Metal (Pb, Cd, and Zn) Binding to Diverse Organic Matter Samples and Implications for Speciation Modeling.

This study evaluated the influence of dissolved organic matter (DOM) properties on the speciation of Pb, Zn, and Cd. A total of six DOM samples were categorized into autochthonous and allochthonous sources based on their absorbance and fluorescence properties. The concentration of free metal ions ( CM2+) measured by titration using the absence of gradients and Nernstian equilibrium stripping (AGNES) method was compared with that predicted by the Windermere humic aqueous model (WHAM). At the same binding condition (pH, dissolved organic carbon, ionic strength, and total metal concentration) the allochthonous DOM showed a higher level of Pb binding than the autochthonous DOM (84- to 504-fold CPb2+ variation). This dependency, however, was less pronounced for Zn (12- to 74-fold CZn2+ variation) and least for Cd (2- to 14-fold CCd2+ variation). The WHAM performance was affected by source variation through the active DOM fraction ( F). The commonly used F = 1.3 provided reliable CPb2+ for allochthonous DOMs and acceptable CCd2+ for all DOM, but it significantly under-predicted CPb2+ and CZn2+ for autochthonous DOM. Adjusting F improved CM2+ predictions, but the optimum F values were metal-specific (e.g., 0.03-1.9 for Pb), as shown by linear correlations with specific optical indexes. The results indicate a potential to improve WHAM by incorporating rapid measurement of DOM optical properties for site-specific F.

Speciation of Zn, Fe, Ca and Mg in wine with the Donnan Membrane Technique.

Free concentrations of Zn2+, Fe3+, Ca2+ and Mg2+ in a red wine (Raimat, Catalonia, Spain) have been determined, with the Donnan Membrane Technique (DMT) for the first time. The required equilibration time benefits from the acceptor solution including major cations. K+ and Na+, mainly unbound to any ligand in the sample, have been identified as suitable reference ions. A free Zn concentration of 1.76µmolL-1 determined with DMT was in excellent agreement with the free Zn concentration independently provided by the electroanalytical technique Absence of Gradients and Nernstian Equilibrium Stripping (AGNES), 1.7µmolL-1, amounting to 14.4% of the total Zn. The free concentrations found in this wine were 1.79µmolL-1 Fe3+, 1.11mmolL-1 Ca2+ and 3.4mmolL-1Mg2+ (8.82%, 40% and 57% of their total concentrations). Prior to the application of the techniques to the red wine, they had been cross-validated in Zn-tartrate solutions.

Determination of the complexing capacity of wine for Zn using the absence of gradients and nernstian equilibrium stripping technique.

The complexing capacity of synthetic (0.011 M tartrate in 13.5% ethanol) and real wine (Raimat Abadia) in titrations with added total Zn concentrations up to 0.03 M has been determined following the free Zn concentrations with AGNES (absence of gradients and Nernstian equilibrium stripping) technique. A correction to find the preconcentration factor or gain (Y(1)) really applied at each one of the ionic strengths reached due to Zn additions along the titration has been applied. The standard implementation of AGNES to real wine led to the observation of two anomalous behaviors: (a) an increasingly negative current in the deposition stage (labeled as "HER" effect) and (b) a minimum in the currents of the stripping stage plot (labeled as the "dip" effect). A practical strategy to apply AGNES avoiding the dip effect has been developed to quantify properly free Zn concentrations. The van den Berg-Ruzic-Lee linearization method (assuming the existence of just 1:1 complexes) has been adapted to consider the dilution effect and the ionic strength changes. Aggregated stability constants and total ligand concentrations have been calculated from synthetic and wine titration data. The found complexing capacity in the studied wine (c(T,L) = 0.0179 ± 0.0007 M) indicates the contribution of ligands other than tartrate (which is confirmed to be the main one).

Determination of free Zn2+ concentration in synthetic and natural samples with AGNES (Absence of Gradients and Nernstian Equilibrium Stripping) and DMT (Donnan Membrane Technique).

The determination of free Zn(2+) ion concentration is a key in the study of environmental systems like river water and soils, due to its impact on bioavailability and toxicity. AGNES (Absence of Gradients and Nernstian Equilibrium Stripping) and DMT (Donnan Membrane Technique) are emerging techniques suited for the determination of free heavy metal concentrations, especially in the case of Zn(2+), given that there is no commercial Ion Selective Electrode. In this work, both techniques have been applied to synthetic samples (containing Zn and NTA) and natural samples (Rhine river water and soils), showing good agreement. pH fluctuations in DMT and N(2)/CO(2) purging system used in AGNES did not affect considerably the measurements done in Rhine river water and soil samples. Results of DMT in situ of Rhine river water are comparable to those of AGNES in the lab. The comparison of this work provides a cross-validation for both techniques.

Evaluation of thin mercury film rotating disk electrode to perform absence of gradients and Nernstian equilibrium stripping (AGNES) measurements.

In the present work, the applicability of thin mercury film on a rotating disk electrode (TMF-RDE), to assess the free metal ion concentration by the absence of gradients and Nernstian equilibrium stripping (AGNES), is evaluated. The thickness of the mercury film and several AGNES parameters has been optimized. A nominal 16 nm film is chosen due to the higher signal (faradaic current) relative to the value of the noise (capacitive current). Due to the smaller volume to area ratio, the deposition time needed to reach a certain preconcentration factor (Y) is much shorter than in larger electrodes, like the HMDE. The limit of detection (3 sigma) for lead(II) is 7.4 x 10(-9)M and 7.2 x 10(-8)M for a Y of 5000 (deposition time of 150 s) and 1000 (deposition time of 100 s), respectively. A specific mathematical treatment is developed in order to subtract a corrected blank taking into account the degradation of the thin film (presumably, falling down of drops). The couple TMF-RDE/AGNES is successfully applied for speciation purposes in the systems Pb(II)-latex nanospheres and Pb(II)-IDA (iminodiacetic acid), where the stability constants calculated for both systems agree with values reported in the literature.

Application of the new electroanalytical technique AGNES for the determination of free Zn concentration in river water.

Absence of gradients and Nernstian equilibrium stripping (AGNES) is a recently developed electroanalytical technique specifically designed for the direct determination of free concentrations of metal ions. AGNES is applied here to the determination of free Zn concentration in a river water sample. The method has been validated with synthetic solutions of low ionic strengths containing Zn and 2,6-pyridinedicarboxylic acid and then applied to synthetic river waters and to a natural sample collected from Besòs River in Montcada i Reixac (Catalonia, North-Eastern Spain). In the river sample, an average free Zn concentration of 12.8(4) nM was obtained, while the total dissolved Zn concentration was 0.51(8) microM. To control and maintain pH and pCO(2) constant during AGNES measurements, a novel device for N(2)/CO(2) mixed purging has been developed.

Measurement of free zinc concentration in wine with AGNES.

AGNES (absence of gradients and Nernstian equilibrium stripping), a voltammetric technique recently introduced to measure free metal concentration in solution and checked with different natural and synthetic aqueous media, has been applied here to determine free Zn concentration in wine. The content of ethanol in a solution increases its viscosity, and, so, the diffusion coefficient decreases. Another added effect in ethanolic solutions is the increase of the activity of the metal ions, due to the decrease of the permittivity in the alcoholic medium with respect to the aqueous one. With this taken into account, a specific methodology has been developed to apply AGNES in ethanolic media. A relevant point in this methodology has been the introduction of a new kind of blank, the EDTA blank, able to be applied in the same natural sample and with the same potential program. The free Zn concentrations of the two wines analyzed, a red and a white Raimat wine, were 4.5(2) x 10 (-7) and 7.2(4) x 10 (-7) M, respectively. These represent around 5% of the total Zn content. In the wine samples analyzed, it was checked that intermetallic formation of Zn-Cu does not affect the measurement of free Zn in a significant way.

Competitive Cd2+/H+ complexation to polyacrylic acid described by the stepwise and intrinsic stability constants.

Stepwise constants can be used to describe competitive proton and metal binding to macromolecules with a large number of sites. With the aim of accessing information on the microscopic binding model, we report an expression that connects the stepwise constants to the site-specific metal constants. This expression holds for a very general complexation model including heterogeneity, interactions, and chelate complexation. Assuming bidentate binding of the Cd ions to adjacent carboxylate groups in poly(acrylic acid), stepwise and intrinsic stability constants for proton and cadmium binding were estimated from the experimental data. Intrinsic values were split into specific and electrostatic contributions (by means of the Poisson-Boltzmann equation under cylindrical geometry). Free of the electrostatic contribution, the remaining Cd binding energy showed almost no dependence on the coverage and ionic strength, and the corresponding average values allowed for a reasonable reproduction of raw binding data. Small systematic discrepancies from the homogeneous behavior are critically discussed.

Conditional affinity spectra of Pb2+-humic acid complexation from data obtained with AGNES.

The new electroanalytical technique AGNES (Absence of Gradients and Nernstian Equilibrium Stripping) has been applied to follow Pb2+ complexation to Purified Aldrich Humic Acid. A refined methodology of AGNES, allowing considerably larger gains, reached free metal ion concentrations down to subnanomolar values in a reasonable deposition time due to the lability and mobility of these complexes. Further insights into the meaning of the binding data, fitted to a NICA (Non Ideal Competitive Adsorption) isotherm, can be obtained with the concept of conditional affinity spectrum (CAS). For this purpose, we present the analytical expression for the CAS of NICA isotherm and show the CAS distributions for the Pb binding at fixed pH. Results reveal that the underlying spectra of each elementary distribution of the bimodal NICA evolve with pH yielding different overlapping and nonsymmetrical distributions. A non-negligible occupation of phenolic and carboxylic sites by Pb2+ takes place in the range of 4 < pH < 9.

A comparison between the determination of free Pb(II) by two techniques: absence of gradients and Nernstian equilibrium stripping and resin titration.

Absence of gradients and Nernstian equilibrium stripping (AGNES) is an emerging electroanalytical technique designed to measure free metal ion concentration. The practical implementation of AGNES requires a critical selection of the deposition time, which can be drastically reduced if the contribution of the complexes is properly taken into account. The resin titration (RT) is a competition method based on the sorption of metal ions on a complexing resin. The competitor here considered is the resin Chelex 100 whose sorbing properties towards Pb(II) are well known. The RT is a consolidated technique especially suitable to perform an intercomparison with AGNES, due to its independent physicochemical nature. Two different ligands for Pb(II) complexation have been analyzed here: nitrilotriacetic acid (NTA) and pyridinedicarboxylic acid (PDCA). The complex PbNTA is practically inert in the diffusion layer, so, for ordinary deposition potentials, its contribution is almost negligible; however, at potentials more negative than -0.8 V vs. Ag/AgCl the complex dissociates on the electrodic surface giving rise to a second wave in techniques such as normal pulse polarography. The complex Pb-PDCA is partially labile, so that its contribution can be estimated from an expression of the lability degree of the complex. These new strategies allow us to reduce the deposition time. The free Pb(II) concentrations obtained by AGNES and by RT are in full agreement for both systems here considered. The main advantage of the use of AGNES in these systems lies in the reduction of the time of the experiment, while RT can be applied to non-amalgamating elements and offers the possibility of simultaneous determinations.

Competitive ion complexation to polyelectrolytes: determination of the stepwise stability constants. The Ca2+/H+/polyacrylate system.

This work presents a new methodology aimed at obtaining the stepwise stability constants corresponding to the binding of ions (or other small molecules) to macromolecular ligands having a large number of sites. For complexing agents with a large number of sites, very simple expressions for the stepwise stability constants arise. Such expressions are model-independent; that is, they allow the determination of the stepwise stability constants without making any previous assumption of the detailed complexation mechanism. The formalism is first presented for a single complexing ion and further extended to competitive systems where the competing ions can display, in general, different stoichiometric relationships. These ideas are applied to the analysis of experimental titrations corresponding to competitive binding of calcium ions to poly(acrylic acid) for different pH values and ionic strengths. Intrinsic stability constants were estimated from the stepwise stability constants (by removing the corresponding statistical factor), and split into specific and electrostatic contributions (by means of the Poisson-Boltzmann equation). After this treatment, the specific proton binding energies showed almost no dependence on the coverage and ionic strength. Likewise, for the range of concentrations studied, the specific component of the intrinsic stability constants of the calcium ions, calculated assuming bidentate binding of Ca to neighboring groups of a linear chain, is almost independent of the calcium and proton coverage and ionic strength.

Ligand mixture effects in metal complex lability.

The degree of lability of a given metal complex species is modified in the presence of a mixture of ligands. This modification is a consequence of the coupling of the association and dissociation processes of all of the complexes according to the competitive complexation reaction scheme. We show that, because of the mixture effect, the lability of a given complex usually increases when another more labile complex is added into the system, while it decreases upon addition of a less labile one. Typically, complexes tend to adapt to the global lability of the mixture. A quantitative evaluation of these effects for diffusion-limited conditions in a finite domain by rigorous numerical simulation in a system with two complexes indicates that the lability degree of a complex can change by more than 100% with respect to that in the single ligand system. The impact of the mixture effect on the metal flux depends at least on two main factors: the respective abundance of the metal species and the particular values of their lability degrees. Dominant complexes (i.e., those most abundant when these complexes have equal diffusion coefficients) undergo smaller changes in their own lability degree, but these changes have the greater impact on the overall metal flux. Partially labile complexes are more easily influenced by the mixture than labile or inert ones. Some mixture effects can be qualitatively predicted by an analytical expression for the lability index derived using the reaction layer approximation. For a mixture of many complexes, the change in the lability degree of a complex due to the mixture effect can be understood as a combination of the changes due to all of the complexes present.