The feasibility of employing a porous polyurethane–keratin hybrid membrane for the removal of hexavalent chromium was investigated. Keratin was extracted from chicken feathers and incorporated onto a synthetic polyurethane polymer to synthesize a hybrid membrane. Keratin supply active sites to bioadsorb Cr(VI) and polyurethane play an important role as the support to protein. Also, polyurethane–keratin biofiber membranes were synthesized. Biofibers obtained from chicken feathers were modified to activate their surface. The effective pore in membranes is less than 50 nm, which places these materials in the mesopore range. Scanning electron microscopy (SEM) was used to study the morphology of membranes, and mechanical dynamical analysis (DMA) was used to evaluate the viscoelastic properties. NH, C=O, S–S and C–S were determined via Fourier-transform infrared (FTIR) analysis as functional groups of keratin, which participate in the linking sorption of hexavalent chromium. Adsorption of Cr(VI) was carried out in a filtering system at low contact time in continuous flux; the maximum removal reached was 38% at neutral pH of chromium solution. Results indicate that the isoelectric point of keratin is relevant in the adsorption process. pH of keratin solution above the isoelectric point brings about higher adsorption of heavy metals, whereas lower pH causes minor adsorptions, due to the functional groups’ ion charges. Based on the results, keratin extracted from feathers is a natural biosorbent that can be incorporated onto synthetic polymers to develop novel membranes and improve its applications in the heavy metal separation process.

The presence of sexual hormones (female estrogens) was assessed in sediments of a mangrove located in the urban region of southern Brazil. The estrogens are involved in human sexual reproduction. They act as the chemical messengers, and they are classified as natural and synthetic. The estrogens inputs in the environment are from treated and untreated sewage. The presence of estrogens in sewage is excretion from the female due to natural production and use of contraceptives (synthetic estrogens). With the indiscriminate release of sewage into the environment, estrogens can be found in rivers, lakes, and even in oceans. In this work, the presence of estrone (E1), 17-β-estradiol (E2), and 17-α-ethynilestradiol (EE2) in eight sedimentary stations in Itacorubi mangrove located on Santa Catarina Island, south Brazil, was investigated. Historically, the Itacorubi mangrove has been impacted by anthropogenic activities because the mangrove is inserted in the urban area of the Florianopolis. The estrogen EE2, used as contraceptive, had the highest concentration in mangrove sediment, 129.75 ± 3.89 ng/g. E2 was also found, with its concentration ranging from 0.90 ± 0.03 to 39.77 ± 1.19 ng/g. Following the mechanism, under aerobic or anaerobic conditions, E2 will first be oxidized to E1, which is further oxidized to unknown metabolites and finally to CO2 and water (mineralized). EE2 is oxidized to unknown metabolites and also finally mineralized. Theoretically, under anaerobic conditions, EE2 can be reduced to E1 even in environments such as mangrove which is essentially anaerobic.

Mixed microbial culture was isolated from heavy metal-contaminated ground soils located inside iron, vinyl and cement factory area. Isolated mixed microbial culture was used for the heavy metal ions (Fe²⁺, Cu²⁺, Ni²⁺ and Zn²⁺) removal process in horizontal rotating tubular bioreactor (HRTB). In this research, the effect of bioreactor process parameters on the bioprocess dynamics in the HRTB was studied. Results of this research have shown that profiles of heavy metals concentration were gradually reduced along HRTB at all combinations of bioreactor process parameters [inflow rates (0.5-2.0 L h⁻¹) and rotation speed (5-30 min⁻¹)]. Hydrodynamic conditions and biomass sorption capacity have main impact on the metal ions removal efficiency that was varied in the range of 38.1% to 95.5%. Notable pH gradient (cca 0.7 pH unit) along the HRTB was only observed at the inflow rate of 2.0 L h⁻¹. On the basis of obtained results, it is clear that medium inflow rate (F) has higher impact on the heavy metal removal process than bioreactor rotation speed (n) due to the fact that increase of inflow rate was related to the reduction of equilibrium time for all examined metal ions. Furthermore, equilibrium times for all metal ions are significantly shorter than medium residence times at all examined combinations of bioreactor process parameters. The main impact on the biofilm sorption capacity has covalent index of metal ions and biofilm volumetric density. The sorption capacity of suspended microbial biomass is closely related to its concentration. Results of this research have also shown that the removal of heavy metals ion can be successfully conducted in an HRTB as a one-step process.

Resistivity of plastic litter to chemical weathering, mechanical erosion, and biological degradation poses a critical environmental threat. Plastic debris has increased in abundance over the past several decades along shorelines and at sea, where organisms mistake small particles including plastic pellets as a potential food supply. These pellets have been shown to adsorb persistent organic pollutants such as PCBs, which may endanger the organism and become ingested higher in the food chain. Although several studies have been conducted to determine the amount and effects of plastics pollution in marine environments, relatively little is known concerning fresh water plastics pollution. This study represents the first detailed examination of the distribution, types, and physical and chemical degradation processes of plastic particles in a fresh water setting. In conducting field surveys along the shoreline of Lake Huron, Canada, we were able to ascertain that the total number of pellets over multiple sampling localities comprise 94% of plastic debris. The majority of the pellets were found proximal to an industrial sector along the southeastern margin of the lake and their abundance steadily decreased northward, following the dominant lake current patterns. Laboratory analyses using Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy indicate predominant mechanical abrasion textures, including grooves, gauges, pits, and flakes, and less common chemical weathering features such as linear and crescentic fractures that developed from shrinkage during subaerial exposure. The predominant type of plastic, polyethylene, appears to be much more resistant to chemical weathering than polypropylene, as indicated by oxidation peaks on FTIR spectra suggesting that polypropylene degrades more readily under natural conditions on freshwater beaches.

Hexavalent chromium is a heavy metal used in a variety of industrial applications which is highly toxic to humans, animals, plants and microorganisms. Moreover, it is a well-established human carcinogen by the inhalation route of exposure and a possible human carcinogen by the oral route of exposure. Therefore, it should be removed from contaminated waters. Its reduction to trivalent chromium can be beneficial because a more mobile and more toxic chromium species is converted to a less mobile and less toxic form. During the last two decades, there has been important interest in using zero-valent iron (ZVI) as a Cr(VI)-reducing agent. A considerable volume of research has been carried out in order to investigate the mechanism and kinetics of Cr(VI) reduction with ZVI, as well as the influence of various parameters controlling the reduction efficiency. Therefore, the purpose of this review was to provide updated information regarding the developments and innovative approaches in the use of ZVI for the treatment of Cr(VI)-polluted waters.

In recent years, human pharmaceutical substances have been increasingly detected in the aquatic environment. Specific attention has been drawn to the occurrence of pharmaceutical substances at bank filtration sites which are used for drinking water production. In the course of the authorisation application for new pharmaceutical compounds, an environmental risk assessment is required. Currently, the expected concentration of the human pharmaceutical compound in groundwater at bank filtration sites is calculated following the guideline Pre-Authorisation Evaluation of Medicines for Human Use issued by the European Medicines Agency (EMEA 2006). A simple estimation is applied: The predicted environmental concentration (PECGW) is the predicted environmental concentration in surface water (PECSW) multiplied with 0.25. A new approach considering the hydraulic and hydrogeological characteristics of bank filtration sites as well as transport processes is presented in this study. First, a numerical groundwater flow model was developed to simulate the groundwater flow processes at bank filtration sites in general. Flow times were calculated as a function of the hydraulic and hydrogeological parameters: hydraulic conductivity, shore-well distance, screen depth and extraction rate. In a second step, the PECGW was calculated based on the compound concentration in surface water and the modelled groundwater flow times considering linear sorption and first-order decay. Sorption and degradation can only be calculated based on the data provided by the pharmaceutical company in the course of the authorisation application. The current approach following the EMEA guideline invariably connects the PECGW with the PECSW without considering sorption and/or degradation processes. We introduce an approach that incorporates the hydraulic process bank filtration and the main transport processes sorption and degradation. The new approach is compound specific as well as aquifer, flow and transport specific resulting in a more realistic PECGW value compared to the old approach.

Retardation of tritium migration in the Chinese loess media was studied through column experiments by comparison of the migration velocity with other three “non-adsorptive” tracers of Br−, 99Tc, and 131I. Results showed that the transport peak of Br− was 1.25 times earlier than that of tritium when the tracers were simultaneously injected into the column, and the migration of 99Tc was even 1.60 times faster than 3H when the tracers were simultaneously injected. For iodine, it was only 1.02 times faster than that of tritium, but it should not be ignored. It reflected that the transport of 3H, compared to that of Br−, 99Tc, or 131I in the loess media, was retarded. In order to validate the adsorption behavior of tritium on loess, batch tests were carried out using Chinese loess soil. The experimental results indicated that the adsorption of tritium was actual existence, and the distribution coefficient of tritium is influenced by initial activity of tritium, pH, water/solid ratio, and the content of humic and fulvic acids.

A major input in intensive organic agriculture is nutrient-rich liquid fertilizers. Guano and other fowl manure are frequently digested in water extracts, and the supernatant is supplied as fertilizer. The resultant manure biowaste (MBW) is commonly disposed of to the environment, posing potential pollution and health risks. The study aims were to determine two types of fowl MBWs for their chemical properties before and after lime treatment and to test their reuse potential as soil amendment. Guano and layer manure were digested, and the residues’ chemical properties were analyzed before and after lime treatment. MBWs were then air-dried and used as a soil amendment in a parsley-growing experiment. The lime-treated MBW composition met the European standards for high-quality biowaste compost. Both digested and lime-treated MBWs had residual nitrogen, 3% and 1% in guano and layer manure, respectively. Parsley grown in soil amended with layer MBW had 100% survival, high yield, and good crop quality compared with controls. Plants grown with soil amended with guano biowaste exhibited lower yield and only 50% survival. These findings indicate that the current practice of disposing guano biowaste to the environment may pollute soil and water bodies, while the land spread of lime-treated layer MBW is safe and may improve soil fertility.

This paper explores the regulation of water quality protection downstream from the Ranger Uranium Project in the Alligator Rivers Region, an area of high conservation value which is both World Heritage- and Ramsar-listed. Available historical monitoring data for surface water quality in Magela Creek downstream of Ranger have been compiled and analysed with respect to hydrologic data and the Australian and New Zealand Environment and Conservation Council–Agricultural and Resource Management Council of Australia and New Zealand (ANZECC–ARMCANZ) regulatory guidelines, introduced in late 2000. The paper focuses on the underlying scientific basis for the current approach and examines the complex inter-relationships of minesite water management, hydrology, climate, monitoring design, implementation and interpretation which are used to differentiate between natural variability and potential mine-derived solutes. The research found that the application of the ANZECC–ARMCANZ guidelines has clearly improved the regulation of water quality protection downstream from the Ranger Uranium Project. The scientific basis is more coherent than the previous regulatory regime; however, for U (a key parameter of indigenous Mirarr-Gundjeihmi and public concern), higher downstream concentrations are permitted than those observed through natural variability, leaving open the potential for an influence of mine-derived U loads while still being within regulatory limits. Another improvement that could be made to the current regulatory regime, to provide enhanced protection of the water quality in Magela Creek downstream of Ranger, would be to explicitly link the water quality monitoring regime with hydrologic flow conditions. The paper makes a valuable case study for the application of water quality guidelines, especially for controversial projects such as uranium mining surrounded by a World Heritage- and Ramsar-listed region on indigenous land—a context of clear relevance for many places around the world.

The use of multiwall carbon nanotubes (MWCNT) as an efficient solid extractor in preconcentration/cleanup studies for tin determination in water samples by electrothermal atomic absorption spectrometry (ETAAS) is proposed. In the proposed method, tin adsorption onto MWCNT was carried out by percolating the solution previously buffered (pH 4.79 with 0.24 mol L−1 acetic acid/acetate buffer) at 4.0-mL min−1 flow rate, followed by elution with 1.0 mL of 2.7 mol L−1 HNO3. Factors such as sample pH, preconcentration/cleanup flow rate, type and concentration of eluent, and buffer concentration were appraised and optimized from chemometric tools based on fractional factorial design and Doehlert design. A limit of detection of 0.73 μg L−1 and precision (n = 8) assessed as relative standard deviation of 8.6% and 7.0% for tin concentration of 8.0 and 43.0 μg L−1, respectively, were achieved. Foreign metallic ions (Ni2+, Pb2+, Co2+, Zn2+, Cd2+, Mn2+, and Fe3+) were checked as potential interferents, and no interference was observed up to an analyte/interference ratio of 1:10 (m/v). Direct tin determination by ETAAS in water samples containing high salt amount is drastically affected by background signal. However, previous cleanup of sample by MWCNT has promoted a significant improvement and makes the method useful for tin monitoring in water samples (mineral, lake, mine, and natural waters) by ETAAS. Quantitative recovery values ranging from 91.5% to 103.0% attested the applicability of the proposed preconcentration/cleanup for tin determination in water samples.