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Catalytic Performance of One-Pot Synthesized Fe-MWW Layered Zeolites (MCM-22, MCM-36, and ITQ-2) in Selective Catalytic Reduction of Nitrogen Oxides with Ammonia

The application of layered zeolites of MWW topology in environmental catalysis has attracted growing attention in recent years; however, only a few studies have explored their performance in selective catalytic reduction with ammonia (NH(3)-SCR). Thus, our work describes, for the first time, the one...

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Detalles Bibliográficos
Autores principales: Szymaszek-Wawryca, Agnieszka, Díaz, Urbano, Samojeden, Bogdan, Motak, Monika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9104601/
https://www.ncbi.nlm.nih.gov/pubmed/35566333
http://dx.doi.org/10.3390/molecules27092983
Descripción
Sumario:The application of layered zeolites of MWW topology in environmental catalysis has attracted growing attention in recent years; however, only a few studies have explored their performance in selective catalytic reduction with ammonia (NH(3)-SCR). Thus, our work describes, for the first time, the one-pot synthesis of Fe-modified NH(3)-SCR catalysts supported on MCM-22, MCM-36, and ITQ-2. The calculated chemical composition of the materials was Si/Al of 30 and 5 wt.% of Fe. The reported results indicated a correlation between the arrangement of MWW layers and the form of iron in the zeolitic structure. We have observed that one-pot synthesis resulted in high dispersion of Fe(3+) sites, which significantly enhanced low-temperature activity and prevented N(2)O generation during the reaction. All of the investigated samples exhibited almost 100% NO conversion at 250 °C. The most satisfactory activity was exhibited by Fe-modified MCM-36, since 50% of NO reduction was obtained at 150 °C for this catalyst. This effect can be explained by the abundance of isolated Fe(3+) species, which are active in low-temperature NH(3)-SCR. Additionally, SiO(2) pillars present in MCM-36 provided an additional surface for the deposition of the active phase.