The heterogeneous nucleation of polypropylene homopolymer and disconti
nuous glass fibre (critical fibre length, L(c) greater-than-or-equal-t
o 3 mm) reinforced polypropylene was performed by using sodium benzoat
e as the nucleating agent. Isothermal crystallization of the compressi
on-moulded nucleated polypropylene, non-nucleated polypropylene, nucle
ated composite and non-nucleated composite was carried out over a temp
erature range of 370-398 K. Comparison of the shift in the bulk crysta
llization peak temperatures, as well as the rate of isothermal crystal
lization of the samples, showed that the incorporation of the nucleati
ng agent resulted in a significant improvement in the crystallization
of the polypropylene homopolymer. The short glass fibres nucleated the
polypropylene matrix to the extent that the crystallization and morph
ology of the matrix differ appreciably from those of the homopolymer.
Detailed Avrami kinetic analysis was carried out at 390 K for the samp
les and values of the Avrami constants K and n, ranging from 2.3 x 10(
-5) to 2.4 x 10(-3) and 2.01 to 1.66 for the polypropylene homopolymer
to the nucleated composite, respectively, were obtained. Optical micr
oscopic analysis showed spherulitic crystallization for the homopolyme
r, crystallitic crystallization for the nucleated polypropylene, and m
ixed crystallitic and axialitic crystallization for the discontinuous
composite.