Rietveld refinement and catalytic properties of of nanosized WO3 and V2O5 dispersed on SBA15 mesoporous solid

Jin A Wang

Abstract

Rietveld refinement and catalytic properties of of nanosized WO3 and V2O5 dispersed on SBA15 mesoporous solid

In the present work, two sets of transition metal oxides dispersed on SBA-15 were synthesized and their crystallite sizes, phase composition, textural properties, and morphological features were characterized with XRD, N₂ phsisorption isotherms, TEM, XPS and Raman spectroscopic techniques. Their crystalline structures were refined with the Rietveld method on the basis of X-ray diffraction analysis. Oxygen defect concentrations in the crystalline structure were calculated. The surface acidity including Brφnsted and Lewis acidity were measured by in situ FTIR of pyridine adsorption technique. In the crystals of WO₃ and V₂O₅, oxygen defects were formed during the synthesis procedure. All the (WO₃,V₂O₅)/SBA15 catalysts predominantly contained a great number of Lewis acid sites with Brφnsted acid sites as minor. Creation of Lewis acidity can be correlated with the structural defects. In the oxidation of 4,6-dimethyldibenzothiophene (4,6âÂÂÃâÃâ¬ÂÂÃâÃâDMDBT) in a model diesel, the 4,6âÂÂÃâÃâ¬ÂÂÃâÃâDMDBT oxidation was correlated with the number of Lewis acid sites and the concentration of oxygen defects. When formic acid was added into the reaction system, 4,6âÂÂÃâÃâ¬ÂÂÃâÃâDMDBT oxidation was significantly improved. Formic acid may react with hydrogen peroxide to produce performic acid which interacts with W⁵⁺ /W⁶⁺ or V⁴⁺/V⁵⁺ ions in the catalyst surface to form peroxometallic complexes. With respect to the H₂O₂ oxidant, the peroxometallic complexes are more active for sulfur oxidation due to its asymmetrical character in the bond MâÂÂÃâÃâ¬ÂÂÃâÃâOâÂÂÃâÃâ¬ÂÂÃâÃâOâÂÂÃâÃâ¬ÂÂÃâÃâH (M =W or V) and thus benefits to enhancement of the oxidative desulfurization efficiency. A surface reaction mechanism involving peroxometallic complexes formation, 4,6âÂÂÃâÃâ¬ÂÂÃâÃâDMDBT molecules adsorption, and surface oxidation reaction on structural defects or Lewis acid sites of the catalysts was proposed. This biphasic reaction system consisting of a catalyst bearing Lewis acid sites, a green oxidant, an oxidant promoter, and a polar solvent would simultaneously perform the oxidation and separation of polyaromatic sulfur compounds in one operation which was very practical for ultralow sulfur diesel production.