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Hydrotalcite-derived mixed oxides as catalysts for different C-C bond formation reactions from bioorganic materials

机译:水滑石衍生的混合氧化物作为生物有机材料不同的C-C键形成反应的催化剂

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摘要

The performance of a hydrotalcite-derived mixed oxide (Mg3AlO_x) for the three different aldolization reactions, concerned with the valorisation of biomass derivatives, has been studied in this work. The studied reactions were acetone self-condensation, ethanol condensation for the synthesis of C4 chemicals, and the aldolization of aqueous mixtures of acetone and furfural. The gas phase condensation of acetone generates mesityl oxide (C6) and isophorones (C9) as main products, with high selectivities for mesityl oxide (up to 80%). Reaction of ethanol leads to butanol and 1,3-butadiene, although important amounts of undesired ethylene were found at the highest temperatures. Concerning to the liquid-phase condensation of furfural with acetone, C8 and C_(13) species were found as reaction products. The performance of the catalysts can be explained in terms of the distribution of acid and basic sites determined by NH3- and CO2-TPD, being needed medium strength basic sites (M~(n+)-O~(2-) pairs) for the condensation reactions, whereas the presence of acid-base pairs are needed for alcohols dehydrogenation (previous step for the condensation when ethanol is used as reactant). The presence of acid sites also leads to lateral reactions, such as the dehydration of ethanol or the rearrangement of lineal phorones into cyclic compounds (isophorones) in the reaction of acetone.
机译:在这项工作中,研究了水滑石衍生的混合氧化物(Mg3AlO_x)在三种不同的醛醇缩合反应中的性能,涉及生物质衍生物的增值。所研究的反应是丙酮自缩合,乙醇缩合以合成C4化学品以及丙酮和糠醛的水性混合物醛醇缩合。丙酮的气相缩合生成异丁烯二氧化物(C6)和异佛尔酮(C9)作为主要产物,对异丁烯二氧化物的选择性高(高达80%)。乙醇反应生成丁醇和1,3-丁二烯,尽管在最高温度下发现了大量不希望的乙烯。关于糠醛与丙酮的液相缩合,发现C8和C_(13)物种为反应产物。催化剂的性能可以用酸的分布和由NH3-和CO2-TPD确定的碱性位点来解释,这是催化剂所需的中等强度碱性位点(M〜(n +)-O〜(2-)对)。缩合反应,而醇脱氢则需要酸碱对的存在(当使用乙醇作为反应物时,缩合的先前步骤)。酸位的存在还导致副反应,例如乙醇的脱水或在丙酮反应中将线型佛尔酮重新排列成环状化合物(异佛尔酮)。

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