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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Veröffentlicht in:Energy conversion and management 2018-05, Vol.163, p.420-427
Hauptverfasser: 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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container_start_page 420
container_title Energy conversion and management
container_volume 163
creator 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
description •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.
doi_str_mv 10.1016/j.enconman.2018.02.078
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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 (&lt;500 °C), resulting in higher primary coke yields than that of the fast heating rates. Decomposition reaction was found to be pronounced at fast heating rates, causing decreases in the tar yields and abundance of light compounds. 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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 (&lt;500 °C), resulting in higher primary coke yields than that of the fast heating rates. Decomposition reaction was found to be pronounced at fast heating rates, causing decreases in the tar yields and abundance of light compounds. The increases in the yields of the secondary coke, the formations of more condensed aromatic structures and macromolecules (m/z &gt; 500) were also promoted at fast heating rates via the more intense secondary reactions.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.enconman.2018.02.078</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-0627-1528</orcidid><orcidid>https://orcid.org/0000-0002-9952-0131</orcidid><orcidid>https://orcid.org/0000-0003-4329-2050</orcidid><orcidid>https://orcid.org/0000-0001-9485-1700</orcidid><orcidid>https://orcid.org/0000-0003-3523-8222</orcidid></addata></record>
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source ScienceDirect Journals (5 years ago - present)
subjects Aromatics
Bio-oil
Biomass
Coke
Cyclotron resonance
Decomposition reactions
Fluorescence
Fluorescence spectroscopy
Fourier transforms
Gas chromatography
Heating
Heating rate
High temperature
Low temperature
Macromolecules
Mass spectroscopy
Natural gas
Oil
Organic chemistry
Polymerization
Pyrolysis
Synthesis gas
Tar
Vegetable oils
Yield
title Effects of heating rate on the evolution of bio-oil during its pyrolysis
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