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Magnetic Nanoparticles Coated with Ionic Liquid as a Sorbent for Solid Phase Extraction of Chromium(VI) Prior to Its Determination by Electrothermal Atomic Absorption Spectrometry

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Resumo:A simple, sensitive and reliable method for the separation, preconcentration and determination of ultra trace amounts of chromium species has been developed. Chromium(VI) in aqueous sample was reacted with 9-phenyl-2,3,7-trihydroxy-6-fluorone to produce a chelate at pH of 5.0 and extracted onto the magnetic nanoparticles coated with the ionic liquid 1-hexadecyl-3- methylimidazolium bromide. The trapped analyte was back extracted using 350 µL of nitric acid solution (2 mol L-1) and was determined by electrothermal atomic absorption spectrometry. Total chromium was determined by oxidizing CrIII to CrVI using KMnO4 in acidic media. Under the optimum conditions, the method exhibited a linear dynamic range of 0.01-0.50 µg L-1 with an enhancement factor of 112 and a detection limit of 0.003 µg L-1 for CrVI. The coefficient of variation (n = 6) at 0.3 µg L-1 concentration level of CrVI was 3.2%.
Autores principais:Karimi,Mehdi
Outros Autores:Shabani,Ali M. H.; Dadfarnia,Shayessteh
Assunto:chromium speciation electrothermal atomic absorption spectrometry ionic liquid solid phase extraction magnetic nanoparticle
Ano:2016
País:Brasil
Tipo de documento:artigo
Tipo de acesso:acesso aberto
Instituição associada:IBICT
Idioma:inglês
Origem:Oasisbr
Descrição
Resumo:A simple, sensitive and reliable method for the separation, preconcentration and determination of ultra trace amounts of chromium species has been developed. Chromium(VI) in aqueous sample was reacted with 9-phenyl-2,3,7-trihydroxy-6-fluorone to produce a chelate at pH of 5.0 and extracted onto the magnetic nanoparticles coated with the ionic liquid 1-hexadecyl-3- methylimidazolium bromide. The trapped analyte was back extracted using 350 µL of nitric acid solution (2 mol L-1) and was determined by electrothermal atomic absorption spectrometry. Total chromium was determined by oxidizing CrIII to CrVI using KMnO4 in acidic media. Under the optimum conditions, the method exhibited a linear dynamic range of 0.01-0.50 µg L-1 with an enhancement factor of 112 and a detection limit of 0.003 µg L-1 for CrVI. The coefficient of variation (n = 6) at 0.3 µg L-1 concentration level of CrVI was 3.2%.

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