Silica–alumina (SA) was used as support for dispersing CuO, Ga2O3, SnO2 oxide phases and the corresponding binary couplings (CuGa/SA and CuSn/SA samples). The acidity of uncovered SA and of SA-supported oxides was studied from a qualitative (nature of acid sites) and quantitative (number, acid strength, and strength distribution of acid sites) points of view by an integrated approach. The adsorption and desorption of basic probes (ammonia and pyridine) onto the acidic surfaces were monitored by the coupled volumetric–calorimetric technique, and by XPS and FT-IR spectroscopy. The results show that the Broensted acidity of the SA support was converted into predominantly Lewis acidity upon metal oxide deposition. The high dispersion of the copper oxide phase was responsible for this phenomenon. Differences of acid strength distribution were noticed among the samples. Moderate acidity was associated with the Cu sites (100 kJ/mol< qdiff < 150 kJ/mol), whereas the most acidic fraction of the sites (qdiff > 150 kJ/mol) increased with the presence of Ga and Sn. The experimental results are discussed in the light of the intrinsic acidity of the Cu, Ga, and Sn metal ions derived from electronic parameters.

Surface acidic properties of supported binary oxides containing CuO coupled with Ga2O3 and SnO2 studied by complementary techniques / A. Gervasini, S. Bennici, A. Auroux, C. Guimon. - In: APPLIED CATALYSIS A: GENERAL. - ISSN 0926-860X. - 331:1(2007), pp. 129-137.

Surface acidic properties of supported binary oxides containing CuO coupled with Ga2O3 and SnO2 studied by complementary techniques

A. Gervasini
Primo
;
S. Bennici
Secondo
;
2007

Abstract

Silica–alumina (SA) was used as support for dispersing CuO, Ga2O3, SnO2 oxide phases and the corresponding binary couplings (CuGa/SA and CuSn/SA samples). The acidity of uncovered SA and of SA-supported oxides was studied from a qualitative (nature of acid sites) and quantitative (number, acid strength, and strength distribution of acid sites) points of view by an integrated approach. The adsorption and desorption of basic probes (ammonia and pyridine) onto the acidic surfaces were monitored by the coupled volumetric–calorimetric technique, and by XPS and FT-IR spectroscopy. The results show that the Broensted acidity of the SA support was converted into predominantly Lewis acidity upon metal oxide deposition. The high dispersion of the copper oxide phase was responsible for this phenomenon. Differences of acid strength distribution were noticed among the samples. Moderate acidity was associated with the Cu sites (100 kJ/mol< qdiff < 150 kJ/mol), whereas the most acidic fraction of the sites (qdiff > 150 kJ/mol) increased with the presence of Ga and Sn. The experimental results are discussed in the light of the intrinsic acidity of the Cu, Ga, and Sn metal ions derived from electronic parameters.
Supported metal oxides ; Copper oxide ; Gallium oxide ; Tin oxide ; Surface acidity ; Adsorption microcalorimetry ; X-ray spectrophotometry ; Fourier transform infrared spectroscopy
Settore CHIM/02 - Chimica Fisica
2007
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/42449
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