Conclusions
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1.
The method of photoelectron spectroscopy has been used to show that the Co and Mo ions of CoO-MoO3-Al2O3 catalysts interact with the γ-Al2O3 lattice, the Mo ions blocking the penetration of the Co ions. Formation of metallic Co promotes extensive Mo ion reduction.
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2.
Thermal treatment of the CoO-MoO3-Al2O3 catalyst in air tends to enrich the surface with respect to Mo ions, while reduction enriches the surface with respect to Co ions.
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3.
Oxidational treatment of the CoO-MoO3-Al2O3 and MoO3-Al2O3 catalysts is required for formation of anthracene radical-cations. A description is given of an oxidizing center structure which accounts for the reduction in acceptor activity of the Mo6+ ions in the ternary system.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 10, pp. 2225–2233, October, 1978.
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Slinkin, A.A., Antoshin, G.V., Loktev, M.I. et al. The phase composition and reduction of CoO-Al2O3, MoO3-Al2O3, and CoO-MoO3-A12O3 catalysts. Russ Chem Bull 27, 1965–1972 (1978). https://doi.org/10.1007/BF00946507
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DOI: https://doi.org/10.1007/BF00946507