Pilot-scale performance of a UV-regenerable Iron-based activated carbon system for pharmaceutical and PFAS removal

Emerging contaminants (ECs), particularly per - and polyfluoroalkyl substances (PFAS) and pharmaceuticals (PhACs), are challenging to treat because of their persistence, mobility, and weak adsorption. We constructed and continuously operated a 200 m 3 ·day −1 pilot at a municipal wastewater treatment plant (WWTP) in Daegu, South Korea, coupling iron-impregnated powdered activated carbon (Fe-PAC) with ultraviolet (UV)/H₂O₂ photo-regeneration to restore adsorption in situ. Bench tests verified Fe-site-enabled photo-Fenton reactions, and pilot-assessed robustness under actual, variable influent fluctuations. Without regeneration, short-chain PFAS (PFHxA and PFHpA) showed limited, unstable removal, whereas long-chain PFNA and PFOA decreased over time owing to site saturation. Most PhACs (diclofenac, and florfenicol) sustained ≥90% removal; hydrophilic caffeine decreased transiently but recovered after regeneration, whereas atenolol exhibited lower long-term stability. With periodic UV/H₂O₂ treatment, PFAS removal exceeded 95% after three months; aggregate removal reached 97.7 and 99.1% at three and five months, respectively, without deterioration of water-quality indicators. Mechanistically, Fe-PAC acted as a dual adsorbent–catalyst: pores captured contaminants, and Fe sites generated radicals that decomposed surface residues and reopened adsorption sites, providing pilot-scale evidence that the UV-regenerable Fe-PAC hybrid can overcome adsorption limitations and deliver robust control of persistent micropollutants. We recommend optimizing the regeneration frequency and intensity and performing techno-economic evaluations to support full-scale deployment. • A 200 m 3 ·day −1 Fe-PAC/UV pilot ran >6 months on real WWTP effluent. • Fe-PAC: dual adsorbent–catalyst; enables in-situ UV/H₂O₂ regeneration. • UV/H₂O₂ regeneration restored sites; PFAS removal >95% after 3 months. • Most pharmaceuticals kept >90% long-term removal. • Demonstrated scalable control of persistent micropollutants in practice.

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Publication Details

Journal
Journal of Water Process Engineering
Published
2026-01-14
DOI
https://doi.org/10.1016/j.jwpe.2026.109468
Citations
1
Primary Topic
Per- and polyfluoroalkyl substances research
Type
article
Field-Weighted Citation Impact
23.84
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article

Pilot-scale performance of a UV-regenerable Iron-based activated carbon system for pharmaceutical and PFAS removal

TaeHwa Jung, Soyoung Beak, Jiyeol Bae, Eunji Kim et al.
1 citations
Journal of Water Process Engineering
Per- and polyfluoroalkyl substances research
23.84
article

Pilot-scale performance of a UV-regenerable Iron-based activated carbon system for pharmaceutical and PFAS removal

TaeHwa Jung, Soyoung Beak, Jiyeol Bae, Eunji Kim, Jungbeom Lee
article en
1 citations

Abstract

Emerging contaminants (ECs), particularly per - and polyfluoroalkyl substances (PFAS) and pharmaceuticals (PhACs), are challenging to treat because of their persistence, mobility, and weak adsorption. We constructed and continuously operated a 200 m 3 ·day −1 pilot at a municipal wastewater treatment plant (WWTP) in Daegu, South Korea, coupling iron-impregnated powdered activated carbon (Fe-PAC) with ultraviolet (UV)/H₂O₂ photo-regeneration to restore adsorption in situ. Bench tests verified Fe-site-enabled photo-Fenton reactions, and pilot-assessed robustness under actual, variable influent fluctuations. Without regeneration, short-chain PFAS (PFHxA and PFHpA) showed limited, unstable removal, whereas long-chain PFNA and PFOA decreased over time owing to site saturation. Most PhACs (diclofenac, and florfenicol) sustained ≥90% removal; hydrophilic caffeine decreased transiently but recovered after regeneration, whereas atenolol exhibited lower long-term stability. With periodic UV/H₂O₂ treatment, PFAS removal exceeded 95% after three months; aggregate removal reached 97.7 and 99.1% at three and five months, respectively, without deterioration of water-quality indicators. Mechanistically, Fe-PAC acted as a dual adsorbent–catalyst: pores captured contaminants, and Fe sites generated radicals that decomposed surface residues and reopened adsorption sites, providing pilot-scale evidence that the UV-regenerable Fe-PAC hybrid can overcome adsorption limitations and deliver robust control of persistent micropollutants. We recommend optimizing the regeneration frequency and intensity and performing techno-economic evaluations to support full-scale deployment. • A 200 m 3 ·day −1 Fe-PAC/UV pilot ran >6 months on real WWTP effluent. • Fe-PAC: dual adsorbent–catalyst; enables in-situ UV/H₂O₂ regeneration. • UV/H₂O₂ regeneration restored sites; PFAS removal >95% after 3 months. • Most pharmaceuticals kept >90% long-term removal. • Demonstrated scalable control of persistent micropollutants in practice.

Journal of Water Process EngineeringVol. 82
Science and Technology Policy Institute (KR), Korea Electric Power Corporation (South Korea) (KR), Korea Institute of Civil Engineering and Building Technology (KR), Korea University of Science and Technology (KR)
Clean water and sanitation
Openalex Percentile: Top 3%
Per- and polyfluoroalkyl substances research
23.84
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