极限抗拉强度
琼脂
复合数
延伸率
葡甘露聚糖
材料科学
复合材料
乙酰化
微晶
傅里叶变换红外光谱
化学
化学工程
食品科学
生物化学
生物
基因
遗传学
工程类
冶金
细菌
作者
Dongling Qiao,Jieyi Lu,Wen‐Juan Shi,Hao Li,Liang Zhang,Fatang Jiang,Binjia Zhang
标识
DOI:10.1016/j.carbpol.2021.118776
摘要
From a microstructural point of view, this work concerns how deacetylation improves the practical characteristics of deacetylated-konjac glucomannan/agar (DK/A) composite films. As disclosed by infrared spectroscopy and X-ray diffraction, the deacetylation of konjac glucomannan (KGM) enhanced the chain interactions in DK/A composites and suppressed the realignment of agar molecules into crystallites. The enhanced associations between acetyl-free regions of KGM and agar reduced the exposure of OH groups and thus increased the hydrophobicity of the composites. Besides, the partial removal of acetyl groups allowed shortened distances between chains; consequently, denser composite matrices emerged with lower water vapor permeability and higher tensile strength. Also, the KGM deacetylation increased the matrix flexibility and elongation at break for DK/A composites, associated with the hindered rearrangement of agar chains. Thus, altering the deacetylation degree of KGM may be an effective way to design KGM-based composites with improved hydrophobicity and mechanical performance.
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