Capabilities of several phosphonium ionic liquids for arsenic species determination in water by liquid-liquid microextraction and electrothermal atomic absorption spectrometry

Autores
Castro Grijalba, Alexander; Escudero, Leticia Belén; Wuilloud, Rodolfo German
Año de publicación
2015
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The capabilities of several phosphonium-ionic liquids (PILs) to form ion-pairs with a complex obtained by reaction of arsenate species with molybdate were evaluated. Phosphonium-ILs containing the tetradecyl(trihexyl)phosphonium cation but different anions (dicyanamide and decanoate) and tributyl(methyl)phosphonium methylsulphate IL were studied. Size, polarity and localization of charges in PILs cations showed to influence their capability to form ion-pairs with arsenomolybdate (AsMo12O403-) complex and to extract As(V). The performance of PILs was compared with that showed by a widely used ion-pairing reagent such as cethyltrimethylamonium bromide (CTAB). Finally, the IL tetradecyl(trihexyl)phosphonium dicyanamide was chosen to develop a liquid-liquid microextraction (LLME) procedure using only 80 μL of tetrachloroethylene as extractant. The organic phase was directly injected into the graphite furnace of an electrothermal atomic absorption spectrometer (ETAAS) for As determination. An extraction efficiency of 100% and a preconcentration factor of 130 were obtained with 5 mL of sample. The detection limit was 1.9 ng L-1 and the relative standard deviation for six replicate measurements of 1.0 μg L-1 for As were 4.9%, 5.0% and 5.1% for As(V), As(III) and organic As species, respectively.
Fil: Castro Grijalba, Alexander. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de Cuyo. Facultad de Ciencias Exactas y Naturales. Laboratorio de Química Analítica para Investigación y Desarrollo; Argentina
Fil: Escudero, Leticia Belén. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de Cuyo. Facultad de Ciencias Exactas y Naturales. Laboratorio de Química Analítica para Investigación y Desarrollo; Argentina
Fil: Wuilloud, Rodolfo German. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de Cuyo. Facultad de Ciencias Exactas y Naturales. Laboratorio de Química Analítica para Investigación y Desarrollo; Argentina
Materia
Ionics Liquids
Microextraction
Arsenic
Water
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:11336/5747
Acceder
id CONICETDig_9f92115e280942005af3d831bbebd1cb
oai_identifier_str oai:ri.conicet.gov.ar:11336/5747
network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Capabilities of several phosphonium ionic liquids for arsenic species determination in water by liquid-liquid microextraction and electrothermal atomic absorption spectrometryCastro Grijalba, AlexanderEscudero, Leticia BelénWuilloud, Rodolfo GermanIonics LiquidsMicroextractionArsenicWaterhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1The capabilities of several phosphonium-ionic liquids (PILs) to form ion-pairs with a complex obtained by reaction of arsenate species with molybdate were evaluated. Phosphonium-ILs containing the tetradecyl(trihexyl)phosphonium cation but different anions (dicyanamide and decanoate) and tributyl(methyl)phosphonium methylsulphate IL were studied. Size, polarity and localization of charges in PILs cations showed to influence their capability to form ion-pairs with arsenomolybdate (AsMo12O403-) complex and to extract As(V). The performance of PILs was compared with that showed by a widely used ion-pairing reagent such as cethyltrimethylamonium bromide (CTAB). Finally, the IL tetradecyl(trihexyl)phosphonium dicyanamide was chosen to develop a liquid-liquid microextraction (LLME) procedure using only 80 μL of tetrachloroethylene as extractant. The organic phase was directly injected into the graphite furnace of an electrothermal atomic absorption spectrometer (ETAAS) for As determination. An extraction efficiency of 100% and a preconcentration factor of 130 were obtained with 5 mL of sample. The detection limit was 1.9 ng L-1 and the relative standard deviation for six replicate measurements of 1.0 μg L-1 for As were 4.9%, 5.0% and 5.1% for As(V), As(III) and organic As species, respectively.Fil: Castro Grijalba, Alexander. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de Cuyo. Facultad de Ciencias Exactas y Naturales. Laboratorio de Química Analítica para Investigación y Desarrollo; ArgentinaFil: Escudero, Leticia Belén. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de Cuyo. Facultad de Ciencias Exactas y Naturales. Laboratorio de Química Analítica para Investigación y Desarrollo; ArgentinaFil: Wuilloud, Rodolfo German. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de Cuyo. Facultad de Ciencias Exactas y Naturales. Laboratorio de Química Analítica para Investigación y Desarrollo; ArgentinaRoyal Society of Chemistry2015info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/5747Castro Grijalba, Alexander; Escudero, Leticia Belén; Wuilloud, Rodolfo German; Capabilities of several phosphonium ionic liquids for arsenic species determination in water by liquid-liquid microextraction and electrothermal atomic absorption spectrometry; Royal Society of Chemistry; Analytical Methods; 7; 2; 2015; 490-4991759-9660enginfo:eu-repo/semantics/altIdentifier/doi/10.1039/c4ay02324binfo:eu-repo/semantics/altIdentifier/url/http://pubs.rsc.org/en/Content/ArticleLanding/2015/AY/C4AY02324Binfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:03:48Zoai:ri.conicet.gov.ar:11336/5747instacron: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 10:03:48.904CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Capabilities of several phosphonium ionic liquids for arsenic species determination in water by liquid-liquid microextraction and electrothermal atomic absorption spectrometry
title Capabilities of several phosphonium ionic liquids for arsenic species determination in water by liquid-liquid microextraction and electrothermal atomic absorption spectrometry
spellingShingle Capabilities of several phosphonium ionic liquids for arsenic species determination in water by liquid-liquid microextraction and electrothermal atomic absorption spectrometry
Castro Grijalba, Alexander
Ionics Liquids
Microextraction
Arsenic
Water
title_short Capabilities of several phosphonium ionic liquids for arsenic species determination in water by liquid-liquid microextraction and electrothermal atomic absorption spectrometry
title_full Capabilities of several phosphonium ionic liquids for arsenic species determination in water by liquid-liquid microextraction and electrothermal atomic absorption spectrometry
title_fullStr Capabilities of several phosphonium ionic liquids for arsenic species determination in water by liquid-liquid microextraction and electrothermal atomic absorption spectrometry
title_full_unstemmed Capabilities of several phosphonium ionic liquids for arsenic species determination in water by liquid-liquid microextraction and electrothermal atomic absorption spectrometry
title_sort Capabilities of several phosphonium ionic liquids for arsenic species determination in water by liquid-liquid microextraction and electrothermal atomic absorption spectrometry
dc.creator.none.fl_str_mv Castro Grijalba, Alexander
Escudero, Leticia Belén
Wuilloud, Rodolfo German
author Castro Grijalba, Alexander
author_facet Castro Grijalba, Alexander
Escudero, Leticia Belén
Wuilloud, Rodolfo German
author_role author
author2 Escudero, Leticia Belén
Wuilloud, Rodolfo German
author2_role author
author
dc.subject.none.fl_str_mv Ionics Liquids
Microextraction
Arsenic
Water
topic Ionics Liquids
Microextraction
Arsenic
Water
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 capabilities of several phosphonium-ionic liquids (PILs) to form ion-pairs with a complex obtained by reaction of arsenate species with molybdate were evaluated. Phosphonium-ILs containing the tetradecyl(trihexyl)phosphonium cation but different anions (dicyanamide and decanoate) and tributyl(methyl)phosphonium methylsulphate IL were studied. Size, polarity and localization of charges in PILs cations showed to influence their capability to form ion-pairs with arsenomolybdate (AsMo12O403-) complex and to extract As(V). The performance of PILs was compared with that showed by a widely used ion-pairing reagent such as cethyltrimethylamonium bromide (CTAB). Finally, the IL tetradecyl(trihexyl)phosphonium dicyanamide was chosen to develop a liquid-liquid microextraction (LLME) procedure using only 80 μL of tetrachloroethylene as extractant. The organic phase was directly injected into the graphite furnace of an electrothermal atomic absorption spectrometer (ETAAS) for As determination. An extraction efficiency of 100% and a preconcentration factor of 130 were obtained with 5 mL of sample. The detection limit was 1.9 ng L-1 and the relative standard deviation for six replicate measurements of 1.0 μg L-1 for As were 4.9%, 5.0% and 5.1% for As(V), As(III) and organic As species, respectively.
Fil: Castro Grijalba, Alexander. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de Cuyo. Facultad de Ciencias Exactas y Naturales. Laboratorio de Química Analítica para Investigación y Desarrollo; Argentina
Fil: Escudero, Leticia Belén. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de Cuyo. Facultad de Ciencias Exactas y Naturales. Laboratorio de Química Analítica para Investigación y Desarrollo; Argentina
Fil: Wuilloud, Rodolfo German. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de Cuyo. Facultad de Ciencias Exactas y Naturales. Laboratorio de Química Analítica para Investigación y Desarrollo; Argentina
description The capabilities of several phosphonium-ionic liquids (PILs) to form ion-pairs with a complex obtained by reaction of arsenate species with molybdate were evaluated. Phosphonium-ILs containing the tetradecyl(trihexyl)phosphonium cation but different anions (dicyanamide and decanoate) and tributyl(methyl)phosphonium methylsulphate IL were studied. Size, polarity and localization of charges in PILs cations showed to influence their capability to form ion-pairs with arsenomolybdate (AsMo12O403-) complex and to extract As(V). The performance of PILs was compared with that showed by a widely used ion-pairing reagent such as cethyltrimethylamonium bromide (CTAB). Finally, the IL tetradecyl(trihexyl)phosphonium dicyanamide was chosen to develop a liquid-liquid microextraction (LLME) procedure using only 80 μL of tetrachloroethylene as extractant. The organic phase was directly injected into the graphite furnace of an electrothermal atomic absorption spectrometer (ETAAS) for As determination. An extraction efficiency of 100% and a preconcentration factor of 130 were obtained with 5 mL of sample. The detection limit was 1.9 ng L-1 and the relative standard deviation for six replicate measurements of 1.0 μg L-1 for As were 4.9%, 5.0% and 5.1% for As(V), As(III) and organic As species, respectively.
publishDate 2015
dc.date.none.fl_str_mv 2015
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/11336/5747
Castro Grijalba, Alexander; Escudero, Leticia Belén; Wuilloud, Rodolfo German; Capabilities of several phosphonium ionic liquids for arsenic species determination in water by liquid-liquid microextraction and electrothermal atomic absorption spectrometry; Royal Society of Chemistry; Analytical Methods; 7; 2; 2015; 490-499
1759-9660
url http://hdl.handle.net/11336/5747
identifier_str_mv Castro Grijalba, Alexander; Escudero, Leticia Belén; Wuilloud, Rodolfo German; Capabilities of several phosphonium ionic liquids for arsenic species determination in water by liquid-liquid microextraction and electrothermal atomic absorption spectrometry; Royal Society of Chemistry; Analytical Methods; 7; 2; 2015; 490-499
1759-9660
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1039/c4ay02324b
info:eu-repo/semantics/altIdentifier/url/http://pubs.rsc.org/en/Content/ArticleLanding/2015/AY/C4AY02324B
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
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
_version_ 1842269821275734016
score 13.13397

Publicaciones similares