Modeling of the kinetics for methanol synthesis using Cu/ZnO/Al2O3/ZrO2 catalyst / Hye-Won Lim in Industrial & engineering chemistry research, Vol. 48 N° 23 (Décembre 2009)  

Public ISBD [article]  inIndustrial & engineering chemistry research > Vol. 48 N° 23 (Décembre 2009) . - pp. 10448–10455 Titre : Modeling of the kinetics for methanol synthesis using Cu/ZnO/Al2O3/ZrO2 catalyst : influence of carbon dioxide during hydrogenation Type de document : texte imprimé Auteurs : Hye-Won Lim, Auteur ; Myung-June Park, Auteur ; Suk-Hwan Kang, Auteur Année de publication : 2010 Article en page(s) : pp. 10448–10455 Note générale : Industrial chemistry Langues : Anglais (eng) Mots-clés : Modeling--Kinetics--Methanol--Synthesis--using--Cu/ZnO/Al2O3/ZrO2--Catalyst--Influence--Carbon Dioxide--during Hydrogenation Résumé : A kinetic model for methanol (MeOH) synthesis over Cu/ZnO/Al2O3/ZrO2 catalyst has been developed and selected to evaluate the effect of carbon dioxide on the reaction rates due to its high activity and stability. Detailed kinetic mechanism, on the basis of different sites on Cu for the adsorption of carbon monoxide and carbon dioxide, is applied, and the water−gas shift (WGS) reaction is included in order to provide the relationship between the hydrogenations of carbon monoxide and carbon dioxide. Parameter estimation results show that, among 48 reaction rates from different combinations of rate determining steps (RDSs) in each reaction, the surface reaction of a methoxy species, the hydrogenation of a formate intermediate HCO2, and the formation of a formate intermediate are the RDS for CO and CO2 hydrogenations and the WGS reaction, respectively. It is shown that the CO2 hydrogenation rate is much lower than the CO hydrogenation rate, and this affects the methanol production rate. However, carbon dioxide decreases the WGS reaction rate, which prevents methanol from converting to dimethyl ether, a byproduct. In such a way, a small fraction of carbon dioxide accelerates the production of methanol indirectly within a limited range, showing a threshold value of the CO2 fraction for the maximum methanol synthesis. ISSN : 0888-5885 En ligne : http://pubs.acs.org/doi/abs/10.1021/ie901081f [article] Modeling of the kinetics for methanol synthesis using Cu/ZnO/Al2O3/ZrO2 catalyst : influence of carbon dioxide during hydrogenation [texte imprimé] / Hye-Won Lim, Auteur ; Myung-June Park, Auteur ; Suk-Hwan Kang, Auteur . - 2010 . - pp. 10448–10455. Industrial chemistry Langues : Anglais (eng) in Industrial & engineering chemistry research > Vol. 48 N° 23 (Décembre 2009) . - pp. 10448–10455 Mots-clés : Modeling--Kinetics--Methanol--Synthesis--using--Cu/ZnO/Al2O3/ZrO2--Catalyst--Influence--Carbon Dioxide--during Hydrogenation Résumé : A kinetic model for methanol (MeOH) synthesis over Cu/ZnO/Al2O3/ZrO2 catalyst has been developed and selected to evaluate the effect of carbon dioxide on the reaction rates due to its high activity and stability. Detailed kinetic mechanism, on the basis of different sites on Cu for the adsorption of carbon monoxide and carbon dioxide, is applied, and the water−gas shift (WGS) reaction is included in order to provide the relationship between the hydrogenations of carbon monoxide and carbon dioxide. Parameter estimation results show that, among 48 reaction rates from different combinations of rate determining steps (RDSs) in each reaction, the surface reaction of a methoxy species, the hydrogenation of a formate intermediate HCO2, and the formation of a formate intermediate are the RDS for CO and CO2 hydrogenations and the WGS reaction, respectively. It is shown that the CO2 hydrogenation rate is much lower than the CO hydrogenation rate, and this affects the methanol production rate. However, carbon dioxide decreases the WGS reaction rate, which prevents methanol from converting to dimethyl ether, a byproduct. In such a way, a small fraction of carbon dioxide accelerates the production of methanol indirectly within a limited range, showing a threshold value of the CO2 fraction for the maximum methanol synthesis. ISSN : 0888-5885 En ligne : http://pubs.acs.org/doi/abs/10.1021/ie901081f

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