SCR performance and mechanism study with multiple poisoning gases on CeOx promoted V2O5-WO3/TiO2 monolithic honeycomb catalyst of NOx removal

• Multiple poisoning gases of monolithic SCR catalysts was studied, combining fundamental research and practical application. • CeO x enhanced the SCR performance in the low temperature region and in the presence of multiple poisoning gases. • Reaction with C 3 H 8 promoted the formation of Ce 3+ and active oxygen on the 7CeVWTi surface. • SO 2 affected NH 3 adsorption and slowed down the reaction rate, leading to the decreased SCR performance lower than 275 ℃. • The C 3 H 8 and H 2 O deactivation was due to the competed adsorption with NH 3 on the V=O and W=O sites of 7CeVWTi catalysts. The V 2 O 5 -WO 3 -TiO 2 catalysts are commonly used in the selective catalytic reduction of ammonia for NO x removal. Coated VWTi and Ce promoted VWTi monolithic catalysts were prepared to compare the SCR performance and anti-poisoning properties. The VWTi catalyst demonstrated more than 90 % NO conversion in the range of 300–500 ℃, which decreased to about 50 % NO conversion after multiple gases poisoning. However, the CeVWTi catalyst demonstrated more than 90 % NO removal efficiency in the range of 250–500 ℃, remaining about 60 % after multiple gases poisoning. In contrast to the fresh catalysts, the presence of SO 2 /H 2 O/C 3 H 8 caused the catalysts redox properties decreased and the inert acid sites formated on the VWTi surface. However, CeO 2 provided surface adsorbed oxygen and mitigated these negative effects to some extent. The in situ DRIFTs results indicated that SO 2 inhibited the reaction and prevented the NH 3 and NO adsorption on the surface of the 7CeVWTi catalyst. The decreased NO conversion in the presence of H 2 O and C 3 H 8 was due to the competition adsorption with NH 3 species. Overall, the doping of CeO 2 improved the catalytic activity and poisoning resistance ability of the VWTi catalyst.

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Publication Details

Journal
Separation and Purification Technology
Published
2025-02-15
DOI
https://doi.org/10.1016/j.seppur.2025.132087
Citations
16
Primary Topic
Catalytic Processes in Materials Science
Type
article
Field-Weighted Citation Impact
8.28

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article

SCR performance and mechanism study with multiple poisoning gases on CeOx promoted V2O5-WO3/TiO2 monolithic honeycomb catalyst of NOx removal

Yingjie Zhao, Wei Ye, Shaoping Cui, Xiao Meng et al.
16 citations
Separation and Purification Technology
Catalytic Processes in Materials Science
8.28
article

SCR performance and mechanism study with multiple poisoning gases on CeOx promoted V2O5-WO3/TiO2 monolithic honeycomb catalyst of NOx removal

Yingjie Zhao, Wei Ye, Shaoping Cui, Xiao Meng, Jing Gao, Boqun Liu, Yidan Huang, Ke Niu
article en
16 citations

Abstract

• Multiple poisoning gases of monolithic SCR catalysts was studied, combining fundamental research and practical application. • CeO x enhanced the SCR performance in the low temperature region and in the presence of multiple poisoning gases. • Reaction with C 3 H 8 promoted the formation of Ce 3+ and active oxygen on the 7CeVWTi surface. • SO 2 affected NH 3 adsorption and slowed down the reaction rate, leading to the decreased SCR performance lower than 275 ℃. • The C 3 H 8 and H 2 O deactivation was due to the competed adsorption with NH 3 on the V=O and W=O sites of 7CeVWTi catalysts. The V 2 O 5 -WO 3 -TiO 2 catalysts are commonly used in the selective catalytic reduction of ammonia for NO x removal. Coated VWTi and Ce promoted VWTi monolithic catalysts were prepared to compare the SCR performance and anti-poisoning properties. The VWTi catalyst demonstrated more than 90 % NO conversion in the range of 300–500 ℃, which decreased to about 50 % NO conversion after multiple gases poisoning. However, the CeVWTi catalyst demonstrated more than 90 % NO removal efficiency in the range of 250–500 ℃, remaining about 60 % after multiple gases poisoning. In contrast to the fresh catalysts, the presence of SO 2 /H 2 O/C 3 H 8 caused the catalysts redox properties decreased and the inert acid sites formated on the VWTi surface. However, CeO 2 provided surface adsorbed oxygen and mitigated these negative effects to some extent. The in situ DRIFTs results indicated that SO 2 inhibited the reaction and prevented the NH 3 and NO adsorption on the surface of the 7CeVWTi catalyst. The decreased NO conversion in the presence of H 2 O and C 3 H 8 was due to the competition adsorption with NH 3 species. Overall, the doping of CeO 2 improved the catalytic activity and poisoning resistance ability of the VWTi catalyst.

Separation and Purification TechnologyVol. 363
Tianjin Research Institute of Water Transport Engineering (CN)
Natural Science Foundation of Tianjin City
Openalex Percentile: Top 2%
Catalytic Processes in Materials Science
8.28
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