0000000000671273
AUTHOR
V. Cortés Corberán
Catalytic combustion of ethane over high surface area Ln1−xKxMnO3 (Ln = La, Nd) perovskites: The effect of potassium substitution
Publisher Summary As a general trend, the substitution of the rare earth cation by potassium decreased the intrinsic activity, reduced the reaction order in oxygen, and, for the more substituted samples (x>0.10), it increased the selectivity to ethene. Supported platinum or palladium catalysts have so far been used almost exclusively, because of their excellent activity. However, their high price, tendency to be poisoned, and volatility in some applications have estimulated the search for suitable substitutes. LaCoO3, as a potential auto exhaust catalyst, starting a wide interest in the catalytic properties of perovskites. Their specific application as catalysts in flameless combustion has …
Synthesis of high surface area perovskite catalysts by non-conventional routes
Abstract The use of rare earth-containing perovskite oxides as total oxidation catalysts faces to the difficulty of obtaining high surface area materials and the need of calcination at high temperatures for its synthesis. In this work, perovskite NdCoO3 catalysts with relatively high surface areas were synthesized at soft calcination conditions by two non-conventional routes: heteronuclear organic complexes and amorphous precursors obtained by freeze-drying of nitrates solutions. Depending on the method used, different degrees of homogeneity in the bulk distribution of the component cations, oxygen non-stoichiometry as well as surface Co/Nd atomic ratios are obtained. In this way, the synth…
Selective oxidative activation of isobutane on a novel vanadium-substituted bimodal mesoporous oxide V-UVM-7
Abstract New vanado-silicates with a bimodal mesoporous system (V-UVM-7) and high vanadium contents (Si/V ≥ 7) have been prepared by a modification of the so-called atrane method. Its morphology consists of aggregation of nano-particles with V-MCM-41 structure, creating a second broader porous system in their interparticle space. Its structure allows to incorporate a high V contents into tetrahedral sites of the framework while keeping vanadium dispersion. V-UVM-7 catalysts are very active and selective for the direct transformation of isobutane to isobutene and methacrolein. Total conversion and methacrolein-to-isobutene ratio in the products increased with increasing vanadium contents. Th…
Oxidative dehydrogenation of isobutane over Co-MCM-41 catalysts
Abstract Cobalt-containing mesoporous silicates with MCM-41-like structure, with Si/Co≥49, are active and selective catalysts for the oxidative dehydrogenation (ODH) of isobutane. The formation of dehydrogenation products is analysed in terms of the nature of the cobalt species, tetrahedral Co(II), and heterogeneously initiated gas-phase reactions inside the mesopores.
Direct oxidation of isobutane to methacrolein over V-MCM-41 catalysts
High vanadium content mesoporous vanado-silicates with MCM-41-like structure, obtained by the atrane route, catalyse the direct oxidation of isobutane to methacrolein with 30% selectivity, and a total dehydrogenation (olefin plus methacrolein) selectivity up to 74%.