Iron speciation analysis in seawater is a fundamental step to understand the cycling of this element in oceanic waters, in view of its central role in regulating primary productivity and its connection to global planetary cycles. At present, analytical procedures are the bottleneck for speciation analysis, in term of both time and sample size requirement. Here we present a novel instrumental configuration for the speciation analysis of iron by the Competitive Ligand Equilibration - Cathodic Stripping Voltammetry (CLE-CSV) procedure. The new system features a 1 mL microcell and a silver wire pseudoreference enabling a tenfold reduction of the sample volume. 2,3-dihydroxynaphthalene was used as the complexing ligand and atmospheric oxygen as the catalytic enhancer because they ensured the best analytical performances in terms of detection capabilities. The side reaction coefficient for the FeDHN complex αFe'DHN was calibrated against EDTA and an average value of 9.25 for logK’Fe'DHN was calculated. The method was successfully validated in UV digested seawater using diethylenetriaminepentaacetic acid (DTPA), which has known stability constant for iron. The method was lastly applied to six samples from the Ross Sea water column (Antarctica), demonstrating its fit for purpose for the detection of trace amounts of iron ligands in seawater. Thanks to the employed instrumental configuration and the high sensitivity, the proposed method achieved a tenfold reduction in sample size, a tenfold increase in sensitivity compared with other methods employing DHN and halved the analysis time with respect to the fastest method reported in the literature. Half an hour is enough to measure a 12 point titration, making the analysis of at least three titrations per day feasible. It is expected that the application of this procedure will foster the sample throughput, thanks to the reduced analysis time, and make possible the analysis of limitedly available and challenging samples, like porewater and vent fluids via the tenfold reduction in sample size.
Fast iron speciation in seawater by catalytic Competitive Ligand Equilibration-Cathodic Stripping Voltammetry with tenfold sample size reduction
Sanvito F.Primo
;Monticelli D.
Ultimo
2020-01-01
Abstract
Iron speciation analysis in seawater is a fundamental step to understand the cycling of this element in oceanic waters, in view of its central role in regulating primary productivity and its connection to global planetary cycles. At present, analytical procedures are the bottleneck for speciation analysis, in term of both time and sample size requirement. Here we present a novel instrumental configuration for the speciation analysis of iron by the Competitive Ligand Equilibration - Cathodic Stripping Voltammetry (CLE-CSV) procedure. The new system features a 1 mL microcell and a silver wire pseudoreference enabling a tenfold reduction of the sample volume. 2,3-dihydroxynaphthalene was used as the complexing ligand and atmospheric oxygen as the catalytic enhancer because they ensured the best analytical performances in terms of detection capabilities. The side reaction coefficient for the FeDHN complex αFe'DHN was calibrated against EDTA and an average value of 9.25 for logK’Fe'DHN was calculated. The method was successfully validated in UV digested seawater using diethylenetriaminepentaacetic acid (DTPA), which has known stability constant for iron. The method was lastly applied to six samples from the Ross Sea water column (Antarctica), demonstrating its fit for purpose for the detection of trace amounts of iron ligands in seawater. Thanks to the employed instrumental configuration and the high sensitivity, the proposed method achieved a tenfold reduction in sample size, a tenfold increase in sensitivity compared with other methods employing DHN and halved the analysis time with respect to the fastest method reported in the literature. Half an hour is enough to measure a 12 point titration, making the analysis of at least three titrations per day feasible. It is expected that the application of this procedure will foster the sample throughput, thanks to the reduced analysis time, and make possible the analysis of limitedly available and challenging samples, like porewater and vent fluids via the tenfold reduction in sample size.
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