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Effects of heating rate on the evolution of bio-oil during its pyrolysis

•Slow heating rates promote primary reactions during bio-oil pyrolysis.•Fast heating rate promote the secondary cracking of vapor.•A proposed reaction mechanism of bio-oil pyrolysis is provided.•The characteristics of primary and secondary products varied with the heating rate. Bio-oil from the fast...

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Bibliographic Details
Published in:Energy conversion and management 2018-05, Vol.163, p.420-427
Main Authors: Xiong, Zhe, Wang, Yi, Syed-Hassan, Syed Shatir A., Hu, Xun, Han, Hengda, Su, Sheng, Xu, Kai, Jiang, Long, Guo, Junhao, Berthold, Engamba Esso Samy, Hu, Song, Xiang, Jun
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Language:English
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Summary:•Slow heating rates promote primary reactions during bio-oil pyrolysis.•Fast heating rate promote the secondary cracking of vapor.•A proposed reaction mechanism of bio-oil pyrolysis is provided.•The characteristics of primary and secondary products varied with the heating rate. Bio-oil from the fast pyrolysis of biomass can be converted to solid carbon materials, chemicals and syngas by various thermochemical conversion methods. As a first step in all of these processes, bio-oil undergoes drastic components changes due to its exposure to the elevated temperature. Understanding the effects of heating rate on bio-oil transformation during its pyrolysis is therefore crucial for effective utilization of bio-oil. In this study, a bio-oil sample produced from the fast pyrolysis of rice husk at 500 °C was pyrolyzed in a fixed-bed reactor at temperatures between 300 and 800 °C at three different heating rates: fast (≈200 °C/s), medium (≈20 °C/s), and slow (≈0.33 °C/s). In addition to the quantification of coke and tar yields, the tar was characterized with an ultraviolet (UV) fluorescence spectroscopy, a gas chromatography/mass spectrometer (GC/MS) and a Fourier transform ion cyclotron resonance mass spectrometer (FT-ICR MS). Our results indicate that slow heating rates promote polymerization of bio-oil components, particularly at low temperatures ( 500) were also promoted at fast heating rates via the more intense secondary reactions.
ISSN:0196-8904
1879-2227
DOI:10.1016/j.enconman.2018.02.078