The high-temperature reaction of NO with H-2 has been studied behind r
eflected shock waves in the temperature range of 1760-2160 K at total
pressures of 1.4 to 2.0 bar by monitoring the time-dependent H-atom co
ncentrations in the postshock reaction zone using atomic resonance abs
orption spectroscopy (ARAS). Mixtures of NO and H-2 highly diluted in
argon were used as initial reactants. The rate coeffficient, k(1), of
the initiation reaction: NO + H-2 --> HNO + H has been determined from
the measured initial H-atom concentration slopes to be k(1) = 1.5 x 1
0(13) exp(-26165K/T) cm(3) mol(-1) s(-1), taking the fast decompositio
n of HNO into account. This direct determination of the rate coefficie
nt k(1) was possible, because the contribution of H-2 dissociation to
the total H atom concentration of the system was relatively small in t
he temperature and concentration ranges of this study. Measured O-atom
concentrations in the high-temperature H-2/NO/Ar reaction system (256
0 K less than or equal to T less than or equal to 4040 K) were sensiti
ve to the reaction NO + H --> OH + N, resulting in an estimate of its
rate coefficient. A simplified mechanism of 15 elementary reactions wa
s able to predict all measured H and O atom profiles with reasonable a
ccuracy.