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

  • 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*
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

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.

Original languageEnglish
Pages (from-to)323-333
Number of pages11
JournalCatalysis Science & Technology
Volume15
Issue number2
Early online date6 Nov 2024
DOIs
Publication statusPublished - 2025

Bibliographical note

Publisher Copyright:
© 2024 The Royal Society of Chemistry.

Funding

CJK was funded at the Advanced Research Center for Chemical Building Blocks consortium (project number 2021.032.A.UU), which is co-founded and co-financed by the Dutch Research Council (NWO) and the Netherlands Ministry of Economic Affairs and Climate Policy. SEM and STEM-EDX measurements were performed at the Electron Microscopy Centre at Utrecht University. The authors would like to thank Eric Hellebrand and Chris Schneijdenberg (SEM) for technical support. Dennis Becker (Bruker AXS) is acknowledged for his help with resolving an error in the PDF+ database. Julie Cao and Litao Bai (Shell) are acknowledged for setting up and conducting the XPS measurements.

FundersFunder number
Advanced Research Center for Chemical Building Blocks consortium2021.032

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