Magnetic nanoparticles of CoFe₂O₄ were synthesized by co-precipitation method. The magnetic material silicalite-2@CoFe₂O₄ (SC) was prepared by using tetrabutylammonium hydroxide as the template, tetraethoxysilane as the silica source and CoFe₂O₄ as the magnetic core. TiO₂/silicalite-2@CoFe₂O₄ (TSC) magnetic photocatalyst was prepared by sol-gel technique using SC particles as the supporter and tetrabutyltitanate as the titanium source. The samples were characterized by X-ray diffraction, scanning electron microscopy, N₂ adsorption-desorption, Fourier transform infrared spectroscopy, and ultraviolet (UV)–visible diffuse reflectance spectra. The reduction of Cr(VI) in aqueous solution by UV/TSC process was studied under various operating conditions. The results demonstrate that the as-synthesized TSC has high photocatalytic activity due to the high dispensability of TiO₂ provided by silicalite-2@CoFe₂O₄. The removal of Cr(VI) reached 72.9 % by using 0.6 g/L of TSC under the optimum conditions within 180 min. The photocatalytic reduction of Cr(VI) by TSC followed the Langmuir–Hinshelwood kinetic model. At the end of the reaction, TSC could easily be recovered and could be reused without the significant loss of the catalytic activity.

The growing pollution mainly caused by the discharge of industrial, sanitary, and agricultural wastes has become one of the main current environmental issues. Thus, the use of bioindicators has become an important tool for investigating environmental imbalance. In this context, microorganisms have shown to be important for the identification of altered environments because of their ubiquity and their ability to grow in inhospitable habitats. Yeasts of the genus Candida are potential bioindicators because of their ability to survive in contaminated freshwater environments. Besides, they are more frequently recovered than fecal coliforms. It is noteworthy that the nonspecific activity of efflux pumps, which help in cellular detoxification processes, may be associated with the presence of chemical compounds in contaminated environments. Thus, the activity of efflux pumps may be the main mechanism involved in the resistance to azole derivatives in Candida spp. and the assessment of their activity may also be a tool for environmental monitoring. As a result, the phenotypical and molecular evaluation of this antifungal resistance in Candida species has been pointed as a promising tool for monitoring the quality of aquatic environments. Hence, the objective of this study was to collect and systematize data pointing to an alternative use of Candida spp. as bioindicators by assessing the occurrence of azole resistance among environmental Candida as a strategy to monitor the quality of freshwater environments.

The estimated diffusion fluxes of methane (CH₄) and carbon dioxide (CO₂) at the sediment–water interface in the Rzeszów Reservoir in southeastern Poland are presented. The relevant studies were conducted during 2009, 2010, and 2011. Calculated fluxes ranged from 0.01 to 2.19 mmol m⁻² day⁻¹and from 0.36 to 45.33 mmol m⁻² day⁻¹for methane and carbon dioxide, respectively. While the values for calculated diffusion fluxes of methane are comparable with those reported for other eutrophic reservoirs, much higher values were obtained here for carbon dioxide. The resulting values of δ¹³C-CH₄and the fractionation coefficients between methane and carbon dioxide (αCH₄-CO₂) suggest that methane in the sediment of the Rzeszów Reservoir is produced by acetate fermentation, while the hydrogenotrophic methanogenic process is of successively greater importance with increasing depth. In the top layer of the sediment, 24–72 % of CO₂came from methanogenesis, while the contribution made by the degradation of organic matter by methanogenesis to CO₂was greater in the deeper layer.

Rhizoctonia zeae SOL3 fungus was isolated from contaminated soil based on its ability to decolorize remazol brilliant blue R in solid medium. This fungus has been used to degrade pyrene a four-ring polycyclic aromatic hydrocarbon. R. zeae SOL3 could biodegrade pyrene as a sole source of carbon and energy. Different parameters were investigated to study their effect on the biodegradation rate. The highest biodegradation rate reached at 28 °C, non-agitated culture, 20 g/L glucose, 24 g/L NaCl, and 20 mg/L pyrene. The metabolites of pyrene were detected by thin layer chromatography (TLC) and confirmed by gas chromatography–mass spectrometry (GC-MS), which were identified as benzoic acid, 4-hydroxybenzoic acid and botanic acid.

We analysed nutrients and basic ions (Na, Cl, K, Mg, Si, Ca, and SO₄) for a period of 1 year, including every precipitation event, and sampled stream water every 2 weeks from a forest catchment in Shimane Prefecture, Japan. Backward-trajectory analysis revealed that some air masses originated within Japan, but did not affect the precipitation chemistry. Air masses originating from northern China were positively correlated with nutrients and all basic ions. Concentrations of ammonium and dissolved organic nitrogen were much lower in stream water than in precipitation, while those of nitrate and particulate nitrogen were similar in stream water and precipitation. Unlike nitrogen, the dissolved phosphorus concentration was much higher in stream water than in precipitation. Both phosphate and dissolved organic phosphorus (DOP) levels were higher in stream water than in precipitation. Particulate phosphorus (PP) concentrations were very similar in precipitation and stream water. PP showed stronger correlations than potassium with suspended solids (SS) and flow rate, while phosphate and DOP were more strongly correlated with potassium than with SS or flow rate. Stream silica concentrations were not correlated with phosphate but did exhibit a significant negative correlation with DOP. Neither phosphate nor DOP was correlated with calcium. These results suggest that phosphorus is not leaching with silica or calcium as a paired cation, but rather with potassium in this area. Lower nitrogen concentrations in stream water than in precipitation can be attributed to an enhanced uptake of nitrogen by forest soils owing to the increased atmospheric deposition of phosphorus.

The majority of the existing water bodies around the world are increasingly polluted with oily wastewater. The aim of this study was to investigate the role of single protozoan isolates (Aspidisca, Trachelophyllum and Peranema) and of a consortium of these three protozoan isolates in the biodegradation of fats and oils present in polluted domestic wastewater. The biomass of protozoan isolates, chemical oxygen demand (COD), dissolved oxygen (DO) and concentrations of fats and oils were determined in triplicate before and after the inoculation of isolates in oily wastewaters, using standard methods. Results revealed optimum growth of protozoan cell densities under favourable conditions of 30 °C, pH 6 and 8 (from 1.00 to 4.00, 3.96, 3.80 and 4.20 × 10²cells/ml for Aspidisca, Trachelophyllum, Peranema and a consortium of the three isolates, respectively). The average percentage uptake of DO by Aspidisca, Trachelophyllum, Peranema and their consortium was 95, 96, 96 and 100 %, respectively, for both 30 and 25 °C and at pH levels of (4, 6, 8 and 10), respectively. The results revealed that the COD removal rates of the isolates at various pH levels were ≥20 and ≤90 %, respectively, for 30 and 25 °C. At a temperature of 30 °C, the biodegradation capabilities of the isolates ranged from 3.0 to 8.0, 3.0 to 6.0, 7.0 to 11.0 and 8.0 to 22.0 %, while at 25 °C, the biodegradation rates were 3.0 to 6.0, 4.0 to 7.0, 3.0 to 8.0 and 4.0 to 15.0 % for Aspidisca, Trachelophyllum, Peranema and the consortium of these three isolates, respectively.

Chemical contamination of water resources on the planet generates a range of environmental disturbances which impair ecosystems. Humans ingest such chemicals often present in water. Conventional treatments fail to remove these contaminants from water, requiring complementary methods such as activated carbon filters, reverse osmosis, or distillation, which are expensive and seldom used in the public water supply. In recent years, there has been a search for alternative eco-friendly, low-cost methods which can effectively remove these contaminants. This study was conducted to test the effectiveness of biotite (black mica), an igneous mineral of the mica group, in removing pesticides from water. A trial was designed to assess the rate of pesticide removal using a methodology based on axes of variation of pH, temperature, concentration, and time. The pesticides tested were atrazine, fluazifop-p-butyl, lambda-cyhalothrin, chlorpyrifos, and lactofen. The results showed higher removal rates in acidic conditions (pH 3) and temperatures between 20 and 30 °C, requiring about 6 h to reach maximum adsorption. More than 80 % of all the pesticides were adsorbed. The best result was obtained for fluazifop (94.2 %) in 6 h, under pH 3, and temperature of 25 °C. The study revealed that biotite has a high absorption capacity of complex and varied compounds. These findings signal the need for further studies and tests. Due to the high cost of pesticide analysis, which can only be made using a chromatograph mass spectrometer, financial resources will be required.

The analysis of 18 elements in muscle, liver, gills, and gonads of sichel (Pelecus cultratus), ruffe (Gymnocephalus cernua), and European perch (Perca fluviatilis), caught at a polluted segment of the Danube River near Belgrade, was carried out with the aim to expand the knowledge about the ecotoxicology of these species for monitoring purposes and the possible impact on human health. Generally, the elemental concentration significantly differed between species and tissues (p < 0.0001), and a statistical interaction between these two factors was observed (p < 0.0001). In muscle and liver, concentrations of Hg and Se were statistically higher in ruffe than in sichel and European perch. In gills, statistically highest concentrations of Mn, Sr, and Zn were found in sichel, and of Fe in European perch. In gonads, statistically highest concentrations of As were detected in sichel, of Zn in ruffe, and of Mn and Mo in European perch. The highest number of coefficients of partial correlations between fish weight and element levels was found in sichel (11 in total). Of all analyzed elements, Al and B had the highest number of partial correlations in tissues. The levels of Hg exceeded the maximum acceptable concentration (0.5 mg kg⁻¹) in all muscle samples, which can pose a risk for human consumption. Different diet preferences of the investigated fish species resulted in a different accumulation of elements in tissues, and ruffe (as a species that consume mainly benthic macroinvertebrates) accumulated the highest level of Hg, which makes it suitable for monitoring of this element in water bodies.

Biochar has attracted recent research interest as a metal adsorbent. The heavy metal adsorption capacity of biochar can be controlled by the carbonization of biochar. The adsorption characteristics of heavy metals (Pb, Cu, and Cd) by peat moss-derived biochars produced under different carbonization conditions were investigated by a series of batch experiments. Biochars were produced by the pyrolysis of peat moss over a temperature range of 400–1000 °C for 30–90 min. Biochar produced at 800 °C for 90 min was the most efficient for the removal of Pb and Cu, when weight loss ratio was considered. The pseudo-second-order and Langmuir models adequately described kinetics and isotherms, respectively, of heavy metal adsorption on peat moss-derived biochar, indicating that heavy metal ions were chemically adsorbed on the adsorption sites as uniform monolayer. The peat moss-derived biochar showed the highest maximum adsorption capacity for Pb (81.3 mg/g), followed by Cd and Cu, which were 39.8 and 18.2 mg/g, respectively. This study shows that peat moss-derived biochar is an effective adsorbent to remediate heavy metal-contaminated water.

To develop an efficient adsorbent for humic acid, the present study represents the first attempt to investigate the capability of zeolitic imidazole frameworks to remove humic acid from water. Zeolitic imidazole framework-8 (ZIF-8) is particularly selected as a prototype ZIF to adsorb humic acid owing to its high stability in aqueous solutions. ZIF-8 was synthesized and characterized using scanning electronic microscopy (SEM), powder X-ray diffraction pattern (PXRD), Fourier transform infrared spectroscopy (FT-IR), and thermogravimetric analyzer (TGA) and then used to adsorb humic acid under various conditions. The structure of ZIF-8 was found to remain intact after the exposure to humic acid in water. Factors affecting the adsorption were examined, including solid-to-liquid ratio, mixing time, temperature, pH, presence of salt, and surfactants. The adsorption capacity of ZIF-8 was found to be much higher than that of activated carbon, fly ash, zeolites, graphite, etc., showing its promising potential for removal of humic acid. The adsorption mechanism could be attributed to the electrostatic interaction between the positive surface of ZIF-8 and the acidic sites of humic acid, as well as the π–π stacking interaction between imidazole of ZIF-8 and benzene rings of humic acid. The humic acid adsorption to ZIF-8 could be enhanced in the acidic conditions, and the adsorption process remained highly stable in the solutions of a wide range of NaCl concentrations. ZIF-8 can be also regenerated by simple ethanol-washing process and reused for humic acid adsorption. These features enable ZIF-8 to be an efficient and stable adsorbent to remove humic acid from water.