Peroxide activation by microbially synthesized sulfidated iron: Comparison against abiotic iron-based materials in terms of treatment efficiency and oxidative degradation pathway

Authors
Yang, BowenSuh, Sae-InLee, JeonggilRyoo, Hwa-SooHam, So-YoungKim, JaesungKo, Young-JinWoo, HeesooChoi, JaeminOh, Hyung-SukLee, Sang-HoonPark, Hee-DeungKwon, Man JaeLee, HongshinLee, Jaesang
Issue Date
2022-04
Publisher
Elsevier BV
Citation
Applied Catalysis B: Environmental, v.303, pp.1 - 13
Abstract
This study demonstrated the application of biogenic sulfidated iron (B-FeS), produced via anaerobic digestion of Desulfovibrio desulfuricans using sulfate as the terminal electron acceptor, for peroxide activation. B-FeS was assessed against chemically prepared zerovalent and sulfidated iron (ferrous sulfide and pyrite) with respect to their ability to activate peroxydisulfate (PDS) and H2O2. Regardless of the peroxide type, B-FeS outperformed benchmark iron activators in treating 4-chlorophenol due to its resistance to iron corrosion and the high content of reduced sulfur. The roles of oxidizing radicals were confirmed based on the effects of alcohol-based quenchers, multi-activity assessment, electron paramagnetic resonance spectral features, and product analysis. The pHdependent efficiency of sulfoxide-to-sulfone conversion suggested that high-valent iron species acted as the secondary oxidant in all iron/peroxide systems, and the contribution was more pronounced when PDS and B-FeS were used. Microbial sulfidation as a catalyst regeneration strategy recovered the peroxide activation capacity of oxidized B-FeS.
Keywords
ZERO-VALENT IRON; ZEROVALENT IRON; WATER-TREATMENT; SPECTROPHOTOMETRIC DETERMINATION; 2,4-DICHLOROPHENOXYACETIC ACID; PEROXYMONOSULFATE ACTIVATION; CONTAINING MINERALS; OXIDIZING CAPACITY; HYDROXYL RADICALS; RATE CONSTANTS; Biogenic sulfidated iron; Sulfate-reducing bacteria; Peroxide activation; Sulfate radical; High-valent iron
ISSN
0926-3373
URI
https://pubs.kist.re.kr/handle/201004/115498
DOI
10.1016/j.apcatb.2021.120884
Appears in Collections:
KIST Article > 2022
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