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Kinetic Investigation of the Photocatalytic Reduction of Nitric Oxide by Carbon Monoxide at Low Pressure on Silica-Supported Molybdenum Oxide
Authors:Lisachenko  A.A.  Chikhachev  K.S.  Zakharov  M.N.  Basov  L.L.  Shelimov  B.N.  Subbotina  I.R.  Che  M.  Coluccia  S.
Affiliation:(1) Institute of Physics, St Petersburg State University, 198904 St Petersburg, Russia;(2) Laboratoire de Réactivité de Surface, UMR 7609, CNRS, Université Pierre et Marie Curie, 4 Place Jussieu, 75252 Paris Cedex 05, France;(3) Dipartimento di Chimica Inorganica, Chimica Fisica e Chimica dei Materiali, Università di Torino, Via Pietro Giuria 7, 10125 Torino, Italy
Abstract:The kinetics of photoinduced reactions that occur upon UV irradiation (gamma<360 nm) of a MoO3/SiO2 catalyst (2.5 wt% Mo) in CO-NO mixtures and CO alone are studied at gas pressures from 0.05 to 2 torr and for CO/NO ratios from 0.3 to 3.0 in the temperature interval 20-150C. The data obtained are consistent with a previously proposed two-stage redox mechanism. In the first stage NO is reduced to N2O through the reaction CO+2NO rarr CO2+N2O, while in the second stage the N2O formed is further reduced to N2 via the reaction CO+N2O rarr CO2+N2. The ratio of rate constants for quenching of a transient excited state (Mo5+-O-)* by NO and CO molecules is found to be 2.8. The reaction rates decrease with increasing temperature, apparently because of a lower concentration of adsorbed species and/or a reduction of the steady-state concentration of (Mo5+-O-)*.
Keywords:NO  CO  MoOx/SiO2  reduction  photocatalysis  kinetics
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