Abstract
The synthesis of graft copolymers by the grafting ‘‘onto'' process in the molten state was described. Functional oligomers obtained by telomerization or by ATRP were reacted onto maleic anhydride grafted polypropylene (PP-g-MAH) and poly(ethylene-ter-maleic anhydride-ter-methyl acrylate) (P(E-ter-MAHter- MeA)) to obtain PP-g-PMMA and P(E-ter-MAH-ter-MeA)-g-PMMA graft copolymers, respectively. The grafting of different mono-functional oligomers bearing hydroxyl, aliphatic amine or aromatic amine functions was investigated at 180 C and at 200 C. The grafting efficiency was very low in the case of hydroxyl-terminated PMMA, while the amine-terminated PMMA led to high yields. In the last part, PP-g- PMMA and P(E-ter-MAH-ter-MeA)-g-PMMA graft copolymers were synthesized by the reaction of aliphatic amine functional PMMA oligomers onto PP-g-MAH and P(E-ter-MAH-ter-MeA), respectively. The influence of the molecular weight of PMMA oligomers was investigated and showed that he grafting efficiency slightly decreases with the increasing molecular weight. However, this process allows the synthesis of PP-g-PMMA graft copolymers containing 6–45 wt% of PMMA side chains. The microstructure of the nanostructured PP-g-PMMA and P(E-ter-MAH-ter-MeA)-g-PMMA graft copolymers was investigated by TEM and SEM. This was established that the addition of PP-g-PMMA in PP/PMMA binary blends allows to control their morphologies and stabilities.