The kinetics of the catalytic reduction of NO by CO on Rh(111) surfaces was investigated by using dynamic Monte Carlo simulations. Our model takes into account recent experimental findings and introduces relevant modifications to the classical reaction scheme, including an alternative pathway to produce N2 through an (N-NO)* intermediate, the formation of atomic nitrogen islands in the adsorbed phase, and the influence of coadsorbed species on the dissociation of NO. All elementary steps are expressed as activated processes with temperature-dependent rates and realistic values dictated by experiments. Calculated steady-state phase diagrams are presented for the NO + CO reaction showing the windows for the conditions under which the reaction is viable. The model predicts variations in both production rates and adsorbate coverages with temperature consistent with experimental data. The effect of varying the individual kinetic parameters and the importance of each step in the reaction scheme were probed.
Taking as starting point the complete analysis of mean residence times in linear compartmental systems performed by Garcia-Meseguer et al. (Bull. Math. Biol. 65:279-308, 2003) as well as the fact that enzyme systems, in which the interconversions between the different enzyme species involved are of first or pseudofirst order, act as linear compartmental systems, we hereby carry out a complete analysis of the mean lifetime that the enzyme molecules spend as part of the enzyme species, forms, or groups involved in an enzyme reaction mechanism. The formulas to evaluate these times are given as a function of the individual rate constants and the initial concentrations of the involved species at the onset of the reaction. We apply the results to unstable enzyme systems and support the results by using a concrete example of such systems. The practicality of obtaining the mean times and their possible application in a kinetic data analysis is discussed.
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