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Registros recuperados : 8 | |
3. | | MAZZEI, J. R. F.; FREIRE, E.; SERRA, E. G.; MACEDO, J. R. de; OLIVEIRA, A. C. de; BASTOS, L. H. P.; CARDOSO, M. H. W. M. Pesquisa de campo: uma análise comparativa entre os métodos de plantio convencional, orgânico e sustentável da produção de tomates. Revista Científica Multidisciplinar Núcleo do Conhecimento, ano 6, v. 5, n. 2, 5, p. 125-146, fev. 2021. Biblioteca(s): Embrapa Solos. |
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4. | | MAZZEI, J. R. F.; FREIRE, E.; SERRA, E. G.; MACEDO, J. R. de; OLIVEIRA, A. C. de; BASTOS, L. H. P.; CARDOSO, M. H. W. M. Multiresidue method for analysis of 240 pesticides in tomato planting soils by ultra performance liquid chromatography coupled to mass spectrometry. In: SOUTH FLORIDA CONGRESS OF DEVELOPMENT, 1., 2021. Proceedings [...]. Deerfield Beach: South Florida Publishing, 2021. Evento on-line. Biblioteca(s): Embrapa Solos. |
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5. | | MAZZEI, J. R. F.; FREIRE, E.; SERRA, E. G.; MACEDO, J. R. de; OLIVEIRA, A. C. de; BASTOS, L. H. P. Método multirresíduos para análise de 240 agrotóxicos em solos do plantio de tomate por cromatografia líquida de ultra desempenho acoplada à espectrometria de massa. Revista Científica Multidisciplinar Núcleo do Conhecimento, ano 6, v. 8, n. 1, p. 34-67, jan. 2021. Biblioteca(s): Embrapa Solos. |
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6. | | MAZZEI, R. R. F.; FREIRE, E.; SERRA, E. G.; MACEDO, J. R. de; OLIVEIRA, A. C. de; BASTOS, L. H. P.; CARDOSO, M. H. W. M. Estudo comparativo das concentrações de agrotóxicos no solo provenientes dos métodos de plantio do tomate convencional, orgânico e sustentável. Brazilian Journal of Development, v. 7, n. 3, p. 22981-23000, mar. 2021. Biblioteca(s): Embrapa Solos. |
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7. | | MACEDO, J. R. de; BRANDÃO, E. S.; COSTA, J. R. P. F. da; ZAMBERLAN, F.; BASTOS, L. H. P.; NÓBREGA, A. W.; SILVA, Z.; BHERING, S. B. Sistema conservacionista de produção de tomate em São José do Ubá (RJ/ Brasil) e a consequente redução dos riscos ambientais e de saúde. In: CONGRESSO LUSO-AFRO-BRASILEIRO DE CIÊNCIAS SOCIAIS, 10., 2009, Braga. Sociedades desiguais e paradigmas em confronto: globalização, política e riscos: segurança, ambiente e saúde. Braga: Universidade do Minho, 2009. v. 5, p. 633-640. Biblioteca(s): Embrapa Solos. |
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8. | | CASTRO, I. M. de; BASTOS, L. H. P.; ANJOS, M. R. dos; OLIVEIRA, A. C. DE; COSTA, D. M. S. F. DA; CARDOSO, M. H. W. M.; CARVALHO, L. M. J. DE. Multi-residue method of pesticides by UPLC-MS/MS in bivalve mollusks samples as a tool for food quality and safety. Food Science and Technology, v. 43, e116722, 2023. Biblioteca(s): Embrapa Agroindústria de Alimentos. |
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Registros recuperados : 8 | |
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Registro Completo
Biblioteca(s): |
Embrapa Solos. |
Data corrente: |
31/08/2022 |
Data da última atualização: |
31/08/2022 |
Tipo da produção científica: |
Artigo em Anais de Congresso |
Autoria: |
MAZZEI, J. R. F.; FREIRE, E.; SERRA, E. G.; MACEDO, J. R. de; OLIVEIRA, A. C. de; BASTOS, L. H. P.; CARDOSO, M. H. W. M. |
Afiliação: |
JOÃO ROBERTO FORTES MAZZEI, UFRJ; ESTEVÃO FREIRE, UFRJ; EDUARDO GONÇALVES SERRA, UFRJ; JOSE RONALDO DE MACEDO, CNPS; ANGÉLICA CASTANHEIRA DE OLIVEIRA, FIOCRUZ; LUCIA HELENA PINTO BASTOS, FIOCRUZ; MARIA HELENA WOHLERS MORELLI CARDOSO, FIOCRUZ. |
Título: |
Multiresidue method for analysis of 240 pesticides in tomato planting soils by ultra performance liquid chromatography coupled to mass spectrometry. |
Ano de publicação: |
2021 |
Fonte/Imprenta: |
In: SOUTH FLORIDA CONGRESS OF DEVELOPMENT, 1., 2021. Proceedings [...]. Deerfield Beach: South Florida Publishing, 2021. Evento on-line. |
Idioma: |
Inglês |
Conteúdo: |
In this work, an analytical method for the determination of residues was optimized for the focus pesticides: Azoxystrobin, Boscalid, Carbendazim, Chlorantraniliprole, Clothianidin, Diafenthiuron, Difenoconazole, Dimethomorph, Spinetoram, Spinosad A, Spinosad D, Fenuron, Imidacloprid, Indoxacarb, Metalaxyl M, Methoxyfenozide, Thiamethoxan in soil derived from the tomato crop, to compare the contamination levels of these compounds in samples. The modified QuEChERS extraction method and Ultra Performance Liquid Chromatography coupled to Sequential Mass Spectrometry were used (CLUE-MS/MS), with an electronebulization ionization source in ESI (+/-) mode. The method consisted of extracting 15.0 g of soil with 15 mL of saturated calcium hydroxide solution pH 12.3 and 15 mL of acetonitrile, with consequent partitioning in a "salting out" effect using 6.0 g anhydrous magnesium sulfate and 1.5 g sodium chloride. The phases were separated by centrifugation at 3700 rpm for 7 min. Linearity between 0.2 and 20.0 ug L-1, coefficients of determination greater than 0.99. The LOQ values for the method were 13 ug kg-1 for Spinosad and 7.0 ug kg- 1 for the other pesticides. The method showed good precision, with RSD values < 20%, and accuracy, with recoveries between 70 and 120% for the vast majority of the compounds analyzed. The analytical curves were prepared with reference blank soil extracts to minimize the Matrix Effect. The method was found to be suitable for the analysis of pesticide residues in the soil since it meets the validation parameters for chromatographic methods (European Comission, 2018). After validation, the method was used for residue analysis of these pesticides in soil samples from conventional, organic, and sustainable tomato crops. Making it possible to compare the levels of environmental impacts generated. In addition to validating the analytical method for the pesticides that were the focus of the study, validation was also achieved for another 240 compounds, including those authorized and those not authorized for use on tomato crops. MenosIn this work, an analytical method for the determination of residues was optimized for the focus pesticides: Azoxystrobin, Boscalid, Carbendazim, Chlorantraniliprole, Clothianidin, Diafenthiuron, Difenoconazole, Dimethomorph, Spinetoram, Spinosad A, Spinosad D, Fenuron, Imidacloprid, Indoxacarb, Metalaxyl M, Methoxyfenozide, Thiamethoxan in soil derived from the tomato crop, to compare the contamination levels of these compounds in samples. The modified QuEChERS extraction method and Ultra Performance Liquid Chromatography coupled to Sequential Mass Spectrometry were used (CLUE-MS/MS), with an electronebulization ionization source in ESI (+/-) mode. The method consisted of extracting 15.0 g of soil with 15 mL of saturated calcium hydroxide solution pH 12.3 and 15 mL of acetonitrile, with consequent partitioning in a "salting out" effect using 6.0 g anhydrous magnesium sulfate and 1.5 g sodium chloride. The phases were separated by centrifugation at 3700 rpm for 7 min. Linearity between 0.2 and 20.0 ug L-1, coefficients of determination greater than 0.99. The LOQ values for the method were 13 ug kg-1 for Spinosad and 7.0 ug kg- 1 for the other pesticides. The method showed good precision, with RSD values < 20%, and accuracy, with recoveries between 70 and 120% for the vast majority of the compounds analyzed. The analytical curves were prepared with reference blank soil extracts to minimize the Matrix Effect. The method was found to be suitable for the analysis of pesticide re... Mostrar Tudo |
Palavras-Chave: |
Contaminants in soils; QuEChERS; UPLC-MS/MS. |
Thesaurus NAL: |
Pesticide residues. |
Categoria do assunto: |
P Recursos Naturais, Ciências Ambientais e da Terra |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/doc/1145910/1/Multiresidue-method-for-analysis-of-240-pesticides-in-tomato-planting-soils-2021.pdf
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Marc: |
LEADER 02918nam a2200229 a 4500 001 2145910 005 2022-08-31 008 2021 bl uuuu u00u1 u #d 100 1 $aMAZZEI, J. R. F. 245 $aMultiresidue method for analysis of 240 pesticides in tomato planting soils by ultra performance liquid chromatography coupled to mass spectrometry.$h[electronic resource] 260 $aIn: SOUTH FLORIDA CONGRESS OF DEVELOPMENT, 1., 2021. Proceedings [...]. Deerfield Beach: South Florida Publishing, 2021. Evento on-line.$c2021 520 $aIn this work, an analytical method for the determination of residues was optimized for the focus pesticides: Azoxystrobin, Boscalid, Carbendazim, Chlorantraniliprole, Clothianidin, Diafenthiuron, Difenoconazole, Dimethomorph, Spinetoram, Spinosad A, Spinosad D, Fenuron, Imidacloprid, Indoxacarb, Metalaxyl M, Methoxyfenozide, Thiamethoxan in soil derived from the tomato crop, to compare the contamination levels of these compounds in samples. The modified QuEChERS extraction method and Ultra Performance Liquid Chromatography coupled to Sequential Mass Spectrometry were used (CLUE-MS/MS), with an electronebulization ionization source in ESI (+/-) mode. The method consisted of extracting 15.0 g of soil with 15 mL of saturated calcium hydroxide solution pH 12.3 and 15 mL of acetonitrile, with consequent partitioning in a "salting out" effect using 6.0 g anhydrous magnesium sulfate and 1.5 g sodium chloride. The phases were separated by centrifugation at 3700 rpm for 7 min. Linearity between 0.2 and 20.0 ug L-1, coefficients of determination greater than 0.99. The LOQ values for the method were 13 ug kg-1 for Spinosad and 7.0 ug kg- 1 for the other pesticides. The method showed good precision, with RSD values < 20%, and accuracy, with recoveries between 70 and 120% for the vast majority of the compounds analyzed. The analytical curves were prepared with reference blank soil extracts to minimize the Matrix Effect. The method was found to be suitable for the analysis of pesticide residues in the soil since it meets the validation parameters for chromatographic methods (European Comission, 2018). After validation, the method was used for residue analysis of these pesticides in soil samples from conventional, organic, and sustainable tomato crops. Making it possible to compare the levels of environmental impacts generated. In addition to validating the analytical method for the pesticides that were the focus of the study, validation was also achieved for another 240 compounds, including those authorized and those not authorized for use on tomato crops. 650 $aPesticide residues 653 $aContaminants in soils 653 $aQuEChERS 653 $aUPLC-MS/MS 700 1 $aFREIRE, E. 700 1 $aSERRA, E. G. 700 1 $aMACEDO, J. R. de 700 1 $aOLIVEIRA, A. C. de 700 1 $aBASTOS, L. H. P. 700 1 $aCARDOSO, M. H. W. M.
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