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   <subfield code="a">On the influence of the acid-base character of catalysts on the oxidative dehydrogenation of alkanes</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[P. Concepción, A. Galli, J. Nieto, A. Dejoz, M. Vazquez]</subfield>
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   <subfield code="a">Vanadium oxides supported on metal oxide, i.e. Al2O3, MgO and Mg-Al mixed oxide, and V-containing microporous materials (VAPO-5 and MgVAPO-5) have been tested in the oxidative dehydrogenation of C2-C4 alkanes. In all cases, tetrahedral vanadium species (isolated and/or associated) were mainly observed from51V-NMR and diffuse reflectance spectroscopies. The reducibility of V5+-species, determined from the onset-reduction temperature, decreases as follows: VOx/AL &gt; VAPO-5 &gt; MgVAPO-5 =VOx/MG &gt; VOx/MG + AL. The acid character of catalysts, determined from the FTIR spectra of pyridine adsorbed, decreases as: MgVAPO-5 &gt; VOx/AL &gt; VAPO-5 &gt; VOx/MG + AL &gt; VOx/MG. A similar trend between V-reducibility of the catalyst and its catalytic activity for the alkane conversion was observed. However, the selectivity to olefins depends on the acid-base character of catalyst and the alkane fed. In the ODH ofn-butane, the higher the acid character of the catalyst the lower the selectivity to C4-olefins, while in the ODH of ethane an opposite trend between the catalyst acidity and the selectivity to ethene was observed.</subfield>
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