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Dehydrogenation of Ethylbenzene over Vanadium Oxide-Loaded MgO Catalyst: Promoting Effect of Carbn Dioxide

机译:氧化钒负载的MgO催化剂上乙苯的脱氢:二氧化碳的促进作用

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摘要

The dehydrogenation of ethylbenzene over a vanadium oxide-loaded MgO catalyst was investigated using carbon dioxide. The styrene yield in the presence of carbon dioxide was 2.5 times higher than that in the absence of carbon dioxide (argon atmosphere) at 823 K, indicating that carbon dioxide markedly promoted the dehydrogenation of ethylbenzene. At 873 K, the same catalyst afforded the highest styrene yield, 73.8% with a selectivity of 90.1%, in the presence of carbon dioxide. In order to elucidate the role of carbon dioxide in this reaction, characterization of the catalyst was carried out via methods such as temperature-programmed reduction, temperature-programmed reaction with carbon dioxide, and UV-visible, FT-IR, and XRD spectroscopies. Carbon dioxide behaved as an oxidant for the vanadium species, and the surface vanadium species were kept in a high oxidation state with carbon dioxide during the dehydrogenation reaction. Active phases of vanadium in the dehydrogenation reaction were believed to be V~(5+) species in V_2O_5 or Mg_3V_2O_8 on highly dispersed MgO. The reduced species, V~(4+) and V~(3+), were less reactive sites for the dehydrogenation.
机译:使用二氧化碳研究了在负载钒氧化物的MgO催化剂上乙苯的脱氢作用。在存在二氧化碳的情况下,在823 K时,苯乙烯的收率是在没有二氧化碳的情况下(氩气)的收率高2.5倍,表明二氧化碳显着促进了乙苯的脱氢。在二氧化碳存在下,在873 K下,相同的催化剂提供了最高的苯乙烯产率,为73.8%,选择性为90.1%。为了阐明二氧化碳在该反应中的作用,通过诸如程序升温还原,与二氧化碳的程序升温反应以及紫外可见光谱,FT-IR和XRD光谱学等方法对催化剂进行了表征。二氧化碳充当钒物种的氧化剂,并且在脱氢反应期间,表面钒物种被二氧化碳保持在高氧化态。认为在脱氢反应中钒的活性相是高度分散的MgO上V_2O_5或Mg_3V_2O_8中的V〜(5+)物种。还原的物质V〜(4+)和V〜(3+)的脱氢活性较低。

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