@article{zhang_tang_knappe_2023, title={Oxidation of Per- and Polyfluoroalkyl Ether Acids and Other Per- and Polyfluoroalkyl Substances by Sulfate and Hydroxyl Radicals: Kinetic Insights from Experiments and Models}, volume={5}, ISSN={["1520-5851"]}, url={https://doi.org/10.1021/acs.est.3c00947}, DOI={10.1021/acs.est.3c00947}, abstractNote={Per- and polyfluoroalkyl substances (PFAS) are widely used anthropogenic chemicals. Because of the strength of the carbon-fluorine bond, PFAS are not destroyed in typical water treatment processes. Sulfate (SO4•-) and hydroxyl (•OH) radicals can oxidize some PFAS, but the behavior of per- and polyfluoroalkyl ether acids (PFEAs) in processes involving SO4•- and •OH is poorly understood. In this study, we determined second-order rate constants (k) describing the oxidation of 18 PFAS, including 15 novel PFEAs, by SO4•- and •OH. Among the studied PFAS, 6:2 fluorotelomer sulfonate reacted most readily with •OH [k•OH = (1.1-1.2) × 107 M-1 s-1], while polyfluoroalkyl ether acids containing an -O-CFH- moiety reacted more slowly [k•OH = (0.5-1.0) × 106 M-1 s-1]. In the presence of SO4•-, polyfluoroalkyl ether acids with an -O-CFH- moiety reacted more rapidly [kSO4•- = (0.89-4.6) × 106 M-1 s-1] than perfluoroalkyl ether carboxylic acids (PFECAs) and a chloro-perfluoro-polyether carboxylic acid (ClPFPECA) [kSO4•- = (0.85-9.5) × 104 M-1 s-1]. For homologous series of perfluoroalkyl carboxylic acids, linear and branched monoether PFECAs, and multiether PFECAs, PFAS chain length had little impact on second-order rate constants. SO4•- reacted with the carboxylic acid headgroup of perfluoroalkyl carboxylic acids and PFECAs. In contrast, for polyfluoroalkyl ether carboxylic and sulfonic acids with an -O-CFH- moiety, the site of SO4•- attack was the -O-CFH- moiety. Perfluoroalkyl ether sulfonic acids were not oxidized by SO4•- and •OH under the conditions evaluated in this study.}, journal={ENVIRONMENTAL SCIENCE & TECHNOLOGY}, author={Zhang, Chuhui and Tang, Tiffany and Knappe, Detlef R. U.}, year={2023}, month={May} }
 @misc{zhi_zhang_hjorth_baun_duckworth_call_knappe_jones_grieger_2020, title={Emerging lanthanum (III)-containing materials for phosphate removal from water: A review towards future developments}, volume={145}, ISSN={["1873-6750"]}, url={http://www.scopus.com/inward/record.url?eid=2-s2.0-85090951095&partnerID=MN8TOARS}, DOI={10.1016/j.envint.2020.106115}, abstractNote={The last two decades have seen a rise in the development of lanthanum (III)-containing materials (LM) for controlling phosphate in the aquatic environment. >70 papers have been published on this topic in the peer-reviewed literature, but mechanisms of phosphate removal by LM as well as potential environmental impacts of LM remain unclear. In this review, we summarize peer-reviewed scientific articles on the development and use of 80 different types of LM in terms of prospective benefits, potential ecological impacts, and research needs. We find that the main benefits of LM for phosphate removal are their ability to strongly bind phosphate under diverse environmental conditions (e.g., over a wide pH range, in the presence of diverse aqueous constituents). The maximum phosphate uptake capacity of LM correlates primarily with the La content of LM, whereas reaction kinetics are influenced by LM formulation and ambient environmental conditions (e.g., pH, presence of co-existing ions, ligands, organic matter). Increased La solubilization can occur under some environmental conditions, including at moderately acidic pH values (i.e., < 4.5–5.6), highly saline conditions, and in the presence of organic matter. At the same time, dissolved La will likely undergo hydrolysis, bind to organic matter, and combine with phosphate to precipitate rhabdophane (LaPO4·H2O), all of which reduce the bioavailability of La in aquatic environments. Overall, LM use presents a low risk of adverse effects in water with pH > 7 and moderate-to-high bicarbonate alkalinity, although caution should be applied when considering LM use in aquatic systems with acidic pH values and low bicarbonate alkalinity. Moving forward, we recommend additional research dedicated to understanding La release from LM under diverse environmental conditions as well as long-term exposures on ecological organisms, particularly primary producers and benthic organisms. Further, site-specific monitoring could be useful for evaluating potential impacts of LM on both biotic and abiotic systems post-application.}, journal={ENVIRONMENT INTERNATIONAL}, author={Zhi, Yue and Zhang, Chuhui and Hjorth, Rune and Baun, Anders and Duckworth, Owen W. and Call, Douglas F. and Knappe, Detlef R. U. and Jones, Jacob L. and Grieger, Khara}, year={2020}, month={Dec} }
 @article{zhang_maness_cuthbertson_kimura_liberatore_richardson_stanford_sun_knappe_2020, title={Treating water containing elevated bromide and iodide levels with granular activated carbon and free chlorine: impacts on disinfection byproduct formation and calculated toxicity}, volume={6}, ISSN={["2053-1419"]}, url={https://doi.org/10.1039/D0EW00523A}, DOI={10.1039/d0ew00523a}, abstractNote={Granular activated carbon effectively controlled disinfection byproduct formation and calculated toxicity, especially at high influent bromide levels.}, number={12}, journal={ENVIRONMENTAL SCIENCE-WATER RESEARCH & TECHNOLOGY}, publisher={Royal Society of Chemistry (RSC)}, author={Zhang, Chuhui and Maness, J. Clark and Cuthbertson, Amy A. and Kimura, Susana Y. and Liberatore, Hannah K. and Richardson, Susan D. and Stanford, Benjamin D. and Sun, Mei and Knappe, Detlef R. U.}, year={2020}, month={Dec}, pages={3460–3475} }