Abstract
Using molecular beam sampling mass spectrometry the structure of a quasi-equimolar ammonianitric oxide flat flame burning at 54 torr has been determined. From the mole fraction profiles of major species (H, H 2, NH 2, NH 3, H 2O, N 2, NO, Ar, N 2O) and from the rates of NO consumption or N 2 formation, the overall rate constant k 1 of the reaction NH 2 + NO → products has been measured between 1500 and 2100 K. In that temperature range the rate coefficient k 1 remains practically constant 3 × 10 12 cm 3 mol −1 s −1. The “pool flux” concept, based on the variation of the total bonds flux throughout the flame, has allowed us to determine the impact of the decomposition reaction in this flame. This event can be ascribed to the process NH 2 + NO → H 2 + h + or through the decomposition of N 2H originating from NH 2 + NO → N 2 H + OH The branching ratio β = ( k 1 c k 1 ) has been deduced and varies from 0.5 at 1500 K to 0.8 at 2150 K. The reaction r.1c plays an essential role on the burning abilities of NH 3 NO mixtures by providing the essential hydrogen atoms and hydroxyl radicals for the primary attack of NH 3. Reaction r.1c replaces the classical H + O 2 branching reaction occurring in all O 2 containing systems. The flame structure has been simulated using the PREMIX code with the experimental temperature profile as an input parameter. Calculated data compared with experimental ones agree very well when Bian et al.'s modified model is used while substantial disagreements are noticed with Miller and Bowman's mechanism.
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