The NH3-SCR (selective catalytic reduction) reactions were systematically investigated over a commercial copper zeolite catalyst in view of its application to the DeNO(x), aftertreatment of exhaust gases from light- and heavy-duty Diesel engines. Catalytic activity data were collected at high space velocities in both steady state and dynamic runs over the catalyst in the form of powder, in order to derive intrinsic kinetic information in a wide temperature range. Results were also compared to those obtained over a commercial iron zeolite catalyst under similar conditions. With respect to the iron-based catalyst, the copper zeolite system showed a higher ammonia storage capacity, a higher activity in the ammonia oxidation reaction and in the Standard SCR reaction, and its DeNO(x) activity was found less sensitive to the NO2 feed content. As opposite to the iron zeolite, over the copper zeolite no inhibiting effect of ammonia on the Standard SCR reaction was observed, while formation of some N2O was detected even in the absence of NO2 in the gas feed mixture. (C) 2010 Elsevier B.V. All rights reserved.
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Politecn Milan, Lab Catalysis & Catalyt Proc, Dipartimento Energia, Via La Masa 34, I-20156 Milan, ItalyPolitecn Milan, Lab Catalysis & Catalyt Proc, Dipartimento Energia, Via La Masa 34, I-20156 Milan, Italy
Ruggeri, Maria Pia
Nova, Isabella
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Politecn Milan, Lab Catalysis & Catalyt Proc, Dipartimento Energia, Via La Masa 34, I-20156 Milan, ItalyPolitecn Milan, Lab Catalysis & Catalyt Proc, Dipartimento Energia, Via La Masa 34, I-20156 Milan, Italy
Nova, Isabella
Tronconi, Enrico
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Politecn Milan, Lab Catalysis & Catalyt Proc, Dipartimento Energia, Via La Masa 34, I-20156 Milan, ItalyPolitecn Milan, Lab Catalysis & Catalyt Proc, Dipartimento Energia, Via La Masa 34, I-20156 Milan, Italy
Tronconi, Enrico
Schmeisser, Volker
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Daimler AG, HPC G206, D-70546 Stuttgart, GermanyPolitecn Milan, Lab Catalysis & Catalyt Proc, Dipartimento Energia, Via La Masa 34, I-20156 Milan, Italy
Schmeisser, Volker
Weibel, Michel
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Daimler AG, HPC G206, D-70546 Stuttgart, GermanyPolitecn Milan, Lab Catalysis & Catalyt Proc, Dipartimento Energia, Via La Masa 34, I-20156 Milan, Italy
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Politecn Milan, Dipartimento Energia, Lab Catalysis & Catalyt Proc, Via La Masa 34, I-20156 Milan, ItalyPolitecn Milan, Dipartimento Energia, Lab Catalysis & Catalyt Proc, Via La Masa 34, I-20156 Milan, Italy
Marchitti, Fabio
Nova, Isabella
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Politecn Milan, Dipartimento Energia, Lab Catalysis & Catalyt Proc, Via La Masa 34, I-20156 Milan, ItalyPolitecn Milan, Dipartimento Energia, Lab Catalysis & Catalyt Proc, Via La Masa 34, I-20156 Milan, Italy
Nova, Isabella
Tronconi, Enrico
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Politecn Milan, Dipartimento Energia, Lab Catalysis & Catalyt Proc, Via La Masa 34, I-20156 Milan, ItalyPolitecn Milan, Dipartimento Energia, Lab Catalysis & Catalyt Proc, Via La Masa 34, I-20156 Milan, Italy
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Politecn Milan, Dipartimento Energia, Lab Catalysis & Catalyt Proc, Via La Masa 34, I-20156 Milan, ItalyPolitecn Milan, Dipartimento Energia, Lab Catalysis & Catalyt Proc, Via La Masa 34, I-20156 Milan, Italy
Ruggeri, M. P.
Nova, I.
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Politecn Milan, Dipartimento Energia, Lab Catalysis & Catalyt Proc, Via La Masa 34, I-20156 Milan, ItalyPolitecn Milan, Dipartimento Energia, Lab Catalysis & Catalyt Proc, Via La Masa 34, I-20156 Milan, Italy
Nova, I.
Tronconi, E.
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Politecn Milan, Dipartimento Energia, Lab Catalysis & Catalyt Proc, Via La Masa 34, I-20156 Milan, ItalyPolitecn Milan, Dipartimento Energia, Lab Catalysis & Catalyt Proc, Via La Masa 34, I-20156 Milan, Italy
Tronconi, E.
Collier, J. E.
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Johnson Matthey Technol Ctr, Blounts Court Rd, Reading RG4 9NH, Berks, EnglandPolitecn Milan, Dipartimento Energia, Lab Catalysis & Catalyt Proc, Via La Masa 34, I-20156 Milan, Italy
Collier, J. E.
York, A. P. E.
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Johnson Matthey Technol Ctr, Blounts Court Rd, Reading RG4 9NH, Berks, EnglandPolitecn Milan, Dipartimento Energia, Lab Catalysis & Catalyt Proc, Via La Masa 34, I-20156 Milan, Italy