4.8 Article

Inhibition Effect of Phosphorus Poisoning on the Dynamics and Redox of Cu Active Sites in a Cu-SSZ-13 NH3-SCR Catalyst for NOx Reduction

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 55, Issue 18, Pages 12619-12629

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.1c03630

Keywords

Cu mobility; DRIFTS; UV-vis; impedance spectroscopy; Cu redox cycle; in situ

Funding

  1. National Natural Science Foundation of China [21976058, 21806039]
  2. Natural Science Foundation of Guangdong Province [2018A030313302, 2020A1414010005]
  3. DFG (German Research Foundation) [EXC 2186, 390919832]
  4. Pearl River Talent Recruitment Program of Guangdong Province [2019QN01L170]
  5. Innovation & Entrepreneurship Talent Program of Shaoguan City

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Cu-SSZ-13 catalyst was found to be deactivated by phosphorus poisoning in NH3-SCR reactions, leading to both loss of Cu active sites and restricted dynamic motion of Cu species. This inhibition significantly affects the redox cycling of Cu sites, especially the formation of key dimeric Cu intermediates, ultimately resulting in decreased NH3-SCR activity at low temperatures.
Phosphorus (P) stemming from biodiesel and/or lubricant oil additives is unavoidable in real diesel exhausts and deactivates gradually the Cu-SSZ-13 zeolite catalyst for ammonia-assisted selective catalytic NOx reduction (NH3-SCR). Here, the deactivation mechanism of Cu-SSZ-13 by P-poisoning was investigated by ex situ examination of the structural changes and by in situ probing the dynamics and redox of Cu active sites via a combination of impedance spectroscopy, diffuse reflection infrared Fourier transform spectroscopy, and ultraviolet-visible spectroscopy. We unveiled that strong interactions between Cu and P led to not only a loss of Cu active sites for catalytic turnovers but also a restricted dynamic motion of Cu species during low-temperature NH3-SCR catalysis. Furthermore, the Cu-II <-> Cu-I redox cycling of Cu sites, especially the Cu-I <->(CI)-I-uI reoxidation half-cycle, was significantly inhibited, which can be attributed to the restricted Cu motion by P-poisoning disabling the formation of key dimeric Cu intermediates. As a result, the NH3-SCR activity at low temperatures (200 degrees C and below) decreased slightly for the mildly poisoned Cu-SSZ-13 and considerably for the severely poisoned Cu-SSZ-13.

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