Polyfluoroalkyl Substances Concentrations Research Articles

Association between per- and polyfluoroalkyl substance exposures and thyroid homeostasis parameters

Abstract Context Prevailing studies have shown the disruption effect of per- and polyfluoroalkyl substances (PFAS) on thyroid homeostasis. However, most studies focused on individual thyroid hormones. Objective To explore the associations between PFAS exposures and thyroid homeostasis parameters. Methods A total of 2386 adults from NHANES (2007-2008 and 2011-2012) were included. Thyroid homeostasis parameters included central and peripheral thyroid hormone sensitivity, calculated by thyroid hormones. Multivariable survey-weighted linear regressions were performed to determine the association between PFAS exposure and thyroid homeostasis parameters. The weighted quantile sum (WQS) and the quantile g-computation (QGC) models were used to estimate the mixed effects of co-exposures to PFAS. Results The ratio of free triiodothyronine/free thyroxine (FT3/FT4) and the sum activity of peripheral deiodinases (SPINA-GD) were positively associated with perfluorooctanoic acid (PFOA), perfluorooctanesulfonic acid, perfluorononanoic acid and perfluorohexane sulfonic acid, respectively. However, no significant associations were observed between PFAS exposure and central thyroid sensitivity parameters. PFAS co-exposures was positively associated with FT3/FT4 (β = 0.013, P < 0.001) and SPINA-GD (β = 1.230, P < 0.001) in WQS models. Consistently, PFAS concentrations per quantile was linked to an increase in FT3/FT4 (β = 0.004, P = 0.002) and SPINA-GD (β = 0.392, P = 0.008) in GQC models, with PFOA having the highest weight in all models. Conclusion This study revealed that PFAS exposures may affect peripheral thyroid hormone sensitivity instead of central among U.S. general adults, enhancing our understanding of the correlation between PFAS exposure and thyroid hormones and providing insights into potential health implications.

Enhanced removal of trace-level per- and polyfluoroalkyl substances (PFAS) from drinking water using granular activated carbon (GAC): the role of ozonation.

Granular activated carbon (GAC) is a promising approach for removing per- and polyfluoroalkyl substances (PFAS) from drinking water. However, GAC filters usually suffer early PFAS breakthroughs due to the competition between PFAS and natural organic matter (NOM) during sorption. The present study investigated the possibility of using ozonation to enhance the GAC performance for PFAS removal. Rapid-small-scale-column tests were performed for three GACs using filtered or filtered and ozonated water. NOM was fractionated using liquid chromatography-organic carbon detection (LC-OCD), and 76 ambient PFAS were quantified using ultra-high-performance liquid chromatography coupled with high-resolution mass spectrometry (UHPLC-HRMS). Although ozonation did not remove either NOM or PFAS, it altered their composition in water. Ozonation reduced the hydrophobicity and the molecular size of natural organic matter (NOM). On the other hand, ozonation oxidized some PFAS precursors, leading to a higher total detected PFAS concentration in the filtered and ozonated water than in filtered water (10.2 ± 0.7 ng/L vs. 9.5 ± 0.7 ng/L). The impact of ozonation on GAC performance for NOM and PFAS removal mainly depended on GAC properties. GAC with a lower micropore volume showed an improvement in NOM and PFAS removal when ozonation was applied, approaching the performance of GACs with higher micropore volumes.

Occurrence of per- and polyfluoroalkyl substances in wheat, maize, rice, and soybean from chinese major grain producing regions.

Dietary exposure to per- and polyfluoroalkyl substances (PFAS) has been a concern for many years. Previous studies demonstrated that foods such as meat, milk, fish, vegetables, and tuber crops could be potential sources of human exposure to PFAS. However, research on PFAS contamination in grains remains limited. Therefore, this study conducted a comprehensive investigation of PFAS contamination in raw grains from major grain-producing regions in China. Among all grain species, soybeans exhibited the highest Σ16PFAS level (1.01ng/g dw), followed by rice (0.570ng/g dw), wheat (0.542ng/g dw), and maize (0.245ng/g dw). Short-chain perfluoroalkyl carboxylates (PFCAs) displayed higher detection frequencies compared to their long-chain homologues and perfluoroalkyl sulfonates (PFSAs). Perfluorobutanoic acid (PFBA) and perfluorooctanoic acid (PFOA) were dominant in wheat, maize, and soybean samples, while sodium p-perfluorous nonenoxybenzenesulfonate (OBS) was predominant in rice. OBS contributed approximately 70% to Σ16PFAS concentrations in rice. The concentration difference of OBS was not significant between indica rice and japonica rice, however, a disparity was observed between early indica rice and mid-late indica rice, suggesting that the growing period potentially affects OBS level in rice grains. Compared to other regions, east China displayed relatively higher PFAS concentrations in grain samples. This finding is consistent with previous studies and may be attributed to the intensive industrial and human activities. The estimated daily intake (EDI) of Σ16PFAS in grains from this study ranged from 0.0829 to 3.32ng/kg bw/day. The dietary health risks associated with PFOA in wheat and OBS in rice warrant further attention.

Bioturbation Affects Bioaccumulation: PFAS Uptake from Sediments by a Rooting Macrophyte and a Benthic Invertebrate.

Despite the widespread presence of per- and polyfluoroalkyl substances (PFAS) in freshwater environments, only a few studies have addressed their bioaccumulation in macrophytes and benthic invertebrates. This study therefore aimed at investigating the presence of 40 PFAS in sediments, assessing their bioaccumulation in a rooting macrophyte (Myriophyllum spicatum) and a benthic invertebrate (Lumbriculus variegatus) and examining the effects of the presence and bioturbation activity of the invertebrate on PFAS bioaccumulation in the plants. The macrophytes were exposed to sediments originating from a reference and a PFAS-contaminated site. The worms were introduced in half of the replicates, and at the end of the experiment, PFAS were quantified in all environmental compartments. Numerous targeted PFAS were detected in both sediments and taken up by both organisms, with summed PFAS concentrations in organisms largely exceeding concentrations in the original sediments. Bioaccumulation differed between organisms and the two sediments. The presence of the worms significantly reduced the PFAS concentrations in the plant tissues, but for some compounds, root bioaccumulation increased in the presence of the worms. This effect was most prominent for the degradable PFAS precursors. It is concluded that organisms affect the environmental fate of PFAS, emphasizing that contaminant-macroinvertebrate interactions are two-sided.

Persistent organic pollutants among seafood processing workers in West Greenland

The Greenlandic population is highly exposed to persistent organic pollutants (POPs) through the consumption of traditional marine food, including marine mammals. Central to Greenland's economy and cultural identity, the fishing industry employes about 15% of the working population.This study investigated POP exposure, including polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs), and per- and polyfluoroalkyl substances (PFASs), among seafood processing workers at the Greenlandic west coast. We examined determinants for the POPs including age, smoking habits, ethnicity, and working place. Additionally, we explored the association between POPs and the prevalence of asthma, allergy, and lung function.With samples taken during 2016–2018, the study encompassed 382 workers, primarily of Inuit descent (93%), employed across three large factories located in Nuuk, Sisimiut, and Ilulissat, four smaller factories in settlements (Kangaatsiaq, Ikerasaarsuk, Sarfannguaq, Qeqertarsuaq), and four factory trawlers. Data collected include clinical examinations, questionnaires on ethnicity, occupational exposure status, health indicators, and smoking habits, and serum selenium and POP analyses. We used ANCOVA with adjustment for relevant confounders to assess differences in POPs between groups (e.g. ethnic groups and working place), and multiple linear and logistic regressions were used to assess associations between POPs and lung function, allergy and asthma.Significant differences in POPs were observed among ethnic groups; Faroese workers had the highest concentrations of lipophilic POPs (lipPOPs; PCBs and OCPs), while Inuit workers exhibited highest PFASs. All subsequent analyses were focused on the Inuit workers (n = 337). The PFASs were significantly higher in workers at small factories, followed by large factories and trawlers, whereas no differences were seen for lipPOPs. The differences between the working places were most likely due to differences in lifestyle and diet, but occupational exposures cannot be excluded.LipPOP and PFAS concentrations associated positively with selenium, and PFASs positively associated with lung function. However, upon adjustment of selenium, the associations between PFASs and lung function became non-significant and attenuated towards null. No significant associations were found between POPs and the prevalence of asthma or allergy.Compared to the general population in the same area and period, the seafood processing workers exhibited 2–6 times higher POP levels. The higher exposure level among seafood processing workers, as well as the difference across workplaces, underscore the need for further investigation of environmental and occupational sources of POPs in this population. These findings may contribute to future public health strategies and regulatory measures to reduce POP exposure in Arctic populations.

Occurrence, transformation, and transport of PFAS entering, leaving, and flowing past wastewater treatment plants with diverse land uses

Per- and polyfluoroalkyl substances (PFAS) have been detected ubiquitously throughout the environment. Wastewater treatment plants (WWTPs) have been identified as potential hotspots for the introduction of PFAS into the environment. Therefore, the occurrence, transformation, and transport of 18 PFAS in two WWTPs with varying treatment processes, prevailing land uses, and during two distinct time periods were investigated. Polar Organic Chemical Integrative Samplers (POCIS) were installed at two WWTPs in Central Kentucky during April and July of 2022. PFAS concentrations typically increased from influent to effluent at both WWTPs, regardless of wastewater treatment processes, but changes in surface water concentrations from upstream to downstream of the effluent mixing zones varied. Both WWTPs discharged the 18 PFAS at higher loads than received, indicating prevalent transformation of PFAS precursors and non-measured PFAS analytes into measurable PFAS. Nearly all measured PFAS persisted in aqueous (86–98%) compartments rather than sediment or biosolids (2–14%). All biosolids had low content of PFAS with the dominant compound being PFOS (1.59–2.60 ng/g). Based on recent US EPA proposed maximum contaminant levels, hazard indexes for drinking water were exceeded in effluent and downstream surface waters at both WWTPs. The WWTP located in a heavily developed area and downstream from a firefighting training facility, had significantly higher concentrations of most PFAS species at most monitoring sites and was less impacted by sampling period compared to the WWTP located in a moderately developed, pastured area. Findings support the importance of WWTPs and land use practices as contributing to PFAS impact to downstream ecosystems along with potentially increasing strains on downstream drinking water source waters in regions that are surface water dependent.

Application of coniferous bark as sorbent material for per- and polyfluoroalkyl substances – A case study in Sweden

Per- and polyfluoroalkyl substances (PFAS) are anthropogenic contaminants commonly found in drainage water from waste management facilities. Within the European Union, these facilities either treat the water locally or transfer it to wastewater treatment plants to reduce harmful emissions. However, PFAS are a broad class of compounds with varying physicochemical properties, leading to different removal efficiencies for adsorbents. Activated carbon and ion exchange resins are effective but costly, and they can become saturated with other contaminants. Therefore, this study aims to explore inexpensive, abundant alternatives for reducing PFAS concentrations in the environment. In Sweden, bark is a by-product of forestry activities, primarily used as fuel in heat and power plants. This study evaluates the ability of pine and spruce bark to remove PFAS from contaminated drainage water. Initial laboratory experiments employed liquid-to-solid ratios of 10 and 20 to assess the performance of both materials. Results indicated that pine bark exhibited better removal efficiencies, particularly when a layered column with pine bark followed by spruce bark was utilized. The overall removal efficiencies for short-chain PFAS (perfluorinated carbons: PFCA C3–C6 and PFSA C4–C5) and long-chain PFAS (PFCA > C7 and PFSA > C6) were below 20%, except for perfluorooctane sulfonic acid (PFOS), which showed reductions of 40%–80%. The pH of the treated water decreased from 7 to 4 (pine bark) and 5 (spruce bark) after treatment. In a larger-scale trial, a combination of 50% pine bark and 50% spruce bark was tested, achieving similar reductions for PFOS. Although the removal efficiencies were insufficient for exclusive treatment, these materials may be useful in specific applications targeting long-chain PFAS or in conjunction with other treatment methods.

A Prospective Analysis of Per- and Polyfluoroalkyl Substances from Early Pregnancy to Delivery in the Atlanta African American Maternal-Child Cohort.

Longitudinal trends in per- and polyfluoroalkyl substances (PFAS) serum concentrations across pregnancy have not been thoroughly examined, despite evidence linking prenatal PFAS exposures with adverse birth outcomes. We sought to characterize longitudinal PFAS concentrations across pregnancy and to examine the maternal-fetal transfer ratio among participants in a study of risk and protective factors for adverse birth outcomes among African Americans. In the Atlanta African American Maternal-Child cohort (2014-2020), we quantified serum concentrations of four PFAS in 376 participants and an additional eight PFAS in a subset of 301 participants during early (8-14 weeks gestation) and late pregnancy (24-30 weeks gestation). Among these, PFAS concentrations were also measured among 199 newborns with available dried blood spot (DBS) samples. We characterized the patterns, variability, and associations in PFAS concentrations at different time points across pregnancy using intraclass correlation coefficients (ICCs), maternal-newborn pairs transfer ratios, linear mixed effect models, and multivariable linear regression, adjusting for socioeconomic and prenatal predictors. Perfluorohexane sulfonic acid (PFHxS), perfluorooctane sulfonic acid (PFOS), perfluorooctanoic acid (PFOA), and perfluorononanoic acid (PFNA) were detected in of maternal samples, with PFHxS and PFOS having the highest median concentrations. We observed high variability in PFAS concentrations across pregnancy time points (). All median PFAS concentrations increased from early to late pregnancy, except for PFOA and N-methyl perfluorooctane sulfonamido acetic acid (NMFOSAA), which decreased [paired -test for all PFAS except for PFOA and perfluorobutane sulfonic acid (PFBS)]. Prenatal serum PFAS were weakly to moderately correlated with newborn DBS PFAS ( ). The median maternal-fetal PFAS transfer ratio was lower for PFAS with longer carbon chains. After adjusting for socioeconomic and prenatal predictors, in linear mixed effect models, the adjusted mean PFAS concentrations significantly increased during pregnancy, except for PFOA. In multivariable linear regression, PFAS concentrations in early pregnancy significantly predicted the PFAS concentrations in late pregnancy and in newborns. We found that the concentrations of most PFAS increased during pregnancy, and the magnitude of variability differed by individual PFAS. Future studies are needed to understand the influence of within-person PFAS variability during and after pregnancy on birth outcomes. https://doi.org/10.1289/EHP14334.

Mid-Childhood Plasma Concentrations of Per- and Polyfluoroalkyl Substances, Modifiable Lifestyle Factors, and Bone Mineral Density Through Late Adolescence.

There is limited research on associations of per- and polyfluoroalkyl substances (PFAS) with areal bone mineral density (aBMD) through adolescence and whether bone-strengthening factors ameliorate effects. In the Project Viva cohort (N = 484; 50% female), we used sex-stratified linear regression and quantile g-computation mixture models to examine associations of mid-childhood (median: 7.8 years; 2007-2010) plasma PFAS concentrations with a dual-energy X-ray absorptiometry total-body aBMD Z-score in early and late adolescence (median: 12.9 and 17.6 years, respectively). We explored stratum-specific estimates by parent/self-reported physical activity and dairy intake. Using linear mixed models, we evaluated associations with aBMD accrual from mid-childhood through late adolescence. Females with higher perfluorooctanoate (PFOA) and perfluorodecanoate (PFDA) had lower early adolescent aBMD Z-score [e.g., β(95%CI)] per doubling PFOA: -0.19(-0.41, 0.03)]. Youth with higher PFOA and PFDA had lower late adolescent aBMD Z-score, but CIs were wide [e.g., PFOA: females, -0.12(-0.40, 0.16); males, -0.10(-0.42, 0.21)]. Mixture models generally corroborated single PFAS results, and in linear mixed models, females with higher PFAS concentrations, and males with higher PFOA, had slower aBMD accrual. Less active males with higher PFOA, PFDA, and the PFAS mixture had lower late adolescent aBMD Z-score. Some PFAS appeared more negatively associated with the aBMD Z-score among those who consumed less dairy, but there was not consistent evidence of effect modification. Exposure to select PFAS may affect bone accrual through adolescence, with possible resilience conferred by greater physical activity and dairy intake.

Increasing disparities in human exposure to perfluorooctanesulfonic acid: findings from per- and polyfluoroalkyl substance concentrations in 1999-2018 NHANES

The disparities in exposure to environmental hazards have fueled the environmental justice movement, which has garnered increasing attention and momentum over the past few decades. However, research addressing exposure disparities pertaining to chemicals remains notably limited. Here, leveraging data from the National Health and Nutrition Examination Survey spanning the period from 1999 to 2018, we unveiled that the perfluorooctanesulfonic acid (PFOS) exhibited the highest concentration in human biomonitoring in general U.S. population, with a mean value of 14.54 ± 19.59ng/ml. Subsequently, the mean concentrations of Perfluorooctanoic acid (PFOA), perfluorohexane sulfonic acid (PFHxS), perfluorononanoic acid (PFNA), and perfluorodecanoic acid (PFDA) were 3.33 ± 3.19, 2.29 ± 3.13, 1.07 ± 1.30, and 0.34 ± 0.71, respectively. Meanwhile, although females or Non-hispanic White exhibited relatively higher levels for most per- and polyfluoroalkyl substances (PFASs) compared to other groups. The individuals with higher household incomes demonstrated elevated exposure to PFASs. Interestingly, despite lower exposure burdens were observed in Non-Hispanic Black individuals, females, and individuals with low family income, we identified relatively higher exposure disparities in these populations. In particular, exposure disparities for general U.S. population exposure to PFOS exhibited an approximate 50% increase from 1999 to 2018, despite a concurrent decline of 84% in biomonitoring levels. Meanwhile, the population aging has led to an exacerbation of human exposure to PFOS by 12.4%. Our findings underscore the necessity of ensuring equitable protection from PFAS exposure for all populations, although further investigation is required to understand the underlying mechanisms driving these disparities.

Fate of biosolids-bound PFAS through pyrolysis coupled with thermal oxidation for air emissions control.

Pyrolysis has been identified as a possible thermal treatment process for reducing perfluoroalkyl and polyfluoroalkyl substances (PFAS) from wastewater solids, though off-gas from the pyrolysis unit can still be a source of PFAS emissions. In this work, the fate of PFAS through a laboratory-scale pyrolysis unit coupled with a thermal oxidizer for treatment of off-gasses is documented. Between 91.5% and >99.9% reduction was observed through the entire system for specific compounds based on targeted analyses. Overall, the pyrolysis and thermal oxidizer system removed 99.4% of the PFAS moles introduced. Furthermore, shorter chain variants comprised the majority of reportable PFAS in the thermal oxidizer flue gas, indicating the longer chain compounds present in the dried biosolids fed to pyrolyzer decompose through the system. PRACTITIONER POINTS: Thermal oxidation is a promising treatment technology for exhaust systems associated with thermal biosolids treatments. Thermal oxidation demonstrated significant degradation capabilities, with gas phase emissions comprising only 0.200% of initial PFAS concentrations to the system. Short-chain PFAS made up a higher percent of thermal oxidizer emissions, ranging between 54.4% and 79.5% of PFAS in the exhaust on a molar basis. The possibility of recombinant PFAS formation and partial thermal decomposition of PFAS in thermal oxidation is a needed area of research.

Aptamer-Triggered Nucleic Acid Amplification Strategy for the Electrochemiluminescence Detection of Perfluorooctanoic Acid.

Per- and polyfluoroalkyl substances (PFASs) are a class of persistent micropollutants. Due to their chemical stability and bioaccumulation, concentrations of PFASs in environmental media, even at ultratrace levels, pose significant environmental and health risks. However, currently reported detection methods lack an effective signal amplification strategy, and the detection sensitivity is limited, which can not meet the requirements of ultratrace detection. Herein, a groundbreaking aptamer-recognition-driven nucleic acid strategy was developed to significantly amplify the detection signal of perfluorooctanoic acid (PFOA). Furthermore, step pulse (SP) was used instead of cyclic voltammetry (CV) as an electrochemical excitation method to modulate the low electrochemiluminescence (ECL) triggering potential of poly [9,9-bis (3'-(N, N-dimethylamino) propyl) -2,7-fluorene]-alt-2,7-(9,9-dioctylfluorene)] (PFN) nanoparticles (NPs) so that a strong signal of +0.80 V was emitted without any exogenous coreactants. PFN NPs coupled rolling circle amplification-assisted PAM-free CRISPR/Cas12a system to construct an ultrasensitive ECL aptasensor for PFOA detection and the limit of detection was as low as 1.97 × 10-15 M. This ECL system integrated the advantages of no exogenous coreactants, low trigger potential, and nucleic acid amplification strategy and provided an ultrasensitive method for monitoring trace PFOA in the real water sample.

Large scale study on PFASs levels in fruits, vegetables and soil from allotments and gardens contaminated by atmospheric deposition from a Dutch fluorochemical production plant

Citizens grow their own fruits and vegetables in allotment gardens in the vicinity of a fluorochemical production plant (FCPP) in The Netherlands. Historic emissions and the subsequent atmospheric deposition of perfluorooctanoic acid (PFOA) and GenX (hexafluoropropylene oxide-dimer acid / HFPO-DA) from the FCPP have resulted in the nearby environment being contaminated with per- and polyfluoroalkyl substances (PFASs). This research aimed to investigate the levels of PFASs in garden produce and whether a gradient can be observed in relation to distance from the FCPP. Furthermore, differences between certain types of fruits and vegetables were explored, as well as a potential relation between the measured concentrations in garden produce and soil. 737 fruit and vegetable samples were collected from 17 allotments and 4 gardens up to 20 kilometres from the FCPP, along with soil and water samples. Garden produce included fruits, potatoes, fruiting vegetables, brassicas, leafy vegetables, root vegetables, bulb vegetables, legumes and stem vegetables. PFASs concentrations in the samples were quantified using a very sensitive UPLC-MS/MS method. PFASs were detected in most samples above the analytical limit of detection (0.3 to 12.5 pg/g ww). PFOA and GenX were found in the highest concentrations (up to 5280 pg/g ww GenX and 3020 pg/g ww PFOA) in garden produce sampled downwind and close to the FCPP. Other PFASs were also found, but at (much) lower levels. Field-derived bioaccumulation factors (BAFs) were calculated for PFOA and GenX. The BAFs for PFOA were shown to be approximately 1 order of magnitude lower than BAFs from other studies. This may be explained by aging of the PFASs contamination and the intense cultivation of the garden plots. This study shows that PFOA and GenX can end up in garden produce and this will result in human exposure when the garden produce is consumed.

Occurrence and efficient removal of PFAS from landfill leachates using on-site DTRO systems: A comprehensive analysis across 11 Chinese cities

Per- and polyfluoroalkyl substances (PFAS), known for their persistent toxicity and mobility, pose significant environmental and human health risks. Here we explored the occurrence and efficacy of on-site Double-Pass Reverse Osmosis (DTRO) systems in removing 30 different PFAS from landfill leachates in 11 diverse cities across China. PFAS concentrations in landfill leachate ranged from 938 to 32,491 ng/L, averaging 6,486 ng/L, predominantly comprising short-chain PFAS, notably perfluorobutane sulfonate (PFBS). Notable emerging substitutes like 6:2 fluorotelomer sulfonate, fluorobutane sulfonamide, and 9-chlorohexadecafluoro-3-oxanone sulfonate were also identified. The PFAS levels correlated positively (r2 = 0.79, p < 0.01) with regional economic development, with coastal areas exhibiting higher concentrations than inland regions. The DTRO membrane filtration and ion exchange resin achieved an average removal efficiency of 94 % for ∑30PFAS and even 99.97 % for PFBS (the concentration of PFBS in the raw leachate ranged from 226.36 ng/L to 27,935.61 ng/L, with an average concentration of 4,506.88 ng/L). The Na ion exchange resin had a limited effect on further reducing the PFAS concentration. Our findings not only contribute to the theoretical understanding of PFAS behavior in landfill leachates but also offer a practical engineering applications for global waste management practices.

Predictions of groundwater PFAS occurrence at drinking water supply depths in the United States.

Per- and polyfluoroalkyl substances (PFAS), known colloquially as "forever chemicals", have been associated with adverse human health effects and have contaminated drinking water supplies across the United States owing to their long-term and widespread use. People in the United States may unknowingly be drinking water that contains PFAS because of a lack of systematic analysis, particularly in domestic water supplies. We present an extreme gradient boosting model for predicting the occurrence of PFAS in groundwater at the depths of drinking water supply for the conterminous United States. Our model results indicate that 71 to 95 million people in the conterminous United States potentially rely on groundwater with detectable concentrations of PFAS for their drinking-water supplies prior to any treatment.

Efficient Online TurboFlow Method for Simultaneous Determination of 60 Emerging Per- and Polyfluoroalkyl Substances in Milk.

Emerging perfluoroalkyl and polyfluoroalkyl substances (PFASs) have received much attention in recent years. Milk has usually low concentrations of PFASs, but it remains an important PFAS exposure route due to its high consumption. In this study, a method for simultaneous determination of 60 PFASs in milk was developed by online TurboFlow liquid chromatography-tandem mass spectrometry. A pH-dependent cold-induced liquid-liquid extraction was developed for precleanup and enrichment. Method quantification limits ranged from 0.003 to 0.500 ng/mL. For PFASs without corresponding isotope-labeled internal standards, Tanimoto coefficient and logP were introduced for the selection of internal standards. The matrix spiked recoveries ranged from 47 to 190%. The method was applied for PFAS analysis in 35 milk samples. PFBS, perfluorohexanesulfonic acid, perfluorooctanesulfonic acid, PFNS, PFPeA, perfluorooctanoic acid, PFNA, and 6:2 FTS were detected. The developed online TurboFlow method was simple, reliable, efficient, and applicable for trace analysis of PFASs in milk.

Partitioning of Neutral PFAS in Homes and Release to the Outdoor Environment: Results from the IPA Campaign.

The distribution and fate of per- and polyfluoroalkyl substances (PFAS) in homes are not well understood. To address this, we measured nine neutral PFAS in dust, airborne particles, dryer lint, and on heating and air conditioning (HAC) filters in 11 homes in North Carolina as part of the Indoor PFAS Assessment (IPA) Campaign and compared them with concurrently collected gas and cloth measurements. Fluorotelomer alcohols (FTOHs) contributed most (≥75%) to total (∑) measured neutral PFAS concentrations in dust, HAC filter, and dryer lint samples, with mean ∑(FTOH) concentrations of 207 ng/g, 549 ng/g, and 84 ng/g, respectively. In particles, perfluorooctane sulfonamidoethanols (FOSEs) dominated, with a mean ∑(FOSE) concentration of 0.28 ng/m3 or 75,467 ng/g. For FTOHs and FOSEs, resulting mean dust-air, HAC filter-air, dryer lint-air and particle-air partition coefficients in units of log(m3/μg) ranged (across species) from -5.1 to -3.6, -4.9 to -3.5, -5.4 to -4.1, and -3.2 to -0.78, respectively. We estimate that cloth, gas phase, and HAC filters are the largest reservoirs for FTOHs, while cloth, HAC filters, and dust are the largest reservoirs for FOSEs. Release rates of neutral PFAS from homes to the outdoor environment are reported.

Per- and poly-fluoroalkyl substances in aquatic ecosystems and wastewater treatment works in Africa: Occurrence, ecological implications, and future perspectives

The increasing levels of industrialization and urbanization have led to the generation of significant amounts of wastewater and waste products, often containing chemicals like per- and poly-fluoroalkyl substances (PFASs) commonly found in consumer products. PFASs are known for their persistence, ubiquity, and ecotoxicological impacts, raising concerns about potential harm to ecosystems. This paper reports the occurrence and evaluates the ecological risks of PFASs in aquatic ecosystems and wastewater treatment works (WWTWs) across Africa. We reviewed 32 papers published in the period 2009–2024 and identified a total of 35 PFAS compounds in surface waters, wastewater, sediments, fish, crocodiles, and invertebrates. Much of the reported studies came from South Africa, followed by Kenya and Nigeria. PFAS concentrations in Africa were <0.7–390.0 ng L−1 in surface waters, 0.05–772 ng g−1 dw in sediments, and <0.2–832 ng L−1 in wastewater, while the highest levels in fish and invertebrates were 460.7 and 35.5 ng g−1 ww, respectively. The PFAS levels were in the same range of data as those reported globally. However, the high concentrations of PFASs in sediments and wastewater suggest areas of point contamination and a growing risk to aquatic ecosystems from effluent discharges. Calculated risk quotients suggested that, in Africa, organisms in river systems face greater risks due to exposure to PFASs compared to those in lakes, while marine organisms might face higher risks compared to freshwater organisms. Future studies should focus on PFAS contamination sources, especially WWTWs, as emerging sources of PFASs in aquatic systems.

Characterizing the Areal Extent of PFAS Contamination in Fish Species Downgradient of AFFF Source Zones.

Most monitoring programs next to large per- and polyfluoroalkyl substances (PFAS) sources focus on drinking water contamination near source zones. However, less is understood about how these sources affect downgradient hydrological systems and food webs. Here, we report paired PFAS measurements in water, sediment, and aquatic biota along a hydrological gradient away from source zones contaminated by the use of legacy aqueous film-forming foam (AFFF) manufactured using electrochemical fluorination. Clustering analysis indicates that the PFAS composition characteristic of AFFF is detectable in water and fishes >8 km from the source. Concentrations of 38 targeted PFAS and extractable organofluorine (EOF) decreased in fishes downgradient of the AFFF-contaminated source zones. However, PFAS concentrations remained above consumption limits at all locations within the affected watershed. Perfluoroalkyl sulfonamide precursors accounted for approximately half of targeted PFAS in fish tissues, which explain >90% of EOF across all sampling locations. Suspect screening analyses revealed the presence of a polyfluoroketone pharmaceutical in fish species, and a fluorinated agrochemical in water that likely does not accumulate in biological tissues, suggesting the presence of diffuse sources such as septic system and agrochemical inputs throughout the watershed in addition to AFFF contamination. Based on these results, monitoring programs that consider all hydrologically connected regions within watersheds affected by large PFAS sources would help ensure public health protection.

PFAS profiles in biosolids, composts, and chemical fertilizers intended for agricultural land application in Quebec (Canada)

Biosolids, sewage sludge, and composts are applied to agricultural land for nutrient recovery and soil organic matter replenishment, aligning with sustainable development goals. However, they may contain per- and polyfluoroalkyl substances (PFAS) that can enter the food chain through plant bioaccumulation and leaching into the groundwater. This study analyzed 80 PFAS compounds in sewage sludge, biosolids, commercial composts, and chemical fertilizers in Quebec, Canada, using UHPLC-HRMS (Orbitrap Q-Exactive). PFAS concentrations ranged from 18 to 59 µg/kg in commercial composts, 9.8 to 213 µg/kg in pulp and paper sludge, 15 to 705 µg/kg in sewage sludge, 12 to 1310 µg/kg in biosolids, and 14.6 µg/kg on average in biosolids ash. Dominant PFAS classes included diPAPs, sulfonamides, PFCAs, and PFSAs. High diPAPs concentrations indicated widespread use in domestic, commercial, or industrial applications. This study also observed a negligible correlation between soil organic carbon and PFAS concentration in the biowastes signifying a stronger influence due to different WWTP configurations, the quality of the wastewater inputs and other medium’s properties that could affect PFAS partitioning to the biowastes. Environmental assessments showed PFAS loads of up to 30 µg/kg soil from a single application, within some regulatory limits. However, repeated applications could lead to PFAS accumulation in soil, posing risks to crops and groundwater.