Ionic liquid as ion-pairing reagent for liquid-liquid microextraction and preconcentration of arsenic species in natural waters followed by ETAAS

Autores
Monasterio, Romina Paula; Wuilloud, Rodolfo German
Año de publicación
2010
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
A simple and highly efficient microextraction methodology was developed for arsenate [As(V)], arsenite [As(III)] and organic arsenic (i.e., DMA and MMA) preconcentration and determination based on the novel use of tetradecyl(trihexyl)phosphonium chloride ionic liquid (CYPHOS® IL 101) as an ionpairing reagent. As(V) species was selectively separated by forming As(V)-molybdate heteropoly acid [As(V)-MHPA] complex with molybdenum, followed by ion-pairing reaction with CYPHOS® IL 101 and microextraction in chloroform. Arsenic detection was performed by electrothermal atomic absorption spectrometry (ETAAS). Under optimum conditions, the analyte extraction efficiency was 99% and yielded a preconcentration factor of 125 with only 5.00 mL of sample. The detection limit was 0.002 mg L-1 as As(V). The relative standard deviation (RSD) for six replicate measurements at 1.5 mg L-1 of As were 4.1%, 4.9% and 5.0% for As(V), As(III) and total organoarsenicals, respectively. The proposed methodology was successfully applied for As speciation analysis in several types of water samples.
Fil: Monasterio, Romina Paula. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Regional de Investigaciones Científicas y Tecnológicas. Laboratorio de Investigaciones y Servicios Ambientales Mendoza; Argentina
Fil: Wuilloud, Rodolfo German. Universidad Nacional de La Pampa. Facultad de Ciencias Exactas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Materia
IONIC LIQUID
ARSENATE-MOLYBDATE HETEROPOLY ACID (As(V)-MHPA)
ARSENIC SPECIATION
MICROEXTRACTION
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:11336/104944
Acceder
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network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Ionic liquid as ion-pairing reagent for liquid-liquid microextraction and preconcentration of arsenic species in natural waters followed by ETAASMonasterio, Romina PaulaWuilloud, Rodolfo GermanIONIC LIQUIDARSENATE-MOLYBDATE HETEROPOLY ACID (As(V)-MHPA)ARSENIC SPECIATIONMICROEXTRACTIONhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1A simple and highly efficient microextraction methodology was developed for arsenate [As(V)], arsenite [As(III)] and organic arsenic (i.e., DMA and MMA) preconcentration and determination based on the novel use of tetradecyl(trihexyl)phosphonium chloride ionic liquid (CYPHOS® IL 101) as an ionpairing reagent. As(V) species was selectively separated by forming As(V)-molybdate heteropoly acid [As(V)-MHPA] complex with molybdenum, followed by ion-pairing reaction with CYPHOS® IL 101 and microextraction in chloroform. Arsenic detection was performed by electrothermal atomic absorption spectrometry (ETAAS). Under optimum conditions, the analyte extraction efficiency was 99% and yielded a preconcentration factor of 125 with only 5.00 mL of sample. The detection limit was 0.002 mg L-1 as As(V). The relative standard deviation (RSD) for six replicate measurements at 1.5 mg L-1 of As were 4.1%, 4.9% and 5.0% for As(V), As(III) and total organoarsenicals, respectively. The proposed methodology was successfully applied for As speciation analysis in several types of water samples.Fil: Monasterio, Romina Paula. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Regional de Investigaciones Científicas y Tecnológicas. Laboratorio de Investigaciones y Servicios Ambientales Mendoza; ArgentinaFil: Wuilloud, Rodolfo German. Universidad Nacional de La Pampa. Facultad de Ciencias Exactas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaRoyal Society of Chemistry2010-06info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/104944Monasterio, Romina Paula; Wuilloud, Rodolfo German; Ionic liquid as ion-pairing reagent for liquid-liquid microextraction and preconcentration of arsenic species in natural waters followed by ETAAS; Royal Society of Chemistry; Journal of Analytical Atomic Spectrometry; 25; 9; 6-2010; 1485-14900267-9477CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1039/c000040jinfo:eu-repo/semantics/altIdentifier/url/https://pubs.rsc.org/en/content/articlelanding/2010/JA/c000040j#!divAbstractinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:47:14Zoai:ri.conicet.gov.ar:11336/104944instacron: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 09:47:14.372CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Ionic liquid as ion-pairing reagent for liquid-liquid microextraction and preconcentration of arsenic species in natural waters followed by ETAAS
title Ionic liquid as ion-pairing reagent for liquid-liquid microextraction and preconcentration of arsenic species in natural waters followed by ETAAS
spellingShingle Ionic liquid as ion-pairing reagent for liquid-liquid microextraction and preconcentration of arsenic species in natural waters followed by ETAAS
Monasterio, Romina Paula
IONIC LIQUID
ARSENATE-MOLYBDATE HETEROPOLY ACID (As(V)-MHPA)
ARSENIC SPECIATION
MICROEXTRACTION
title_short Ionic liquid as ion-pairing reagent for liquid-liquid microextraction and preconcentration of arsenic species in natural waters followed by ETAAS
title_full Ionic liquid as ion-pairing reagent for liquid-liquid microextraction and preconcentration of arsenic species in natural waters followed by ETAAS
title_fullStr Ionic liquid as ion-pairing reagent for liquid-liquid microextraction and preconcentration of arsenic species in natural waters followed by ETAAS
title_full_unstemmed Ionic liquid as ion-pairing reagent for liquid-liquid microextraction and preconcentration of arsenic species in natural waters followed by ETAAS
title_sort Ionic liquid as ion-pairing reagent for liquid-liquid microextraction and preconcentration of arsenic species in natural waters followed by ETAAS
dc.creator.none.fl_str_mv Monasterio, Romina Paula
Wuilloud, Rodolfo German
author Monasterio, Romina Paula
author_facet Monasterio, Romina Paula
Wuilloud, Rodolfo German
author_role author
author2 Wuilloud, Rodolfo German
author2_role author
dc.subject.none.fl_str_mv IONIC LIQUID
ARSENATE-MOLYBDATE HETEROPOLY ACID (As(V)-MHPA)
ARSENIC SPECIATION
MICROEXTRACTION
topic IONIC LIQUID
ARSENATE-MOLYBDATE HETEROPOLY ACID (As(V)-MHPA)
ARSENIC SPECIATION
MICROEXTRACTION
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv A simple and highly efficient microextraction methodology was developed for arsenate [As(V)], arsenite [As(III)] and organic arsenic (i.e., DMA and MMA) preconcentration and determination based on the novel use of tetradecyl(trihexyl)phosphonium chloride ionic liquid (CYPHOS® IL 101) as an ionpairing reagent. As(V) species was selectively separated by forming As(V)-molybdate heteropoly acid [As(V)-MHPA] complex with molybdenum, followed by ion-pairing reaction with CYPHOS® IL 101 and microextraction in chloroform. Arsenic detection was performed by electrothermal atomic absorption spectrometry (ETAAS). Under optimum conditions, the analyte extraction efficiency was 99% and yielded a preconcentration factor of 125 with only 5.00 mL of sample. The detection limit was 0.002 mg L-1 as As(V). The relative standard deviation (RSD) for six replicate measurements at 1.5 mg L-1 of As were 4.1%, 4.9% and 5.0% for As(V), As(III) and total organoarsenicals, respectively. The proposed methodology was successfully applied for As speciation analysis in several types of water samples.
Fil: Monasterio, Romina Paula. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Regional de Investigaciones Científicas y Tecnológicas. Laboratorio de Investigaciones y Servicios Ambientales Mendoza; Argentina
Fil: Wuilloud, Rodolfo German. Universidad Nacional de La Pampa. Facultad de Ciencias Exactas y Naturales. Departamento de Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
description A simple and highly efficient microextraction methodology was developed for arsenate [As(V)], arsenite [As(III)] and organic arsenic (i.e., DMA and MMA) preconcentration and determination based on the novel use of tetradecyl(trihexyl)phosphonium chloride ionic liquid (CYPHOS® IL 101) as an ionpairing reagent. As(V) species was selectively separated by forming As(V)-molybdate heteropoly acid [As(V)-MHPA] complex with molybdenum, followed by ion-pairing reaction with CYPHOS® IL 101 and microextraction in chloroform. Arsenic detection was performed by electrothermal atomic absorption spectrometry (ETAAS). Under optimum conditions, the analyte extraction efficiency was 99% and yielded a preconcentration factor of 125 with only 5.00 mL of sample. The detection limit was 0.002 mg L-1 as As(V). The relative standard deviation (RSD) for six replicate measurements at 1.5 mg L-1 of As were 4.1%, 4.9% and 5.0% for As(V), As(III) and total organoarsenicals, respectively. The proposed methodology was successfully applied for As speciation analysis in several types of water samples.
publishDate 2010
dc.date.none.fl_str_mv 2010-06
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/11336/104944
Monasterio, Romina Paula; Wuilloud, Rodolfo German; Ionic liquid as ion-pairing reagent for liquid-liquid microextraction and preconcentration of arsenic species in natural waters followed by ETAAS; Royal Society of Chemistry; Journal of Analytical Atomic Spectrometry; 25; 9; 6-2010; 1485-1490
0267-9477
CONICET Digital
CONICET
url http://hdl.handle.net/11336/104944
identifier_str_mv Monasterio, Romina Paula; Wuilloud, Rodolfo German; Ionic liquid as ion-pairing reagent for liquid-liquid microextraction and preconcentration of arsenic species in natural waters followed by ETAAS; Royal Society of Chemistry; Journal of Analytical Atomic Spectrometry; 25; 9; 6-2010; 1485-1490
0267-9477
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1039/c000040j
info:eu-repo/semantics/altIdentifier/url/https://pubs.rsc.org/en/content/articlelanding/2010/JA/c000040j#!divAbstract
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
application/pdf
dc.publisher.none.fl_str_mv Royal Society of Chemistry
publisher.none.fl_str_mv Royal Society of Chemistry
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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score 13.13397

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