Abstract
Catalytic reduction of NO2 in the presence of excess oxygen and NO has been studied over a 0.2% Pd/SiO2 catalyst between 120 and 260 °C. CO is effective in selective reduction of NO2 at temperatures below 180 °C. Temperature programmed desorption (TPD) and FT-IR studies have been used to investigate the adsorption sites during the reaction conditions. A Langmuir¿Hinshelwood mechanism involving oxidised Pd sites is proposed for the reduction of NO2 with CO, where both reactants adsorb competitively on Pd2+ sites. Cl deactivates the catalyst for the reduction of NO2 with CO. This problem can be overcome by using propylene as a co-reductant. Furthermore, addition of propylene widens the temperature window of operation.
Original language | Undefined |
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Pages (from-to) | 143-151 |
Number of pages | 9 |
Journal | Applied catalysis B: environmental |
Volume | 50 |
Issue number | 3 |
DOIs | |
Publication status | Published - 2004 |
Keywords
- IR-49070
- METIS-221052