Understanding the reversible and irreversible deactivation of methane oxidation catalysts

Rasmus Lykke Mortensen, Hendrik-David Noack, Kim Pedersen, Maja A. Dunstan, Fabrice Wilhelm, Andrei Rogalev, Kasper S. Pedersen, Jerrik Mielby*, Susanne Mossin*

*Corresponding author for this work

Research output: Contribution to journalJournal articleResearchpeer-review

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Abstract

Catalytic oxidation is a promising technology for controlling methane emissions from natural gas engines, but fast and severe deactivation prevents implementation. We investigated a commercial Pd on alumina oxidation catalyst under realistic conditions and identified two deactivation phenomena: fast, reversible inhibition and slow, irreversible loss of active sites. The loss of active sites occurs only during methane conversion, fortunately a brief oxygen cut-off is enough to regenerate the catalyst. Both types of deactivation increase the reduction temperature of PdO. From 36 kinetic experiments we propose a simple kinetic model encompassing both types of deactivation. The inhibition is confirmed to be due to water coverage of the active sites whereas dispersion of Pd on the surface is the cause of the irreversible loss of active sites. The new insight shows a pathway toward designing more durable catalysts for complete methane oxidation.
Original languageEnglish
Article number123646
JournalApplied Catalysis B: Environmental
Volume344
Number of pages10
ISSN0926-3373
DOIs
Publication statusPublished - 2024

Keywords

  • Methane oxidation
  • Palladium
  • Deactivation
  • Kinetic model
  • CH4-TPR

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