材料科学
胶粘剂
木质素
复合材料
粘接
复合数
化学工程
湿强度
共价键
机械强度
溶剂
聚合物
乙醚
稳健性(进化)
分子
堆积
三羟甲基丙烷
粘结强度
纳米技术
沸腾
缩放比例
工作(物理)
基质(化学分析)
作者
Fangyuan Tang,Jiajun Qiu,Xunxiao Wu,Yongfei Liu,Qingdi Hu,Chenchen Cai,Jiaao Zhang,Bingbing Guan,Zhixin Wang,Xusheng Li
标识
DOI:10.1002/adfm.202527965
摘要
Abstract The weather resistance of bonding interfaces is a crucial prerequisite for scaling up bio‐based adhesives in the plywood industry; however, achieving a balance between mechanical robustness and green sustainability remains a major challenge. Inspired by the hierarchical composite interfaces of natural wood cell walls, a bioinspired lignin–carbohydrate matrix interfacial design strategy is proposed. Through controlled etherification between trimethylolpropane triglycidyl ether (TMPTE), lignin, and cellulose, lignin molecules are covalently anchored onto wood fibers, constructing a robust cross‐linked network analogous to natural cell wall architecture. The resulting bio‐adhesive exhibits exceptional bonding performance, with the dry strength enhanced from 1.11 ± 0.15 to 12.57 ± 1.25 MPa and the wet strength increased from 0 to 3.06 ± 0.38 MPa, surpassing most conventional petroleum‐based adhesives. Moreover, the adhesive maintains structural integrity under extreme conditions, including boiling water, cryogenic, high‐temperature, acidic/alkaline, and organic solvent environments. This work breaks through the long‐standing limitation of poor weather resistance in bio‐based adhesives and establishes a feasible and sustainable pathway toward robustness, low‐carbon structural bonding materials.
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