Modification Effect of Pt on the Active Sites of Sulfated CeO2 Nanorods for the Selective Catalytic Reduction of NO
Source abstract
Abstract
Although the surface acidity of CeO 2 has been increased by H 2 SO 4 to increase its acid sites, the low-temperature (<250 °C) activity of sulfated CeO 2 catalysts still needs to be improved. In this study, a Pt-modified CeO 2 catalyst was prepared by impregnation or reduction methods to increase its catalytic activity. The results showed the Pt-modified CeO 2 catalyst significantly widened its low-temperature catalytic window. The NO conversion and N 2 selectivity of the Pt 1.0% /SCe-I sample were both more than 90% at 200–350 °C because of its numerous acid sites, excellent redox ability, and higher Pt 2+ content. NH 3, NH 4+, –NH 2, and bridging nitrates and monodentate nitrates on the Pt 1.0% /SCe-I catalyst surface acted as the active substances. Among them, coordinated NH 3 at the Lewis acid sites reacted first. This study highlights the interactions among metals, sulfates, and carriers and supplies a useful method to improve the low-temperature activity of sulfated CeO 2 .
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Catalytic Processes in Materials Science · Advanced Photocatalysis Techniques · Nanomaterials for catalytic reactions
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Xi’an Key Laboratory of Solid Waste Recycling and Resource Recovery, Department of Environmental Sciences and Engineering, Xi’an Jiaotong University, Xi’an 710049, China
Instrumental Analysis Center of Xi’an Jiaotong University, Xi’an Jiaotong University, Xi’an 710049, China
Funding
Key Research and Development Projects of Shaanxi Province · State Key laboratory of Loess and Quaternary Geology, Chinese Academy of Sciences · Science and Technology plan project of Xiâ??an city
References (49)
Show source-provided references
1. 10.1021/acs.est.9b0121710.1021/acs.est.9b01217 ↗
2. 10.1016/j.cej.2021.13369410.1016/j.cej.2021.133694 ↗
3. 10.1021/acs.chemrev.9b0020210.1021/acs.chemrev.9b00202 ↗
4. 10.1021/acsami.1c1962510.1021/acsami.1c19625 ↗
5. 10.1021/acs.est.8b0563710.1021/acs.est.8b05637 ↗
6. 10.1006/jcat.1995.102410.1006/jcat.1995.1024 ↗
7. 10.1021/acscatal.0c0190010.1021/acscatal.0c01900 ↗
8. 10.1039/C5CP04570C10.1039/C5CP04570C ↗
9. 10.1016/j.apsusc.2022.15519510.1016/j.apsusc.2022.155195 ↗
10. 10.1002/cctc.20200130710.1002/cctc.202001307 ↗
11. 10.1016/j.seppur.2020.11718110.1016/j.seppur.2020.117181 ↗
12. 10.1007/s11244-020-01342-810.1007/s11244-020-01342-8 ↗
13. 10.3390/catal904037110.3390/catal9040371 ↗
14. 10.1016/j.apcatb.2020.11880810.1016/j.apcatb.2020.118808 ↗
15. 10.1016/j.jcis.2021.06.11410.1016/j.jcis.2021.06.114 ↗
16. 10.1016/j.cej.2019.12291010.1016/j.cej.2019.122910 ↗
17. 10.1016/j.apr.2022.10158210.1016/j.apr.2022.101582 ↗
18. 10.1021/acscatal.3c0010610.1021/acscatal.3c00106 ↗
19. 10.1021/acscatal.9b0555910.1021/acscatal.9b05559 ↗
20. 10.1016/j.cej.2011.01.00110.1016/j.cej.2011.01.001 ↗
21. 10.1016/j.apcatb.2021.12075410.1016/j.apcatb.2021.120754 ↗
22. 10.1021/acsami.2c2098510.1021/acsami.2c20985 ↗
23. 10.1021/acscatal.2c0491810.1021/acscatal.2c04918 ↗
24. 10.1021/acs.jpcc.6b0294510.1021/acs.jpcc.6b02945 ↗
25. 10.1039/D1RA00059D10.1039/D1RA00059D ↗
26. 10.1039/c3nr00831b10.1039/c3nr00831b ↗
27. 10.1021/acs.iecr.8b0255310.1021/acs.iecr.8b02553 ↗
28. 10.1016/j.apcatb.2018.02.03510.1016/j.apcatb.2018.02.035 ↗
29. 10.1016/j.jcis.2012.12.03410.1016/j.jcis.2012.12.034 ↗
30. 10.1007/s11164-018-3635-210.1007/s11164-018-3635-2 ↗
31. 10.1002/bio.126910.1002/bio.1269 ↗
32. 10.1016/j.apcatb.2014.10.02910.1016/j.apcatb.2014.10.029 ↗
33. 10.1016/j.apcatb.2020.11919410.1016/j.apcatb.2020.119194 ↗
34. 10.1021/acs.est.0c0174910.1021/acs.est.0c01749 ↗
35. 10.1016/j.cej.2019.12239810.1016/j.cej.2019.122398 ↗
36. 10.1016/j.apcatb.2017.02.04110.1016/j.apcatb.2017.02.041 ↗
37. 10.1109/TDEI.2022.318365910.1109/TDEI.2022.3183659 ↗
38. 10.1016/j.fuel.2014.08.06010.1016/j.fuel.2014.08.060 ↗
39. 10.1016/j.catcom.2017.06.03810.1016/j.catcom.2017.06.038 ↗
40. 10.1016/j.apcata.2022.11875410.1016/j.apcata.2022.118754 ↗
41. 10.1016/j.jcis.2021.10.07810.1016/j.jcis.2021.10.078 ↗
42. 10.1016/j.apcatb.2023.12254410.1016/j.apcatb.2023.122544 ↗
43. 10.1016/j.matchemphys.2011.10.03210.1016/j.matchemphys.2011.10.032 ↗
44. 10.1016/j.cej.2017.06.07910.1016/j.cej.2017.06.079 ↗
45. 10.1016/j.apcatb.2021.12028610.1016/j.apcatb.2021.120286 ↗
46. 10.1021/acscatal.9b0177610.1021/acscatal.9b01776 ↗
47. 10.1038/s41929-020-00508-710.1038/s41929-020-00508-7 ↗
48. 10.1016/j.apcatb.2013.01.02810.1016/j.apcatb.2013.01.028 ↗
49. 10.1016/j.apsusc.2017.03.16410.1016/j.apsusc.2017.03.164 ↗