热解
纤维素
烧焦
化学工程
化学
有机化学
原材料
材料科学
热稳定性
碳纤维
复合材料
复合数
工程类
作者
Chenting Zhang,Chao Li,Zhanming Zhang,Qian Zhang,Qingyin Li,Huailin Fan,Shu Zhang,Qing Liu,Yingyun Qiao,Yuanyu Tian,Yi Wang,Xun Hu
标识
DOI:10.1016/j.rser.2020.110416
摘要
The pyrolysis of cellulose at 200–800 °C with an increment of 50 °C was conducted in this study, aiming to understand impacts of temperature on evolution of the of organics and the structures of bio-char. Extensively pyrolysis of cellulose to bio-oil initiated at 300 °C, reached maximum at 450 °C, and shifted to gasification to produce gases as the main products above 650 °C. Dehydrate sugars were the initial products formed below 350 °C, which soon dehydrated to form furans at ca. 400 °C and then generate aliphatic aldehydes, ketones and carboxylic acids at ca. 650 °C via the session of the C–C bonds. Aromatization of the volatiles initiated at 350 °C, producing phenolics and then further to aromatic hydrocarbons. The medium pyrolysis temperature (i.e. 450 °C) tended to produce the heavier bio-oil. The in situ DRIFTS characterization of cellulose pyrolysis showed that the structural reconstruction of the feedstock occurred at ca. 430–440 °C, forming abundant CO functionalities in bio-char. The increasing pyrolysis temperature led to staged change of carbon, hydrogen and oxygen contents in bio-char. The bio-char produced at the low temperature was quite aliphatic, and increasing pyrolysis temperature enhanced the formation of graphite structure, thermal stability and the porosity of bio-char. The bio-char from cellulose had a compact structure with small surface area and very limited mesopores. The results of kinetic analysis showed that the pyrolysis of cellulose was a complex multi-step reaction process.
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