Effect of treatment temperature on structures and properties of zirconia-supported ruthenium oxide catalysts for selective oxidation of methanol to methyl formate

Abstract

The structures of the RuOx species supported on monoclinic ZrO2 (m-ZrO2) after treatment in a wide temperature range 673–1323K were characterized by X-ray diffraction, Raman, infrared and X-ray photoelectron spectroscopies, and temperature-programmed reduction in H2. Their catalytic properties were examined in the selective oxidation of methanol to methyl formate at 373K. The RuOx species were present as highly dispersed RuO42− on m-ZrO2 with Ru surface densities of 0.2–2.2Ru/nm2, irrespective of the treatment temperatures. Their molecular structures evolved from umbrella-like dioxo (O)2Ru(OH)–O–Zr (containing a Ru–OH bond and a Ru–O–Zr bond to m-ZrO2 surface) into tetrahedral dioxo (O)2Ru–(O–Zr)2 with increasing the treatment temperatures from 673 to 773K, and into pyramidic mono-oxo ORu–(O–Zr)4 above 1173K, induced by the stronger interaction between the RuOx species and underlying m-ZrO2 surface at the higher temperatures. Following such structural changes, the turnover rates of the methanol oxidation increased markedly, and reached the greatest value (39.0mol/mol Ru-h) on the catalyst treated at 1223K, as a result of the parallel increase in the reducibility of the RuOx species, consistent with the known Mars–van Krevelen redox mechanism using lattice oxygen atoms on RuOx. These understandings may be useful for improving the reactivity of the RuOx-based catalysts for the selective oxidation of methanol as well as of other alcohols and probably light hydrocarbons, for instance, by synthesis and tuning of the more reducible di-oxo RuO42− structures.