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Flexibility Improvement of Poly(L‐lactide) by Reactive Blending With Poly(ether urethane) Containing Poly(ethylene glycol) Blocks
Authors:Lidong Feng  Xinchao Bian  Yi Cui  Zhiming Chen  Gao Li  Xuesi Chen
Affiliation:1. Key Laboratory of Polymer Ecomaterials, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, Jilin, China;2. Zhejiang Hisun Biomaterials Co., Ltd, Taizhou 31800, Zhejing, China;3. Graduate University of Chinese Academy of Sciences, Beijing 100039, China
Abstract:Poly(L ‐lactide) (PLLA) is melt blended with poly(ether urethane) (PEU) based on poly(ethylene glycol) blocks via a chain‐extension reaction by diisocyanate as a chain extender to improve its flexibility without sacrificing comprehensive performance. The elongation at break of the blends with triphenyl phosphate (TPP) as a reactive blending additive is much higher than that without TPP by physical blending. When 10 wt% PEU is blended, the former elongation reaches to 298%, while the latter one is only approximately 20%. The reactive blending forms a PLLA–PEU block copolymer, thus improving their compatibility. When the weight‐average molecular weight (M w) of PEUs is 18–90 kg mol?1, the effect of M w is very little on tensile properties of blends. The rheological properties of the blends are modified through the content and molecular weight of PEU. The complex viscosity (η*) of PLLA/PEU blends increases with increasing M w of PEU. The η* of the PLLA blend containing 5 wt% PEU in M w 73 kg mol?1 is higher than that of neat PLLA. The water absorption of the PLLA/PEU blends enhances because of the hydrophilicity of PEUs versus neat PLLA.
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Keywords:microstructure  poly(ether urethane)  poly(L‐lactide)  reactive processing  toughness
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