TY - JOUR
T1 - Catalytic diesel engine emission control. - studies on model reactions over a europt-1 (Pt/SiO2) catalyst
AU - Xue, E.
AU - Seshan, K.
AU - van Ommen, J. G.
AU - Ross, J. R.H.
PY - 1993/1/1
Y1 - 1993/1/1
N2 - Catalytic oxidation of NO to NO2in the presence of SO2over a standard Pt/SiO2catalyst (EUROPT-1) was studied. The gas phase reactions between NO, SO2and O2were found to be insignificant under the experimental conditions concerned. The Pt/SiO2catalyst was observed to be very active in catalyzing the reactions of both NO+O2to NO2and SO2+O2to SO3In the presence of SO2the catalytic activity for NO oxidation dropped dramatically, and in contrast, the presence of NO promoted SO2oxidation. Formation of a complex surface species of the type (NO)x(SO2)yattached on Pt, was observed when both NO and SO2were present in the gas phase. It is proposed that this species reacts towards SO3rather than NO2and is responsible for the mutual effect between NO and SO2Deactivation of the catalyst was also observed during activity test. It is believed that the deactivation was mainly due to the built-up of non-active nitrogen- and sulphur-compounds on the catalyst surface and the sintering of Pt particles under the reaction environment. This has been confirmed by XPS, TPR and H2chemisorption measurements.
AB - Catalytic oxidation of NO to NO2in the presence of SO2over a standard Pt/SiO2catalyst (EUROPT-1) was studied. The gas phase reactions between NO, SO2and O2were found to be insignificant under the experimental conditions concerned. The Pt/SiO2catalyst was observed to be very active in catalyzing the reactions of both NO+O2to NO2and SO2+O2to SO3In the presence of SO2the catalytic activity for NO oxidation dropped dramatically, and in contrast, the presence of NO promoted SO2oxidation. Formation of a complex surface species of the type (NO)x(SO2)yattached on Pt, was observed when both NO and SO2were present in the gas phase. It is proposed that this species reacts towards SO3rather than NO2and is responsible for the mutual effect between NO and SO2Deactivation of the catalyst was also observed during activity test. It is believed that the deactivation was mainly due to the built-up of non-active nitrogen- and sulphur-compounds on the catalyst surface and the sintering of Pt particles under the reaction environment. This has been confirmed by XPS, TPR and H2chemisorption measurements.
UR - http://www.scopus.com/inward/record.url?scp=77956893428&partnerID=8YFLogxK
U2 - 10.1016/S0167-2991(08)64375-X
DO - 10.1016/S0167-2991(08)64375-X
M3 - Article
AN - SCOPUS:77956893428
SN - 0167-2991
VL - 75
SP - 2665
EP - 2668
JO - Studies in Surface Science and Catalysis
JF - Studies in Surface Science and Catalysis
IS - C
ER -