There is a current debate on whether the toxicity of engineered ZnO nanoparticles (NPs) can be traced back to their nanoscale properties or rather to the simple fact of their relatively high solubility and consequent release of Zn2+ ions. In this work, the emerging electroanalytical technique AGNES (Absence of Gradients and Nernstian Equilibrium Stripping), which is specially designed to determine free metal ion concentration, is shown to be able to measure the Zn2+ concentration resulting from dissolution of ZnO nanoparticles dispersed in aqueous salt solutions. Three NP samples from different sources (having average primary particle diameters of 6, 20, and 71 nm) were tested and compared with bulk ZnO material. The enhanced solubility of the nanoparticles with decreasing primary radius allows for an estimation of the surface energy of 0.32 J/m2. AGNES also allows the study of the kinetics of Zn2+ release as a response to a change in the solution parameters (e.g., pH, ZnO concentration). A physicochemical model has been developed to account for the observed kinetic behavior. With this model, only one kinetic parameter is required to describe the time dependence of the free Zn2+ concentration in solution. Good agreement with this prediction is obtained when, starting from an equilibrated NP dispersion, the pH of the medium is lowered. Also, the independence of this parameter from pH, as expected from the model, is obtained at least in the pH range 7–9. When dissolution is studied by dispersing ZnO nanoparticles in the medium, the kinetic parameter initially decreases with time. This decrease can be interpreted as resulting from the increase of the radius of the clusters due to the agglomeration/aggregation phenomena (independently confirmed). For the larger assayed NPs (i.e., 20 and 71 nm), a sufficiently large pH increase leads to a metastable solubility state, suggesting formation of a hydroxide interfacial layer.

ZnO nanoparticles (NPs) are prone to dissolution, and uncertainty remains whether biological/cellular responses to ZnO NPs are solely due to the release of Zn(2+) or whether the NPs themselves have additional toxic effects. We address this by establishing ZnO NP solubility in dispersion media (Dulbecco's modified Eagle's medium, DMEM) held under conditions identical to those employed for cell culture (37 °C, 5% CO2, and pH 7.68) and by systematic comparison of cell-NP interaction for three different ZnO NP preparations. For NPs at concentrations up to 5.5 μg ZnO/mL, dissolution is complete (with the majority of the soluble zinc complexed to dissolved ligands in the medium), taking ca. 1 h for uncoated and ca. 6 h for polymer coated ones. Above 5.5 μg/mL, the results are consistent with the formation of zinc carbonate, keeping the solubilized zinc fixed to 67 μM of which only 0.45 μM is as free Zn(2+), i.e., not complexed to dissolved ligands. At these relatively high concentrations, NPs with an aliphatic polyether-coating show slower dissolution (i.e., slower free Zn(2+) release) and reprecipitation kinetics compared to those of uncoated NPs, requiring more than 48 h to reach thermodynamic equilibrium. Cytotoxicity (MTT) and DNA damage (Comet) assay dose-response curves for three epithelial cell lines suggest that dissolution and reprecipitation dominate for uncoated ZnO NPs. Transmission electron microscopy combined with the monitoring of intracellular Zn(2+) concentrations and ZnO-NP interactions with model lipid membranes indicate that an aliphatic polyether coat on ZnO NPs increases cellular uptake, enhancing toxicity by enabling intracellular dissolution and release of Zn(2+). Similarly, we demonstrate that needle-like NP morphologies enhance toxicity by apparently frustrating cellular uptake. To limit toxicity, ZnO NPs with nonacicular morphologies and coatings that only weakly interact with cellular membranes are recommended.

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The effective distribution of affinities (Conditional Affinity Spectrum, CAS) seen by a metal ion binding to a humic substance under natural water conditions is derived and discussed within the NICA-Donnan model. Analytical expressions for the average affinity of these distributions in general multi-ion mixtures are reported here for the first time. These expressions enable a simple evaluation of the effect of all interfering cations on the affinity distribution of a given one. We illustrate this methodology by plotting the affinity spectra of a generic fulvic acid for 14 different cations in the presence of major inorganic ions and trace metals at pH and concentration values representative of a river water. The distribution of occupied sites and their average affinity at the typical freshwater conditions are also reported for each ion. The CAS allows usto distinguish three groups of cations: (a) Al, H, Pb, Hg, and Cr, which are preferentially bound to the phenolic sites of the fulvic ligand; (b) Ca, Mg, Cd, Fe(II), and Mn, which display a greater effective affinity for carboxylic sites, in contrast to what would be expected from their individual complexation parameters; and (c) Fe(III), Cu, Zn, and Ni, for which phenolic and carboxylic distributions are overlapped.

a b s t r a c t AGNES (Absence of Gradients and Nernstian Equilibrium Stripping) determination of free Zn(II) in a solution can be affected by the reaching of high Zn°concentrations inside the amalgam. At concentrations about the solubility limit of Zn°in mercury, the formation of dendrites and powders around the mercury surface can be seen with an optical microscope. At concentrations of Zn°quite below the solubility limit, an anomalous stripping current appears which increases with decreasing supporting electrolyte concentration. The current along the stripping time exhibits a convex shape, which is labelled here as ''anomalous convex behaviour" (acb). The origin of acb is tentatively ascribed to different kinetic reasons (amongst which the electroneutrality limitation due to low ionic strength outstands), but more than one cause is necessary for a full account of the experimental observations. With various strategies, like monitoring the charge as response function or by application of lower gains, AGNES can successfully probe these high concentrations.

As the measurement of metals by DGT (diffusion gradients in thin films) in low salinity media has been controversial, a thorough study of the impact of ionic strength (I) is timely. DGT accumulations of Cd, Co, and Ni in the presence of NTA at pH 7.5 with I in the range from 10(-4) to 0.5 M were obtained. An observed decrease in the metal accumulation as the ionic strength of the system decreased is partially explained by the electrostatic repulsion between the negatively charged resin domain and the dominant negatively charged complex species M-NTA. This electrostatic effect reduces the complex penetration into the resin domain, especially for nonlabile complexes, which do not fully dissociate in the gel domain. Analytical expressions, based on the Donnan model, were able to quantify these electrostatic effects. Additionally, the data indicate that the kinetic dissociation constant of M-NTA complexes in the resin layer is higher than Eigen predictions, suggesting a ligand-assisted dissociation mechanism. As the ionic strength decreases, the rate of reaction in the resin layer decreases due to the repulsion between the negatively charged resin sites and the complex species. This decrease contributes to the decrease in metal accumulation. These novel, previously unconsidered, effects of ionic strength and the ligand-assisted dissociation mechanism in the resin domain will affect DGT measurements made in freshwaters and soils.

The index of refraction, the optical band edge and the Raman scattering of strontium barium niobate, Sr x Ba 1-x Nb 2 O 6 with 0 38 0 77 x . < < . have been studied. The ordinary refractive index does not depend on x, while the extra-ordinary one increases with increasing x. The band edge is almost unaffected by the Baor Sr-content and shows a weak band bowing. Both the index of refraction and the band edge may be used for an optical determination of the composition of the crystal. Raman spectra show the typical behavior of tungsten bronze type crystals with broad bands and complicated spectral shapes.

The temperature dependence of the spontaneous polarization in strontium-barium-niobate single crystals with varying Sr/Ba ratio is presented. The temperature of the relaxor phase-transition is determined from the inflexion point of the curve of the ferroelectric polarization versus temperature. The influence of the Sr/Ba ratio in the crystal on the transition temperature is discussed within an effective field approach.