Claudia J Keijzer, Pim T Weide, Kristiaan H Helfferich, Justyna Zieciak, Marco de Ridder, Remco Dalebout, Tracy L Lohr, John R Lockemeyer, Peter van den Brink, Petra E de Jongh
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引用次数: 0
摘要
商用乙烯环氧化催化剂由α-氧化铝支撑的银颗粒组成,通常含有促进剂混合物。高选择性催化剂通常含有少量铼。我们研究了一系列以 Re(Re/(Re + Ag))负载量高达 4% 的银催化剂,有意将其高于优化的商用催化剂,以方便表征并扩大对催化的影响。顺序浸渍使 Re 和 Ag 紧密接触,从而形成了新的 AgReO4 特征相。化学吸附实验表明,ReO x 和 AgReO4 物种都是氧气的可逆储层。乙烯环氧化反应是在进料中不含工业上至关重要的氯乙烷促进剂和含氯乙烷促进剂的情况下进行的。在不加入氯化物(Cl)的情况下,有 Re 存在时环氧乙烷的选择性会增加,而在 Re 含量较高时,Re 和 Cl 的组合会降低环氧乙烷的选择性。系统的环氧乙烷异构化实验表明,Re 和 Cl 可单独抑制银表面的异构化。然而,Re 和 Cl 结合在一起会增加异构化,这可以解释为表面变得过于亲电。因此,研究单独和组合的促进剂非常重要。
Insight into the influence of Re and Cl on Ag catalysts in ethylene epoxidation.
Commercial ethylene epoxidation catalysts consist of α-alumina supported Ag particles and usually contain a mixture of promoters. High selectivity catalysts typically include a small amount of rhenium species. We studied a series of Ag catalysts promoted with Re loadings up to 4 at% (Re/(Re + Ag)), which is intentionally higher than in optimized commercial catalysts to facilitate characterization and to amplify the influence on catalysis. Sequential impregnation brought Re and Ag in such close contact that they formed a new characterized phase of AgReO4. Chemisorption experiments showed that both ReO x and AgReO4 species act as a reversible reservoir for O2. Ethylene epoxidation was performed without and with the industrially crucial ethyl chloride promoter in the feed. Without the chloride (Cl), the ethylene oxide selectivity increased when Re was present, whereas the combination of Re and Cl decreased the ethylene oxide selectivity at higher Re loadings. Systematic ethylene oxide isomerization experiments revealed that Re and Cl individually inhibit the isomerization on the Ag surface. However, Re and Cl combined increased the isomerization, which can be explained by the surface becoming overly electrophilic. This hence shows the importance of studying promoters both individually and combined.
期刊介绍:
A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis.
Editor-in-chief: Bert Weckhuysen
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