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Determination of iron(III) in water samples by microsequential injection solid phase spectrometry using an hexadentate 3-hydroxy-4-pyridinone chelator as reagent

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Resumo:In this work, the hexadentate 3,4–hydroxypyridinone ligand was used as reagent for the spectrophotometric quantification of iron(III) in fresh and sea waters, using a micro sequential injection lab-on-valve (μSI-LOV) system in a solid phase spectrometry (SPS) mode. To implement SPS, thus eliminating the sample matrix, a packed column in the flow cell was used; the chosen sorbent was Nitrilotriacetic Acid Superflow resin (NTA). The possibility of performing an analytical curve resorting to just one standard was also demonstrated. The consumption of the hexadentante ligand was about 30 μg per determination and the effluent production lower than 2.5 mL. The dynamic concentration range was 0.45–9.0 μmol L−1, with a limit of detection of 0.13 μmol L−1 and limit of quantification 0.43 μmol L−1. The proposed μSI-LOV-SPS methodology was successfully applied to river, ground, estuarine, tap, and sea waters.
Autores principais:Miranda, Joana L. A.
Outros Autores:Mesquita, Raquel B. R.; Nunes, Ana; Rangel, Maria; Rangel, António O. S. S.
Assunto:Hexadentate 3,4-hydroxypyridinone ligand Iron(III) quantification Solid phase spectrometry Fresh and saline water samples
Ano:2019
País:Portugal
Tipo de documento:artigo
Tipo de acesso:acesso restrito
Instituição associada:Universidade Católica Portuguesa
Idioma:inglês
Origem:Veritati - Repositório Institucional da Universidade Católica Portuguesa
Descrição
Resumo:In this work, the hexadentate 3,4–hydroxypyridinone ligand was used as reagent for the spectrophotometric quantification of iron(III) in fresh and sea waters, using a micro sequential injection lab-on-valve (μSI-LOV) system in a solid phase spectrometry (SPS) mode. To implement SPS, thus eliminating the sample matrix, a packed column in the flow cell was used; the chosen sorbent was Nitrilotriacetic Acid Superflow resin (NTA). The possibility of performing an analytical curve resorting to just one standard was also demonstrated. The consumption of the hexadentante ligand was about 30 μg per determination and the effluent production lower than 2.5 mL. The dynamic concentration range was 0.45–9.0 μmol L−1, with a limit of detection of 0.13 μmol L−1 and limit of quantification 0.43 μmol L−1. The proposed μSI-LOV-SPS methodology was successfully applied to river, ground, estuarine, tap, and sea waters.