Preferential oxidation of carbon monoxide on Co/CeO2 nanoparticles

• Published in: Applied catalysis. B, Environmental Vol. 97; no. 1-2; pp. 28 - 35
• Main Authors: Woods, Matthew P., Gawade, Preshit, Tan, Bing, Ozkan, Umit S.
• Format: Journal Article
• Language: English
• Published: Kidlington Elsevier B.V 09-06-2010; Elsevier
• Subjects: Catalysis; CeO2; Ceria; Chemistry; CO oxidation; Co/CeO2; Co3O4; Cobalt; Cobalt oxide; Colloidal state and disperse state; Exact sciences and technology; General and physical chemistry; H2 combustion; Physical and chemical studies. Granulometry. Electrokinetic phenomena; PROX; Surface physical chemistry; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry; Cobalt oxide; H2 combustion; CO oxidation; Ceria; Co/CeO2; CeO2; Cobalt; PROX; Co3O4; Binary compound; Methanation; Hydrogen; Nanoparticle; H; Combustion; Cerium oxide; Co; Co/CeO; O; Lanthanide compound; Oxidation; Raman spectrometry; Carbon monoxide; Activation energy; Transition metal; Conversion; X ray diffraction; Ce0; Heterogeneous catalysis; Adsorption; Surface area; Catalyst activity; Catalyst; Environmental protection
• ISSN: 0926-3373; 1873-3883
• DOI: 10.1016/j.apcatb.2010.03.015

A highly active CoOx/CeO2 nanoparticle catalyst with high surface area (78m2/g) has been prepared and tested in the preferential oxidation of carbon monoxide (PROX) in the presence of hydrogen. Three distinct temperature regions of catalyst activity are observed corresponding to CO oxidation, H2 oxidation and methanation. The catalyst achieves near 100% CO conversion under a wide range of reaction conditions demonstrating peak activity near 175°C. The catalyst is stable with time-on-stream at the temperature of highest CO conversion. The presence of H2 decreases the CO oxidation rate, possibly due to competitive adsorption between H2 and CO. CO oxidation and H2 oxidation activation energies were 52 and 74kJ/mol, respectively. Raman spectroscopy and X-ray diffraction experiments have demonstrated that the cobalt takes the form of Co3O4 and no CoO was detected under any experimental conditions.