Polymer coagulation is studied by a Monte Carlo diffusion model in whi
ch coagulant, solvent, and polymer particles move on nearest neighbor
lattice sites according to the change in local interaction energy. Our
approach has allowed, for the first time, to describe the coagulation
process beyond the initial quench state and to reproduce the wide var
iety of different polymer structures that can be obtained, ranging fro
m dust- to finger- to spongelike morphologies. We show that these morp
hologies are fully controlled by the coagulation rate which is itself
strongly dependent on the degree of miscibility between solvent and co
agulant. (C) 1995 John Wiley and Sons, Inc.