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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/77810
Ver los metadatos del registro completo
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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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1846083487586582528 |
score |
13.22299 |