Corinne Parat

Determination of trace metal speciation parameters by using screen-printed electrodes in stripping chronopotentiometry without deaerating

The objective of this study was to exploit the advantages of stripping chronopotentiometry (SCP) and stripping chronopotentiometry at scanned deposition potential (SSCP) for trace metal speciation analyses by using thin-film mercury screen-printed electrodes (TMF-SPE). At first, the SCP parameters were optimised for TMF-SPE, in order to reach the complete depletion regime. It has been shown that a stripping current higher than or equal to 10 μA allows this regime to be attained without removing oxygen from the solution. Then, these analytical conditions were used for the construction of SSCP curves for Cd-PDCA and Cd-NTA. When the concentration of free ligand in solution was known, the knowledge of the model describing the SSCP curves in absence and presence of a complex and the use of an effective fitting tool enabled estimating the stability constant and the rate constants for complexation. Further studies with complexes of restricted mobility are however necessary to assess the usefulness of this procedure to also estimate the diffusion coefficient of the complexes. Besides, this study showed that this approach was valid even when ligands were not in excess at the electrode during stripping.

Cadmium speciation assessed by voltammetry, ion exchange and geochemical calculation in soil solutions collected after soil rewetting

Analytical techniques and speciation models have been developed to characterize the speciation of Cd in soil solution. They provide an estimate of operationally defined species of Cd that need to be compared, especially for soil solutions highly concentrated in organic matter as are the solutions collected after soil rewetting. This work deals with the comparison between the speciation of Cd measured by anodic stripping voltammetry (ASV) and ion exchange and the speciation of Cd calculated using Visual MINTEQ. The aim of this study was to quantify and explain the differences in Cd speciation observed between the three approaches. Cd speciation was assessed in soil solutions collected 4, 8, 24, 48, 96 and 144h after the rewetting of an air-dried contaminated soil. To optimize the computed speciation of Cd, other physico-chemical parameters were followed (e.g. pH, ionic strength and the concentrations of major anions, major cations and dissolved organic carbon) and a brief characterisation of dissolved organic matter (DOM) was performed. The discrepancy between model predictions and analytical measurements highlighted the need for caution in the interpretation of geochemical speciated data for Cd. The major result of this study was that a characterization of DOM based on its specific UV-absorbance at 254 nm improved the accuracy of model predictions. Another finding is that labile Cd complexes, even organic, may have been included in the electrochemically labile fraction of Cd measured by ASV.

Comparison of two experimental speciation methods with a theoretical approach to monitor free and labile Cd fractions in soil solutions.

This work focused on the suitability of two techniques to monitor cadmium speciation in soil solutions collected during a 7-day incubation of a contaminated soil. Anodic stripping voltammetry (ASV) and ion exchange were performed on soil solutions collected daily and results were compared with calculations obtained with the speciation software Visual MINTEQ. The electrochemically labile Cd fraction was greater than the exchange-estimated free Cd fraction during the first 6 days, after which it decreased sharply during the last 2 days to reach values close to the exchange-estimated free Cd fraction. Further investigations showed that the increase in pH was mainly responsible for the reduction. However, calculations performed with Visual MINTEQ software clearly demonstrated that a change in the nature of organic matter and/or its complexing capacity also needed to be taken into consideration.

Free Zn2+ determination in natural freshwater of the Pyrenees: towards on-site measurements with AGNES

An on-site methodology has been developed for the direct determination of free Zn2+ with AGNES (Absence of Gradients and Nernstian Equilibrium Stripping) in freshwaters. This implementation includes: (i) the use of screen-printed electrodes, which provide good limits of detection and easy transportation and deployment; (ii) no need for sample purging; (iii) a calibration in a synthetic river solution that reproduces the speciation changes of the natural samples well and allows oxygen interference to be minimised; (iv) the addition of a background electrolyte up to 0.01 mol L–1 in both the calibration and freshwater samples; (v) chemical stripping chronopotentiometry as the quantification stage of AGNES. This procedure minimises the effects of working at low ionic strength and in the presence of dissolved oxygen. In the laboratory, the methodology was checked with different natural samples taken from rivers Garonne, Gave de Cauterets and Gave de Pau in the Pyrenees. Results appeared in good agreement with theoretical estimations computed from Visual Minteq. On-site measurements were performed for the first time with AGNES in the Gave de Cauterets in Soulom (France) and the results were corroborated with purged measurements performed in the laboratory.

ISIDORE, a probe for in situ trace metal speciation based on Donnan membrane technique with related electrochemical detection part 1: Equilibrium measurements.

This work presents the development of a new probe (ISIDORE probe) based on the hyphenation of a Donnan Membrane Technique device (DMT) to a screen-printed electrode through a flow-cell to determine the free zinc, cadmium and lead ion concentration in natural samples, such as a freshwater river. The probe displays many advantages namely: (i) the detection can be performed on-site, which avoids all problems inherent to sampling, transport and storage; (ii) the low volume of the acceptor solution implies shorter equilibration times; (ii) the electrochemical detection system allows monitoring the free ion concentration in the acceptor solution without sampling.