生物塑料
纤维素
材料科学
石油化工
生物降解
热成型
纤维素乙醇
共价键
极限抗拉强度
纤维素纤维
玻璃化转变
高分子科学
复合材料
化学工程
聚合物
有机化学
废物管理
纤维
化学
工程类
作者
Guowen Zhou,Haishan Zhang,Zhiping Su,Xiaoqian Zhang,Haonan Zhou,Le Yu,Chaoji Chen,Xiaohui Wang
标识
DOI:10.1002/adma.202301398
摘要
The growing environmental concern over petrochemical-based plastics continuously promotes the exploration of green and sustainable substitute materials. Compared with petrochemical products, cellulose has overwhelming superiority in terms of availability, cost, and biodegradability; however, cellulose's dense hydrogen-bonding network and highly ordered crystalline structure make it hard to be thermoformed. A strategy to realize the partial disassociation of hydrogen bonds in cellulose and the reassembly of cellulose chains via constructing a dynamic covalent network, thereby endowing cellulose with thermal processability as indicated by the observation of a moderate glass transition temperature (Tg = 240 °C), is proposed. Moreover, the cellulosic bioplastic delivers a high tensile strength of 67 MPa, as well as excellent moisture and solvent resistance, good recyclability, and biodegradability in nature. With these advantageous features, the developed cellulosic bioplastic represents a promising alternative to traditional plastics.
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