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Abstract
The oxidation of NO toNO2 and CO to CO2 in quartz gas-sampling microprobes drawing gases from fuel-lean flames of CH4/air and CO/air has been modeled and measured. The kinetic model includes surface recombination of O- and H-atoms. Confirming measurements were obtained by gas-sampling a jet-stirred reactor. It was predicted that as the gas sample was rapidly quenched sufficient levels of HO2 were formed within the probe to oxidize NO to NO2. The transient HO2 concentration limited the NO2 formation to ca. 25 ppm. Ozone may have exerted a similar influence. Carbon monoxide tended to oxidize to CO2 due to reaction with OH in the warmer regions of the probe. Modeling indicated that sample distortions could be eliminated at probe pressures below 10 torr.
