An experimental and theoretical study of the impact of NO, NO2 and H2O
on CO oxidation has been carried out. The experiments were performed
in an isothermal quartz flow reactor at atmospheric pressure in the te
mperature range 800-1400 K. Inlet concentrations of NO and NO2 were 0-
1% (vol) and 0-622 ppmv, respectively, while the water vapor level was
varied in the ranges 1-32% (NO absent) and 1-10% (NO present). The re
sults show that the concentration of water vapor has a strong effect o
n the CO oxidation process, partly because it controls the O/OH ratio
of the radical pool, and partly due to the high efficiency of H2O in p
romoting H + O-2 recombination, which causes a strong inhibition of CO
oxidation at high levels. Presence of NO and NO2 has a significant im
pact on moist CO oxidation. In low concentrations NO enhances CO consu
mption in the 900-1100 K range by converting HO2 to OH. In higher conc
entrations NO may catalyze recombination of radicals, thereby inhibiti
ng the CO oxidation. The overall effect of NO depends on the radical p
ool composition, particularly the HO2 level and the O/OH ratio. NO2 is
much more efficient than NO in removing radicals and presence of NO,
has a strong inhibiting effect on CO oxidation. A chemical kinetic mod
el has been established, which provides a good description of the effe
ct of NO, NO2 and H2O on CO oxidation. Based on the calculations, the
rate determining steps in the system have been identified. The present
results are significant for understanding the impact of NOx on fuel o
xidation and CO burnout in practical systems. Furthermore, they indica
te that presence of NO2 impurities may affect significantly experiment
s on NO containing systems.