TY - JOUR
T1 - Determination of iron(III) in water samples by microsequential injection solid phase spectrometry using an hexadentate 3-hydroxy-4-pyridinone chelator as reagent
AU - Miranda, Joana L. A.
AU - Mesquita, Raquel B. R.
AU - Nunes, Ana
AU - Rangel, Maria
AU - Rangel, António O. S. S.
N1 - Funding Information:
J. L. A. Miranda thanks for the grant NORTE-08-5369-FSE-000007_BD_1, R. B. R. Mesquita thanks to Fundação para a Ciência e a Tecnologia (FCT) and Programa Operacional de Capital Humano (POCH) of Fundo Social Europeu (FSE) for the grant SFRH/BPD/112032/2015. This work was supported by National Funds from FCT through project PTDC/AAG-MAA/5887/2014; scientific collaboration from FCT project UID/Multi/50016/2013 is also acknowledged.
Funding Information:
J. L. A. Miranda thanks for the grant NORTE-08-5369-FSE-000007_BD_1 , R. B. R. Mesquita thanks to Fundação para a Ciência e a Tecnologia ( FCT ) and Programa Operacional de Capital Humano (POCH) of Fundo Social Europeu ( FSE ) for the grant SFRH/BPD/112032/2015 . This work was supported by National Funds from FCT through project PTDC/AAG-MAA/5887/2014 ; scientific collaboration from FCT project UID/Multi/50016/2013 is also acknowledged.
Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2019/1/1
Y1 - 2019/1/1
N2 - 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.
AB - 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.
KW - Fresh and saline water samples
KW - Hexadentate 3,4-hydroxypyridinone ligand
KW - Iron(III) quantification
KW - Solid phase spectrometry
UR - http://www.scopus.com/inward/record.url?scp=85052963374&partnerID=8YFLogxK
U2 - 10.1016/j.talanta.2018.08.063
DO - 10.1016/j.talanta.2018.08.063
M3 - Article
C2 - 30262077
AN - SCOPUS:85052963374
SN - 0039-9140
VL - 191
SP - 409
EP - 414
JO - Talanta
JF - Talanta
ER -