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Detection of key transient Cu intermediates in SSZ-13 during NH(3)-SCR deNO(x) by modulation excitation IR spectroscopy

The small pore zeolite Cu-SSZ-13 is an efficient material for the standard selective catalytic reduction of nitrogen oxides (NO(x)) by ammonia (NH(3)). In this work, Cu-SSZ-13 has been studied at 250 °C under high conversion using a modulation excitation approach and analysed with phase sensitive de...

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Detalles Bibliográficos
Autores principales: Greenaway, Alex G., Marberger, Adrian, Thetford, Adam, Lezcano-González, Inés, Agote-Arán, Miren, Nachtegaal, Maarten, Ferri, Davide, Kröcher, Oliver, Catlow, C. Richard A., Beale, Andrew M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7067242/
https://www.ncbi.nlm.nih.gov/pubmed/32190265
http://dx.doi.org/10.1039/c9sc04905c
Descripción
Sumario:The small pore zeolite Cu-SSZ-13 is an efficient material for the standard selective catalytic reduction of nitrogen oxides (NO(x)) by ammonia (NH(3)). In this work, Cu-SSZ-13 has been studied at 250 °C under high conversion using a modulation excitation approach and analysed with phase sensitive detection (PSD). While the complementary X-ray absorption near edge structure (XANES) spectroscopy measurements showed that the experiments were performed under cyclic Cu(+)/Cu(2+) redox, Diffuse Reflectance Infrared Fourier Transform Spectroscopy (DRIFTS) experiments provide spectroscopic evidence for previously postulated intermediates Cu–N([double bond, length as m-dash]O)–NH(2) and Cu–NO(3) in the NH(3)-SCR deNO(x) mechanism and for the role of [Cu(2+)(OH(–))](+). These results therefore help in building towards a more comprehensive understanding of the reaction mechanism which to date has only been postulated in silico.