Graft copolymerization of methacrylic acid (MAA) onto starch using a p
otassium persulfate/sodium thiosulfate redox initiation system was inv
estigated. Emphasis was placed on the promotion of graft formation whi
le minimizing homopolymerization. This could be achieved through a tho
rough investigation into the major factors affecting the polymerizatio
n reaction such as the state of the starch, redox ratio of the initiat
or, monomer and initiator concentrations, time and temperature of poly
merization, and material-to-liquor ratio. The results obtained imply t
hat the magnitude of the polymer yield including total conversion, gra
ft yield, and homopolymer are determined by these factors. The yield i
s favored under the influence of higher temperature, longer time, shor
t liquor, and increased monomer and initiator concentrations. A poly(M
AA)-starch graft copolymer is the main product of the polymerization r
eactions only when starch was preswelled (through cooking prior to gra
fting). Moreover, this grafted product could be precipitated by more d
ilution with water and easily separated by filtration. Hence, the resu
lts of the current work formed the basis of a novel method for the syn
thesis of poly(MAA)-starch graft copolymers. The mechanisms involved i
n the synthesis are reported. (C) 1998 John Wiley & Sons, Inc.