纳米纤维素
微观结构
氢键
材料科学
催化作用
化学工程
纳米纤维
硅烷
比表面积
纳米技术
保温
复合材料
化学
纤维素
有机化学
图层(电子)
分子
工程类
作者
Yiwen Cao,Xinyi Chen,Linping Zhang,Yaping Wang,Hou‐Yong Yu,Ziheng Li,Ying Zhou
出处
期刊:ACS Sustainable Chemistry & Engineering
[American Chemical Society]
日期:2023-01-19
卷期号:11 (4): 1581-1590
被引量:25
标识
DOI:10.1021/acssuschemeng.2c06544
摘要
Because of the fascinating properties and tremendous application potential of nanocellulose aerogels (CAs), research into them has exploded. However, regulating and controlling their microstructure remain challenging. Herein, the strategy of regulating the strength of hydrogen bonding was used to investigate the cause of cellulose nanofiber (CNF) aggregation. Three kinds of silane coupling agents with different tail functional groups were employed to modify CNFs. The hydrogen bond fraction of CAs decreased from 0.41 to 0.33, indicating a decrease in the intensity of hydrogen bonding. Also, the CA with a 3D-web-like structure was obtained. The specific surface area of the aerogels increased from 44.36 to 99.37 m2/g, showing that the aggregation was limited. In parallel, superior mechanical properties and thermal insulation were obtained. These results showed that varying the intensity of the hydrogen bond could inhibit the aggregation of the CA skeleton structure. The improvement of the specific surface area will expand its application in catalyst support, environmental remediation, heat insulation, and other fields. This method paved the way for future studies on the control of the micro-structure of CAs.
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