Stability Constants of Tetravalent Germanium Complexes in Aqueous Solution: Small Organic Oxygen and Nitrogen Donor Ligands.

The formation constants of about 100 different complexes of Ge(IV) with some 50 organic, low-molecular-weight ligands, principally bidentate oxygen and/or nitrogen donors, are determined by potentiometric titrations at 25 °C and an ionic strength of 0.1 mol L-1 (KNO3). In the few cases for which literature data are available, these older data are critically discussed and completed in light of our new experimental data. The overall picture emerging from our work is that such complexes are comparatively weak, except when a chelate effect comes into play, as is observed with aminopolyols, α-hydroxocarboxylic acids, and carbohydrate derivatives, where even quantitative chelation of Ge is possible. No binding to amino acids or peptides is detected. An important finding is our evidence for the existence of a bridged dinuclear germanium(IV) tartrate complex in the aqueous phase, whose occurrence in solids was confirmed by X-ray diffraction beforehand. Our work has implications for the general understanding of the aqueous coordination chemistry of Ge, its geochemical cycling, and its behavior in environmental and biological systems. Potentiometric raw data for use by other researchers are publicly accessible in the repository Zenodo at CERN.

Chemical-genomic profiling identifies genes that protect yeast from aluminium, gallium, and indium toxicity.

Aluminium, gallium, and indium are group 13 metals with similar chemical and physical properties. While aluminium is one of the most abundant elements in the Earth's crust, gallium and indium are present only in trace amounts. However, the increased use of the latter metals in novel technologies may result in increased human and environmental exposure. There is mounting evidence that these metals are toxic, but the underlying mechanisms remain poorly understood. Likewise, little is known about how cells protect themselves from these metals. Aluminium, gallium, and indium are relatively insoluble at neutral pH, and here we show that they precipitate in yeast culture medium at acidic pH as metal-phosphate species. Despite this, the dissolved metal concentrations are sufficient to induce toxicity in the yeast Saccharomyces cerevisiae. By chemical-genomic profiling of the S. cerevisiae gene deletion collection, we identified genes that maintain growth in the presence of the three metals. We found both shared and metal-specific genes that confer resistance. The shared gene products included functions related to calcium metabolism and Ire1/Hac1-mediated protection. Metal-specific gene products included functions in vesicle-mediated transport and autophagy for aluminium, protein folding and phospholipid metabolism for gallium, and chorismate metabolic processes for indium. Many of the identified yeast genes have human orthologues involved in disease processes. Thus, similar protective mechanisms may act in yeast and humans. The protective functions identified in this study provide a basis for further investigations into toxicity and resistance mechanisms in yeast, plants, and humans.

A Comprehensive Potentiometric Study of the Tartrate Complexes of Trivalent Arsenic, Antimony, and Bismuth in Aqueous Solution.

The tartrate complexes of trivalent arsenic, antimony, and bismuth were studied potentiometrically. The existing, fragmentary data on the antimony/l-(+)-tartrate system were confirmed. Nine complexes of arsenic and bismuth with optically active, racemic, and meso-tartrate, as well as complexes of antimony with meso-tartrate, were newly identified, and their formation constants computed. Difficulties arising from the poor stability of the arsenic complexes and precipitation in the Sb(III)/meso-tartrate system were overcome by titrating at very high concentrations [As(III) systems] and using an auxiliary ligand [Sb(III) in the presence of catechol]. All data were obtained at 25.0 °C and at constant ionic strength [0.1 mol L-1 for Sb(III) and Bi(III) complexes and 1 mol L-1 for As(III) complexes]. Speciation diagrams of all systems at millimolar concentrations were computed on the basis of the newly obtained constants and the results discussed.

Antimony release from polyester textiles by artificial sweat solutions: A call for a standardized procedure.

Polyester fibres are usually contaminated by antimony because of its use as a catalyst in the production of polyethylene terephthalate and as a flame retardant synergist in a variety of new and recycled polymers. The present study determined the release of antimony (at total concentrations ranging from about 125 to 470 µg g-1) from polyester textile samples designed to be in contact with human skin using standard artificial sweat solutions (ISO 105-E04 and EN 1811). The study also examined the role of different experimental parameters on the release of the metalloid. Overall, and using the default parameters, between about 0.05 and 2% of total antimony (or 0.1-1 µg g-1) was mobilized into artificial sweat. A reduction in time (from 24 to 12 h) and temperature (from 37 to 20 or 4 °C) and an increase in pH (from 5.5 to 7) resulted in a decline in antimony mobilization from textiles, while altering textile mass to solution volume and the presence of lactate had little impact on the results. Removal of a filtration step increased antimony mobilization but this was attributed to artefacts associated with release from microfibres during extract storage and analysis. In general, antimony mobilization was sufficiently repeatable using either EN 1811 or ISO 105-E04 but the latter is recommended for an assessment of antimony mobilization and potential exposure because its pH is closer to that of human sweat. Since the first fraction of either extractions mobilized the greatest quantity of antimony, exposure can be minimized by washing articles before use.

Selective determination of niobium in natural waters at the low ngL-1 level by differential pulse cathodic stripping voltammetry in the presence of pyrogallol red.

A completely selective method for electrochemical determination of very low concentrations (ngL-1) of niobium is presented. The method relies on the cathodic reduction of the pyrogallol red­niobium complex at pH3. Virtually no sample preparation (apart from cation exchange) is required. The method is both free from interferences (particularly from Ta) and affordable. Time consuming preconcentration and separation procedures as well as the use of hydrofluoric acid, fluorides or problematic solvents are avoided. The applicability of the method is illustrated through analysis of mineral waters containing niobium concentrations ranging from 1 to several hundred ngL-1.

Bulk Dissolution Rates of Cadmium and Bismuth Tellurides As a Function of pH, Temperature and Dissolved Oxygen.

The toxicity of Cd being well established and that of Te suspected, the bulk, surface-normalized steady-state dissolution rates of two industrially important binary tellurides-polycrystalline cadmium and bismuth tellurides- were studied over the pH range 3-11, at various temperatures (25-70 °C) and dissolved oxygen concentrations (0-100% O2 in the gas phase). The behavior of both tellurides is strikingly different. The dissolution rates of CdTe monotonically decreased with increasing pH, the trend becoming more pronounced with increasing temperature. Activation energies were of the order of magnitude associated with surface controlled processes; they decreased with decreasing acidity. At pH 7, the CdTe dissolution rate increased linearly with dissolved oxygen. In anoxic solution, CdTe dissolved at a finite rate. In contrast, the dissolution rate of Bi2Te3 passed through a minimum at pH 5.3. The activation energy had a maximum in the rate minimum at pH 5.3 and fell below the threshold for diffusion control at pH 11. No oxygen dependence was detected. Bi2Te3 dissolves much more slowly than CdTe; from one to more than 3.5 orders of magnitude in the Bi2Te3 rate minimum. Both will readily dissolve under long-term landfill deposition conditions but comparatively slowly.

Direct determination of tellurium and its redox speciation at the low nanogram level in natural waters by catalytic cathodic stripping voltammetry.

Tellurium is one of the elements recently identified as technologically critical and is becoming a new emergent contaminant. No reliable method exists for its determination in environmental samples such as natural waters. This gap is filled by the method described here; it allows the rapid detection of trace concentrations of Te(IV) and Te(VI) in surface waters by differential pulse cathodic stripping voltammetry. It is based on the proton reduction catalysed by the absorption of Te(IV) on the mercury electrode. Under our conditions (0.1 mol L(-1) HCl) a detection limit of about 5 ng L(-1) for a deposition time of 300 s is achieved. Organic matter does not represent a problem at low concentrations; higher concentrations are eliminated by adsorptive purification. Tellurium occurs primarily as Te(IV) and Te(VI) in natural waters. Thus, determining total Te requires the reduction of Te(VI) that it is not electroactive. A number of reduction procedures have been carefully evaluated and a method based on the addition of TiCl3 to the acidified samples has been proven to reduce Te(VI) at the trace level to Te(IV) reliably and quantitatively. Therefore, the procedure described allows the direct determination of total Te and its redox speciation. It is flexible, reliable and cost effective compared to any possible alternative method based on the common preconcentration-ICPMS approach. It is readily implementable as a routine method and can be deployed in the field with relative ease.

The desorption of antimony(V) from sediments, hydrous oxides, and clay minerals by carbonate, phosphate, sulfate, nitrate, and chloride.

The desorption of antimony, Sb(V), from two sediment samples by phosphate, carbonate, sulfate, chloride, and nitrate at pH 8 was examined. One highly contaminated sediment sample was taken from an Sb mine (Goesdorf, Luxembourg); the other sample was the certified reference material PACS-2 (marine sediment). Phosphate was found to have a strong mobilizing ability, whereas that of carbonate was in general weaker. For comparison, and to understand better the possible importance of individual components of the sediments, desorption experiments were performed on pure phases (i.e., hydrous oxides of Fe, Mn, and Al) and the clay minerals kaolinite and montmorillonite. In the cases of hydrous metal oxides, Sb(V) was most effectively desorbed by phosphate, followed by carbonate. Phosphate also desorbed Sb(V) from the clay minerals, whereas carbonate had no effect. The pH dependence of adsorption of Sb(V) in the absence and presence of carbonate revealed that adsorption densities were higher (except in the case of montmorillonite) in the absence of carbonate, suggesting a competition between carbonate and [Sb(OH)] for surface sites generally and a lowering of surface charge in the case of hydrous aluminum oxide. The observations are unlikely to be due to ionic strength effects because activity coefficients in the blank and spiked solutions differ by <4%. Desorption experiments on sediments with varying concentrations of phosphate and carbonate demonstrated that at environmentally relevant concentrations, desorption by phosphate is negligible, whereas the effect of carbonate is not. Sulfate, chloride, and nitrate generally had little effect. The proportion of Sb desorbed in blank experiments coincides with that mobilized in the first fraction of the Bureau Communautaire de Référence (BCR) sequential extraction (easily exchangeable and carbonate-bound fraction).