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dc.contributor.author
Arroyave Rodriguez, Jeison Manuel
dc.contributor.author
Avena, Marcelo Javier
dc.contributor.author
Tan, Wenfeng
dc.contributor.author
Wang, Mingxia
dc.date.available
2023-07-13T14:38:57Z
dc.date.issued
2022-11
dc.identifier.citation
Arroyave Rodriguez, Jeison Manuel; Avena, Marcelo Javier; Tan, Wenfeng; Wang, Mingxia; The two-species phosphate adsorption kinetics on goethite; Pergamon-Elsevier Science Ltd; Chemosphere; 307; 1; 11-2022; 1-7
dc.identifier.issn
0045-6535
dc.identifier.uri
http://hdl.handle.net/11336/203789
dc.description.abstract
Studying the adsorption-desorption kinetics of ions and molecules is crucial to understand the mobility of nutrients and pollutants in the environment. This article reports the adsorption-desorption kinetics of phosphate on goethite, as measured by ATR-FTIR spectroscopy at pH 4.5, 7.0 and 9.5. The system phosphate-goethite has become a model system to test new experimental setups and theories to understand the behavior of pollutants with phosphonic or phosphinic moieties such as glyphosate or glufosinate. One of the main difficulties in the analysis of ATR-FTIR spectra in adsorption-desorption kinetics is to calibrate the equipment to convert absorbance vs. t curves into adsorption vs. t curves, and thus the methodology to achieve a good calibration using spectroscopic data in combination with adsorption isotherms is clearly described. The time evolution of the different surface species was monitored simultaneously during adsorption and desorption at different pH, showing the advantages of this spectroscopy over traditional adsorption methods that only quantify total adsorption. Results were analysed in terms of a simple adsorption-desorption model that takes into account transport, attachment, detachment and surface transformation of the adsorbed species. The same rate parameters at a given pH could predict well the adsorption-desorption kinetics of the two formed surface species and the corresponding adsorption isotherm, giving new insights into the dynamics of phosphate on the surface of goethite. It was found that phosphate desorbed faster from goethite at low pH than at high pH, which is counterintuitive, but has good practical and environmental applications.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Pergamon-Elsevier Science Ltd
dc.rights
info:eu-repo/semantics/restrictedAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
dc.subject
ADSORPTION-DESORPTION KINETICS
dc.subject
OXIDE-WATER INTERFACE
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SURFACE COMPLEXES
dc.subject
SURFACE SPECIATION
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Otras Ciencias Químicas
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Ciencias Químicas
dc.subject.classification
CIENCIAS NATURALES Y EXACTAS
dc.title
The two-species phosphate adsorption kinetics on goethite
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2023-07-06T21:12:45Z
dc.journal.volume
307
dc.journal.number
1
dc.journal.pagination
1-7
dc.journal.pais
Países Bajos
dc.journal.ciudad
Amsterdam
dc.description.fil
Fil: Arroyave Rodriguez, Jeison Manuel. 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
dc.description.fil
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
dc.description.fil
Fil: Tan, Wenfeng. University Wuhan; China
dc.description.fil
Fil: Wang, Mingxia. University Wuhan; China
dc.journal.title
Chemosphere
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.chemosphere.2022.135782
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0045653522022755
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