The current study included the investigation of several metals and their distribution in urban soils from parks and green areas in the city of Belgrade. The soils were sampled in January and February 2008. The concentrations of Cd, Co, Cu, Pb, Mn and Zn were measured, as well as the pH values and organic matter contents. The obtained results showed that there was a significant level of contamination in some samples, especially with lead, and that it was most probably caused by anthropogenic activities, mostly from traffic. The results were compared with the National legislation and Netherlands standards. Also, the recent results were compared with the data from previous work and it was concluded that there has been a certain increase of the Pb concentration in the past three years. The level of pollution in playground soil was very high and each analyzed sample exceeded the Dutch target value for Cd, Co and Pb.

Considering the rising demand for rare earth elements (REEs), researchers are looking for new sources for their extraction, thereby fostering economic and environmentally justified processing solutions. Among potential industrial sources, coal fly ash emerges as one of the most promising. The recovery of REEs from coal fly and bottom ashes derived from different thermal power plants was the main focus of this study. A dual-step methodology was conducted on ash samples, which involved an ultrasonic roasting process to disintegrate the silica matrix, followed by a microwave-assisted acid leaching step to extract REEs. The roasting procedure was studied using the Plackett–Burman design, and the Box–Behnken design was subsequently implemented to optimize the leaching procedure. The optimized ultrasonic roasting procedure was set up at 95 °C for 10 min with an ash-to-roasting agent (3M NaOH) ratio of 0.5:1 (m/V). For acid leaching, the optimal conditions were obtained at 174 °C for 30 min with an HCl ÷ HNO₃ mixture (1:1 V/V). The standard reference material (NIST 1633c) was used in the conclusive experiments to estimate the average recovery (80%) of REEs. The green aspects of this methodology were evaluated using several metrics (atom economy, E-factor, and energy consumption). The proposed process outperforms high-temperature roasting procedures in terms of greenness; however, the REE recovery rate is lower.

In this work multiwalled carbon nanotubes (MWCNTs) modified by oxidation (o-MWCNTs) and by aminofunctionalization (e-MWCNTs) were examined as potential adsorbents for arsenate removal from water. Adsorption characteristics of raw and modified MWCNTs were investigated in batch adsorption experiments. The influence of solution pH (pH range 3–10), contact time, and temperature (25, 35, and 45°C) were studied. Ethylenediamine-functionalized MWCNTs have the greatest affinity for arsenate ions, followed by o-MWCNTs and raw-MWCNTs. The obtained experimental data for raw- and o-MWCNTs fitted Sips isotherm model, while for the e-MWCNTs, the Freundlich model provided the best fit to the experimental points. The maximum adsorption capacity for arsenate ions was achieved using e-MWCNTs, 12.18 mg g⁻¹. The presence of the arsenate on the adsorbent is confirmed by FTIR spectroscopy. Thermodynamic studies indicated the spontaneity and endothermic nature of the adsorption. Sodium hydroxide solution (0.1 M) was found to desorb about 70% of arsenate from e-MWCNTs. The results with spiked drinking water samples demonstrated that e-MWCNTs, due to the present basic and acidic groups, were very efficient for the removal of arsenate ions, as well as of some cations, at pH 4.

This study investigated the occurrence and distribution of rare earth elements (REEs), including 14 lanthanoids, scandium (Sc), and yttrium (Y), in groundwater around a large coal-fired thermal power plant (TPP). The ICP-MS technique was used to analyze 16 REEs in groundwater samples collected from monitoring wells. REE concentrations ranged from 59.9 to 758 ng/L, with an average of 290 ng/L. The most abundant was Sc, followed by La, accounting for 54.2% and 21.4% of the total REE concentration, respectively. Geospatial analysis revealed the REE enrichment at several hotspots near the TPP. The highest REE concentrations were observed near the TPP and ash landfill, decreasing with the distance from the plant and the landfill. REE fractionation ratios and anomalies suggested the Light REE dominance, comprising over 78% of the total REEs. Correlation and principal component analyses indicated similar behavior and sources for most REEs. Health risk assessment found hazard indices (HI) of 1.36 × 10⁻³ and 1.98 × 10⁻³ for adults and children, respectively, which are far below the permissible limit (HI = 1). Likewise, incremental lifetime cancer risks (ILCR) were all below 1 × 10⁻⁶. Nevertheless, ongoing ash disposal and potential accumulation in the environment could elevate the REE exposure over time.

Emission factors (EFs) of gaseous pollutants, particulate matter, certain harmful trace elements, and polycyclic aromatic hydrocarbons (PAHs) from three thermal power plants (TPPs) and semi-industrial fluidized bed boiler (FBB) were compared. EFs of particulate matter, trace elements (except Cd and Pb), benzo[a]pyrene, and benzo[b]fluoranthene exceed the upper limits specified in the EMEP inventory guidebook for all combustion facilities. The comparison of trace elements and PAHs content in fly ashes (FAs) from lignite and coal waste combustion in TPPs and FBB, respectively, as well as the potential environmental impact of FAs disposal, was performed by employing a set of ecological indicators such as crustal enrichment factor, risk assessment code, risk indices for trace elements, and benzo[a]pyrene equivalent concentration for PAHs. Sequential analysis shows that the trace elements portion is the lowest for water-soluble and exchangeable fractions. The highest enrichment levels in FAs are noticed for As and Hg. Based on toxic trace elements content, FAs from TPPs represent a very high ecological risk, whereas fly ash from FBB poses a moderate ecological risk but has the highest benzo[a]pyrene equivalent concentration, indicating its increased carcinogenic potential. Lead isotope ratios for Serbian coals and FAs can contribute to a lead pollution global database.

Eight selected trace elements, which are generally included in regulations, were analyzed in 23 types of bottled waters. Ten mineral and seven spring bottled waters were from the Serbian market and six mineral bottled waters were obtained in different EU countries. For the purpose of comparison, selected tap waters were also analyzed. Inductively coupled plasma mass spectrometry (ICP-MS) was used for the analysis of trace elements (arsenic, cadmium, copper, manganese, nickel, lead and antimony). Results were compared with the Serbian regulations for bottled water, EU regulations and guideline values set by the World Health Organization for drinking water. With few exceptions, the trace element levels of most bottled waters were below the guideline values. However, a higher content of antimony was observed in waters from polyethylene terephthalate (PET) containers, indicating a potential leaching of this element from the plastic packaging.