Volume 27, Issue 28
Physical Inorganic Chemistry
Full Access

ChemInform Abstract: Stationary Kinetics of Essential Reactions on Automobile Exhaust Pt-Rh/ Al2O3 Catalyst.

P. MANNILA

P. MANNILA

Dep. Chem. Eng., Aabo Akad., SF-20500 Turku, Finland

Search for more papers by this author
T. SALMI

T. SALMI

Dep. Chem. Eng., Aabo Akad., SF-20500 Turku, Finland

Search for more papers by this author
H. HAARIO

H. HAARIO

Dep. Chem. Eng., Aabo Akad., SF-20500 Turku, Finland

Search for more papers by this author
M. LUOMA

M. LUOMA

Dep. Chem. Eng., Aabo Akad., SF-20500 Turku, Finland

Search for more papers by this author
M. HAERKOENEN

M. HAERKOENEN

Dep. Chem. Eng., Aabo Akad., SF-20500 Turku, Finland

Search for more papers by this author
J. SOHLO

J. SOHLO

Dep. Chem. Eng., Aabo Akad., SF-20500 Turku, Finland

Search for more papers by this author
First published: July 9, 1996

Abstract

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

ChemInform Abstract

The kinetics of CO and propene oxidation and of NO reduction are studied over ceria-promoted Pt-Rh/Al2O3 catalysts under steady-state conditions at 10-400 °C and at atmospheric pressure under dry and wet gas conditions by measuring the CO, CO2, total hydrocarbons, NO/NOx, and O2 concentrations for different gas feeds at the three-way catalyst outlet. Water enhances the oxidation reactions at low temperatures while water-gas shift and steam reforming reactions proceed at high temperatures under wet conditions. From the proposed steady-state equations based on plausible surface reaction mechanisms for CO and propene oxidation, water-gas shift, and NO reduction, the steady-state kinetics on the commercial catalyst can be described as shown by the good agreement of experimental and predicted concentrations.

    The full text of this article hosted at iucr.org is unavailable due to technical difficulties.