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dc.contributor.authorYang, Bowen-
dc.contributor.authorSuh, Sae-In-
dc.contributor.authorLee, Jeonggil-
dc.contributor.authorRyoo, Hwa-Soo-
dc.contributor.authorHam, So-Young-
dc.contributor.authorKim, Jaesung-
dc.contributor.authorKo, Young-Jin-
dc.contributor.authorWoo, Heesoo-
dc.contributor.authorChoi, Jaemin-
dc.contributor.authorOh, Hyung-Suk-
dc.contributor.authorLee, Sang-Hoon-
dc.contributor.authorPark, Hee-Deung-
dc.contributor.authorKwon, Man Jae-
dc.contributor.authorLee, Hongshin-
dc.contributor.authorLee, Jaesang-
dc.date.accessioned2024-01-19T12:30:57Z-
dc.date.available2024-01-19T12:30:57Z-
dc.date.created2022-01-25-
dc.date.issued2022-04-
dc.identifier.issn0926-3373-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/115498-
dc.description.abstractThis 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.-
dc.languageEnglish-
dc.publisherElsevier BV-
dc.titlePeroxide activation by microbially synthesized sulfidated iron: Comparison against abiotic iron-based materials in terms of treatment efficiency and oxidative degradation pathway-
dc.typeArticle-
dc.identifier.doi10.1016/j.apcatb.2021.120884-
dc.description.journalClass1-
dc.identifier.bibliographicCitationApplied Catalysis B: Environmental, v.303, pp.1 - 13-
dc.citation.titleApplied Catalysis B: Environmental-
dc.citation.volume303-
dc.citation.startPage1-
dc.citation.endPage13-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000720473800006-
dc.identifier.scopusid2-s2.0-85118896977-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryEngineering, Environmental-
dc.relation.journalWebOfScienceCategoryEngineering, Chemical-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaEngineering-
dc.type.docTypeArticle-
dc.subject.keywordPlusZERO-VALENT IRON-
dc.subject.keywordPlusZEROVALENT IRON-
dc.subject.keywordPlusWATER-TREATMENT-
dc.subject.keywordPlusSPECTROPHOTOMETRIC DETERMINATION-
dc.subject.keywordPlus2,4-DICHLOROPHENOXYACETIC ACID-
dc.subject.keywordPlusPEROXYMONOSULFATE ACTIVATION-
dc.subject.keywordPlusCONTAINING MINERALS-
dc.subject.keywordPlusOXIDIZING CAPACITY-
dc.subject.keywordPlusHYDROXYL RADICALS-
dc.subject.keywordPlusRATE CONSTANTS-
dc.subject.keywordAuthorBiogenic sulfidated iron-
dc.subject.keywordAuthorSulfate-reducing bacteria-
dc.subject.keywordAuthorPeroxide activation-
dc.subject.keywordAuthorSulfate radical-
dc.subject.keywordAuthorHigh-valent iron-
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