材料科学
乙二醇
共聚物
极限抗拉强度
韧性
纤维素
聚合物
化学工程
PEG比率
结晶
高分子化学
纳米晶
复合材料
纳米技术
工程类
经济
财务
作者
Guanhang Qu,Yafei Wei,Lifen Zhao,Jie Liu,Xin Liu,Haifeng He,Haotian Ma,Shengxue Qin
出处
期刊:Polymer
[Elsevier]
日期:2023-12-28
卷期号:292: 126609-126609
被引量:1
标识
DOI:10.1016/j.polymer.2023.126609
摘要
As a green and renewable resource, cellulose nanocrystals (CNC) possess excellent mechanical properties, rendering them a favorable option for modifying polymer materials. However, improving their dispersibility in the matrix and enhancing the interface are the crucial to exploit their advantages. The physically modified CNC (mCNC) are prepared by exploiting hydrogen bonding between CNC and the block copolymer of poly(d-lactic acid) and poly(ethylene glycol) (PDLA-PEG-PDLA) through a solvent exchange method. The incorporation of the copolymer not only enhances the dispersity of CNC, but also facilitates the formation of the stereocomplex crystal (SC) structure in PLA, thereby concurrently enhancing the interface. Consequently, the PLA/mCNC nanocomposites demonstrate a notable increase in crystallization ability and the mechanical properties. In comparison to neat PLA, the yield strength, elongation at break, and tensile toughness experienced significant enhancements of 11.2 %, 265.9 %, and 280.2 %, respectively. This facile method provides a good basis for the large-scale application of cellulose nanocrystals.
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