The impact of the distributions of surface oxides and their migration on characterization of the heterogeneous carbon–oxygen reaction

• Published in: Combustion and flame 2008-07, Vol.154 (1), p.47-66
• Main Authors: Campbell, P.A., Mitchell, R.E.
• Format: Article
• Language: English
• Subjects: 01 COAL, LIGNITE, AND PEAT; ACTIVATION ENERGY; Adsorbed oxygen; ADSORPTION; ALGORITHMS; Applied sciences; BUILDUP; CARBON; CARBON DIOXIDE; CARBON MONOXIDE; Char oxidation; CHARS; COAL; Coal combustion; COMBUSTION; Combustion of solid fuels; Combustion. Flame; COMPLEXES; DESORPTION; DISTRIBUTION; Energy; Energy. Thermal use of fuels; EVOLUTION; Exact sciences and technology; Mathematical models; Migration; Oxidation; Oxides; OXYGEN; REACTION KINETICS; SPECIFIC SURFACE AREA; SURFACE AREA; Surface chemistry; Surface migration; SURFACES; Theoretical studies. Data and constants. Metering
• ISSN: 0010-2180; 1556-2921
• DOI: 10.1016/j.combustflame.2007.11.002

A study was undertaken to characterize the impact of the heterogeneity and migration of surface oxides on the char oxidation process. The char employed in the study was subjected to a series of kinetics-limited oxidation tests in a pressurized thermogravimetric analyzer (PTGA). Temperature-programmed desorption and BET-CO 2 gas adsorption tests were also performed in order to characterize surface oxide complexes and specific surface areas. In agreement with other studies, the experiments indicated that the surface-oxide populations may be characterized in terms of a distribution of desorption activation energies and that migration of the surface oxide complexes is significant. A heterogeneous reaction mechanism was developed to account for the observed rates of O 2 adsorption, CO and CO 2 desorption, and surface-oxide accumulation and was used in a numerical algorithm that modeled the PTGA reaction environment. Surface species were characterized by activation-energy-based distributions; allowance was made for the impact of surface area evolution on surface species concentrations. Analysis of calculated results indicate that a quasi-steady surface area assumption tends to underpredict surface species concentrations, especially at late conversions, but can overpredict these concentrations at early conversions. Calculated results also indicate that using less than five sites to approximate activation energy distributions yields results that are inconsistent with oxidation behaviors that are based on the full distributions.