Over the last decades, removal of potentially toxic and hazardous materials has received a great deal of attention in the field of environmental pollution. Problems associated with the disposal of the wastes of different kinds of industries led to studies of the sorption–uptake properties of clay minerals and zeolites. In the present research, the behavior of vermiculite particles ranging between 425 and 500 μm in a laboratory-scale fluidized bed column for uptake of Cs, Hg, and Mn ions from aqueous solutions and wastes in the presence of competing cations has been studied in order to investigate techniques for decontamination of liquid phases. Vermiculite selectively removed high percentages of Cs even from low concentrations in the presence of competing cations. Also removed were up to 60 % of added Hg²⁺ at concentrations of 5 ppm from drinking water and about 84 % from seawater, and furthermore, Mn²⁺ was selectively removed from low-concentration (ca 10 ppm) industrial wastes even when the ratio of Mn²⁺ to competing cations was 1:94. The results suggest the potential use of vermiculite as decontaminating agent in well-designed fluidized bed columns.

The relative transport and attenuation of bacteria, bacteriophages, and bromide was determined in a 5 m long × 0.3 m diameter column of saturated, heterogeneous gravel. The average pore velocity (V), longitudinal dispersivity (α x ), and total removal rate (λ) were derived from the breakthrough curves at 1, 3, and 5 m, at a flow rate of 24.8 L h−1. The experiments largely confirmed the differences in transport and attenuation patterns among bacteria, phages, and bromide, and between colloid-associated and “free” microorganisms, previously observed in a study using homogeneous pea gravel. Cultured Escherichia coli J6-2 cells were transported faster than phage MS2 and bromide, consistent with velocity enhancement of the larger particles. The evidence for velocity enhancement of phage MS2 compared with bromide was less conclusive, with some evidence of retardation of the phage as a result of adsorption–desorption processes in the finer media. On average, phage in sewage and adsorbed to kaolin particles were transported faster than free phage, suggesting that most sewage phage are adsorbed to colloids. However, average velocities of cultured and sewage E. coli differed far less, suggesting that most E. coli in sewage exist as individual (non colloid-associated) cells. There was no conclusive evidence that the wider pore size range in the heterogeneous mixture compared with pea gravel increased velocity enhancement effects. Removal rates of free phage were far higher than in the pea gravel, and were attributed to adsorption in the finer materials. Equivalent increases in removal of cultured and sewage E. coli and colloid-associated phage were attributed to straining in finer materials and settling in quiescent zones. Inactivation (μ) rates (determined in the pea gravel study) indicated little contribution to removal of either free or attached microorganisms. The results showed the importance of association with colloids in determining the relative transport of bacteria and viruses in alluvial gravels.

Two types of hydrogels with different functional groups, trimethylamine on quaternary ammonium and dimethylethoxyamine on quaternary ammonium, were synthesized. Type 1 and type 2 hydrogels were characterized with Fourier transform infrared, X-ray photoelectron spectroscopy and zeta potential analysis. The anion selectivity of these two hydrogels was investigated. The surface charges of the type 2 hydrogel were lower than those of type 1, probably because of the presence of the hydroxyl group in the ethoxy group. The Cr(VI) removal capacity of type 2 hydrogel was, therefore, less than that of type 1 hydrogel, although their adsorption rates were similar. The anion selectivity of the hydrogels was found to have a similar order: Cr(VI) > sulphate > bromide > As(V). Under the co-presence of Cr(VI) and sulphate conditions, type 2 hydrogel shows a higher selectivity towards Cr(VI). The higher hydrophobicity was caused by the presence of the ethoxy group on the quaternary ammonium in type 2 hydrogel and thus increased in selectivity towards monovalent ions (i.e. HCrO 4 − ). In addition, the hydrogels have a high reusability. Compared with type 1 hydrogel, type 2 hydrogel has an advantage for applications in Cr(VI) removal and recovery processes.

Phosphate from agricultural runoff is a major contributor to eutrophication in aquatic systems. Vegetated drainage ditches lining agricultural fields have been investigated for their potential to mitigate runoff, acting similarly to a wetland as they filter contaminants. It is hypothesized that some aquatic macrophytes will be more effective at removing phosphate than others. In a mesocosm study, three aquatic macrophyte species, cutgrass (Leersia oryzoides), cattail (Typha latifolia), and bur-reed (Sparganium americanum), were investigated for their ability to mitigate phosphate from water. Mesocosms were exposed to flowing phosphate-enriched water (10 mg L⁻¹) for 6 h, left stagnant for 42 h, and then flushed with non-nutrient enriched water for an additional 6 h to simulate flushing effects of a second storm event. Both L. oryzoides and T. latifolia decreased the load of dissolved phosphate (DP) in outflows by greater than 50 %, significantly more than S. americanum, which only decreased DP by 15 ± 6 % (p ≤ 0.002). All treatments decreased concentrations inside mesocosms by 90 % or more after 1 week, though the decrease occurred more rapidly in T. latifolia and L. oryzoides mesocosms. By discovering which species are better at mitigating phosphate in agricultural runoff, planning the community composition of vegetation in drainage ditches and constructed wetlands can be improved for optimal remediation results.

We evaluated the imbalance of the oxidative status in zebra mussel (Dreissena polymorpha) specimens exposed for 96 h to environmentally relevant concentrations (0.1, 0.5, and 1 μg/L) of the 2,2′,4,4′,5,6′-hexa BDE (BDE-154). The activities of three antioxidant enzymes, catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GPx), and the phase II detoxifying enzyme glutathione S-transferase (GST), were measured in the cytosolic fraction from a pool of zebra mussels. Significant variations in the activity of each single enzyme were noticed at each treatment, indicating that exposure to BDE-154 was able to impair the oxidative status of treated bivalves through the increase of reactive oxygen species. In detail, SOD and GPx were significantly induced, while CAT and GST were depressed with respect to the baseline levels. These data have confirmed that the raise of oxidative stress is the main cause of the BDE-154-induced genetic damage observed in a previous study on the zebra mussel.

Crosslinking carboxymethyl starch (CCMS) powder of degree of substitution (DS) 0.43–0.59 was prepared by the process of two steps of alkali addition synthesis. The technique of powder coupling with ultrafiltration was used to absorb Cu2+, Zn2+, Ni2+, Pb2+, and Cd2+ from aqueous solutions. FTIR was used to demonstrate the successfully grafting of carboxymethyl groups, and the technique of microwave plasma torch atomic emission spectrometer was applied in rapid determination of the aforementioned heavy metals ions. The results revealed that the removal sequence of heavy metal ions followed the order of Pb2+>Cu2+>Cd2+>Zn2+>Ni2+. By assistant of diethylene triamine penlaacetic acid, the quaternary system of Pb2+/Ni 2+/Cd2+/Cu2+ mixture solution could have the ideal separation. Besides, the influence of pH, ζ potential, DS value, and membranes molecular weight cut-off on removal of 20 mg L−1 Pb2+ or Ni2+ was also investigated.

Electrical resistivity tomography (2D ERT) is a powerful tool for the diagnosis of the subsoil state and to pursue an environmental monitoring in time to detect and follow a temporal evolution of plumes in hydrocarbon-contaminated soils. In situ, 2D ERT was conducted to investigate the electrical properties of the subsoil in three petrol stations in Murcia semiarid Region (SE Spain), which have been active for many years, in order to look for anomalous areas that could be related to the presence of a non-aqueous phase liquid (NAPL) contaminant plume in the subsoil. A total of 18 ERT profiles in wet and dry season were conducted to study the seasonal effects in the resistivity values of the subsoil. Dipole–dipole array was set up to make the soil diagnosis, achieving a good vertical and lateral resistivity distributions for the sites investigated. Interpretations obtained from ERT pseudo-sections, after a processing and inversion data process with PROSYS II and RES2DINV software, show delimited highly resistive regions above 2,000 Ω·m at 2 m deep related to the underground storage tanks (USTs) position and the filling ports and anomalous resistivity areas where boreholes and further GC–FID determination in soil samples have been done. No significant differences have been found between results obtained in dry and wet seasons. Thus, the geo-electrical non-destructive technique ERT is presented as a tool to delineate the USTs positions and to point out anomaly in the subsoil that could contain NAPL, helping to design sampling strategies, saving cost and time.

The aim of this study is to assess the premature mortality risks caused by exposure to particulate matter with aerodynamic diameter less than 2.5 μm (PM2.5) and ozone elevated concentrations for the years 2000, 2005, and 2020 in East Asia. The spatial distributions and temporal variations of PM2.5 and ozone concentrations are simulated using the Models-3 Community Multiscale Air Quality Modeling System coupled with the Regional Emission Inventory in Asia. The premature mortality risks caused by exposure to PM2.5 and ozone are calculated based on a relative risk (RR) value of 1.04 (95 % confidence interval (CI): 1.01–1.08) for PM2.5 concentrations above the annual mean limit of 10 μg m−3 taken from the World Health Organization–Air Quality Guideline and based on a RR value of 1.003 (95 % CI: 1.001–1.004) for ozone concentration above 35 ppb of the SOMO35 index (the sum of ozone daily maximum 8-h mean concentrations above 35 ppb). We demonstrate one of the implications of the policy making in the area of environmental atmospheric management in East Asia by highlighting the annual premature mortalities associated with exposure to PM2.5 concentrations that just meet an annual mean concentration of 10 μg m−3, as well as ozone concentrations that have a daily zero SOMO35 index in vulnerable places. Our results point to a growing health risk that may endanger human life in East Asia. We find that the effect of PM2.5 on human health is greater than the effect of ozone for the age group of 30 years and above. We estimate the corresponding premature mortality due to the effects of both ozone and PM2.5 in East Asia for the years 2000 and 2005 to be around 316,000 and 520,000 cases, respectively. For future scenarios of the year 2020, policy succeed case, reference, and policy failed case, the estimated annual premature mortality rates are 451,000, 649,000, and 1,035,000 respectively.

After the accident in Fukushima reactors, a daily monitoring programme was initiated in two laboratories in Belgrade, one at the Vinčа Institute for Nuclear Sciences and the other at Institute for Occupational Health Karajovic. Samples of aerosol and fallout, as well as the random samples of food and water, were collected and analysed, using gross alpha/beta and gamma spectrometry, in order to establish the presence of traces of isotopes indicating Fukushima fallout. Gamma spectrometry measurement of these samples showed clear evidence of fission products ¹³¹I, ¹³⁴Cs and ¹³⁷Cs wtihin 2 weeks after the accident. The activity diminished with time due to dispersion in air and, in case of ¹³¹I, short half-life.

Biocovers are an alternative for mitigating fugitive and residual emissions of methane from landfills. In this study, we evaluated the performance of two experimental passive methane oxidation biocovers (PMOBs) constructed within the existing final cover of the St-Nicéphore landfill (Quebec, Canada). The biocovers were fed in a controlled manner with raw biogas and surface fluxes were obtained using static chambers. This enabled calculating mass balances of CH₄ and oxidation efficiencies (f ₒ_MB). Most of the time, f ₒ_MB ≥ 92 % were obtained for loadings as high as 818 g CH₄ m⁻² day⁻¹ (PMOB-2) and 290 g CH₄ m⁻² day⁻¹ (PMOB-3B). The lowest efficiencies (f ₒ_MB = 45.5 % and 34.0 %, respectively) were obtained during cold days (air temperature ~0 °C). Efficiencies were also calculated using stable isotopes (f ₒ_SI); the highest f ₒ_SI were 66.4 % for PMOB-2 and 87.3 % for PMOB-3B; whereas the lowest were 18.8 % and 23.1 %, respectively. However, f ₒ_SI values reflect CH₄ oxidation up to a depth of 0.10 m, which may partly explain the difference in regards to mass balance-derived efficiencies. Indeed, it is expected that a significant fraction of the total CH₄ oxidation occurs within the zone near the surface, where there is greater O₂ availability. The influence of the values of fractionation factors α ₒₓ and α ₜᵣₐₙₛ were also evaluated in this paper.