1. Kinetics of the selective catalytic reduction of NO by NH3 on a Cu-faujasite catalyst
- Author
-
Philippe Trens, Gérard Delahay, Stéphane Kieger, Nathalie Tanchoux, Bernard Coq, Laboratoire de Matériaux Catalytiques et Catalyse en Chimie Organique (LMCCCO), and Université Montpellier 1 (UM1)-Ecole Nationale Supérieure de Chimie de Montpellier (ENSCM)-Centre National de la Recherche Scientifique (CNRS)
- Subjects
Kinetics ,Inorganic chemistry ,02 engineering and technology ,engineering.material ,010402 general chemistry ,01 natural sciences ,7. Clean energy ,Catalysis ,Ammonia ,chemistry.chemical_compound ,Zeolite ,General Environmental Science ,Selective catalytic reduction ,Atmospheric pressure ,Process Chemistry and Technology ,Cationic polymerization ,Nitric oxide ,[CHIM.CATA]Chemical Sciences/Catalysis ,Faujasite ,021001 nanoscience & nanotechnology ,0104 chemical sciences ,chemistry ,engineering ,0210 nano-technology ,Copper - Abstract
International audience; The kinetics of the selective catalytic reduction (SCR) of NO by NH3 in the presence of O2 has been studied on a 5.5% Cu-faujasite (Cu-FAU) catalyst. Cu-FAU was composed of cationic and oxocationic Cu species. The SCR was studied in a gas phase-flowing reactor operating at atmospheric pressure. The reaction conditions explored were: 458 < TR < 513 K, 250 < NO (ppm) < 3000, 1000 < NH3 (ppm)< 4000, 1 < O2 (%) < 4. The kinetic orders were 0.8–1 with respect to NO, 0.5–1 with respect to O2, and essentially 0 with respect to NH3. Based on these kinetic partial orders of reactions and elementary chemistry, a wide variety of mechanisms were explored, and different rate laws were derived. The best fit between the measured and calculated rates for the SCR of NO by NH3 was obtained with a rate law derived from a redox Mars and van Krevelen mechanism. The catalytic cycle is described by a sequence of three reactions: (i) CuI is oxidized by O2 to “CuII-oxo”, (ii) “CuII-oxo” reacts with NO to yield “CuII-NxOy”, and (iii) finally “CuII-NxOy” is reduced by NH3 to give N2, H2O, and the regeneration of CuI (closing of the catalytic cycle). The rate constants of the three steps have been determined at 458, 483, and 513 K. It is shown that CuI or “CuII-oxo” species constitute the rate-determining active center.
- Published
- 2004