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An investigation on the role of Re as a promoter in Ag-Cs-Re/alpha-Al2O3 high-selectivity, ethylene epoxidation catalysts

机译:Re在Ag-Cs-Re /α-Al2O3高选择性乙烯环氧化催化剂中作为助催化剂的作用研究

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A series of Cs-Ag, Re-Ag, Cs-Re-Ag, and Cs-Re-Mo-Ag (supported on alpha-Al2O3) catalysts has been prepared and evaluated for ethylene epoxidation to determine the mechanism of selectivity enhancement for high-selectivity ethylene oxide (EO) catalysts which contain high-valent Re oxyanions and other copromoters, such as MoO42-. Optimal amounts of Re (as NH4ReO4) and Mo [as (NH4)(2)MoO4] on Cs-promoted, Ag/alpha-Al2O3 increase EO selectivity from approximately 79% to 83%. Analyses by XPS and SEM suggest the origin of both Re and Cs promotion is electronic. SEM shows that neither Re nor Mo changes the morphology or particle sizes of the Ag particles. XPS analyses show that Re shifts Ag 3d BE to higher values, which enhances electrophilic attack by oxygen adsorbed on Ag (Ag-O) at the electron-rich C=C bond of C2H4. In the subsequent step, Cs lowers the Ag 3d BE to facilitate desorption of the EO precursor to form gas phase EO. That is, Re and Cs promote different steps of the mechanism of EO formation. A reaction scheme detailing the mechanism of EO formation over Re-modified, Cs-promoted Ag catalysts is presented. (C) 2014 Elsevier Inc. All rights reserved.
机译:制备了一系列Cs-Ag,Re-Ag,Cs-Re-Ag和Cs-Re-Mo-Ag(负载在α-Al2O3上)催化剂,并对乙烯环氧化进行了评估,以确定提高高选择性的机理。选择性环氧乙烷(EO)催化剂,其中包含高价的Re氧阴离子和其他助助剂,例如MoO42-。在Cs促进的Ag /α-Al2O3上,最适量的Re(以NH4ReO4形式)和Mo [以(NH4)(2)MoO4]形式可以将EO选择性从大约79%提高至83%。 XPS和SEM的分析表明,Re和Cs促进的起源都是电子的。 SEM显示,Re和Mo均不改变Ag颗粒的形态或粒径。 XPS分析表明,Re将Ag 3d BE移至更高的值,这增强了C2H4的富电子C = C键吸附在Ag(Ag-O)上的氧的亲电子攻击。在随后的步骤中,Cs降低Ag 3d BE,以促进EO前体的解吸,形成气相EO。也就是说,Re和Cs促进了EO形成机理的不同步骤。提出了详细说明在改性后的Cs促进的Ag催化剂上EO形成机理的反应方案。 (C)2014 Elsevier Inc.保留所有权利。

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