Effect of Hydrophobic Cross-Linkers in Strong Base Gel-Type Resins on the Adsorption Kinetics and Capacity for Perfluoroalkyl Substances

The persistence and water mobility of per- and polyfluoroalkyl substances (PFAS) have led authorities worldwide to lower regulatory limits to prevent adverse health effects. Removal via adsorption on activated carbon can be inefficient due to the unspecific surface interaction, while ion exchange resins with positive charges and hydrophobic chains can offer faster kinetics and improved removal. In here, novel cationic resins were synthesized by cross-linking polyethylenimine, followed by methylation. To obtain cross-linked particles and introduce hydrophobic interacting moieties in one single synthetic step, aliphatic, fluorous, and silicone-based oligoethers were used as cross-linkers. These cationic adsorbents were compared with two state-of-the-art strong base gel-type ion exchange resins and granular activated carbon in isotherm and kinetic studies. The newly developed adsorbents showed significantly faster removals of all tested long- and short-chain PFAS. The fluorous cationic adsorbent achieved equilibrium loadings that were comparable to those of the state-of-the-art adsorbents for all PFAS with five or more perfluorinated carbon atoms.

Authors

Institutions

Publication Details

Journal
ACS ES&T Water
Published
2025-06-13
DOI
https://doi.org/10.1021/acsestwater.5c00094
Primary Topic
Per- and polyfluoroalkyl substances research
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Effect of Hydrophobic Cross-Linkers in Strong Base Gel-Type Resins on the Adsorption Kinetics and Capacity for Perfluoroalkyl Substances

Rainer Haag, Olaf Wagner, Regina Gnirß, Florian Junge et al.
ACS ES&T Water
Per- and polyfluoroalkyl substances research
article

Effect of Hydrophobic Cross-Linkers in Strong Base Gel-Type Resins on the Adsorption Kinetics and Capacity for Perfluoroalkyl Substances

Rainer Haag, Olaf Wagner, Regina Gnirß, Florian Junge, Fiona Elena Rückbeil, F.W. Lorenz, Aki Sebastian Ruhl, Alexander Sperlich, Sunil Paul M. Menacherry, Alejandro Lorente, Ana Zidar
article en

Abstract

The persistence and water mobility of per- and polyfluoroalkyl substances (PFAS) have led authorities worldwide to lower regulatory limits to prevent adverse health effects. Removal via adsorption on activated carbon can be inefficient due to the unspecific surface interaction, while ion exchange resins with positive charges and hydrophobic chains can offer faster kinetics and improved removal. In here, novel cationic resins were synthesized by cross-linking polyethylenimine, followed by methylation. To obtain cross-linked particles and introduce hydrophobic interacting moieties in one single synthetic step, aliphatic, fluorous, and silicone-based oligoethers were used as cross-linkers. These cationic adsorbents were compared with two state-of-the-art strong base gel-type ion exchange resins and granular activated carbon in isotherm and kinetic studies. The newly developed adsorbents showed significantly faster removals of all tested long- and short-chain PFAS. The fluorous cationic adsorbent achieved equilibrium loadings that were comparable to those of the state-of-the-art adsorbents for all PFAS with five or more perfluorinated carbon atoms.

ACS ES&T WaterVol. 5(8)
German Environment Agency (DE), Berliner Wasserbetriebe (Germany) (DE), Technische Universität Berlin (DE), Freie Universität Berlin (DE)
Deutsche Forschungsgemeinschaft, Einstein Stiftung Berlin, Berlin University Alliance, H2020 Societal Challenges
Clean water and sanitation
Openalex Percentile: Top 88%
Per- and polyfluoroalkyl substances research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.