The tailings produce acid mine drainage (AMD) due to sulfide minerals, especially pyrite oxidation. AMD has caused serious pollution to the surrounding aquatic and terrestrial ecosystems because of its famous low pH value and high metal and sulfate concentration, which is an urgent environmental problem faced by the world’s ore mining industry. Here, we show that silicic protective surface films can suppress the oxidation of pyrite-bearing tailings for AMD control at-source without pre-oxidation of pyrite and solution pH adjuster and buffer. We found that the silicic protective surface films formed by calcium silicate can inhibit the oxidation of pyrite-bearing tailings and reduce the production of AMD through chemical leaching tests. Fourier transform infrared (FTIR) analyses and scanning electron microscopy with energy-dispersive spectrometry (SEM/EDS) confirmed the presence of silicic protective surface films of calcium silicate on the surface of pyrite-bearing tailings.

The removal of Acid Orange 51 (AO 51) dye in aqueous solution by microscale zero-valent iron (m-ZVI) was investigated. The m-ZVI powder was characterized granulometrically by laser particle sizer and morphologically by transmission electron microscopy (TEM). The effects of pH, m-ZVI concentration, H₂O₂ addition, and dye concentration on the decolorization of AO 51 were experimentally investigated. Results indicate that the removal efficiency is independent from pH values, increases with increasing ZVI dosage, and decreases with dye concentration. With 1 g/L of m-ZVI, AO 51 was effectively removed without and with addition of 25 mM H₂O₂, yielding a decolorization efficiency of around 70% and 98%, respectively, at pH 3 within 60 min of reaction time. The involvement of ˙OH in oxidizing AO 51 was examined by measuring the removal rates based on ˙OH scavenging molecule. Finally, the disappearance of AO 51 was estimated by monitoring the UV–Vis spectral evolution after 120 min of treatment while the Fourier-Transform Infrared spectroscopy (FT-IR) was performed to verify the occurrence of organic sorption on m-ZVI surface. The scanning electron microscope (SEM) images before and after the reaction illustrated morphological changes on m-ZVI surface. The detoxification of the treated solution was demonstrated using phytotoxicity test.

Mechanochemical degradation (MCD) technology has shown its remarkable potential in the disposal of persistent organochlorines in a non-combustion manner. In the present study, endosulfan, as the newly listed persistent organic pollutants (POPs) in the Stockholm Convention, was investigated for its feasibility of mechanochemical destruction using high-energy ball milling. Using calcium oxide (CaO) as a co-milling reagent, the degradation efficiency of endosulfan was nearly 100% after ball milling for 60 min, while the dechlorination efficiency and the sulfate formation efficiency were delayed for endosulfan degradation. After ball milling for 120 min, the dechlorination efficiency and sulfate formation efficiency reached 87.55% and 26.28%, respectively. Based on the measurement results from various material characterization approaches, the main degradation pathway of endosulfan was proposed as sequential dechlorination followed by the destruction of hydrocarbon skeleton. The GC-MS analysis confirmed that complete desulfurization and dechlorination had been realized finally. This study provides an option for the way toward the efficient and rapid destruction of endosulfan as a new POPs using mechanochemical technology.

Nowadays, the extensive use of pesticides in crops production puts a significant challenge to minimize its side effects along with safe production, storage, and after-use treatment. This paper reports results related to the emission of certain pesticide formulations through the PET containers, as well as, their mitigation to the PET containers during their storage. The influence of storage time on cypermethrin migration to and through the PET was studied in short-term Collaborative International Pesticides Analytical Council test lasting up to 30 days. The PET containers were filled with pure xylene and pesticide formulations, where the amount of active substance, cypermethrin (CY), varied from 5 to 20 wt%, while the amount of emulsifier was kept constant. The results indicate that pesticide formulations diffuse to PET containers with an average increase of its initial mass up to 1.5%. The most intensive diffusion is in the first 24 months of storage, after its rate significantly decreases. It should be noted that the diffusion studied pesticide formulations are also very dependent on CY concentration. Besides the migration to the PET containers, it was also found that pesticide formulation was emitted through the PET containers in the first 17 to 24 months of storage depending on CY concentration. Emission rates were also dependent on CY concentration and were in the range of 15.3 to 38.0 mg/month·container. The emission through the PET containers was successfully predicted using artificial neural networks with R² = 0.94 and the mean absolute percentage error (MAPE) of only 6.2% on testing.

Milk can be considered as an indicator of the degree of environmental contamination of the place where it is produced and this is especially important when assessing its content in toxic metals. Therefore, 36 bovine milk samples from 7 farms with a semi-extensive grazing system were analysed, located in Asturias (Spain), in an area with high probability of being highly contaminated due to a mining zone, with important industrial activity and near high-density highway traffic. The samples were lyophilised to achieve total dehydration, further analysed using inductively coupled plasma mass spectrometry (ICP-MS). The metals titrated were aluminium (Al), arsenic (As), molybdenum (Mo) and mercury (Hg) in the lyophilised samples and subsequently extrapolated their values to whole milk. All samples analysed showed levels of Al and Mo above the limit of detection, with mean values of Al of 140.89 ± 157.07 in liquid milk and 1065.76 ± 1073.45 in lyophilised milk and Mo of 20.72 ± 14.61 μg/kg and 152.26 ± 96.82 μg/kg in whole and lyophilised milk. Only As was detected in four samples with mean values of 18.45 ± 6.89 and 166.45 ± 42.30 μg/kg in liquid and lyophilised milk, respectively, and no Hg was found in any of them. In no case do the values found indicate a significant hazard to the population and are in agreement with those found in other investigations. Although the various anthropogenic activities of the area (industrial, mining, traffic density) could, a priori, indicate a possibly contaminated area.

Anthropogenic activities have resulted in severe environmental degradation. Untreated wastewater from tanneries is hazardous to all kinds of life on earth. Effluent from tanning industries, containing large amount of Cr, is used to irrigate the crops in Pakistan. The current experiment was carried out to study the effects of tannery wastewater on spinach and the role of lysine-Zn in mitigating the severity of stress. The plants were grown in soil and the following treatments were used: irrigation with 0%, 33%, 66%, and 100% wastewater (ww) along with two doses (0 mM, 10 mM) of Zn-lysine. Foliar application of zinc-lysine enhanced the plant growth, biomass, Zn contents, photosynthesis, and enzyme activities in different tissues of plant. Zinc-lysine (10 mM) considerably decreased the Cr content in roots and shoots, along with ameliorating the oxidative stress by enhancing the activities of antioxidant enzymes in plants. Addition of Zn-lys (10 mM) improved the plant height by 19%, root length by 57%, leaf dry weight by 19%, and root dry weight by33% under 100% Cr treatment. Zn-lys significantly reduces the oxidative stress and concentration of Cr as compared with the Cr treatments alone. Application of Zn-lys (10 mM) reduced the Cr contents in roots by 27 and 22 under 33 and 66% Cr treatment, respectively. Taken together, Zn-lys chelates efficiently ameliorated the toxic effects of chromium. Zn-lysine has the extravagant potential of mitigating the heavy metal toxicity without harming the normal growth and development of the plants.

This study reports on acetylsalicylic acid (ASA) biosorption onto fungal-bacterial biofilm supported on two types of activated carbons (one commercial type made of coconut fibers, CAC, and one other manufactured from fruit rinds of Hymenaea stigonocarpa Mart., HYAC, which after biofilm inoculation, they were named CAC-b and HYAC-b), via batch and fixed-bed experiments. These materials were characterized by BET Specific Surface Area and Scanning Electronic Microscopy (SEM). Biosorption onto HYAC-b was 57.2% higher than HYAC. Despite presenting the highest biosorption capacity over time (qₜ = 85.4 ± 0.82 mg g⁻¹), CAC-b had a lower increase in efficiency (32.4%) compared to CAC. Kinetic data from the biosorption experiments responded well to the pseudo-first-order model thus suggests the predominance of physisorption, while without biofilm presence, there was a better agreement with the pseudo-second-order model, suggesting chemisorption. The possible interaction mechanism of ASA to biofilm was attributed to ionic forces between the drug in anionic form and eventual presence of cationic by-products of the biologically active surface metabolism. Biosorption equilibrium data responded better to the Sips model and CAC-b presented the highest biosorption capacity (qₑ = 292.4 ± 2.01 mg g⁻¹). A combination of faster volumetric flow rates, higher inlet concentrations and shorter beds accelerated the breakthrough time of ASA biosorption in the fixed-bed experiments. These operational conditions affected C/Cₒ ratio in the following magnitude order: volumetric flow rate < inlet concentration < bed height. Breakthrough data responded better to the modified dose-response model compared to Thomas and Yoon-Nelson models.

This study evaluates the filtration potential of the biomass obtained from Andropogon grass (Andropogon gayanus Kunth cv. Planaltina) that was converted to biochar by pyrolysis. The biochar is used in filtration systems for the post-treatment of paint industry effluents. The biomass is characterized by elemental analysis (CHSN-O), determination of specific compounds (cellulose/hemicellulose/lignin), FTIR, and SEM. The produced biochar is characterized by SEM, TGA, and surface area analysis. The efficiency of the filters is evaluated by the following parameters: color, turbidity, removal of total solids (suspended and sedimentable), chemical oxygen demand (COD), and metals (Al, Cu, Zn, Co, Cd, and Cr(VI)). Over 99% removal of aluminum, cadmium, and hexavalent chromium is achieved. Moreover, almost 100% of COD and solids are removed, whereas turbidity and color are reduced by over 90%.

The occurrence of plastic particles in aquatic environment has led to enormous concern in the past few years. The sorption behaviors of harmful organic compounds by plastic particles can increase their concentrations by several orders of magnitude influencing their global transport in the marine environment. Five types of mesoplastics (5–20 mm) and five types of microplastics (< 5 mm) were selected to investigate the sorption behaviors of three typical organic compounds (phenanthrene, nitrobenzene, and naphthalene). For phenanthrene, most microplastics have stronger sorption ability than that of mesoplastics due to the higher specific surface area (SSA). However, the sorption ability of nitrobenzene on low-density polyethylene (LDPE) mesoplastics was higher than that on LDPE microplastics, and the sorption ability of naphthalene on polyvinyl chloride (PVC) mesoplastics was higher than that on PVC microplastics, which were attributed to the presence of functional groups on the surface of mesoplastics, induced by adding slip agents, lubricant, plasticizer, stabilizer, etc. during film production. Talcum-filled polypropylene (PP) microplastics had strongest sorption ability to nitrobenzene and naphthalene due to the presence of talcum and high SSA. For unmodified microplastics, the sorption abilities of phenanthrene, nitrobenzene, and naphthalene were all followed the order of high-density polyethylene (HDPE) > polystyrene (PS) > LDPE > PVC after SSA normalization. Thus, SSA and the functional groups on the surface of plastic particles should be considered when the sorption behaviors of harmful organic compounds on plastic particles are studied.

Atmospheric precipitation is a very important link in the water cycle. The characteristics of major ions (n = 341) and stable isotopes (δ²H, δ¹⁸O; n = 157) were analysed in Hangzhou and Huzhou, which are economically prosperous cities in East China. The δ²H and δ¹⁸O values of precipitation ranged from − 109.70 to 21.30‰ and from − 14.87 to − 0.95‰, respectively. Compared with the local meteoric water line (LMWL) of China, the slope and intercept of the LMWL were much higher in Hangzhou and Huzhou, which is related to the effects of the humid climate and less secondary evaporation. The δ²H and δ¹⁸O values were highest in spring because of the influence of air masses from the northern Asian continent and other nearby sources. In contrast, the air masses from the South China Sea and the western Pacific Ocean in the summer had the lowest δ²H and δ¹⁸O. The dominant ions in precipitation indicate that Ca²⁺, HCO₃⁻, SO₄²⁻, NH₄⁺ and NO₃⁻ are the main ions of precipitation in Hangzhou and Huzhou, and the dilution of precipitation leads to lower concentrations of ions in spring and summer, similar to the values found in most Chinese cities. The increase in motor vehicle use resulted in a lower [SO₄²⁻]/[NO₃⁻] ratio (1.64) of precipitation, indicating mixed acid rain in Hangzhou and Huzhou (HZS). Based on a combination of the correlation analysis, enrichment factors and source contributions, we determined that SO₄²⁻ and NO₃⁻ were introduced mainly from anthropogenic activities such as coal combustion and vehicle exhaust, accounting for 89% and 99%, respectively. The strong correlation between Cl⁻ and Na⁺, as well as Ca²⁺, Mg²⁺ and K⁺, indicates that these ions commonly have marine and crustal origins, respectively, and 40% of Mg²⁺ comes from a marine source.