Abstract

Graft copolymers of poly(vinyl acetate)-graft-poly(l-lactide) (PVAc-g-PLLA) comprising biodegradable graft chains were synthesized through the ring-opening polymerization of lactide. The partially hydrolyzed PVAcs, that is, poly(vinyl acetate-co-alcohol) [P(VAc-co-VA)], having degrees of hydrolysis of 5.2 and 9.6% were used as the macromolecular multifunctional initiator. The chemical structure and crystallization behavior of PVAc-g-PLLA were investigated. Graft length and density in PVAc-g-PLLA can be controlled by varying the lactide/P(VAc-co-VA) feed ratio and the degree of hydrolysis of P(VAc-co-VA). Graft length of PLLA chain and molecular weight of graft copolymer increased with the lactide/P(VAc-co-VA) feed ratio. The graft length and density of PVAc-g-PLLA had a significant effect on its crystallization behavior. The crystallization and spherulitic growth of PVAc-g-PLLA were decelerated with decreasing the length of PLLA graft chain or increasing the graft density, due to the branching effects and...

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call