The storage of nitrogen oxides on alumina-supported barium oxide

Noel W. Cant*, Michael J. Patterson

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

161 Citations (Scopus)

Abstract

The storage and release of NO2 on alumina-supported barium oxide has been studied with particular attention to the stoichiometry of the two processes. At 400 °C the storage process is characterised by a short period of complete uptake, possibly as nitrito or nitro species, followed by a slower partial uptake in which approximately one NO is released for every three NO2 lost. The latter reaction appears to supply the oxygen necessary to store NO2 as nitrate ions. Molecular O2 has little direct involvement even if in large excess. The second storage reaction also occurs, but to a much lesser extent, with Al2O3 alone. During temperature programmed desorption, release of NOx from Al2O3 peaks at ∼430 °C with evolution of NO2 and some O2. Release from BaO/Al2O3 exhibits an additional peak near 520 °C corresponding to formation of NO and a higher O2 concentration. The NO may arise from NO2 since BaO/Al2O3 has activity for NO2 decomposition by 500 °C. Although CO2 at low concentration is rapidly taken up by BaO/Al2O3 at 400 °C it is displaced by NO2 and does not interfere with storage. Thermodynamic calculations show that the formation of Ba(NO3)2 by the reaction of NO2 with bulk BaCO3 under the conditions used here is more favourable above 380 °C if NO is evolved than if O2 is consumed.

Original languageEnglish
Pages (from-to)271-278
Number of pages8
JournalCatalysis Today
Volume73
Issue number3-4
DOIs
Publication statusPublished - 15 Apr 2002

Keywords

  • Aluminium oxide
  • Barium carbonate
  • Barium oxide
  • Decomposition of stored nitrate
  • NO storage catalysts

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