极限抗拉强度
氢键
无定形固体
纤维素
分子动力学
化学
粘结强度
材料科学
化学工程
高分子化学
高分子科学
复合材料
结晶学
计算化学
有机化学
分子
胶粘剂
图层(电子)
工程类
作者
Tomoka Nakamura,Tatsuya Ishiyama
标识
DOI:10.1021/acs.biomac.4c00950
摘要
Molecular dynamics (MD) simulations were conducted to investigate the hydrogen-bond (H-bond) structure and its impact on the tensile strength of hydrated amorphous cellulose. The study identifies a stable intramolecular H-bond between the hydroxyl group at position 3 and the ether oxygen at position 5 (OH3···O5). Intermolecularly, the hydroxyl groups at positions 2 (OH2) and 6 (OH6) form stable H-bonds. Young's modulus, maximum tensile strength, and corresponding strain were calculated as functions of moisture content, while the H-bond network, water cluster formation, and cellulose chain orientation during tensile simulations were analyzed to elucidate mechanical properties. The substitution effect of cellulose on Young's modulus is also examined, revealing that the substitution of OH3 for a hydrophobic group minimally affects Young's modulus, but substitutions at OH2 and OH6 significantly reduce tensile strength due to their roles as key intermolecular H-bond donor sites.
科研通智能强力驱动
Strongly Powered by AbleSci AI