These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Search MEDLINE/PubMed
Title: Spectroscopic identification and catalytic relevance of NH4+ intermediates in selective NOx reduction over Cu-SSZ-13 zeolites. Author: Rizzotto V, Chen D, Tabak BM, Yang JY, Ye D, Simon U, Chen P. Journal: Chemosphere; 2020 Jul; 250():126272. PubMed ID: 32109703. Abstract: Reduction of harmful nitrogen oxides (NOx) from diesel engine exhausts is one of the key challenges in environmental protection, and can be achieved by NH3-assisted selective catalytic reduction (NH3-SCR) using copper-exchanged chabazite zeolites (i.e. Cu-CHA, including Cu-SSZ-13 and Cu-SAPO-34) as catalysts. Understanding the redox chemistry of Cu-CHA in NH3-SCR catalysis is crucial for further improving the NOx reduction efficiency. Here, a series of Cu-SSZ-13 catalysts with different Cu ion exchange levels were prepared, thoroughly characterized by different techniques such as X-ray diffraction, diffuse reflectance ultraviolet-visible spectroscopy and temperature-programmed desorption using NH3 as a probe molecule, etc., and tested in NH3-SCR reactions under steady-state conditions. In situ studies by diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS), supplemented with density-functional theory calculations, provided solid evidence for the formation of ammonium ion (NH4+) intermediates resulting from the reduction of Cu2+ to Cu+ by co-adsorbed NH3 and NO molecules on Cu-SSZ-13. Catalytic relevance of the NH4+ intermediates, as demonstrated by an increase of NO conversion over Cu-SSZ-13 pre-treated in NH3/NO atmosphere, can be attributed to the formation of closely coupled Cu+/NH4+ pairs promoting the Cu+ re-oxidation and, consequently, the overall NH3-SCR process. This study thus paves a new route for improving the NH3-SCR efficiency over Cu-CHA zeolite catalyst.[Abstract] [Full Text] [Related] [New Search]