Selective oxidation of CO in hydrogen-rich stream over Cu–Ce catalyst promoted with transition metals

• DOI: 10.1016/j.ijhydene.2004.04.016
• Publication Date: 2004-06-25T12:31:36Z
• Authors: Jong Won Park; Jin Hyeok Jeong; Wang Lai Yoon; Chang Soo Kim; Deuk Ki Lee; Yong-Ki Park; Young Woo Rhee
• Keywords: 13. Climate action; 02 engineering and technology; 0210 nano-technology; 7. Clean energy

Abstract Cu–Ce/γ-Al2O3 catalysts promoted with Co were tested for the low temperature selective oxidation of CO in excess hydrogen. The effects of Cu–Ce composition, Co as a dopant, stoichiometric ratio (λ=2O2/CO), water vapor and CO2 on the selective oxidation of CO to CO2, O2 consumption and selectivity of O2 to CO oxidation as a function of temperature are presented. Also, the catalytic properties of the catalysts were investigated by using X-ray diffraction, CO-/H2-temperature programmed reduction, temperature programmed oxidation, CO-/CO2-/H2O-temperature programmed desorption (TPD). Small addition (0.2 wt ) of Co onto the Cu–Ce/γ-Al2O3 brought large increase in selective CO oxidation activity. In the presence of either CO2 (13 vol%) or H2O (10 vol%) in the reformed gas feed, both Cu–Ce/γ-Al2O3 and Cu–Ce-Co/γ-Al2O3 showed decreased activity in CO oxidation at low temperatures, especially, under 200°C. Compared with the Cu–Ce/γ-Al2O3, however, the Cu–Ce-Co/γ-Al2O3 gives higher resistivity for the CO2 and H2O. From the CO2/H2O-TPD results, it could be explained that the main cause for the decrease in catalytic activity with CO2 and H2O in the feed may be attributed to the competitive adsorption of CO and CO2 as well as the blockage of the active sites by water vapor at low reaction temperatures.