Effects of pH, As species, and Fe/Mn minerals on the fractions of adsorbed As in aquifer sediments were evaluated. Kinetic data showed that As adsorption was controlled by diffusion through the external film. Isothermal data of both As(III) and As(V) fitted the Langmuir isotherm well, revealing a monolayer adsorption process. Sequential extraction demonstrated that water-soluble As and non-specifically sorbed As were the major fractions of adsorbed As. Assessing the relationship between the Freundlich K F and the increases in the amounts of As fractions showed that the pH played a key role in weakly adsorbed As, especially water-soluble As. Although inorganic As species converted each other during the adsorption processes, more non-specifically sorbed As was adsorbed in As(V)-treated sediment than in As(III)-treated sediment, showing that the electrostatic selectivity controlled the non-specific adsorption. Additionally, specifically sorbed As and As associated with the amorphous phases were predominated by Fe/Mn minerals, especially Fe(III) (hydr)oxides. These results suggested that pH, As species, and Fe/Mn minerals would regulate the As fractions in aquifer sediments, and therefore control As cycling in aquifer systems.

The impact of Fe₂O₃and TiO₂nanoparticles (NPs) on the removal of trichloroethylene (TCE) in a granular activated carbon (GAC)-fixed bed adsorber was investigated in the presence of humic acid (HA). The surface charges of GAC and NPs were obtained in the presence and absence of HA with the NPs behaving similarly. Isotherm and column studies were conducted in the presence and absence of the NPs and HA. NPs had no effect on TCE adsorption during isotherm studies. However, in the column studies conducted with organic-free water, the presence of NPs resulted in a reduction in TCE capacity most likely due to pore blockage by aggregating NPs. This effect was completely mitigated in the presence of HAs that prevented an association between the GAC and the NPs, and between NPs. The presence of HA provided a high negative charge on the GAC and on the nanoparticles resulting in repulsive forces between the GAC and the NPs, and between NPs, thereby preventing pore blockage. Both Fe₂O₃and TiO₂NPs demonstrated that charge characteristics are more important than chemical characteristics. Pore-size distribution of the fresh and the spent GAC confirmed the adsorption data but points to some HA and NP interaction with the carbon.

This study examined a single underground coal mine and investigated two aspects of its operation: the disposal of the mine waste through a discharge to a nearby river and the impact of subsidence from an underground longwall to a small waterway above. Water quality of the two waterways was monitored over a 2-year period with a monthly investigation over a 6-month period, which included collection of stream macroinvertebrates. Both mine activities modified surface water geochemistry and macroinvertebrate communities. Mean electrical conductivity (EC) increased in surface waters below the mine discharge, rising 4.8 times from (186 μS/cm) upstream to 1078 μS/cm below the waste inflow. Mean EC increased in a small stream that was disturbed by subsidence from longwall mining, rising 3.8 times from (247 μS/cm) upstream to 1195 μS/cm below. The mineral constituents of the increased salinities were different. The coal mine wastewater discharge was enriched with sodium and bicarbonate ions compared to sodium and chloride ions in the subsidence affected creek. Both the waste discharge and the subsidence caused increases in the concentrations of zinc by about four times and nickel by 20 to 30 times the background levels. The subsidence reduced dissolved oxygen to ecologically stressful levels and increased iron and manganese concentrations by about 20 times the background levels. Two of the key changes in stream ecosystems were a reduction in the proportion of mayfly larvae downstream of the mine waste discharge and mosquito larvae dominating (60–70 % of total abundance) the invertebrate community in the subsidence affected creek.

Featured with biodegradability and biocompatibility properties, gelatin (GE) was selected as the backbone to graft poly(acrylic acid) (PAA) to fabricate a granular hydrogel at room temperature in air. Using attapulgite (APT) as an inorganic component, the resulting GE-g-PAA/APT hydrogel was characterized by means of Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), and zeta potential analysis and then used as the adsorbent to be applied in a mixed dye solution containing malachite green and orange G. The addition of APT can significantly reduce the swelling degree during the adsorption process, though its influences on the adsorption capacity are not so expectable. The as-prepared hydrogel shows a wide pH-independent adsorption from 3.0 to 10.0, with the maximum adsorption capacity of 1370 mg/g for GE-g-PAA and 1190 mg/g for GE-g-PAA/APT (5 wt%). More importantly, the as-prepared hydrogel shows high adsorption selectivity for cationic dyes and the dye-loaded hydrogel can be easily regenerated and recovered for successive adsorption cycles. Graphical Abstract Gelatin-based granular hydrogel for selective removal of MG in a mixed dyes containing MG and OG-G.

To facilitate the mapping of pollution fluxes under different flow conditions when a limited number of gauging stations are available, a method relying on geographic data was developed to estimate the mean daily stream discharge at each sampling station. It has been tested on a rural river watershed that is located in northeast France (Madon River). The stretch of 100 km is equipped with three gauging stations. Surface water samples were collected at 30 stations under different flow conditions. In a participatory research project, samples were also collected by school children at one of the stations (once a week during the school year over a 2-year period). Dissolved organic carbon and nitrogen species were measured for all samples. These data illustrate the variation in the pollution in the river that is associated with agricultural activities and discharges of untreated wastewater. This method was used to obtain localized points of nutrient discharge, to identify the zones that favor nutrient removal, and to propose remediation work.

Multifunctional sorbents, activated carbons (AC), were prepared by one-step microwave activation utilizing peanut shells and sunflower seed husks. The influence of the original particle size of raw materials on the yield and specific surface area of AC was studied, which reached 33.5 % and 1133.27 m²/g, respectively. The repetitive and competitive uptakes of perfluorooctane sulfonate (PFOS) and chromium were applied to investigate the sorption properties of AC. The sorption mechanisms were demonstrated using sulfur K-edge X-ray absorption near edge structure analysis (XANES). In the repetitive experiment, AC made from peanut shells (ACP₀₅) still retained 70 % removal efficiency of PFOS after the fourth sorption because sorbed PFOS might form a new organic phase that supplied effective sites for the hydrophobic partition of PFOS. However, the removal efficiency of Cr(VI) decreased dramatically from 60 to 11 % after the fourth uptake because electrostatic attraction was its only removal pathway. In the binary solutes system, ACP₀₅ possessed perfect sorption performance for both PFOS and Cr(VI), which were 885 and 192 mg/g, respectively. In the multivariate solutes system, the XANES spectra indicated that the thiol functional group existed in the resulting AC and a metal chelate was formed between thiol and Zn²⁺/Cu²⁺. Hence, the presence of Zn²⁺/Cu²⁺ further promoted the removal of PFOS and Cr(VI) through the electrostatic attraction between the anions and positive metal chelate.

The first uranium extraction mine of Brazil, nowadays found in decommissioning phase, has caused several negative environmental impacts in its area, as a result of mining, treatment, and beneficiation processes. The generation of acid mine drainage in waste rock pile 4 (WR-4) is one of the negative impacts with the most critical situation. The acidic water, product of this drainage, presents heavy metals and radioactive elements and it may be infiltrated by the basis of the impoundment basin, where this water is collected for treatment. The objective of this study was to investigate a typical tropical soil, located in the area of Ores Treatment Unit of Caldas in the southwestern state of Minas Gerais, Brazil, in order to use it as a mineral liner for a retention basin to minimize leakage of acidic water through the foundation of a containment dam. In this way, geotechnical, chemical, and mineralogical tests were performed in order to characterize a soil sample collected in the area. In addition, adsorption tests were conducted with solutions of aluminum (Al), manganese (Mn), and iron (Fe), and with and without adjustment of the initial pH (pHₜₒ) of the solutions. The results indicated a well-weathered soil composed of kaolinite, gibbsite, and iron oxides. The adsorption tests showed different behaviors for Al, Mn, and Fe considering or not the adjustment of the pHₜₒ. Aluminum showed low adsorption by soil; because of this, only the adsorption isotherms of Mn and Fe for test with adjustment of the pHₜ₀were determinate. The coefficient of distribution (KD) of Mn was 0.0364 L g⁻¹and Fe 0.0281 L g⁻¹. As for the retardation factor (Rd), its values ranged from 81 to 91 for Mn and from 61 to 79 for Fe, considering different behaviors of the adsorption isotherm models.

Solid organic carbon and zero-valent iron (ZVI) have been used separately as reactive media in permeable reactive barriers (PRBs) to degrade nitrate in groundwater, but few studies have examined the combination of the two materials in one system for nitrate remediation. In the present study, batch tests are conducted to evaluate three common solid organic carbons and their combination with ZVI for nitrate removal from water. The results show that the combined system achieves better denitrification efficiency than that measured with sawdust or cotton alone. However, no obvious difference is noted between the cornstalk alone and its mixture with ZVI treatment. When complete nitrate removal is achieved in the system that combined ZVI with sawdust or cotton, only 72 and 62.6 % of nitrate removal, respectively, are obtained in which the carbon (C) source is used alone. The results indicate that there are synergistic effects in the combined denitrification system, and the effects depend on the type of carbon material used. Sawdust is an alternative carbon source for nitrate removal in a C-ZVI-combined system. In a sawdust-ZVI system, the accumulation of nitrite and ammonium is affected greatly by nitrate concentration, C/N ratio, and Fe/N ratio.

The objectives of the survey were to analyse the structure of the mollusc communities in the mining subsidence reservoirs that were created as a result of land subsidence over exploited hard coal seams and to determine the most predictive environmental factors that influence the distribution of mollusc species. The reservoirs are located in urbanised and industrialised areas along the Trans-Regional Highway, which has a high volume of vehicular traffic. They all have the same sources of supply but differ in the physical and chemical parameters of the water. In total, 15 mollusc species were recorded including four bivalve species. Among them Anodonta cygnea is classified as Endangered according to the Polish Red Data Book of Animals and also as Near Threatened according to the European Red List of Non-marine Molluscs. Eleven of the 15 mollusc species are included on the European Red List of Non-marine Molluscs as Least Concern. Conductivity, pH and the concentration of calcium were the parameters most associated with the distribution of mollusc species. Canonical correspondence analysis showed that Potamopyrgus antipodarum, Radix balthica, Physella acuta, Gyraulus crista and Pisidium casertanum were associated with higher conductivity and lower pH values. A. cygnea, Anodonta anatina and Ferrissia fragilis were negatively influenced by these parameters of the water. The results of this survey showed that the mining subsidence reservoirs located in urbanised and industrialised areas provide refuges for rare and legally protected species and that they play an essential role in the dispersal of alien species as well.

The effect of humic acid (HA), on the adsorption and transport of arsenic (As) onto and within a model iron oxide-based adsorbent, iron oxide-coated diatomite (IOCD), is investigated. Experimental results indicate that the adsorption of both As and HA is highly pH-dependent. As uptake was suppressed by HA, with the level of suppression increasing with HA concentration. The suppression is attributed to the partial coverage of the adsorption sites, as confirmed by elemental analysis. Adsorption energy analysis indicates that for As(III), the main interaction with IOCD is physical adsorption, whereas for As(V), it is more likely ion exchange. The presence of HA may alter the adsorption energy and interaction of As with the adsorbent, particularly at higher HA concentrations. Kinetic results indicate that HA did not affect the diffusional transport of As in systems with both As and HA. However, for IOCD preloaded with HA, the adsorption kinetics of As was significantly slower, although the As uptake was similar to the conditions of co-sorption with HA. The slower kinetics and similar equilibrium uptake of As in the HA-preloaded IOCD system may be attributed to the partial blockage of the intraparticular pores within IOCD, which slowed down the diffusion of As.