Optimization and validation of liquid–liquid extraction with low temperature partitioning for determination of carbamates in water
Autor(a) principal: | |
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Data de Publicação: | 2010 |
Outros Autores: | , , , , |
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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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 |
_version_ |
1822610666478895104 |