Chromia/zirconia catalysts with Cr content exceeding the monolayer. A comparison with chromia/alumina and chromia/silica for isobutane dehydrogenation

• Published in: Applied catalysis. A, General Vol. 167; no. 2; pp. 257 - 270
• Main Authors: De Rossi, Sergio, Pia Casaletto, Maria, Ferraris, Giovanni, Cimino, Alessandro, Minelli, Giuliano
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier B.V 27-02-1998; Elsevier
• Subjects: Alkane dehydrogenation; Catalysis; Catalysts: preparations and properties; Chemistry; Chromia on alumina; Chromia on silica; Chromia on zirconia; Exact sciences and technology; General and physical chemistry; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry; Alkane dehydrogenation; Chromia on silica; Chromia on zirconia; Chromia on alumina; Binary compound; Transition metal Compounds; Experimental study; Ultraviolet spectrometry; X ray diffraction; Silica; Supported catalyst; Characterization; Zirconia; Heterogeneous catalysis; Chromium Oxides; Dehydrogenation; Alkane; Isobutane; Catalyst activity; Alumina
• ISSN: 0926-860X; 1873-3875
• DOI: 10.1016/S0926-860X(97)00315-3

CrO
x
/ZrO
2, CrO
x
/γ-Al
2O
3 and CrO
x
/SiO
2 catalysts were prepared by wet impregnation in the loading range 0.05–14
atoms Cr
nm
−2, that is below and above the monolayer capacity of support. The samples were characterized by chemical analysis, including carbon monoxide reduction and Cr
VI extraction with sodium hydroxide or water, and by XRPD, UV-Vis DRS and ESR. Several Cr species were identified, namely Cr
VI, Cr
V (ESR γ-signal), Cr
III (ESR δ-signal), small Cr
III oxide clusters (ESR β-signal) and α-chromia. The relative abundance of these Cr species was found to be mainly controlled by the specific support employed and the Cr concentration. The catalytic activity in the isobutane dehydrogenation was studied at 723 and 773
K in a flow microreactor. It was found that the activity per total Cr atom was markedly higher for the zirconia-based catalysts compared with the other two systems in all the explored Cr concentration range. That is, the CrO
x
/ZrO
2 interaction maintains its positive effect well beyond the monolayer capacity of this support. Moreover, the catalytic activity correlated with the amount of high-oxidation state chromium (Cr
VI and Cr
V), evaluated by the quantity of extractable Cr or by the consumption of carbon monoxide in the catalyst reduction. The larger concentration of mononuclear Cr
V species on zirconia, confirmed here, is thought to be responsible for the higher activity of the zirconia-based catalysts, through reduction to active mononuclear Cr
III species under reaction conditions.