Coagulation/flocculation is a widely used water and wastewater treatment process due to its low cost, simplicity, and effectiveness. However, the process is not effective in the treatment of per- and polyfluoroalkyl substances (PFAS), the presence and treatment of which is an ongoing challenge for water providers. Here, we explore cationic surfactant-enhanced coagulation as a process modification to target the removal of PFAS in existing coagulation/flocculation systems. Batch experiments, in jar testing apparatus, were performed to assess the removal of two short-chain and two long-chain PFAS at an initial concentration of 10 µg/L with the addition of cetyltrimethylammoniumg chloride (CTAC) as the coagulant-aid. Our findings suggest that elevated coagulant dose (60 mg/L of alum or 100 mg/L of FeCl3) coupled with the addition of a cationic surfactant (1 mg/L of CTAC) significantly enhanced the removal of both short-chain (perfluorobutane sulfonate: PFBS removal to >40%) and long-chain PFAS (perfluorooctanoic acid: PFOA and perfluorooctane sulfonate: PFOS removal to >80%), with FeCl3 showing better performance than alum. Sulfonates (PFBS, PFOS) were shown to be removed more efficiently compared to carboxylates (PFBA, PFOA), presumably due to their higher hydrophobicity leading to better interactions with the flocs. Furthermore, CTAC in combination with traditionally used additives such as Powdered Activated Carbon (PAC), served as a better aid for PFAS treatment and improved the removal of PFBS, PFOA, and PFOS to >98%. This study highlights that introducing a cost-effective pre-treatment with a cationic surfactant to existing conventional treatment systems can improve the performance efficiency in treating PFAS-contaminated waters.
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Rapid Capture of Per- and Polyfluoroalkyl Substances Using a Self-Assembling Zirconium-Based Metal-Organic Cage
Legacy and emerging per- and polyfluoroalkyl substances (PFAS) are widely detected in environmental and human samples because of their widespread use and resistance to degradation. Due to the increasing concern on health impacts of PFAS resulting from exposure to contaminated water, the development of novel materials to capture and remove PFAS from the environment is needed. Here, we present a self-assembling, fluorinated, zirconium-based metal–organic cage (F-ZrMOC) capable of capturing 37 different PFAS species, at an average of 82% removal from a solution that contains 400 ng/mL of each individual PFAS. The F-ZrMOC captured different classes of PFAS within 30 s, including perfluoroalkyl carboxylates, sulfonates, sulfonamides, ethoxylates, and fluorotelomer carboxylates/sulfonates/alcohols from water during in-vial, static, and flow through exposures (in which the F-ZrMOC is used as a solid phase extraction sorbent). Removal efficiency is higher for PFAS with chain lengths of seven carbons or higher; the presence of complex matrices such as untreated wastewater and groundwater samples did not significantly reduce the removal efficiencies for PFAS. The F-ZrMOC was characterized using 1H and 19F nuclear magnetic resonance (NMR) spectroscopy, and the stoichiometry of the synthesized cage was confirmed using Fourier transform-ion cyclotron resonance mass spectrometry. The surface area and pore size of F-ZrMOC were further determined by N2 and CO2 sorption measurements. 19F-NMR spectroscopy revealed that solvent plays an important role in the capture of PFAS; once the cages are in contact with methanol solution, captured PFAS are released.
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- Award ID(s):
- 1905274
- PAR ID:
- 10511980
- Publisher / Repository:
- American Chemical Society
- Date Published:
- Journal Name:
- ACS Applied Engineering Materials
- Volume:
- 2
- Issue:
- 1
- ISSN:
- 2771-9545
- Page Range / eLocation ID:
- 87 to 95
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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