Affiliation:
1. Department of Chemistry, Sharif University of Technology, Tehran;
2. Geological Survey of Iran, Tehran;
3. Institute of Water and Energy, Sharif University of Technology, Tehran, Iran
Abstract
TiO2, transition metal (Cr, Mn, Fe, Co, Ni, Cu, and Zn)– and aluminum-doped TiO2 nanoparticles were prepared by the sol–gel technique. The sulfated catalysts were prepared by the impregnation method with H2SO4 solution. The catalysts were characterised by X-ray diffraction (XRD), BET surface area measurement, diffuse reflectance spectroscopy (DRS), and Fourier transform infrared (FTIR) techniques. The sulfate content of the metal–incorporated samples was considerably higher than for SO42-/TiO2. The metal doping brought about a considerable reduction in the extent of sulfate loss from the catalyst surface due to the wide dispersion on the surface. The SO42-/TiO2 and SO42-/M/TiO2 nanoparticles have smaller crystalline size and higher surface area than pure TiO2. Sulfation increases the acidity of pure titania. Addition of metal cations also changes the acidity of sulfated titania, which may be related to the interaction of the metal ions with titania and their incorporation into the lattice. The sulfation and addition of transition metals to nanocrystalline TiO2 enhances the extent of esterification of phthalic anhydride with octan-2-ol. The SO42-/Al/TiO2 catalyst has the highest activity towards esterification.
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3 articles.
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