Determining the storage, availability and reactivity of NH3 within Cu-Chabazite-based Ammonia Selective Catalytic Reduction systems

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Access status: Embargo until 2050-01-01 , c3cp54132k.pdf (3.29 MB)

Publication date

2014-11-28

Authors

Lezcano-Gonzalez, I.ISNI 0000000436417676
Deka, U.ISNI 0000000390808611
Arstad, B
Van Yperen-De Deyne, A
Hemelsoet, K
Waroquier, M
Van Speybroeck, V
Weckhuysen, BertORCID 0000-0001-5245-1426ISNI 0000000110540180
Beale, AMISNI 000000039664243X

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Abstract

Three different types of NH3 species can be simultaneously present on Cu(2+)-exchanged CHA-type zeolites, commonly used in Ammonia Selective Catalytic Reduction (NH3-SCR) systems. These include ammonium ions (NH4(+)), formed on the Brønsted acid sites, [Cu(NH3)4](2+) complexes, resulting from NH3 coordination with the Cu(2+) Lewis sites, and NH3 adsorbed on extra-framework Al (EFAl) species, in contrast to the only two reacting NH3 species recently reported on Cu-SSZ-13 zeolite. The NH4(+) ions react very slowly in comparison to NH3 coordinated to Cu(2+) ions and are likely to contribute little to the standard NH3-SCR process, with the Brønsted groups acting primarily as NH3 storage sites. The availability/reactivity of NH4(+) ions can be however, notably improved by submitting the zeolite to repeated exchanges with Cu(2+), accompanied by a remarkable enhancement in the low temperature activity. Moreover, the presence of EFAl species could also have a positive influence on the reaction rate of the available NH4(+) ions. These results have important implications for NH3 storage and availability in Cu-Chabazite-based NH3-SCR systems.

Keywords

Ammonia, Catalysis, Copper, Models, Molecular, Organometallic Compounds, Oxidation-Reduction, Surface Properties, Temperature, Zeolites

Citation

Lezcano-Gonzalez, I, Deka, U, Arstad, B, Van Yperen-De Deyne, A, Hemelsoet, K, Waroquier, M, Van Speybroeck, V, Weckhuysen, B M & Beale, A M 2014, 'Determining the storage, availability and reactivity of NH3 within Cu-Chabazite-based Ammonia Selective Catalytic Reduction systems', Physical Chemistry Chemical Physics, vol. 16, no. 4, pp. 1639-1650. https://doi.org/10.1039/c3cp54132k