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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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Published in: | Energy conversion and management 2018-05, Vol.163, p.420-427 |
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Main Authors: | , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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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. |
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ISSN: | 0196-8904 1879-2227 |
DOI: | 10.1016/j.enconman.2018.02.078 |