Pseudopolarograms of lead (II) constructed from the voltammograms measured in situ in the sediment and in the interstitial water by using an Ir solid microelectrode with a thin mercury film have shown as a kind of fingerprints of the sample. Despite shortcomings when compared to measurements with the mercury drop electrode and in model solutions, the measurement procedure was adapted for enough signal repeatability, avoiding to a reasonable extent the memory effect and electrode surface blocking. To make the best use of the information available, besides the classical pseudopolarograms, i.e. besides the dependence of the peak-height on the deposition potential, it is necessary to analyze the peak-area, the peak-position and the half-peak width versus deposition potential, and combine them with the knowledge from various theoretical and model situations. They have shown to contain interesting information about speciation. This information is not always unambiguous, it is often semi-quantitative, and cannot be reached by other methods, however, in combination with other methods it could be useful for the characterization of the sample solution. Pseudopolarograms of lead (II) in different liquid fractions of the sediment were measured and compared, the electrode sensitivity varying from 4 to 20 nA/mol L −1 of lead (II). The differences in half-wave potentials recorded were ranging up to 0.6 V and those in the slopes of pseudopolarograms were threefold , having interesting relationships with the peak potentials of single voltammetric curves.
Detailed investigation of Cu (II) binding with natural lipid phosphatidylglycerol (PG) in aqueous solution was carried out by voltammetric measurements at the mercury drop electrode, complemented by monolayer studies in a Langmuir trough and electrophoretic measurements, all used as models for hydrophobic cell membranes. Penetration of copper ions into the PG layer was facilitated by the formation of hydrophilic Cu-Phenanthroline (Phen) complex in the subphase, followed by the mixed ligand Cu-Phen-PG complex formation at the hydrophobic interface. Electrophoretic measurements indicated a comparatively low abundance of the formed mixed ligand complex within the PG vesicles, resulting it the zeta potential change of +0.83mV, while monolayer studies confirmed their co-existence at the interface. The Cu-Phen-PG complex was identified in the pH range from 6 to 9. The stoichiometry of the complex ([PhenCuOHPG]), as well as its stability and kinetics of formation, were determined at the mercury drop electrode. Cu-Phen-PG reduces quasireversibly at about -0.7V vs. Ag/AgCl including reactant adsorption, followed by irreversible mixed complex dissociation, indicating a two-electron transfer - chemical reaction (EC mechanism). Consequently, the surface concentration (γ) of the adsorbed [PhenCuOHPG] complex at the hydrophobic electrode surface was calculated to be (3.35±0.67)×10molcm. Information on the mechanism of Cu (II) - lipid complex formation is a significant contribution to the understanding of complex processes at natural cell membranes.
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