Passive NOx Reduction with CO Using Pd/TiO2/Al2O3 + WGSR Catalysts Under Simulated Post-Euro IV Diesel Exhaust Conditions
- Authors
- Hong, Yoon-Ki; Lee, Dae-Won; Ko, Young-Chul; Yinghua, Li; Han, Hyun-Sik; Lee, Kwan-Young
- Issue Date
- 5월-2010
- Publisher
- SPRINGER
- Keywords
- DeNO(x); Selective catalytic reduction (SCR); Pd/TiO2/Al2O3; Cu/ZnO/Al2O3; Post-Euro IV
- Citation
- CATALYSIS LETTERS, v.136, no.1-2, pp.106 - 115
- Indexed
- SCIE
SCOPUS
- Journal Title
- CATALYSIS LETTERS
- Volume
- 136
- Number
- 1-2
- Start Page
- 106
- End Page
- 115
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/116493
- DOI
- 10.1007/s10562-010-0312-5
- ISSN
- 1011-372X
- Abstract
- This study deals with diesel DeNO(x) catalysis by physically mixed Pd/TiO2/Al2O3 and water-gas-shift reaction (WGSR) catalysts under CO-rich conditions at a CO/NOx ratio of 16. In the post-Euro IV era, many diesel engines are expected to produce CO-rich exhaust emissions due to the trend toward emission regulation and limitations in related technologies. Under these circumstances, the passive DeNOx strategy utilizing CO as a single reductant can be considered appropriate. The Pd/TiO2/Al2O3 catalyst is well known for its high DeNO(x) performance when CO and H-2 are available as NOx reductants. However, when CO is used as a single reductant, the catalyst shows poor DeNOx activity, even if the CO concentration is exceptionally high (CO/NOx = 16). In this study, the DeNO(x) activity of Pd/TiO2/Al2O3 was noticeably improved by physically mixing it with a proper WGSR catalyst (Cu/ZnO/Al2O3), which is capable of producing H-2 and feeding it to Pd/TiO2/Al2O3 successfully even in the presence of O-2. The NOx conversion exceeded 70% at 400-450 degrees C using a Pd/TiO2/Al2O3 + Cu/ZnO/Al2O3 catalyst mixture at a weight ratio of 33:67. The reaction gas consisted of 500 ppm NO, 8000 ppm CO, 8 vol.% O-2, 5 vol.% CO2 and 10 vol.% H2O and w/f was 0.1 g s/cm(3).
- Files in This Item
- There are no files associated with this item.
- Appears in
Collections - College of Engineering > Department of Chemical and Biological Engineering > 1. Journal Articles
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.