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34, 104.17, 109.89, and 121.95 mg·g-1, respectively. The LODs for the analysis of EDCs with HPLC-DAD by using 57%TCPP@MOF-808 as sorbent were achieved in the range of 0.01-0.03 ng·mL-1. The recoveries were obtained in the range of 74.63-98.00%. Enrichment factors were calculated in the range of 146-312. This work provides an effective strategy for design and preparation of multifunctional nanomaterials to improve their potential applications in the detection of environmental pollutants.The arsenic-rich biomass of Pteris vittata is a heavy burden to phytoremediation, but the compositions of extracts recycled from arsenic-rich biomass, such as rutin, may promote broiler growth. As such, this extract can be used to reduce the usage of antibiotics in the broiler industry and the cost of phytoremediation at the same time. Therefore, the critical issues for using extract from arsenic-rich biomass as a growth promoter have been studied, including its effective composition, health and environmental risks, and potential benefits and feasibility. Forty-five compounds were identified in the extract, and they were mainly flavonoids, chlorogenic acids, and proanthocyanidins, which can directly or indirectly influence the growth of broiler. The lifetime carcinogenic risks of broiler edible parts may be maximally increased by 4.75 × 10-9 due to feeding the extract. The arsenic concentration of the farmland fertilized with the excrement from the broiler fed with the extract may increase by 0.00003-0.01857 mg/kg per year. Results revealed a feasible scenario that the sustainability of phytoremediation and broiler industry could be benefited through wastes from each other.Photocatalytic oxidation of contaminants in water has recently gained extensive attentions. In this study, Cu2+-doped BiOCl microsphere photocatalysts were prepared using solvothermal method. The effects of Cu2+ doping ratio on the morphological structures and photoelectric and photocatalytic properties of BiOCl were studied in detail. Results showed that Cu2+ doping affected the particle size of BiOCl microspheres. The introduction of Cu2+ ions gradually increased the light absorption range and decreased the electron recombination rate of photocatalysts as shown by ultraviolet-visible diffuse reflection and photoluminescence spectra. The best doping ratio was 0.25 Cu2+-BiOCl, showing the highest photocatalytic activity for rhodamine B (14.25 time higher than BiOCl) and a good inhibition of algal growth. The main reactants in the photocatalytic system were·OH and h+ (electron holes). Density functional theory (DFT) calculations further demonstrated that the doping of Cu2+ ions made the photogenerated carriers in BiOCl easier to generate and ensured the charge was transferred more rapidly. In conclusion, a novel high-efficiency multifunctional photocatalyst is proposed for the efficient organic pollutants removal and algae growth inhibition from water.Antibiotics, antibiotic resistant bacteria (ARB) and antibiotic resistance genes (ARGs) are ubiquitous in the reclaimed water, posing a potential threat to human and ecological health. Nowadays, the reuse technology of reclaimed water has been widely concerned, but the removal of antibiotics, ARB and ARGs in reclaimed water has not been sufficiently studied. This study used TiO2 nanotube arrays (TNTs) decorated with Ag/SnO2-Sb nanoparticles (TNTs-Ag/SnO2-Sb) as the anode and Ti-Pd/SnO2-Sb as the cathode to construct an efficient photoelectrocatalytic (PEC) system. In this system, 99.9% of ARB was inactivated in 20 min, meanwhile, ARGs was removed within 30 min, and antibiotics were almost completely degraded within 1 h. Furthermore, the effects of system parameters on the removals of antibiotics, ARB and ARGs were also studied. The redox performance of the system was verified by adding persulfate. Escherichia coli, as a representative microorganism in aquatic environments, was used to evaluate the ecotoxicity of PEC treated chloramphenicol (CAP) solution. The ecotoxicity of CAP solution was significantly reduced after being treated by PEC. In addition, transformation intermediates of CAP were identified using liquid chromatography-tandems mass spectrometry (LC-MS/MS) and the possible degradation pathways were proposed. This study could provide a potential alternative method for controlling antibiotic resistance and protecting the quality of reclaimed water.N-nitrosodimethylamine (NDMA) and N-nitrosomorpholine (NMOR) and their specific precursors (N,N-dimethylformamide [DMF] for NDMA and morpholine [MOR] for NMOR) were widely identified in runoff of urban area around the southern Lake Biwa basin, Japan. It was thought that this runoff might constitute a non-point source of the four compounds in rivers and sewage treatment plants (STPs) during heavy rainfall events. We investigated the spatiotemporal patterns of NDMA, NMOR, DMF and MOR in runoff and rivers in rainy days. NDMA and NMOR were detected in concentrations of up to 295 ng/L, while DMF and MOR were detected in concentrations of up to 33.7 µg/L. Continuous sequential sampling over periods of 24 or 48 h at the largest STP in the study area revealed that the four compounds in the primary effluent (PE) each had higher mass fluxes during heavy rainfall events than on dry days. This phenomenon might be contributed to non-point sources (e.g., runoff) from infiltration/inflow related to rainwater into sanitary sewers. Moreover, the four compounds were confirmed to have higher mass fluxes in the final effluent of the STP during periods of PE bypass (1.3-1.7 times for NDMA, NMOR, and MOR; over 200 times for DMF; on average) than that on dry days because of increasing inflow during heavy rain than during periods without PE bypass in dry weather.Recently, rice contamination by heavy metals (HMs) has become a severe problem. Taking the Western Fujian region as an example in this study, a total of 1311 rice samples containing eight HMs were collected from 2015 to 2019, then used to explore their pollution characteristics, health risks, and Spatio-temporal variations, finally derive the target remediation areas of the key pollutants. The results showed that average concentrations of all the HMs had not reached the limits of the National Standards of Food Safety, but pollution indexes of As (0.783) and Cu (0.665) were at accumulation level (>0.6), which posed high pollution risks. Furthermore, locations of higher HMs concentrations coincided with those of higher pollution estimation probabilities. The non-carcinogenic risk (4.150, 2.434) and carcinogenic risk (4.96 × 10-3, 2.92 × 10-3) for children and adults cannot be negligible, As and Cd were the largest contributors. Children were more susceptible than adults due to the metal concentrations and rice intake rate. The spatio-temporal changes indicated that a decreasing trend in average concentrations of HMs (except Cr), but As (0.37%-0.88%) contents increased in the west and northeast parts, and so did Cd (1.92%-5.11%) in the central region during monitoring. For the target remediation, particular regions in the western and eastern were used as risky areas of As and Cd, respectively. Our results will provide theoretical support for the pollution management of HMs in rice.Studies have demonstrated the worldwide presence of bisphenol A (BPA) and its toxic effects on human health. BPA may exist as several structural isomers, which are byproducts in industrial BPA production. However, nearly nothing is known about the occurrence of BPA isomers in human blood and the partitioning of BPA metabolites between human serum and whole blood. In this study, BPA, BPA-sulfate (BPA-S), and BPA-glucuronide (BPA-G) were quantified in 144 pairs of serum and whole blood samples from Chinese participants. BPA was detected in 115 serum and 121 whole blood samples, with mean concentrations of 0.53 and 0.88 ng/mL, respectively. A structural isomer of BPA, tentatively termed B1-BPA, was identified for the first time, and measurable in 53% and 57% of serum ( less then LOD-1.9 ng/mL) and whole blood ( less then LOD-1.4 ng/mL) samples, respectively. BPA-S was the predominant BPA metabolite (mean 2.3 and 1.4 ng/mL, respectively), significantly higher (p less then 0.01) than BPA-G (1.3 and 0.64 ng/mL) in both serum and whole blood. The calculated partitioning coefficients between serum and whole blood were the highest for B1-BPA (mean ± SD, 1.8 ± 0.25), followed by BPA-S (1.6 ± 0.36), BPA-G (1.4 ± 0.37), and BPA (1.3 ± 0.39), indicating their preferential enrichment in the serum fraction. Overall, this study first identifies a BPA isomer, which has not been previously reported in any environmental or human samples. Measuring BPA isomers in human serum and whole blood is critical for accurate human BPA exposure risk assessment.It is of great interest to explore physiological metabolism of electrochemically active bacteria (EAB) for combined organics and heavy metals in single-chamber microbial electrolysis cells (MECs). Four pure culture EAB varying degrees responded to the combined acetate (1.0-5.0 g/L) and Cd(II) (20-150 mg/L) at different initial concentrations in the single-chamber MECs, shown as significant relevance of Cd(II) removal (2.57-7.35 mg/L/h) and H2 production (0-0.0011 m3/m3/h) instead of acetate removal (73-130 mg/L/h), to these EAB species at initial Cd(II) below 120 mg/L and initial acetate below 3.0 g/L. A high initial acetate (5.0 g/L) compensated the Cd(II) inhibition and broadened the removal of Cd(II) to 150 mg/L. These EAB physiologically released variable amounts of extracellular polymeric substances with a compositional diversity in response to the changes of initial Cd(II) and circuital current whereas the activities of typical intracellular enzymes were more apparently altered by the initial Cd(II) than the circuital current. These results provide experimental validation of the presence, the metabolic plasticity and the physiological response of these EAB directed by the changes of initial Cd(II) and acetate concentrations in the single-chamber MECs, deepening our understanding of EAB physiological coping strategies in metallurgical microbial electro-ecological cycles.In recent decades, much attention has been paid to microplastic pollution, and research on microplastics has begun to grow exponentially. However, microplastics research still suffers from the lack of standardized protocols and methods for investigation of microplastics under laboratory conditions. Therefore, in this review, we summarize and critically discuss the results of 715 laboratory studies published on microplastics in the last five years to provide recommendations for future laboratory research. selleckchem Analysis of the data revealed that the majority of microplastic particles used in laboratory studies are manufactured spheres of polystyrene ranging in size from 1 to 50 µm, that half of the studies did not characterize the particles used, and that a minority of studies used aged particles, investigated leaching of chemicals from microplastics, or used natural particles as a control. There is a large discrepancy between microplastics used in laboratory research and those found in the environment, and many laboratory studies suffer from a lack of environmental relevance and provide incomplete information on the microplastics used.