Sulfated tin oxide was synthesized from a hydroxylated tin oxide obtained by the precipitation method, followed by ion exchange of OH groups by SO4 species with a sulfuric acid solution. The samples were characterized by X-ray diffraction, transmission electron microscopy, thermoanalysis, and nitrogen physisorption by the Brunauer-Emmett-Teller method. The rutile crystalline structure was refined by the Rietveld method. Thermal analysis suggests the following stoichiometric formulas: SnO2-x(OH)2x and SnO2-x(OH)x(HSO4)x with X = 0.35 and 0.17 for non-sulfated and sulfated samples, respectively. The SO4 species remained strongly bonded at the SnO2 surface stabilizing its crystallite size against sintering, inhibiting the crystallite aggregation, and it acts as a structure porogen director mediating nanoparticle growth and assembly yielding a mesostructure form of SnO2 with wormhole morphology and high thermal stability. The interaction between SO4(2-) and the SnO2 surface changes the symmetry of the representative tin-oxygen octahedron. It relaxes the four tin-oxygen bond lengths located at the basal plane of the octahedron while the two apical Sn-O bonds decrease, producing a strong deformed octahedron, which could be transformed into a higher asymmetry in the electronic distribution around the Sn4+ nuclei. The elimination of SO4 groups brings about the coalescence and crystallite growth, which collapse the mesostructure form of SnO2, decreasing the surface area and porosity.
WO3-ZrO2 catalysts were synthesized by precipitating the aqueous solutions of zirconium oxynitrate and ammonium metatungstate with ammonium hydroxide. The white slurry precipitate was treated under three different conditions. In the as-made materials, the amorphous phase was formed in the aged and refluxed samples, while well-crystallized tetragonal and monoclinic phases were obtained in the hydrothermally treated sample. The real amount of tungsten loaded in the samples was similar for the three samples, independently of the treatments; however, the tungsten surface atomic density in the annealed WO3-ZrO2 samples varied between 6 and 9 W atoms/nm2. Two different contrast types of aggregates were determined by scanning electron microscopy, the white particles which are rich in W, and the gray ones which are rich in zirconium; both of them were formed in the calcined solids prepared under aging or reflux condition. A very high dispersion of tungsten species on the zirconia surface was achieved in the hydrothermally treated sample. The degree of the interaction between WO(x) and ZrO2 surface strongly modified the Zr-O bond lengths and bond angles in the structure of tetragonal zirconia as proved by X-ray diffraction analysis and the Rietveld refinement. The catalyst obtained under hydrothermal condition exhibited the highest dispersion of tungsten species in the zirconia, which in turn causes strong structural deformation of the tetragonal ZrO2 phase responsible of the strongest surface acidity and, consequently, the optimum catalytic activity for n-hexane isomerization.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.