TEMPERATURE CO OXIDATION;
DENSITY-FUNCTIONAL THEORY;
WATER-GAS SHIFT;
CRYSTALLITE SIZE;
METAL-OXIDES;
DEPOSITION-PRECIPITATION;
CALCINATION TEMPERATURE;
AU/FE2O3;
CATALYSTS;
AU/TIO2;
CATALYST;
AU CATALYSTS;
D O I:
10.1021/jp111483v
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070305 [高分子化学与物理];
摘要:
Au/rutile catalysts were activated in hydrogen and in air, and their catalytic activity for the oxidation of CO was analyzed as a function of time. The catalysts were characterized with X-ray powder diffraction, the refinement of the crystalline structures, transmission electron microscopy, and infrared spectroscopy. The activation atmosphere determined the interaction between the gold atoms and the support, which in turn determined the mobility of the gold particles with time and, with that, the gold particle dimensions and, consequently, their catalytic activity for the oxidation of CO. This catalytic activity was also affected by the adsorption, with time, of carbonate species on the active sites, species that were eliminated by heating the aged catalysts in air at 200 degrees C, recovering the catalytic activity.