In this study, we propose the dispersive ("long-tail") kinetics concept as
a possible candidate for elucidating qualitatively some experimentally noti
ced departures from the constancy in a polymer crystal growth rate against
time behavior. It turns out to be a consequence of some more detailed consi
deration of the polymer (colloid) mass-dependent diffusion coefficient, whi
ch is consistent with a microscopic picture of the entire crystallization p
henomenon, that is basically a nucleation-and-growth process. The phenomeno
n under consideration appears to be solution controlled, with a dominant ro
le of solute or solute-solvent interactions. The random adsorption of macro
molecules cannot drastically change this picture. (C) 2000 Elsevier Science
B.V. All rights reserved.