分子内力
草酸
氯化胆碱
分子间力
纤维素
材料科学
范德瓦尔斯力
高分子化学
化学
有机化学
分子
作者
Zhenke Wei,Daiqi Wang,Yehong Chen,Dongmei Yu,Qijun Ding,Ronggang Li,Chaojun Wu
出处
期刊:Cellulose
[Springer Science+Business Media]
日期:2022-03-27
卷期号:29 (7): 3675-3687
被引量:19
标识
DOI:10.1007/s10570-022-04517-6
摘要
The fracture and recombination of its H-bond network have significant influence on the pore structure of nanocellulose and its materials. Deep eutectic solvents (DESs) have been widely used in the cellulose dissolution and nanocellulose treatment because of their efficient H-bond cleavage in cellulose; however, the H-bond evolution mechanism is still not fully understood. The main objective of the present work was to treat cellulose nanofibrils (CNFs) using a DES system based on choline chloride and oxalic acid. The effect of DES treatment on the H-bond, micro-structure, and properties of CNFs were analyzed. The results confirmed that choline chloride/oxalic acid effectively destroyed the intermolecular and intramolecular H-bonds in CNFs, thereby reducing the H-bond energy. This resulted in a decrease in the intramolecular H-bond contents, and an increase in the intermolecular H-bond contents of the CNFs. The changes in the three types of H-bond were independent, and their fracture sequence was of the order v(O(3)H…O(5) intramolecular H-bond) > v(O(6)H…O(3′) intermolecular H-bond) > v(O(2)H…O(6) intramolecular H-bond). Moreover, H-bond destruction improved the crystallinity index and crystallite size of the CNFs. The changes in the crystal parameters further led to an increase in the thermal stability. This work provides a theoretical basis for the treatment of CNFs by DESs, which is critical for the H-bond evolution principle of CNFs.Graphic Abstract
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