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Preparation and characterization of biodegradable poly(lactic acid)‐ block‐poly(ε‐caprolactone) multiblock copolymer
Authors:Tao Yu  Jie Ren  Shuying Gu  Ming Yang
Institution:1. Institute of Nano‐ and Bio‐polymeric Materials, School of Material Science and Engineering, Tongji University, 1239 Siping Road, Shanghai 200092, P R China;2. Key Laboratory of Advanced Civil Engineering Materials, Ministry of Education, Tongji University, 1239 Siping Road, Shanghai 200092, P R China
Abstract:Biodegradable copolymers of poly(lactic acid)‐block‐poly(ε‐caprolactone) (PLA‐b‐PCL) were successfully prepared by two steps. In the first step, lactic acid monomer is oligomerized to low molecular weight prepolymer and copolymerized with the (ε‐caprolactone) diol to prepolymer, and then the molecular weight is raised by joining prepolymer chains together using 1,6‐hexamethylene diisocyanate (HDI) as the chain extender. The polymer was carefully characterized by using 1H‐NMR analysis, gel permeation chromatography (GPC), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and Fourier transform infrared spectroscopy (FTIR). The results of 1H‐NMR and TGA indicate PLA‐b‐PCL prepolymer with number average molecular weights (Mn) of 4000–6000 were obtained. When PCL‐diols are 10 wt%, copolymer is better for chain extension reaction to obtain the polymer with high molecular weight. After chain extension, the weight average molecular weight can reach 250,000 g/mol, as determined by GPC, when the molar ratio of –NCO to –OH was 3:1. DSC curve showed that the degree of crystallization of PLA–PCL copolymer was low, even became amorphous after chain extended reaction. The product exhibits superior mechanical properties with elongation at break above 297% that is much higher than that of PLA chain extended products. Copyright © 2009 John Wiley & Sons, Ltd.
Keywords:poly(lactic acid)  poly(ε  ‐caprolactone) diols  polycondensation  chain extension  copolymer
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