Activated carbons are receiving great attention in the last decades as catalysts and catalyst supports due to some advantages, such as, their very high specific surface area, high thermal and chemical stability and the presence of stable basic and acid surface sites as oxygen surface groups. We havepreviou sly reported the preparation and characterization of activated carbons by chemical activation of different lignocelullosic waste and by-products with phosphoric acid [1,2]. The carbons obtained
showed a particular surface chemistry due to acid surface phosphorus groups of high thermal
stability that remain over the carbon surface, providing the carbons a high oxidation resistance and surface acidity.
In this work, we study the catalytic conversion of ethanol and methanol over an acid carbon-based
catalyst obtained by chemical activation of olive stone with H3PO4. The carbon catalyst is active for both reactions, yielding mainly dehydration products, that is, dimethyl ether (SDME>82% at 350ºC) and ethylene (Sethylene>91% at 325ºC), with lower amounts of diethyl ether, for methanol and
ethanol decomposition, respectively.
The activated carbon catalytic activity and stability, under inert and oxidant atmospheres, as well as, different regeneration procedures were analyzed. Results evidence that catalytic performance strongly depends on the type of atmosphere in which the reaction proceeds and suggest that oxygen would play a key role on theses catalytic processes. In the absence of oxygen, catalyst suffers a progressive deactivation by coke deposition on the active acid
sites, being faster and more pronounced for methanol decomposition (Fig. 1). However, in the presence of air, the carbon surface chemistry is modified, probably through oxygen spillover on the catalyst surface, where the availability of labile
oxygen would inhibit catalyst deactivation and allow steady state conditions to be reached. Furthermore, the presence of oxygen leads to significant enhancements of both alcohol conversions and could even partially regenerate the catalyst.Universidad de Málaga. Campus de Excelencia Internacional Andalucía Tec
