Effect of poly(ε-caprolactone-co-L-lactide) on thermal and functional properties of poly(L-lactide)

被引:14
作者
Qin, Yuyue [1 ]
Liu, Shiqi [1 ]
Zhang, Yingjie [2 ]
Yuan, Mingwei [1 ]
Li, Hongli [1 ]
Yuan, Minglong [1 ]
机构
[1] Yunnan Univ Nationalities, Engn Res Ctr Biopolymer Funct Mat Yunnan, Kunming 650500, Peoples R China
[2] Kunming Univ Sci & Technol, Kunming 650550, Peoples R China
基金
中国国家自然科学基金;
关键词
Poly(L-lactide); Star-shaped; poly(epsilon-caprolactone-co-L-lactide); Blend; Thermal properties; Mechanical properties; POLY(LACTIC ACID); MECHANICAL-PROPERTIES; MOLECULAR-WEIGHT; BLENDS; FILMS; PLA; PLASTICIZATION; DEGRADATION; NANOFIBERS; COPOLYMERS;
D O I
10.1016/j.ijbiomac.2014.07.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A blend of poly(L-lactide) (PLLA) with star-shaped poly(epsilon-caprolactone-co-L-lactide) (s-PCLA) at different contents (PLLA/s-PCLA = 100/0, 90/10, 80/20, and 70/30, w/w) were prepared by torque rheometer. Thermal and functional properties of the blends were investigated by FTIR, SEM, DSC, TGA, DMA, tensile, optical, and water vapor permeability tests. FTIR results showed that intermolecular hydrogen bonds existed between two components in the blends. SEM indicated that PLLA and s-PCLA showed limited miscibility. DSC showed that T-g occurred at lower temperatures in the PLLA/s-PCLA blends than in neat PLLA, and the crystallinity of PLLA phase increased by the presence of s-PCLA in the PLLA/s-PCLA blends. TGA indicated that s-PCLA improved the thermal stability of the PLLA/s-PCLA blends. DMA results revealed that the storage modulus of the composites decreased with respect to the pure polymer. The result of tensile tests suggested that the PLLA/s-PCLA blends showed better elongation at break than neat PLLA. The effect of s-PCLA on the color and opacity of films could be considered as negligible. The WVP of PLLA/s-PCLA blend films increased with the increase in s-PCLA, and they were still lower than that of commercial LDPE films. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:327 / 333
页数:7
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