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DeNO(x) Abatement over Sonically Prepared Iron-Substituted Y, USY and MFI Zeolite Catalysts in Lean Exhaust Gas Conditions

Iron-substituted MFI, Y and USY zeolites prepared by two preparation routes—classical ion exchange and the ultrasound modified ion-exchange method—were characterised by micro-Raman spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), and ultraviolet (UV)/visible diffuse reflect...

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Detalles Bibliográficos
Autores principales: Chlebda, Damian K., Stachurska, Patrycja, Jędrzejczyk, Roman J., Kuterasiński, Łukasz, Dziedzicka, Anna, Górecka, Sylwia, Chmielarz, Lucjan, Łojewska, Joanna, Sitarz, Maciej, Jodłowski, Przemysław J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5791108/
https://www.ncbi.nlm.nih.gov/pubmed/29301370
http://dx.doi.org/10.3390/nano8010021
Descripción
Sumario:Iron-substituted MFI, Y and USY zeolites prepared by two preparation routes—classical ion exchange and the ultrasound modified ion-exchange method—were characterised by micro-Raman spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), and ultraviolet (UV)/visible diffuse reflectance spectroscopy (UV/Vis DRS). Ultrasound irradiation, a new technique for the preparation of the metal salt suspension before incorporation to the zeolite structure, was employed. An experimental study of selective catalytic reduction (SCR) of NO with NH(3) on both iron-substituted reference zeolite catalysts and those prepared through the application of ultrasound conducted during an ion-exchange process is presented. The prepared zeolite catalysts show high activity and selectivity in SCR deNO(x) abatement. The MFI-based iron catalysts, especially those prepared via the sonochemical method, revealed superior activity in the deNO(x) process, with almost 100% selectivity towards N(2). The hydrothermal stability test confirmed high stability and activity of MFI-based catalysts in water-rich conditions during the deNO(x) reaction at 450 °C.