4.6 Article

Enhanced performance of iron-cerium NOx reduction catalysts by sulfuric acid treatment: The synergistic effect of surface acidity and redox capacity

Journal

APPLIED CATALYSIS A-GENERAL
Volume 621, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.apcata.2021.118200

Keywords

FeOx-CeO2; Sulfuric acid treatment; Ammonia oxidation; NH3-SCR

Funding

  1. Opening Project of the Key Laboratory of Green Catalysis of the Sichuan Institutes of Higher Education [LZJ1808]

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CeO2-based catalysts have garnered attention in the selective catalytic reduction of NO with NH3, but their poor T-90 operation window hinders industrial application. A study introducing sulfuric acid treatment to FeOx-CeO2 mixed oxides for NH3-SCR showed significantly improved high temperature activity and broadened operation window, attributed to increased redox capacity and surface acidity. This enhancement in performance was associated with the synergistic effect of these two parameters, favoring the formation of active intermediate species for N2 generation and inhibiting the formation of N2O and NOx, resulting in high catalytic activity and N2 selectivity.
CeO2-based catalysts have raised extensive attention in selective catalytic reduction of NO with NH3 but the poor T-90 operation window limits their industrial application. In present work, FeOx-CeO2 mixed oxides were prepared by a sol-gel method for NH3-SCR, and the effects of sulfuric acid treatment on the catalytic performance were systematically investigated. The results showed that sulfuric acid treatment significantly improved the high temperature activity. Compared to the FeOx-CeO2 sample, the T-90 operation window of FeOx-CeO2-S was greatly broadened from 200-300 degrees C to 250-450 degrees C. Various characterizations demonstrated that sulfuric acid introduction increased redox capacity and also enhanced surface acidity. The synergistic effect of these two parameters was closely associated with the enhanced performance. Further investigations revealed that the sulfuric acid modification favored the formation of active intermediate species for N-2 generation, while inhibited the formation of N2O and NOx, thus contributing to the high catalytic activity and N-2 selectivity.

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