Super-tough polylactic acid (PLA)/poly(butylene succinate) (PBS) materials prepared through reactive blending with epoxy-functionalized PMMA-GMA copolymer

材料科学 甲基丙烯酸缩水甘油酯 聚乳酸 共聚物 环氧树脂 增容 复合材料 艾氏冲击强度试验 甲基丙烯酸甲酯 复配 甲基丙烯酸酯 高分子化学 聚合物 聚合物混合物 极限抗拉强度
作者
Tao Zhao,Jinshuo Yu,Hongwei Pan,Yan Zhao,Qingxin Zhang,Xiaoyan Yu,Junjia Bian,Lijing Han,Huiliang Zhang
出处
期刊:International Journal of Biological Macromolecules [Elsevier BV]
卷期号:251: 126150-126150 被引量:35
标识
DOI:10.1016/j.ijbiomac.2023.126150
摘要

High-performance biosourced polylactic acid (PLA)/poly(butylene succinate) (PBS) blends with small amounts of compatibilizer, epoxy-functionalized methyl methacrylate-co-glycidyl methacrylate copolymer (PMMA-GMA), were fabricated by melt compounding. The properties of the modified PLA/PMMA-GMA, PBS/PMMA-GMA, and PLS(PLA/PBS)/PMMA-GMA blends were investigated systematically. DSC combined with X-ray diffraction revealed a low-order semi-crystalline structure for all samples. SEM and DMA showed that the compatibility between PLA and PBS was improved after addition of PMMA-GMA. Rheological behavior of blends showed that the addition of PMMA-GMA resulted in a significant improvement in the viscoelasticity. FT-IR spectra confirmed that the interfacial compatibilization between PLA and PBS phases was improved due to the reaction of epoxy groups with terminal groups of PLA and PBS. Finally, the toughness and notched impact strength of the PLA materials were increased significantly. The elongation at break and notched impact strength of PLS/PMMA-GMA was about 55.7 and 6.2 times than neat PLA after incorporation of 7 wt% PMMA-GMA, respectively.
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