Synergistic Promotion Effect between NOx and Chlorobenzene Removal on MnOx–CeO2 Catalyst
Source abstract
Abstract
Developing new technologies for the simultaneous removal of NOx and dioxins from metallurgical facility and waste incinerator emissions remains challenging. Here, we present a new synergistic improvement effects of NOx and chlorobenzene (CB) on the MnOx–CeO2 catalyst. CB promoted both the NOx conversion and N2 selectivity below 300 °C during the NOx reduction process, in which the MnOx–CeO2 catalyst caused the undesired side reactions due to the over-oxidation of NH3. Meanwhile, NOx and NH3 promoted the CB oxidation activity above 100 °C in the presence of O2. On the basis of the diffuse reflectance infrared Fourier transforms and kinetic studies, the promotion was due to the separation of the MnOx–CeO2 catalyst into different temperature windows: NOx reduction at 100–200 °C and CB oxidation at 200–300 °C. The side reactions mainly occurred above 200 °C, which is suppressed by the coverage and activation of CB on catalyst surface.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Catalytic Processes in Materials Science · Industrial Gas Emission Control · Catalysis and Oxidation Reactions
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
National Engineering Laboratory for Multi Flue Gas Pollution Control Technology and Equipment, State Key Joint Laboratory of Environment Simulation and Pollution Control, School of Environment, Tsinghua University, Beijing 100084, China
Department of Chemical and Environmental Engineering, Yale University, New Haven, Connecticut 06520, United States
Funding
China Postdoctoral Science Foundation · National Natural Science Foundation of China
References (33)
Show source-provided references
1. 10.1016/j.atmosenv.2008.08.02110.1016/j.atmosenv.2008.08.021 ↗
2. 10.1021/es102474w10.1021/es102474w ↗
3. 10.1021/es903334210.1021/es9033342 ↗
4. 10.1016/S0926-3373(98)00040-X10.1016/S0926-3373(98)00040-X ↗
5. 10.1016/j.apcatb.2008.08.00910.1016/j.apcatb.2008.08.009 ↗
6. 10.1016/j.catcom.2012.06.02210.1016/j.catcom.2012.06.022 ↗
7. 10.1016/j.jcat.2005.01.00910.1016/j.jcat.2005.01.009 ↗
8. 10.1016/j.apcatb.2005.11.02210.1016/j.apcatb.2005.11.022 ↗
9. 10.1039/C4CY01194E10.1039/C4CY01194E ↗
10. 10.1016/j.chemosphere.2016.05.07210.1016/j.chemosphere.2016.05.072 ↗
11. 10.1016/j.cattod.2015.02.02910.1016/j.cattod.2015.02.029 ↗
12. 10.1016/j.apcatb.2015.11.00610.1016/j.apcatb.2015.11.006 ↗
13. 10.1016/j.apcatb.2016.12.02010.1016/j.apcatb.2016.12.020 ↗
14. 10.1039/C7CC08705E10.1039/C7CC08705E ↗
15. 10.1021/es304732h10.1021/es304732h ↗
16. 10.1016/j.apcatb.2004.01.02310.1016/j.apcatb.2004.01.023 ↗
17. 10.1016/j.ces.2017.01.00910.1016/j.ces.2017.01.009 ↗
18. 10.1016/j.apsusc.2016.07.02210.1016/j.apsusc.2016.07.022 ↗
19. 10.1021/acs.jpcc.7b0860010.1021/acs.jpcc.7b08600 ↗
20. 10.1021/es502585s10.1021/es502585s ↗
21. 10.1016/j.apcatb.2015.08.02310.1016/j.apcatb.2015.08.023 ↗
22. 10.1021/jp512407k10.1021/jp512407k ↗
23. 10.1021/jp506248910.1021/jp5062489 ↗
24. 10.1016/j.jcat.2004.01.03210.1016/j.jcat.2004.01.032 ↗
25. 10.1016/j.cattod.2014.04.00210.1016/j.cattod.2014.04.002 ↗
26. 10.1016/j.apcatb.2016.05.07610.1016/j.apcatb.2016.05.076 ↗
27. 10.1016/j.jcat.2007.01.01510.1016/j.jcat.2007.01.015 ↗
28. 10.1016/j.apcata.2010.09.03410.1016/j.apcata.2010.09.034 ↗
29. 10.1016/j.jcat.2012.04.01910.1016/j.jcat.2012.04.019 ↗
30. 10.1021/acs.jpcc.5b1057710.1021/acs.jpcc.5b10577 ↗
31. 10.1006/jcat.1997.178810.1006/jcat.1997.1788 ↗
32. 10.1016/j.apcatb.2010.06.01210.1016/j.apcatb.2010.06.012 ↗
33. 10.1016/S0926-3373(98)00040-X10.1016/S0926-3373(98)00040-X ↗