聚乳酸
材料科学
极限抗拉强度
木质素
复合数
共聚物
热稳定性
聚合
单体
复合材料
聚合物
化学工程
高分子化学
化学
有机化学
工程类
作者
Kang Shi,Guoshuai Liu,Hui Sun,Biao Yang,Yunxuan Weng
出处
期刊:ACS omega
[American Chemical Society]
日期:2023-07-23
卷期号:8 (30): 26926-26937
被引量:6
标识
DOI:10.1021/acsomega.3c01738
摘要
The development of low-cost and high-performance bio-based composites derived from forestry waste lignin and polylactic acid has emerged as a topic of central attention. However, the weak compatibility between lignin and polylactic acid often resulted in high brittleness of the composites. Graft copolymerization is not only the most effective way to modify lignin but also can significantly improve the compatibility of lignin and polylactic acid. In this study, bio-based monomer lauryl methacrylate was grafted onto lignin by feasible radical polymerization to prepare lignin graft copolymers with excellent thermal stability and hydrophobicity, which are expected to improve the compatibility with polylactic acid. Wholly bio-based composites were prepared by compounding this graft copolymer with polylactic acid. The results showed that the crystallization ability of the composite was improved, and the highest crystallinity was increased from 6.42% to 17.46%. With addition of LG-g-PLMA lower than 9%, the thermal stability of the composites was slightly improved. At 5% copolymer addition, the elongation at break and tensile toughness of the composites increased by 42% and 36%, respectively. Observation of the frozen fracture surface of the composite by SEM found that wire drawing and ductile deformation appeared when a small amount of LG-g-PLMA was added. The thus prepared composites also showed excellent UV barrier properties. This approach provides a new idea for the high-value application of lignin.
科研通智能强力驱动
Strongly Powered by AbleSci AI