4.8 Article

Mathematical modeling of the oxygen storage capacity phenomenon studied by CO pulse transient experiments over Pd/CeO2 catalyst

Journal

JOURNAL OF CATALYSIS
Volume 219, Issue 2, Pages 259-272

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/S0021-9517(03)00151-9

Keywords

oxyen storage capacity; three-way catalysts; supported-Pd; transient CO oxidation; mathematical modeling of OSC; pulse CO oxidation

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A mathematical model has been developed for the first time to study the oxygen storage capacity (OSC) phenomenon by the CO pulse injection technique over a 1 wt% Pd/CeO2 model catalyst in the 500-700 degreesC range. A two-step reaction path that involves the reaction of gaseous CO with the oxygen species of PdO (pre-oxidized supported palladium particles in the 500-700 degreesC range) and of the backspillover of the oxygen process from ceria to the oxygen vacant sites of surface PdO has been proven to better describe the outlet CO pulse transient response and the experimentally measured quantity of OSC (muatoms of O/g) obtained in a CSTR microreactor. With the proposed mathematical model, the transient rates of the CO oxidation reaction and of the back-spillover of the oxygen process can be calculated. In the 500-700 degreesC range, the transient rate of CO oxidation was always greater than that of the back-spillover of oxygen. The ratio, p, of the maximum CO oxidation rate to the maximum back-spillover of the oxygen rate was found to decrease with increasing reaction temperature in the 500-700 degreesC range. In particular, at 500 and 700 degreesC the value of p was found to be 1.6 and 1.2, respectively. The present mathematical model allows also the calculation of the intrinsic rate constant k(1) (s(-1)) of the Eley-Rideal step for the reaction of gaseous CO with surface oxygen species of PdO to form CO2. An activation energy of 9.2 kJ/moI was estimated for this reaction step. In addition, an apparent rate constant k(2)(app) (s(-1)) was estimated for the process of back-spillover of oxygen. The ratio of the two rate constants (k(1)/k(app)) was found to be 2 2 greater than 100 in the 500-700 'C range. A Langmuir-Hinshelwood surface elementary reaction step of adsorbed CO with atomic oxygen of PdO failed to describe the experimental transient kinetics of CO oxidation in the 500-700 degreesC range. The results of the present work provide the means for a better understanding of the effects of various additives and contaminants present in a three-way commercial catalytic converter and other related model catalysts on their OSC kinetic behavior. In addition, intrinsic effects of a given regeneration method for a commercial three-way catalyst on the OSC phenomenon could better be studied by making use of the results of the present mathematical model. (C) 2003 Elsevier Inc. All rights reserved.

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