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DGEBA—See Diglycidyl ether

DGEBA. See Bisphenol A, diglycidyl ether. Bisphenol A, diglycidyl ether (DGEBA) [1675-54-3]... [Pg.291]

Dezincing, lead refining by, 14 754-755 DGEBA-aromatic polyamine adduct system, 10 416, 417. See also Diglycidyl ether of bisphenol A (DGEBA)... [Pg.257]

The prepolymer stage in most cases is DGEBA (diglycidyl ether bisphenol A) (see Fig. 15.2a). [Pg.661]

Some of the first commercial conductive epoxy adhesives were simply based on silver powder dispersed in a liquid epoxy resin [e.g., diglycidyl ether of bisphenol A (DGEBA)] with an aliphatic amine [e.g., triethylene tetramine (TETA)] as a curing agent. Although capable of room-temperature cure, commercialization of this type of system was hampered by severe mix ratio disparity (typically, 50 1 by weight), problematic mixing due to viscosity differences, short pot life, and safety concerns. See Table 3 for typical properties of this type of formulation. [Pg.849]

Table 10.6 Comparison of some stoichiometric, fully cured epoxide-amine networks Tg, glass transition temperature [Ar], aromatic group concentration F, flex parameter (see text) n, crosslink density and [OH], hydroxyl concentration. Note DGEBD = diglycidyl ether of butane diol DGEBA = diglycidyl ether of bisphenol A (i = degree of polymerization) and TGAP = triglycidyl derivative of p-aminophenol ... Table 10.6 Comparison of some stoichiometric, fully cured epoxide-amine networks Tg, glass transition temperature [Ar], aromatic group concentration F, flex parameter (see text) n, crosslink density and [OH], hydroxyl concentration. Note DGEBD = diglycidyl ether of butane diol DGEBA = diglycidyl ether of bisphenol A (i = degree of polymerization) and TGAP = triglycidyl derivative of p-aminophenol ...
The best-known vinyl ester is made by reacting the diglycidyl ether of bisphenol-A (DGEBA see Section 16.4.2) with a monocarboxylic unsaturated acid such as methacrylic or acrylic acid see Scheme 16.24. This addition reaction occurs at a temperature of 120-140°C. The vinyl ester urethanes, on the other hand, are synthesized from a low molecular weight (unsaturated) polyester diol, mostly based on bisphenol-A, a diisocyanate, and a hydroxyalkyl (meth)acrylate (see also Schemes 16.30 and 16.31, Section 16.8.3.3). As for standard UP resins, the most commonly used reactive solvent is styrene. Both types of products have only a few ester linkages (which are the points of greatest vulnerability to chemical attack) in the mole-... [Pg.873]


See other pages where DGEBA—See Diglycidyl ether is mentioned: [Pg.531]    [Pg.269]    [Pg.142]    [Pg.312]    [Pg.74]    [Pg.158]    [Pg.24]    [Pg.1195]    [Pg.142]    [Pg.2236]    [Pg.178]    [Pg.2597]   


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DGEBA ether

Diglycidyl ether

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