Journal
JOURNAL OF PHYSICAL CHEMISTRY C
Volume 116, Issue 7, Pages 4642-4654Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jp210312r
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Funding
- IFP Energies nouvelles
- ANRT (CIFRE)
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Kinetic parameters for soot oxidation by O-2 and NO are estimated by fitting for product selectivity and global rates. Depending on the gas mixture, the competition of two surface reactions for lumped C*(NO) complexes determines whether N-2 or NO2 and CO2 are produced. NO adsorption and soot conversion are much improved when 02 is added to NO because the presence of oxygen on soot favors the competing step of reaction with C*(NO). For NO, the adsorption/desorption steps are rate determining,: the importance of CO and CO2 formation steps grows with increasing O-2 concentration. For soot + NO2, adsorption/desorption of NO2 controls the rate above 600 degrees C; below this temperature, it is the surface formation of C*(ONO2). Experiments with soot and graphite show that differences in BET area are not sufficient to model tendencies in NO chemisorption and CO and CO2 formation.
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