Photocatalytic degradation of PFAS under field water matrix conditions using an adsorptive photocatalyst

• Tested an adsorptive photocatalyst (Ga/TNTs@AC) for treating PFAS in field water • Field water matrix impeded column adsorption and photocatalysis of PFAS • Addition of Fe 3+ during photocatalysis enhanced PFAS degradation and mineralization • Column tests confirmed effective sorption of all PFAS from the surface water • PFAS retained by the column were effectively photodegraded, regenerating the media Per- and polyfluoroalkyl substances (PFAS) are ubiquitous in surface waters. While numerous technologies have been investigated to mitigate human exposure, limited information is available for treatment of PFAS in actual field waters. Based on the “concentrate-and-destroy” strategy, we prepared and evaluated an adsorptive photocatalyst, namely gallium-doped activated carbon-supported titanate nanotubes (Ga/TNTs@AC), for treatment of six PFAS in a model surface water. Being most prevalent in the field water, perfluorooctane sulfonate (PFOS) was selected as a representative compound for feasibility and optimization studies. Batch experiments revealed that at a dosage of 1 g/L, Ga/TNTs@AC adsorbed 98% of 100 µg/L PFOS in the surface water within 10 min. Background cations enhanced PFOS removal by suppressing repulsive forces and enabling the cation-bridging effects. Upon UV irradiation, 35.5% of adsorbed PFOS was effectively degraded and 25.8% defluorinated. The photocatalytic defluorination of PFOS was boosted to 70.0% by addition of 60 µM Fe 3+ during the photodegradation, where formation of Fe 3+ −PFOS and Fe 3+ −DOM complexes reduced the energy barrier, facilitated activation of PFOS, and diminished inhibitory effects of DOM. Acidic conditions were found favorable for both adsorption and photocatalysis of PFOS. Fixed-bed column tests confirmed the effective adsorption of PFOS and other PFAS in the field water, with complete PFOS breakthrough occurred after 5,100 bed volumes. Subsequently, the PFAS-laden Ga/TNTs@AC successfully degraded the pre-concentrated PFAS, which also regenerated the Ga/TNTs@AC media for reuse. Ga/TNTs@AC appeared to be a promising material for enabling the “concentrate-&-destroy” strategy for more efficient removal and degradation of PFAS in field waters.

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Publication Details

Journal
Water Research X
Published
2026-01-01
DOI
https://doi.org/10.1016/j.wroa.2026.100485
Primary Topic
Per- and polyfluoroalkyl substances research
Type
article
Field-Weighted Citation Impact
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article

Photocatalytic degradation of PFAS under field water matrix conditions using an adsorptive photocatalyst

Rodney Nelson Leary, Dongye Zhao, Lee Blaney, Tianyuan Xu et al.
Water Research X
Per- and polyfluoroalkyl substances research
article

Photocatalytic degradation of PFAS under field water matrix conditions using an adsorptive photocatalyst

Rodney Nelson Leary, Dongye Zhao, Lee Blaney, Tianyuan Xu, Yangmo Zhu, Ke He, Xiaodi Hao
article en

Abstract

• Tested an adsorptive photocatalyst (Ga/TNTs@AC) for treating PFAS in field water • Field water matrix impeded column adsorption and photocatalysis of PFAS • Addition of Fe 3+ during photocatalysis enhanced PFAS degradation and mineralization • Column tests confirmed effective sorption of all PFAS from the surface water • PFAS retained by the column were effectively photodegraded, regenerating the media Per- and polyfluoroalkyl substances (PFAS) are ubiquitous in surface waters. While numerous technologies have been investigated to mitigate human exposure, limited information is available for treatment of PFAS in actual field waters. Based on the “concentrate-and-destroy” strategy, we prepared and evaluated an adsorptive photocatalyst, namely gallium-doped activated carbon-supported titanate nanotubes (Ga/TNTs@AC), for treatment of six PFAS in a model surface water. Being most prevalent in the field water, perfluorooctane sulfonate (PFOS) was selected as a representative compound for feasibility and optimization studies. Batch experiments revealed that at a dosage of 1 g/L, Ga/TNTs@AC adsorbed 98% of 100 µg/L PFOS in the surface water within 10 min. Background cations enhanced PFOS removal by suppressing repulsive forces and enabling the cation-bridging effects. Upon UV irradiation, 35.5% of adsorbed PFOS was effectively degraded and 25.8% defluorinated. The photocatalytic defluorination of PFOS was boosted to 70.0% by addition of 60 µM Fe 3+ during the photodegradation, where formation of Fe 3+ −PFOS and Fe 3+ −DOM complexes reduced the energy barrier, facilitated activation of PFOS, and diminished inhibitory effects of DOM. Acidic conditions were found favorable for both adsorption and photocatalysis of PFOS. Fixed-bed column tests confirmed the effective adsorption of PFOS and other PFAS in the field water, with complete PFOS breakthrough occurred after 5,100 bed volumes. Subsequently, the PFAS-laden Ga/TNTs@AC successfully degraded the pre-concentrated PFAS, which also regenerated the Ga/TNTs@AC media for reuse. Ga/TNTs@AC appeared to be a promising material for enabling the “concentrate-&-destroy” strategy for more efficient removal and degradation of PFAS in field waters.

Water Research XVol. 30
China University of Mining and Technology (CN), San Diego State University (US), Beijing University of Civil Engineering and Architecture (CN), University of Maryland, Baltimore County (US), Auburn University (US)
Clean water and sanitation
Openalex Percentile: Top 95%
Per- and polyfluoroalkyl substances research
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