Journal
POLYMER
Volume 45, Issue 24, Pages 8231-8237Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.polymer.2004.08.076
Keywords
poly(L-lactide); blends; reactive compatibilization
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This paper describes a new reactive blending approach to improve the compatibility Of poly(L-lactide) (PLLA) and poly(epsilon-caprolacton) (PCL). For this purpose, the ring-opening polymerization of L-lactide (LLA) was carried out in the presence of PCL-OH (OH groups on one end). The P(CL-b-LLA) block copolymers were in situ formed during polymerization, and as a result, PLLA/P(CL-b-LLA) blends were obtained. The characterization of GPC and H-1 NMR verified the synthesis of PLLA/P(CL-b-LLA) blends. Furthermore, the C-13 NMR spectroscopy showed that no transesterification reaction occurred to a significant extent during LLA polymerization process. The in situ formed P(CL-b-LLA) compatibilizes the phase separated structure of PCL domains in PLLA matrix. The size of PCL domains in PLLA matrix became much smaller than that in a solution blended sample. The average sizes of PCL domains are controllable in the level of sub-micron scale. (C) 2004 Elsevier Ltd. All rights reserved.
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