Resumen
N 2O formation and consumption were investigated over a coupled LNT-SCR system consisting of a low-precious metal loaded Pt/Rh LNT catalyst and a commercial Cu-zeolite SCR catalyst. Under lean-rich cycling conditions, N 2O emissions from the LNT were found to be partially mitigated by the downstream SCR catalyst. N 2O decomposition over the SCR catalyst was observed in the absence of reductant immediately after the switch to rich conditions, while N 2O reduction occurred after subsequent breakthrough of the reductant from the LNT. Steady-state data indicate that the former process is weakly promoted by NO which breaks through the LNT at the same time as the N 2O. Steady-state experiments revealed the order H 2>NH 3>CO>C 3H 6 for the efficacy of N 2O reduction with different reductants. These findings suggest that coupled LNT-SCR systems can not only improve overall NO x conversion levels but can also mitigate N 2O emissions from the LNT catalyst under actual driving conditions.
| Idioma original | English |
|---|---|
| Páginas (desde-hasta) | 1167-1174 |
| Número de páginas | 8 |
| Publicación | Catalysis Letters |
| Volumen | 142 |
| N.º | 10 |
| DOI | |
| Estado | Published - oct 2012 |
Nota bibliográfica
Funding Information:Acknowledgments This project was funded by the U.S. Department of Energy (DOE) under award No. DE-EE0000205. The authors thank BASF for providing the catalysts used in this study. Dr. R. McCabe of Ford Motor Co. is thanked for helpful discussions.
Financiación
Acknowledgments This project was funded by the U.S. Department of Energy (DOE) under award No. DE-EE0000205. The authors thank BASF for providing the catalysts used in this study. Dr. R. McCabe of Ford Motor Co. is thanked for helpful discussions.
| Financiadores | Número del financiador |
|---|---|
| Michigan State University-U.S. Department of Energy (MSU-DOE) Plant Research Laboratory | DE-EE0000205 |
ASJC Scopus subject areas
- Catalysis
- General Chemistry
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