P. Punchaipetch, N.A. D'Souza, W. Brostow, A. E. Akinay, Jonathan Reed

Department of Materials Science, University of North Texas, Denton, TX 76203-5310, USA

ABSTRACT

Curing reactions of diglycidyl ether of bisphenol F (DGEBP-F) and pre-catalyzed methyltetrahydrophtalic anhydride (MTHPA) with benzyl triethyl ammonium chloride (BTEAC) were studied and effects of glass fibers evaluated. The influence on the kinetics of glass fibers and a hybrid blend of maleated polypropylene + glass fibers is studied. Isothermal and dynamic kinetic parameters are determined by differential scanning calorimetry (DSC). Applicability of the autocatalytic model is investigated. The model serves well in the range of degrees of conversion between 25 and 80%. At high conversion rates the diffusion control becomes apparent. Glass fibers accelerate the curing, shortening the time needed to reach the maximum reaction rate; this is reflected in lower activation energies for curing in comparison to the neat resin. The effects observed can be explained by a reaction between the amine group present on the fiber surfaces and the epoxy glycidyl groups. The result of both isothermal and non-isothermal curing of resin + glass fibers commingled with polypropylene are close to those for the neat resin. The reinforcement increases the elastic modulus 12 times, the tensile strength 2 times, and the impact strength 285 times. The glass fibers + commingled polypropylene reinforcement provides comparable mechanical properties as glass fibers alone when normalized with respect to the density fraction of the fibers.