J. Dudowicz et al., Lattice model of living polymerization. II. Interplay between polymerization and phase stability, J CHEM PHYS, 112(2), 2000, pp. 1002-1010
Representative spinodal curves and polymerization lines for the equilibrium
polymerization of linear polymers in a solvent have been calculated using
a Flory-Huggins-type mean-field theory. The calculations are primarily rest
ricted to systems that polymerize upon cooling, but examples are also given
for systems that polymerize upon heating. In the former case, we find that
an increase in the magnitude of enthalpy of propagation \Delta h\ ("sticki
ng energy") leads to an elevation of the critical temperature T-c and to a
decrease of the critical composition phi(c) when \Delta h\ exceeds a critic
al value \Delta h(c)\. The shifts in the critical temperature and compositi
on, Delta T-c = T-c(Delta h) - T-c(Delta h = 0) and Delta phi(c) = phi(c)(D
elta h)-phi(c)(Delta h = 0), vary linearly with Delta h for \Delta h\>\Delt
a h(c)\ over a large range of sticking energies \Delta h\, so that Delta T-
c is proportional to Delta phi(c) for a sufficiently large sticking energy.
Variations in the phase boundaries with Delta h are also evaluated for sys
tems that polymerize upon heating, but the presence of multiple critical po
ints in this case renders a general description of these changes difficult.
The polymerization line is found to be independent of solvent quality (chi
interaction parameter) within the simple Flory-Huggins model, but the phas
e stability is strongly influenced by the magnitude of both chi and Delta h
. Similarities between living polymers and other types of associating polym
ers (thermally reversible gels, micelles) suggest that some of the thermody
namic consequences of particle association in these self-assembling systems
are insensitive to the detailed nature of the clustering process. Thus, ou
r results may have a much broader range of applicability than living polyme
r solutions (e.g., gelation in clay and other colloidal suspensions, polyel
ectrolyte solutions, cell aggregation, and self-organization of biologicall
y significant structures that exist at equilibrium). (C) 2000 American Inst
itute of Physics. [S0021-9606(00)50102-0].