In this work, the determination of moving averages is proposed as a method for quantifying metal, arsenic, and sulfate discharges into a water course undergoing acid mine drainage processes which flows into a public water supply dam in the Iberian Pyrite Belt. The analysis of the results obtained by applying moving averages shows that the highest metal and sulfate concentrations occur in October, coinciding with the first rainfall and the sponging of mine dumps, with November and December being the months when the highest contributions to the Andevalo Dam take place. The discharge of acid mine waters with its corresponding metal load into the Andevalo Dam means, for a single hydrological year, more than 6,000 t of sulfates, almost 600 t of iron, and 1 t of As, of special relevance for the hydrochemical quality of the stored waters. When they arrive at the dam, these metals precipitate, since the water pH is near 7, and remain latent in the bottom sediment as long as the chemical makeup of the dam water does not change.

Urban soils are an essential element of the city environment. However, studies on urban soils are scattered in terms of geographical distribution, sampling pattern, analytical dataset, etc. One of the major issues arising from the studies on this ecosystem is the diffusion of its contamination. In cities, in fact, the proximity to humans may cause a serious danger for citizens. In the present study, results from the literature about trace elements in urban soils are presented to compare methodologies and results and to offer a basis for the harmonization of investigation approaches and establishment of remediation thresholds. A total of 153 studies on the urban ecosystem published in the last 10 years were collected and data on trace elements in soils of 94 world cities were compared and discussed. Data highlights the discrepancies among different studies (sampling strategies, analytical procedures) and the extreme variability of urban soils. Most cities are contaminated by one or more trace elements, revealing the environmental relevance of the urban soil system. While Pb is still one of the major concerns in many locations, new contaminants are on the rise and would deserve more attention from the researchers. While in fact some contaminants are almost ubiquitous in world cities and could be used as tracers for urban contamination, some traffic-related elements such as platinum, rhodium, and palladium, whose reactivity and toxicity is still unknown, are becoming of concern. Collation of literature data highlights the need for the harmonization of sampling, analytical, and rendering procedures for regulatory purposes and provides a useful dataset for environmental scientists dealing with the urban ecosystem and for city planners. A sampling design adapted to local urban patterns, a prescribed sampling depth, and a minimum set of elements that deserve to be measured could be the core of a common methodology.

It is well known that mass transfer of a solid compound into a liquid phase is characterized by mutual properties of both sides. Solubilization capacity of the liquid phase is primary affected by its composition in inorganic species inducing salting in/out effect evaluated by Setschenow constant, generally defined at 298.15 K. On the other hand, the equilibrium process is highly influenced by polar compatibility issue. Therefore, the study of such transfer is essential in order to set the role of each party participating in the solid-liquid equilibrium. Thus, a comparison of transfer magnitude and feasibility of carbaryl from pure water, to seawater, and lab-made seawater was held. To do so, solubility of the compound was experimented at different temperature in multiple media. Solubility determination is based on the saturation of a specific heated fluid passing through a saturation cell. The solute transported is subsequently trapped in a specific extraction column. Back flashing method is then applied to dissolve the compound. After validation, aqueous solubility of carbaryl was studied as function of temperature ranging from (273.15 to 318.15 K) at atmospheric pressure. In addition, solubility was determined in pure, seawater, and corresponding lab-made water, thus solubility values ranged from 3.57E-06 to 3.49E-05 in pure water, from 3.04E-06 to 2.53E-05 in seawater and from 6.51E-06 to 3.61E-05 in lab-made water. As a result, thermophysical properties of transfer and usage of lab-made water on the mass transfer properties divergence was spotted. The Salting out phenomenon observed for carbaryl was interpreted by the internal pressure theory that suggests the reduction of internal cavities in the presence of salt, making solubilization process more difficult to achieve. Thus, showing an overall endogenic process with a positive Gibbs free energy of transfer that is highly affected by the magnitude of salting out effect and the temperature. The molar entropy of transfer increases versus temperature caused by the disorder of solvent molecules due to the dissolution process.

The effects of anthropogenic activities on water, environment, and consequently quality of life can be evaluated using genetic, biochemical, and microbiological parameters. Regarding genetic parameters, the micronucleus test is a fast, efficient, inexpensive method for detecting alterations in genetic material induced by a variety of genotoxic agents. In the present study, blood cells from Poecilia vivipara from the Belém River in the city of Curitiba, Paraná, Brazil were evaluated for genotoxic effects stemming from human-produced pollution, as expressed by the micronucleus. The water in the river was evaluated with regard to physiochemical and microbiological parameters as well as for heavy metals. The analysis revealed the presence of copper, zinc, and nickel, with high concentrations of copper. The micronucleus analysis revealed significant differences in relation to the groups (study and control), suggesting a positive relation between the water quality of the Belém River and micronucleus expression as a result of the pollution to which this river is subjected.

The preparation, characterization, and environmental application of crosslinked chitosan-coated bentonite (CCB) beads for tartrazine adsorption have been investigated. CCB beads were characterized by using Fourier transform infrared spectrophotometer (FTIR), scanning electron microscope (SEM), and Brunauer-Emmett-Teller (BET) surface area and Barrett-Joyner-Halenda (BJH) pore size distribution analyses were also determined. The values of pH of the aqueous slurry and pH of zero point charge (pHZPC) were almost equal. The adsorption at equilibrium of tartrazine was found to be a function of pH of the solution, stirring rate, contact time, and tartrazine concentration. The optimum conditions for tartrazine adsorption were pH 2.5, stirring rate of 400 rpm and contact time of 80 min. Pseudo-first-order and pseudo-second-order models were used to analyze the kinetics of adsorption with the latter found to agree well with the kinetics data, suggesting that the rate determining step may be chemisorption. The two most common isotherm models, Langmuir and Freundlich, were used to describe the adsorption equilibrium data. On the basis of Langmuir isotherm model, the maximum adsorption capacities were determined to be 250.0, 277.8, and 294.1 mg g⁻¹ at 300, 310, and 320 K, respectively. Desorption studies were carried out at different concentrations of EDTA, H₂SO₄, and NaOH. All desorbing solutions showed poor recovery of tartrazine.

Composting municipal wastewater sludge may generate composting wastewater (acid washer water and tunnel wastewater) with high ammonium-nitrogen (NH₄-N) concentration; this kind of wastewater is usually generated in a rather small daily amount. A procedure of air stripping with catalytic oxidation was developed and tested with pilot-scale and full-scale units for synthetic disposal of the high NH₄-N wastewaters from composting facilities. In air stripping, around 90% NH₄-N removal efficiency was reliably achieved with a maximum of 98%. A model to describe the stripping process efficiency was constructed, which can be used for process optimization. After catalytic oxidation, the concentrations in the outlet gas were acceptable for NH₃, NOX, NO₂, and N₂O, but the NH₃ and N₂O concentrations limited the feasible loading range. The treatment costs were estimated in detail. The results indicate that air stripping with the catalytic oxidation process can be applied for wastewater treatment in composting facilities.

We evaluated the applicability of a simple passive sampling method to quantify HNO₃(g) in ambient air. The method has the advantages of not only ease of operation but also low cost. A sampling velocity of 214 m day⁻¹ was determined based on the concentration of HNO₃(g) measured by the four-stage filter-pack method at nine sites located within a 250 × 250-km area in Japan. This sampling velocity was applied at sites located outside of area to verify the applicability and accuracy of the simple passive sampling method. The variation in the results for the application of the sampling velocity ranged from 0.39 to 0.95. The simple passive sampling method should be applied to sites with different meteorological conditions, and the obtained data should be used to obtain more significant information and/or to indicate the need for further developments in the methodology.

Actually, there is a growing interest in finding efficient low-cost materials that allow the removal of chemical substances from water in order to decrease the environmental impact. The use of nanoscale systems is a new area of investigation for the elimination of polluting agents from water among other useful applications in science and technology. In this work, removal of indigo blue in water solutions has been evaluated using Fe/Cu nanoparticles and composites of C/Fe–Cu nanoalloy. The first composite was using carbon obtained by pyrolysis of sewage sludge with Fe/Cu nanoparticles (MCL-NP); the second one was made with commercial activated carbon and Fe–Cu nanoparticles (CAC-NP). Synthesis of materials were carried out by the sodium borohydride reduction of FeSO4[Symbol: see text]7H2O and CuSO4[Symbol: see text]5H2O aqueous mixture. Batch adsorption and isotherm experiments were carried out in order to know the behavior of each adsorbent material employed. The experimental data were adjusted to Langmuir, Freundlich, and BET models.

Arsenic (As) contamination of the environment has emerged as a concerning issue recently for which phytoremediation has been suggested as a viable solution. Hydrilla verticillata (L.f.) Royle is a widely distributed rapidly growing aquatic weed possessing significant potential to accumulate As and is thus a potential candidate for the purpose of As phytoremediation. In the present study, an investigation of thiol metabolism was conducted in H. verticillata, which revealed differential effects upon exposure to arsenite [As(III)] and arsenate [As(V)]. The accumulation of arsenic was found to be higher upon exposure to As(III) than to As(V). Besides, As(III) was found to induce the activities of enzymes, such as cysteine synthase and γ-glutamylcysteine synthetase and the amounts of cysteine and glutathione (GSH) to higher levels than that observed with As(V). The activity of glutathione-S-transferase was, however, stimulated to a higher level upon exposure to As(V) than As(III). The activity of arsenate reductase was found to increase upon As(V) exposure at all concentrations and durations. In addition, a significant stimulation in the activity of phytochelatin synthase was noticed in vitro with an increase in As/GSH concentration and time of incubation. Arsenic detoxification in H. verticillata thus appeared to involve an induction of thiol synthesis and consumption in a coordinated manner, though differentially upon exposure to As(III) and As(V). The information gained through this study would help in better designing of the pilot experiment at the field level depending on the chemical composition of the contaminated water.

This work aimed to determine the sensitivity of acetylcholinesterase (AChE) and glutathione S-transferases (GST) activities of Crangon crangon (L.) to the water-accommodated fraction (WAF) of the fuel oil spilled by the oil tanker Prestige, in order to assess their usefulness as markers for this kind of pollution. Laboratory exposure of shrimps to WAF of weathered Prestige fuel oil showed no significant interference with AChE activity. Significant induction of GST activity was observed, potentially as a result of high concentrations of polycyclic aromatic hydrocarbons. However, these results were only obtained with the higher WAF concentrations tested. It was concluded that AChE and GST activities of C. crangon were not useful biomarkers for short-term exposure to the WAF of fuel oil spilled by the tanker Prestige and carried to the beaches of Galicia (NW Spain).