Complexation at the edges of hydrotalcite: the cases of arsenate and chromate

Autores
Jobbagy, Matias; Regazzoni, Alberto Ernesto
Año de publicación
2012
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Sorption of CrO2 4 and HAsO2 4 by hydrotalcite, in its chloride form, was studied as a function of anion concentration. In both cases, the shape of the isotherms is langmuirian. The maximum uptake of CrO2 4 equals the ion-exchange capacity of the solid, whereas sorption of HAsO2 4 saturates at a higher value. Chloride ions inhibit the uptake of both anions, the amount of sorbed CrO2 4 declining rapidly to zero. The uptake of HAsO2 4 , however, attains a constant value at high chloride concentrations. The excess of arsenate uptake follows, at constant pH, a langmuirian dependence with equilibrium concentration and decreases with increasing pH, depicting a marked change in slope at pH pQa3. CrO2 4 and HAsO2 4 have notable, albeit different, effects on the electrophoretic behavior of hydrotalcite; the positive particle charge is screened almost completely by CrO2 4 , whereas sorption of HAsO2 4 produces charge reversal. These results reflect the formation of inner-sphere arsenate surface complexes at the edges of hydrotalcite particles. The underlying rationale is discussed in terms of the crystal structure of hydrotalcite surfaces.
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
Fil: Regazzoni, Alberto Ernesto. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes; Argentina. Universidad Nacional de San Martín. Instituto Sabato; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Materia
Layered Double Hydroxides
Chromate
Surface Complexation
Arsenate
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:11336/26308

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spelling Complexation at the edges of hydrotalcite: the cases of arsenate and chromateJobbagy, MatiasRegazzoni, Alberto ErnestoLayered Double HydroxidesChromateSurface ComplexationArsenatehttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1Sorption of CrO2 4 and HAsO2 4 by hydrotalcite, in its chloride form, was studied as a function of anion concentration. In both cases, the shape of the isotherms is langmuirian. The maximum uptake of CrO2 4 equals the ion-exchange capacity of the solid, whereas sorption of HAsO2 4 saturates at a higher value. Chloride ions inhibit the uptake of both anions, the amount of sorbed CrO2 4 declining rapidly to zero. The uptake of HAsO2 4 , however, attains a constant value at high chloride concentrations. The excess of arsenate uptake follows, at constant pH, a langmuirian dependence with equilibrium concentration and decreases with increasing pH, depicting a marked change in slope at pH pQa3. CrO2 4 and HAsO2 4 have notable, albeit different, effects on the electrophoretic behavior of hydrotalcite; the positive particle charge is screened almost completely by CrO2 4 , whereas sorption of HAsO2 4 produces charge reversal. These results reflect the formation of inner-sphere arsenate surface complexes at the edges of hydrotalcite particles. The underlying rationale is discussed in terms of the crystal structure of hydrotalcite surfaces.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; ArgentinaFil: Regazzoni, Alberto Ernesto. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes; Argentina. Universidad Nacional de San Martín. Instituto Sabato; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaElsevier Inc2012-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/26308Jobbagy, Matias; Regazzoni, Alberto Ernesto; Complexation at the edges of hydrotalcite: the cases of arsenate and chromate; Elsevier Inc; Journal of Colloid and Interface Science; 393; 11-2012; 314-3180021-9797CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.jcis.2012.10.069info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0021979712012647info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:02:38Zoai:ri.conicet.gov.ar:11336/26308instacron: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:34982025-09-03 10:02:39.034CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Complexation at the edges of hydrotalcite: the cases of arsenate and chromate
title Complexation at the edges of hydrotalcite: the cases of arsenate and chromate
spellingShingle Complexation at the edges of hydrotalcite: the cases of arsenate and chromate
Jobbagy, Matias
Layered Double Hydroxides
Chromate
Surface Complexation
Arsenate
title_short Complexation at the edges of hydrotalcite: the cases of arsenate and chromate
title_full Complexation at the edges of hydrotalcite: the cases of arsenate and chromate
title_fullStr Complexation at the edges of hydrotalcite: the cases of arsenate and chromate
title_full_unstemmed Complexation at the edges of hydrotalcite: the cases of arsenate and chromate
title_sort Complexation at the edges of hydrotalcite: the cases of arsenate and chromate
dc.creator.none.fl_str_mv Jobbagy, Matias
Regazzoni, Alberto Ernesto
author Jobbagy, Matias
author_facet Jobbagy, Matias
Regazzoni, Alberto Ernesto
author_role author
author2 Regazzoni, Alberto Ernesto
author2_role author
dc.subject.none.fl_str_mv Layered Double Hydroxides
Chromate
Surface Complexation
Arsenate
topic Layered Double Hydroxides
Chromate
Surface Complexation
Arsenate
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Sorption of CrO2 4 and HAsO2 4 by hydrotalcite, in its chloride form, was studied as a function of anion concentration. In both cases, the shape of the isotherms is langmuirian. The maximum uptake of CrO2 4 equals the ion-exchange capacity of the solid, whereas sorption of HAsO2 4 saturates at a higher value. Chloride ions inhibit the uptake of both anions, the amount of sorbed CrO2 4 declining rapidly to zero. The uptake of HAsO2 4 , however, attains a constant value at high chloride concentrations. The excess of arsenate uptake follows, at constant pH, a langmuirian dependence with equilibrium concentration and decreases with increasing pH, depicting a marked change in slope at pH pQa3. CrO2 4 and HAsO2 4 have notable, albeit different, effects on the electrophoretic behavior of hydrotalcite; the positive particle charge is screened almost completely by CrO2 4 , whereas sorption of HAsO2 4 produces charge reversal. These results reflect the formation of inner-sphere arsenate surface complexes at the edges of hydrotalcite particles. The underlying rationale is discussed in terms of the crystal structure of hydrotalcite surfaces.
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
Fil: Regazzoni, Alberto Ernesto. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes; Argentina. Universidad Nacional de San Martín. Instituto Sabato; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
description Sorption of CrO2 4 and HAsO2 4 by hydrotalcite, in its chloride form, was studied as a function of anion concentration. In both cases, the shape of the isotherms is langmuirian. The maximum uptake of CrO2 4 equals the ion-exchange capacity of the solid, whereas sorption of HAsO2 4 saturates at a higher value. Chloride ions inhibit the uptake of both anions, the amount of sorbed CrO2 4 declining rapidly to zero. The uptake of HAsO2 4 , however, attains a constant value at high chloride concentrations. The excess of arsenate uptake follows, at constant pH, a langmuirian dependence with equilibrium concentration and decreases with increasing pH, depicting a marked change in slope at pH pQa3. CrO2 4 and HAsO2 4 have notable, albeit different, effects on the electrophoretic behavior of hydrotalcite; the positive particle charge is screened almost completely by CrO2 4 , whereas sorption of HAsO2 4 produces charge reversal. These results reflect the formation of inner-sphere arsenate surface complexes at the edges of hydrotalcite particles. The underlying rationale is discussed in terms of the crystal structure of hydrotalcite surfaces.
publishDate 2012
dc.date.none.fl_str_mv 2012-11
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/11336/26308
Jobbagy, Matias; Regazzoni, Alberto Ernesto; Complexation at the edges of hydrotalcite: the cases of arsenate and chromate; Elsevier Inc; Journal of Colloid and Interface Science; 393; 11-2012; 314-318
0021-9797
CONICET Digital
CONICET
url http://hdl.handle.net/11336/26308
identifier_str_mv Jobbagy, Matias; Regazzoni, Alberto Ernesto; Complexation at the edges of hydrotalcite: the cases of arsenate and chromate; Elsevier Inc; Journal of Colloid and Interface Science; 393; 11-2012; 314-318
0021-9797
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.jcis.2012.10.069
info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0021979712012647
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
application/pdf
application/pdf
dc.publisher.none.fl_str_mv Elsevier Inc
publisher.none.fl_str_mv Elsevier Inc
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
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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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