催化作用
1,3-丁二烯
巴豆醛
乙醛
化学
脱氢
选择性
乙醇
氧化物
多相催化
酒
金属
无机化学
有机化学
作者
Vitaly L. Sushkevich,І. І. Іванова,Vitaly V. Ordomsky,Esben Taarning
出处
期刊:Chemsuschem
[Wiley]
日期:2014-08-14
卷期号:7 (9): 2527-2536
被引量:171
标识
DOI:10.1002/cssc.201402346
摘要
Abstract The synthesis of buta‐1,3‐diene from ethanol has been studied over metal‐containing (M=Ag, Cu, Ni) oxide catalysts (MO x =MgO, ZrO 2 , Nb 2 O 5 , TiO 2 , Al 2 O 3 ) supported on silica. Kinetic study of a wide range of ethanol conversions (2–90 %) allowed the main reaction pathways leading to butadiene and byproducts to be determined. The key reaction steps of butadiene synthesis were found to involve ethanol dehydrogenation, acetaldehyde condensation, and the reduction of crotonaldehyde with ethanol into crotyl alcohol. Catalyst design included the selection of active components for each key reaction step and merging of these components into multifunctional catalysts and adjusting the catalyst functions to achieve the highest selectivity. The best catalytic performance was achieved over the Ag/ZrO 2 /SiO 2 catalyst, which showed the highest selectivity towards butadiene (74 mol %).
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