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A magnetic covalent organic framework (Fe 3 O 4 @COF) with core–shell structure was fabricated at room temperature and used as an adsorbent for magnetic solid-phase extraction of polar endocrine-disrupting phenols (4-n-nonylphenol, 4-n-octylphenol, bisphenol A and bisphenol AF). The sorbent was characterized by transmission electron microscopy, FTIR, powder X-ray diffraction and other techniques. The main parameters governing the extraction efficiency were optimized. The phenols were quantified by HPLC with fluorometric detection. The method has attractive features such as low limits of detection (0.08–0.21 ng.mL −1 ), wide linear ranges (0.5–1000 ng.mL −1 ), and good repeatability (intra-day: 0.39%–4.99%; inter-day: 1.57%–5.21%). Satisfactory results were obtained when the developed method was applied to determine the four target pollutants in real world drink samples with spiked recoveries over the range of 81.3~118.0%. This indicates that the method is a powerful tool for the enrichment and determination of endocrine-disrupting phenols in drink samples. Graphical abstract A magnetite based covalent organic framework (Fe 3 O 4 @COFs) was synthesized with TPAB, TPA and Fe 3 O 4 . It was used for magnetic solid-phase extraction of endocrine-disrupting phenols from plastic-packaged tea drink samples coupled with liquid chromatography (LC) for determination.

Nonylphenol (NP), nonylphenol monoethoxylate (NP1EO), and nonylphenol diethoxylate (NP2EO) are widely used in various daily products and have been cataloged as endocrine-disrupting chemicals. Due to their high lipophilicity and low biodegradability, these compounds remain in the environment and enter the human body through the food chain. Growing concerns regarding the potential negative effects of NP, NP1EO, and NP2EO on human health have raised the need for biomonitoring to investigate human exposure to these compounds. In this study, a simultaneous analysis method using solid-phase extraction (SPE) combined with gas chromatography-mass spectrometry (GC–MS) was established by controlling the background contamination of NP, NP1EO, and NP2EO, which are ubiquitous in laboratory environments. The proposed method showed proper linearity of over 0.999 and a recovery greater than 85.8% for all analytes. Accuracy and precision were verified in ranges of 92.97–116.30% and 0.65–9.29%, respectively. The detection limits for NP, NP1EO, and NP2EO were 0.0363 μg L −1 , 0.0401 μg L −1 , and 0.0364 μg L −1 , respectively, which were suitable for determining the trace analytes in human urine. Therefore, this simple and integrated analytical method was applied to measure the free and total forms of the target analytes in 25 human urine samples collected in Korea. Overall, free NP, NP1EO, and NP2EO were detected with average contents of 3.94 ± 4.14 μg L −1 , 4.63 ± 2.62 μg L −1 , and 0.293 ± 0.638 μg L −1 , respectively, and with total NP, NP1EO, and NP2EO contents of 6.14 ± 8.24 μg L −1 , 5.99 ± 2.91 μg L −1 , and 0.806 ± 1.10 μg L −1 , respectively. These data showed that these compounds are prevalent in human urine, and indicate the need for further studies.

Alkylphenols (APs) are ultimate breakdown products of alkylphenol polyethoxylate (APEs) that are used in cleaning and industrial processes. The most commonly used APEs in the market are the nonylphenol ethoxylates (NPEs) and octylphenol ethoxylates (OPEs). As a result of their widespread use and their lipophilic nature, these compounds are ubiquitous in the environment and are currently of concern because of their toxicity, oestrogenic properties and widespread contamination. This review summarizes the concentrations of NPE and NP in different environmental media. The sources of NPE in the environment and toxicity are reviewed. Their distribution patterns in the environment as well as exposure pathways are discussed with a view to provide better understanding of these emerging environmental contaminants. It is envisaged that this review will heighten the importance of identifying emerging issues and data gaps, and generate a future research agenda on APEs.

The suspected endocrine disruptor nonylphenol (NP) is closely associated with anthropogenic activities; therefore, studies on this compound have been clustered in urban areas. This study investigated the NP concentrations in drinking water sources ( n  = 8), terminal tap water ( n  = 36), and human urine samples ( n  = 127) collected from urban and rural areas in Wuhan, China. The mean concentrations of NP measured in drinking water sources in urban and rural areas were 92.3 ± 7.5 and 11.0 ± 0.8 ng/L (mean ± SD), respectively, whereas the mean levels in urban and rural tap waters were 5.0 ± 0.7 and 44.2 ± 2.6 ng/L (mean ± SD), respectively. Nevertheless, NP was detected in 74.1% and 75.4% of the human urine samples from urban and rural participants, with geometric mean concentrations of 0.19 ng/mL (0.26 µg/g creat) and 0.27 ng/mL (0.46 µg/g creat), respectively. Although the NP concentrations measured in the drinking water sources of urban areas were significantly higher than those in rural areas ( P  < 0.05), the tap water and urine NP concentrations measured in urban areas were unexpectedly lower than those of rural areas ( P  < 0.05). Additionally, this investigation showed that the materials comprising household water supply pipelines and drinking water treatment processes in the two areas were also different. Our results indicated that the levels of exposure to NP in drinking water and human urine in rural areas were not necessarily lower than those in urban areas. Thus, particular attention should be paid to rural areas in future studies of NP.

Endocrine-disrupting chemicals (EDC) are a wide group of chemicals that interfere with the endocrine system. Their similarity to natural steroid hormones makes them able to attach to hormone receptors, thereby causing unfavorable health effects. Among EDC, bisphenol A (BPA), bisphenol S (BPS), and nonylphenol (NP) seem to be particularly harmful. As the industry is experiencing rapid expansion, BPA, BPS, and NP are being produced in growing amounts, generating considerable environmental pollution. White rot fungi (WRF) are an economical, ecologically friendly, and socially acceptable way to remove EDC contamination from ecosystems. WRF secrete extracellular ligninolytic enzymes such as laccase, manganese peroxidase, lignin peroxidase, and versatile peroxidase, involved in lignin deterioration. Owing to the broad substrate specificity of these enzymes, they are able to remove numerous xenobiotics, including EDC. Therefore, WRF seem to be a promising tool in the abovementioned EDC elimination during wastewater treatment processes. Here, we review WRF application for this EDC removal from wastewater and indicate several strengths and limitations of such methods.

The study evaluated the co-metabolism of nonylphenol polyethoxylate (NPEO) within a main substrate stream subjected to biodegradation in an activated sludge system. Peptone mixture simulating sewage was selected as the synthetic substrate. As a novel approach, the NPEO concentration was magnified to match the COD level of the peptone mixture, so that co-metabolism could be evaluated by respirometry and modeling. A sequencing batch reactor (SBR) set-up at high sludge age to also allow nitrification was operated for this purpose. A long acclimation phase was necessary to start NPEO biodegradation, which was completed with 15% residual by-products. Modeling of respirometric data could identify COD fractions of NPEO with corresponding process kinetics for the first time, where the biodegradation of by-products could be interpreted numerically as a hydrolysis mechanism. Nonylphenol diethoxylate (NP2EO) was observed as the major by-product affecting the biodegradation of NPEO, because NPEO and NP2EO accounted for 60 to 70% of the total soluble COD in the solution during the course of biological reactions. The co-metabolism characteristics basically defined NPEO as a substrate, with no appreciable inhibitory action on the microbial culture both in terms of heterotrophic and autotrophic activities.

Tannery wastewater (TWW) is of serious environmental concern to pollution control authorities, because it contains highly toxic, recalcitrant organic and inorganic pollutants. The nature and characteristics of recalcitrant organic pollutants (ROPs) are not fully explored to date. Hence, the purpose of this study was to characterize and identify the ROPs present in the treated TWW. Gas chromatography–mass spectrometry data analysis showed the presence of a variety of ROPs in the treated TWW. Results unfolded that benzyl chloride, butyl octyl phthalate, 2,6-dihydroxybenzoic acid 3TMS, dibutyl phthalate, benzyl alcohol, benzyl butyl phthalate, 4-chloro-3-methyl phenol, phthalic acid, 2′6′-dihydroxyacetophenone, diisobutyl phthalate, 4-biphenyltrimethylsiloxane, di-(-2ethy hexyl)phthalate, 1,2-benzenedicarboxylic acid, dibenzyl phthalate, and nonylphenol were present in the treated TWW. Due to endocrine disrupting nature and aquatic toxicity, the U.S. Environmental Protection Agency classified many of these as “priority pollutants” and restricted their use in leather industries. In addition, the physicochemical analysis of the treated TWW also showed very high BOD, COD, and TDS values along with high Cr and Pb content beyond the permissible limits for industrial discharge. Furthermore, phytotoxicity assessment unfolds the inhibitory effects of TWW on the seed germination, seedling growth parameters, and α-amylase activity in Phaseolus aureus L. This indicates that the TWW discharged even after secondary treatment into the environment has very high pollution parameters and may cause a variety of serious health threats in living beings upon exposure. Overall, the results reported in this study will be helpful for the proper treatment and management of TWW to combat the environmental threats.

Migration of emerging contaminants (ECs) from pipes into water is a global concern due to potential human health effects. Nevertheless, a review of migration ECs from pipes into water distribution systems is presently lacking. This paper reviews, the reported occurrence migration of ECs from pipes into water distribution systems in the world. Furthermore, the results related to ECs migration from pipes into water distribution systems, their probable sources, and their hazards are discussed. The present manuscript considered the existing reports on migration of five main categories of ECs including microplastics (MPs), bisphenol A (BPA), phthalates, nonylphenol (NP), perfluoroalkyl, and polyfluoroalkyl substances (PFAS) from distribution network into tap water. A focus on tap water in published literature suggests that pipes type used had an important role on levels of ECs migration in water during transport and storage of water. For comparison, tap drinking water in contact with polymer pipes had the highest mean concentrations of reviewed contaminants. Polyvinyl chloride (PVC), polyamide (PA), polypropylene (PP), polyethylene (PE), and polyethylene terephthalate (PET) were the most frequently detected types of microplastics (MPs) in tap water. Based on the risk assessment analysis of ECs, levels of perfluorooctanoic acid (PFOA), perfluorononanoic acid (PFNA), perfluorodecanoic acid (PFDA), perfluorohexane sulfonate (PFHxS), and perfluorooctane sulfonate (PFOS) were above 1, indicating a potential non-carcinogenic health risk to consumers. Finally, there are still scientific gaps on occurrence and migration of ECs from pipes used in distribution systems, and this needs more in-depth studies to evaluate their exposure hazards on human health.

Exposure to endocrine disruptor substances will alter the function of the endocrine system and then cause adverse effects on human health. Among these endocrine disrupting chemicals, hexestrol, nonylphenol, and bisphenol A are most commonly used worldwide. In this study, we aim to develop a simple, rapid, and efficient analytical method for the simultaneous determination of trace hexestrol, nonylphenol, and bisphenol A in lake water and milk samples. A magnetic molecularly imprinted polymer-assisted magnetic solid-phase extraction technique was applied. The magnetic molecularly imprinted polymer was prepared and characterized by electron scanning microscopy and Fourier transform infrared spectroscopy. Subsequently, different experiments were conducted to optimize the magnetic solid-phase extraction conditions. High-performance liquid chromatography with UV detection was employed to determine hexestrol, nonylphenol, and bisphenol A. Limits of detection of the developed method were from 0.1 to 0.3 μg L−1 and spiked recoveries ranged from 89.9 to 102.5%, with a relative standard deviation of < 2.5% (intraday). Results obtained from this study showed that the proposed magnetic solid-phase extraction method was a simple, rapid, and sensitive sample pre-treatment method for the determination of trace hexestrol, nonylphenol, and bisphenol in different aqueous samples.

Nonylphenol is a typical endocrine-disrupting chemical that has received considerable attention from government officials, scientists and the public due to its estrogenicity and ubiquitous occurrence in water environments. Here we review the current knowledge on nonylphenol occurrence, distribution, toxic effects and water quality criteria related to the protection of freshwater organisms. Nonylphenol enters the water ecosystem mainly via wastewater treatment plant effluents, agricultural runoff, groundwater discharge from air, soil, water and agricultural sources. Toxic effects of nonylphenol on aquatic organisms include acute toxic effects, growth and development effects, estrogenic effect and reproductive effects, neurotoxicity, liver toxicity and immunotoxicity.