The combustion of lean, stoichiometric and rich hydrogen-air mixtures in we
ll-stirred reactors has been modeled in the temperature range 1500-2200 K e
mploying a detailed N/N/O reaction scheme, and a H/O reaction scheme togeth
er with algebraic expressions for the NO production rate as a function of l
ocal gas composition and temperature. Thermal-NO. nitrous oxide, and NNH me
chanisms of nitric oxide formation have been taken into account, it is demo
nstrated that explicit expressions of the NO formation rate correctly repro
duce the prediction of the detailed mechanism for residence times longer th
an about 100 mus at all temperatures of this study in rich, stoichiometric
and lean mixtures. With time increase the reduced mechanism deviates from t
he full one in rich mixtures at residence times longer than about 10 ms. Th
e evaluation of the NNH route showed that this pathway is important at all
temperatures at short residence times. At temperatures of 2100 K and higher
the thermal-NO mechanism becomes dominant after about 1 ms. Sensitivity an
alysis clearly demonstrates the validity of the assumptions employed in the
development of the explicit expressions for the instantaneous NO formation
rates in hydrogen combustion in the range of residence times from 1 to 25
ms. A possible new route for NO formation in rich hydrogen mixtures via N2H
3 radicals is identified. (C) 2000 Elsevier Science Ltd. All rights reserve
d.