Abstract
An investigation was carried out on the curing reaction of a liquid crystalline epoxy monomer, N, N '-bis[4-(2,3-epoxypropoxy)benzylydene]-1,4-phenylenediamine, with an aromatic diamine, sulfanilamide (SAA). The complexity of the curing involves the competition of the reactivities of a primary amine and a secondary amine and also a difference in reactivity of the amine and the amide functional groups from SAA. These phenomena have been studied by differential scanning calorimetry (DSC) under isothermal and non-isothermal conditions. The stability of the mesophase during cross-linking reaction was investigated by polarized optical microscopy (POM) and X-ray diffraction (WAXS).
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