Effect of alkali metal poisoning on Cu-SSZ-13 in selective catalytic reduction with ammonia (NH 3 -SCR)

Abstract

Cu-SSZ-13 is widely recognized as an efficient catalyst for the selective catalytic reduction of NO x with ammonia (NH 3 -SCR). However, in practical stationary applications, it is frequently exposed to alkali metal contaminants, which can significantly influence its catalytic performance. In this study, the effects of different alkali metal salts (NaNO 3 , KNO 3 , NaCl and KCl) on Cu-SSZ-13 were systemically investigated (regarding the variation in the physicochemical properties and NH 3 -SCR activity). A slight promotional effect (about 10% increase in NO x conversion) was observed at low temperatures (< 250 °C) for alkali metal poisoned samples, which is attributed to the enhanced presence of active ZCu II OH species, as evidenced by H 2 -TPR analysis. Conversely, a marked deactivation (up to 50% decline in NO x conversion) was observed at high temperatures (> 400 °C), primarily due to the loss of Brøsted acid sites and isolated Cu 2+ species, as indicated by NH 3 -TPD, pyridine-IR, H 2 -TPR and UVvis spectroscopy. Notably, alkali metal chlorides (KCl, NaCl) induced more severe deactivation than their nitrate counterparts, likely due to a synergistic effect between framework dealumination and transformation of Cu 2+ species, leading to the formation of CuAlO x species. These findings provide deeper insight into the effect of alkali metal poisoning on NH 3 -SCR activity of Cu-SSZ-13, highlighting the necessity of preventing alkali metal chlorides from entering SCR systems to maintain catalyst efficiency.

Supplementary files

Article information

Article type
Paper
Submitted
04 Sep 2025
Accepted
30 Oct 2025
First published
31 Oct 2025
This article is Open Access
Creative Commons BY-NC license

Phys. Chem. Chem. Phys., 2025, Accepted Manuscript

Effect of alkali metal poisoning on Cu-SSZ-13 in selective catalytic reduction with ammonia (NH 3 -SCR)

B. Wang, S. Chansai, H. Xiang, Y. Jiao, J. Zhan, Y. Zhang, T. He, Y. Zhang and X. Fan, Phys. Chem. Chem. Phys., 2025, Accepted Manuscript , DOI: 10.1039/D5CP03404C

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