Journal
PHYSICAL CHEMISTRY CHEMICAL PHYSICS
Volume 4, Issue 13, Pages 3136-3145Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b110444f
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ZrO(2)-SO(4) (SZ) powders were prepared by calcining at 740, 820, and 900 K hydrous precursors, obtained by a hydrothermal precipitation route from ZrCl(4) solutions at 334 K, and subsequently sulfated with H(2)SO(4) (1 M). The samples were characterised as to phase composition (XRD, Raman spectroscopy), surface area (BET) and total sulfur content. Surface functionalities and acidity features were investigated by FTIR spectroscopy of the powders themselves and of probe molecules ( carbon monoxide, pyridine) adsorbed thereon. By a revised Hammett-Bertolacini technique, both the density and strength of the (protonic) surface sites were obtained. XPS analyses of the samples were performed by elaboration of the sulfur 2p, oxygen 1s and zirconium 3d spectral regions. Catalytic tests were performed both in the gas phase, for the isomerisation of n-butane at 423 and 523 K, and in liquid media, for the esterification of benzoic acid to methylbenzoate. Correlations were obtained with the samples calcination temperature, catalytic activity, distribution of Lewis/Bronsted acid sites, and spectral features of the XPS Zr 3d doublet.
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