Abstract
Direct formation of 3–30% (w/w) LaFeO3/MCM−41, nanocomposite catalysts were performed by a sol−gel process, followed by calcination at 550 and 750 °C. The nanocomposites were characterized through different techniques including LAXRD, WAXRD, EDX, simultaneous TG−DTA, ATR−FTIR, nitrogen adsorption/desorption, and TEM. The nanocomposites featured high surface areas (up to 1000 m2/g) and enhanced thermal stability. The direct formation method led to nanodispersion and size confinement of LaFeO3 in MCM−41 mesopores. The nanocomposites showed very high catalytic activity for isopropanol conversion, whereas their parent materials (blank MCM-41 or bulk LaFeO3) were totally inactive under the same reaction conditions. Thus, nanocomposite catalysts with low loading ratios and low calcination temperature produced pure dehydration product (propene) with very high conversion and total selectivity. Nanocomposite catalysts with high loading ratios and high calcination temperature produced an appreciable amount of the dehydrogenation product (acetone) as well as the dehydration products. Moreover, high loading ratios at high reaction temperatures in air atmosphere led to the formation of oxidation products. The different reactivities of the nanocomposite catalysts were discussed and correlated to their nanostructure, in terms of enhancing of the mesoporous textures with surface acidity, oxidation ability and thermal stability.
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•The method led to nanodispersion and size confinement of LaFeO3 in MCM-41 pores.•Catalytic products of isopropanol conversion were based on dispersion case of LaFeO3.•Low LaFeO3/MCM-41 w/w catalysts led to pure dehydration with 100% yield.•High LaFeO3/MCM-41 w/w catalysts calcined at high temperature led to oxidation.•The method can be generalized for different perovskites -type mixed metal oxides.