A general, mechanistic, kinetic model is presented to predict polymer micro
structure formation during processing. Applications of the model are presen
ted for three specific cases. The model represents polymer molecules as Kra
mers chains which may or may not have nucleated. Three forces (hydrodynamic
, Brownian, and intermolecular) that act on polymer molecules during proces
sing were considered, which resulted in the presentation of the model as a
diffusion equation. The input parameters account for the rheological and th
ermal history of the polymer melt, the specific type of polymer molecule, a
nd the initial morphology. The solution of the diffusion equation yields a
probability distribution function from which the transient and equilibrium
morphology can be determined. The three specific cases were chosen to illus
trate the versatility of the model and include: the extensional flow-induce
d growth of extended chain crystals; the orientation of stiff molecules in
solution undergoing shear flow well above the crystallization temperature;
and the formation of folded chain vs. extended chain crystals in an extensi
onal flow. Data are available for the first two cases and agree favorably w
ith the model predictions. (C) 1999 John Wiley & Sons, Inc.