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Unraveling the poisoning effects of different lead species on MnCeOx catalysts in low-temperature NH3-SCR coupled with CO oxidation

  • Shan Ren* (Co-first Author)
  • , Xiaodi Li (Co-first Author)
  • , Manyi Liu
  • , Liang Wang
  • , Guangwei Wang
  • , Wenxue Wang
  • , Yifan Chai
  • , Chunbao Charles Xu
  • *Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

Abstract

Lead poisoning represents a major limitation for MnCeOx catalyst used in low-temperature flue gas treatment. In this work, the effects of different Pb species on the physicochemical properties, catalytic performance, and reaction pathways of MnCeOx catalyst were systematically investigated for the simultaneous removal of NO and CO. The catalytic performance results demonstrated that the poisoning severity strongly depended on Pb speciation, following the order of PbCl2 > PbSO4 > Pb(NO3)2 > PbCO3. Although Pb deposition exerted little influence on the crystal structure of MnCeOx, it induced notable changes in surface texture and electronic structure, leading to distinct deactivation behaviors. PbCl2 caused the most severe loss of catalytic activity owing to extensive pore blockage, active site coverage, suppression of surface acidity, and deterioration of redox properties. In contrast, PbCO3 exhibited the weakest poisoning effect and preserved relatively favorable surface characteristics. XPS and Raman analyses further demonstrated that Pb species decreased the surface Mn4+ concentration and hindered the Ce4+/Ce3+ redox cycle, leading to reduced oxygen vacancy density and impaired oxygen mobility. In situ DRIFTS analysis revealed that Pb species significantly altered surface reaction pathways. PbCO3 maintained effective NO oxidation and NH3 adsorption, enabling a nitrate mediated L-H route for NH3-SCR, whereas PbCl2 and PbSO4 markedly suppressed nitrate formation and NH3 activation, favoring a less efficient E-R pathway. In addition, Pb species modified carbonate formation and oxygen participation during CO oxidation reaction, leading to distinct oxidation behaviors among the poisoned catalysts. These results provided mechanistic insights into Pb poisoning and offer a guidance for the rational design of Pb-tolerant MnCeOx catalysts for low-temperature flue gas purification. © 2026 Elsevier B.V.
Original languageEnglish
Article number178596
JournalChemical Engineering Journal
Volume543
Online published19 Jun 2026
DOIs
Publication statusPublished - 1 Sept 2026

Funding

This work was financially supported by the National Natural Science Foundation of China (No. 52374411), the Outstanding Youth Science Foundation of Shaanxi Province (No. 2025JC-JCQN-031), the Inner Mongolia Autonomous Region Science and Technology Planning Project (No. 2025YFHH0055), and the Key Research and Development Program Project of Shaanxi Province (No. 2025CY-GJHX2-12).

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Research Keywords

  • CO oxidation
  • MnCeOx catalysts
  • NH3-SCR
  • Pb poisoning
  • Reaction mechanism

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