Catechol (CC), resorcinol (RC) and hydroquinone (HQ) are dihydroxybenzene isomers that usually coexist in different samples and can be determined using voltammetric techniques taking profit of their fast response, high sensitivity and selectivity, cheap instrumentation, simple and timesaving operation modes. However, a strong overlapping of CC and HQ signals is observed hindering their accurate analysis. In the present work, the combination of differential pulse voltammetry with graphene screen-printed electrodes (allowing detection limits of 2.7, 1.7 and 2.4µmolL(-1) for HQ, CC and RC respectively) and the data analysis by partial least squares calibration (giving root mean square errors of prediction, RMSEP values, of 2.6, 4.1 and 2.3 for HQ, CC and RC respectively) has been proposed as a powerful tool for the quantification of mixtures of these dihydroxybenzene isomers. The commercial availability of the screen-printed devices and the low cost and simplicity of the analysis suggest that the proposed method can be a valuable alternative to chromatographic and electrophoretic methods for the considered species. The method has been applied to the analysis of these isomers in spiked tap water.
To evaluate plant response to Hg stress, glutathione, phytochelatins, and their Hg complexes were analyzed using HPLC with amperometric detection in samples of Asparagus acutifolius grown in the Almadén mining district (Ciudad Real, Spain), one of the most Hg-contaminated sites in the world. Soils of the Almadén mining district, and specifically from the Almadenejos zone, are highly contaminated, with some zones having values above 4,000 μg Hg g(-1) soil. Although soils have an extremely high concentration of mercury, generally less than 2% is available for plants, as is shown by various soil extractions simulating bioavailability. In plants, Hg concentration increases depending on the content of Hg in soils. In addition, Hg levels in roots are higher than in aerial parts, which is a strategy of plants for protecting their more sensitive aerial parts from the deleterious effects of metal stress. The total content of phytochelatins (PCs) and their complexes are directly related with the amount of mercury in soils. These findings highlight the important role of thiol compounds and their metal complexes in capturing and fixing Hg from soils, giving plants the capacity to deal with the heavy metal toxicity of polluted soils.
Indium is increasingly used in electronic devices, from which it can be mobilized towards environmental compartments. Speciation of In in waters is important for its direct ecotoxicological effects, as well as for the fate of this element in the environment (e.g. fluxes from or towards sediments). Free indium concentrations in the environment can be extremely low due to hydrolysis, especially important in trivalent cations, to precipitation and to complexation with different ligands. In this work, the free indium concentration (which is a toxicologically and geochemically relevant fraction) in aqueous solutions at pH3 has been measured with an adapted version of the electroanalytical technique AGNES (Absence of Gradients and Nernstian Equilibrium Stripping). Speciation measurements in mixtures of indium with the ligands NTA (nitrilotriacetic acid) and oxalate indicate that the values of their stability constants in the NIST46.6 database are less adequate than those published in some more recent literature. The extraordinary lability and mobility of In-oxalate complexes allow the measuring of free indium concentrations below nmol/L in just 25s of deposition time.
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