Loading Eu2O3 Enhances the CO Oxidation Activity and SO2 Resistance of the Pt/TiO2 Catalyst

Pt/TiO2 and Pt-Eu2O3/TiO2 catalysts were prepared via the impregnation method for catalytic oxidation of CO. The Pt-2Eu2O3/TiO2 catalyst exhibited better CO oxidation activity as well as greater SO2 resistance than the Pt/TiO2 catalyst. For the inlet gas consisting of 0.8% CO, 5% O2, and balanced N2, the lowest complete conversion temperatures (T100) of CO were 120 °C and 140 °C for the Pt-2Eu2O3/TiO2 and Pt/TiO2 catalysts, respectively. During the 72 h SO2-resistance test at 200 °C under an inlet gas composition of 0.8% CO, 5% O2, 15% H2O, 50 ppm SO2, and balanced N2, the CO conversion on the Pt-2Eu2O3/TiO2 catalyst remained >99%, while that on the Pt/TiO2 catalyst gradually decreased to 77.8%. Pre-loading 2 wt% Eu2O3 on TiO2 enhanced the dispersion of Pt, increased the proportion of Pt0, and facilitated the adsorption and dissociation of H2O, all of which promoted CO oxidation. SO2 preferentially occupied the Eu2O3 sites by forming stable sulfates on the Pt-2Eu2O3/TiO2 catalyst, which protected the Pt active sites from poisoning. The OH* species produced from the dissociation of H2O played a significant role in promoting CO oxidation through the formation of COOH* as the key reaction intermediate. The developed Pt-2Eu2O3/TiO2 catalyst has great application potential in terms of the removal of CO from industrial flue gases.

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Publication Details

Journal
Catalysts
Published
2025-08-16
DOI
https://doi.org/10.3390/catal15080783
Citations
6
Primary Topic
Catalytic Processes in Materials Science
Type
article
Field-Weighted Citation Impact
3.11

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article

Loading Eu2O3 Enhances the CO Oxidation Activity and SO2 Resistance of the Pt/TiO2 Catalyst

Yudong Meng, Xing Fan, Jianyu Cai, Wenjun Liang et al.
6 citations
Catalysts
Catalytic Processes in Materials Science
3.11
article

Loading Eu2O3 Enhances the CO Oxidation Activity and SO2 Resistance of the Pt/TiO2 Catalyst

Yudong Meng, Xing Fan, Jianyu Cai, Wenjun Liang, Jian Li, Zehui Yu
article en
6 citations

Abstract

Pt/TiO2 and Pt-Eu2O3/TiO2 catalysts were prepared via the impregnation method for catalytic oxidation of CO. The Pt-2Eu2O3/TiO2 catalyst exhibited better CO oxidation activity as well as greater SO2 resistance than the Pt/TiO2 catalyst. For the inlet gas consisting of 0.8% CO, 5% O2, and balanced N2, the lowest complete conversion temperatures (T100) of CO were 120 °C and 140 °C for the Pt-2Eu2O3/TiO2 and Pt/TiO2 catalysts, respectively. During the 72 h SO2-resistance test at 200 °C under an inlet gas composition of 0.8% CO, 5% O2, 15% H2O, 50 ppm SO2, and balanced N2, the CO conversion on the Pt-2Eu2O3/TiO2 catalyst remained >99%, while that on the Pt/TiO2 catalyst gradually decreased to 77.8%. Pre-loading 2 wt% Eu2O3 on TiO2 enhanced the dispersion of Pt, increased the proportion of Pt0, and facilitated the adsorption and dissociation of H2O, all of which promoted CO oxidation. SO2 preferentially occupied the Eu2O3 sites by forming stable sulfates on the Pt-2Eu2O3/TiO2 catalyst, which protected the Pt active sites from poisoning. The OH* species produced from the dissociation of H2O played a significant role in promoting CO oxidation through the formation of COOH* as the key reaction intermediate. The developed Pt-2Eu2O3/TiO2 catalyst has great application potential in terms of the removal of CO from industrial flue gases.

CatalystsVol. 15(8)
Beijing University of Technology (CN), Beijing Municipal Ecology and Environment Bureau (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 8%
Catalytic Processes in Materials Science
3.11
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