Epoxy resins are normally used in what is called an epoxy-resin system. This system consists of the epoxy resin and a hardener, and reactive diluent or other additives, such as fillers, modifiers, pigments and reinforcements.
Epoxy ResinsEpoxy resins contain at least two cyclic three-membered ring structures containing oxygen, called epoxy groups, oxirane or epoxide groups, in their molecules. The term "epoxy resin" may refer to the resins in both the uncured thermoplastic and cured thermoset state. The uncured resins can be cross linked through the use of a variety of curing agents or hardeners to form cured plastics with insoluble three-dimensional structures.The reaction products of epichlorohydrin [CAS 106-89-8] and bisphenol A [CAS 80-05-7] resulted in the first commercial epoxy resins, which are generally mixtures of monomeric diglycidyl ether of bisphenol A (DGEBA), with a molecular weight (MW) of 340 Da, and oligomers with a higher MW (Fig. 1). Apart from the DGEBA and higher oligomers, side reactions result in the formation of low levels of impurities.DGEBA epoxy resins with a low average MW of 350-400 Da are liquids with a relatively high viscosity, and they contain up to and more than 90% monomeric DGEBA. Resins with a high average MW of over than 900 Da are solids (Muskopf and McCollister 1987), but may contain more than 15% DGEBA (Henriks-Eckerman and Laijoki 1986b).DGEBA epoxy resins account for about 75% of the epoxy resins used worldwide. Non-DGEBA epoxy resins possess special properties that have made them competitive with DGEBA resins for certain applications. A list of chemical names and CAS numbers of available epoxy resins is given in Table 1. The resin or mixture of resins chosen for a particular application depends on the desired balance of properties. For example, brominated epoxy resins are semisolids and resistant to ignition, and epoxy resins based on diglycidyl ether of bisphenol F (DGEBF) are less viscous and exhibit better chemical resistance than DGEBA epoxy resins (Ponten and Bruze 2001). Triglycidyl isocyanurate (TGIC) is one of the non-DGE-32 L. Kanerva et al. (eds.), Condensed Handbook of Occupational Dermatology