Highly dispersed gold on zirconia: characterization and activity in low-temperature water gas shift tests.

Gold-loaded zirconia and sulfated zirconia catalysts were tested in the low-temperature water gas shift reaction. The samples were characterized by N2 adsorption analysis, temperature-programmed reduction, X-ray diffraction, pulse-flow CO chemisorption, FTIR spectroscopy, and high-resolution transmission electron microscopy. A reference catalyst, Au/TiO2, provided by the World Gold Council was investigated for comparison. CO chemisorption and FTIR data indicate the presence of only highly dispersed gold clusters on the sulfated sample and both small clusters and small particles on the non-sulfated sample. Both gold-zirconia catalysts are much more active than the Au/TiO2 reference sample over all the temperature range investigated. The sample prepared on sulfated zirconia exhibits higher stability than the catalyst on unmodified zirconia. The prominent role in the water gas shift reaction of gold clusters in close contact with the support was deduced.

CO adsorption on gold clusters stabilized on ceria-titania mixed oxides: comparison with reference catalysts.

Fourier transform infrared spectra of CO adsorption from 120 K up to room temperature on two gold catalysts supported on different mixed ceria-titania oxides are discussed in comparison with those obtained on Au/TiO(2) and Au/Fe(2)O(3) reference catalysts provided by the World Gold Council. The spectra of adsorbed CO, run on the different samples before preliminary treatment, are shown and compared with those of the untreated catalysts and of the samples reduced either in CO or in hydrogen. Big differences have been found between the ceria-titania supported samples and the reference ones: unusual absorption bands, irreversible to outgassing, have been detected after CO interaction on the untreated and oxidized ceria containing samples. These absorptions are assigned to CO on Au(n)(+) small clusters stabilized at the ceria defects. By reduction in hydrogen, negatively charged Au(n)(-) species are produced on the same sample. Oxidized small particles are present on the reference catalysts, but only on the untreated samples; after treatment, only metallic step sites are evident.