2018
DOI: 10.1016/j.cej.2017.10.011
|View full text |Cite
|
Sign up to set email alerts
|

Mechanistic aspects of NH3-SCR reaction over CeO2/TiO2-ZrO2-SO42− catalyst: In situ DRIFTS investigation

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
74
0

Year Published

2018
2018
2023
2023

Publication Types

Select...
8

Relationship

3
5

Authors

Journals

citations
Cited by 153 publications
(74 citation statements)
references
References 53 publications
0
74
0
Order By: Relevance
“…This facilitated the oxidation of NO to NO 2 and consequently, increased the NH 3 -SCR performance. 48,49 Moreover, there is a shi to higher binding energies for Mn/Ti-Zr samples, which could be ascribed to the interaction between the manganese oxide and Ti-Zr support.…”
Section: 44mentioning
confidence: 99%
“…This facilitated the oxidation of NO to NO 2 and consequently, increased the NH 3 -SCR performance. 48,49 Moreover, there is a shi to higher binding energies for Mn/Ti-Zr samples, which could be ascribed to the interaction between the manganese oxide and Ti-Zr support.…”
Section: 44mentioning
confidence: 99%
“…Sample blank displayed a main peak at 633 °C with a small peak at 135 °C, meanwhile, Mo possessed a main peak at 645 °C and two smaller peaks at 110, 438 °C. NH 3 ‐desoprtion peaks shifted to higher temperature for Mo sample, indicating more and stronger acid sites . This could be owing to the interaction between Mo and MnCe, which led to the increase of the metal–oxygen coordination bond length and surface acidity .…”
Section: Resultsmentioning
confidence: 94%
“…ZrO 2 has been previously used as SCR catalyst carrier due to its excellent thermal stability, surface acidity, although its redox ability should be neglected in the low temperature SCR because Zr 4+ ions were unreducible below 800 °C. ZrO 2 can interact with the metallic active components which lead to the change of electronic structure and oxidative states of the metallic components and promote NO x conversion …”
Section: Introductionmentioning
confidence: 99%
“…Then, the fourth peak was associated to the interaction between bulk CeO 2 and Fe species (777 °C). Thereby, the broad peak around 777 °C were mainly regarded as the redox reaction between Fe 3+ /Fe 2+ and Ce 4+ /Ce 3+ , which was driven by the generation of Fe‐O‐Ce . However, with the addition of HSiW, a shift of reduction peaks toward higher temperature was observed on the rest of four catalysts, demonstrated the existence of the synergetic reactions among HSiW and Ce‐Fe‐O x and oxygen species .…”
Section: Resultsmentioning
confidence: 99%