TY - JOUR
T1 - Iron speciation in natural waters by sequential injection analysis with a hexadentate 3-hydroxy-4-pyridinone chelator as chromogenic agent
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 and R.B.R. Mesquita thank Fundação para a Ciência e a Tecnologia (FCT) for the Grants PTDC/AAG-MAA/3978/2012_BI_2 and PTDC/AAG-MAA/3978/2012_BI_3 respectively. This work was also supported by National Funds from FCT through projects PTDC/AAG-MAA/3978/2012 , PEst-OE/EQB/LA0016/2013 and PEst-OE/EQB/LA006/2013 .
Publisher Copyright:
© 2015 Elsevier B.V.
PY - 2016/2/1
Y1 - 2016/2/1
N2 - A sequential injection method for iron speciation in various types of natural waters was developed using a synthesised hexadentate 3-hydroxy-4-pyridinone chelator (CP256). The denticity of the ligand that allow formation of the corresponding iron(III) complex in a 1:1 stoichiometry proved to be highly advantageous, in comparison with parent bidentate, hydroxy-4-piridinone chelators, with a two fold increase of reaction sensitivity and over 65% decrease of the LOD. A solid phase extraction approach was employed to attain matrix elimination, facilitating iron(III) determination and application to high salinity waters. The combination with the total iron determination obtained by the direct reaction of the ligand resulted in iron speciation. Two detection spectrophotometric cells were tested, a conventional flow cell (CFC) and a liquid waveguide capillary cell (LWCC). The dynamic concentration ranges were 0.1-2 mg/L with the CFC detection and 0.005-0.1 mg/L with the LWCC, with limit of detection of 30 μg/L and 6 μg/L, respectively. The developed method was successfully applied to a variety of natural waters.
AB - A sequential injection method for iron speciation in various types of natural waters was developed using a synthesised hexadentate 3-hydroxy-4-pyridinone chelator (CP256). The denticity of the ligand that allow formation of the corresponding iron(III) complex in a 1:1 stoichiometry proved to be highly advantageous, in comparison with parent bidentate, hydroxy-4-piridinone chelators, with a two fold increase of reaction sensitivity and over 65% decrease of the LOD. A solid phase extraction approach was employed to attain matrix elimination, facilitating iron(III) determination and application to high salinity waters. The combination with the total iron determination obtained by the direct reaction of the ligand resulted in iron speciation. Two detection spectrophotometric cells were tested, a conventional flow cell (CFC) and a liquid waveguide capillary cell (LWCC). The dynamic concentration ranges were 0.1-2 mg/L with the CFC detection and 0.005-0.1 mg/L with the LWCC, with limit of detection of 30 μg/L and 6 μg/L, respectively. The developed method was successfully applied to a variety of natural waters.
KW - Fresh and saline water samples
KW - Hexadentate 3,4-hydroxypiridinone ligand
KW - Iron speciation
KW - Solid phase extraction
UR - http://www.scopus.com/inward/record.url?scp=84949093095&partnerID=8YFLogxK
U2 - 10.1016/j.talanta.2015.05.062
DO - 10.1016/j.talanta.2015.05.062
M3 - Article
C2 - 26653494
AN - SCOPUS:84949093095
SN - 0039-9140
VL - 148
SP - 633
EP - 640
JO - Talanta
JF - Talanta
ER -