Changing active sites in Cu–CHA catalysts: deNOx selectivity as a function of the preparation method

Autores
Deka, Upakul; Lezcano Gonzalez, Ines; Warrender, Stewart J.; Picone, Andrea Lorena; Wright, Paul A.; Weckhuysen, Bert M.; Beale, Andrew M.
Año de publicación
2013
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The selective catalytic reduction of NO x with ammonia (NH 3-SCR) has been studied over Cu-CHA catalysts in which the loading of copper species was achieved using three different synthetic routes: two are based on post-synthetic treatment of the zeolite material (via aqueous or vapor phase) and a third involves the direct synthesis of a Cu-loaded SAPO-34. The catalysts were subsequently characterized by XRD, solid-state NMR, UV-vis and XAFS spectroscopies. Whilst the catalysts prepared via wet chemical routes show excellent deNO x activity and high selectivity to N 2, the one prepared via chemical vapor deposition gave the undesired product N 2O in significant quantities. Isolated mononuclear Cu 2+ ions in the vicinity of six-membered rings (6mrs, part of the d6r sub-units of CHA) were found to be active sites in both catalysts prepared via the wet chemical approaches. In contrast, XAFS data revealed that the catalyst prepared via chemical vapor deposition possesses Cu in two different environments: isolated Cu 2+ cations and CuAlO 2-type species. Catalytic experiments revealed a strong correlation between the number of isolated mononuclear Cu 2+ in or near the plane of the 6m rings and N 2 production, whereas the presence of CuAlO 2 species appears to promote the formation of undesired N 2O.
Fil: Deka, Upakul. Materials Innovation Institute; Países Bajos. Utrecht University; Países Bajos
Fil: Lezcano Gonzalez, Ines. Materials Innovation Institute; Países Bajos. Utrecht University; Países Bajos
Fil: Warrender, Stewart J.. University of St. Andrews; Reino Unido
Fil: Picone, Andrea Lorena. University of St. Andrews; Reino Unido. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Wright, Paul A.. University of St. Andrews; Reino Unido
Fil: Weckhuysen, Bert M.. Utrecht University; Países Bajos
Fil: Beale, Andrew M.. Utrecht University; Países Bajos
Materia
Active Sites
Cu-Sapo-34
Cu-Ssz-13
Cvd-Ie
Nh 3-Scr
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/77810

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network_name_str CONICET Digital (CONICET)
spelling Changing active sites in Cu–CHA catalysts: deNOx selectivity as a function of the preparation methodDeka, UpakulLezcano Gonzalez, InesWarrender, Stewart J.Picone, Andrea LorenaWright, Paul A.Weckhuysen, Bert M.Beale, Andrew M.Active SitesCu-Sapo-34Cu-Ssz-13Cvd-IeNh 3-Scrhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1The selective catalytic reduction of NO x with ammonia (NH 3-SCR) has been studied over Cu-CHA catalysts in which the loading of copper species was achieved using three different synthetic routes: two are based on post-synthetic treatment of the zeolite material (via aqueous or vapor phase) and a third involves the direct synthesis of a Cu-loaded SAPO-34. The catalysts were subsequently characterized by XRD, solid-state NMR, UV-vis and XAFS spectroscopies. Whilst the catalysts prepared via wet chemical routes show excellent deNO x activity and high selectivity to N 2, the one prepared via chemical vapor deposition gave the undesired product N 2O in significant quantities. Isolated mononuclear Cu 2+ ions in the vicinity of six-membered rings (6mrs, part of the d6r sub-units of CHA) were found to be active sites in both catalysts prepared via the wet chemical approaches. In contrast, XAFS data revealed that the catalyst prepared via chemical vapor deposition possesses Cu in two different environments: isolated Cu 2+ cations and CuAlO 2-type species. Catalytic experiments revealed a strong correlation between the number of isolated mononuclear Cu 2+ in or near the plane of the 6m rings and N 2 production, whereas the presence of CuAlO 2 species appears to promote the formation of undesired N 2O.Fil: Deka, Upakul. Materials Innovation Institute; Países Bajos. Utrecht University; Países BajosFil: Lezcano Gonzalez, Ines. Materials Innovation Institute; Países Bajos. Utrecht University; Países BajosFil: Warrender, Stewart J.. University of St. Andrews; Reino UnidoFil: Picone, Andrea Lorena. University of St. Andrews; Reino Unido. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Wright, Paul A.. University of St. Andrews; Reino UnidoFil: Weckhuysen, Bert M.. Utrecht University; Países BajosFil: Beale, Andrew M.. Utrecht University; Países BajosElsevier Science2013-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/77810Deka, Upakul; Lezcano Gonzalez, Ines; Warrender, Stewart J.; Picone, Andrea Lorena; Wright, Paul A.; et al.; Changing active sites in Cu–CHA catalysts: deNOx selectivity as a function of the preparation method; Elsevier Science; Microporous and Mesoporous Materials; 166; 1-2013; 144-1521387-1811CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.micromeso.2012.04.056info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S1387181112002831info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-15T15:36:25Zoai:ri.conicet.gov.ar:11336/77810instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-15 15:36:25.814CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Changing active sites in Cu–CHA catalysts: deNOx selectivity as a function of the preparation method
title Changing active sites in Cu–CHA catalysts: deNOx selectivity as a function of the preparation method
spellingShingle Changing active sites in Cu–CHA catalysts: deNOx selectivity as a function of the preparation method
Deka, Upakul
Active Sites
Cu-Sapo-34
Cu-Ssz-13
Cvd-Ie
Nh 3-Scr
title_short Changing active sites in Cu–CHA catalysts: deNOx selectivity as a function of the preparation method
title_full Changing active sites in Cu–CHA catalysts: deNOx selectivity as a function of the preparation method
title_fullStr Changing active sites in Cu–CHA catalysts: deNOx selectivity as a function of the preparation method
title_full_unstemmed Changing active sites in Cu–CHA catalysts: deNOx selectivity as a function of the preparation method
title_sort Changing active sites in Cu–CHA catalysts: deNOx selectivity as a function of the preparation method
dc.creator.none.fl_str_mv Deka, Upakul
Lezcano Gonzalez, Ines
Warrender, Stewart J.
Picone, Andrea Lorena
Wright, Paul A.
Weckhuysen, Bert M.
Beale, Andrew M.
author Deka, Upakul
author_facet Deka, Upakul
Lezcano Gonzalez, Ines
Warrender, Stewart J.
Picone, Andrea Lorena
Wright, Paul A.
Weckhuysen, Bert M.
Beale, Andrew M.
author_role author
author2 Lezcano Gonzalez, Ines
Warrender, Stewart J.
Picone, Andrea Lorena
Wright, Paul A.
Weckhuysen, Bert M.
Beale, Andrew M.
author2_role author
author
author
author
author
author
dc.subject.none.fl_str_mv Active Sites
Cu-Sapo-34
Cu-Ssz-13
Cvd-Ie
Nh 3-Scr
topic Active Sites
Cu-Sapo-34
Cu-Ssz-13
Cvd-Ie
Nh 3-Scr
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv The selective catalytic reduction of NO x with ammonia (NH 3-SCR) has been studied over Cu-CHA catalysts in which the loading of copper species was achieved using three different synthetic routes: two are based on post-synthetic treatment of the zeolite material (via aqueous or vapor phase) and a third involves the direct synthesis of a Cu-loaded SAPO-34. The catalysts were subsequently characterized by XRD, solid-state NMR, UV-vis and XAFS spectroscopies. Whilst the catalysts prepared via wet chemical routes show excellent deNO x activity and high selectivity to N 2, the one prepared via chemical vapor deposition gave the undesired product N 2O in significant quantities. Isolated mononuclear Cu 2+ ions in the vicinity of six-membered rings (6mrs, part of the d6r sub-units of CHA) were found to be active sites in both catalysts prepared via the wet chemical approaches. In contrast, XAFS data revealed that the catalyst prepared via chemical vapor deposition possesses Cu in two different environments: isolated Cu 2+ cations and CuAlO 2-type species. Catalytic experiments revealed a strong correlation between the number of isolated mononuclear Cu 2+ in or near the plane of the 6m rings and N 2 production, whereas the presence of CuAlO 2 species appears to promote the formation of undesired N 2O.
Fil: Deka, Upakul. Materials Innovation Institute; Países Bajos. Utrecht University; Países Bajos
Fil: Lezcano Gonzalez, Ines. Materials Innovation Institute; Países Bajos. Utrecht University; Países Bajos
Fil: Warrender, Stewart J.. University of St. Andrews; Reino Unido
Fil: Picone, Andrea Lorena. University of St. Andrews; Reino Unido. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Wright, Paul A.. University of St. Andrews; Reino Unido
Fil: Weckhuysen, Bert M.. Utrecht University; Países Bajos
Fil: Beale, Andrew M.. Utrecht University; Países Bajos
description The selective catalytic reduction of NO x with ammonia (NH 3-SCR) has been studied over Cu-CHA catalysts in which the loading of copper species was achieved using three different synthetic routes: two are based on post-synthetic treatment of the zeolite material (via aqueous or vapor phase) and a third involves the direct synthesis of a Cu-loaded SAPO-34. The catalysts were subsequently characterized by XRD, solid-state NMR, UV-vis and XAFS spectroscopies. Whilst the catalysts prepared via wet chemical routes show excellent deNO x activity and high selectivity to N 2, the one prepared via chemical vapor deposition gave the undesired product N 2O in significant quantities. Isolated mononuclear Cu 2+ ions in the vicinity of six-membered rings (6mrs, part of the d6r sub-units of CHA) were found to be active sites in both catalysts prepared via the wet chemical approaches. In contrast, XAFS data revealed that the catalyst prepared via chemical vapor deposition possesses Cu in two different environments: isolated Cu 2+ cations and CuAlO 2-type species. Catalytic experiments revealed a strong correlation between the number of isolated mononuclear Cu 2+ in or near the plane of the 6m rings and N 2 production, whereas the presence of CuAlO 2 species appears to promote the formation of undesired N 2O.
publishDate 2013
dc.date.none.fl_str_mv 2013-01
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/77810
Deka, Upakul; Lezcano Gonzalez, Ines; Warrender, Stewart J.; Picone, Andrea Lorena; Wright, Paul A.; et al.; Changing active sites in Cu–CHA catalysts: deNOx selectivity as a function of the preparation method; Elsevier Science; Microporous and Mesoporous Materials; 166; 1-2013; 144-152
1387-1811
CONICET Digital
CONICET
url http://hdl.handle.net/11336/77810
identifier_str_mv Deka, Upakul; Lezcano Gonzalez, Ines; Warrender, Stewart J.; Picone, Andrea Lorena; Wright, Paul A.; et al.; Changing active sites in Cu–CHA catalysts: deNOx selectivity as a function of the preparation method; Elsevier Science; Microporous and Mesoporous Materials; 166; 1-2013; 144-152
1387-1811
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1016/j.micromeso.2012.04.056
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S1387181112002831
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Elsevier Science
publisher.none.fl_str_mv Elsevier Science
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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