Formation of reaction intermediates and primary volatiles during acid-catalysed fast pyrolysis of cellulose in a wire-mesh reactor

被引:10
作者
Cao, Jinxiu [1 ]
Liaw, Sui Boon [1 ]
Long, Yu [1 ]
Yu, Yun [1 ]
Wu, Hongwei [1 ]
机构
[1] Curtin Univ, Western Australian Sch Mines Minerals Energy & Ch, Discipline Chem Engn, GPO Box U1987, Perth, WA 6845, Australia
基金
澳大利亚研究理事会;
关键词
Cellulose; Fast pyrolysis; Acid catalysis; Reaction intermediates; Primary volatiles;
D O I
10.1016/j.proci.2020.07.035
中图分类号
O414.1 [热力学];
学科分类号
摘要
This study aims to understand the fundamental reaction mechanisms during fast pyrolysis of the acid impregnated cellulose in a wire-mesh reactor at 40-450 degrees C and 20 degrees C/s, via quantifying key compounds in the reaction intermediates and primary volatiles. Acid impregnation reduces the onset reaction temperature of cellulose pyrolysis. During acid-catalysed cellulose pyrolysis, 1,6-anhydro-beta-D-glucofuranose (AGF), levoglucosenone (LGO) and 5-hydroxymethylfurfural (5-HMF) are identified as major products in the primary volatiles, and the formation of levoglucosan is greatly suppressed. At temperatures < 100 degrees C, acid catalyses hydrolysis reactions to produce glucose, which is further dehydrated to AGF at 120 degrees C. At temperatures > 160 degrees C, acid enhances the dehydration of glucose, levoglucosan and AGF to produce 5-HMF and LGO as major primary products. Once produced, those products can be easily released into the vapour phase, as either aerosols via thermal ejection or vapours via evaporation. As the pyrolysis temperature increases to 240 degrees C, aromatic compounds can be identified in the primary volatiles, indicating condensation reactions also play important roles during acid-catalysed cellulose pyrolysis under the conditions. As a result, char formation becomes the favoured pathway during acid-catalysed cellulose pyrolysis at temperatures > 300 degrees C. (C) 2020 The Combustion Institute. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:4301 / 4308
页数:8
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