Persistent and emerging organic pollutants were sampled in September 2012 and 2013 at a sampling site in front of the Three Gorges Dam near Maoping (China) in a water depth between 11 and 61 m to generate a depth profile of analytes. A novel compact water sampling system with self-packed glass cartridges was employed for the on-site enrichment of approximately 300 L of water per sample to enable the detection of low analytes levels in the picogram per liter-scale in the large water body. The overall performance of the sampling system was acceptable for the qualitative detection of polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs), perfluoroalkylic acids (PFAAs), pharmaceutical residues and polar pesticides. Strongly particle-associated analytes like PAHs and PCBs resided mainly in the glass wool filter of the sampling system, whereas all other compounds have mainly been enriched on the XAD-resin of the self-packed glass cartridges. The sampling results revealed qualitative information on the presence, depth distribution and origin of the investigated compounds. Although the depth profile of PAHs, PCBs, OCPs, and PFAAs appeared to be homogeneous, pharmaceuticals and polar pesticides were detected in distinct different patterns with water depth. Source analysis with diagnostic ratios for PAHs revealed their origin to be pyrogenic (burning of coal, wood and grass). In contrast, most PCBs and OCPs had to be regarded as legacy pollutants which have been released into the environment in former times and still remain present due to their persistence. The abundance of emerging organic pollutants could be confirmed, and their most abundant compounds could be identified as perfluorooctanoic acid, diclofenac and atrazine among investigated PFAAs, pharmaceuticals and polar pesticides, respectively.

The sorption behavior of 17α-ethinylestradiol by a surface-modified zeolitic tuff with hexadecyltrimethylammonium (HDTMA) was investigated. The zeolitic material (clinoptilolite) was treated with 0.1 M of sodium chloride solution and then with 25 and 50 mM of HDTMA solutions. The sorption kinetics shows that the maximum removal percentage of 96.87 % was reached at 36 h for the zeolite with 25 mM HDTMA, while with 50 mM of HDTMA, the maximum removal of 98.34 % was achieved at 44 h. Furthermore, pseudo-first-order, pseudo-second-order, and Elovich models were analyzed and the kinetic data exhibited a good fit with the pseudo-second-order model, indicating that the sorption mechanism is chemisorption. The isotherms for the sorption of 17α-ethinylestradiol showed that sorption capacity was 0.7073 and 0.6943 mg/g for 25 and 50 mM, respectively, at 25 °C and showed a partition mechanism. Moreover, the pH influence on the sorption process was studied and the sorption capacity was increased as the pH decreases.

This study examined two underground coal mines in the Sydney basin and investigated the water chemistry impact from their wastewater discharges to surface receiving waters. One mine closed 17 years prior to the study, and the other was still active. The geology of both mine locations shared many similarities and some important differences that influenced their wastewater chemistry and its subsequent impact on receiving waterways. Water quality of wastewater discharges from the two mines and their receiving waterways was investigated over a 6-month period. Both mine discharges caused comprehensive modification to receiving water chemistry. The closed mine increased electrical conductivity (EC) 3.3 times from upstream (33 μS/cm) compared to downstream (108 μS/cm). In comparison, the active mine increased EC by 9.4 times (173 μS/cm) upstream to 1628 μS/cm downstream. Both coal mine wastes increased the concentration of different contaminants to levels that are potentially hazardous for receiving water ecosystems. The active mine increased bicarbonate concentration in the receiving water by more than 60 times to 743 mg/L. The closed mine increased zinc and nickel concentrations in its receiving stream by 70 and 20 times to 318 and 360 μg/L. The active coal mine discharge was dominated by sodium and bicarbonate ions compared to magnesium and sulphate ions in the closed mine drainage. Although both receiving waters were sodium and chloride dominated upstream of the mine waste, their ionic composition was strongly modified due to the inflow of coal mine wastes. Results from this study are a reminder that water pollution from coal mines is important for both active mines and for closed mines decades after mining activity ceases.

Research was carried out on the granulometric, mineral composition and fractional distribution of some elements in surface sediments of the Zeya River basin (Far East, Russia). The order of sediments’ pollution by heavy metals due to man-caused impact on the Zeya River’s ecosystem was determined. The compound forms of heavy metals in sediments were studied. It presented the most of the Fe, Ni, Cr, Mn, Co, Cu and Zn accumulated in bottom fraction; Pb and Cd—also in Fe and Mn hydroxides and bottom fractions. On average, 56% Pb, 83% Cd, 27–37% Cu, Co and Zn (of total amount) are held in geochemical moving forms.

This 3-year study was aimed to understand the factors and mechanisms that cause the temporal changes in the concentration of microbiological indicators of water quality and nutrient concentration in selected sites of the Białka river catchment (southern Poland) situated in direct vicinity of the largest ski station in the region. The analysis comprised 35 sampling campaigns conducted in five sites. Water temperature, pH, and electrical conductivity were measured during sampling, laboratory analyses included determination of the selected nutrients content (NH₄, NO₃, NO₂, PO₄); and the number of mesophilic and psychrophilic bacteria, coliforms, fecal coliforms, and Escherichia coli. Based on the cluster analysis, the collected samples were grouped into three to four groups, depending on the most characteristic features. Seasonal variation was evident, showing the predominance of either anthropogenic or natural-environment factors, depending on the considered season. On the other hand, principal component analysis revealed clear effect of various forms of land use in different sites.

This study focused on the treatment of effluent contaminated with chromium, being driven by the application of magnetic field studies in living cells and organisms. The objective was to quantify the removal of chromium(VI), total chromium, and total organic carbon (TOC) by applying a magnetic field generated by permanent magnets of neodymium in mixed culture. The resistance of microorganisms was evaluated for 4 h and 17 min against the application of a magnetic field at frequencies of 3, 5, and 10 Hz, which correspond to flow rates of 3.93, 7.07, and 14.92 cm³ s⁻¹ in the system loop, respectively. The initial concentration of Cr(VI) was 100 mg L⁻¹. The magnetic field frequency of 5 Hz showed a higher removal of Cr(VI) (100 %), total chromium (82 %), and TOC (34 %) compared with frequencies of 3 and 10 Hz and the absence of magnetic field exposure.

This is a green method for determination of mercury ion (Hg²⁺) in environmental samples. The method of exchangeable water based on liquid-liquid microextraction (EW-LLME) was first time introduced as a green analytical separation technique. Exchangeable water was made by the reaction of carbon dioxide with diethylenetriamine. The exchanging phenomena from low polarity to high polarity were confirmed by Fourier transforms infrared spectrometry. The complex formation between Hg²⁺ and 1, 5-diphenylcarbazone was achieved under the optimized experimental conditions. The enrichment factor and limits of detection of the present method were obtained to be 45.2 and 0.5 ng L⁻¹, respectively. The accuracy of the present method was confirmed with certified reference materials. The EW-LLME was successfully applied for determination of Hg²⁺ in solid matrices of block-III and V of Thar coalfield.

Industrial synthesis processes produce high concentration of hazardous organic pollutants into water body, which must be removed before being discharged. Advanced oxidation processes (AOPs) using heterogeneous catalysts has been widely utilized for wastewater treatment. Here, RuO₂-based catalyst was synthesized by a general impregnation method and used to oxidize phenol by peroxymonosulfate (PMS) as an oxidant in aqueous solution. The properties of this supported catalyst were characterized by SEM (scanning electron microscopy), XRD (powder X-ray diffraction), and nitrogen adsorption-desorption. The mesoporous Al₂O₃ support had large surface area and high thermal stability. It is found that ruthenium oxide-based catalyst is highly effective to activate PMS to related sulfate radicals. The effects of catalyst loading, phenol concentration, PMS concentration, reaction temperature, and reusability of the as-prepared catalyst on phenol degradation have been investigated. Overall, our findings demonstrate that in RuO₂/Al₂O₃ mesoporous catalyst, Oxone (PMS) is effectively activated, and 100% phenol degradation occurs in 60 min. To regenerate the deactivated catalyst and improve its catalytic properties, three different methods involving annealing in air, washing with water, and applying ultrasonics were used. The catalyst was recovered thoroughly by heating treatment.

Since the industrial revolution, the impact of effluents produced by human activities on ecosystems has been a major international environmental concern. This study was aimed at observing the changes in water and sediment qualities at a watershed level of two different river systems facing the same land use practices, but impacted to different degrees. Samples were collected at strategically selected sites within the mainstream of both rivers, the major tributaries draining into them, as well as a major impoundment in each system. A distinct difference between the two different rivers was observed. It was established that certain variables, for example pH, contributed to the differential water and sediment quality signatures in the upper Olifants and Mokolo rivers, having important considerations for the future management of both river ecosystems. Other abiotic factors, such as alkalinity and sulphate levels, were also found to be important. The tributaries were found to play an important role in the purification and/or pollution of the mainstream rivers. On the other hand, the present impoundments in the Mokolo River were observed to affect the water and sediment qualities downstream. Overall, through the use of comparative models, it was observed that the upper Olifants River was in a different state than the Mokolo River and the information from this study may aid in the future management of the Mokolo River to prevent a shift to an undesirable state.

To provide growing population with sufficient food, greenhouse vegetable production has expanded rapidly in recent years in China and sustainability of its farming practices is a major concern. Therefore, this study assessed the sustainability of greenhouse vegetable farming practices from environmental, economic, and socio-institutional perspectives in China based on selected indicators. The empirical data were collected through a survey of 91 farm households from six typical greenhouse vegetable production bases and analysis of environmental material samples. The results showed that heavy fertilization in greenhouse vegetable bases of China resulted in an accumulation of N, P, Cd, Cu, Pb, and Zn in soil, nutrient eutrophication in irrigation water, and high Cd in some leaf vegetables cultivated in acidic soil. Economic factors including decreased crop yield in conventional farming bases, limited and site-dependent farmers’ income, and lack of complete implementation of subsidy policies contributed a lot to adoption of heavy fertilization by farmers. Also, socio-institutional factors such as lack of unified management of agricultural supplies in the bases operated in cooperative and small family business models and low agricultural extension service efficiency intensified the unreasonable fertilization. The selection of cultivated vegetables was mainly based on farmers’ own experience rather than site-dependent soil conditions. Thus, for sustainable development of greenhouse vegetable production systems in China, there are two key aspects. First, it is imperative to reduce environmental pollution and subsequent health risks through integrated nutrient management and the planting strategy of selected low metal accumulation vegetable species especially in acidic soil. Second, a conversion of cooperative and small family business models of greenhouse vegetable bases to enterprises should be extensively advocated in future for the unified agricultural supplies management and improved agricultural extension service efficiency, which in turn can stabilize vegetable yields and increase farmers’ benefits.