The poorly reversible risks to human health and ecosystems from contamination with per- and polyfluoroalkyl substances (PFAS) have led many researchers and regulators worldwide to call for a classwide ban of these so-called forever chemicals. As part of the EU Chemicals Strategy for Sustainability, the national authorities of five European countries submitted a broad restriction proposal on PFAS under REACH in January 2023. This restriction proposal is unique in its scope by including the vast majority of uses for >10 000 substances that meet the OECD definition of PFAS. (1) In parallel, several countries and multiple states in the United States have proposed or enacted broad PFAS restrictions for all non-essential uses or for specific uses and reporting requirements for a range of consumer products. Although the regulatory frameworks underpinning these restrictions contain many differences, the proposed restrictions have the common objective to ban the intentional use of all PFAS and thus avoid regrettable substitution with other PFAS. Given that the proposed restrictions apply to chemical products and articles (both hereafter termed simply “products”) that are imported from other states, countries, or regions, they may also trigger substitution and an increased demand for supply chain information on a global level. Direct communication with manufacturers and distributors is typically the primary approach for companies to ensure compliance with chemical regulations. Nevertheless, companies and authorities require reliable analytical methods to independently verify supply chain information and capture products that are noncompliant with PFAS restrictions.

Perfluoroalkyl acids (PFAAs) are highly persistent anthropogenic pollutants that have been detected in the global oceans. Our previous laboratory studies demonstrated that PFAAs in seawater are remobilized to the air in sea spray aerosols (SSAs). Here, we conducted field experiments along a north-south transect of the Atlantic Ocean to study the enrichment of PFAAs in SSA. We show that in some cases PFAAs were enriched >100,000 times in the SSA relative to seawater concentrations. On the basis of the results of the field experiments, we estimate that the secondary emission of certain PFAAs from the global oceans via SSA emission is comparable to or greater than estimates for the other known global sources of PFAAs to the atmosphere from manufacturing emissions and precursor degradation.

Fluoropolymers are a group of fluorinated polymers within the broad class of substances known as per- and polyfluoroalkyl substances (PFASs). During their production, a wide array of additional fluorinated organic substances (many PFASs and some not defined as PFASs) are used, formed and emitted to air and water. This study aims to assess, and make an inventory of, all emissions of PFASs and other fluorinated organic substances by the fluoropolymer production industry in Europe using available emission databases and permits. Air emissions of the fluorinated gases (i.e., chlorofluorocarbons, hydrofluorocarbons, hydrochlorofluorocarbons and perfluorocarbons (CFCs, H(C)FCs and PFCs)) by this industry have reportedly decreased between 2007 and 2021 from roughly 500 to 150 tonnes per year. Emissions of fluorosurfactants to air and water have also been reduced significantly. However, large uncertainties remain regarding the emissions of substances that are neither fluorinated gases nor fluorosurfactants but are classified as PFASs, such as polymerization by-products, chain transfer agents and fluorinated solvents. The available data indicate that the release of these substances is not decreasing but remains relatively stable. As this inventory probably underestimates emissions, further research, improved data availability and more harmonized reporting of emissions are necessary to obtain more accurate emission data for these substances. Nevertheless, based on the available data, it is clear that the emissions from fluoropolymer production plants to air and water are still significant and that the production of fluoropolymers continues to introduce persistent substances to the environment. This study assesses the environmental impact of the fluoropolymer industry in Europe by making an inventory of their emissions of PFASs and other fluorinated organic substances.

The process by which perfluoroalkyl acids (PFAAs) become enriched on sea spray aerosol (SSA) is complex and likely influenced by several factors. In this study, we utilized a plunging water jet in a controlled laboratory setup to generate SSA. We investigated the enrichment process of PFAAs on nascent SSA by systematically varying three key parameters: 1) total organic carbon (TOC), 2) water jet flow rate, and 3) inorganic ion composition. The results showed a significant enhancement in enrichment when organic matter was introduced into artificial seawater. However, this enhancement did not exhibit a consistent trend when increasing the TOC from 1 to 2 mg L^–1. The enrichment was increased at higher water jet flow rates (3.2 L min^–1) compared to lower flow rates (1.6 and 2.4 L min^–1), and the effect was particularly pronounced for submicrometer SSA particles. There was minimal difference in the enrichment of PFAAs when SSA was generated using sodium chloride solution instead of artificial seawater at the same salinity. Overall, these findings shed light on the complex process of PFAA enrichment on SSA and improved our understanding of the uncertainties associated with varying dissolved organic matter, water jet flow rate, and inorganic ion composition.

Hydrofluorocarbons (HFCs) and so-called hydrofluoroolefins (HFOs) are used as refrigerants in air conditioning, refrigeration, chillers, heat pumps and devices for dehumidification and drying. However, many HFCs, including R-134a and R-125, have a high global warming potential and some of the HFCs and HFOs degrade atmospherically and form trifluoroacetic acid (TFA) as a persistent degradation product. Rising levels of TFA around the globe reveal an urgent need to replace fluorinated refrigerants with non-fluorinated working fluids to avoid direct emissions due to leakage, incorrect loading or removal. It is important, however, also to select refrigerants with high efficiencies to avoid increasing indirect CO2 emissions due to higher energy consumption during the use phase. The present study investigates the available non-fluorinated alternatives to fluorinated refrigerants and shows that a transition to non-fluorinated refrigerants, in general, is possible and has happened in many sectors already. Technically, there are only slight barriers to overcome in order to replace fluorinated refrigerants in almost all newly developed systems conforming to existing standards. Additionally, we show that alternatives are available even for some use cases for which derogations have been proposed in the EU PFAS restriction proposal and suggest making these derogations more specific to support a speedy transition to non-fluorinated refrigerants in all sectors.

Total fluorine was determined in 45 consumer product samples from the Swedish market which were either suspected or known to contain fluorinated polymers. Product categories included cookware (70–550 000 ppm F), textiles (10–1600 ppm F), electronics (20–2100 ppm F), and personal care products (10–630 000 ppm F). To confirm that the fluorine was organic in nature, and deduce structure, a qualitative pyrolysis-gas chromatography-mass spectrometry (pyr-GC/MS) method was validated using a suite of reference materials. When applied to samples with unknown PFAS content, the method was successful at identifying polytetrafluoroethylene (PTFE) in cookware, dental products, and electronics at concentrations as low as 0.1–0.2 wt%. It was also possible to distinguish between 3 different side-chain fluorinated polymers in textiles. Several products appeared to contain high levels of inorganic fluorine. This is one of the few studies to quantify fluorine in a wide range of consumer plastics and provides important data on the concentration of fluorine in materials which may be intended for recycling, along with insights into the application of pyr-GC/MS for structural elucidation of fluorinated polymers in consumer products.

Per- and polyfluoroalkyl substances (PFAS) are a broad group of persistent organic compounds with vastly differing physicochemical and toxicological properties. Some jurisdictions have proposed to regulate PFAS as a single class to overcome the limitations of regulating such a diverse group on a chemical-by-chemical basis. Implications of regulating PFAS as a single class have been discussed for PFAS production and use, but equivalent discussion of implications for managing contaminated sites is largely lacking. This opinion piece summarizes the views of a group of environmental consultants, environmental regulators, land managers, and academics with significant experience in researching or managing PFAS. The group considered that neither a single PFAS class approach nor a chemical-by-chemical approach is well suited to managing risks from PFAS in a contaminated site setting, and defining PFAS subgroups would have value. Second, some but not all in the group, hypothesize that PFAS properties that drive fate and transport are those that influence toxicity and bioaccumulation in animals. This may be a valuable observation for future discussions on dividing PFAS into subclasses for contaminated site regulation based on physicochemical properties rather than purely structural definitions.

We argue that a seismic shift in the landscape of per- and polyfluoroalkyl substances (PFAS) uses can be observed. From conversations with representatives of the fluorochemical industry and of large brands of consumer products; from recent statements made in the general discussion among industry, consumer groups, environmental NGOs, and academic scientists; from various analyses of the availability of alternatives to PFASs in many use areas, including our own work; (1−4) and from the decision of a major PFAS manufacturer (3M) to leave entirely the production of PFAS, (5) we conclude that in many PFAS use areas, the transition to nonfluorinated alternatives is underway and is gaining more and more momentum.

The ongoing transition to PFAS-free alternatives includes uses such as surface treatment for a wide range of materials (food-contact materials, textiles, carpets, leather, metals, and cookware), lubrication, personal care products and cosmetics, firefighting foams, components of electrical devices (e.g., in fuel cells), ski waxes, cleaning products, building materials, refrigerants, and many other uses not highlighted here.

While the extent of environmental contamination by per- and polyfluoroalkyl substances (PFAS) has mobilized considerable efforts around the globe in recent years, publicly available data on PFAS in Europe were very limited. In an unprecedented experiment of “expert-reviewed journalism” involving 29 journalists and seven scientific advisers, a cross-border collaborative project, the “Forever Pollution Project” (FPP), drew on both scientific methods and investigative journalism techniques such as open-source intelligence (OSINT) and freedom of information (FOI) requests to map contamination across Europe, making public data that previously had existed as “unseen science”. The FPP identified 22,934 known contamination sites, including 20 PFAS manufacturing facilities, and 21,426 “presumptive contamination sites”, including 13,745 sites presumably contaminated with fluorinated aqueous film-forming foam (AFFF) discharge, 2911 industrial facilities, and 4752 sites related to PFAS-containing waste. Additionally, the FPP identified 231 “known PFAS users”, a new category for sites with an intermediate level of evidence of PFAS use and considered likely to be contamination sources. However, the true extent of contamination in Europe remains significantly underestimated due to a lack of comprehensive geolocation, sampling, and publicly available data. This model of knowledge production and dissemination offers lessons for researchers, policymakers, and journalists about cross-field collaborations and data transparency.