Effects of ball milling on the structure of cotton cellulose

被引:1
|
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
机构
[1] Beijing Forestry University,Beijing Key Laboratory of Lignocellulosic Chemistry
[2] Southern Regional Research Center,Department of Chemistry
[3] Agricultural Research Service,Department of Chemical Engineering, Materials Science Research Institute
[4] USDA,Department of Chemistry, Division of Chemistry of Renewable Resources
[5] Louisiana State University,undefined
[6] The Pennsylvania State University,undefined
[7] University of Natural Resources and Life Sciences,undefined
来源
Cellulose | 2019年 / 26卷
关键词
Amorphous cellulose; Ball milling; Cellulose degradation; Crystal structure; Rietveld refinement;
D O I
暂无
中图分类号
学科分类号
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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页码:305 / 328
页数:23
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