Persistence of aqueous-phase, short-chain per- and polyfluoroalkyl substances (PFAS) and their abatement by heterogeneous photocatalysisShow others and affiliations
2026 (English)In: Journal of Materials Chemistry A, ISSN 2050-7488, E-ISSN 2050-7496Article in journal (Refereed) Epub ahead of print
Abstract [en]
Short-chain (C4-C6) per- and polyfluoroalkyl substances (PFAS) have become the dominant PFAS fraction in the environment following the phase-out of long-chain analogues. Their exceptional chemical stability, amphiphilic character and resistance to degradation have led to ubiquitous occurrence of short-chain PFAS across the global hydrological cycle. At the same time, their enhanced aqueous solubility, mobility and persistence resulted in poor removal by conventional water treatment leading to widespread detection in drinking water. By first providing the general classification of PFAS, this Review summarises the physicochemical properties of short-chain PFAS and their interactions to elucidate their removal challenges. While heterogeneous photocatalysis has long been the vanguard technology for the abatement of aqueous-phase micropollutants, it now finds itself in uncharted territory. Previously, photocatalysts that efficiently generate hydroxyl radicals generally exhibit strong activity toward hydrocarbon-based micropollutants; however, in the absence (or lacking) of C-H bonds in PFAS, this paradigm may no longer apply. Hence, this Review presents an up-to-date understanding of short-chain PFAS and their abatement through heterogeneous photocatalysis. As the field remains in its infancy, critical knowledge gaps must be addressed before the rational design of PFAS-targeted photocatalysts and treatment processes can be realized.
Place, publisher, year, edition, pages
Royal Society of Chemistry, 2026.
National Category
Materials Chemistry
Identifiers
URN: urn:nbn:se:oru:diva-130239DOI: 10.1039/d6ta01866aISI: 001809173200001OAI: oai:DiVA.org:oru-130239DiVA, id: diva2:2088277
Funder
Knowledge FoundationSwedish Research Council Formas, 2023–00522
Note
The work is supported by the Ministry of Higher Education Malaysia via the Fundamental Research Grant Scheme (FRGS/1/2022/TK08/UM/02/43), Australian Research Council via the Discovery Project (DP260101375), Southeast Asia-European Joint Funding Scheme (JFS21-123 HYPERMIS), SMART-PFAS – Synergy project (2026-0015) through the Knowledge Foundation (KKS), United Arab Emirates University – Asian University Alliance (UAEU-AUA Scheme; 12R174) and Universiti Malaya (UM) Matching Grants. AQM is thankful of the support from the UM Postdoctoral Fellowship. LYG would like to acknowledge the fund from Formas (2023–00522) and Scandinavian-Japan Sasagawa Foundation (GA24-SWE-0097).
2026-07-272026-07-272026-07-27Bibliographically approved