Synthesis, Characterization and Catalytic Activity of Ternary Oxide Catalysts Using the Microwave-Assisted Solution Combustion Method.

Ni-Co-Al, Ni-Cu-Al and Co-Cu-Al ternary oxide catalysts, with a fixed 5 wt% transition metal loading, were prepared by the microwave-assisted solution combustion method and tested in CO oxidation. The bulk and surface properties of the catalysts were investigated, using XRD, N2 adsorption-desorption, SEM, XPS and TEM techniques. XRD, XPS and TEM results revealed that nickel and cobalt were present as spinels on the surface and in the bulk. Differently, copper was preferentially present in "bulk-like" CuO-segregated phases. No interaction between the couples of transition metal species was detected, and the introduction of Cu-containing precursors into the Ni-Al or Co-Al combustion systems was not effective in preventing the formation of NiAl2O4 and CoAl2O4 spinels in the Ni- or Co-containing catalysts. Copper-containing catalysts were the most active, indicating that copper oxides are the effective active species for improving the CO oxidation activity.

Binary Oxides Prepared by Microwave-Assisted Solution Combustion: Synthesis, Characterization and Catalytic Activity.

Three different alumina-based Ni, Cu, Co oxide catalysts with metal loading of 10 wt %, and labeled 10Ni⁻Al, 10Co⁻Al and 10Cu⁻Al, were prepared by microwave-assisted solution combustion. Their morphological, structural and surface properties were deeply investigated by complementary physico-chemical techniques. Finally, the three materials were tested in CO oxidation used as test reaction for comparing their catalytic performance. The 10Cu⁻Al catalyst was constituted of copper oxide phase, while the 10Ni⁻Al and 10Co⁻Al catalysts showed the presence of "spinels" phases on the surface. The well-crystallized copper oxide phase in the 10Cu⁻Al catalyst, obtained by microwave synthesis, allowed for obtaining very high catalytic activity. With a CO conversion of 100% at 225 °C, the copper containing catalyst showed a much higher activity than that usually measured for catalytic materials of similar composition, thus representing a promising alternative for oxidation processes.

Rheological behavior of organic suspensions of fluorapatite.

A fluorapatite suspension prepared in the azeotrope methyl ethyl ketone-ethyl alcohol (MEK:EtOH) in the presence of the phosphoric ester was investigated. Electrical conductivity, adsorption isotherms, and sedimentation technique showed that the amount of phosphoric ester adsorbed on the fluorapatite surface was equal to, or higher than, 1 wt%. This dispersant concentration led to a good particle packing. The rheological properties of fluorapatite suspensions were studied as a function of phosphoric ester concentration. The data obtained from the viscosity measurements and those previously collected correlated well. In the case of suspensions prepared with 60 wt% in fluorapatite, the dispersion was optimal for a phosphoric ester content of about 1.3 wt%.