Search Results (514)

The performance of a sequencing batch biofilter granular reactor (SBBGR), followed by a dual media granular activated carbon (GAC) column, was evaluated in terms of its ability to remove selected per- and polyfluoroalkyl substances (PFAS) from landfill leachate. The results show that the SBBGR achieved an overall reduction of 51%, with the preferential removal of long-chain PFAS, while short-chain PFAS were only partially removed. Subsequent GAC treatment exhibited compound-specific breakthrough behavior, which was governed by chain length. Short-chain PFAS (e.g., perfluorobutanoic acid) exhibited rapid bed volumes at 50% breakthrough (BV₅₀ ≈ 88), whereas long-chain PFAS (e.g., perfluorooctanoic acid and perfluorooctanesulfonic acid) were substantially more retained (BV₅₀ ≈ 446 and 361, respectively), with perfluorohexanesulfonic acid and perfluorodecanoic acid failing to reach BV₅₀ within the monitored period. Mass balance analysis showed that the hybrid GAC column captured ~73% of the influent PFAS mass. This resulted in >80–95% retention of long-chain PFAS and <40% retention of short-chain PFAS. Although long-chain PFAS were preferentially adsorbed, mobile short-chain species dominated residual effluent loads. These findings highlight the need for optimized contact times or dual-media strategies to control the breakthrough of short-chain PFAS. Full article

Global climate change and air pollution jointly threaten respiratory health. Asthma, a prevalent chronic inflammatory airway disease, is exacerbated by both traditional air pollutants such as particulate matter (PM_2.5), ozone (O₃), nitrogen dioxide (NO₂), sulfur dioxide (SO₂) and emerging contaminants like microplastics (MPs) and per- and polyfluoroalkyl substances (PFAS), with effects amplified under extreme temperature conditions. In reality, individuals face complex combined exposures, yet the synergistic effects of these factors on asthma pathogenesis remain poorly understood. This narrative review synthesizes epidemiological and toxicological evidence. It aims to elucidate both the individual and the notably synergistic effects of these factors on asthma pathogenesis. The central mechanistic pathway is initiated by oxidative stress, which activates key inflammatory signaling pathways, thereby driving immune imbalance and airway inflammation. Our review underscores that the combined exposure to traditional pollutants, emerging pollutants, and extreme temperatures may pose a greater threat than individual factors. These findings underscore the critical need for an integrated perspective in asthma research and public health policy. Moving beyond single-pollutant approaches, we advocate for combinatorial risk assessment and synergistic intervention strategies to effectively mitigate the growing burden of asthma in a changing climate. Full article

Per- and polyfluoroalkyl substances (PFASs) are persistent micropollutants whose carbon–fluorine bonds resist conventional advanced oxidation. Nonthermal plasmas have emerged as a promising option for PFAS degradation, but the relative contributions of reactive oxygen species (ROS) and electrons are still being investigated. Herein, we compared sinusoidal alternating-current (AC) and nanosecond-pulsed discharges―in an identical plasma reactor with the same input power (30 W)―through diagnostics including voltage–current characterization, optical emission spectroscopy with vibrational and rotational temperatures and Hα Stark broadening for electron density, and aqueous H₂O₂ quantification. AC discharges produced more aqueous H₂O₂, stronger ·OH emission, and higher vibrational and rotational temperatures, yet showed lower perfluorooctanoic acid (PFOA) removal (85% ± 2%) and lower defluorination (61% ± 1%) than the pulsed discharge (96% ± 2% and 80% ± 2%, respectively). Among the diagnostics examined, electron density tracked the removal trend, being higher under pulsed operation (1.2 × 10¹⁶ vs. 8.3 × 10¹⁵ under AC operation). A pseudo-first-order kinetic model based on electron density qualitatively reproduced the observed PFOA decay rate, suggesting that the waveform may serve as a design variable for tuning electron and ROS-mediated pathways in plasma–water reactors. Full article

Zeolite-based composite nanomaterials represent a versatile and mechanistically rich platform for the removal of organic micropollutants (OMPs)—including pharmaceuticals, endocrine-disrupting compounds, pesticides, and per- and polyfluoroalkyl substances (PFAS)—from contaminated water systems. Although pristine zeolite frameworks provide well-defined microporous architectures, tunable Si/Al ratios, and ion-exchange capacity, their intrinsic hydrophilicity restricts interaction diversity and limits performance toward the structurally heterogeneous OMPs prevalent in real aquatic environments. Composite integration with carbonaceous nanophases, functional polymers and surfactants, and catalytically active metal oxide nanoparticles substantially extends this interaction repertoire, yielding multifunctional materials whose adsorption performance exceeds that of the individual components. Drawing on a systematic survey of peer-reviewed literature published between 2016 and 2026, this review develops a mechanism-oriented, structure–property–performance framework examining five dominant adsorption mechanisms—electrostatic attraction, π–π stacking, hydrogen bonding, hydrophobic partitioning, and micropore confinement—in relation to composite nanoarchitecture, surface chemistry, and structural parameters. The modulating influence of realistic water matrix conditions on adsorption efficiency is critically assessed, alongside challenges of regeneration, long-term stability, metal leaching, and the persistent gap between laboratory-scale synthesis and scalable deployment. Priority research directions are identified, including standardized performance evaluation under environmentally representative conditions and rational design of hierarchical multifunctional nanocomposites from earth-abundant and waste-derived precursors. Full article

Per- and polyfluoroalkyl substances (PFAS) have been extensively used for many years in the manufacturing of industrial and commercial goods. Their toxicity and their extensive use, stability, durability, persistence, and bioaccumulation are responsible for the contamination of water, soil, air, and food, causing significant harm to human health and the environment. The objective of this chapter is to evaluate the ability of advanced (bio)sensing strategies for the sensitive, accurate, rapid, simple, and low-cost detection of PFAS in drinking water and the environment. We address advanced bio(sensing) strategies by emphasizing the electrochemical (bio)sensing strategies and the optical bio(sensing) strategies. The principle of each method, the mechanisms involved in the detection, the linear range, the limit of detection, and the applicability are underlined. Finally, this review outlines the major challenges and outlook to move advanced (bio)sensing strategies from the laboratory stage to practical applications in the environment, food, and health. Full article

Green Bay, Wisconsin, USA, is a popular waterfowl hunting location with thousands of waterfowl hunters visiting the area annually. Despite its popularity, the potential exposure to per- and polyfluoroalkyl substances (PFAS) through the consumption of waterfowl harvested in the area is unknown. Between 2022 and 2024, mallard duck (Anas platyrhynchos) breast tissue was collected from Green Bay and an unimpacted reference location to better understand waterfowl hunters’ exposure to PFAS. Results indicate that PFAS exposure is site-specific, as only two mallards from the reference location had detectable levels of perfluorooctane sulfonate (PFOS) in the breast tissue, while mallard breast tissue detection rates ranged from 67% to over 90% in two Green Bay locations. PFOS concentrations in the duck breast tissue were high enough to warrant a “one meal per month” (10 ng/g) and a “do not eat” (40 ng/g) advisory for mallards from Middle and Lower Green Bay, respectively, based on current consumption advisory thresholds used in Wisconsin. Paired water samples at the Lower Green Bay mallard collection site had PFOS concentrations higher than the Wisconsin surface water criteria of 8 ng/L, and the relative composition of PFAS in the water indicated multiple sources of PFAS to the area. Full article

This study evaluated the impact of a fire at a plastic recycling plant in the suburbs of Osijek on the concentrations of per- and polyfluoroalkyl substances (PFAS) in home-produced eggs (HPE) collected from nearby settlements exposed to smoke. The assessment was conducted over three time periods following the fire. Commercial eggs from supermarkets and HPE from northwestern Croatia were also analyzed. Thirteen out of 30 compounds were quantified. In both HPE groups—the one closer to and more exposed to smoke (Zone A) and the one farther from fire (Zone B)—linear perfluorooctane sulfonic acid (L-PFOS) showed the highest detection frequency (91–100%). The highest mean concentrations of L-PFOS and the sum of the four main PFAS (∑4PFAS: PFOS, perfluorooctanoic acid (PFOA), perfluorononanoic acid (PFNA), and perfluorohexane sulfonic acid (PFHxS)), at 1.33 μg/kg, were measured in HPE from Zone A one month after the fire. In Zone B, a lower total ∑4PFAS of 0.93 μg/kg was detected. After eight months, concentrations of all quantified compounds decreased. The sums of ∑4PFAS decreased to 0.41 μg/kg (A) and 0.37 μg/kg (B), respectively. Concentrations are higher than those from northwestern Croatia and the previously determined national average. Weekly intakes of ∑4PFAS exceeded the tolerable weekly intake for toddlers and children even eight months after the fire. Full article

Ultrashort-chain (USC) per- and polyfluoroalkyl substances (PFAS) are highly polar, mobile, and persistent emerging pollutants. While the environmental distribution of USC species is well-documented, their presence in widely consumed beverages remains under-characterized due to the analytical difficulty of capturing such highly polar species. This study established a robust workflow for the simultaneous determination of C1 to C14 perfluoroalkyl carboxylic and sulfonic acids, alongside other PFAS classes, in diverse beverage matrices including teas and fruit juices. Chromatographic separation was achieved using a mixed-mode inert-coated alkyl-phase LC column to enhance USC retention while maintaining performance for longer-chain analytes. A high-throughput, minimal-handling sample preparation was optimized to mitigate matrix effects and contamination. Method performance was evaluated using fortified beverage samples across 2–500 ng/L, with calibration ranges of 1–2000 ng/L and incorporation of 13 isotopically labeled internal standards. Results demonstrated acceptable accuracy (recoveries within 30% of nominal values) and optimal precision (%RSD < 12%). Application to commercial samples revealed frequent PFAS occurrence, specifically highlighting the prevalence of previously overlooked USC species in the human diet. These results demonstrate that ready-to-drink beverages are a significant pathway for human exposure, necessitating the inclusion of USC compounds in future food safety monitoring and risk assessments. Full article

Per- and polyfluoroalkyl substances (PFASs) in fluorinated firefighting wastewater (FFW), which are difficult to remediate using conventional technologies, represent a critical environmental hazard due to the extreme persistence and bioaccumulation potential of soil–groundwater systems. Niobium-supported boron-doped diamond (BDD) anodes were synthesized by microwave plasma chemical vapor deposition, and their performance in the electrochemical advanced oxidation processes (EAOPs) of FFW were systematically investigated. Under optimized conditions (100 mM Na₂SO₄ electrolyte with 100 mM peroxymonosulfate (PMS), current density of 33.3 mA/cm², pH = 6), the BDD anode achieved near-complete mineralization, with 92.5% total organic carbon (TOC) removal and significant defluorination (77.5% F⁻ release) within 240 min in simulated FFW-contaminated groundwater. For FFW-contaminated soil remediation, 90.2% TOC removal and 41.6% defluorination were achieved after 720 min under optimal treatment (water-to-soil ratio of 20:1). Quenching experiments and electron paramagnetic resonance (EPR) tests revealed that hydroxyl radicals (·OH) and singlet oxygen (¹O₂) were the predominant reactive species. Liquid chromatography–mass spectrometry/mass spectrometry (LC-MS/MS) analysis indicated that PFASs were removed by shortened carbon chains, ultimately mineralizing to CO₂ and F⁻. Toxicity assessment using Vibrio fischeri luminescence demonstrated a reduction in toxicity (from 99.8% to 20.9%), confirming the effective detoxification of BDD-based EAOPs. This work establishes BDD-based EAOPs as a promising technology for eliminating PFASs in groundwater and soil, offering theoretical insights into EAOPs and engineering solutions for PFAS remediation. Full article

Background/Objectives: Per- and polyfluoroalkyl substances (PFAS) are environmentally persistent chemicals widely detected in aquatic systems and drinking water. Perfluorononanoic acid (PFNA), a long-chain PFAS, has been reported globally in environmental matrices and fish tissues. Although PFNA has been linked to developmental, metabolic, and neurological toxicity, its effects on lipid-related pathways and neurotoxicity remain poorly characterized. Methods: This study evaluated the developmental and neurotoxic effects of PFNA exposure in zebrafish embryos and larvae following a 7-day exposure to environmentally relevant PFNA concentrations. Results: PFNA exposure did not significantly affect survival or deformity rates at the concentrations tested. Apoptosis was significantly increased in larvae exposed to 1 µg/L PFNA compared to controls, whereas reactive oxygen species levels were unaffected. Two concentrations (0.1 µg/L and 10 µg/L) were further examined for transcriptomic responses, and the transcriptome response was largely different for each concentration. Low-dose PFNA exposure primarily affected lipid transport, cholesterol metabolism, sphingolipid signaling, and neurodegeneration-related pathways, whereas high-dose PFNA altered transcripts related to synaptic signaling, axon guidance, and thyroid hormone synthesis. Hypoactivity was observed in the movement of larval zebrafish based on a Visual Motor Response test. Conclusions: Taken together, PFNA exposure induced molecular changes related to neurotoxicity and lipid metabolism in zebrafish, which may contribute to adverse neurodevelopmental outcomes. Full article

Reverse osmosis (RO) membranes are widely applied in reuse facilities, but the management of RO concentrate remains a major sustainability challenge. Conventional brine disposal methods, such as deep well injection or evaporation ponds, are costly, energy intensive, and often ineffective at addressing the accumulation of contaminants of emerging concern (CEC) and per- and polyfluoroalkyl substances (PFAS). Bioelectrochemical systems, such as microbial fuel cells (MFCs), offer a promising pathway for sustainable brine organic load management by simultaneously reducing organic load and recovering energy. In this study, a pilot-scale MFC system (Aquacycl BETT^®, Escondido, CA, USA, unit, 12 modular reactors) was evaluated for treatment of RO concentrate produced by a combined ultrafiltration and closed-circuit reverse osmosis pilot train at the San Jacinto Valley Regional Water Reclamation Facility (San Jacinto, CA, USA). Operating with a 4-h hydraulic retention time, the MFC achieved an average chemical oxygen demand (COD) removal of 40% and biochemical oxygen demand (BOD₅) removal of 52%. Coulombic efficiency ranged from 2.8% to 15.5%, with an average energy recovery value of about 8.1 Wh per kg of COD removed. PFOS concentrations decreased by 36% across the MFC, and PFAS were not detected in the harvested anode biomass. The mechanism of PFOS attenuation (e.g., adsorption vs. transformation) was not directly evaluated. These findings highlight the potential of MFCs as a bioelectrochemical solution for sustainable water reuse RO brine management. Full article

Environmental contaminants such as per- and polyfluoroalkyl substances (PFAS) and toxic metals have been implicated in biological aging, yet their combined effects remain poorly understood. This study evaluated the associations of PFAS, lead, and cadmium mixtures with multiple DNA methylation-based measures of epigenetic aging in a nationally representative sample of U.S. adults aged ≥ 50 years. Data were obtained from the 1999–2000 and 2001–2002 National Health and Nutrition Examination Survey (NHANES). The analytic sample included 1119 participants with available data on seven PFAS, blood lead, cadmium, and DNA methylation measures. Epigenetic aging outcomes included HannumAge, HorvathAge, SkinBloodAge, PhenoAge, GrimAge, and DunedinPoAm. Multivariable linear regression and Bayesian Kernel Machine Regression (BKMR) were used to assess individual and joint exposure–response relationships. Cadmium showed the most consistent positive associations with epigenetic aging measures, particularly for the second-generation clocks PhenoAge and GrimAge. Lead was positively associated with GrimAge, while PFAS showed more variable and generally weaker associations, with PFNA demonstrating the most consistent signal. Mixture analyses indicated that higher combined exposure levels were associated with higher DNA methylation age estimates, with stronger patterns observed for second-generation clocks. These findings suggest that combined exposure to PFAS, lead, and cadmium is associated with higher epigenetic aging in older U.S. adults, with cadmium emerging as a key contributor to the observed mixture effects. Evaluating environmental exposures as mixtures may provide important insight into how co-occurring contaminants jointly influence biological aging. Full article

Endocrine-disrupting chemicals (EDCs) are a diverse group of environmental pollutants capable of interfering with hormonal and immune system regulation. In recent years, increasing concern has been raised about the effects of chemicals, including bisphenols, phthalates, per- and polyfluoroalkyl substances (PFAS), insecticides, and parabens, on maternal and fetal health, primarily due to their widespread exposure in human populations. Pregnancy represents a critical window characterized by tightly regulated hormonal and immunological adaptations. Emerging evidence suggests that EDC exposure during this period may alter maternal microbiota, disrupt immune responses, and interfere with endocrine signaling. These changes may increase susceptibility to bacterial and viral infections, including bacterial vaginosis, urinary tract infections, and intrauterine infections, all of which are associated with adverse pregnancy outcomes. This review summarizes the current evidence on the sources and mechanisms of exposure to endocrine disruptors during pregnancy and examines the potential biological pathways linking endocrine disruption to the development of infections. Particular emphasis is placed on the interactions between immune regulation, hormonal signaling, and changes in the microbiome, which may contribute to increased susceptibility to infections. A deeper understanding of these complex mechanisms is critical to improve risk assessment, develop effective public health strategies, and ultimately protect maternal and fetal health in an environment of increasing chemical exposure. A literature search was conducted using PubMed/MEDLINE, Scopus, and Web of Science, including studies published up to January 2026. Full article

Wastewater is a complex and dynamic issue, particularly at the human–animal–environment interface, bearing biological and chemical hazards that may serve as a resource for transmission pathways for pathogens, antimicrobial resistance (AMR) determinants, heavy metals, pharmaceutical residues, per- and polyfluoroalkyl substances (PFAS), and microplastics. Rising global health issues necessitate effective wastewater treatment and advanced research to support risk-informed circular management within a one health framework, incorporating wastewater-based epidemiology (WBE), multi-omics approaches, nanobiotechnology, and green technologies. Inadequate wastewater treatment and uncontrolled discharge result in the generation of more than 380 billion cubic meters of wastewater annually worldwide, contributing to ecological degradation, the spread of AMR, and long-term toxicological risks. Despite significant advances in wastewater treatment, several challenges remain, including complex contaminant mixtures, limited detection and monitoring technologies, variable treatment efficiency, and weak regulatory and governance frameworks. This review highlights key wastewater treatment issues and presents recent advances in WBE and multi-omics approaches, such as metagenomics, resistome profiling, virome analysis, and chemical fingerprinting for contaminant monitoring and public health risk assessment. This review also examines circular reuse strategies focused on water reclamation, nutrient recovery, bioenergy production, and resource recovery, with particular emphasis on nature-based systems, hybrid biological–physicochemical treatment platforms, and green nanobiotechnology as promising approaches to improve treatment performance while minimizing environmental impacts. In conclusion, this review highlights the importance of integrated and sustainable wastewater management approaches within the One Health framework to address emerging challenges and promote environmental resilience, public health protection, and circular resource recovery. Full article

Per- and polyfluoroalkyl substances (PFAS) are a class of synthetic chemicals notable for their high persistence and extensive applications. With the advancement of detection technologies in recent years, PFAS have been frequently identified in environmental media and human biological samples, raising significant global concerns about their potential health risks. PFAS exhibit distinctive toxicokinetic behaviors, including efficient absorption, strong protein binding, limited metabolism, and slow excretion, which lead to prolonged biological half-lives and considerable bioaccumulation in humans. These properties contribute to a range of adverse health outcomes, such as endocrine disruption, immune suppression, liver damage, reproductive toxicity, carcinogenic potential, and cardiovascular disease. This review synthesizes evidence on PFAS-associated health risks from a multisystem, multitarget perspective, elucidating the key molecular pathways involved, thereby providing a scientific basis for understanding their complex toxicological effects and for developing targeted prevention and control strategies. Future research should prioritize characterizing the toxicological profiles of individual PFAS compounds, evaluating the health impacts of combined (mixture) exposures, and assessing risks associated with chronic, low-dose exposure to support the development of public health strategies and regulatory decisions. Full article