The ultrasonic degradation of poly(vinyl acetate) was carried out in six di
fferent solvents and two mixtures of solvents. The evolution of molecular w
eight distribution (MWD) with time was determined with gel permeation chrom
atography. The observed MWDs were analyzed by continuous distribution kinet
ics. A stoichiometric kernel that accounts for preferential mid-point break
age of the polymer chains was used. The degradation rate coefficient of the
polymer in each solvent was determined from the model. The variations of r
ate coefficients were correlated with vapor pressure of the solvent, the Fl
ory-Huggins polymer-solvent interaction parameter and the kinematic viscosi
ty of the solution. A lower saturation vapor pressure resulted in higher de
gradation rates of the polymer. The degradation rate increased with increas
ing kinematic viscosity. (C) 2001 Elsevier Science Ltd. All rights reserved
.