Article ID Journal Published Year Pages File Type
1398580 European Polymer Journal 2007 8 Pages PDF
Abstract

Microstructural studies of Poly(vinyl alcohol-co-vinyl acetate)-g-polycaprolactone (PVA-Ac)-g-(PCL) were realized principally using NMR. Initial PVA-Ac has a rather blocky structure with an average sequence length of PVA units equal to 12.5. During the synthesis of the studied (PVA-Ac)-g-(PCL), alcoholysis and transesterification reactions led to PCL grafts with acetate end groups. These reactions typically concern 2–5.5% of the total acetate groups. The influence of the local tacticity on the alcohol triad reactivity was evidenced and explained the incomplete functionalization of the PVA-Ac hydroxyl groups. Alcoholysis reactions were also evidenced but with a very low rate in the tested conditions. Caprolactone homopolymerization was not observed. Other properties of the final synthesized copolymers were also presented. Crystallinity totally disappeared in the (PVA-Ac)-g-(PCL). The glass transition temperature was perfectly adjustable by the Fox law without significant modification of the viscoelastic properties characterized by dynamic rheology.

Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
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