Insight into the influence of Re and Cl on Ag catalysts in ethylene epoxidation.

IF 4.4 3区 化学 Q2 CHEMISTRY, PHYSICAL
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
{"title":"Insight into the influence of Re and Cl on Ag catalysts in ethylene epoxidation.","authors":"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","doi":"10.1039/d4cy00858h","DOIUrl":null,"url":null,"abstract":"<p><p>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 AgReO<sub>4</sub>. Chemisorption experiments showed that both ReO <sub><i>x</i></sub> and AgReO<sub>4</sub> species act as a reversible reservoir for O<sub>2</sub>. 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.</p>","PeriodicalId":66,"journal":{"name":"Catalysis Science & Technology","volume":" ","pages":""},"PeriodicalIF":4.4000,"publicationDate":"2024-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11563198/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysis Science & Technology","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d4cy00858h","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

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.

深入了解 Re 和 Cl 对乙烯环氧化中银催化剂的影响。
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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Catalysis Science & Technology
Catalysis Science & Technology CHEMISTRY, PHYSICAL-
CiteScore
8.70
自引率
6.00%
发文量
587
审稿时长
1.5 months
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 Impact factor: 5.0 Time to first decision (peer reviewed only): 31 days
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信