Journal
PROCEEDINGS OF THE COMBUSTION INSTITUTE
Volume 39, Issue 3, Pages 3379-3388Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.proci.2022.07.122
Keywords
Coal; Char; Oxy-fuel combustion; Gasification
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Previous research has shown that CO2 and H2O gasification reactions play a significant role in the combustion of pulverized coal (pc) char, especially in oxy-fuel environments. This study aims to quantify the influence of CO2 gasification reaction by combining experimental measurements and simulations. The results demonstrate a consistent relationship between the gasification reaction rate and the char particle temperatures and burnout rates in oxy-fuel combustion environments.
Previous research has provided strong evidence that CO 2 and H 2 O gasification reactions can provide nonnegligible contributions to the consumption rates of pulverized coal (pc) char during combustion, particularly in oxy-fuel environments. Fully quantifying the contribution of these gasification reactions has proven to be difficult, due to the dearth of knowledge of gasification rates at the elevated particle temperatures associated with typical pc char combustion processes, as well as the complex interaction of oxidation and gasification reactions. Gasification reactions tend to become more important at higher char particle temperatures (because of their high activation energy) and they tend to reduce pc oxidation due to their endothermicity (i.e. cooling effect). The work reported here attempts to quantify the influence of the gasification reaction of CO 2 in a rigorous manner by combining experimental measurements of the particle temperatures and consumption rates of size-classified pc char particles in tailored oxy-fuel environments with simulations from a detailed reacting porous particle model. The results demonstrate that a specific gasification reaction rate relative to the oxidation rate (within an accuracy of approximately + /- 20% of the pre-exponential value), is consistent with the experimentally measured char particle temperatures and burnout rates in oxy-fuel combustion environments. Conversely, the results also show, in agreement with past calculations, that it is extremely difficult to construct a set of kinetics that does not substantially overpredict particle temperature increase in strongly oxygen-enriched N 2 environments. This latter result is believed to result from deficiencies in standard oxidation mechanisms that fail to account for falloff in char oxidation rates at high temperatures.& COPY; 2022 The Combustion Institute. Published by Elsevier Inc. All rights reserved.
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