Optimization and validation of liquid–liquid extraction with low temperature partitioning for determination of carbamates in water

Detalhes bibliográficos
Autor(a) principal: Goulart, Simone Machado
Data de Publicação: 2010
Outros Autores: Alves, Renata Domingos, Neves, Antônio Augusto, Queiroz, José Humberto de, Assis, Tamires Condé de, Queiroz, Maria Eliana L.R. de
Tipo de documento: Artigo
Idioma: eng
Título da fonte: LOCUS Repositório Institucional da UFV
Texto Completo: https://doi.org/10.1016/j.aca.2010.05.003
http://www.locus.ufv.br/handle/123456789/19437
Resumo: Using a 23 experimental design, liquid–liquid extraction with low temperature partitioning (LLE-LTP) was optimized and validated for analysis of three carbamates (aldicarb, carbofuran and carbaryl) in water samples. In this method, 2.0 mL of sample is placed in contact with 4.0 mL of acetonitrile. After agitation, the sample is placed in a freezer for 3 h for phase separation. The organic extract is analyzed by high performance liquid chromatography with ultraviolet detection (HPLC-UV). For validation of the technique, the following figures of merit were evaluated: accuracy, precision, detection and quantification limits, linearity, sensibility and selectivity. Extraction recovery percentages of the carbamates aldicarb, carbofuran and carbaryl were 90%, 95% and 96%, respectively. Even though extremely low volumes of sample and solvent were used, the extraction method was selective and the detection and quantification limits were between 5.0 and 10.0 μg L−1, and 17.0 and 33.0 μg L−1, respectively.
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spelling Optimization and validation of liquid–liquid extraction with low temperature partitioning for determination of carbamates in waterCarbamatesWaterLow temperature partitioningAldicarbCarbofuranCarbarylUsing a 23 experimental design, liquid–liquid extraction with low temperature partitioning (LLE-LTP) was optimized and validated for analysis of three carbamates (aldicarb, carbofuran and carbaryl) in water samples. In this method, 2.0 mL of sample is placed in contact with 4.0 mL of acetonitrile. After agitation, the sample is placed in a freezer for 3 h for phase separation. The organic extract is analyzed by high performance liquid chromatography with ultraviolet detection (HPLC-UV). For validation of the technique, the following figures of merit were evaluated: accuracy, precision, detection and quantification limits, linearity, sensibility and selectivity. Extraction recovery percentages of the carbamates aldicarb, carbofuran and carbaryl were 90%, 95% and 96%, respectively. Even though extremely low volumes of sample and solvent were used, the extraction method was selective and the detection and quantification limits were between 5.0 and 10.0 μg L−1, and 17.0 and 33.0 μg L−1, respectively.Analytica Chimica Acta2018-05-10T12:09:58Z2018-05-10T12:09:58Z2010-05-10info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlepdfapplication/pdf00032670https://doi.org/10.1016/j.aca.2010.05.003http://www.locus.ufv.br/handle/123456789/19437engv. 671, Issues 1–2, p. 41-47, June 2010Elsevier B.V.info:eu-repo/semantics/openAccessGoulart, Simone MachadoAlves, Renata DomingosNeves, Antônio AugustoQueiroz, José Humberto deAssis, Tamires Condé deQueiroz, Maria Eliana L.R. dereponame:LOCUS Repositório Institucional da UFVinstname:Universidade Federal de Viçosa (UFV)instacron:UFV2024-07-12T07:51:28Zoai:locus.ufv.br:123456789/19437Repositório InstitucionalPUBhttps://www.locus.ufv.br/oai/requestfabiojreis@ufv.bropendoar:21452024-07-12T07:51:28LOCUS Repositório Institucional da UFV - Universidade Federal de Viçosa (UFV)false
dc.title.none.fl_str_mv Optimization and validation of liquid–liquid extraction with low temperature partitioning for determination of carbamates in water
title Optimization and validation of liquid–liquid extraction with low temperature partitioning for determination of carbamates in water
spellingShingle Optimization and validation of liquid–liquid extraction with low temperature partitioning for determination of carbamates in water
Goulart, Simone Machado
Carbamates
Water
Low temperature partitioning
Aldicarb
Carbofuran
Carbaryl
title_short Optimization and validation of liquid–liquid extraction with low temperature partitioning for determination of carbamates in water
title_full Optimization and validation of liquid–liquid extraction with low temperature partitioning for determination of carbamates in water
title_fullStr Optimization and validation of liquid–liquid extraction with low temperature partitioning for determination of carbamates in water
title_full_unstemmed Optimization and validation of liquid–liquid extraction with low temperature partitioning for determination of carbamates in water
title_sort Optimization and validation of liquid–liquid extraction with low temperature partitioning for determination of carbamates in water
author Goulart, Simone Machado
author_facet Goulart, Simone Machado
Alves, Renata Domingos
Neves, Antônio Augusto
Queiroz, José Humberto de
Assis, Tamires Condé de
Queiroz, Maria Eliana L.R. de
author_role author
author2 Alves, Renata Domingos
Neves, Antônio Augusto
Queiroz, José Humberto de
Assis, Tamires Condé de
Queiroz, Maria Eliana L.R. de
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Goulart, Simone Machado
Alves, Renata Domingos
Neves, Antônio Augusto
Queiroz, José Humberto de
Assis, Tamires Condé de
Queiroz, Maria Eliana L.R. de
dc.subject.por.fl_str_mv Carbamates
Water
Low temperature partitioning
Aldicarb
Carbofuran
Carbaryl
topic Carbamates
Water
Low temperature partitioning
Aldicarb
Carbofuran
Carbaryl
description Using a 23 experimental design, liquid–liquid extraction with low temperature partitioning (LLE-LTP) was optimized and validated for analysis of three carbamates (aldicarb, carbofuran and carbaryl) in water samples. In this method, 2.0 mL of sample is placed in contact with 4.0 mL of acetonitrile. After agitation, the sample is placed in a freezer for 3 h for phase separation. The organic extract is analyzed by high performance liquid chromatography with ultraviolet detection (HPLC-UV). For validation of the technique, the following figures of merit were evaluated: accuracy, precision, detection and quantification limits, linearity, sensibility and selectivity. Extraction recovery percentages of the carbamates aldicarb, carbofuran and carbaryl were 90%, 95% and 96%, respectively. Even though extremely low volumes of sample and solvent were used, the extraction method was selective and the detection and quantification limits were between 5.0 and 10.0 μg L−1, and 17.0 and 33.0 μg L−1, respectively.
publishDate 2010
dc.date.none.fl_str_mv 2010-05-10
2018-05-10T12:09:58Z
2018-05-10T12:09:58Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv 00032670
https://doi.org/10.1016/j.aca.2010.05.003
http://www.locus.ufv.br/handle/123456789/19437
identifier_str_mv 00032670
url https://doi.org/10.1016/j.aca.2010.05.003
http://www.locus.ufv.br/handle/123456789/19437
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv v. 671, Issues 1–2, p. 41-47, June 2010
dc.rights.driver.fl_str_mv Elsevier B.V.
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Elsevier B.V.
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv pdf
application/pdf
dc.publisher.none.fl_str_mv Analytica Chimica Acta
publisher.none.fl_str_mv Analytica Chimica Acta
dc.source.none.fl_str_mv reponame:LOCUS Repositório Institucional da UFV
instname:Universidade Federal de Viçosa (UFV)
instacron:UFV
instname_str Universidade Federal de Viçosa (UFV)
instacron_str UFV
institution UFV
reponame_str LOCUS Repositório Institucional da UFV
collection LOCUS Repositório Institucional da UFV
repository.name.fl_str_mv LOCUS Repositório Institucional da UFV - Universidade Federal de Viçosa (UFV)
repository.mail.fl_str_mv fabiojreis@ufv.br
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