2022
DOI: 10.1016/j.cej.2021.133928
|View full text |Cite
|
Sign up to set email alerts
|

Synergy of the successive modification of cryptomelane MnO2 by potassium insertion and nitrogen doping for catalytic formaldehyde oxidation

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

0
3
0

Year Published

2022
2022
2024
2024

Publication Types

Select...
10

Relationship

0
10

Authors

Journals

citations
Cited by 23 publications
(5 citation statements)
references
References 57 publications
0
3
0
Order By: Relevance
“…From mapping tests in Figures a–e and S2a, we can understand the distribution status of elements on MnO x -S-A, where Mn, O, Na, K, and S all exhibit a uniformly distributed state. It has been shown that small amount of alkali metal (Na + , K + ) doping can generate additional surface-adsorbed oxygen on the catalyst surface, while element S mainly exists on the catalyst surface in the form of SO 4 2– (as shown in Figure S2b), which may occupy some active sites of the catalyst. As shown in Table S1, the elemental contents of Na, K, and S of MnO x -S-A after multiple deionized water rinses were 0.005, 0.222, and 0.575%, respectively, all of which were slightly lower than those of unrinsed MnO x -S-A. By testing the catalytic performance of MnO x -S-A without rinsing and with multiple rinses (shown in Figure S3), the performance of both was the same, indicating that the trace change in impurity content on the surface of the MnO x -S-A catalyst is not the main factor affecting its catalytic performance.…”
Section: Resultsmentioning
confidence: 99%
“…From mapping tests in Figures a–e and S2a, we can understand the distribution status of elements on MnO x -S-A, where Mn, O, Na, K, and S all exhibit a uniformly distributed state. It has been shown that small amount of alkali metal (Na + , K + ) doping can generate additional surface-adsorbed oxygen on the catalyst surface, while element S mainly exists on the catalyst surface in the form of SO 4 2– (as shown in Figure S2b), which may occupy some active sites of the catalyst. As shown in Table S1, the elemental contents of Na, K, and S of MnO x -S-A after multiple deionized water rinses were 0.005, 0.222, and 0.575%, respectively, all of which were slightly lower than those of unrinsed MnO x -S-A. By testing the catalytic performance of MnO x -S-A without rinsing and with multiple rinses (shown in Figure S3), the performance of both was the same, indicating that the trace change in impurity content on the surface of the MnO x -S-A catalyst is not the main factor affecting its catalytic performance.…”
Section: Resultsmentioning
confidence: 99%
“…In the development of a heterogeneous Fenton reaction, the key problem is to develop high-activity nanocatalysts. MnO 2 , as a metal oxide, has been used widely as a nanocatalyst [12] due to its unique properties such as multiple valences of manganese, low toxicity, large surface area, primary adaptability, strong adsorption, and catalytic performance [13,14]. For example, Li et al prepared highly porous α-MnO 2 nanorods by selective acid etching from Mn-containing spinel, and 90.9% of 4-chlorophenol can be degraded within 12 min by catalytic ozonation in a wide range of pH of 4.5-10.5 [15].…”
Section: Introductionmentioning
confidence: 99%
“…[8][9][10][11][12][13] Manganese oxides have recently emerged as promising materials for diverse applications in pollution abatement. [14][15][16][17][18][19][20][21][22] However, it is still a great challenge to achieve high catalytic activity and long-term stability at ambient temperature for HCHO oxidation over MnO x -based catalysts.…”
Section: Introductionmentioning
confidence: 99%