Ionic liquids (ILs), also known as green solvents, are widely acknowledged in several fields, such as chemical separation, synthesis, and electrochemistry, owing to their excellent physiochemical properties. However, their poor biodegradability may lead to environmental and health risks, posing a severe threat to humans, thus requiring further research. In this study, the biotoxicities of the imidazolium-based ILs were evaluated in Tetrahymena pyriformis. Moreover, IL detoxification was investigated by addition of glutathione (GSH), cysteine, and nicotinamide adenine dinucleotide (NADH). Reactive oxygen species (ROS) initiated by different IL types caused damage to Tetrahymena, while glutathione, cysteine, and NADH eliminated ROS, achieving the detoxification purposes. Detoxification results showed that NADH exhibited the best detoxification ability, followed by glutathione and cysteine. Finally, RT-PCR results suggested that metallothionein might have participated in IL detoxification.

Tetraconazole, a chiral triazole fungicide, is widely used for the prevention of plant disease in wheat fields. However, the chirality of pesticides like tetraconazole can cause diverse biological responses. Therefore, it is important that research is conducted to investigate the enantioselective effects of chiral enantiomers in this regard. The absolute configurations of two tetraconazole enantiomers were initially confirmed by ECD (Electrostatic circular dichroism). The bioassay test showed that the fungicidal activity of (R)-(+)-tetraconazole against two pathogens (R. cerealis and F. graminearum) was approximately 1.49–1.98 times greater than that for (S)-(−)- tetraconazole. Following recovery experiments, a modified QuEchERS (Quick, easy, cheap, effective, rugged, safe) method was established using UPLC-MS/MS (ultra-performance liquid chromatography tandem mass spectrometry). The mean recoveries from plant and soil sample ranged from 78.9% to 100.5% with intraday relative standard (RSDᵣ) values of 0.8%–6.9% and interday relative standard (RSDR) values of 3.0%–5.2% respectively. The stereoselective degradation of tetraconazole in wheat meant that (S)-(−)-tetraconazole was more rapidly degraded than (R)-(+)-tetraconazole. Conversely, (R)-(+)-tetraconazole was preferentially degraded in wheat soil. These results will provide us with a greater understanding when assessing future environmental risk assessments and strategies that invoke pesticide reduction.

This work reports the architecture of a novel class of membrane-supported 1D MOF hollow superstructures, by using the bio-inspired polydopamine (PDA) mediated contra-diffusion synthetic strategy, for facile and efficient separation of uranium in a flow-through mode. PDA chemistry was firstly employed to modify the inner surfaces of the cylindrical pore channels of polycarbonate track-etched membrane (PCTM), thereby regulating the heterogeneous nucleation and interfacial growth of ZIF-8 crystals. ZIF-8 hollow superstructures embedded in membrane matrix with well-defined 1D channels were obtained. These membrane-supported MOF hollow superstructures then, for the first time, served as integrated chromatographic micro-column arrays for effective entrapment of uranium from aqueous solutions. It is highlighted that the PCTM supported ZIF-8 superstructures exhibited outstanding uranium entrapment ability in both traditional batch mode (capacity 62.3 mg/g) and fast flow-through mode (removal rate over 90% for 3 level). Moreover, new insights into the interaction between ZIF-8 and uranyl ions were obtained, suggesting that an ion-exchange mechanism involved synergistic effect was responsible for uranium binding, especially in a long-term exposure. The membrane-supported 1D MOF hollow superstructures developed in this work represent a new category of organic-inorganic composite membrane. And, it is envisioned that the methodology established in this work would be versatile for preparing more MOF superstructures with deployable form for separation applications.In summary, a novel class of membrane-supported ZIF-8 hollow superstructure was fabricated for effective separation of uranyl ions.

Microplastics (plastic particles, 0.1 μm–5 mm in size) are widespread marine pollutants, accumulating in benthic sediments and shorelines the world over. To gain a clearer understanding of microplastic availability to marine life, and the risks they pose to the health of benthic communities, ecological processes and food security, it is important to obtain accurate measures of microplastic abundance in marine sediments. To date, methods for extracting microplastics from marine sediments have been disadvantaged by complexity, expense, low extraction efficiencies and incompatibility with very fine sediments.Here we present a new, portable method to separate microplastics from sediments of differing types, using the principle of density floatation. The Sediment-Microplastic Isolation (SMI) unit is a custom-built apparatus which consistently extracted microplastics from sediments in a single step, with a mean efficiency of 95.8% (±SE 1.6%; min 70%, max 100%). Zinc chloride, at a density of 1.5 g cm−3, was deemed an effective and relatively inexpensive floatation media, allowing fine sediment to settle whilst simultaneously enabling floatation of dense polymers. The method was validated by artificially spiking sediment with low and high density microplastics, and its environmental relevance was further tested by extracting plastics present in natural sediment samples from sites ranging in sediment type; fine silt/clay (mean size 10.25 ± SD 3.02 μm) to coarse sand (mean size 149.3 ± SD 49.9 μm). The method presented here is cheap, reproducible and is easily portable, lending itself for use in the laboratory and in the field, eg. on board research vessels. By employing this method, accurate estimates of microplastic type, distribution and abundance in natural sediments can be achieved, with the potential to further our understanding of the availability of microplastics to benthic organisms.

Microplastics are omnipresent in the terrestrial and aquatic environment, and are considered as a potentially serious threat to the biodiversity and ecosystem. Pollution of plastic debris and microplastics in the inland and marine environment has raised concerns in Bangladesh, which is one of the most densely populated countries in the world. This review summarizes the research progress on separation and characterization of microplastics, as well as their occurrence and sources in Bangladesh. Despite of the first total ban on plastic bags in the world introduced back in 2002, microplastics have been ubiquitously detected in the country's inland and marine environment, with the majority of them coming from secondary sources. The microplastics observed in Bangladesh were dominated by fibers, which were derived mainly from textile sources. Polyethylene (PE), polyethylene terephthalate (PET), polypropylene (PP), and polyvinylchloride (PVC) were the most abundant polymers found for microplastics in the marine and freshwater environment of Bangladesh. Along with the identified research priorities to improve the understanding on the ecotoxicological effect and fate of microplastics, extensive and in-depth studies are required to bridge the knowledge gaps to enable comprehensive risk assessment of microplastic pollution on local ecosystems and human health, while effective management of plastic wastes and their recycling are necessary to alleviate this problem in the country.

Soil and sludge are important pools for microplastics (MPs), however standard separation methods for MPs from these pools are still missing. We tested the widely used methods for MPs extraction from water and sediment to six agriculture surface soils and three sewage sludges from municipal wastewater treatment plants and included an additional pre-digestion procedure with 30% H₂O₂ before floatation to remove soil or sludge organic matter (OM). Extraction efficiency of MPs were evaluated under different separation conditions, including floatation solution (NaCl, ZnCl₂, and NaI), filtration membrane, and oxidation solution. Results showed that H₂O₂ pre-digestion significantly increased MPs extraction in soil and sludge, especially the samples with high OM contents, particularly sludge. Floatation solution with higher densities recovered more MPs. The extra released MPs were mainly small fibrous MPs, probably because they are easily retained by aggregates. Our results provide an feasible separation method for MPs in soil and sludge, i.e., pre-digestion with 30% H₂O₂ at 70 °C, floatation with NaI solution, filtration through nylon membrane, and further oxidation with 30% H₂O₂ + H₂SO₄ or 30% H₂O₂ at 70 °C. About 420–1290 MP items/kg soil were detected in soil samples, while much higher numbers (5553–13460 MP items/kg) were found in sludge samples. The dominate morphology of MPs was white fiber with a size of 0.02–0.25 mm, while the main types of MPs, identified by a micro-Fourier transformed infrared spectroscopy (μ-FTIR), were polyethylene and polypropylene in soil samples and polyethylene, polyethylene terephthalate, and polyacrylonitrile in sludge samples.

Oil is principally one of the most important energy sources in the world. However, as long as oil is explored and transported for being used, there will be the risk of the spillage into the marine environment. The use of technical textiles, i.e. fibrous beds, is a conventional separation technique for oil/water emulsion since it is efficient and easy to design. In this paper, the recovery of oil by technical textiles was mathematically modeled based on the structural parameters of textile and the capillary mechanism. Eleven types of commercial technical textiles with different properties were prepared for the experimental program. The experimental design included fiber type (polypropylene and polyester), fabric type (woven and/or nonwoven), fabric thickness and fabric areal density. Consequently, the absorption capacities of different technical textile samples were derived by the use of theoretical and experimental methods. The results show that there is a well fitness between theoretical outputs and experimental data.

The growths of oil and gas exploration and production activities have increased environmental problems, such as oil spillage and the resulting pollution. The study of the methods for cleaning up oil spills is a critical issue to protect the environment. Various techniques are available to contain oil spills, but they are typically time consuming, energy inefficient and create secondary pollution. The use of a sorbent, such as a nanofibre sorbent, is a technique for controlling oil spills because of its good physical and oil sorption properties. This review discusses about the application of nanofibre sorbent for oil removal from water and its current developments. With their unique physical and mechanical properties coupled with their very high surface area and small pore sizes, nanofibre sorbents are alternative materials for cleaning up oil spills.