Jinxiu Wang
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Jinxiu Wang has a total of 34 co-authors. Here are the top co-authors by number of shared publications:
- Jinsheng Chen
State Key Laboratory of Advanced Environmental Technology Institute of Urban Environment Chinese Academy of Sciences Xiamen China
13 shared publications Yanting Chen
7 shared publicationsJianyi Zhang
6 shared publicationsXianfang Yi
5 shared publicationsYuqiu Liu
5 shared publications- Yanke Yu
Department of Environmental Science and Engineering
4 shared publications
Latest Publications
- 4 February 2026
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry A
- Vol. 14 (20) , 12036-12050
Unveiling the distinct effect mechanisms of H 2 O: aggravating and mitigating SO 2 poisoning of Fe 2 O 3 and α-MnO 2 catalysts in low-temperature NH 3 -SCR
Elucidating the mechanisms of coexisting SO 2 and H 2 O, especially H 2 O's dual function in aggravating or mitigating SO 2 poisoning pathways, is pivotal for the rational design of high-performance, poison-resistant low-temperature SCR catalysts.
- 4 February 2026
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry A
- Vol. 14 (20) , 12036-12050
Unveiling the distinct effect mechanisms of H 2 O: aggravating and mitigating SO 2 poisoning of Fe 2 O 3 and α-MnO 2 catalysts in low-temperature NH 3 -SCR
Elucidating the mechanisms of coexisting SO 2 and H 2 O, especially H 2 O's dual function in aggravating or mitigating SO 2 poisoning pathways, is pivotal for the rational design of high-performance, poison-resistant low-temperature SCR catalysts.
- 25 January 2024
- Published by American Chemical Society (ACS) in Industrial & Engineering Chemistry Research
- Vol. 63 (5) , 2167-2176
Effect of Various Acid Anions on Potassium Poisoning and the Mechanism of Commercial V2O5–WO3/TiO2 Catalysts for SCR of NOx
- 25 January 2024
- Published by American Chemical Society (ACS) in Industrial & Engineering Chemistry Research
- Vol. 63 (5) , 2167-2176
Effect of Various Acid Anions on Potassium Poisoning and the Mechanism of Commercial V2O5–WO3/TiO2 Catalysts for SCR of NOx
- 1 September 2023
- Published by Elsevier in Journal of Rare Earths
- Vol. 42 (9) , 1682-1692
Excellent alkali resistance of Fe, Ce and sulfates co-modified V2O5–WO3/TiO2 catalyst for selective catalytic reduction of NO with NH3
- 1 September 2023
- Published by Elsevier in Journal of Rare Earths
- Vol. 42 (9) , 1682-1692
Excellent alkali resistance of Fe, Ce and sulfates co-modified V2O5–WO3/TiO2 catalyst for selective catalytic reduction of NO with NH3
- 8 August 2023
- Published by Royal Society of Chemistry (RSC) in Catalysis Science & Technology
- Vol. 13 (18) , 5374-5386
Improved NH 3 -SCR activity by the cooperation of FeVO 4 and CeO 2 nanosheet catalysts: structure and mechanism
The cooperation of FeVO 4 and CeO 2 nanosheets significantly improves NH 3 -SCR activity via the nanosheet structure with lattice defects and Fe–V–Ce interaction.
- 8 August 2023
- Published by Royal Society of Chemistry (RSC) in Catalysis Science & Technology
- Vol. 13 (18) , 5374-5386
Improved NH 3 -SCR activity by the cooperation of FeVO 4 and CeO 2 nanosheet catalysts: structure and mechanism
The cooperation of FeVO 4 and CeO 2 nanosheets significantly improves NH 3 -SCR activity via the nanosheet structure with lattice defects and Fe–V–Ce interaction.
- 25 May 2022
- Published by Royal Society of Chemistry (RSC) in Catalysis Science & Technology
- Vol. 12 (13) , 4169-4180
Promotional effect of Fe and Ce co-doping on a V2O5–WO3/TiO2 catalyst for SCR of NOx with high K and Pb resistance
The cooperation of Fe and Ce on V2O5–WO3/TiO2 improves the K and Pb resistance by promoting the redox and NOx adsorption ability.
- 25 May 2022
- Published by Royal Society of Chemistry (RSC) in Catalysis Science & Technology
- Vol. 12 (13) , 4169-4180
Promotional effect of Fe and Ce co-doping on a V2O5–WO3/TiO2 catalyst for SCR of NOx with high K and Pb resistance
The cooperation of Fe and Ce on V2O5–WO3/TiO2 improves the K and Pb resistance by promoting the redox and NOx adsorption ability.
- Open Access
Improved Sulfur Resistance of COMMERCIAl V2O5-WO3/TiO2 SCR Catalyst Modified by Ce and Cu
The accumulation of NH4HSO4 leads to the deactivation of commercial V2O5-WO3/TiO2 catalyst (VWTi) in practical application. The commercial catalyst is modified with 0.3 wt. % Ce and 0.05 wt. % Cu (donated as VWCeCuTi), and its sulfur resistance is noticeably improved. After loading 20 wt. % NH4HSO4, the NOx conversion of VWCeCuTi-S remains 40% at 250 °C, higher than that of VWTi-S (25%). Through a series of characterization analyses, it was found that the damaged surface areas and acid sites are the key factors for the deactivation of S-poisoned samples. However, surface-active oxygen and NO adsorption are increased by NH4HSO4 deposition, and the L–H mechanism is promoted over S-poisoned samples. Due to the interaction between V, Ce and Cu, the surface-active oxygen over VWCeCuTi-S is increased, and then NO adsorption is promoted. In addition, VWCeCuTi-S obtains a higher V5+ ratio and a better redox property than VWTi-S, which in turn accelerates the NH3-SCR reaction. More NO adsorption and encouraged reaction contribute to the better sulfur resistance of VWCeCuTi.
Open AccessImproved Sulfur Resistance of COMMERCIAl V2O5-WO3/TiO2 SCR Catalyst Modified by Ce and Cu
The accumulation of NH4HSO4 leads to the deactivation of commercial V2O5-WO3/TiO2 catalyst (VWTi) in practical application. The commercial catalyst is modified with 0.3 wt. % Ce and 0.05 wt. % Cu (donated as VWCeCuTi), and its sulfur resistance is noticeably improved. After loading 20 wt. % NH4HSO4, the NOx conversion of VWCeCuTi-S remains 40% at 250 °C, higher than that of VWTi-S (25%). Through a series of characterization analyses, it was found that the damaged surface areas and acid sites are the key factors for the deactivation of S-poisoned samples. However, surface-active oxygen and NO adsorption are increased by NH4HSO4 deposition, and the L–H mechanism is promoted over S-poisoned samples. Due to the interaction between V, Ce and Cu, the surface-active oxygen over VWCeCuTi-S is increased, and then NO adsorption is promoted. In addition, VWCeCuTi-S obtains a higher V5+ ratio and a better redox property than VWTi-S, which in turn accelerates the NH3-SCR reaction. More NO adsorption and encouraged reaction contribute to the better sulfur resistance of VWCeCuTi.
- 7 June 2021
- Published by Royal Society of Chemistry (RSC) in Catalysis Science & Technology
- Vol. 11 (15) , 5125-5134
Application of ReOx/TiO2 catalysts with excellent SO2 tolerance for the selective catalytic reduction of NOx by NH3
The adsorption of SO2 on ReOx/TiO2 catalysts was rather weak; thus, ReOx/TiO2 catalysts exhibited excellent SO2 tolerance in the NH3-SCR reaction.
- 7 June 2021
- Published by Royal Society of Chemistry (RSC) in Catalysis Science & Technology
- Vol. 11 (15) , 5125-5134
Application of ReOx/TiO2 catalysts with excellent SO2 tolerance for the selective catalytic reduction of NOx by NH3
The adsorption of SO2 on ReOx/TiO2 catalysts was rather weak; thus, ReOx/TiO2 catalysts exhibited excellent SO2 tolerance in the NH3-SCR reaction.