TY - JOUR
T1 - Surface properties of catalytic aluminas modified by alkaline-earth metal cations
T2 - A microcalorimetric and IR-spectroscopic study
AU - Bolis, Vera
AU - Magnacca, Giuliana
AU - Morterra, Claudio
N1 - Funding Information:
Acknowledgements The authors gratefully acknowledge the Italian "Consiglio Nazionale delle Ricerche (CNR)" for financial support (Comitato Nazionale per le Ricerche Tecnologiche; Contributo di ricerca N. 94.00544.CT11, Effect of form on the surface chemistry of finely divided solids).
PY - 1999
Y1 - 1999
N2 - Lewis acidic properties of transition aluminas whose surfaces have been doped with alkaline-earth metal cations (Ca2+ and Ba2+) were studied by means of the room temperature adsorption of carbon monoxide. The vibrational features of CO adsorbed at the surface of doped aluminas were investigated by IR spectroscopy in comparison with pure parent aluminas, while the quantitative and energetic features were studied by adsorption microcalorimetry. Various CO adspecies were found to form at the surface of both pure and doped-alumina, owing to the structural heterogeneity of the Al2O3 surface and to the presence of alkaline-earth metal cations. The surface heterogeneity was revealed by different νCO stretching frequencies, namely νCO ≈ 2230, 2218 and 2205 cm-1 for coordinatively unsaturated tetrahedral Al3+ cations in different crystallographic configurations, and νCO ≈ 2186 and 2172 cm-1 for coordinatively unsaturated Ca2+ and Ba2+ cations, respectively. Heats of adsorption of ≈ 80, 70 and 55 kJ/mol were assigned to the formation of Al3+/CO complexes, ≈ 45 kJ/mol for Ca2+/CO and ≈ 30 kJ/mol for Ba2+/CO complexes. The latter value was estimated through a correlation curve existing between νCO stretching frequencies and adsorption enthalpies. This correlation, already proposed in the past for CO adsorbed on non-d/d0/d10 metal cations, has been revisited and confirmed here, by including Al2O3 data for which an apparent lack of correlation between the two parameters was first observed. With respect to pure alumina, the population of Lewis acidic sites was found to be significantly depressed by the presence of alkaline-earth cus metal cations. These acidic sites are intrinsically weaker than tetrahedral eus Al3+ cations, as witnessed by smaller upward shifts of the νCO stretching frequencies with respect to CO gas and lower heats of adsorption, in accordance with expectations from the charge/ionic radius ratios. Ca2+ cations were found to compete in adsorbing CO with Al3+ cations more efficiently than the larger Ba2+ cations. In the case of CaO/Al2O3 systems outgassed at 1023 K, a thin surface layer of calcium aluminate, not detected by XRD or HRTEM, was suggested to form.
AB - Lewis acidic properties of transition aluminas whose surfaces have been doped with alkaline-earth metal cations (Ca2+ and Ba2+) were studied by means of the room temperature adsorption of carbon monoxide. The vibrational features of CO adsorbed at the surface of doped aluminas were investigated by IR spectroscopy in comparison with pure parent aluminas, while the quantitative and energetic features were studied by adsorption microcalorimetry. Various CO adspecies were found to form at the surface of both pure and doped-alumina, owing to the structural heterogeneity of the Al2O3 surface and to the presence of alkaline-earth metal cations. The surface heterogeneity was revealed by different νCO stretching frequencies, namely νCO ≈ 2230, 2218 and 2205 cm-1 for coordinatively unsaturated tetrahedral Al3+ cations in different crystallographic configurations, and νCO ≈ 2186 and 2172 cm-1 for coordinatively unsaturated Ca2+ and Ba2+ cations, respectively. Heats of adsorption of ≈ 80, 70 and 55 kJ/mol were assigned to the formation of Al3+/CO complexes, ≈ 45 kJ/mol for Ca2+/CO and ≈ 30 kJ/mol for Ba2+/CO complexes. The latter value was estimated through a correlation curve existing between νCO stretching frequencies and adsorption enthalpies. This correlation, already proposed in the past for CO adsorbed on non-d/d0/d10 metal cations, has been revisited and confirmed here, by including Al2O3 data for which an apparent lack of correlation between the two parameters was first observed. With respect to pure alumina, the population of Lewis acidic sites was found to be significantly depressed by the presence of alkaline-earth cus metal cations. These acidic sites are intrinsically weaker than tetrahedral eus Al3+ cations, as witnessed by smaller upward shifts of the νCO stretching frequencies with respect to CO gas and lower heats of adsorption, in accordance with expectations from the charge/ionic radius ratios. Ca2+ cations were found to compete in adsorbing CO with Al3+ cations more efficiently than the larger Ba2+ cations. In the case of CaO/Al2O3 systems outgassed at 1023 K, a thin surface layer of calcium aluminate, not detected by XRD or HRTEM, was suggested to form.
UR - http://www.scopus.com/inward/record.url?scp=0002110263&partnerID=8YFLogxK
U2 - 10.1163/156856799X00374
DO - 10.1163/156856799X00374
M3 - Article
SN - 0922-6168
VL - 25
SP - 25
EP - 56
JO - Research on Chemical Intermediates
JF - Research on Chemical Intermediates
IS - 1
ER -