A method using a miniature analytical system based on hydride generation capacitively coupled plasma microtorch optical emission spectrometry with a QE65 Pro microspectrometer was developed and evaluated for the simultaneous determination of As and Sb in soil samples. The use of this microspectrometer allows the examination of the spectral range between 190 and 220 nm where the continuum background emission of the plasma is low and the most intense resonance lines As 193.759; 197.262 nm and Sb 206.833; 217.581 nm are located. The method involves microwave-assisted digestion of samples in aqua regia, prereduction of As(V) and Sb(V) to their (+3) species with 0.3% L-cysteine by heating in a boiling water bath at 90 ± 5 °C and hydride generation in 0.01 mol L⁻¹ HCl (pH = 2.00 ± 0.01) medium with 0.5% NaBH₄ solution. The method was optimized in order to provide the simultaneous determination of As and Sb. The figures of merit were evaluated at different emission wavelengths under the optimum conditions of plasma microtorch operation (10 W, 150 mL min⁻¹ Ar), and the best performances were obtained at 193.759 nm (As) and 217.581 nm (Sb). The figures of merit of the method were compared to those of the traditional hydride generation inductively coupled plasma optical emission spectrometry taken as a reference method. Analysis of CRMs revealed recoveries of 101 ± 9% As and 102 ± 3% Sb comparable to 102 ± 7% As and 98 ± 4% Sb in the reference method. The precision of determinations was 2–10% for 90–210 mg kg⁻¹ As and 40–130 mg kg⁻¹ Sb, close to 3–8% in hydride generation inductively coupled plasma optical emission spectrometry. The Bland and Altman test performed on 10 soil samples indicated no significant difference between the results obtained by the two methods, so that the miniature analytical system could be successfully applied for As and Sb monitoring in environmental samples. The proposed method is attractive in terms of analytical costs due to limited consumption of high purity HCl, power and Ar to sustain the plasma, and therefore more advantageous than hydride generation inductively coupled plasma optical emission spectrometry.

The objective of this study was to examine the potential environmental risk of tailings resulted after precious and base metal ores processing, stored in seven impoundments located in the Aries river basin, Romania. The tailings were characterized by mineralogical and elemental composition, contamination indices, acid rock drainage generation potential and water leachability of hazardous/priority hazardous metals and ions. Multivariate statistical methods were used for data interpretation.

The paper presents the evaluation of soil contamination with total, water-available, mobile, semi-mobile and non-mobile Hg fractions in the surroundings of a former chlor-alkali plant in connection with several chemical soil characteristics. Principal Component Analysis and Cluster Analysis were used to evaluate the chemical composition variability of soil and factors influencing the fate of Hg in such areas. The sequential extraction EPA 3200-Method and the determination technique based on capacitively coupled microplasma optical emission spectrometry were checked.