Evidence map›Paper›PMID 40808832›Full record

ArticleACS ES&T water2025

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

Florian Junge, Fiona E Rückbeil, Regina Gnirss, Rainer Haag, Alejandro Lorente, Fabio Lorenz, Sunil P M Menacherry, Aki S Ruhl, Alexander Sperlich, Ana Zidar and 1 more

Abstract read
In one paragraph

Article in ACS ES&T water, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Florian JungeInstitut für Chemie und Biochemie, Freie Universität Berlin, Arnimallee 22, 14195 Berlin, Germany.
Fiona E RückbeilBerliner Wasserbetriebe, Neue Jüdenstraße 1, 10179 Berlin, Germany.
Regina GnirssBerliner Wasserbetriebe, Neue Jüdenstraße 1, 10179 Berlin, Germany.
Rainer HaagInstitut für Chemie und Biochemie, Freie Universität Berlin, Arnimallee 22, 14195 Berlin, Germany.ORCID https://orcid.org/0000-0003-3840-162X
Alejandro LorenteInstitut für Chemie und Biochemie, Freie Universität Berlin, Arnimallee 22, 14195 Berlin, Germany.
Fabio LorenzInstitut für Chemie und Biochemie, Freie Universität Berlin, Arnimallee 22, 14195 Berlin, Germany.
Sunil P M MenacherryGerman Environment Agency, Section II 3.3, Schichauweg 58, 12307 Berlin, Germany.
Aki S RuhlTechnische Universität Berlin, Water Treatment, KF4, Fasanenstraße 1A, 10623 Berlin, Germany.ORCID https://orcid.org/0000-0002-2443-4722
Alexander SperlichBerliner Wasserbetriebe, Neue Jüdenstraße 1, 10179 Berlin, Germany.ORCID https://orcid.org/0000-0001-5329-9948
Ana ZidarInstitut für Chemie und Biochemie, Freie Universität Berlin, Arnimallee 22, 14195 Berlin, Germany.
Olaf WagnerInstitut für Chemie und Biochemie, Freie Universität Berlin, Arnimallee 22, 14195 Berlin, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

fluorine−fluorine interactionsion exchange resinsPFAS adsorptionpolyethyleniminesiloxanewater treatment

Identifiers

PMID40808832
PMCPMC12340944

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.