The use of carbon-rich sorbents to remove and/or immobilize perfluoroalkyl substances (PFAS) in contaminated environmental scenarios is attracting increasing interest. The identification of key sorbent properties responsible for PFAS sorption and the development of models that can predict the distribution coefficients (K) for PFAS sorption in these materials are crucial in the screening of candidate materials for environmental remediation. In this study, sorption kinetics, sorption isotherms, and the effects of pH, calcium concentration and dissolved organic carbon (DOC) content on PFAS sorption were evaluated in four representative carbon-rich materials: two biochars with contrasting properties, a compost, and charcoal fines rejected by the metallurgical industry. Subsequently, the sorption of seven PFAS with numbers of fluorinated carbons ranging from 4 to 11 was evaluated in a total of ten carbon-rich materials, including activated carbons, so as to build up a K prediction model. The sorption of PFAS increased with greater fluorinated chain length, suggesting that hydrophobic interactions play a major role in sorption and electrostatic interactions a minor one. These results were confirmed by a principal component analysis, which revealed that the C/O molar ratio and the specific surface area of the material were the two main sorbent properties affecting PFAS sorption. Furthermore, the DOC content in solution had a negative effect on PFAS sorption. Using this information, a simple K prediction model applicable to a wide range of materials and PFAS was developed, using only a few easily-derived physicochemical properties of sorbent (C/O molar ratio and SSA) and PFAS (number of CF), and was externally validated with data gathered from the literature.
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http://dx.doi.org/10.1016/j.chemosphere.2022.134733 | DOI Listing |
Environ Sci Technol
January 2025
State Key Laboratory of Soil and Sustainable Agriculture, Institute of Soil Science, Chinese Academy of Sciences, Nanjing 211135, China.
Microplastics (MPs) and per- and polyfluoroalkyl substances (PFASs) are ubiquitous contaminants in environments, yet their co-occurrence and interactions remain insufficiently understood. In this study, we confirmed the concurrent presence of MPs and PFASs and their distinct distribution patterns in a wastewater treatment plant (WWTP) through a comprehensive sampling and analysis effort. Significant correlations ( < 0.
View Article and Find Full Text PDFWater Res
December 2024
Department of Civil and Environmental Engineering, University of California, Berkeley, CA, 94720, United States. Electronic address:
Military bases and airports are often contaminated by per- and polyfluoroalkyl substances (PFAS) due to the repeated use of aqueous film forming foams (AFFFs) from decades of training exercises, equipment testing, and extinguishing of fuel- and solvent-based fires. Pump-and-treat systems combined with sorption processes are common ex situ remediation strategies; however, they can be expensive and may require decades of operation, particularly at sites where long-term diffusion and desorption of contaminants are the primary release processes. Alternatively, in situ chemical oxidation is an effective remediation strategy in which oxidants (e.
View Article and Find Full Text PDFWater Res
December 2024
State Environmental Protection Key Laboratory of Environmental Health Impact Assessment of Emerging Contaminants, School of Environmental Science and Engineering, Shanghai Jiao Tong University, Shanghai 200240, PR China. Electronic address:
The effective protocol for treating per- and polyfluoroalkyl substances (PFAS) in water at environmentally relevant concentrations (∼ ng L) has received unprecedented attention due to the stringent drinking water standards. In order to ensure safe water treatment, sorption using quaternary ammonium functionalized strong-base anion exchange resins (SB-AERs) is considered a viable option for treating PFAS when compared to commercialized activated carbon, as SB-AERs can be in situ regenerated with long-term operation capabilities. However, the harsh conditions required for traditional direct synthesis of SB-AERs (such as prolonged reaction times, complex processes, and environmental pollution caused by the organic reagents used) limit their applications.
View Article and Find Full Text PDFHeliyon
December 2024
IAEA Marine Environment Laboratories, 4a Quai Antoine 1er, 98000, Principality of Monaco, Monaco.
Adv Mater
November 2024
Institut Européen des Membranes (IEM), Univ Montpellier, CNRS, ENSCM, Montpellier, 34090, France.
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