Interplay of charge density and relative humidity on the structure of nitrate layered double hydroxides
- Autores
- Jobbagy, Matias; Iyi, Nobuo
- Año de publicación
- 2010
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- The structure of several crystalline Ni(II)-Al(III) and Mg(II)-Al(III) layered double hydroxides (LDHs) intercalated with nitrate anions was studied as a function of the relative humidity. For low charge density LDHs, the electrostatic attraction between the anions and the positive LDH layers prevails over any other interaction, and the anions remain flat, F, with their C 3 axis perpendicular to the xy planes, irrespective of water activity. For LDHs bearing higher charge densities, the incoming water molecules drive an abrupt phase expansion in which the anions tilt their C3 axis with respect to the interlamellar xy plane, thus resulting in an expanded, T, form. The structural F-T transition is discontinuous, and involves a second staging phase intermediate, with alternated F and T galleries. For intermediate charge density LDHs, the hydration process easily reverts, once the samples are resubmitted to a dry atmosphere. Dehydration of high charge density LDHs is however kinetically hindered; this behavior is explained in terms of the structural features of the involved phases. For all samples, the maximum net gallery expansion is proportional to the layer charge density, irrespective of the nature of the divalent cation. © 2010 American Chemical Society.
Fil: Jobbagy, Matias. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina. Centro Interdisciplinario de Nanociencia y Nanotecnología; Argentina
Fil: Iyi, Nobuo. Tsukuba University. National Institute For Materials Science; Japón - Materia
-
Layered Double Hydroxides
Surface Sorption
Structure
Kinetics - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/71962
Ver los metadatos del registro completo
id |
CONICETDig_1150ee1978bae6894f479b08b58bad80 |
---|---|
oai_identifier_str |
oai:ri.conicet.gov.ar:11336/71962 |
network_acronym_str |
CONICETDig |
repository_id_str |
3498 |
network_name_str |
CONICET Digital (CONICET) |
spelling |
Interplay of charge density and relative humidity on the structure of nitrate layered double hydroxidesJobbagy, MatiasIyi, NobuoLayered Double HydroxidesSurface SorptionStructureKineticshttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1The structure of several crystalline Ni(II)-Al(III) and Mg(II)-Al(III) layered double hydroxides (LDHs) intercalated with nitrate anions was studied as a function of the relative humidity. For low charge density LDHs, the electrostatic attraction between the anions and the positive LDH layers prevails over any other interaction, and the anions remain flat, F, with their C 3 axis perpendicular to the xy planes, irrespective of water activity. For LDHs bearing higher charge densities, the incoming water molecules drive an abrupt phase expansion in which the anions tilt their C3 axis with respect to the interlamellar xy plane, thus resulting in an expanded, T, form. The structural F-T transition is discontinuous, and involves a second staging phase intermediate, with alternated F and T galleries. For intermediate charge density LDHs, the hydration process easily reverts, once the samples are resubmitted to a dry atmosphere. Dehydration of high charge density LDHs is however kinetically hindered; this behavior is explained in terms of the structural features of the involved phases. For all samples, the maximum net gallery expansion is proportional to the layer charge density, irrespective of the nature of the divalent cation. © 2010 American Chemical Society.Fil: Jobbagy, Matias. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina. Centro Interdisciplinario de Nanociencia y Nanotecnología; ArgentinaFil: Iyi, Nobuo. Tsukuba University. National Institute For Materials Science; JapónAmerican Chemical Society2010-10info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/71962Jobbagy, Matias; Iyi, Nobuo; Interplay of charge density and relative humidity on the structure of nitrate layered double hydroxides; American Chemical Society; Journal of Physical Chemistry C; 114; 42; 10-2010; 18153-181581932-7447CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1021/jp1078778info:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/jp1078778info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-15T14:38:44Zoai:ri.conicet.gov.ar:11336/71962instacron: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 14:38:44.848CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Interplay of charge density and relative humidity on the structure of nitrate layered double hydroxides |
title |
Interplay of charge density and relative humidity on the structure of nitrate layered double hydroxides |
spellingShingle |
Interplay of charge density and relative humidity on the structure of nitrate layered double hydroxides Jobbagy, Matias Layered Double Hydroxides Surface Sorption Structure Kinetics |
title_short |
Interplay of charge density and relative humidity on the structure of nitrate layered double hydroxides |
title_full |
Interplay of charge density and relative humidity on the structure of nitrate layered double hydroxides |
title_fullStr |
Interplay of charge density and relative humidity on the structure of nitrate layered double hydroxides |
title_full_unstemmed |
Interplay of charge density and relative humidity on the structure of nitrate layered double hydroxides |
title_sort |
Interplay of charge density and relative humidity on the structure of nitrate layered double hydroxides |
dc.creator.none.fl_str_mv |
Jobbagy, Matias Iyi, Nobuo |
author |
Jobbagy, Matias |
author_facet |
Jobbagy, Matias Iyi, Nobuo |
author_role |
author |
author2 |
Iyi, Nobuo |
author2_role |
author |
dc.subject.none.fl_str_mv |
Layered Double Hydroxides Surface Sorption Structure Kinetics |
topic |
Layered Double Hydroxides Surface Sorption Structure Kinetics |
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 structure of several crystalline Ni(II)-Al(III) and Mg(II)-Al(III) layered double hydroxides (LDHs) intercalated with nitrate anions was studied as a function of the relative humidity. For low charge density LDHs, the electrostatic attraction between the anions and the positive LDH layers prevails over any other interaction, and the anions remain flat, F, with their C 3 axis perpendicular to the xy planes, irrespective of water activity. For LDHs bearing higher charge densities, the incoming water molecules drive an abrupt phase expansion in which the anions tilt their C3 axis with respect to the interlamellar xy plane, thus resulting in an expanded, T, form. The structural F-T transition is discontinuous, and involves a second staging phase intermediate, with alternated F and T galleries. For intermediate charge density LDHs, the hydration process easily reverts, once the samples are resubmitted to a dry atmosphere. Dehydration of high charge density LDHs is however kinetically hindered; this behavior is explained in terms of the structural features of the involved phases. For all samples, the maximum net gallery expansion is proportional to the layer charge density, irrespective of the nature of the divalent cation. © 2010 American Chemical Society. Fil: Jobbagy, Matias. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina. Centro Interdisciplinario de Nanociencia y Nanotecnología; Argentina Fil: Iyi, Nobuo. Tsukuba University. National Institute For Materials Science; Japón |
description |
The structure of several crystalline Ni(II)-Al(III) and Mg(II)-Al(III) layered double hydroxides (LDHs) intercalated with nitrate anions was studied as a function of the relative humidity. For low charge density LDHs, the electrostatic attraction between the anions and the positive LDH layers prevails over any other interaction, and the anions remain flat, F, with their C 3 axis perpendicular to the xy planes, irrespective of water activity. For LDHs bearing higher charge densities, the incoming water molecules drive an abrupt phase expansion in which the anions tilt their C3 axis with respect to the interlamellar xy plane, thus resulting in an expanded, T, form. The structural F-T transition is discontinuous, and involves a second staging phase intermediate, with alternated F and T galleries. For intermediate charge density LDHs, the hydration process easily reverts, once the samples are resubmitted to a dry atmosphere. Dehydration of high charge density LDHs is however kinetically hindered; this behavior is explained in terms of the structural features of the involved phases. For all samples, the maximum net gallery expansion is proportional to the layer charge density, irrespective of the nature of the divalent cation. © 2010 American Chemical Society. |
publishDate |
2010 |
dc.date.none.fl_str_mv |
2010-10 |
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/11336/71962 Jobbagy, Matias; Iyi, Nobuo; Interplay of charge density and relative humidity on the structure of nitrate layered double hydroxides; American Chemical Society; Journal of Physical Chemistry C; 114; 42; 10-2010; 18153-18158 1932-7447 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/71962 |
identifier_str_mv |
Jobbagy, Matias; Iyi, Nobuo; Interplay of charge density and relative humidity on the structure of nitrate layered double hydroxides; American Chemical Society; Journal of Physical Chemistry C; 114; 42; 10-2010; 18153-18158 1932-7447 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1021/jp1078778 info:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/jp1078778 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
American Chemical Society |
publisher.none.fl_str_mv |
American Chemical Society |
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 |
_version_ |
1846082868495777792 |
score |
13.22299 |