibers used in the preparation of carbon fiber-epoxy matrix composites. was expressed as ... [Pg.42]


See other pages where Epoxy number is mentioned: [Pg.299]    [Pg.327]    [Pg.327]    [Pg.321]    [Pg.321]    [Pg.299]    [Pg.327]    [Pg.327]    [Pg.321]    [Pg.321]    [Pg.38]    [Pg.6]    [Pg.495]    [Pg.335]    [Pg.45]    [Pg.361]    [Pg.35]    [Pg.204]    [Pg.321]    [Pg.9]    [Pg.20]    [Pg.49]    [Pg.262]    [Pg.452]    [Pg.745]    [Pg.769]    [Pg.28]    [Pg.158]    [Pg.375]    [Pg.427]   
See also in sourсe #XX -- [ Pg.327 ]

See also in sourсe #XX -- [ Pg.321 ]




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