Investigação da adequabilidade da cromatografia de íons para a determinação de espécies de halogênios em saliva

Detalhes bibliográficos
Ano de defesa: 2019
Autor(a) principal: Mendes, Ana Luiza Garcia lattes
Orientador(a): Mello, Paola de Azevedo lattes
Banca de defesa: Mesko, Márcia Foster lattes, Bolzan, Rodrigo Cordeiro 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:
Palavras-chave em Inglês:
Área do conhecimento CNPq:
Link de acesso: http://repositorio.ufsm.br/handle/1/20632
Resumo: In this work, ion chromatography was investigated for halogens speciation analysis in human saliva. Initially, it was used an isocratic ion chromatography system (“IC 1 System”), being evaluated: the chromatographic column (Metrosep A Supp 7 or Metrosep A Supp 5), the composition of the mobile phase (Na2CO3 or Na2CO3 + NaHCO3), the mobile phase flow rate (between 0.4 to 0.8 mL min-1, depending on the column), the temperature of the column compartment (30 to 45 °C), and the use of mobile phase modifiers (acetone). A system that allows operating in gradient mode (“IC 2 System”) was also evaluated, being optimized: the temperature of the column compartment (20 to 45 °C), the eluent flow rate (0.15 to 0.40 mL min-1) and different gradient programs (1 to 60 mmol L-1 KOH). Microwave-assisted alkaline dissolution was used to obtain the total halogen concentration by inductively coupled plasma mass spectrometry (ICP-MS). The best condition found for the “IC 1 System” was obtained with the Metrosep A Supp 7 column at 45 °C using Na2CO3 (3.6 mmol L-1) as the mobile phase, at 0.8 mL min-1. However, this condition did not provide the separation of fluoride and iodate and also, bromide, chlorate and perchlorate. The “IC 2 System” enabled the separation of bromide from chlorate and perchlorate according to the gradient elution program. The optimized conditions for the “IC 2 System” were 1 to 60 mmol L-1 KOH gradient, 0.3 mL min-1 mobile phase flow rate and column compartment temperature at 35 °C. In addition to chromatographic evaluations, the stability of halogens in saliva was also studied, as well as the use of different filtration membranes for sample pretreatment. The stability study demonstrated the viability of storage for up to 90 days under refrigeration (4 °C), without leading to losses in total Cl, Br and I concentration. Regarding the use of a filtration step as pretreatment, different membrane types were investigated and no influence was observed for Cl and Br. However, Cl contamination was observed in some filters and underestimated results were observed for iodine. Additionally, the IC systems presented wide linear range (5-10000 μg L-1), as well as low limits of detection and quantification for the investigated species. With the developed method, it was possible to identify chloride and bromide, as well as sulfate and phosphate in human saliva.
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spelling 2021-04-20T09:40:56Z2021-04-20T09:40:56Z2019-08-15http://repositorio.ufsm.br/handle/1/20632In this work, ion chromatography was investigated for halogens speciation analysis in human saliva. Initially, it was used an isocratic ion chromatography system (“IC 1 System”), being evaluated: the chromatographic column (Metrosep A Supp 7 or Metrosep A Supp 5), the composition of the mobile phase (Na2CO3 or Na2CO3 + NaHCO3), the mobile phase flow rate (between 0.4 to 0.8 mL min-1, depending on the column), the temperature of the column compartment (30 to 45 °C), and the use of mobile phase modifiers (acetone). A system that allows operating in gradient mode (“IC 2 System”) was also evaluated, being optimized: the temperature of the column compartment (20 to 45 °C), the eluent flow rate (0.15 to 0.40 mL min-1) and different gradient programs (1 to 60 mmol L-1 KOH). Microwave-assisted alkaline dissolution was used to obtain the total halogen concentration by inductively coupled plasma mass spectrometry (ICP-MS). The best condition found for the “IC 1 System” was obtained with the Metrosep A Supp 7 column at 45 °C using Na2CO3 (3.6 mmol L-1) as the mobile phase, at 0.8 mL min-1. However, this condition did not provide the separation of fluoride and iodate and also, bromide, chlorate and perchlorate. The “IC 2 System” enabled the separation of bromide from chlorate and perchlorate according to the gradient elution program. The optimized conditions for the “IC 2 System” were 1 to 60 mmol L-1 KOH gradient, 0.3 mL min-1 mobile phase flow rate and column compartment temperature at 35 °C. In addition to chromatographic evaluations, the stability of halogens in saliva was also studied, as well as the use of different filtration membranes for sample pretreatment. The stability study demonstrated the viability of storage for up to 90 days under refrigeration (4 °C), without leading to losses in total Cl, Br and I concentration. Regarding the use of a filtration step as pretreatment, different membrane types were investigated and no influence was observed for Cl and Br. However, Cl contamination was observed in some filters and underestimated results were observed for iodine. Additionally, the IC systems presented wide linear range (5-10000 μg L-1), as well as low limits of detection and quantification for the investigated species. With the developed method, it was possible to identify chloride and bromide, as well as sulfate and phosphate in human saliva.Neste trabalho, a cromatografia de troca iônica foi investigada para análise de especiação de halogênios em saliva humana. Inicialmente, foi utilizado um sistema de cromatografia de íons que opera no modo isocrático (“Sistema IC 1”), sendo avaliados: a coluna cromatográfica (Metrosep A Supp 7 ou Metrosep A Supp 5), a composição da fase móvel (Na2CO3 e Na2CO3 + NaHCO3), a vazão da fase móvel (entre 0,4 a 0,8 mL min-1, dependendo da coluna), a temperatura do compartimento da coluna (30 a 45 °C), e, ainda, o uso de modificador na fase móvel (acetona). Na sequência foi avaliado um sistema que permite operar no modo gradiente (“Sistema IC 2”), sendo otimizados: a temperatura do compartimento da coluna (20 a 45 °C), a vazão do eluente (0,15 a 0,40 mL min-1) e diferentes programas de eluição por gradiente (1 a 60 mmol L-1 de KOH). A dissolução alcalina assistida por micro-ondas foi utilizada para obter a concentração de halogênios total por espectrometria de massa com plasma indutivamente acoplado (ICP-MS). A melhor condição obtida com o “Sistema IC 1” foi obtida com a coluna Metrosep A Supp 7, a 45 °C, utilizando Na2CO3 (3,6 mmol L-1) como fase móvel, a 0,8 mL min-1. Contudo, esta condição não proporcionou a separação entre fluoreto e iodato e, entre brometo, clorato e perclorato. O “Sistema IC 2”, possibilitou a separação de brometo do par cloratoperclorato devido ao programa de eluição por gradiente. Com o “Sistema IC 2”, a melhor condição de separação foi obtida com eluição por gradiente de 1 a 60 mmol L-1 de KOH, vazão de fase móvel de 0,3 mL min-1 e temperatura do compartimento da coluna em 35 °C. Além das avaliações cromatográficas, foi avaliada também a estabilidade dos halogênios na saliva, bem como o uso de diferentes membranas de filtração para o pré-tratamento da amostra. O estudo de estabilidade demonstrou a viabilidade de armazenamento por até 90 dias, quando a amostra é armazenada sob refrigeração (4 °C), sem representar perdas na concentração de Cl, Br e I total. Quanto ao uso de uma etapa de filtração como pré-tratamento, foram investigados diferentes tipos de membrana e não foi observada influência para Cl e Br. Contudo, foi observada contaminação para Cl em alguns filtros e resultados subestimados foram observados para iodo. Adicionalmente, os sistemas de IC apresentaram ampla faixa linear (5-10000 μg L-1), bem como baixos limites de detecção e de quantificação para as espécies investigadas. Com o método desenvolvido, foi possível identificar cloreto e brometo, além de sulfato e fosfato em saliva humana.Conselho Nacional de Pesquisa e Desenvolvimento Científico e Tecnológico - CNPqporUniversidade 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/openAccessAnálise de especiaçãoHalogêniosCromatografia de íonsSalivaEstabilidadeSpeciation analysisHalogensIon chromatographySalivaStabilityCNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICAInvestigação da adequabilidade da cromatografia de íons para a determinação de espécies de halogênios em salivaInvestigation of the adequability of ion chromatography for halogens speciation analysis in salivainfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisMello, Paola de Azevedohttp://lattes.cnpq.br/2189500441942469Mesko, Márcia FosterXXXXXXXXXXXXXXXBolzan, Rodrigo CordeiroXXXXXXXXXXXXXXhttp://lattes.cnpq.br/6670439791922140Mendes, Ana Luiza Garcia1006000000006000128b934-4b3f-43d6-8526-fb278da0f6739450a632-f169-495d-981c-fd73058d28554691aa1d-cefe-4480-a95e-4e5300bd23800b6036d2-a4c4-4565-bfc3-5fef0aae6060reponame:Biblioteca Digital de Teses e Dissertações do UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSMORIGINALDIS_PPGQUIMICA_2019_MENDES_ANA.pdfDIS_PPGQUIMICA_2019_MENDES_ANA.pdfDissertação de Mestradoapplication/pdf1336636http://repositorio.ufsm.br/bitstream/1/20632/1/DIS_PPGQUIMICA_2019_MENDES_ANA.pdffaa9af9d9e8b7d49949851bcff5319f5MD51CC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; 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dc.title.por.fl_str_mv Investigação da adequabilidade da cromatografia de íons para a determinação de espécies de halogênios em saliva
dc.title.alternative.eng.fl_str_mv Investigation of the adequability of ion chromatography for halogens speciation analysis in saliva
title Investigação da adequabilidade da cromatografia de íons para a determinação de espécies de halogênios em saliva
spellingShingle Investigação da adequabilidade da cromatografia de íons para a determinação de espécies de halogênios em saliva
Mendes, Ana Luiza Garcia
Análise de especiação
Halogênios
Cromatografia de íons
Saliva
Estabilidade
Speciation analysis
Halogens
Ion chromatography
Saliva
Stability
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
title_short Investigação da adequabilidade da cromatografia de íons para a determinação de espécies de halogênios em saliva
title_full Investigação da adequabilidade da cromatografia de íons para a determinação de espécies de halogênios em saliva
title_fullStr Investigação da adequabilidade da cromatografia de íons para a determinação de espécies de halogênios em saliva
title_full_unstemmed Investigação da adequabilidade da cromatografia de íons para a determinação de espécies de halogênios em saliva
title_sort Investigação da adequabilidade da cromatografia de íons para a determinação de espécies de halogênios em saliva
author Mendes, Ana Luiza Garcia
author_facet Mendes, Ana Luiza Garcia
author_role author
dc.contributor.advisor1.fl_str_mv Mello, Paola de Azevedo
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/2189500441942469
dc.contributor.referee1.fl_str_mv Mesko, Márcia Foster
dc.contributor.referee1Lattes.fl_str_mv XXXXXXXXXXXXXXX
dc.contributor.referee2.fl_str_mv Bolzan, Rodrigo Cordeiro
dc.contributor.referee2Lattes.fl_str_mv XXXXXXXXXXXXXX
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/6670439791922140
dc.contributor.author.fl_str_mv Mendes, Ana Luiza Garcia
contributor_str_mv Mello, Paola de Azevedo
Mesko, Márcia Foster
Bolzan, Rodrigo Cordeiro
dc.subject.por.fl_str_mv Análise de especiação
Halogênios
Cromatografia de íons
Saliva
Estabilidade
topic Análise de especiação
Halogênios
Cromatografia de íons
Saliva
Estabilidade
Speciation analysis
Halogens
Ion chromatography
Saliva
Stability
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
dc.subject.eng.fl_str_mv Speciation analysis
Halogens
Ion chromatography
Saliva
Stability
dc.subject.cnpq.fl_str_mv CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
description In this work, ion chromatography was investigated for halogens speciation analysis in human saliva. Initially, it was used an isocratic ion chromatography system (“IC 1 System”), being evaluated: the chromatographic column (Metrosep A Supp 7 or Metrosep A Supp 5), the composition of the mobile phase (Na2CO3 or Na2CO3 + NaHCO3), the mobile phase flow rate (between 0.4 to 0.8 mL min-1, depending on the column), the temperature of the column compartment (30 to 45 °C), and the use of mobile phase modifiers (acetone). A system that allows operating in gradient mode (“IC 2 System”) was also evaluated, being optimized: the temperature of the column compartment (20 to 45 °C), the eluent flow rate (0.15 to 0.40 mL min-1) and different gradient programs (1 to 60 mmol L-1 KOH). Microwave-assisted alkaline dissolution was used to obtain the total halogen concentration by inductively coupled plasma mass spectrometry (ICP-MS). The best condition found for the “IC 1 System” was obtained with the Metrosep A Supp 7 column at 45 °C using Na2CO3 (3.6 mmol L-1) as the mobile phase, at 0.8 mL min-1. However, this condition did not provide the separation of fluoride and iodate and also, bromide, chlorate and perchlorate. The “IC 2 System” enabled the separation of bromide from chlorate and perchlorate according to the gradient elution program. The optimized conditions for the “IC 2 System” were 1 to 60 mmol L-1 KOH gradient, 0.3 mL min-1 mobile phase flow rate and column compartment temperature at 35 °C. In addition to chromatographic evaluations, the stability of halogens in saliva was also studied, as well as the use of different filtration membranes for sample pretreatment. The stability study demonstrated the viability of storage for up to 90 days under refrigeration (4 °C), without leading to losses in total Cl, Br and I concentration. Regarding the use of a filtration step as pretreatment, different membrane types were investigated and no influence was observed for Cl and Br. However, Cl contamination was observed in some filters and underestimated results were observed for iodine. Additionally, the IC systems presented wide linear range (5-10000 μg L-1), as well as low limits of detection and quantification for the investigated species. With the developed method, it was possible to identify chloride and bromide, as well as sulfate and phosphate in human saliva.
publishDate 2019
dc.date.issued.fl_str_mv 2019-08-15
dc.date.accessioned.fl_str_mv 2021-04-20T09:40:56Z
dc.date.available.fl_str_mv 2021-04-20T09:40:56Z
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http://creativecommons.org/licenses/by-nc-nd/4.0/
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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
dc.publisher.country.fl_str_mv Brasil
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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