Effects of ball milling on the structure of cotton cellulose

结晶度 材料科学 傅里叶变换红外光谱 纤维素 无定形固体 热重分析 微晶 化学工程 拉曼光谱 副晶态 极限抗拉强度 复合材料 分析化学(期刊) 有机化学 结晶学 化学 光学 物理 工程类 冶金
作者
Zhe Ling,Tuo Wang,Mohamadamin Makarem,Michael Santiago Cintrón,H. N. Cheng,Xue Kang,Markus Bacher,Antje Potthast,Thomas Rosenau,Holly King,Christopher D. Delhom,Sunghyun Nam,J. Vincent Edwards,Seong H. Kim,Feng Xu,Alfred D. French
出处
期刊:Cellulose [Springer Science+Business Media]
卷期号:26 (1): 305-328 被引量:357
标识
DOI:10.1007/s10570-018-02230-x
摘要

Cellulose is often described as a mixture of crystalline and amorphous material. A large part of the general understanding of the chemical, biochemical and physical properties of cellulosic materials is thought to depend on the consequences of the ratio of these components. For example, amorphous materials are said to be more reactive and have less tensile strength but comprehensive understanding and definitive analysis remain elusive. Ball milling has been used for decades to increase the ratio of amorphous material. The present work used 13 techniques to follow the changes in cotton fibers (nearly pure cellulose) after ball milling for 15, 45 and 120 min. X-ray diffraction results were analyzed with the Rietveld method; DNP (dynamic nuclear polarization) natural abundance 2D NMR studies in the next paper in this issue assisted with the interpretation of the 1D analyses in the present work. A conventional NMR model’s paracrystalline and inaccessible crystallite surfaces were not needed in the model used for the DNP studies. Sum frequency generation (SFG) spectroscopy also showed profound changes as the cellulose was decrystallized. Optical microscopy and field emission-scanning electron microscopy results showed the changes in particle size; molecular weight and carbonyl group analyses by gel permeation chromatography confirmed chemical changes. Specific surface areas and pore sizes increased. Fourier transform infrared (FTIR) and Raman spectroscopy also indicated progressive changes; some proposed indicators of crystallinity for FTIR were not in good agreement with our results. Thermogravimetric analysis results indicated progressive increase in initial moisture content and some loss in stability. Although understanding of structural changes as cellulose is amorphized by ball milling is increased by this work, continued effort is needed to improve agreement between the synchrotron and laboratory X-ray methods used herein and to provide physical interpretation of the SFG results.
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