Structural Features of Styrene-Functionalized Cyclodextrin Polymers That Promote the Adsorption of Perfluoroalkyl Acids in Water.

Autor: Lin ZW; Department of Chemistry, Northwestern University, Evanston, Illinois 60208, United States., Wang J; School of Civil and Environmental Engineering, Cornell University, Ithaca, New York 14853, United States., Dyakiv Y; Department of Chemistry, Northwestern University, Evanston, Illinois 60208, United States., Helbling DE; School of Civil and Environmental Engineering, Cornell University, Ithaca, New York 14853, United States., Dichtel WR; Department of Chemistry, Northwestern University, Evanston, Illinois 60208, United States.
Jazyk: angličtina
Zdroj: ACS applied materials & interfaces [ACS Appl Mater Interfaces] 2024 Jun 05; Vol. 16 (22), pp. 28409-28422. Date of Electronic Publication: 2024 May 20.
DOI: 10.1021/acsami.4c01969
Abstrakt: Cross-linked β-cyclodextrin (β-CD) polymers are promising adsorbents for the removal of per- and polyfluoroalkyl substances (PFAS) from contaminated water sources, including contaminated groundwater, drinking water, and wastewater. We previously reported porous, styrene-functionalized β-cyclodextrin (StyDex) polymers derived from radical polymerization with vinyl comonomers. Because of the versatility of these polymerizations, StyDex polymer compositions are tunable, which facilitates efforts to establish structure-adsorption relationships and to discover improved materials. Here, we evaluate the material properties and PFAS adsorption of 20 StyDex derivatives with varied comonomer structure and loading, regiochemistry of styrene placement on the CD monomer, and CD size. A StyDex polymer containing N , N '-dimethylbutyl ammonium ions exhibited the most effective PFAS adsorption in batch experiments. Furthermore, a StyDex polymer containing β-CD exhibited size-selective host-guest interactions with perfluoroalkyl acids (PFAAs) and neutral contaminants in aqueous electrolyte when compared to similar polymers containing either α-CD or γ-CD. Polymers based on β-CD monomers with an average of seven styrene groups randomly positioned over the 21 available hydroxyl groups performed similarly to those based on a β-CD monomer functionalized regiospecifically at each of the seven 6' positions. The former β-CD monomer is prepared in a single step from unmodified β-CD, so the ability to use it without compromising performance demonstrates promise for developing economically competitive adsorbents. These results offered important insights into structure-adsorption properties of StyDex polymers and will inform the design of improved StyDex formulations.
Databáze: MEDLINE