Post-Synthetically Treated ERI and SSZ-13 Zeolites Modified with Copper as Catalysts for NH3-SCR-DeNOx

Author:

Robles Alejandro Mollá1ORCID,Deplano Gabriele2ORCID,Góra-Marek Kinga3ORCID,Rotko Marek4ORCID,Wach Anna5ORCID,Lukman Muhammad Fernadi6ORCID,Bertmer Marko6,Signorile Matteo2ORCID,Bordiga Silvia2,Pöppl Andreas6,Gläser Roger1ORCID,Jabłońska Magdalena1ORCID

Affiliation:

1. Institute of Chemical Technology, Universität Leipzig, Linnéstr. 3, 04103 Leipzig, Germany

2. Department of Chemistry, NIS Center and INSTM Reference Center, University of Turin, Via P. Giuria 7, 10125 Turin, Italy

3. Faculty of Chemistry, Jagiellonian University in Krakow, Gronostajowa 2, 30-387 Krakow, Poland

4. Department of Chemical Technology, Institute of Chemical Sciences, Faculty of Chemistry, Maria Curie-Sklodowska University, 3 Maria Curie-Sklodowska Sq., 20-031 Lublin, Poland

5. Paul Scherrer Institute, 5232 Villigen, Switzerland

6. Felix Bloch Institute for Solid State Physics, Universität Leipzig, Linnéstr. 5, 04103 Leipzig, Germany

Abstract

ERI and SSZ-13 were subjected to post-synthetic treatments (depending on the zeolite topology) to create micro-/mesoporous materials. The results in terms of NH3-SCR-DeNOx show that the applied treatments improved the catalytic activity of the Cu-containing ERI-based materials; however, the NO conversion did not vary for the different materials treated with NaOH or NaOH/HNO3. For the micro-/mesoporous Cu-containing SSZ-13, a lower NO conversion in NH3-SCR-DeNOx was observed. Thus, our findings challenge the current paradigm of enhanced activity of micro-/mesoporous catalysts in NH3-SCR-DeNOx. The modification of the supports results in the presence of different amounts and kinds of copper species (especially isolated Cu2+ and aggregated Cu species) in the case of ERI- and SSZ-13-based samples. The present copper species further differentiate the formation of reactive reaction intermediates. Our studies show that besides the μ-η2,η2-peroxo dicopper(II) complexes (verified by in situ DR UV-Vis spectroscopy), copper nitrates (evidenced by in situ FT-IR spectroscopy) also act as reactive intermediates in these catalytic systems.

Funder

DFG

NCN

MUR

Publisher

MDPI AG

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