Abstract

The one‐step selective oxidation of methanol to dimethoxymethane (DMM) was demonstrated over titania‐supported molybdenum oxide catalysts, containing different amounts of molybdenum and prepared using two different impregnation techniques, namely wet impregnation and incipient wetness impregnation. The corresponding catalysts exhibited both acidic and redox properties, which are necessary for the oxidation of methanol to formaldehyde with subsequent condensation of the latter with excess methanol to finally yield DMM. The formation of well‐dispersed polyoxomolybdate species on the catalyst surface was evidenced using IR‐Raman, X‐ray diffraction, and nitrogen physisorption. Varying the amount of these polyoxomolydate species was associated with a modulation of the acidic and redox properties, as shown by NH₃‐TPD and H₂‐TPR. With respect to the catalytic performances, the best balance between acid and redox properties was observed over the samples containing 8 wt.% Mo, which corresponds to a theoretical MoO _x species coverage close to a monolayer.

Two series of oxomolybdate species supported on TiO₂ were synthesized by incipient wetness impregnation and wet impregnation, respectively. After detailed characterizations of the catalysts physical and chemical properties, the catalytic activity tests evidenced that the 8 wt.% Mo/TiO₂ was the most efficient solid in dimethoxymethane synthesis from methanol (81% in selectivity at 5% in conversion at 170°C). The results showed that a submonolayer was required to optimized the dimethoxymethane synthesis.