In the reaction between NO and O-atoms, the concentration of NO remains essentially unaltered. The reaction can therefore be considered as a NO-catalyzed recombination of O-atoms. Its rate can be conveniently studied by following the disappearance of O-atoms by an isothermal calorimetric technique. The reaction was found to be third order, first order in the concentrations of O, NO, and M, where M is some third body. The third-order rate constant was found to be 1.85 × 10 16 cc 2 mole −2 sec −1 when M = O 2 , A, or He and 2.0 × 10 16 cc 2 mole −2 sec −1 when M = CO 2 The rate constant was found to have a slight negative temperature coefficient which corresponded to a negative Arrhenius activation energy of about 0.2 kcal/mole. A detailed mechanism for the reaction has been proposed.
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Ogryzlo et al. (1959) studied this question.