Origin of double dinitrogen release feature during fast switching between lean and rich cycles for NOx storage reduction catalysts

Sarayute Chansai*, R. Burch, C. Hardacre, Shuichi Naito

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

7 Citations (Scopus)

Abstract

The performance of NOx storage and reduction over 1.5 wt% Pt/20 wt% KNO3/K2Ti8O17 and 1.5 wt% Pt/K2Ti8O17 catalysts has been investigated using combined fast transient kinetic switching and isotopically labelled (NO)-N-15 at 350 degrees C. The evolution of product N-2 has revealed two significant peaks during 60 s lean/1.3 s rich switches. It also found that the presence of CO2 in the feed affects the release of N-2 in the second peak. Regardless of the presence/absence of water in the feed, only one peak of N-2 was observed in the absence of CO2. Gas-phase NH3 was not observed in any of the experiments. However, in the presence of CO2 the results obtained from in situ DRIFTS-MS analysis showed that isocyanate species are formed and stored during the rich cycles, probably from the reaction between NOx and CO, in which CO was formed via the reverse water-gas shift reaction. 

Original languageEnglish
Pages (from-to)91-98
Number of pages8
JournalJournal of Catalysis
Volume317
Early online date10 Jul 2014
DOIs
Publication statusPublished - Aug 2014

Keywords

  • NOx storage reduction
  • Lean/rich cycles
  • CO
  • H-2
  • K2Ti8O17
  • Fast transient kinetics
  • DRIFTS-MS
  • Isocyanates
  • Reverse water-gas shift
  • IN-SITU FTIR
  • NSR CATALYSTS
  • STORAGE/REDUCTION CATALYST
  • PT/BAO/AL2O3 CATALYSTS
  • TRAP CATALYST
  • NO(X) STORAGE
  • LNT CATALYST
  • STORED NOX

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