0000000000374295

AUTHOR

Albert Frederick Carley

Niobium phosphates as new highly selective catalysts for the oxidative dehydrogenation of ethane

Several niobium phosphate phases have been prepared, fully characterized and tested as catalysts for the selective oxidation of ethane to ethylene. Three distinct niobium phosphate catalysts were prepared, and each was comprised predominantly of a different bulk phase, namely Nb(2)P(4)O(15), NbOPO(4) and Nb(1.91)P(2.82)O(12). All of the niobium phosphate catalysts showed high selectivity towards ethylene, but the best catalyst was Nb(1.91)P(2.82)O(12), which was produced from the reduction of niobium oxide phosphate (NbOPO(4)) by hydrogen. It was particularly selective for ethylene, giving ca. 95% selectivity at 5% conversion, decreasing to ca. 90% at 15% conversion, and only produced low l…

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The significance of the order of impregnation on the activity of vanadia promoted palladium-alumina catalysts for propane total oxidation

The increased activity of alumina-supported palladium catalysts promoted with vanadium oxide has been investigated. Three different vanadium promoted Pd/Al2O3 catalysts with the same composition but synthesized employing sequential and co-impregnation were tested for the total oxidation of propane. The order of impregnation was critical to produce high activity catalysts. Vanadium and palladium co-impregnation on the Al2O3 support led to the most active catalyst, whereas the step-wise impregnated catalysts show a catalytic performance similar to or slightly better than unpromoted palladium catalysts. The high activity of the co-impregnated catalysts is related to the particle size and oxida…

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Synergy between tungsten and palladium supported on titania for the catalytic total oxidation of propane

Titania-supported palladium catalysts modified by tungsten have been tested for the total oxidation of propane. The addition of tungsten significantly enhanced the catalytic activity. Highly active catalysts were prepared containing a low loading of 0.5 wt.% palladium, and activity increased as the tungsten loading was increased up to 6 wt.%. Catalysts were characterised using a variety of techniques, including powder X-ray diffraction, laser Raman spectroscopy, X-ray photoelectron spectroscopy, temperature-programmed reduction and aberration-corrected scanning transmission electron microscopy. Highly dispersed palladium nanoparticles were present on the catalyst with and without the additi…

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Influence of the preparation method on the activity of ceria zirconia mixed oxides for naphthalene total oxidation

Cerium/zirconium mixed oxides, with different Ce/Zr ratios, have been synthesised by a co-precipitation method using two different precipitating agents (sodium carbonate and urea) and tested for the total oxidation of naphthalene. Catalysts were characterized by N2 adsorption, XRD, Raman, TPR, XPS and DRIFTS. Ceria prepared by carbonate precipitation had low activity and this is likely to be related to the high concentration of residual surface carbonate that covers catalytic sites and inhibits reaction. For carbonate precipitation, increasing the Zr content to 1% resulted in a significant increase of activity, which is related to the decrease of surface carbonate. Increasing the Zr content…

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Deep oxidation of propane using palladium–titania catalysts modified by niobium

Abstract Pd/TiO 2 catalysts modified by niobium have been prepared and tested for the complete oxidation of propane. The catalysts have been characterised by BET, XRD, laser Raman spectroscopy, XPS, DRS and TPR. The incorporation of niobium into Pd/TiO 2 catalysts resulted in a marked increase in the catalytic activity compared to the Nb-free Pd/TiO 2 catalysts, and the activity increased as the niobium and/or palladium loading increased. The addition of Nb significantly modified the nature of the palladium and niobium species. There was a marked increase in the oxygen mobility after niobium addition. This could not only promote the presence of palladium species in a totally oxidized state …

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