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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/26308
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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) |
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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1842269767523631104 |
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13.13397 |