Abstract
The acidic properties of alumina-supported molybdenum oxide (MoO3/Al2O3) calcined at high temperatures, with MoO3 loadings of 5–30wt%, were investigated using acid-catalyzed reactions (benzylation of anisole and isomerization of α-pinene), and Fourier-transformed infrared spectroscopy (FT-IR). The structure of MoO3 on Al2O3 was characterized by X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectra (XPS), and X-ray absorption fine structure (XAFS) analysis. The correlation between acidic property and structure is discussed. Brønsted acid sites, where acid-catalyzed reactions take place, are generated on MoO3/Al2O3 by calcination at high temperatures. 11wt% MoO3/Al2O3 calcined at 1073K exhibited the highest activity, and the largest numbers of Brønsted acid sites were generated. XPS and Mo K-edge XAFS revealed that molybdenum oxide monolayer domains with distorted MoO6 units and small MoO3 clusters were formed and molybdenum oxide monolayer domains were stabilized on alumina below 11wt% of MoO3 loading. Brønsted acid sites are probably generated at boundaries between molybdenum oxide monolayer domains and/or small MoO3 clusters. When the MoO3 loading was sufficient to form two-dimensional molybdenum oxide overlayers (>11wt%), some of the Brønsted acid sites on MoO3/Al2O3 was covered with Al2Mo3O12 having no Brønsted acid site, resulting in a lowering of the catalytic activity.
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