The characterization of fluoride-modified Mo/Al2O3 catalysts was performed in order to investigate on the effect that low levels of fluoridation of the alumina support (0-2.0 wt.%) cause on the support itself and on the supported Mo oxide and sulfide phases. Fluoride-modified Al-2-O-3 supports and Mo/Al-2-O-3 catalysts where characterized by nitrogen physisorption, scanning electronic microscopy (SEM-EDX), isoelectric point (IEP), Fourier transform infrared spectroscopy (FT-IR), infrared spectroscopy of adsorbed CO2 (IR-CO2) and temperature programmed reduction (TPR). The dispersion of the sulfided catalysts was estimated by dynamic NO chemisorption. The results indicate that the different hydroxyl types present on the alumina surface react to a different extent with fluoride and that it is the most basic hydroxyl groups that are titrated first. The consumption of the alumina OH by F-, inhibits, during the deposition of Mo, the formation of tetrahedral molybdenum oxide species in strong interaction with the support, leading to an increased number of polymeric octahedral Mo surface species. The NO adsorption results put in evidence a drop in the dispersion of the MOS2 phase present in the sulfided samples. (C) 2003 Elsevier Science B.V. All rights reserved.
Fluoride modification of Mo/Al2O3 catalysts characterization of the changes induced in support and Mo phases
BUSCA, GUIDO
2003-01-01
Abstract
The characterization of fluoride-modified Mo/Al2O3 catalysts was performed in order to investigate on the effect that low levels of fluoridation of the alumina support (0-2.0 wt.%) cause on the support itself and on the supported Mo oxide and sulfide phases. Fluoride-modified Al-2-O-3 supports and Mo/Al-2-O-3 catalysts where characterized by nitrogen physisorption, scanning electronic microscopy (SEM-EDX), isoelectric point (IEP), Fourier transform infrared spectroscopy (FT-IR), infrared spectroscopy of adsorbed CO2 (IR-CO2) and temperature programmed reduction (TPR). The dispersion of the sulfided catalysts was estimated by dynamic NO chemisorption. The results indicate that the different hydroxyl types present on the alumina surface react to a different extent with fluoride and that it is the most basic hydroxyl groups that are titrated first. The consumption of the alumina OH by F-, inhibits, during the deposition of Mo, the formation of tetrahedral molybdenum oxide species in strong interaction with the support, leading to an increased number of polymeric octahedral Mo surface species. The NO adsorption results put in evidence a drop in the dispersion of the MOS2 phase present in the sulfided samples. (C) 2003 Elsevier Science B.V. All rights reserved.
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
