|dc.description.abstract||The aim of this work was to characterize an alumina supported Pt catalyst
before and after post- and pre-modification with WO3. A 2wt%Ru/Al2O3
and a WO3/ZrO2 catalyst were also characterized.
Pt/Al2O3 with a loading of 1wt%Pt was prepared by one step aqueous incipient
wetness impregnation. Post and pre-modified 1wt%Pt-1.3wt%WO3 catalyst
was prepared by two step aqueous incipient wetness impregnation. In this work,
characterization by N2 adsorption, H2 and CO chemisorption, X-ray
fluorescence (XRD), Scanning electron microscopy (SEM), energy-dispersive X-ray
analysis (EDS), X-ray diffraction (XRD), temperature programmed reduction (TPR),
Fourier transform infra-red Attenuated Total Reflectance (FTIR-ATR) and in-situ
Diffuse Reflectance Infrared Fourier Transform Spectroscopy (DRIFTS) with
pyridine adsorption were performed.
Nitrogen adsorption showed that the addition of platinum and tungsten oxide did
not alter the surface area, pore size or pore volume of the support.
Chemisorption showed a good dispersion of platina on alumina, but this
decreased slightly when modified by WO3, indicating blockage of active
sites. XRF measurements shows a metal loading of 1.2wt\%Pt for unmodified
catalyst, and 0.8wt%Pt and 0.7%wtWO3 for both post- and pre-modified
catalyst. No reliable results were obtained from TPR, which could mean that
platinum was already in its elemental state. Due to the low Pt and WO3
content and highly amorphous alumina, assignment of phase type or calculation
of crystallite size with XRD was not feasible. Ex-situ investigation with ATR
did not detect changes in the surface structure after addition of Pt and WO3.
DRIFT investigations shows that band associated with strong and medium Lewis
acid sites are barely present in Pt/Al2O3 catalyst. By contrast, these
bands increased in intensity for post- and pre-modified catalyst. This
indicates increased acidity of the alumina after WO3 addition.
These results will later be used in the investigation of a suitable catalyst
for the current non-catalytic NO oxidation step in nitric acid production.||