The gas-phase oxidation of o-xylene over a commercial V205-Ti02 catalyst was studied in tied bed non-isothermal reactor. The experiments were carried out at initial o-xylene concentrations which differed greatly from each other. The following reaction network was suggested.
Surface Characterisation of V2O5/TiO2 Catalytic System
✍ Scribed by Rodella, C.B. ;Nascente, P.A.P. ;Franco, R.W.A. ;Magon, C.J. ;Mastelaro, V.R. ;Florentino, A.O.
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 133 KB
- Volume
- 187
- Category
- Article
- ISSN
- 0031-8965
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✦ Synopsis
Samples of the V 2 O 5 /TiO 2 system were prepared by the sol-gel method and calcined at different temperatures. Surface species of vanadium, their dispersion, as well as the structural evolution of the system were analysed by XRD, Raman, EPR, and XPS techniques. The results of XRD showed the evolution of TiO 2 from anatase phase to rutile phase. The Raman spectra for calcination temperatures up to 500 C showed a good dispersion of vanadium over titania in the form of monomeric vanadyl groups (V 4þ ) and polymeric vanadates (V 5þ ). At least three families of V 4þ ions were identified by EPR investigations. Two kinds of isolated V 4þ species are placed in sites of octahedral symmetry, substituting Ti 4þ in the rutile phase. The third is formed by pairs of V 4þ species on the surface of titania. Above 500 C part of superficial V 4þ is inserted into the matrix of titania and part is oxidized to V 5þ . The XPS results showed that the V/Ti ratio rises with increasing calcination temperature, indicating a smaller dispersion of vanadium.
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