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THERMOSETS


                             3.28                        CHAPTER 3


                                      TABLE 3.25  Vinyl Ester Formulations
                                         Ingredients  Standard  Acid-modified  Rubber-modified
                                       Epoxy resin  1032       1032        609

                                       Methacrylic acid  195    171         76
                                       Maleic acid              32
                                       CTBN                                228
                                       Styrene       970        970
                                       Hydroquinone    0.45      0.45        0.17


                                         TABLE 3.26  Vinyl Ester Properties

                                                                   Cast  Reinforced
                                          Tensile modulus, kpsi    460     1590
                                          Tensile strength, kpsi    11       24
                                          Ultimate elongation, %    6        1
                                          Impact strength, fpi       0.4     28
                                          Heat deflection temperatures, °C  102  260

                             lecular flexibility, increasing elongation and impact strength, at the expense of modulus,
                             strength, and heat deflection temperature. Conversely, novolac epoxy gives much higher
                             cross-linking, increasing modulus, strength, and heat deflection temperature (148°C) at the
                             expense of elongation and impact strength. Acrylic acid is used instead of methacrylic acid
                             to produce vinyl esters for UV-cured coatings. Tetrabromobisphenol A builds flame-retar-
                             dance into the polymer. Use of some maleic acid in place of methacrylic acid builds some
                             acid groups onto the ends of the vinyl ester molecule; this permits MgO gelation for sheet
                             molding compound. Use of some carboxy-terminated butadiene-nitrile oligomer (CTBN)
                             in place of methacrylic acid builds nitrile rubber structure into the polymer, increasing im-
                             pact strength. And the –OH groups of the epoxy resin can be cross-linked by diisocyanate
                             to build some polyurethane structure and properties into the cured polymer. A number of
                             these variations are available commercially.

                               3.1.3.2.4 Processing. Reinforcement, shaping, and cure of vinyl esters is quite simi-
                             lar to processes described earlier for polyesters (Sec. 3.1.3.1.3).
                             3.1.3.3 Allyls. The allyl group CH =CH-CH - is less reactive than conventional vinyl
                                                               2
                                                        2
                             monomers CH =CH-X, which offers both advantages and disadvantages. Several allyl
                                        2
                             monomers have found unique applications in plastics: diallyl phthalate, triallyl cyanurate,
                             and diethylene glycol bis(allyl carbonate).
                               3.1.3.3.1 Diallyl phthalate. Glass-fiber-reinforced diallyl phthalate (DAP) is supe-
                             rior to unsaturated polyesters in shelf life and especially resistance to heat and moisture





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