Perfluoroalkyl Substances Research Articles

Life Cycle Assessment of Per- and Polyfluoroalkyl Substances (PFAS) Remediation Technologies: A Literature Review

The remediation of environments contaminated with per- and polyfluoroalkyl substances (PFAS) has become a growing priority due to the persistent, bioaccumulative, and toxic characteristics of these compounds. To promote green and sustainable remediation practices, it is crucial to assess and minimize the environmental impacts of PFAS remediation projects through life cycle assessment (LCA) at the early stages of planning. So far, no systematic literature review has been published to assess the current state of the art or identify the challenges associated with applying LCA to PFAS remediation. This article provides a review of the recent literature on LCAs of PFAS remediation, following the ISO 14040 and 14044 standards. The results indicate that the application of LCA to PFAS remediation remains in its infancy and is highly fragmented. Significant methodological variations, including differences in system boundaries and data quality, hinder the comparability and benchmarking of LCA results across studies. To enhance the use of LCA as a decision support tool for environmental assessment, there is a pressing need for methodological harmonization and improved practices. Key areas for improvement include enhancing data quality, reducing uncertainties, and increasing the robustness of PFAS LCAs, thereby enabling more informed and sustainable decision-making in PFAS remediation efforts.

Analysis of wastewater treatment plant data identifies the drivers of PFAS enrichment in foams

The concept of incorporating foam fractionation in aerated bioreactors at wastewater treatment plants (WWTPs) for the removal of per- and polyfluoroalkyl substances (PFAS) has recently been proposed. The extent of PFAS enrichment in aerated bioreactors’ foams, as indicated by enrichment factors (EFs), has been observed to vary widely. Laboratory evidence has shown that factors affecting PFAS enrichment in foams include conductivity, surfactant concentrations and initial PFAS concentrations. However, real wastewaters are complex heterogenous matrices with physical, chemical and biological characteristics potentially contributing to the phenomenon of PFAS partitioning into foams. In this study, we characterised mixed liquor suspensions, including conductivity, filament content, aqueous PFAS concentrations, surface tension and total suspended solids concentrations (TSS) as well as foams, including bubble size and half-life. We used statistical tools – linear mixed-effects model – to establish relationships between PFAS enrichment in aerated bioreactor foams and the examined characteristics. We found that some of the examined characteristics, specifically filament content, surface tension and TSS concentrations measured in mixed liquor suspension and foam half-life, are negatively and significantly associated with the enrichment of longer chain PFAS (with perfluorinated carbon number ≥ 6). Of these, filament content is the important determinant of PFAS enrichment, potentially leading to an increase in, for example, perfluorooctanoic acid (PFOA) EF from 3 to 100 between typical filamentous and non-filamentous suspended biomass. However, enrichment of shorter chain PFAS (with perfluorinated carbon number ≤ 5) is negligible and is not affected by the characteristics that were measured. The findings of our study may serve as valuable information for the implementation of foam fractionation at WWTPs by elucidating the drivers that contribute to the enrichment of longer chain PFAS, under conditions typically found at WWTPs.

Using a Time-of-Travel Sampling Approach to Quantify Per- and Polyfluoroalkyl Substances (PFAS) Stream Loading and Source Inputs in a Mixed-Source, Urban Catchment

Using a Time-of-Travel Sampling Approach to Quantify Per- and Polyfluoroalkyl Substances (PFAS) Stream Loading and Source Inputs in a Mixed-Source, Urban Catchment

Environmental toxicants modulate disease severity in pediatric metabolic dysfunction-associated steatohepatitis.

Metabolic dysfunction-associated steatotic liver disease (MASLD) is common in children. We hypothesized environmental toxins could drive progression to metabolic dysfunction-associated steatohepatitis (MASH), and assayed serum toxins and metabolites in children with histologically characterized MASLD/MASH. Environmental chemicals, common in household items, perfluoroalkyl substances (PFAS), brominated flame retardants (PBDEs), and metabolic profiles were assayed in children enrolled in the multicenter NASH Clinical Research Network Pediatric Database 2. Mixture models, using repeated holdout weighted quantile sum regression (WQSrh) were run in addition to single chemical/metabolite logistic regression. For metabolomic analyses, random subset version of WQSrh was used for the large number of predictors versus participants. Nominal and false discovery rate (FDR) p-values (two-sided) were computed. Four hundred and thirty-five children distributed across MASH (n = 293) and MASLD (n = 142), with 304 (69.9%) males. Mean (standard deviation) for Nonalcoholic Steatohepatitis Score (NAS) and alanine aminotransferase (ALT) for MASLD were 3.1 (1.0), 67.9 (43.4), and for MASH 4.2 (1.4), 144 (121). There was an inverse association between PFAS/PBDE mixture and MASH versus MASLD, lobular inflammation (p = 0.026), NAS (p = 0.009, FDR p = 0.04), and log-transformed ALT (p = 0.005, FDR p = 0.025) driven by perfluorohexane sulfonate (PFHxS). Metabolites from positive hydrophilic interaction liquid chromatography mode, biliverdin (p = 0.002) and 1-methylhistidine (associated with meat ingestion, p = 0.02) and reverse phase negative mode, hippuric acid (solvent exposure, p = 0.022) significantly associated with MASH. Significant negative PFAS/PBDE mixture effect and odds of MASH were dominated by PHFXS. Several metabolites are significantly associated with MASH which inform mechanistic pathways and could drive key therapeutic and diagnostic strategies in children.

Methods for Analyzing PFAS in Water

Key TakeawaysAs the hazards of per‐ and polyfluoroalkyl substances—widely known as PFAS—are better understood, regulations and guidelines for addressing them will continue to evolve.Water utilities play a significant role in PFAS mitigation by incorporating detection, monitoring, and treatment techniques into their operations.Many methods for PFAS analysis are in place. A detailed explanation and comparison of each can help utilities determine the best approaches for their particular circumstances.

Spectral induced polarization (SIP) measurements across a PFAS-contaminated source zone

There is a need to develop field-scale, in situ screening technologies for assessing variations in aqueous film-forming foam (AFFF) concentrations in soils at former fire training and storage sites. Field-scale Spectral Induced Polarization (SIP) geophysical measurements were acquired on a transect crossing an AFFF source zone. Soil samples were acquired to determine variations in poly- and per-fluoroalkyl substances (PFAS) concentrations in soils, characterize soil texture, and create triplicate soil columns for laboratory SIP measurements. Field and laboratory observations show that SIP measurements are sensitive to the concentration of AFFF constituents associated with soil pore surface area. The specific polarizability and the phase of the SIP measurements for the laboratory samples were linearly correlated with total soil-sorbed PFAS concentration. The phase from the field SIP measurements was highest over the location of maximum PFAS concentration measured on the laboratory samples. However, a significant correlation between field-measured phase and laboratory-measured total PFAS concentration still needs to be established. These observations, along with the demonstrated sensitivity of the SIP response to the removal of soil PFAS using a methanol wash procedure, support the case for SIP characterization of AFFF source zones.

Decade-long historical shifts in legacy and emerging per- and polyfluoroalkyl substances (PFAS) in surface sediments of China's marginal seas: Ongoing production and ecological risks

Since the addition of perfluorooctane sulfonate (PFOS) to the Stockholm Convention in 2009, it became imperative to reassess the distribution and ecological risk of per- and polyfluoroalkyl substances (PFAS) in coastal sediments over the past decade as sediment records the history of pollutants from human activities. To achieve this, sediments were collected in 2009 and 2021 from China's coastal regions. Despite the consistent geographical pattern where the highest concentrations of ∑PFAS were found in the Yellow Sea, temporal changes have emerged. During the studied period, ∑PFAS levels experienced an increase in the East China Sea while concurrently witnessing a decrease in the South China Sea. Of significance, emerging PFAS compounds displayed not only rising concentrations but also a broader array, pointing towards their intensified production and utilization within China. Alarmingly, PFOS levels in sediments taken from the East China Sea maintained a consistently high ecological risk status over the last ten years. Significant correlations were found between long-chain PFAS and organic carbon content. Comparisons between datasets from 2009 to 2021 uncovered a shifting ecological risk landscape, with heightened concerns for PFOA in the East China Sea, while PFOS-associated risks appeared to diminish in the South China Sea—potentially reflecting the transition to alternative PFAS chemicals. The research reinforces the importance of continuous monitoring and emphasizes the urgent necessity for deeper exploration into the environmental implications and hazards posed by emerging PFAS.

In Vitro Hepatic Clearance Evaluations of Per- and Polyfluoroalkyl Substances (PFAS) across Multiple Structural Categories.

Toxicokinetic (TK) assays and in vitro-in vivo extrapolation (IVIVE) models are New Approach Methods (NAMs) used to translate in vitro points of departure to exposure estimates required to reach equivalent blood concentrations. Per- and polyfluoroalkyl substances (PFAS) are a large chemical class with wide-ranging industrial applications for which only limited toxicity data are available for human health evaluation. To address the lack of TK data, a pooled primary human hepatocyte suspension model was used with targeted liquid chromatography-mass spectrometry to investigate substrate depletion for 54 PFAS. A median value of 4.52 μL/(min x million cells) was observed across those that showed significant clearance, with 35 displaying no substrate depletion. Bayesian modeling propagated uncertainty around clearance values for use in IVIVE models. Structural evaluations showed the fluorotelomer carboxylic acids were the only PFAS carboxylates showing appreciable clearance, and per- and polyfluorosulfonamides were more readily metabolized than other PFAS sulfonates. Biotransformation product prediction, using the chemical transformation simulator, suggested hydrolysis of PFAS sulfonamides to more stable sulfonic acids, which is an important consideration for exposure modeling. This effort greatly expands the PFAS in vitro toxicokinetic dataset, enabling refined TK modeling, in silico tool development, and NAM-based human health evaluations across this important set of emerging contaminants.

Development and validation of a novel HPLC-MS/MS method for the quantitative determination of PFASs in non-hazardous solid waste samples

Perfluoroalkyl substances (PFASs) are a heterogeneous group of fluorinated synthetic compounds characterised by the presence of a hydrophobic carbonyl chain at different fluorination rates and by a terminal hydrophilic group. Because of their persistence and mobility, PFASs have been widely detected in ecosystems and living organisms, leading to their classification as persistent organic pollutants (POPs). Hence, monitoring the PFASs content in solid waste meant for disposal in non-hazardous landfills can be crucial, since leachate can pose a significant pollution threat to farmlands and aquifers.Therefore, a QuEChERS and SPE pretreatment with HPLC-MS/MS detection method for 10 different PFASs in solid waste samples was developed in this study. Different sample preparation approaches have been evaluated, taking into account the lack in the literature of this complex matrix.An innovative application using the Captiva EMR cartridge for the clean up (designed to be applied to lipidic matrix) was proposed and a multiresidual HPLC-MS/MS method for the analysis of PFASs in internal waters was extended to the investigation of non-lipidic samples as solid wastes. The method was then validated through 6 blanks and 6 spiked samples, according to the UNI EN ISO/IEC 17025. The optimized method showed satisfactory performance with recoveries ranging from 89.8 % to 106.5 % and with LOD and LOQ ranging between 0.0023 – 0.09 µg/L and 0.006 – 0.13 µg/L, respectively, for each of the PFASs under consideration. In addition, this approach demonstrated to be reliable and time consuming due to its capability for determining PFASs in waters and in solid wastes simultaneously in a single chromatographic run.

Adsorption of per- and polyfluoroalkyl substances on biochar derived from municipal sewage sludge

Granular activated carbon (GAC) and ion exchange resin (IXR) are widely used as adsorbents to remove PFAS from drinking water sources and effluent waste streams. However, the high cost associated with GAC and IXR generation has motivated the development of less expensive adsorbents for treatment of PFAS-impacted water. Thus, the objective of this research was to create an economically viable and sustainable PFAS adsorbent from sewage sludge. Stepwise pyrolysis at temperatures from 300 °C to 1000 °C yielded biochars whose specific surface area (SSA) and porosity increased from 41 to 148 m2/g, and from 0.062 to 0.193 cm3/g, respectively. On a per organic char basis, the SSA of the biochar was as high as 1183 m2/g, which is comparable to commercially-available activated carbons. The adsorption of perfluorooctane sulfonic acid (PFOS) on sludge biochar increased with increasing pyrolysis temperature, which was positively correlated with increasing porosity and SSA. When 1000 °C processed biochar was tested with a mixture of eight PFAS, preferential adsorption of longer carbon chain-length species was observed, indicating the importance of PFAS hydrophobic interactions with the biochar and the availability of a wide range of mesopores. The adsorption of each PFAS was dependent upon both chain length and head group, with longer chain-length species exhibiting greater adsorption than shorter chain-length species, along with greater adsorption of species with sulfonic acid head groups compared to their chain length counterparts with carboxylic acid head groups. These findings demonstrate that biochar derived from municipal solid waste can serve as a cost-effective and sustainable adsorbent for the removal of PFOS and PFAS mixtures from source waters. The circular economy benefits and waste reduction potential associated with the use of sewage sludge-derived biochar supports the development of a viable sludge-derived biochar for the removal of PFAS from water.

Comparing occurrence of per- and polyfluoroalkyl substances (PFAS) in municipal biosolids and industrial wastewater sludge: A City of Los Angeles study

Biosolids and sludge are what remain after the liquid fraction of wastewater is separated during wastewater treatment. These high organic content matrices are known to contain organic contaminants, a few of which are the hazardous and environmentally persistent per- and polyfluoroalkyl substances (PFAS). The current study investigates whether sludge from a treatment facility serving mostly industrial establishments and biosolids from a facility serving mostly domestic dwellings retain these ‘forever chemicals’ similarly. Using 31 markers covering different classes of PFAS, the sludge was found to contain higher levels of PFAS (869 ± 791 ng/g; 21 of 31) than biosolids (31 ± 7 ng/g, 11 of 31). The most abundant overall was perfluorooctane sulfonic acid (PFOS), mostly in sludge (range: 71–1300 ng/g versus 0–18 ng/g in biosolids). The large PFAS concentration variability in sludge was seasonal and sinusoidal. Sludge, additionally, contained all long chain PFAS, precursors (mostly surfactant ingredients and their transformation byproducts) and short chain PFAS (perhaps because of higher moisture content). By regression, the sludge is shown to consistently contain twice as much PFAS as biosolids when the same amounts are exposed to increasing levels of PFAS. Factors observed to cause differential PFAS retention between sludge and biosolids were moisture (98.6 % and 72.1 %, respectively), chain length, input quality (industrial versus residential) and functional group. Sulfonic acids for instance are one C atom shorter than carboxylates with similar occurrence in sludge and biosolids. More studies are needed to define the roles that organic carbon of sludge/biosolids, water chemistry, temperature and factors not considered here play in partitioning PFAS between the two matrices with respect to inputs. Existing Koc values could not help in explaining observed trends, but the ratio of biosolids-to-influent concentrations was found to correlate positively with PFAS size. Using influent in the ratio, and not effluent, is novel. SynopsisSludge and biosolids are soil amendments; they contain hazardous and persistent PFAS. Methods of decoupling PFAS from these matrices start with understanding matrix-driven PFAS partitioning as shown here.

Development, validation, and clinical assessment of a liquid chromatography-tandem mass spectrometry serum assay for per- and polyfluoroalkyl substances (PFAS) recommended by the National Academies of Science, Engineering, and Medicine (NASEM).

Per- and polyfluoroalkyl substances (PFAS) are widely used in industry, residential, and consumer products. Studies have shown associations between high PFAS exposure and adverse health effects. In 2022, the National Academies of Science, Engineering, and Medicine (NASEM) published Guidance on PFAS Exposure, Testing, and Clinical Follow-up providing laboratory and clinical direction. The Guidance suggests nine PFAS should be measured in serum or plasma specimens and summed to provide a total PFAS concentration using a NASEM-recommended method. Follow-up clinical recommendations are based on the calculated PFAS NASEM summation. We developed and validated a liquid chromatography-tandem mass spectrometry (LC-MS/MS) method in accordance with NASEM recommendations but distinguished by the ability to separate closely related structural isomers. As part of our validation, PFAS prevalence was evaluated in a population survey comprised of clinical donor and remnant specimens (n = 1023 in total). In this study, 82.2% of the specimens had PFAS NASEM summations of 2 to < 20ng/mL and 2.5% had a summation ≥ 20ng/mL. The median PFAS NASEM summation was 4.65ng/mL in this study, lower than the 7.74ng/mL median observed in the 2017-2020 Centers for Disease Control and Prevention, National Health and Nutrition Examination Survey (n = 3072). This lower median PFAS NASEM summation may reflect a decline in PFAS population levels over time or sample population exposure differences.

Mapping Per- and Polyfluoroalkyl Substance Footprint from Cosmetics and Carpets across the Continental United States.

Per- and polyfluoroalkyl substances (PFAS) released from common consumer products, such as cosmetics and carpets, are nonpoint sources of environmental contamination. However, detailed information on PFAS mass and emission rates from these products is limited. Here, we propose a methodology to develop PFAS footprint from the manufacturing and supply chain data of cosmetics and carpets. Our analysis combines geospatial and statistical assessments to understand how the production and consumption of these products contribute to existing PFAS contamination hotspots in the Continental United States (CONUS). Statewide mass estimations revealed that North Carolina and New York contribute to the major PFAS mass released from cosmetics, while Georgia and California contribute to the major PFAS mass released from carpets. The average per capita PFAS footprint from carpets and cosmetics is about 103 mg/year. Upon disposal, over 60% of the mass eventually ends up in landfills. The accumulation of PFAS stocks in landfills, primarily from carpets and to some extent from cosmetics, highlights the critical need to cease the production and use of PFAS in consumer products. Coastal counties are particularly vulnerable due to higher population and therefore higher consumption of these PFAS-tainted consumer products. Additionally, counties with densely populated areas and with preexisting contamination sources would face increased vulnerability to PFAS contamination released from various consumer products.

Cytotoxicity and mechanisms of perfluorobutane sulfonate (PFBS) in umbilical cord fibroblast cells of Yangtze finless porpoise

Yangtze finless porpoises (YFP) accumulate high levels of per- and polyfluoroalkyl substances (PFASs). However, the health impacts of PFASs to YFP are still unknown because it is technically and ethically unfeasible to use the critically endangered YFP in toxicological exposures. To uncover the potential toxicities of PFASs to YFP, this study exposed a YFP umbilical cord fibroblast cell line to perfluorobutane sulfonate (PFBS), an emerging PFASs pollutant in the aquatic environments. After exposure, the cytotoxicity and mechanisms of PFBS were explored. Our preliminary experiments found that PFBS compromised the cell viability in a concentration and duration dependent manner. In an exposure of 48-h duration, the maximum no observed effect concentration (NOEC) of PFBS was determined to be 400 µM. High-throughput proteomics were then conducted to identify the differentially expressed proteins in YFP cells exposed to 400 µM PFBS for 48 h. The results found that PFBS exposure significantly perturbed the proteome fingerprints of YFP umbilical cord fibroblast cells. Functional annotation of differential proteins showed that PFBS had the potential to impair a variety of biological processes associated with the immunity, oxidative stress, metabolism, and proteolysis. Consistently, the intracellular levels of reactive oxygen species (ROS) and proinflammatory cytokine IL-1β were significantly increased by PFBS in YFP umbilical cord fibroblast cells. Overall, this study highlights the toxic effects of emerging PFASs on YFP and provides reference data to evaluate the health risks of aquatic pollution under the context of national YFP protection. To our knowledge, this is the first omics study using YFP umbilical cord fibroblast cells in ecotoxicology of PFASs, which is applicable to various cetacean species and pollutants.

Occurrence, risk assessment and source apportionment of perfluoroalkyl acids in the river of a hill-plain intersection region: The impacts of land use and river network structure

Studying the impacts of land use and river network structure on perfluoroalkyl acids (PFAAs) footprint in rivers is crucial for predicting the fate of PFAAs in aquatic environments. This study investigated the distribution, ecological risks, sources and influence factors of 17 PFAAs in water and sediments of rivers from hills to plain areas. The results showed that the detection frequencies were higher for short-chain PFAAs than long-chain PFAAs in water, whereas an opposite pattern was found in sediments. The concentration of ∑PFAAs ranged from 59.2 to 414 ng/L in water and from 1.4 to 60.1 ng/g in sediments. Perfluorohexanoic acid and perfluorooctanoic acid were identified as the main pollutants in the river. The average concentrations of PFAAs were higher in the aquaculture areas (water: 309.8 ng/L; sediments: 43.27 ng/g) than in residential areas (water: 206.03 ng/L; sediments: 11.7 ng/g) and farmland areas (water: 123.12 ng/L; sediments: 9.4 ng/g). Environmental risk assessment showed that PFAAs were mainly low risk or no risk in water, but were moderate risk and even high risk in sediments, especially for perfluorooctane sulfonate. Source apportionment found that PFAA sources were mostly from industry, wastewater discharge, and surface runoff. Dissolved oxygen, chemical oxygen demand, water system circularity, network connectivity and organic matter were significantly correlated to PFAA concentration, indicating that the physicochemical properties and river network might directly influence the environmental behavior of PFAAs. The built-up area was positively correlated with PFAAs. These findings indicated that a comprehensive understanding of the influences of land use and river network structure on PFAAs in rivers is essential for managers to formulate effective PFAA control strategies.

Prenatal exposure to perfluoroalkyl and polyfluoroalkyl substances and childhood bone mineral density: A prospective birth cohort study

Background and aimPerfluoroalkyl and polyfluoroalkyl substances (PFAS) have demonstrated potential toxicity in skeletal development. However, the relationship between prenatal PFAS exposure and offspring bone health remains unclear in epidemiological studies. Therefore, we aim to investigate whether prenatal exposure to PFAS is associated with bone mineral density (BMD) in offspring. MethodThis study population included 182 mother-child pairs in the Shanghai Obesity and Allergy Cohort, enrolled during 2012–2013. 10 PFAS were measured by liquid chromatography-mass spectrometry (LC-MS) in cord plasma. The child's spinal BMD was measured using a dual-energy X-ray absorptiometry (DXA) scanner at the age of 8. Multivariable linear regression models were used to estimate the associations between individual PFAS concentrations (as a continuous variable or categorized into quartiles) and child BMD. Bayesian kernel machine regression (BKMR) was employed to explore the joint effects of PFAS mixtures on BMD. ResultsAmong the 10 PFAS, 8 of them had a detection rate >90% and were included in the subsequent analysis. We observed no significant associations between individual PFAS (as a continuous variable) and spinal BMD in 8-year-old children using the multivariable linear regression model. When treated as quartile categories, the second and fourth quartiles of perfluorobutane sulfonate (PFBS) was associated with higher BMD in the first lumbar vertebra, compared with the lowest quartile. BKMR analysis revealed no association between the PFAS mixture and child BMD. ConclusionWe observed no associations of prenatal PFAS exposure with child BMD at 8 years of age. Given the inconsistent epidemiological evidence, further research is needed to confirm these findings from other studies or elucidate the potentially toxic effects of PFAS on bone.

Comparative analysis of enhanced adsorption and thermal decomposition of oil-borne PFAS using CeO2 nanoparticles and activated carbon

Per- and poly-fluoroalkyl substances (PFAS) are widely used as surfactants in the oil and gas industry, presenting significant environmental and health risks due to their persistence and mobility. While prevailing research primarily targets PFAS removal from aqueous environments, this study explores the efficacy of nanosized cerium oxide nanoparticles (CeO2 NPs) and traditional activated carbon (AC) in removing PFAS from organic media via adsorption and thermal degradation. Both adsorbents exhibited robust adsorption capabilities; however, their interaction mechanism with PFAS differ significantly. CeO2 NPs primarily engage in chemical adsorption with PFAS, whereas AC relies on hydrophobic interactions. Additionally, CeO2 NPs outperformed AC in thermal degradation experiments, achieving approximately 95 % decomposition of PFOS at 400 °C, compared to only 52 % with AC. Furthermore, the formation of stable Ce−F bonds at high temperatures significantly reduced fluoride ion release from CeO2 NPs, underscoring their potential to minimize environmental impact. This study is the first to apply both AC and CeO2 NPs for PFAS removal from organic media and to elucidate their distinct adsorption and thermal decomposition mechanisms, highlighting the superior performance of CeO2 NPs in environmental remediation of PFAS.

Determination of regulated perfluoroalkyl substances (PFAS) in drinking water according to Directive 2020/2184/EU.

Perfluoroalkyl substances (PFAS) are chemical compounds that have been widely used in industry and manufacture. Occurrence, together with persistence and recent toxicological effects data, has promoted the regulation of 20 PFAS (carboxylic and sulfonic) acids in drinking water through the recent Directive 2020/2184/EU. This Regulation included PFAS with different carbon chain lengths (from C4 to C13) and limited the total PFAS concentration (as sum) to a maximum of 0.1µg/L, for which law-enforcement analytical methods are required. In this work, three different methodologies have been developed and evaluated as regards their performance to determine those 20 PFAS in tap and bottled water, based on on-line and off-line solid-phase extraction (SPE) and direct injection. In all cases, ultra-high pressure liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) was used as a determination technique. Off-line SPE with Oasis Weak Anion Exchange (WAX) cartridges provided the best results in terms of limits of quantification (LOQ ≤ 0.3ng/L) and accuracy (R ≥ 70%) in drinking water samples. On-line SPE and direct injection presented some drawbacks such as background contamination problems and lower accuracies for the least polar compounds. This off-line SPE methodology was then applied to the analysis of 46 drinking water samples (11 commercial bottled samples, 23 Spanish and 12 international tap water samples). Ten PFAS were quantified in such samples at concentrations and detection frequencies ranging from 0.1 to 20.1ng/L and 2 to 91%, respectively. However, the sum concentration did not surpass the established limit in any sample.

Understanding the Selective Removal of Perfluoroalkyl and Polyfluoroalkyl Substances via Fluorine-Fluorine Interactions: A Critical Review.

As regulatory standards for per- and polyfluoroalkyl substances (PFAS) become increasingly stringent, innovative water treatment technologies are urgently demanded for effective PFAS removal. Reported sorbents often exhibit limited affinity for PFAS and are frequently hindered by competitive background substances. Recently, fluorinated sorbents (abbreviated as fluorosorbents) have emerged as a potent solution by leveraging fluorine-fluorine (F···F) interactions to enhance selectivity and efficiency in PFAS removal. This review delves into the designs and applications of fluorosorbents, emphasizing how F···F interactions improve PFAS binding affinity. Specifically, the existence of F···F interactions results in removal efficiencies orders of magnitude higher than other counterpart sorbents, particularly under competitive conditions. Furthermore, we provide a detailed analysis of the fundamental principles underlying F···F interactions and elucidate their synergistic effects with other sorption forces, which contribute to the enhanced efficacy and selectivity. Subsequently, we examine various fluorosorbents and their synthesis and fluorination techniques, underscore the importance of accurately characterizing F···F interactions through advanced analytical methods, and emphasize the significance of this interaction in developing selective sorbents. Finally, we discuss challenges and opportunities associated with employing advanced techniques to guide the design of selective sorbents and advocate for further research in the development of sustainable and cost-effective treatment technologies leveraging F···F interactions.

Concentrations of Per-and Polyfluoroalkyl Substances (PFAS) and Pancreatic Cancer: A Case–Control Study in New York

Concentrations of Per-and Polyfluoroalkyl Substances (PFAS) and Pancreatic Cancer: A Case–Control Study in New York