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This study presents a new, non‐enzymatic electrochemical sensor based on gold‐copper nanobrambles (Au‐CuONBs) for rapid and accurate chemical oxygen demand (COD) monitoring in water. COD, an essential metric of water quality, is typically assessed using labor‐intensive methods with high toxicity and limited tolerance to chloride interference. The Au‐CuONBs‐based sensor here proposed overcomes these limitations by offering high sensitivity, a broad linear detection range (0.1–10.3 mM glucose), and robust tolerance to chloride ions, enabling accurate measurements even in challenging water samples. Tested on real wastewater samples, the sensor delivered results closely aligned with standard COD methods, with a detection limit of 11 μM and response time of only 5 min. This portable, cost‐effective sensor provides a promising solution for sustainable on‐site COD analysis, enhancing water quality management and environmental monitoring. A novel, non‐enzymatic electrochemical sensor employing gold‐copper nano‐brambles enables rapid, accurate, and chloride‐tolerant chemical oxygen demand (COD) detection. Demonstrating high sensitivity and excellent performance in real wastewater samples, this portable platform offers a sustainable and efficient alternative for on‐site COD monitoring in environmental and water quality assessment contexts.

In recent years, due to modern techniques for the distribution, transport, and retail sale of food, the production of large amounts of non-biodegradable and bioaccumulative packaging waste has become a major environmental issue. To address this issue, new food packaging materials based on renewable biomass have been studied as eco-friendly, biodegradable, and biocompatible alternatives to synthetic materials. However, although these materials are not petrochemical derivatives, the presence of contaminants cannot be excluded. This work aims to extend the knowledge on bio-based packaging materials, researching the presence of contaminants potentially able to migrate to food at concentrations of concern. In this study, we focus on two classes of contaminants, organophosphate esters (OPEs) and perfluoroalkyl substances (PFASs), carrying out migration tests toward different simulants, according to the current European regulation. PFAS analysis was performed using high-resolution liquid chromatography coupled to ion trap-tandem mass spectrometry (QTrap). OPE analyses were performed both by gas chromatography–mass spectrometry (GC-MS) and high-resolution liquid chromatography coupled to triple quadrupole mass spectrometry (TQMS). Preliminary findings demonstrate the release of toxic OPEs and PFASs from bio-based food packaging, highlighting the need to investigate the presence of potentially harmful chemicals in these materials.

Objectives: The aim of this study was to provide a comprehensive overview of the nutritional and toxicological aspects of different forms of blueberry products (fresh blueberries, dried blueberries, supplements and herbal teas). Methods: Twelve aglycone and glycoside polyphenolic compounds, such as stilbenoids (resveratrol, astringin), flavonols (quercetin, rutin, isoquercitrin, quercitrin, kaempferol), flavanols (catechin, epicatechin), flavanone (hesperitin), flavone (luteolin), and forty chemical elements were analyzed using high-performance liquid chromatography coupled to a mass spectrometer and inductively coupled plasma mass spectrometry. Total phenolic and flavonoid content and antioxidant activity were also evaluated. Results: Different distributions of polyphenolic compounds were observed in the blueberry samples, with quercetin and its derivatives, as well as catechin and epicatechin, present in all samples. High concentrations of Ca, K, Mg and P (10–5800 mg/kg) were detected, followed by Fe and Mn at levels below the allowable limits in foods (425 and 500 mg/kg, respectively). The daily intake of polyphenols was quantified, and the estimated daily intake (EDI) was calculated for sixteen elements (including As, Cd, Cu, Fe, Ni, Pb, V and Zn). Hazard quotients (HQs), hazard index (HI) and cancer risk (CR) were assessed for carcinogenic and non-carcinogenic risks associated with the EDI of these elements in food products for both adults and young consumers. For all samples, HI values were below 1, and CR values were within acceptable limits. Conclusions: The diversity in polyphenolic profiles and elemental content in blueberry-based products was highlighted by this exploratory study. These findings are valuable for understanding the health benefits and risks of blueberry products.

Poly- and perfluorinated alkyl substances (PFASs) are widely used in the electrical and electronic appliance industry to the point that waste of electrical and electronic equipment (WEEE), also known as e-waste, creates significant potential for PFAS exposure (by inhalation, ingestion, or dermal exposure) for people handling and recycling e-waste. The aim of this work was the development of an untargeted analytical approach in order to detect the presence of possible unknown PFASs in particulate matter collected in three Italian e-waste facilities through liquid chromatography coupled to high-resolution tandem mass spectrometry (LC-HR-MS/MS) in negative ionization mode. By means of three acquisition experiments, nine compounds were detected as candidate PFASs, and three were definitively confirmed by comparison with their authentic standards. Among these, bistriflimide (bis (trifluoromethylsulfonyl) imide), an ionic liquid with several promising technological applications, was the most abundant compound detected in all three recycling plants. This is the first study associating the presence of fluorinated ionic liquids with e-waste, and as these chemicals are not only toxic and persistent but also highly mobile, our results indicate the need to include them in future PFAS research. Only further data on their actual environmental diffusion will determine whether they are emerging pollutants or not.

This study uses a membrane‐less reactor to explore the bioelectrochemical remediation of real contaminated groundwater from chlorinated aliphatic hydrocarbons (CAHs) and nitrates. The research focuses on testing a column‐type bioelectrochemical reactor to stimulate in situ degradation of contaminants through the supply of electrons by a graphite granules biocathode. After a preliminary laboratory characterization and operation with a synthetic feeding solution, a field test is conducted in a real contaminated site, where the reactor demonstrates effective degradation of CAHs and inorganic anions. Notably, the cathodic potential promotes the reductive dechlorination of chlorinated species. Simultaneously, nitrate reduction, sulfate reduction, and methanogenesis occurr, influencing the overall coulombic efficiency of the process. The use of real groundwater, compared to the synthetic medium, significantly decreases the coulombic efficiency of reductive dechlorination, dropping from 2.43% to 0.01%. Concentration profiles along the bioelectrochemical reactor allow for a deeper description of the reductive dechlorination rate at different flow rates, as well as increase the knowledge about reduction and oxidation mechanisms. Scaling up the technology presents several challenges, including the optimization of coulombic efficiency and the management of competing microbial metabolisms. The study provides a valuable contribution toward advancing bioelectrochemical technologies for the bioremediation of complex contaminated sites.

The occurrence of halogenated organic pollutants in indoor dust can be high due to the presence of textile, electronic devices, furniture, and building materials treated with these chemicals. In this explorative study, we focused on emerging organic pollutants, such as novel brominated flame retardants (nBFRs) and some perfluoroalkyl substances, together with legacy polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (BDEs) in settled dust collected in houses and workplaces such as one office and two electrotechnical and mechanical workshops. The total contribution of the investigated pollutants was lower in house and in office dusts except for few nBFRs (such as bis (2-ethylhexyl)-3,4,5,6-tetrabromo-phthalate at a concentration of 464.5 ng/g in a house and hexachlorocyclopentadienyldibromocyclooctane at 40.4 ng/g in the office), whereas in electrotechnical and mechanical workshops a high incidence of PCBs, BDEs, and nBFRs occurred (for example, BDE 209 at a concentration of 2368.0 ng/g and tetrabromobisphenol A at 32,320.1 ng/g in electrotechnical and mechanical workshops). Estimated daily intakes were also calculated, showing that domestic and occupational environments can lead to a similar contribution in terms of human exposure. The higher exposure contribution was associated to nBFRs, whose EDIs were in the range of 3968.2–555,694.2 pg/kg bw/day. To provide a complete view about the indoor contamination, in this investigation, we also included polycyclic aromatic hydrocarbons (PAHs) and their oxygenated and nitrated derivatives. Definitely, dust collection represents a simple, fast, and cost-effective sampling and dust contamination level can be a useful indicator of environment healthiness. Besides, the presented method can be a smart tool to provide a time and money saving technique to characterize 99 pollutants thanks to a single sample treatment.

PFASs are a variety of ecologically persistent compounds of anthropogenic origin loosely included in many industrial products. In these, the carbon chain can be fully (perfluoroalkyl substances) or partially (polyfluoroalkyl substances) fluorinated. Their ubiquitous presence in many environmental compartments over the years and their long-lasting nature have given rise to concerns about the possible adverse effects of PFASs on ecosystems and human health. Among a number of remediation technologies, adsorption has been demonstrated to be a manageable and cost-effective method for the removal of PFASs in aqueous media. This study tested two novel and eco-friendly adsorbents (pinewood and date seeds biochar) on six different PFASs (PFOS, GenX, PFHxA, PFOA, PFDA, and PFTeDA). Batch sorption tests (24 h) were carried out to evaluate the removal efficiency of each PFAS substance in relation to the two biochars. All samples of liquid phase were analyzed by a developed and then a well-established method: (i) pre-treatment (centrifugation and filtration) and (ii) determination by high-performance liquid chromatography coupled with mass spectrometry (HPLC-MS/MS). The results evidenced a comparable adsorption capacity in both materials but greater in the long-chain PFASs. Such findings may lead to a promising path towards the use of waste-origin materials in the PFAS remediation field.

In the last years, many studies have focused on risk assessment of exposure of workers to airborne particulate matter (PM). Several studies indicate a strong correlation between PM and adverse health outcomes, as a function of particle size. In the last years, the study of atmospheric particulate matter has focused more on particles less than 10 μm or 2.5 μm in diameter; however, recent studies identify in particles less than 0.1 μm the main responsibility for negative cardiovascular effects. The present paper deals with the determination of 66 organic compounds belonging to six different classes of persistent organic pollutants (POPs) in the ultrafine, fine and coarse fractions of PM (PM < 0.1 µm; 0.1 < PM < 2.5 µm and 2.5 < PM < 10 µm) collected in three outdoor workplaces and in an urban outdoor area. Data obtained were analyzed with principal component analysis (PCA), in order to underline possible correlation between sites and classes of pollutants and characteristic emission sources. Emission source studies are, in fact, a valuable tool for both identifying the type of emission source and estimating the strength of each contamination source, as useful indicator of environment healthiness. Moreover, both carcinogenic and non-carcinogenic risks were determined in order to estimate human health risk associated to study sites. Risk analysis was carried out evaluating the contribution of pollutant distribution in PM size fractions for all the sites. The results highlighted significant differences between the sites and specific sources of pollutants related to work activities were identified. In all the sites and for all the size fractions of PM both carcinogenic and non-carcinogenic risk values were below acceptable and safe levels of risks recommended by the regulatory agencies.

Wastewater carries different pathogenic and non-pathogenic microorganisms that can be dispersed in the surrounding environment. Workers who frequent sewage treatment plants can therefore be exposed to aerosols that contain a high concentration of potentially dangerous biological agents, or they can come into direct contact with contaminated material. This can lead to allergies, infections and occupational health-associated diseases. A characterization of biological risk assessment of bioaerosol exposure is necessary. The aim of this study was to evaluate the application of an interdisciplinary method that combines chemical and biological approaches for the analysis of a bioaerosol derived from a wastewater treatment plant (WWTP) situated in Italy. Sampled filters were analyzed by HPLC-MS/MS spectroscopy that searched for different chemical biomarkers of airborne microorganisms. The analytical quantification was compared to the biological cultural method that revealed an underrated microbial concentration. Furthermore, next generation sequencing analysis was used also to identify the uncultivable species that were not detected by the culture dependent-method. Moreover, the simple animal model was used to evaluate the pathogenicity of two isolates- and that showed multidrug-resistance. This work represents a starting point for the development of a multidisciplinary approach for the validation of bioaerosol exposure on WWTP workplaces.

Abstract Wastes from electrical and electronic equipment (WEEE) are disposed and dismantled in recycling plants where chemical composition of particulate matter (PM) is different from all the other working places. A first identification of airborne contaminants, associated with size-segregated particles in the fine (aerodynamic diameter < 2.5 µm) and coarse (aerodynamic diameter in the range 2.5–10 µm) fractions, sampled in two sectors of a WEEE facility, was performed. In the two areas of the plant, disassembly and shredding processes produced large amounts of dust, causing mass concentrations of airborne particles particularly high when activities intensified.Analyses of Na, Mg, Al, Si, P, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Ga, As, Se, Br, Rb, Sr, Y, Zr, Mo, Ba, and Pb were performed on PM samples collected by a streaker sampler. PM was collected with hourly and 30-min time resolution in the two sectors of the plant for three consecutive days, night and day.Organic substances belonging to the classes of polycyclic aromatic hydrocarbons (PAHs) and their oxy- and nitro- derivatives (oxy-PAHs and nitro-PAHs), organophosphorus compounds (OPEs), polyfluoralkyl substances (PFASs), and novel-brominated flame retardants (BFRs) were extracted and identified in PM samples collected by PM10 impactors. Particle sampling period for organic analyses was 4 h per day in the same three days, in each sector of the plant, during the working hours.High time resolution records of elemental composition were useful for highlighting the elements strongly depending on the productive process. During working hours, Pb and Ba concentrations reached higher levels and drastically decreased during the night. Their distribution in the coarse and fine fractions consistently increased and decreased, meaning that both fractions were linked to the working activity. Si, as main component of glass, was the most abundant element at both the areas. Though all the elements were below the permissible exposure limits recommended by Occupational Safety and Health Administration (OSHA’s PELs), the concentration of Pb was significantly high, especially at the shredding zone (21.9 µg/m3).The major organic constituents, among the classes of compounds investigated, were organophosphorus compounds (OPEs), especially in the coarse fraction of PM. In particular, triphenylphosphate (TPhP), deriving from computer video display units, was the most abundant organic compound. Interestingly, phenanthrene contributed to 60% of the total polycyclic aromatic hydrocarbons (PAHs), at both the sampling sites. Airborne plastic dust can be a source of PAHs. Products made of polyethylene recycled from post-commercial waste contain high concentrations of phenanthrene, present as impurities. The present study represents a preliminary investigation on WEEE plants airborne PM composition and additional research is necessary to confirm the data, but it is worth developing a method, as high particle concentrations, together with absorbed genotoxins, could constitute an occupational health risk.