Evaluation of commercial nanofiltration and reverse osmosis membrane filtration to remove per‐and polyfluoroalkyl substances (PFAS): Effects of transmembrane pressures and water matrices DOI
Qingquan Ma, Qian Lei, Fangzhou Liu

et al.

Water Environment Research, Journal Year: 2024, Volume and Issue: 96(2)

Published: Jan. 30, 2024

Abstract Perfluoroalkyl and polyfluoroalkyl substances (PFASs) are now widely found in aquatic ecosystems, including sources of drinking water portable water, due to their increasing prevalence. Among different PFAS treatment or separation technologies, nanofiltration (NF) reverse osmosis (RO) both yield high rejection efficiencies (>95%) diverse water; however, technologies affected by many intrinsic extrinsic factors. This study evaluated the carbon chain length (e.g., PFOA PFBA) two commercial RO NF membranes under operational conditions applied pressure initial concentration) feed solution matrixes, such as pH (4–10), salinity (0‐ 1000‐mM NaCl), organic matters (0–10 mM). We further performed principal component analysis (PCA) demonstrate interrelationships molecular weight (213–499 g·mol −1 ), membrane characteristics (RO NF), matrices, on rejection. Our results confirmed that size exclusion is a primary mechanism NF, well fact electrostatic interactions important when molecules have sizes less than pores. Practitioner Points Two were remove 10 PFAS. High transmembrane pressures facilitated permeate recovery RO. Electrostatic repulsion pore dominant mechanisms for removal. pH, ionic strength, Mechanisms with RO/NF explained PCA analysis.

Language: Английский

Influences of Chemical Properties, Soil Properties, and Solution pH on Soil–Water Partitioning Coefficients of Per- and Polyfluoroalkyl Substances (PFASs) DOI Creative Commons
Thi Minh Hong Nguyen, Jennifer Bräunig, Kristie Thompson

et al.

Environmental Science & Technology, Journal Year: 2020, Volume and Issue: 54(24), P. 15883 - 15892

Published: Nov. 28, 2020

The aim of this study was to assess the soil-water partitioning behavior a wider range per- and polyfluoroalkyl substances (PFASs) onto soils covering diverse soil properties. PFASs studied include perfluoroalkyl carboxylates (PFCAs), perfluoroalkane sulfonates (PFSAs), fluorotelomer (FTSs), nonionic sulfonamides (FASAs), cyclic PFAS (PFEtCHxS), ether acids (GenX, ADONA, 9Cl-PF3ONS), three aqueous film-forming foam (AFFF)-related zwitterionic (AmPr-FHxSA, TAmPr-FHxSA, 6:2 FTSA-PrB). Soil-water coefficients (log Kd values) ranged from less than zero approximately three, were chain-length-dependent, significantly linearly related molecular weight (MW) for with MW > 350 g/mol (R2 = 0.94, p < 0.0001). Across all soils, values short-chain (≤5 -CF2- moieties) similar varied (<0.5 log units) compared long-chain (>0.5 1.5 zwitterions AmPr- TAmPr-FHxSA (∼1.5 2 units). Multiple properties described sorption better any single property. effects on different anionic, nonionic, PFASs. Solution pH could change both speciation chemistry affecting surface complexation electrostatic processes. increased when solution decreased eight three. Short-chain sensitive results indicate complex interactions surfaces need consider type describe mobility in environment.

Language: Английский

Citations

302

Spatial Trends of Anionic, Zwitterionic, and Cationic PFASs at an AFFF-Impacted Site DOI
Anastasia Nickerson, Alix E. Rodowa, David T. Adamson

et al.

Environmental Science & Technology, Journal Year: 2020, Volume and Issue: 55(1), P. 313 - 323

Published: Dec. 22, 2020

Soil and groundwater from an aqueous film-forming foam (AFFF)-impacted site were sampled at high resolution (n = 105 for soil, n 58 groundwater) analyzed extensive list of anionic, zwitterionic, cationic poly- perfluoroalkyl substances (PFASs). Spatial trends acids many precursors enabled a better understanding PFAS composition, transport, transformation. All PFASs without analytical standards semi-quantified. Summed individual concentrations often higher depth than near the surface in soil groundwater. Zwitterionic compounds composed majority total mass (up to 97%) firefighter training area (FTA) soil. Composition class, chain length, structural isomers changed with distance FTA, suggesting situ transformation differential transport. The percentage branched perfluorooctane sulfonate increased depth, consistent isomeric However, linear perfluorooctanoic acid (PFOA) was enriched, fluorotelomer precursor PFOA. Perfluorohexane sulfonamide, potential product sulfonamide-based PFASs, present (maximum 448 ng/g 3.4 mg/L groundwater). Precursor may create long-term sources acids, although pathways remain unknown; analysis is critical fate transport understanding.

Language: Английский

Citations

168

Emerging organic contaminants in global community drinking water sources and supply: A review of occurrence, processes and remediation DOI
Anwesha Mukhopadhyay, Srimanti Duttagupta, Abhijit Mukherjee

et al.

Journal of environmental chemical engineering, Journal Year: 2022, Volume and Issue: 10(3), P. 107560 - 107560

Published: March 16, 2022

Language: Английский

Citations

149

Communicating Confidence of Per- and Polyfluoroalkyl Substance Identification via High-Resolution Mass Spectrometry DOI Creative Commons
Joseph A. Charbonnet, Carrie A. McDonough, Feng Xiao

et al.

Environmental Science & Technology Letters, Journal Year: 2022, Volume and Issue: 9(6), P. 473 - 481

Published: May 26, 2022

Per- and polyfluoroalkyl substances (PFASs) are important environmental contaminants, yet relatively few analytical reference standards exist for this class. Nontarget analyses performed by means of high-resolution mass spectrometry (HRMS) increasingly common the discovery identification PFASs in biological samples. The certainty PFAS identifications made via HRMS must be communicated through a reliable harmonized approach. Here, we present confidence scale along with criteria specific to suspect or nontarget analysis HRMS. Confidence levels range from level 1a─"Confirmed Reference Standard," 1b─"Indistinguishable 5─"Exact Masses Interest," which identified screening data filtering, two forms feature prioritization. This is consistent general communicating small organic molecules (e.g., match standards, library MS/MS, and/or retention times) but incorporates conventions tools used classification detection homologous series ranges defects). Our clarifies and, doing so, facilitates more efficient identification.

Language: Английский

Citations

136

Updated review on emerging technologies for PFAS contaminated water treatment DOI
Sudesh Yadav, Ibrar Ibrar, Raed A. Al-Juboori

et al.

Process Safety and Environmental Protection, Journal Year: 2022, Volume and Issue: 182, P. 667 - 700

Published: April 12, 2022

Language: Английский

Citations

98

A juxtaposed review on adsorptive removal of PFAS by metal-organic frameworks (MOFs) with carbon-based materials, ion exchange resins, and polymer adsorbents DOI
Elika Karbassiyazdi, Medha Kasula,

Sweta Modak

et al.

Chemosphere, Journal Year: 2022, Volume and Issue: 311, P. 136933 - 136933

Published: Oct. 21, 2022

Language: Английский

Citations

70

Total Oxidizable Precursor (TOP) Assay─Best Practices, Capabilities and Limitations for PFAS Site Investigation and Remediation DOI
Mohamed Ateia,

Dora Chiang,

Michaela Cashman

et al.

Environmental Science & Technology Letters, Journal Year: 2023, Volume and Issue: 10(4), P. 292 - 301

Published: March 9, 2023

The comprehensive characterization of per- and polyfluoroalkyl substances (PFASs) is necessary for the effective assessment management risk at contaminated sites. While current analytical methods are capable quantitatively measuring a number specific PFASs, they do not provide complete picture thousands PFASs that utilized in commercial products potentially released into environment. These unmeasured include many PFAS precursors, which may be converted related chemicals through oxidation. total oxidizable precursor (TOP) assay offers means bridging this gap by oxidizing unknown precursors intermediates converting them stable with established standards. application TOP to samples from PFAS-contaminated sites has generated several new insights, but it also presented various technical challenges laboratories. Despite increased literature studies assay, there critical growing method beyond researchers academia. This article outlines benefits using aqueous site assessments suggests ways address some its limitations.

Language: Английский

Citations

53

Coexisting ions and long-chain per- and polyfluoroalkyl substances (PFAS) inhibit the adsorption of short-chain PFAS by granular activated carbon DOI
Yi Zhang,

Amanda Thomas,

Onur G. Apul

et al.

Journal of Hazardous Materials, Journal Year: 2023, Volume and Issue: 460, P. 132378 - 132378

Published: Aug. 23, 2023

Language: Английский

Citations

50

A critical science mapping approach on removal mechanism and pathways of per- and poly-fluoroalkyl substances (PFAS) in water and wastewater: A comprehensive review DOI
Chejarla Venkatesh Reddy, Ramesh Kumar,

Prasenjit Chakrabortty

et al.

Chemical Engineering Journal, Journal Year: 2024, Volume and Issue: 492, P. 152272 - 152272

Published: May 16, 2024

Language: Английский

Citations

16

β-Cyclodextrin Polymers with Different Cross-Linkers and Ion-Exchange Resins Exhibit Variable Adsorption of Anionic, Zwitterionic, and Nonionic PFASs DOI
Casey Ching, Max J. Klemes, Brittany Trang

et al.

Environmental Science & Technology, Journal Year: 2020, Volume and Issue: 54(19), P. 12693 - 12702

Published: Sept. 14, 2020

Per- and polyfluoroalkyl substances (PFASs) occur in groundwater as mixtures of anionic, cationic, zwitterionic, nonionic species, although few remediation technologies have been evaluated to assess the removal different types PFASs. In this study, we performance three β-cyclodextrin polymers (CDPs), an anion-exchange (AE) resin, a cation-exchange (CE) resin for PFASs from water. We found that CDP with negative surface charge rapidly removes all zwitterionic log KD values ranging between 2.4 3.1, CE two 1.8 1.9. The CDPs positive remove anionic 2.7 4.1, AE relatively slowly 2.0 2.3. All adsorbents exhibited variable some adsorption inhibition at higher pH presence matrix constituents. Our findings provide insight into how can be combined remediate contaminated complex

Language: Английский

Citations

80