Please use this identifier to cite or link to this item:
Scopus Web of Science® Altmetric
Type: Journal article
Title: The stoichiometry and kinetics of carbon combustion at low temperature: A surface complex approach
Author: Battye, D.
Ashman, P.
Citation: Proceedings of the Combustion Institute, 2009; 32(Part 2):1981-1988
Publisher: The Combustion Institute
Issue Date: 2009
ISSN: 1540-7489
Abstract: The stoichiometry and rate of carbon combustion at low temperature (673 K) were investigated. Oxidation and TPD experimental data provide quantification of gaseous products and stable surface complexes over a broad range of conversion. Our analysis distinguishes between surface complexes forming CO and CO2 and has assumed a certain fraction of each complex type decomposes instantaneously upon formation, leaving the remainder on the surface as stable complexes, C(O) and C(O2). This analysis suggests that a maximum of 25% of CO-complexes and 89% of CO2-complexes are unstable upon formation. At low conversion, unstable complex formation is the dominant pathway for the CO product. As conversion increases, decomposition of stable CO-complexes eventually becomes the main source of CO. Formation of unstable CO2-complexes is the dominant pathway for the CO2 product at all times. The combustion rate is initially high due to a high availability of vacant active sites, decreases sharply as these sites are filled with stable complexes, and gradually increases as the stable complexes promote CO2-complex formation, in turn, driving their decomposition. The dynamics of formation and decomposition of C(O) and C(O2) dictates their ratio on the carbon surface at any moment, which may be measured by TPD. This work may help in developing new kinetic models of carbon combustion which can predict the stoichiometry as well as the rate.
Keywords: Char; Reactivity; Primary product ratio; Surface oxides
Description: Copyright © 2009 Elsevier Inc. All rights reserved.
RMID: 0020090505
DOI: 10.1016/j.proci.2008.07.033
Appears in Collections:Chemical Engineering publications
Environment Institute publications

Files in This Item:
There are no files associated with this item.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.