Desenvolvimento de métodos de preparo de amostras de erva-mate para a posterior determinação de As, Cd e Pb por GF AAS e ICP-MS

Detalhes bibliográficos
Ano de defesa: 2016
Autor(a) principal: Pardinho, Renan Buque lattes
Orientador(a): Flores, Érico Marlon de Moraes lattes
Banca de defesa: Moraes, Diogo Pompéu de lattes, Duarte, Fábio Andrei lattes
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Santa Maria
Centro de Ciências Naturais e Exatas
Programa de Pós-Graduação: Programa de Pós-Graduação em Química
Departamento: Química
País: Brasil
Palavras-chave em Português:
Área do conhecimento CNPq:
Link de acesso: http://repositorio.ufsm.br/handle/1/17689
Resumo: In this work, the following methods for yerba mate digestion/extraction for further determination of As, Cd and Pb by graphite furnace atomic absorption spectrometry (GF AAS) and/or inductively coupled plasma mass spectrometry (ICP-MS) were evaluated: i) wet digestion in open systems ii) wet digestion in closed systems iii) microwave-assisted wet digestion (MAWD) using diluted HNO3 and O2 as auxiliary reagent and iv) ultrasound-assisted extraction (UAE). For the wet digestion method using open and closed systems by conventional heating, the digestion efficiency for several sample masses and HNO3 volume were evaluated in the both systems. For methods “i” and “ii”a low digestion efficiency was observed than the open system was used allowing a high throughput and not necessary predigestion step. The GF AAS technique was used for As, Cd and Pb determination due to the low digestion efficiency of open system method and to avoid possible interferences in the determination step. For MAWD using diluted HNO3 with O2 as auxiliary reagent, several sample masses, variable amount of O2 in gaseous phase and different flow-rates during digestion process were evaluated. After the MAWD evaluation using diluted HNO3 with O2 as auxiliary reagent it was possible to use a relatively high yerba mate mass (1500 mg). For high of sample mass the digestion was not observed influences in the efficiency digestion for different amount of O2 in gaseous phase. On the other hand, it was observed an improvement in the digestion efficiency when the maximum flow-rate allowed by equipment was used. However this condition could cause problems in equipment. For the determination step by ICP-MS it was necessary an interference study due to the high carbon content in solution. For the UAE, extractant solution, sonication time, temperature and sample mass were evaluated. Regarding the recovery of As, Cd and Pb, antagonist effects were observed when sample masses higher the 1000 mg were used. The limit of quantification obtained for three methods evaluated were lower than those established in legislation. Therefore, the proposed methods were considered as feasible for yerba mate digestion/extraction for further determination of As, Cd and Pb by GF AAS and/or ICP-MS.
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spelling 2019-08-02T18:52:51Z2019-08-02T18:52:51Z2016-08-04http://repositorio.ufsm.br/handle/1/17689In this work, the following methods for yerba mate digestion/extraction for further determination of As, Cd and Pb by graphite furnace atomic absorption spectrometry (GF AAS) and/or inductively coupled plasma mass spectrometry (ICP-MS) were evaluated: i) wet digestion in open systems ii) wet digestion in closed systems iii) microwave-assisted wet digestion (MAWD) using diluted HNO3 and O2 as auxiliary reagent and iv) ultrasound-assisted extraction (UAE). For the wet digestion method using open and closed systems by conventional heating, the digestion efficiency for several sample masses and HNO3 volume were evaluated in the both systems. For methods “i” and “ii”a low digestion efficiency was observed than the open system was used allowing a high throughput and not necessary predigestion step. The GF AAS technique was used for As, Cd and Pb determination due to the low digestion efficiency of open system method and to avoid possible interferences in the determination step. For MAWD using diluted HNO3 with O2 as auxiliary reagent, several sample masses, variable amount of O2 in gaseous phase and different flow-rates during digestion process were evaluated. After the MAWD evaluation using diluted HNO3 with O2 as auxiliary reagent it was possible to use a relatively high yerba mate mass (1500 mg). For high of sample mass the digestion was not observed influences in the efficiency digestion for different amount of O2 in gaseous phase. On the other hand, it was observed an improvement in the digestion efficiency when the maximum flow-rate allowed by equipment was used. However this condition could cause problems in equipment. For the determination step by ICP-MS it was necessary an interference study due to the high carbon content in solution. For the UAE, extractant solution, sonication time, temperature and sample mass were evaluated. Regarding the recovery of As, Cd and Pb, antagonist effects were observed when sample masses higher the 1000 mg were used. The limit of quantification obtained for three methods evaluated were lower than those established in legislation. Therefore, the proposed methods were considered as feasible for yerba mate digestion/extraction for further determination of As, Cd and Pb by GF AAS and/or ICP-MS.No presente trabalho foram avaliados os seguintes métodos de decomposição/extração de erva-mate: i) decomposição por via úmida em sistema aberto ii) decomposição por via úmida em sistema fechado, iii) decomposição assistida por radiação micro-ondas (MAWD) empregando HNO3 diluído e O2 como reagente auxiliar e iv) extração assistida por ultrassom para a posterior determinação de As, Cd e Pb por espectrometria de absorção atômica com forno de grafite (GF AAS) e/ou espectrometria de massa com plasma indutivamente acoplado (ICP-MS). No primeiro e segundo método foi avaliada a eficiência de decomposição para massas de amostra até 1000 mg e volumes de HNO3 em ambos os métodos. Os digeridos obtidos após esses estudos apresentaram baixa eficiência de decomposição e valores semelhantes entre os métodos. Assim, foi utilizado o sistema aberto, pela possibilidade de obter uma elevada frequência analítica e não apresentar uma etapa de pré-digestão. Devido a essa má eficiência de decomposição e com o intuito de evitar possíveis interferências na etapa de determinação, para este método foi utilizado a técnica de GF AAS para a determinação de As, Cd e Pb. Para o método de MAWD empregando HNO3 diluído com O2 como reagente auxiliar, foi avaliada a decomposição de diferentes massas de amostras, quantidades de O2 na fase gasosa e a influência da circulação de ar em diferentes vazões externamente aos frascos durante o processo de decomposição. Após as avaliações, foi possível utilizar HNO3 diluído com O2 como reagente auxiliar para a decomposição de massas mais elevadas de erva-mate (até 1500 mg). Foi observado que a quantidade de O2 não influenciou a eficiência de decomposição de 1500 mg de amostra. Por outro lado, a utilização da vazão de ar máxima permitida pelo equipamento, melhorou a eficiência de decomposição. Entretanto, esta condição poderia causar problemas ao equipamento optando-se, assim, pela utilização de condições mais brandas de circulação de ar. Devido à massa de amostra relativamente elevada, houve a necessidade de um estudo de interferências dos elementos C, Cl e K na etapa de determinação por ICP-MS. No método de extração assistida por ultrassom foram avaliadas a solução extratora, o tempo de extração, temperatura e a massa de amostra. A melhor solução extratora foi o HNO3, utilizando 30 min de extração. Também foi possível observar um efeito antagônico da massa de amostra com a recuperação de As, Cd e Pb. Os limites de quantificação obtidos para os métodos propostos foram da ordem de ng g-1 e menores que os valores permitidos pela legislação. Portanto, os resultados obtidos nas avaliações no presente trabalho, mostraram-se que a utilização dos métodos propostos são viáveis para a decomposição/extração de erva-mate para a posterior determinação de As, Cd e Pb por GF AAS e/ou ICP-MS.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESporUniversidade Federal de Santa MariaCentro de Ciências Naturais e ExatasPrograma de Pós-Graduação em QuímicaUFSMBrasilQuímicaAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessQuímicaErva-mateArsênioChumboCádmioQuímica analíticaCNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICADesenvolvimento de métodos de preparo de amostras de erva-mate para a posterior determinação de As, Cd e Pb por GF AAS e ICP-MSinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisFlores, Érico Marlon de Moraeshttp://lattes.cnpq.br/7167629055579212Moraes, Diogo Pompéu dehttp://lattes.cnpq.br/3777062632260326Duarte, Fábio Andreihttp://lattes.cnpq.br/3503633944419329http://lattes.cnpq.br/0617212620483345Pardinho, Renan Buque100600000000600a9c2788c-7913-4d7b-92e1-3429800ac028d95fe6ca-aa5d-4323-ba0e-ff6e1407ed3ca24788db-190b-4118-b5c6-084138df6c807b2cc41c-5584-4228-a9bf-b1eb4d91e1e4reponame:Manancial - Repositório Digital da UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSMCC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; 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dc.title.por.fl_str_mv Desenvolvimento de métodos de preparo de amostras de erva-mate para a posterior determinação de As, Cd e Pb por GF AAS e ICP-MS
title Desenvolvimento de métodos de preparo de amostras de erva-mate para a posterior determinação de As, Cd e Pb por GF AAS e ICP-MS
spellingShingle Desenvolvimento de métodos de preparo de amostras de erva-mate para a posterior determinação de As, Cd e Pb por GF AAS e ICP-MS
Pardinho, Renan Buque
Química
Erva-mate
Arsênio
Chumbo
Cádmio
Química analítica
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
title_short Desenvolvimento de métodos de preparo de amostras de erva-mate para a posterior determinação de As, Cd e Pb por GF AAS e ICP-MS
title_full Desenvolvimento de métodos de preparo de amostras de erva-mate para a posterior determinação de As, Cd e Pb por GF AAS e ICP-MS
title_fullStr Desenvolvimento de métodos de preparo de amostras de erva-mate para a posterior determinação de As, Cd e Pb por GF AAS e ICP-MS
title_full_unstemmed Desenvolvimento de métodos de preparo de amostras de erva-mate para a posterior determinação de As, Cd e Pb por GF AAS e ICP-MS
title_sort Desenvolvimento de métodos de preparo de amostras de erva-mate para a posterior determinação de As, Cd e Pb por GF AAS e ICP-MS
author Pardinho, Renan Buque
author_facet Pardinho, Renan Buque
author_role author
dc.contributor.advisor1.fl_str_mv Flores, Érico Marlon de Moraes
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/7167629055579212
dc.contributor.referee1.fl_str_mv Moraes, Diogo Pompéu de
dc.contributor.referee1Lattes.fl_str_mv http://lattes.cnpq.br/3777062632260326
dc.contributor.referee2.fl_str_mv Duarte, Fábio Andrei
dc.contributor.referee2Lattes.fl_str_mv http://lattes.cnpq.br/3503633944419329
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/0617212620483345
dc.contributor.author.fl_str_mv Pardinho, Renan Buque
contributor_str_mv Flores, Érico Marlon de Moraes
Moraes, Diogo Pompéu de
Duarte, Fábio Andrei
dc.subject.por.fl_str_mv Química
Erva-mate
Arsênio
Chumbo
Cádmio
Química analítica
topic Química
Erva-mate
Arsênio
Chumbo
Cádmio
Química analítica
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
dc.subject.cnpq.fl_str_mv CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
description In this work, the following methods for yerba mate digestion/extraction for further determination of As, Cd and Pb by graphite furnace atomic absorption spectrometry (GF AAS) and/or inductively coupled plasma mass spectrometry (ICP-MS) were evaluated: i) wet digestion in open systems ii) wet digestion in closed systems iii) microwave-assisted wet digestion (MAWD) using diluted HNO3 and O2 as auxiliary reagent and iv) ultrasound-assisted extraction (UAE). For the wet digestion method using open and closed systems by conventional heating, the digestion efficiency for several sample masses and HNO3 volume were evaluated in the both systems. For methods “i” and “ii”a low digestion efficiency was observed than the open system was used allowing a high throughput and not necessary predigestion step. The GF AAS technique was used for As, Cd and Pb determination due to the low digestion efficiency of open system method and to avoid possible interferences in the determination step. For MAWD using diluted HNO3 with O2 as auxiliary reagent, several sample masses, variable amount of O2 in gaseous phase and different flow-rates during digestion process were evaluated. After the MAWD evaluation using diluted HNO3 with O2 as auxiliary reagent it was possible to use a relatively high yerba mate mass (1500 mg). For high of sample mass the digestion was not observed influences in the efficiency digestion for different amount of O2 in gaseous phase. On the other hand, it was observed an improvement in the digestion efficiency when the maximum flow-rate allowed by equipment was used. However this condition could cause problems in equipment. For the determination step by ICP-MS it was necessary an interference study due to the high carbon content in solution. For the UAE, extractant solution, sonication time, temperature and sample mass were evaluated. Regarding the recovery of As, Cd and Pb, antagonist effects were observed when sample masses higher the 1000 mg were used. The limit of quantification obtained for three methods evaluated were lower than those established in legislation. Therefore, the proposed methods were considered as feasible for yerba mate digestion/extraction for further determination of As, Cd and Pb by GF AAS and/or ICP-MS.
publishDate 2016
dc.date.issued.fl_str_mv 2016-08-04
dc.date.accessioned.fl_str_mv 2019-08-02T18:52:51Z
dc.date.available.fl_str_mv 2019-08-02T18:52:51Z
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dc.publisher.none.fl_str_mv Universidade Federal de Santa Maria
Centro de Ciências Naturais e Exatas
dc.publisher.program.fl_str_mv Programa de Pós-Graduação em Química
dc.publisher.initials.fl_str_mv UFSM
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dc.publisher.department.fl_str_mv Química
publisher.none.fl_str_mv Universidade Federal de Santa Maria
Centro de Ciências Naturais e Exatas
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