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Molinari, Ettore and Cramarossa, Francesco and Capitelli, Mario and Pullo, Antonio:
Ossidazione catalitica dell'ammoniaca su ossido di cobalto in presenza di atomi di ossigeno
Atti della Accademia Nazionale dei Lincei. Classe di Scienze Fisiche, Matematiche e Naturali. Rendiconti Serie 8 38 (1965), fasc. n.4, p. 531-539, (Italian)
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Sunto

In order to ascertain whether the presence of unstable species in the gas phase can influence the kinetics of a heterogeneous catalytic process, the oxidation of ammonia has been studied on a CoO catalyst both in the presence and in the absence of atomic oxygen in the gas phase. In accordance with previous results obtained for the same reactionon Pt-Rh catalysts, it is shown that the presence of oxygen atoms significantly lowers the activation energy of the process (from 30 to 9 kcal/mole). It is furthermore shown that oxygen atoms influence the selectivity of the catalyst in the sense of increasing the yield of NO with respect to N2. From the observed kinetics one is lead to the conclusion that the slow step of the process is the reaction: $NH_{3} + O_{ads} \to \text{Intermediates}$ (NH3O, NH, others) and that NO and N2 are formed by successive reactions of the intermediates. The influence of oxygen atoms on the activation energy has previously been discussed for the catalytic oxidation on Pt-Rh gauzes. The influence of the oxygen atoms on the selectivity of the catalyst can be qualitatively understood on the basis of a simplified reaction scheme.
Referenze Bibliografiche
[1] E. MOLINARI, F. CRAMAROSSA, A. PULLO e L. TRIOLO, «J. Catalysis», 4 (1965) (in corso di stampa).
[2] N. GIORDANO, E. CAVATERRA, e D. ZEMA, «Chim. e Ind. (Milano)», 45, 15 (1963).
[3] D. A. FRANCK-KAMENETSKII, Diffusion and heat exchange in chemical kinetics, Princeton University Press, Princeton, New Jersey 1955.
[4] J. K. DIXON e J. E. LONGFIELD, in Catalysis, vol. 7, p. 281. Reinhold, New York 1960.

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