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Experimental and theoretical investigation of controlling regimes during lean oxidation of methane and propylene on Pt /Al2O3 monolithic reactors / Saurabh Y. Joshi in Industrial & engineering chemistry research, Vol. 51 N° 22 (Juin 2012) 

Public ISBD [article]  in Industrial & engineering chemistry research > Vol. 51 N° 22 (Juin 2012) . - pp. 7482–7492 Titre : Experimental and theoretical investigation of controlling regimes during lean oxidation of methane and propylene on Pt /Al2O3 monolithic reactors Type de document : texte imprimé Auteurs : Saurabh Y. Joshi, Auteur ; Yongjie Ren, Auteur ; Michael P. Harold, Auteur Année de publication : 2012 Article en page(s) : pp. 7482–7492 Note générale : Industrial chemistry Langues : Anglais (eng) Mots-clés : Controlling  regimes  Oxidation  methane Résumé : The performance of a catalytic reactor is bounded by the kinetic regime at low temperature (or before light-off) and the mass-transfer-controlled regime at high temperature. Pore diffusion may also be significant at intermediate temperature. We utilize the recently developed criteria (Joshi, S. Y.; Harold, M. P.; Balakotaiah, V. Chem. Eng. Sci.2010, 65, 1729–1747) to characterize the controlling regimes during lean oxidation of CH4 and C3H6 in Pt/Al2O3 monolithic reactors. First, we determine the global kinetics of lean oxidation of CH4 and C3H6 in a Pt/Al2O3 monolithic catalyst. We also present a method for estimation of the effective diffusivity of the limiting reactant and the external mass-transfer coefficient under reacting conditions. Further, we characterize the relative contributions of chemical kinetics, washcoat diffusion, and external mass transfer as a function of the various catalyst design and operating parameters. The analysis reveals that methane oxidation is kinetically controlled over a wide range of temperatures (350–600 °C) whereas propylene oxidation has a more classical transition between the kinetic and mass-transfer-controlled regimes. We use the bench-scale results to analyze the impact of various design and operating variables on transitions between the controlling regimes. ISSN : 0888-5885 En ligne : http://pubs.acs.org/doi/abs/10.1021/ie201653e [article] Experimental and theoretical investigation of controlling regimes during lean oxidation of methane and propylene on Pt /Al2O3 monolithic reactors [texte imprimé] / Saurabh Y. Joshi, Auteur ; Yongjie Ren, Auteur ; Michael P. Harold, Auteur . - 2012 . - pp. 7482–7492. Industrial chemistry Langues : Anglais (eng) in Industrial & engineering chemistry research > Vol. 51 N° 22 (Juin 2012) . - pp. 7482–7492 Mots-clés : Controlling  regimes  Oxidation  methane Résumé : The performance of a catalytic reactor is bounded by the kinetic regime at low temperature (or before light-off) and the mass-transfer-controlled regime at high temperature. Pore diffusion may also be significant at intermediate temperature. We utilize the recently developed criteria (Joshi, S. Y.; Harold, M. P.; Balakotaiah, V. Chem. Eng. Sci.2010, 65, 1729–1747) to characterize the controlling regimes during lean oxidation of CH4 and C3H6 in Pt/Al2O3 monolithic reactors. First, we determine the global kinetics of lean oxidation of CH4 and C3H6 in a Pt/Al2O3 monolithic catalyst. We also present a method for estimation of the effective diffusivity of the limiting reactant and the external mass-transfer coefficient under reacting conditions. Further, we characterize the relative contributions of chemical kinetics, washcoat diffusion, and external mass transfer as a function of the various catalyst design and operating parameters. The analysis reveals that methane oxidation is kinetically controlled over a wide range of temperatures (350–600 °C) whereas propylene oxidation has a more classical transition between the kinetic and mass-transfer-controlled regimes. We use the bench-scale results to analyze the impact of various design and operating variables on transitions between the controlling regimes. ISSN : 0888-5885 En ligne : http://pubs.acs.org/doi/abs/10.1021/ie201653e