Abstract
A series of TiO2–ZrO2 supported V2O5 catalysts with vanadia loadings ranging from 4 to 12 wt% were synthesized by a wet impregnation technique and subjected to various thermal treatments at temperatures ranging from 773 to 1,073 K to understand the dispersion and thermal stability of the catalysts. The prepared catalysts were characterized by X-ray powder diffraction (XRD), BET surface area, oxygen uptake, and X-ray photoelectron spectroscopy (XPS) techniques. XRD results of 773 K calcined samples conferred an amorphous nature of the mixed oxide support and a highly dispersed form of vanadium oxide. Oxygen uptake measurements supported the formation of a monolayer of vanadium oxide over the thermally stable TiO2–ZrO2 support. The O 1s, Ti 2p, Zr 3d, and V 2p core level photoelectron peaks of TiO2–ZrO2 and V2O5/TiO2–ZrO2 catalysts are sensitive to the calcination temperature. No significant changes in the oxidation states of Ti4+ and Zr4+ were noted with increasing thermal treatments. Vanadium oxide stabilized as V4+ at lower temperatures, and the presence of V5+ is observed at 1,073 K. The synthesized catalysts were evaluated for selective oxidation of o-xylene under normal atmospheric pressure in the temperature range of 600–708 K. The TiO2–ZrO2 support exhibits very less conversion of o-xylene, while 12 wt% V2O5 loaded sample exhibited a good conversion and a high product selectivity towards the desired product, phthalic anhydride.
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Acknowledgments
K.N.R. thanks UGC, New Delhi and P.B. and P.V.S. thank CSIR, New Delhi for the award of Research Fellowships. A grant from the Fundamental R&D Program for the core technology of materials, funded by the Ministry of Knowledge Economy of the Republic of Korea, also supported the research.
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Rao, K.N., Venkataswamy, P., Bharali, P. et al. Monolayer V2O5/TiO2–ZrO2 catalysts for selective oxidation of o-xylene: preparation and characterization. Res Chem Intermed 38, 733–744 (2012). https://doi.org/10.1007/s11164-011-0412-x
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DOI: https://doi.org/10.1007/s11164-011-0412-x