A Tunable Porous β-Cyclodextrin Polymer Platform to Understand and Improve Anionic PFAS Removal.

Cross-linked polymers containing β-cyclodextrin (β-CD) are promising adsorbents with demonstrated removal performances for per- and polyfluoroalkyl substances (PFASs) from contaminated water sources. Despite the promising performance of some β-CD-based adsorbents for PFAS removal, many of these materials are not amenable for rational performance improvement or addressing fundamental questions about the PFAS adsorption mechanisms. These ambiguities arise from the poorly defined structure of the cross-linked polymers, especially with respect to the random substitution patterns of the cyclodextrins as well as side reactions that modify the structures of some cross-linkers.

Identifying the physicochemical properties of β-cyclodextrin polymers that determine the adsorption of perfluoroalkyl acids.

Cyclodextrin polymers (CDPs) are emerging adsorbents with demonstrated potential to remove perfluoroalkyl acids (PFAAs) from water. However, little is known about how the physicochemical properties of different types of CDPs determine PFAA adsorption on CDPs. In this study, we investigated the adsorption performance of 34 CDPs which consist of 14 different crosslinkers and exhibit a wide range of physicochemical properties.

Evaluation, optimization, and application of three independent suspect screening workflows for the characterization of PFASs in water.

Suspect screening is a valuable tool for characterizing per- and polyfluoroalkyl substances (PFASs) in environmental media. Although a variety of data mining tools have been developed and applied for suspect screening of PFAS, few suspect screening workflows have undergone a comprehensive performance evaluation or optimization. The goals of this research were to: (1) evaluate and optimize three independent suspect screening workflows for the detection of PFASs in water samples; and (2) apply the optimized suspect screening workflows to an environmental sample to determine the extent to which suspect screening results converge.

β-Cyclodextrin Polymers with Different Cross-Linkers and Ion-Exchange Resins Exhibit Variable Adsorption of Anionic, Zwitterionic, and Nonionic PFASs.

Per- and polyfluoroalkyl substances (PFASs) occur in groundwater as mixtures of anionic, cationic, zwitterionic, and nonionic species, although few remediation technologies have been evaluated to assess the removal of different types of PFASs. In this study, we evaluated the performance of three β-cyclodextrin polymers (CDPs), an anion-exchange (AE) resin, and a cation-exchange (CE) resin for the removal of anionic, zwitterionic, and nonionic PFASs from water. We found that a CDP with a negative surface charge rapidly removes all zwitterionic PFASs with log values ranging between 2.

Reduction of a Tetrafluoroterephthalonitrile-β-Cyclodextrin Polymer to Remove Anionic Micropollutants and Perfluorinated Alkyl Substances from Water.

Organic micropollutants (MPs) are anthropogenic substances that contaminate water resources at trace concentrations. Many MPs, including per- and polyfluorinated alkyl substances (PFASs), have come under increased scrutiny because of their environmental persistence and association with various health problems. A β-cyclodextrin polymer linked with tetrafluoroterephthalonitrile (TFN-CDP) has high affinity for cationic and many neutral MPs from contaminated water because of anionic groups incorporated during the polymerization.

Removal of GenX and Perfluorinated Alkyl Substances from Water by Amine-Functionalized Covalent Organic Frameworks.

Per- and polyfluorinated alkyl substances (PFAS), such as perfluorooctanoic acid (PFOA), perfluorooctanesulfonate (PFOS), and ammonium perfluoro-2-propoxypropionate (GenX), contaminate ground and surface waters throughout the world. The cost and performance limitations of current PFAS removal technologies motivate efforts to develop selective and high-affinity adsorbents. Covalent organic frameworks (COFs) are unexplored yet promising adsorbents because of their high surface area and tunable pore sizes.