Effect of pH, anions and cations on the dissolution kinetics of humic acid particles

Autores
Brigante, Maximiliano Eduardo; Zanini, Graciela Pilar; Avena, Marcelo Javier
Año de publicación
2009
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The dissolution kinetics of solid humic acid (HA) particles under different conditions is reported and analyzed. The dissolution rate at pH 4 and 5 is very slow and several years may take to achieve equilibration. The rate is strongly increased by increasing pH, and at pH 11 complete dissolution is achieved in 30 min. The dissolution rate is also markedly increased by the presence of monocarboxylic acids and anionic herbicides such as glyphosate and 2,4-D. On the contrary, the rate is decreased by inorganic divalent cations (Mg2+, Ca2+, Sr2+, Ba2+). The divalent cation paraquat has a dual behavior, decreasing the dissolution rate at pH >7 but increasing it at pH <7. Simple modeling assuming a surface-controlled dissolution kinetics can reproduce reasonably well the effects of anions and cations. The different ions seem to affect the dissolution rate by modifying intermolecular forces between HA molecules located at the surface of the particles. © 2009 Elsevier B.V. All rights reserved.
Fil: Brigante, Maximiliano Eduardo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Química del Sur. Universidad Nacional del Sur. Departamento de Química. Instituto de Química del Sur; Argentina
Fil: Zanini, Graciela Pilar. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Química del Sur. Universidad Nacional del Sur. Departamento de Química. Instituto de Química del Sur; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Centro de Recursos Naturales Renovables de la Zona Semiárida. Universidad Nacional del Sur. Centro de Recursos Naturales Renovables de la Zona Semiárida; Argentina
Fil: Avena, Marcelo Javier. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Química del Sur. Universidad Nacional del Sur. Departamento de Química. Instituto de Química del Sur; Argentina
Materia
Dissolution Rate
Electrostatic Interactions
Humic Acid-Water Interface
Hydrophobic Associations
Metal Complexes
Solid Humic Acid
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/66021

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spelling Effect of pH, anions and cations on the dissolution kinetics of humic acid particlesBrigante, Maximiliano EduardoZanini, Graciela PilarAvena, Marcelo JavierDissolution RateElectrostatic InteractionsHumic Acid-Water InterfaceHydrophobic AssociationsMetal ComplexesSolid Humic Acidhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1The dissolution kinetics of solid humic acid (HA) particles under different conditions is reported and analyzed. The dissolution rate at pH 4 and 5 is very slow and several years may take to achieve equilibration. The rate is strongly increased by increasing pH, and at pH 11 complete dissolution is achieved in 30 min. The dissolution rate is also markedly increased by the presence of monocarboxylic acids and anionic herbicides such as glyphosate and 2,4-D. On the contrary, the rate is decreased by inorganic divalent cations (Mg2+, Ca2+, Sr2+, Ba2+). The divalent cation paraquat has a dual behavior, decreasing the dissolution rate at pH >7 but increasing it at pH <7. Simple modeling assuming a surface-controlled dissolution kinetics can reproduce reasonably well the effects of anions and cations. The different ions seem to affect the dissolution rate by modifying intermolecular forces between HA molecules located at the surface of the particles. © 2009 Elsevier B.V. All rights reserved.Fil: Brigante, Maximiliano Eduardo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Química del Sur. Universidad Nacional del Sur. Departamento de Química. Instituto de Química del Sur; ArgentinaFil: Zanini, Graciela Pilar. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Química del Sur. Universidad Nacional del Sur. Departamento de Química. Instituto de Química del Sur; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Centro de Recursos Naturales Renovables de la Zona Semiárida. Universidad Nacional del Sur. Centro de Recursos Naturales Renovables de la Zona Semiárida; ArgentinaFil: Avena, Marcelo Javier. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Química del Sur. Universidad Nacional del Sur. Departamento de Química. Instituto de Química del Sur; ArgentinaElsevier Science2009-09info: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/11336/66021Brigante, Maximiliano Eduardo; Zanini, Graciela Pilar; Avena, Marcelo Javier; Effect of pH, anions and cations on the dissolution kinetics of humic acid particles; Elsevier Science; Colloids and Surfaces A: Physicochemical and Engineering Aspects; 347; 1-3; 9-2009; 180-1860927-7757CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.colsurfa.2009.04.003info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0927775709002076info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:10:05Zoai:ri.conicet.gov.ar:11336/66021instacron: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 10:10:05.429CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Effect of pH, anions and cations on the dissolution kinetics of humic acid particles
title Effect of pH, anions and cations on the dissolution kinetics of humic acid particles
spellingShingle Effect of pH, anions and cations on the dissolution kinetics of humic acid particles
Brigante, Maximiliano Eduardo
Dissolution Rate
Electrostatic Interactions
Humic Acid-Water Interface
Hydrophobic Associations
Metal Complexes
Solid Humic Acid
title_short Effect of pH, anions and cations on the dissolution kinetics of humic acid particles
title_full Effect of pH, anions and cations on the dissolution kinetics of humic acid particles
title_fullStr Effect of pH, anions and cations on the dissolution kinetics of humic acid particles
title_full_unstemmed Effect of pH, anions and cations on the dissolution kinetics of humic acid particles
title_sort Effect of pH, anions and cations on the dissolution kinetics of humic acid particles
dc.creator.none.fl_str_mv Brigante, Maximiliano Eduardo
Zanini, Graciela Pilar
Avena, Marcelo Javier
author Brigante, Maximiliano Eduardo
author_facet Brigante, Maximiliano Eduardo
Zanini, Graciela Pilar
Avena, Marcelo Javier
author_role author
author2 Zanini, Graciela Pilar
Avena, Marcelo Javier
author2_role author
author
dc.subject.none.fl_str_mv Dissolution Rate
Electrostatic Interactions
Humic Acid-Water Interface
Hydrophobic Associations
Metal Complexes
Solid Humic Acid
topic Dissolution Rate
Electrostatic Interactions
Humic Acid-Water Interface
Hydrophobic Associations
Metal Complexes
Solid Humic Acid
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 dissolution kinetics of solid humic acid (HA) particles under different conditions is reported and analyzed. The dissolution rate at pH 4 and 5 is very slow and several years may take to achieve equilibration. The rate is strongly increased by increasing pH, and at pH 11 complete dissolution is achieved in 30 min. The dissolution rate is also markedly increased by the presence of monocarboxylic acids and anionic herbicides such as glyphosate and 2,4-D. On the contrary, the rate is decreased by inorganic divalent cations (Mg2+, Ca2+, Sr2+, Ba2+). The divalent cation paraquat has a dual behavior, decreasing the dissolution rate at pH >7 but increasing it at pH <7. Simple modeling assuming a surface-controlled dissolution kinetics can reproduce reasonably well the effects of anions and cations. The different ions seem to affect the dissolution rate by modifying intermolecular forces between HA molecules located at the surface of the particles. © 2009 Elsevier B.V. All rights reserved.
Fil: Brigante, Maximiliano Eduardo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Química del Sur. Universidad Nacional del Sur. Departamento de Química. Instituto de Química del Sur; Argentina
Fil: Zanini, Graciela Pilar. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Química del Sur. Universidad Nacional del Sur. Departamento de Química. Instituto de Química del Sur; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Centro de Recursos Naturales Renovables de la Zona Semiárida. Universidad Nacional del Sur. Centro de Recursos Naturales Renovables de la Zona Semiárida; Argentina
Fil: Avena, Marcelo Javier. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Química del Sur. Universidad Nacional del Sur. Departamento de Química. Instituto de Química del Sur; Argentina
description The dissolution kinetics of solid humic acid (HA) particles under different conditions is reported and analyzed. The dissolution rate at pH 4 and 5 is very slow and several years may take to achieve equilibration. The rate is strongly increased by increasing pH, and at pH 11 complete dissolution is achieved in 30 min. The dissolution rate is also markedly increased by the presence of monocarboxylic acids and anionic herbicides such as glyphosate and 2,4-D. On the contrary, the rate is decreased by inorganic divalent cations (Mg2+, Ca2+, Sr2+, Ba2+). The divalent cation paraquat has a dual behavior, decreasing the dissolution rate at pH >7 but increasing it at pH <7. Simple modeling assuming a surface-controlled dissolution kinetics can reproduce reasonably well the effects of anions and cations. The different ions seem to affect the dissolution rate by modifying intermolecular forces between HA molecules located at the surface of the particles. © 2009 Elsevier B.V. All rights reserved.
publishDate 2009
dc.date.none.fl_str_mv 2009-09
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/11336/66021
Brigante, Maximiliano Eduardo; Zanini, Graciela Pilar; Avena, Marcelo Javier; Effect of pH, anions and cations on the dissolution kinetics of humic acid particles; Elsevier Science; Colloids and Surfaces A: Physicochemical and Engineering Aspects; 347; 1-3; 9-2009; 180-186
0927-7757
CONICET Digital
CONICET
url http://hdl.handle.net/11336/66021
identifier_str_mv Brigante, Maximiliano Eduardo; Zanini, Graciela Pilar; Avena, Marcelo Javier; Effect of pH, anions and cations on the dissolution kinetics of humic acid particles; Elsevier Science; Colloids and Surfaces A: Physicochemical and Engineering Aspects; 347; 1-3; 9-2009; 180-186
0927-7757
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.colsurfa.2009.04.003
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0927775709002076
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/
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application/pdf
application/pdf
application/pdf
dc.publisher.none.fl_str_mv Elsevier Science
publisher.none.fl_str_mv Elsevier Science
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