Abstract
The formation of nitrogen oxides (NOx) during combustion is a topic of substantial fundamental and practical interest, given the complex nature of its formation kinetics and the fact that, as a highly regulated pollutant emission, it is a major constraint in engineering design. To date, there are four known mechanisms by which the strong N–N bond can be broken to facilitate NOx formation from N2 present in air. Here we posit and explore the possibility of a new NOx formation route mediated by an HNNO intermediate whose reactions with common combustion species break the N–N bond. Altogether, we present results from master equation (ME) calculations for HNNO formation from H + N2O (+M), ab initio electronic structure and RRKM/ME calculations for HNNO + O2, and simulations of NO profiles in freely propagating flames using a newly constructed HNNO kinetic sub-model. Our ME results for the H + N2O reaction indicate that HNNO is the favored product channel at lower temperatures and higher pressures – e.g. favored over all other products up to ∼1100 K and over NH + NO up to ∼1500 K above 10 atm. Our ab initio electronic structure calculations for trans-HNNO + O2 show a barrier for abstraction to HO2 + N2O of 18.2 kcal/mol and a barrier for addition of 27.0 kcal/mol to form an HN(OO)NO which can decompose to NO + HNO2 over a barrier of 32.3 kcal/mol (cis-HNNO + O2 shows similar reactivity). Altogether, our rate constant calculations and kinetic modeling, which also includes estimated rate constants for HNNO + radical reactions, suggest that HNNO + O2 mainly recycles HNNO back to N2O but is sufficiently slow that the primary fate of HNNO in many combustion situations likely involves reactions with radical species, which appear likely to occur quickly and with high NOx yields.
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