Dobrzyńska-Mizera Monika, Knitter Monika, Woźniak-Braszak Aneta, Baranowski Mikołaj, Sterzyński Tomasz, Di Lorenzo Maria Laura
Institute of Materials Technology, Polymer Division, Poznan University of Technology, 61-138 Poznan, Poland.
Department of High Pressure Physics, Faculty of Physics, Adam Mickiewicz University, 61-614 Poznan, Poland.
Materials (Basel). 2020 Aug 26;13(17):3776. doi: 10.3390/ma13173776.
Bio-based composites made of poly(-lactic acid) (PLLA) and pine wood were prepared by melt extrusion. The composites were compatibilized by impregnation of wood with γ-aminopropyltriethoxysilane (APE). Comparison with non-compatibilized formulation revealed that APE is an efficient compatibilizer for PLLA/wood composites. Pine wood particles dispersed within PLLA act as nucleating agents able to start the growth of PLLA crystals, resulting in a faster crystallization rate and increased crystal fraction. Moreover, the composites have a slightly lower thermal stability compared to PLLA, proportional to filler content, due to the lower thermal stability of wood. Molecular dynamics was investigated using the solid-state H NMR technique, which revealed restrictions in the mobility of polymer chains upon the addition of wood, as well as enhanced interfacial adhesion between the filler and matrix in the composites compatibilized with APE. The enhanced interfacial adhesion in silane-treated composites was also proved by scanning electron microscopy and resulted in slightly improved deformability and impact resistance of the composites.
采用熔融挤出法制备了由聚(-乳酸)(PLLA)和松木制成的生物基复合材料。通过用γ-氨丙基三乙氧基硅烷(APE)浸渍木材使复合材料增容。与未增容配方的比较表明,APE是PLLA/木材复合材料的有效增容剂。分散在PLLA中的松木颗粒充当能够引发PLLA晶体生长的成核剂,导致更快的结晶速率和增加的晶体分数。此外,由于木材的热稳定性较低,与PLLA相比,复合材料的热稳定性略低,与填料含量成正比。使用固态H NMR技术研究了分子动力学,结果表明添加木材后聚合物链的流动性受到限制,并且在与APE增容的复合材料中填料与基体之间的界面粘附增强。扫描电子显微镜也证明了硅烷处理复合材料中增强的界面粘附,并导致复合材料的可变形性和抗冲击性略有改善。