Trace Molybdenum determination in drinking waters by USN-ICP-OES after solid phase extraction on Ethyl Vinyl Acetate turnings-packed minicolumn

Autores
Escudero, Luis Ariel; Gil, Raul Andres; Gásquez, José A.; Olsina, Roberto Antonio; Martinez, Luis Dante
Año de publicación
2008
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
This study presents the development of a novel on-line preconcentration method for inorganic molybdenum by flow injection solid-phase extraction with detection by inductively coupled plasma optical emission spectrometry and ultrasonic nebulization (SPE-USN-ICP-OES). This method employs a minicolumn filled with ethyl vinyl acetate turnings as the adsorbent material. This system was applied to the on-line preconcentration and determination of molybdenum in water samples with good selectivity and reproducibility; molybdenum was retained on the minicolumn without further complexation. The time required for the preconcentration of a 20-mL sample, injection/data acquisition, and conditioning was about 5.0 minutes, resulting in a sample throughput of 12 samples per hour. A 300-fold total enhancement factor for this sample volume was obtained with respect to the molybdenum determination by ICP-OES without preconcentration. The precision for six replicate measurements of a solution containing 20 µg L-1 Mo was 3.5% relative standard deviation, calculated at peak height. The limit of detection (3σ) was 0.04 µg L-1. This method was successfully applied to trace molybdenum determination in drinking water samples and in a certified reference material (Metals in Natural Waters, NIST CRM 1643e).
Fil: Escudero, Luis Ariel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; Argentina
Fil: Gil, Raul Andres. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; Argentina
Fil: Gásquez, José A.. Universidad Nacional de San Luis; Argentina
Fil: Olsina, Roberto Antonio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; Argentina
Fil: Martinez, Luis Dante. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; Argentina
Materia
MOLYBDENUM DETERMINATION
DRINKING WATERS
ETHYL VINYL ACETATE
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:11336/100263

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repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Trace Molybdenum determination in drinking waters by USN-ICP-OES after solid phase extraction on Ethyl Vinyl Acetate turnings-packed minicolumnEscudero, Luis ArielGil, Raul AndresGásquez, José A.Olsina, Roberto AntonioMartinez, Luis DanteMOLYBDENUM DETERMINATIONDRINKING WATERSETHYL VINYL ACETATEhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1This study presents the development of a novel on-line preconcentration method for inorganic molybdenum by flow injection solid-phase extraction with detection by inductively coupled plasma optical emission spectrometry and ultrasonic nebulization (SPE-USN-ICP-OES). This method employs a minicolumn filled with ethyl vinyl acetate turnings as the adsorbent material. This system was applied to the on-line preconcentration and determination of molybdenum in water samples with good selectivity and reproducibility; molybdenum was retained on the minicolumn without further complexation. The time required for the preconcentration of a 20-mL sample, injection/data acquisition, and conditioning was about 5.0 minutes, resulting in a sample throughput of 12 samples per hour. A 300-fold total enhancement factor for this sample volume was obtained with respect to the molybdenum determination by ICP-OES without preconcentration. The precision for six replicate measurements of a solution containing 20 µg L-1 Mo was 3.5% relative standard deviation, calculated at peak height. The limit of detection (3σ) was 0.04 µg L-1. This method was successfully applied to trace molybdenum determination in drinking water samples and in a certified reference material (Metals in Natural Waters, NIST CRM 1643e).Fil: Escudero, Luis Ariel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; ArgentinaFil: Gil, Raul Andres. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; ArgentinaFil: Gásquez, José A.. Universidad Nacional de San Luis; ArgentinaFil: Olsina, Roberto Antonio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; ArgentinaFil: Martinez, Luis Dante. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; ArgentinaPerkin-elmer Corp2008-01info: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/11336/100263Escudero, Luis Ariel; Gil, Raul Andres; Gásquez, José A.; Olsina, Roberto Antonio; Martinez, Luis Dante; Trace Molybdenum determination in drinking waters by USN-ICP-OES after solid phase extraction on Ethyl Vinyl Acetate turnings-packed minicolumn; Perkin-elmer Corp; Atomic Spectroscopy; 29; 1; 1-2008; 21-260195-5373CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.semanticscholar.org/paper/Trace-Molybdenum-Determination-in-Drinking-Waters-Escudero-Gil/4cbe47c9c7718dd7139fd6e5c8963ee07be82f4einfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:46:51Zoai:ri.conicet.gov.ar:11336/100263instacron: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 09:46:52.063CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Trace Molybdenum determination in drinking waters by USN-ICP-OES after solid phase extraction on Ethyl Vinyl Acetate turnings-packed minicolumn
title Trace Molybdenum determination in drinking waters by USN-ICP-OES after solid phase extraction on Ethyl Vinyl Acetate turnings-packed minicolumn
spellingShingle Trace Molybdenum determination in drinking waters by USN-ICP-OES after solid phase extraction on Ethyl Vinyl Acetate turnings-packed minicolumn
Escudero, Luis Ariel
MOLYBDENUM DETERMINATION
DRINKING WATERS
ETHYL VINYL ACETATE
title_short Trace Molybdenum determination in drinking waters by USN-ICP-OES after solid phase extraction on Ethyl Vinyl Acetate turnings-packed minicolumn
title_full Trace Molybdenum determination in drinking waters by USN-ICP-OES after solid phase extraction on Ethyl Vinyl Acetate turnings-packed minicolumn
title_fullStr Trace Molybdenum determination in drinking waters by USN-ICP-OES after solid phase extraction on Ethyl Vinyl Acetate turnings-packed minicolumn
title_full_unstemmed Trace Molybdenum determination in drinking waters by USN-ICP-OES after solid phase extraction on Ethyl Vinyl Acetate turnings-packed minicolumn
title_sort Trace Molybdenum determination in drinking waters by USN-ICP-OES after solid phase extraction on Ethyl Vinyl Acetate turnings-packed minicolumn
dc.creator.none.fl_str_mv Escudero, Luis Ariel
Gil, Raul Andres
Gásquez, José A.
Olsina, Roberto Antonio
Martinez, Luis Dante
author Escudero, Luis Ariel
author_facet Escudero, Luis Ariel
Gil, Raul Andres
Gásquez, José A.
Olsina, Roberto Antonio
Martinez, Luis Dante
author_role author
author2 Gil, Raul Andres
Gásquez, José A.
Olsina, Roberto Antonio
Martinez, Luis Dante
author2_role author
author
author
author
dc.subject.none.fl_str_mv MOLYBDENUM DETERMINATION
DRINKING WATERS
ETHYL VINYL ACETATE
topic MOLYBDENUM DETERMINATION
DRINKING WATERS
ETHYL VINYL ACETATE
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv This study presents the development of a novel on-line preconcentration method for inorganic molybdenum by flow injection solid-phase extraction with detection by inductively coupled plasma optical emission spectrometry and ultrasonic nebulization (SPE-USN-ICP-OES). This method employs a minicolumn filled with ethyl vinyl acetate turnings as the adsorbent material. This system was applied to the on-line preconcentration and determination of molybdenum in water samples with good selectivity and reproducibility; molybdenum was retained on the minicolumn without further complexation. The time required for the preconcentration of a 20-mL sample, injection/data acquisition, and conditioning was about 5.0 minutes, resulting in a sample throughput of 12 samples per hour. A 300-fold total enhancement factor for this sample volume was obtained with respect to the molybdenum determination by ICP-OES without preconcentration. The precision for six replicate measurements of a solution containing 20 µg L-1 Mo was 3.5% relative standard deviation, calculated at peak height. The limit of detection (3σ) was 0.04 µg L-1. This method was successfully applied to trace molybdenum determination in drinking water samples and in a certified reference material (Metals in Natural Waters, NIST CRM 1643e).
Fil: Escudero, Luis Ariel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; Argentina
Fil: Gil, Raul Andres. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; Argentina
Fil: Gásquez, José A.. Universidad Nacional de San Luis; Argentina
Fil: Olsina, Roberto Antonio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; Argentina
Fil: Martinez, Luis Dante. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; Argentina
description This study presents the development of a novel on-line preconcentration method for inorganic molybdenum by flow injection solid-phase extraction with detection by inductively coupled plasma optical emission spectrometry and ultrasonic nebulization (SPE-USN-ICP-OES). This method employs a minicolumn filled with ethyl vinyl acetate turnings as the adsorbent material. This system was applied to the on-line preconcentration and determination of molybdenum in water samples with good selectivity and reproducibility; molybdenum was retained on the minicolumn without further complexation. The time required for the preconcentration of a 20-mL sample, injection/data acquisition, and conditioning was about 5.0 minutes, resulting in a sample throughput of 12 samples per hour. A 300-fold total enhancement factor for this sample volume was obtained with respect to the molybdenum determination by ICP-OES without preconcentration. The precision for six replicate measurements of a solution containing 20 µg L-1 Mo was 3.5% relative standard deviation, calculated at peak height. The limit of detection (3σ) was 0.04 µg L-1. This method was successfully applied to trace molybdenum determination in drinking water samples and in a certified reference material (Metals in Natural Waters, NIST CRM 1643e).
publishDate 2008
dc.date.none.fl_str_mv 2008-01
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/11336/100263
Escudero, Luis Ariel; Gil, Raul Andres; Gásquez, José A.; Olsina, Roberto Antonio; Martinez, Luis Dante; Trace Molybdenum determination in drinking waters by USN-ICP-OES after solid phase extraction on Ethyl Vinyl Acetate turnings-packed minicolumn; Perkin-elmer Corp; Atomic Spectroscopy; 29; 1; 1-2008; 21-26
0195-5373
CONICET Digital
CONICET
url http://hdl.handle.net/11336/100263
identifier_str_mv Escudero, Luis Ariel; Gil, Raul Andres; Gásquez, José A.; Olsina, Roberto Antonio; Martinez, Luis Dante; Trace Molybdenum determination in drinking waters by USN-ICP-OES after solid phase extraction on Ethyl Vinyl Acetate turnings-packed minicolumn; Perkin-elmer Corp; Atomic Spectroscopy; 29; 1; 1-2008; 21-26
0195-5373
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://www.semanticscholar.org/paper/Trace-Molybdenum-Determination-in-Drinking-Waters-Escudero-Gil/4cbe47c9c7718dd7139fd6e5c8963ee07be82f4e
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
application/pdf
dc.publisher.none.fl_str_mv Perkin-elmer Corp
publisher.none.fl_str_mv Perkin-elmer Corp
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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