Plasticizing effect of poly(ethylene glycol)s with different molecular weights in poly(lactic acid)/starch blends

增塑剂 混溶性 乙二醇 材料科学 淀粉 乳酸 高分子化学 PEG比率 化学工程 甘油 结晶 玻璃化转变 延伸率 聚合物 化学 有机化学 复合材料 极限抗拉强度 经济 工程类 细菌 生物 遗传学 财务
作者
Yunan Yu,Yan Cheng,Jiawei Ren,Enhong Cao,Xiaowei Fu,Weihong Guo
出处
期刊:Journal of Applied Polymer Science [Wiley]
卷期号:132 (16) 被引量:60
标识
DOI:10.1002/app.41808
摘要

ABSTRACT Binary and ternary blends composed of poly(lactic acid) (PLA), starch, and poly(ethylene glycols) (PEGs) with different molecular weights (weight‐average molecular weights = 300, 2000, 4000, 6000, and 10, 000 g/mol) were prepared, and the plasticizing effect and miscibility of PEGs in poly(lactic acid)/starch (PTPS) or PLA were intensively studied. The results indicate that the PEGs were effective plasticizers for the PTPS blends. The small‐molecule plasticizers of PEG300 (i.e., the M w of PEG was 300g/mol) and glycerol presented better plasticizing effects, whereas its migration and limited miscibility resulted in significant decreases in the water resistance and elongation at break. PEG2000, with a moderate molecular weight, was partially miscible in sample PTPS3; this led to better performance in water resistance and mechanical properties. For higher molecular weight PEG, its plasticization for both starch and PLA was depressed, and visible phase separation also occurred, especially for PTPS6. It was also found that the presence of PEG significantly decreased the glass‐transition temperature and accelerated the crystallization of the PLA matrix, depending on the PEG molecular weight and concentration. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132 , 41808.

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