Diao Yifan, Li Manyu, Yu Chenglei, Han Zhenqi, Wang Shuyuan, Liu Yue, Wu Jianguo, Liu Tian
Key Laboratory of Bio-based Material Science & Technology, Northeast Forestry University, Ministry of Education, 26 Hexing Road, Harbin 150040, China.
Engineering Research Center of Advanced Wooden Materials, Ministry of Education, 26 Hexing Road, Harbin 150040, China.
Materials (Basel). 2025 Aug 14;18(16):3817. doi: 10.3390/ma18163817.
In this study, alkali-treated wood flour/dynamic polyurethane composites were successfully prepared through a solvent-free one-pot method and in situ polymerization. The effects of the alkaline treatment process, changes in the flexible long-chain content in the dynamic polyurethane system, and the wood flour filling amount on the interface's bonding, mechanical, and reprocessing properties were investigated. Partial removal of lignin and hemicellulose from the alkali-treated wood flour enhanced rigidity and improved interface bonding and mechanical strength when combined with dynamic polyurethane. The tensile strength was improved from 5.65-11.00 MPa to 13.08-23.53 MPa. As the composite matrix, dynamic polyurethane could not easily infiltrate all wood flour particles when its content was low or its fluidity was poor. Conversely, excessive content or overly high fluidity led to leakage and the formation of large pores, affecting the mechanical strength. As the polyol content increased, the matrix exhibited greater fluidity, which enabled it to accommodate more wood flour and penetrate the cell cavity or even the cell wall. This improved infiltration enhanced the interface bonding performance of the composites and made their mechanical properties sensitive to changes in wood flour content. The reprocessing ability of the prepared composites decreased with the increase in wood flour content, and the interface bonding was enhanced after reprocessing. The tensile strength retention rate of the composites prepared with alkali-treated wood flour was lower. This study provides a theoretical basis for optimizing the performance of wood fiber/dynamic polyurethane composites and an exploration path for developing self-healing and recyclable wood-plastic composites, which can be applied to building materials, automotive interiors, furniture manufacturing, and other fields.
在本研究中,通过无溶剂一锅法和原位聚合法成功制备了碱处理木粉/动态聚氨酯复合材料。研究了碱处理工艺、动态聚氨酯体系中柔性长链含量的变化以及木粉填充量对界面粘结、力学和再加工性能的影响。碱处理木粉中部分木质素和半纤维素的去除提高了刚性,并在与动态聚氨酯结合时改善了界面粘结和机械强度。拉伸强度从5.65 - 11.00MPa提高到13.08 - 23.53MPa。作为复合基体,当动态聚氨酯含量低或流动性差时,其不易渗透到所有木粉颗粒中。相反,含量过高或流动性过大导致泄漏和大孔形成,影响机械强度。随着多元醇含量增加,基体表现出更大的流动性,使其能够容纳更多木粉并渗透到细胞腔甚至细胞壁中。这种改善的渗透增强了复合材料的界面粘结性能,并使其力学性能对木粉含量的变化敏感。制备的复合材料的再加工能力随着木粉含量的增加而降低,再加工后界面粘结增强。用碱处理木粉制备的复合材料的拉伸强度保留率较低。本研究为优化木纤维/动态聚氨酯复合材料的性能提供了理论依据,并为开发具有自修复和可回收性能的木塑复合材料探索了路径,可应用于建筑材料、汽车内饰、家具制造等领域。