1999
DOI: 10.1016/s0255-2701(99)00054-9
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Combined kinetic and potentiometric measurements of the reduction of nitrogen monoxide on vanadia titania catalysts

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Cited by 5 publications
(3 citation statements)
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“…The need for an effective control of hazardous auto exhaust emissions led several research groups to use O 2− SECRs for the reaction of NO x with reducing compounds such as CO, ,, CH 4 , C 2 H 4 , ,, C 3 H 6 , , ,,,,,, and NH 3 . , In most of the above works, NO x was fed at the cathode, together with the reducing compound, and the effect of O 2− pumping on the reaction rate was studied. The highest NEMCA effect was observed during the reduction of NO by C 3 H 6 on Rh when the rate enhancement factor (ρ) reached values as high as 150 …”
Section: Catalytic Studies In Secrsmentioning
confidence: 99%
“…The need for an effective control of hazardous auto exhaust emissions led several research groups to use O 2− SECRs for the reaction of NO x with reducing compounds such as CO, ,, CH 4 , C 2 H 4 , ,, C 3 H 6 , , ,,,,,, and NH 3 . , In most of the above works, NO x was fed at the cathode, together with the reducing compound, and the effect of O 2− pumping on the reaction rate was studied. The highest NEMCA effect was observed during the reduction of NO by C 3 H 6 on Rh when the rate enhancement factor (ρ) reached values as high as 150 …”
Section: Catalytic Studies In Secrsmentioning
confidence: 99%
“…6 gewählten Darstellung verhalten sich beide Grössen praktisch spiegelbildlich zueinander. Dieses Verhalten ist erstmals von Brück [11] [12] bei der Untersuchung der selektiven katalytischen Reduktion von Stick-oxiden an (Vanadium-oxid/Titanoxid)-Katalysatoren beobachtet worden, tritt aber ebenfalls bei partiellen Oxidationen auf, wie Estenfelder und Lintz [22] bei der Bildung von Acrylsäure an oxidischen Katalysatoren feststellen konnten.…”
unclassified
“…8. o-Xylolverbrauchsgeschwindigkeit, O 2 -Verbrauchsgeschwindigkeit und O 2 -Aktivität als Funktion des oXylolmolenbruchs für den undotierten und die mit Li und Cs dotierten Katalysatoren dabei den stationär stabilen Wert der O-Aktivität im Katalysator. Dieser prinzipielle Zusammenhang ist bereits a. o. dargestellt worden[11] …”
unclassified