Examining sorption of perfluoroalkyl substances (PFAS) in biochars and other carbon-rich materials.

Chemosphere

Department of Chemical Engineering and Analytical Chemistry, University of Barcelona, Martí i Franquès 1-11, 08028, Barcelona, Spain. Electronic address:

Published: September 2022

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.2022.134733DOI Listing

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