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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/100263
Ver los metadatos del registro completo
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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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1842268821619998720 |
score |
13.13397 |