结晶度
纤维素
左旋葡糖
热重分析
糠醛
化学工程
材料科学
有机化学
核化学
高分子化学
化学
复合材料
工程类
催化作用
气溶胶
生物质燃烧
作者
Zhouhong Wang,Armando G. McDonald,Roel Johannes Maria Westerhof,Sascha R.A. Kersten,Christian M. Cuba-Torres,Su Ha,M. Brennan Pecha,Manuel Garcı̀a-Pèrez
标识
DOI:10.1016/j.jaap.2012.11.017
摘要
The effect of cellulose crystallinity on the formation of a liquid intermediate and on its thermal degradation was studied thermogravimetrically and by Py-GC/MS using a control cellulose (Avicel, crystallinity at 60.5%) and ball-milled Avicel (low cellulose crystallinity at 6.5%). The crystallinity of the materials studied was quantified by XRD and FTIR. Thermogravimetric analyses (TGA) show the samples with lower crystallinity start to degrade at lower temperatures, exhibiting sharper DTG curves and lower thermal degradation activation energies. Scanning electron microscopy (SEM) studies of the solid residues formed in TGA tests showed that, while the conversion of the ball-milled cellulose (mostly amorphous cellulose) occurs through the formation of a liquid intermediate, in the conversion of the control the fibrous structure is conserved. Py-GC/MS studies showed major differences in the thermal behavior of the samples studied. At 300 °C, amorphous cellulose yielded more levoglucosan. At temperatures between 350 and 450 °C, higher yields of mono-anhydrosugars (levoglucosan and levoglucosenone) were obtained with the samples with higher crystallinity (control). The ball-milled cellulose produced more 5-(hydroxymethyl) furfural, 5-methylfurfural and furfural. The higher yields of these compounds are due to the acceleration of dehydration reactions when a liquid phase intermediate was formed. Fragmentation reactions responsible for the formation of light compounds (glycoaldehyde, acetic acid, methyl-vinyl-ketone and acetol) and the reactions responsible for the formation of cyclopentane do not seem to be affected by cellulose crystallinity and by the formation of a liquid intermediate.
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