Heptafluorobutyric Acid Research Articles

Internal Relative Potency Factors for the Risk Assessment of Mixtures of Per- and Polyfluoroalkyl Substances (PFAS) in Human Biomonitoring.

Background:In human biomonitoring, blood is often used as a matrix to measure exposure to per- and polyfluoroalkyl substances (PFAS). Because the toxicokinetics of a substance (determining the steady-state blood concentration) may affect the toxic potency, the difference in toxicokinetics among PFAS has to be accounted for when blood concentrations are used in mixture risk assessment.Objectives:This research focuses on deriving relative potency factors (RPFs) at the blood serum level. These RPFs can be applied to PFAS concentrations in human blood, thereby facilitating mixture risk assessment with primary input from human biomonitoring studies.Methods:Toxicokinetic models are generated for 10 PFAS to estimate the internal exposure in the male rat at the blood serum level over time. By applying dose–response modeling, these internal exposures are used to derive quantitative internal RPFs based on liver effects.Results:Internal RPFs were successfully obtained for nine PFAS. Perfluorobutanoic acid (PFBA), perfluorohexanoic acid (PFHxA), perfluorononanoic acid (PFNA), perfluorododecanoic acid (PFDoDA), perfluorooctane sulfonic acid (PFOS), and hexafluoropropylene oxide-dimer acid (HFPO-DA, or GenX) were found to be more potent than perfluorooctanoic acid (PFOA) at the blood serum level in terms of relative liver weight increase, whereas perfluorobutane sulfonic acid (PFBS) and perfluorohexane sulfonic acid (PFHxS) were found to be less potent. The practical implementation of these internal RPFs is illustrated using the National Health and Nutrition Examination Survey (NHANES) biomonitoring data of 2017–2018.Discussion:It is recommended to assess the health risk resulting from exposure to PFAS as combined, aggregate exposure to the extent feasible. https://doi.org/10.1289/EHP10009

Abstract 6278: Per- polyfluoroalkyl substance (PFAS) modulates steatosis and fibrogenic signaling in hepatocellular carcinoma cells

Abstract Perfluorooctanoic acid (PFOA), heptafluorobutyric acid (HFBA), and perfluorotetradecanoic acid (PFTA) are the per- and polyfluoroalkyl substances (PFAS) and organic pollutants that predominantly exist in the environment. Exposure to PFAS affects immune, thyroid and kidney function, lipid and insulin dysregulation, liver disease, and cancer. Mechanisms underlying the impact of low and physiologically relevant concentration of PFAS in liver diseases remain elusive. In the current study, we investigated the effect of PFOA, HFBA, and PFTA on cell proliferation, steatosis, and fibrogenic signaling in hepatocytes and liver cancer cell models. Exposure of PFOA and PFBA (10 to 1000 nM) specifically promoted cell proliferation in non-tumor derived HepaRG liver cells and in hepatocellular carcinoma HepG2 cells. PFASs increased the expression of TNFα and IL6 inflammatory markers and produced endogenous reactive oxygen species (ROS) production. Further, PFAS enhanced cell steatosis in liver (HepaRG and HepG2) cells which was accompanied by upregulation of steatotic, and fibrogenic markers as well as activated Unfolded Protein Response (UPR) signaling. RNA-seq data suggested that chronic exposures of PFOA modulated the expression of fatty acid/lipid metabolic gene expression that is involved in the development of fatty liver disease. Collectively our data suggests that chronic exposure to low concentration of PFAS may modulate cell steatosis and fibrogenic signaling in hepatocytes and HCC cells by activation of UPR signaling. Citation Format: Qi Qi, Suryakant Niture, Sashi Gadi, Deepak Kumar. Per- polyfluoroalkyl substance (PFAS) modulates steatosis and fibrogenic signaling in hepatocellular carcinoma cells [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2022; 2022 Apr 8-13. Philadelphia (PA): AACR; Cancer Res 2022;82(12_Suppl):Abstract nr 6278.

Occurrence and contamination profile of legacy and emerging per- and polyfluoroalkyl substances (PFAS) in Belgian wastewater using target, suspect and non-target screening approaches

With the growing concern regarding the health risks of per- and polyfluoroalkyl substances (PFAS), there is an increasing demand for the identification of emerging PFAS. This study provides a comprehensive investigation of legacy and emerging PFAS in 16 wastewater treatment plants (WWTPs) in Belgium using target, suspect, and non-target screening methods. Perfluorobutanoic acid (PFBA) and perfluoropentanoic acid (PFPeA) were the dominant compounds in most locations, whereas perfluorooctanoic acid (PFOA) was the most predominant PFAS in WWTP Deurne (Antwerp region). Using a suspect screening approach, 14 PFAS were annotated as confidence level (CL) of 4 or higher and 4 PFAS were annotated as CL 2a and 2b, including aqueous film forming foam (AFFF)-derived PFAS. The compound group of n:3 unsaturated fluorotelomer carboxylic acid was found using non-target screening in the wastewater from WWTP Deurne. Population exposure in a catchment area estimated using population-normalized mass loads (PNML) showed the highest value in the catchment area of WWTP Deurne, implying a potentially higher exposure to PFAS in this community.

Laboratory batch representation of PFAS leaching from aged field soils: Intercomparison across new and standard approaches

Relating laboratory leaching methods to partitioning and transport of per- and poly-fluoroalkyl substances (PFAS) in field soils is challenging, making estimation of fluxes to groundwater and surface water uncertain. Existing laboratory leaching methods have limitations when assessing field leaching. For 37 aged field soils from five sites historically contaminated with PFAS over decades, we assess PFAS leaching using new and existing laboratory leaching methods to provide alternative methods better reflecting PFAS risks posed by its leaching and movement. Dominant PFAS in the soils were perfluorooctane sulfonic acid, perfluorohexane sulfonic acid, and perfluorohexanoic acid and to a lesser extent perfluorooctanoic acid. Leaching from intact soil cores (Exp 1) was taken to reflect field conditions. These were compared to two new laboratory batch tests, saturate-spin (Exp 2) and saturate-tumble-spin (Exp 3), and two standard approaches; Australian Standard Leaching Procedure (ASLP, Exp 4) and the Leaching Environmental Assessment Framework (LEAF, Exp 5). The tests varied in terms of liquid:soil ratio, tumbling time and pH of the starting solution, with LEAF-1313 conducted across seven pHs (2−12). Correlations between leachate and soil concentrations were highest for Exp 4 and Exp 5 (R2 = 0.72–0.98) and lowest for Exp 3 (R2 = 0.53). The PFAS mass leached as a fraction of the total increased such that: soil core leaching (27 %) < saturate-spin (30 %) < saturate-tumble-spin (65 %) ≤ LEAF-1313 (65 to 88 % at pH 5–9) < ASLP (90 %). As a fraction of individual PFAS compounds in leachate compared with soil, the shorter chain PFAS (e.g., perfluorobutanoic acid) were higher in the leachate in all tests. Across all tests, the saturate-spin batch test most closely represented intact soil core leaching and therefore potentially provides a measure more analogous of in situ soil leaching at field sites. Other methods would apply to broader applications such as landfill disposal.

Perfluoroalkyl substances in the surface water and fishes in Chaohu Lake, China.

The concentration and composition of 13 perfluoroalkyl substances (PFASs) in surface water and fishes in Chaohu Lake, China, were systematically studied in October 2019. Results showed that the PFASs composition has changed greatly. The concentration levels of perfluorooctane sulfonate (PFOS) in the surface water of Chaohu Lake have decreased significantly compared with past years. Perfluorobutanoic acid (PFBA) has become the dominant component, and it was mainly come from industrial wastewater. The highest concentration of perfluorooctanoic acid (PFOA) was measured in the lake inlet of the Baishitian River (southwest part), which mainly received domestic sewage. Different types of wastewater lead to varying compositions of PFASs in the lake water. PFOA and PFBS were homologous in some areas of Chaohu Lake, which reflected the unbalanced promotion of prohibition and substitution of long-chain PFASs around Chaohu Lake. On the basis of the risk quotient and tolerable daily intake assessment, drinking water and eating fish from Chaohu Lake do not lead to apparent PFAS risk, but PFOS in fish has evident bioaccumulation and biomagnification effects. PFOS-based human daily intake of Channa argus accounts for 22.4% of the tolerable daily intake. Thus, the risk caused by PFOS needs close attention. This study is useful for enhancing people's understanding of the environmental behavior and the risk of PFASs in Chaohu Lake.

Assessment of perfluorohexane sulfonic acid (PFHxS)-related compounds degradation potential: Computational and experimental approaches

Perfluorohexane sulfonic acid (PFHxS) and PFHxS-related compounds are listed in Annex A of the Stockholm Convention without specific exemptions. Substances that potentially degrade to PFHxS are considered as their related compounds. Unfortunately, the degradation behavior of PFHxS precursors, an important basis for the corresponding chemical regulation, remains unclear. Herein, based on the hypothesis that bond dissociation enthalpy (BDE) is the determining factor for the degradation of PFHxS precursors, the BDE of PFHxS-related precursors to produceC6F13SO2−groups was calculated. In addition, quantitative structure-activity relationship models based on partial least squares, partial least squares discrimination analysis, and support vector machine algorithms were developed to predict the BDE of 48 PFHxS precursors and distinguish the precursors with different degradation potential. Subsequent photodegradation experiments demonstrated that the order of degradation rates was consistent with that predicted by theoretical models. Importantly, perfluorohexanoic acid (PFHxA) and perfluorobutanoic acid, and not PFHxS, were detected as the degradation products of potential PFHxS precursors. Sulfonamides, phenyl unit, and other radicals in the non-nucleus part of PFHxS precursors were identified as the critical molecular segments that affect their degradation potential. Ultimately, by comparing BDE values, it was theoretically speculated that PFHxS related compounds exhibit a greater potential to generate PFHxA than PFHxS. Results in this study indicated for the first time that not all the compounds containing C6F13SO2− groups were guaranteed to degrade into PFHxS under natural conditions.

Assessment of Bioactive Surfactant Levels in Selected Cereal Products

Per- and polyfluoroalkyl substances (PFASs) are bioactive surfactants that are widespread in the environment and living organisms. This study presents measurements of PFAS in selected food of plant origin that are part of the healthy eating pyramid, including bread, rolls, flour, bran, buckwheat, millet, rice, and noodles. A simple and reliable analytical method was developed for the simultaneous determination of seven perfluorocarboxylic acids (PFCAs) and three perfluoroalkane sulfonates (PFSAs) in cereal-based products. Out of the 10 PFASs, 5 PFASs were detected at levels above LOQ. The most frequently detected compound was perfluorooctanoic acid (PFOA), which was quantified in 65.2% of samples, while none of the others were present in more than 40.0% of tested products. Perfluorobutanoic acid (PFBA) was the predominant PFAS in cereal-based products, and its maximum measured concentration was 202.85 ng/g for wheat bran. The soil–root–shoot interactions in relation to PFAS transfer to the above-ground parts of plants and PFAS’s ability to interfere with proteins are most likely the sources of these compounds in commonly consumed cereal products. As PFBA contributes greatly to total PFAS concentration, this food group should be included in future dietary exposure assessments.

Early breakthrough of short‐chain perfluoroalkyl substances in adsorptive media treatment

AbstractActivated carbon (AC) adsorption continues to be the default technology to remove low levels of per‐ and polyfluoroalkyl substances (PFAS) from water, despite varying reports of the relatively early breakthrough of short‐chain PFAS and high operating costs. Ion‐exchange processes using regenerable and single‐use media have been emerging as practical alternatives which may provide improved treatment and system performance. However, long‐term performance with respect to the more difficult to remove short‐chain PFAS such as perfluorobutanoic acid and perfluorobutanesulfonic acid is less often reported. Treatability testing on PFAS‐impacted groundwater using batch‐equilibration reactors and column flushing apparatus experiments was implemented to compare removal efficiency, breakthrough, and longevity of various media, specifically for shorter chain PFAS. Adsorbents tested included surface‐modified natural media, synthetic resin, and AC. Results indicated that both surface modified natural media and AC achieved &gt;99 percent removal of all detected PFAS after approximately 10,300‐bed volumes (16 weeks) of column flushing, and outperformed the selected resin under site‐specific conditions. In addition, unconventional breakthrough patterns (i.e., the breakthrough of longer chain PFAS before shorter chain PFAS) were observed for some PFAS including perfluoropentanoic acid, perfluorohexanesulfonic acid, and perfluorooctanesulfonic acid. The results of this study suggested that, while the generally accepted breakthrough patterns for PFAS can be reasonably anticipated, column flushing studies were preferred over batch sorption tests to reveal site‐specific or media‐specific breakthrough patterns that can impact overall performance.

Process to separate per‐ and polyfluoroalkyl substances from water using colloidal gas aphrons

AbstractCurrent ex situ per‐ and polyfluoroalkyl substances (PFAS) remediation strategies often involve the treatment of large volumes of PFAS‐impacted water via separation processes to concentrate PFAS for subsequent treatment or disposal. This study presents a new method for concentrating PFAS that relies on colloidal gas aphrons (CGAs), unusual microstructures composed of water, multilayers of surfactants, and air, that can be used for separation via electrostatic and hydrophobic sorption. This study successfully demonstrates the efficacy of CGAs in removing ionic dyes (as PFAS surrogates) (81%–91%), as well as ultra‐short and short‐chain PFAS (60%–90%) and perfluorooctanoic acid (PFOA, 88%) within 10 min. However, poor removal of perfluorooctane sulfonic acid (PFOS, 0%) was observed within 10 min of treatment. Compared to bubbling with nitrogen alone, and nitrogen with cetrimonium bromide (CTAB) in bulk solution, CGAs demonstrate significantly higher removal of perfluorobutanoic acid, a short‐chain PFAS (0% for N2, 11% for N2 + CTAB, and 90% for CGAs). These results suggest that CGAs may serve as a promising new separation and concentration technology for removing a suite of PFAS from water, particularly for difficult to remove short‐chained compounds.

Dual-Functional Nanofiltration and Adsorptive Membranes for PFAS and Organics Separation from Water.

Challenges associated with water separation technologies for per- and polyfluoroalkyl substances (PFASs) require efficient and sustainable processes supported by a proper understanding of the separation mechanisms. The solute rejections by nanofiltration (NF) at pH values near the membrane isoelectric point were compared to the size- and mass-transfer-dependent modeled rejection rates of these compounds in an ionized state. We find that the low pK a value of perfluorooctanoic acid (PFOA) relates to enhanced solute exclusions by minimizing the presence and partitioning of the protonated organic compound into the membrane domain. The effects of Donnan exclusion are moderate, and co-ion transport also contributes to the PFAS rejection rates. An additional support barrier with thermo-responsive (quantified by water permeance variation) adsorption/desorption properties allows for enhanced separations of PFAS. This was possible by successfully synthesizing an NF layer on top of a poly-N-isopropylacrylamide (PNIPAm) pore-functionalized microfiltration support structure. The support layer adsorbs organics (178 mg PFOA adsorbed/m2 membrane at an equilibrium concentration of 70 mg/L), and the simultaneous exclusion from the NF layer allows separations of PFOA and the smaller sized heptafluorobutyric acid from solutions containing 70 μg/L of these compounds at a high water flux of 100 L/m2-h at 7 bar.

Occurrence of per- and polyfluoroalkyl substances (PFASs) in raw milk and feed from nine Chinese provinces and human exposure risk assessment

The per- and polyfluoroalkyl substances (PFASs) are substantially produced and applied in industrial and domestic products, which have recently aroused great public concern for their potential toxicity to humans. In the present study, raw milk (n = 107) and cow feed samples (n = 70) were collected across nine Chinese provinces, in order to investigate the occurrence of PFASs in milk and feed, and the human exposure risk to milk. The concentrations of PFASs are in the range of < method detection limit −9.82 ng/g dw (average: 1.03 ng/g dw) for milk and 0.99–144 ng/g dw (7.68 ng/g dw) for feed. Perfluorobutanoic acid (34.0%) dominates in feed, while perfluorooctanesulfonic acid (67.5%) dominates in milk. No significant positive correlations of PFASs are observed between paired feed and milk (p > 0.05). However, feeds collected around fluorination production area show relatively higher PFAS levels than those from other areas, which also increase PFAS levels in milk. Risk assessment of PFASs through milk consumption is carried out according to evolving reference doses (RfDs). The hazard quotient is more than one for both adults and children when the strictest RfDs are applied. The Monte Carlo Simulation shows that children face higher PFAS exposure risk than adults.

Assessment of Reed Grasses (Phragmites australis) Performance in PFAS Removal from Water: A Phytoremediation Pilot Plant Study

Per- and polyfluoroalkyl substances (PFASs) have multiple emission sources, from industrial to domestic, and their high persistence and mobility help them to spread in all the networks of watercourses. Diffuse pollution of these compounds can be potentially mitigated by the application of green infrastructures, which are a pillar of the EU Green Deal. In this context, a phytoremediation pilot plant was realised and supplied by a contaminated well-located in Lonigo (Veneto Region, Italy) where surface and groundwaters were significantly impacted by perfluoroalkyl acids (PFAAs) discharges from a fluorochemical factory. The investigation involved the detection of perfluorobutanoic acid (PFBA), perfluorooctanoic acid (PFOA), perfluorobutanesulfonic acid (PFBS) and perfluorooctanesulfonic acid (PFOS) inside the inlet and outlet waters of the phytoremediation pilot plant as well as in reed grasses grown into its main tank. The obtained results demonstrate that the pilot plant is able to reduce up to 50% of considered PFAAs in terms of mass flow without an evident dependence on physico-chemical characteristics of these contaminants. Moreover, PFAAs were found in the exposed reed grasses at concentrations up to 13 ng g−1 ww. A positive correlation between PFAA concentration in plants and exposure time was also observed. In conclusion, this paper highlights the potential efficiency of phytodepuration in PFAS removal and recommends improving the knowledge about its application in constructed wetlands as a highly sustainable choice in wastewater remediation.

Review on Per- and Poly-Fluoroalkyl Substances’ (PFASs’) Pollution Characteristics and Possible Sources in Surface Water and Precipitation of China

In recent years, due to the production and use of per- and poly-fluoroalkyl substances (PFASs), the research on the pollution characteristics and sources of PFASs in surface water and precipitation in China has attracted increasing attention. In this study, the related published articles with sampling years from 2010 to 2020 were reviewed, and the concentration levels, composition characteristics and possible sources of PFASs in surface water (rivers and lakes) and precipitation in China were summarized, including those in the Tibetan Plateau region. The results show that the concentrations of PFASs in surface water in different areas of China vary greatly, ranging from 0.775 to 1.06 × 106 ng/L. The production processes of fluorinated manufacturing facilities (FMFs) and sewage discharge from wastewater treatment plants (WWTPS) were the main sources of PFASs in surface water in China, and the concentrations of PFASs in water flowing through cities with high urbanization increased significantly compared with those before water flowed through cities with high urbanization. The compositions of PFASs in surface water gradually changed from long-chain PFASs, such as per-fluoro-octanoic acid (PFOA) and per-fluoro-octanesulfonic acid (PFOS) to short-chain PFASs, such as per-fluorobutanoic acid (PFBA), per-fluorobutanesulfonic acid (PFBS), perfluorohexanoic acid (PFHxA) and per-fluoropentanoic acid (PFPeA). The concentrations of PFASs in precipitation in China ranged from 4.2 to 191 ng/L, which were lower than those of surface water. The precipitation concentrations were relatively high around a fluorination factory and in areas with high urbanization levels. PFASs were detected in the surface water and precipitation in the Tibetan Plateau (TP), which is the global “roof of the world”, but the concentrations were low (0.115–6.34 ng/L and 0.115–1.24 ng/L, respectively). Local human activities and surface runoff were the main sources of PFASs in the surface water of the Tibetan Plateau. In addition, under the influence of the Southeast Asian monsoon in summers, marine aerosols from the Indian Ocean and air pollutants from human activities in Southeast Asia and South Asia will also enter the water bodies through dry and wet depositions. With the melting of glaciers caused by global warming, the concentration of PFASs in the surface water of the TP was higher than that before the melting of glaciers flowed into the surface water of the TP. Generally, this study summarized the existing research progress of PFAS studies on surface water and precipitation in China and identified the research gaps, which deepened the researchers’ understanding of this field and provided scientific support for related research in the future. The concentrations of PFASs in the water bodies after flowing through FMFs were significantly higher than those before water flowed through FMFs, so the discharge of the FMF production process was one of the main sources of PFASs in surface water.

Multiple pollutants in groundwater near an abandoned Chinese fluorine chemical park: concentrations, correlations and health risk assessments

Contamination and adverse effects from various pollutants often appear in abandoned industrial regions. Thus, nine groundwater samples were collected from the vicinity of the fluorochemical industry in Fuxin City, Liaoning Province, to determine concentrations of the ten heavy metals arsenic (As), chromium (Cr), cadmium (Cd), lead (Pb), nickel (Ni), copper (Cu), manganese (Mn), zinc (Zn), iron (Fe) and mercury(Hg), as well as those of fluorine (F−) and eighteen poly- and perfluorinated substances (PFASs), analyse correlation relationships, and assess the health risks for different age groups. The results showed that the levels of fluorine (F−) (0.92–4.42 mg·L−1), Mn (0.0005–4.91 mg·L−1) and Fe (1.45–5.61 mg·L−1) exceeded the standard limits for drinking water. Short chain perfluorobutanoic acid (PFBA) (4.14–2501.42 ng·L−1), perfluorobutane sulfonate (PFBS) (17.07–51,818.61 ng·L−1) and perfluorohexanoic acid (PFHxA) (0.47–936.32 ng·L−1) were the predominant substances from the PFASs group. No individual PFASs levels had significant relationships with F− or heavy metal contents. There was a positive relationship between short chain PFASs concentrations and water depth and a negative relationship between long chain PFASs concentration and water depth. The hazard quotient (HQ) decreased in the order F− > heavy metals > PFASs and also decreased for older age groups. In addition, As, Fe, Mn and perfluorooctanoic acid (PFOA) were the main sources of risk from the heavy metal and PFASs groups, respectively.

Perfluoroalkyl substances in marine food webs from South China Sea: Trophic transfer and human exposure implication

Perfluoroalkyl substances (PFASs) are known to be persistent and toxic, and can be accumulated and trophic magnified in the environments. PFASs are widely distributed, and their coastal input poses a threat to the health of aquatic organisms and local residents. In present study, 17 PFASs including one emerging polyether substitute in water, sediment, and organisms were investigated from the South China Sea. Perfluorobutanoic acid (PFBA) was predominant in water, of which concentration ranged from ND to 10.26 ng/L, with a mean of 5.21 ng/L. Similar to sediment and organisms, PFBA was the substance with the highest concentration detected among PFASs. This result seemingly indicated that use of short-chain PFASs as substitutes for long-chain PFASs in recent years. Trophic magnification factors (TMFs) of PFASs were estimated in the marine food web. TMFs > 1 was observed only in perfluorooctane sulfonic acid (PFOS), indicating a biomagnification potential of PFOS in the given ecosystem. The estimated daily intake (EDI) of PFOS and PFOA were most prevalent in mollusk, whereas the EDI of PFBA was greater in fish and shrimp. The hazard ratio (HR) reported for seven dominant PFASs were lower than 1, which suggests that PFASs via seafood consumption would not cause significant health risk to local residents.

Early Warnings by Liver Organoids on Short- and Long-Chain PFAS Toxicity.

Short-chain per-fluoroalkyl substances (PFAS) have replaced long-chains in many applications, however the toxicity and its mode of action and interactions due to the large number of these compounds and their mixtures is still poorly understood. The paper aims to compare the effects on mouse liver organoids (target organ for bioaccumulation) of two long-chain PFAS (perfluorooctane sulfonate -PFOS-, perfluorooctanoic acid -PFOA) and two short-chain PFAS commonly utilized in the industry (heptafluorobutyric acid -HFBA-, Pentafluoropropionic anhydride-PFPA) to identify the mode of action of these classes of contaminants. Cytomorphological aberrations and ALT/GDH enzyme disruption were identified but no acute toxicity endpoint neither apoptosis was detected by the two tested short-chain PFAS. After cytomorphological analysis, it is evident that short-chain PFAS affected organoid morphology inducing a reduction of cytostructural complexity and aberrant cytological features. Conversely, EC50 values of 670 ± 30 µM and 895 ± 7 µM were measured for PFOS and PFOA, respectively, together with strong ALT/GDH enzyme disruption, caspase 3 and 7 apoptosis activation and deep loss of architectural complexity of organoids in the range of 500–1000 µM. Eventually, biochemical markers and histology analysis confirmed the sensitivity of organoid tests that could be used as a fast and reproducible platform to test many PFAS and mixtures saving time and at low cost in comparison with in vivo tests. Organoids testing could be introduced as an innovative platform to assess the toxicity to fast recognize potentially dangerous pollutants.

Neutral and ionizable per-and polyfluoroalkyl substances in the urban atmosphere: Occurrence, sources and transport

In the atmosphere, the photodegradation of neutral per-and polyfluoroalkyl substances (n-PFASs) is a source of ionizable PFASs (i-PFASs). However, they are not frequently simultaneously analyzed to study their transport and sources. In this study, n-PFASs and i-PFASs were simultaneously analyzed in the atmosphere of China, Japan and Malaysia to investigate the occurrence, seasonal variations, sources and transport. Results showed that n-PFASs ranged from 4.8 to 1400 pg m−3, with an average value of 170 pg m−3, and 8:2 fluorotelomer alcohol (8:2 FTOH) was the most abundant compound. i-PFASs ranged from 3.7 to 330 pg m−3, with an average value of 49 pg m−3, and perfluorobutanoic acid (PFBA) had the highest concentration. Generally, airborne PFASs had a decreasing gradient from cities with high population density toward less industrialized sites. i-PFASs exhibited significantly (P < 0.05) seasonal variations, which were higher in the summer. 8:2 FTOH and 10:2 FTOH had significant (P < 0.05) positive correlations with perfluorooctanoic acid and perfluorodecanoic acid, suggesting that they had same sources, such as co-emission and photodegradation of FTOHs. Urumqi and Selangor were far away from industry, and high percentages (>95%) but low concentrations of PFBA were found in these cities, indicating the long-range atmospheric transport of PFBA due to its high volatility. The Summer Monsoon may promote the transport of high concentrations of PFAS from coastal cities to inland cities.

Association between serum levels of TSH and free T4 and per- and polyfluoroalkyl compounds concentrations in pregnant women

Many per- and polyfluoralkyl substances (PFASs) may disrupt maternal thyroid hormone homeostasis in pregnancy. Concerns should be raised regarding the PFASs exposure in pregnant women because thyroid hormones are involved in the early development of the fetus. In this study, we measured the concentrations of 13 PFASs, including five novel short-chain PFASs, in serum from 123 pregnant women in Beijing, China. Linear regression models were used to investigate the association between thyroid-stimulating hormone (TSH) or free thyroxine (FT4) levels and PFASs concentrations under consideration of the impacts of pregnancy-induced physiological factors. We found that perfluorobutanoic acid (PFBA) (β=0.189, 95%CI=-0.039, 0.417, p=0.10) and perfluorodecanoic acid (PFDA) (β=-0.554, 95%CI=-1.16, 0.049, p=0.071) were suggestive of significant association with TSH in thyroid peroxidase antibody (TPOAb) negative women. No association was observed between all PFASs and FT4 levels after controlling for these confounding factors, such as BMI, gestational weight gain and maternal age. These findings suggest that it should pay more attention to the association between thyroid hormone levels and short-chain PFASs concentrations. Future studies could consider a greater sample and the inclusion of other clinical indicators of thyroid function, such as free T3 and total T3.

Particle size distribution, wet deposition and scavenging effect of per- and polyfluoroalkyl substances (PFASs) in the atmosphere from a subtropical city of China

Per- and polyfluoroalkyl substances (PFASs) as emerging organic pollutants have received great attention, but the scavenging efficiency of particulate PFASs by wet deposition was rarely studied. For the first time, we reported the scavenging efficiency of PFASs on different particle sizes. In this study, both rainwater and particle samples were collected for a whole year from Xiamen, a subtropical city of China. Particulate PFASs ranged from 4.11 to 67.41 pg m−3, with an average value of 26.56 pg m−3, and perfluorooctane sulfonic acid (PFOS), perfluorooctanoic acid (PFOA) were the main compounds. Perfluorocarboxylic acids (PFCAs) were predominantly observed on fine particles (<1 μm), while PFOS and 6:2 chlorinated polyfluoroalkyl ether sulfonic acid (6:2 Cl-PFESA) had large proportions on coarse particles (1–2.5 μm and 2.5–10 μm). In the rainwater, PFASs ranged from 0.20 to 180.65 ng L−1, with an average value of 10.71 ng L−1, and perfluorobutanoic acid (PFBA), PFOA were the main compounds. The wet deposition flux of ∑PFASs was 5200 mg km−2 yr−1, exhibiting high fluxes during the wet season (March to September). The scavenging efficiency of particulate PFOS and PFOA ranged from 68%–98% during the rainfall, and wash-out of the raindrops was found to be one of the main scavenging mechanisms. In addition, the precipitation duration and intensity influenced the scavenging efficiency. The scavenging capacity of PFCAs was large on fine particles, while for per-and polyfluoroalkyl sulfonic acids, the scavenging capacity was high on coarse particles. Our results showed that wet deposition effectively removed medium to long carbon chain (≥C6) PFASs in the atmosphere.

Effect of mono- and di-valent cations on PFAS removal from water using foam fractionation – A modelling and experimental study

Per- and poly-fluoroalkyl substances (PFAS) are a group of recalcitrant compounds whose widespread use in a variety of consumer products has led to contamination of groundwater and surface water systems. Foam fractionation is a potential remediation technology for treatment of PFAS contaminated water, which takes advantage of the high surface activity imparted by the fluorocarbon chain to remove them from solution by adsorption to the surface of air bubbles. In this study, the effect of mono- and di-valent cations on the performance of a PFAS foam fractionation process where sodium dodecyl sulphate (SDS) is used as a co-foaming agent has been evaluated. The results indicated that the separation of PFAS was improved in an order that followed the charge density of the salts with Mg2+ > Na+ > K+. It was also observed that at salt concentrations above 100 mM for Na+, above 10 mM for K+ and Mg2+ but between 0.1 and 10 mM for Ca2+ in the presence of greater than 4 ppm of SDS, the cations can complex with the SDS in the system and suppress foam formation due to the surfactant precipitation. Foam fractionation was able to remove perfluorohexane sulphonic acid (PFHxS), perfluorooctanoic acid (PFOA) and perfluorooctane sulphonic acid (PFOS) from a sample of Australian groundwater to below the analytical detection limit of 0.1 ppb within 60 min with SDS being used as the co-foaming agent, but was unable to remove the short chain perfluorobutanoic acid (PFBA).