Some features of radical ternary copolymerization of maleic anhydride (MA)-
styrene (St)-acrylonitrile (AN) and n-butyl methacrylate (BMA)St-AN accepto
r-donor-acceptor monomer systems have been revealed. The terpolymer composi
tions and kinetics of copolymerizations were studied in the initial and hig
h conversion stages. The considerable divergence in the copolymer compositi
ons was observed when a strong acceptor MA monomer was substituted with BMA
having comparatively low acceptor character in the ternary system studied.
Obtained results show that terpolymerization proceeded mainly through "com
plex" mechanism in the state of near binary copolymerization of St...MA (or
BMA) and AN...St complexes only in the chosen ratios of complexed monomers
. The terpolymers synthesized have high thermal stabilities (295-325 degree
s C), which is explained by possible intermolecular fragmentation of AN-uni
ts through cyclization and crosslinking reactions during thermotreatment in
the isothermal heating conditions. (C) 2000 John Wiley & Sons, Inc.