Affiliation: | a Institute of Physical Chemistry, Splaiul Independentei 202, Bucharest 77208, Romania b Department of Chemical Technology and Catalysis, Faculty of Chemistry, University of Bucharest, B-dul Regina Elisabeta 4-12, Bucharest 70346, Romania c Université catholique de Louvain, Unité de Catalyse et chimie des matériaux divisés, Place Croix du Sud 2, bte 17, 1348 Louvain-la-Neuve, Belgium |
Abstract: | Co–Nb2O5–SiO2 catalysts were prepared using three different sol–gel procedures: (i) the colloidal sol–gel method using NbCl5 and SiCl4 as precursors; (ii) the polymeric sol–gel method using niobium ethoxide and tetraethyl-orthosilicate (TEOS); (iii) an intermediate procedure between the colloidal and polymeric sol–gel method in which the precursors were those utilized in the CSG but dissolved in a mixture of anhydrous ethanol and CCl4. In all procedures, the elimination of the solvent carried out between 80 and 110°C was followed by a reduction in hydrogen flow (30 ml min−1) at 773 K. Following these procedures, samples containing 10 wt.% Co and 15 wt.% niobium oxide (expressed as Nb2O5) were obtained. The characterization of the catalysts was performed using various techniques: N2 adsorption and desorption curves at 77 K, NH3- and H2-chemisorption, TPO, XPS, XRD, and solid state 1H MAS-NMR. Hydrogenolysis of butane was evaluated. The low reaction rates are assigned to the effect of the metal size, whereas the isobutane selectivity as well as the relatively high stability is due to the acidity of the support. |