Cargando…

Rationally tailored redox ability of Sn/γ-Al(2)O(3) with Ag for enhancing the selective catalytic reduction of NO(x) with propene

The development of excellent selective catalytic reduction (SCR) catalysts with hydrocarbons for lean-burn diesel engines is of great significance, and a range of novel catalysts loaded with Sn and Ag were studied in this work. It was found that the synergistic effects of Sn and Ag enabled the 1Sn5A...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Ning, Zhang, Tiantian, Wu, Zuliang, Li, Jing, Wang, Wei, Zhu, Jiali, Yao, Shuiliang, Gao, Erhao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9832442/
https://www.ncbi.nlm.nih.gov/pubmed/36712644
http://dx.doi.org/10.1039/d2ra07316a
Descripción
Sumario:The development of excellent selective catalytic reduction (SCR) catalysts with hydrocarbons for lean-burn diesel engines is of great significance, and a range of novel catalysts loaded with Sn and Ag were studied in this work. It was found that the synergistic effects of Sn and Ag enabled the 1Sn5Ag/γ-Al(2)O(3) (1 wt% Sn and 5wt% Ag) to exhibit superior C(3)H(6)-SCR performance. The de-NO(x) efficiency was maintained above 80% between 336 and 448 °C. The characterization results showed that the presence of AgCl crystallites in the 1Sn5Ag/γ-Al(2)O(3) catalyst helped its redox ability maintain an appropriate level, which suppressed the over-oxidation of C(3)H(6). Besides, the number of surface adsorbed oxygen (O(α)) and hydroxyl groups (O(γ)) were enriched, and their reactivity was greatly enhanced due to the coexistence of Ag and Sn. The ratio of Ag(0)/Ag(+) was increased to 3.68 due to the electron transfer effects, much higher than that of Ag/γ-Al(2)O(3) (2.15). Lewis acid sites dominated the C(3)H(6)-SCR reaction over the 1Sn5Ag/γ-Al(2)O(3) catalyst. The synergistic effects of Sn and Ag facilitated the formation of intermediates such as acetates, enolic species, and nitrates, and inhibited the deep oxidation of C(3)H(6) into CO(2), and the C(3)H(6)-SCR mechanism was carefully proposed.