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Kinetic modeling of CO oxidation on Pt/CeO 2 in a gradientless reactor
Author(s) -
Shalabi Mazen A.,
Harji Bashir H.,
Kenney Christopher N.
Publication year - 1996
Publication title -
journal of chemical technology and biotechnology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.64
H-Index - 117
eISSN - 1097-4660
pISSN - 0268-2575
DOI - 10.1002/(sici)1097-4660(199604)65:4<317::aid-jctb438>3.0.co;2-5
Subject(s) - catalysis , cerium oxide , carbon monoxide , cerium , chemistry , continuous stirred tank reactor , oxygen , activation energy , oxide , inorganic chemistry , catalytic oxidation , adsorption , oxygen storage , oxidation state , organic chemistry
Cerium oxide is a major additive in three‐way catalysts used in emission control of automobile exhaust. Pt/CeO 2 was studied in order to better understand the role of ceria in promoting CO oxidation reaction. The kinetics of carbon monoxide oxidation on Pt/cerium oxide catalyst, was studied over the temperature range 100–170°C. Steady state kinetic measurements of CO oxidation were obtained in a computer controlled micro‐CSTR reactor. Activation energies were reported to vary between 39·5 and 51·2 kJ mol −1 . At low concentrations of either reactant (CO, O 2 ) and total conversion, the catalyst exhibited multiple steady states, similar to the multiplicity behavior of Pt/Al 2 O 3 . The total conversion was reached at 120°C. In comparison, the total conversion at low reactant concentrations was reached at a temperature of 148°C for the alumina‐supported catalyst. Langmuir–Hinshelwood mechanisms gave a good fit to the data. However, no single rate expression could effectively describe the CO oxidation data over the whole concentration in the product of the CSTR reactor. The facts gathered indicate that oxygen adsorbed on interfacial Pt/Ce sites and ceria lattice oxygen provides oxygen for CO oxidation. Cerium oxide has been found to lower CO oxidation activation energy, enhance reaction activity and tends to suppress the usual CO inhibition effect.