异氰酸酯
纤维素
石油化工
极限抗拉强度
生物降解
氨基甲酸酯
聚氨酯
热稳定性
化学
化学工程
有机化学
复合材料
高分子科学
材料科学
工程类
作者
Xinxin Yang,Le Yu,Bowen Zhang,Yongheng Wang,Xiangzheng Jia,Erlantz Lizundia,Chang Chen,Fuhao Dong,Luhe Qi,Lü Chen,Enlai Gao,Xu Xu,He Liu,Chaoji Chen
标识
DOI:10.1038/s41467-025-61722-0
摘要
Abstract In response to the looming concerns of plastic pollution, replacing plastic with paper is a very promising way, but its realization seems a long way off due to the poor water resistance and unsatisfied mechanical strength of cellulose fibril-based materials. Herein, we develop a versatile functionalizing material consisting of mainly biobased cyclic carbonate-bearing compounds and amine compound, which can enable the rapid transformation (within 2 min under microwave radiation) of the cellulose paper into plastic-like material (named paper plastic) having an unprecedently high tensile strength of ~126 MPa. Through a systematic experimental and theoretical study, the paper plastic’s combination of excellent mechanical properties and water/solvent resistance is attributed to the easy formation of carbamate abundant non-isocyanate polyurethane cooperated with the intermolecular bond exchange mechanism between the dynamic carbamate moiety and hydroxyl of the cellulose. Also, benefiting from the high content (>80%) and natural advantages of biobased materials, the paper plastic shows significant thermal stability, processability, and biodegradability than most petrochemical-based plastics, promising the great potential of dynamic carbamate chemistry toward high-performing paper plastic composites.
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