Short-chain per and polyfluoroalkyl substances (PFAS) have been found to be relatively high in water treatment systems compared to long-chain PFAS because of the unsatisfactory adsorption efficiency of short-chain PFAS. Knowledge about why short-chain PFAS are less removed by porous carbon is very limited. The study focused on providing causal mechanisms that link the low adsorption of short-chain PFAS and proposing an improved method for removing both short- and long-chain PFAS. The long-chain PFAS with higher hydrophobicity diffused more quickly than the short-chain PFAS due to stronger partitioning driving forces. In the initial adsorption stage, therefore, pores of activated carbon were blocked by long-chain PFAS, which makes it difficult for the short-chain PFAS to enter the internal pores. Although several short-chain PFAS diffuse into the pores, the relatively more hydrophilic short-chain congeners cannot be fully adsorbed on activated carbon due to limited positively charged sites. Moreover, compared to larger particle sizes, smaller activated carbon particles have shorter pore channels near the surface, reducing the risk of pore-blocking and ensuring the pores remain accessible for more efficient adsorption. Additionally, these smaller particles offer a greater external surface area and more functional groups, which enhance the adsorption capacity. It indicates that the smaller particle size of activated carbon would have a positive effect on the short-chain PFAS removal.
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http://dx.doi.org/10.1016/j.chemosphere.2024.143320 | DOI Listing |
Comp Biochem Physiol C Toxicol Pharmacol
January 2025
Department of Cariology, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences, Saveetha University, Chennai, India. Electronic address:
Per and polyfluoroalkyl substances (PFAS) are anthropogenic chemicals extensively used in consumer products. Perfluorobutane sulfonate (PFBS), a short-chain PFAS, has been introduced as an alternative to long-chain PFAS, but limited studies have investigated its reproductive toxicity in fish. In this study, adult zebrafish were exposed to PFBS at concentrations of 0.
View Article and Find Full Text PDFEnviron Int
January 2025
Département de Chimie, Université de Montréal, Montreal, QC, Canada. Electronic address:
This study investigated the occurrence of perfluoroalkyl and polyfluoroalkyl substances (PFAS), including anionic, cationic, and zwitterionic compounds, in drinking water. Between 2021-2023, an expanded list of 76 target PFAS was screened in tap water samples mainly from Canada, but also including tap water samples from the Eastern United States, Mexico, South America (Argentina), the Caribbean (Dominican Republic, Cuba), Africa (Algeria, Cameroon, Central African Republic, Morocco, Rwanda, Tunisia), Europe (France, Greece, Italy, Spain, and the United Kingdom) and Asia (Japan, Vietnam, Iran, and Türkiye). An additional ∼ 200 suspect-target PFAS were screened using high-resolution Orbitrap mass spectrometry.
View Article and Find Full Text PDFEnviron Sci Technol
January 2025
Department of Agronomy, Ecological Sciences & Engineering Interdisciplinary Graduate Program, Purdue University, 915 Mitch Daniels Blvd, West Lafayette, Indiana 47907, United States.
This study evaluated PFAS occurrence in rural well water and surface water relative to land application of biosolids in a tile-drained agriculture-dominated watershed. Spatial data were used to identify potentially vulnerable rural wells based on their proximity to biosolid-permitted land and location with respect to groundwater flow. Water was collected from 103 private wells in Greater Tippecanoe County Indiana and 168 surface water locations within the Region of the Great Bend of the Wabash River watershed.
View Article and Find Full Text PDFACS Omega
December 2024
Department of Chemistry and Biochemistry, Jackson State University, Jackson, Mississippi 39217, United States.
The short-chain (C to C) and ultrashort-chain (C to C) per- and polyfluoroalkyl substances (PFAS) are bioaccumulative, carcinogenic to humans, and harder to remove using current technologies, which are often detected in drinking and environmental water samples. Herein, we report the development of nonafluorobutanesulfonyl (NFBS) and polyethylene-imine (PEI)-conjugated FeO magnetic nanoparticle-based magnetic nanoadsorbents and demonstrated that the novel adsorbent has the capability for highly efficient removal of six different short- and ultrashort-chain PFAS from drinking and environmental water samples. Reported experimental data indicates that by capitalizing the cooperative hydrophobic, fluorophilic, and electrostatic interaction processes, NFBS-PEI-conjugated magnetic nanoadsorbents can remove ∼100% short-chain perfluorobutanesulfonic acid within 30 min from the water sample with a maximum absorption capacity of ∼234 mg g.
View Article and Find Full Text PDFWater Res
December 2024
State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China; University of Chinese Academy of Sciences, Beijing 100049, China; School of Environment, Hangzhou Institute for Advanced Study, University of Chinese Academy of Sciences, Hangzhou 310024, China.
Per- and polyfluoroalkyl substances (PFAS) enter the Arctic through long-range transport and local pollution. To date, little is known about their behavior in plant and benthic marine food webs in remote Arctic. In this study, we analyzed the environmental distribution and nutrient transfer of 20 PFAS in soil, sediment, plant and benthic biota samples collected between 2014 and 2016 in Svalbard, Arctic.
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