Reaction Engineering, Kinetics, and Catalysis
Polymerization on heating up of bio-oil: A model compound study
Article first published online: 14 JUN 2012
DOI: 10.1002/aic.13857
Copyright © 2012 American Institute of Chemical Engineers (AIChE)
Additional Information
How to Cite
Hu, X., Wang, Y., Mourant, D., Gunawan, R., Lievens, C., Chaiwat, W., Gholizadeh, M., Wu, L., Li, X. and Li, C.-Z. (2013), Polymerization on heating up of bio-oil: A model compound study. AIChE J., 59: 888–900. doi: 10.1002/aic.13857
Publication History
- Issue published online: 20 FEB 2013
- Article first published online: 14 JUN 2012
- Accepted manuscript online: 29 MAY 2012 11:23AM EST
- Manuscript Revised: 13 MAY 2012
- Manuscript Received: 13 DEC 2011
Funded by
- Australian Government funding through the Second Generation Biofuels Research and Development Grant Program
- International Science Linkages (ISL) Program
- Government of Western Australia via the Centre for Research into Energy for Sustainable Transport (CREST)
Keywords:
- bio-oil;
- polymerization;
- upgrading;
- model compounds;
- stabilization
Understanding of the condensation reactions in bio-oil is the key for efficient conversion into transportation fuel or value-added chemicals. In this study, the roles of the typical compounds representing the sugars, sugar derivatives, and aromatics found in bio-oil were investigated for their contribution to condensation reactions. Glucose played a key role for the polymer formation due to its decomposition to reactive compounds with multiple hydroxyl groups, carbonyl groups or conjugated π bonds. The sugar derivatives, including furfural, hydroxyl aldehyde and hydroxyl acetone, were also found to be reactive toward polymerization. The carboxylic acids were shown to be the catalysts for polymerization and formic acid was much more efficient to catalyze polymerization than acetic acid. The phenolic compounds also promoted the acid-catalyzed reactions. Vanillin contains reactive a carbonyl group, leading to its high tendency toward polymerization. In methanol, various kinds of methanolysis reactions dominated, which significantly suppressed the decomposition of glucose and the polymerization of other compounds. © 2012 American Institute of Chemical Engineers AIChE J, 59: 888–900, 2013

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