Optimization of controlled ring-opening polymerization of l-lactide to hydroxyl terminated polylactides using zinc acetate catalyst

Abstract

Hydroxyl terminated polylactide polymers with number of average molecular weights (M n ) varying from 1625 to 3459 g mol−1 were synthesized by ring opening bulk polymerization of lactide in the presence of zinc acetate being a potent catalyst. The use of 1,4 butanediol (BDO) initiator leads to hydroxyl terminated polylactides, thus excellent precursors for shape-memory biodegradable polyurethanes. Different reaction conditions employed for the synthesis of hydroxyl terminated polylactide polymers via activated monomer mechanism may result in differences in M n , percentage mass conversion and percentage degree of crystallinity (%χ c ) of the product. Influence of process parameters, i.e. catalyst concentration, initiator concentration, reaction temperature and time on characteristics of hydroxyl terminated polylactides was studied. These polymers were characterized by Nuclear Magnetic Resonance (1H-NMR) spectroscopy, Fourier transforms infrared (FTIR) spectroscopy, gel permeation chromatography (GPC) and X-ray diffraction (XRD) techniques. FTIR and 1H-NMR confirmed the formation of hydroxyl terminated polylactides. M n was determined by 1H-NMR, GPC and end group analysis. %χ c was calculated from XRD spectra. Maximum mass conversion, M n and %χ c were observed at 5 mol% SnOct2 and 5 mol% BDO concentration. At optimum temperature of 145 °C, these characteristics improved linearly with polymerization time up to 6 h and declined thereafter.