The article draws attention to the problem of the presence of metals: germanium (Ge), tellurium (Te), thallium (Tl), and others (Cd, Ba, Co, Mn, Cr, Cu, Ni, Pb, Sr, and Zn) in selected waste of electrical and electronic equipment (WEEE). As a result of the growing demand for new technologies, the global consumption of TECs has also been increasing. Thus, the amount of metals in circulation, of which the impacts on the environment have not yet been fully understood, is constantly increasing. Due to the low content of these metals in WEEE, they are usually ignored during e-waste analyses. The main aim of this study was to determine the distribution of Ge, Te, and Tl (and other elements) in ground sieve fractions (1.0, 0.5, 0.2, and 0.1 mm) of selected electronic components (solar lamps, solar cell, LED TV screens, LCD screens, photoresistors, photodiodes, phototransistors) and to determine the possible tendency of the concentrations of these metals in fractions. This problem is particularly important because WEEE recycling processes (crushing, grinding, and even collection and transport operations) can lead to dispersion and migration of TCE pollutants into the environment. The quantitative composition of e-waste was identified and confirmed by ICP-MS, ICP-OES and SEM-EDS, and XRD analyses. It was found that Ge, Te, and Tl are concentrated in the finest fractions of ground e-waste, together with Cd and Cr, which may favor the migration of these pollutants in the form of dust during storage and processing of e-waste.

The optimization and validation of a methodology for determining and extracting inorganic ionic Te(VI) and Te(IV) forms in easily-leached fractions of soil by Ion Chromatography-Inductively Coupled Plasma-Mass Spectrometry (IC-ICP-MS) were studied. In this paper, the total concentration of Te, pH, and red-ox potential were determined. Ions were successfully separated in 4 min on a Hamilton PRPX100 column with 0.002 mg/kg and 0.004 mg/kg limits of detection for Te(VI) and Te(IV), respectively. Soil samples were collected from areas subjected to the influence of an electrowaste processing and sorting plant. Sequential chemical extraction of soils showed that tellurium was bound mainly with sulphides, organic matter, and silicates. Optimization of soil extraction allowed 20% average extraction efficiency to be obtained, using 100 mM citric acid as the extractant. In the tested soil samples, both tellurium species were present. In most cases, the soils contained a reduced Te form, or the concentrations of both species were similar.

Background: E-cigarettes (ECs) seem to be a less harmful alternative for conventional cigarettes, however, very little is still known about the exposure to some elements, which are the components of this device and may contaminate the nicotine liquid. The aim of this study is to assess whether e-cigarette users are more exposed to 12 elements detected in aerosol than non-smokers and conventional cigarette smokers, using their concentrations in urine as exposure biomarkers. Methods: A cross-sectional, group-based survey was carried out using 90 volunteers classified into groups of non-smokers, EC-only users, dual EC users-cigarette smokers and cigarette-only smokers. Using inductively coupled plasma mass spectrometry (ICP-MS) and electrothermal atomic absorption spectrometry (ETAAS), Cr, Ni, Co, Ag, In, Mn, Ba, Sr, V, Sb, Cd and Pb levels were measured in spot urine samples. Among the selected groups, a comparison was made using the analysis of covariance and correlations with EC usage pattern were assessed by multiple linear regression. Results: Element concentrations in urine of EC-users were not significantly different from the levels found in non-smokers and smokers. Only in the case of Ba, Ni and Sb was a significant correlation found in relation to some e-cigarette usage patterns. Conclusion: Transfer of the investigated elements to the EC aerosol was not found to be a substantial source of exposure in EC users who quitted smoking.

Migration of metals/metalloids and their inorganic forms from bottom sediments into waters and from waters into bottom sediments is a complex process. Understanding this mechanism is essential for recognising transformations that occur in water reservoir ecosystems. The following research was conducted in 2012–2014. The aim was to define the time and spatial correlations in the changes of total and ionic antimony, arsenic and chromium concentrations in waters and bottom sediments of three water reservoirs located in Upper Silesia (Poland), i.e. Pławniowice, Rybnik and Goczałkowice. The ionic form contents were determined with high-performance liquid chromatography-inductively coupled plasma-mass spectrometry (HPLC-ICP-MS). The research was carried out to verify whether the bottom sediments deposited in the discussed reservoirs could have posed an environmental threat due to the possible release of toxic ionic forms (i.e. As(III), Sb(III) and Cr(VI)) into the pelagic zone. The comparison of the research results obtained for three reservoirs (being under different anthropopressure influence) enabled the researchers to describe the bioavailability of specific elements and their species. It also helped to discern the existing environmental threats for such water reservoirs and their users.

The optimization of new methodology for simultaneous determination of arsenic [As(III), As(V)] and antimony [Sb(III), Sb(V), SbMe₃] species using high-performance liquid chromatography (HPLC) coupled with inductively coupled plasma mass spectrometry (ICP-MS) in water and bottom sediment samples collected from the dam Kozłowa Góra Reservoir (Poland) was studied. Samples were collected monthly from May to September 2018 in four-point (water) and fifth-point (sediment) transects. The contents of Mn, Co, Ni, Cu, Zn, As, Cr, Rb, Sr, Cd, Sb, Ba, Tl, Pb, and Sb were studied in water and bottom sediments using ICP-MS techniques. Additionally, arsenic and antimony fractions were determined in sediments with the BCR method. Pollution Load Index (PLI), Geoaccumulation Index (I_geo), LAWA classification, and Sb/As ratio indicated the presence of extreme sediment pollution for Zn, Cd, Pb, and Cr from anthropogenic sources. Research has shown that the easy-leached bottom sediment fraction contained in most cases more As(V) and Sb(V). But often Sb(V) concentration was equal as Sb(III), which can be released into the pelagic zone under favorable conditions. Even though As(V) and Sb(V) prevail in the reservoir bottom sediments, they can be transformed into As(III) and Sb(III) as a result of drastic changes in pH or redox potential. The Kozłowa Góra sediments are heavily polluted with Pb, Zn, Cd, and As, Cu, and Ni. The highest concentrations of the heavy metals were recorded in the middle of the tank and there was a small spatial variability. The migration of metals along the reservoir transect was closely related to its morphometry.