纳米纤维素
纤维素
材料科学
聚合度
极限抗拉强度
半纤维素
化学工程
聚合
木质素
高分子科学
聚合物
复合材料
化学
有机化学
工程类
作者
Zhiqiang Fang,Bo Li,Yu Liu,Jiatian Zhu,Guanhui Li,Gaoyuan Hou,Jie Zhou,Xueqing Qiu
出处
期刊:Matter
[Elsevier]
日期:2020-04-01
卷期号:2 (4): 1000-1014
被引量:108
标识
DOI:10.1016/j.matt.2020.01.016
摘要
Translation of the outstanding mechanical performance of individual nanocellulose to macroscopic nanocellulose films can be achieved by various alignment techniques. However, attention has seldom been paid to the degree of polymerization (DP) of cellulose that plays a pivotal role in increasing the mechanical strength of nanocellulose films. In this work, nanocellulose film with superior tensile strength (1,014.7 ± 69.1 MPa) is presented by a cellulose DP protection strategy. An alkaline sulfite-anthraquinone-methanol pulping is applied to not only rapidly remove most of lignin and hemicellulose from wood blocks, which facilitates the formation of hydrogen bonds among neighboring fiber cell walls in subsequent mechanical pressing, but also to significantly suppress the decomposition of cellulose DP. Such strong nanocellulose film sheds light on unlocking the exceptional mechanical potential of cellulose and has the potential for use in advanced applications traditionally dominated by nonrenewable materials such as plastics, glass, and metals.
科研通智能强力驱动
Strongly Powered by AbleSci AI