Novel hemin-derived Fe/N–C magnetic catalyst for enhanced peroxymonosulfate activation and diclofenac degradation

dc.contributor.authorAryee. A.A.
dc.contributor.authorKumar. A.V.N.
dc.date.accessioned2025-07-11T10:47:55Z
dc.date.issued2025
dc.descriptionResearch Article
dc.description.abstractIn this study, Fe involved N-doped carbon catalysts labelled as PA@Hemx (x = pyrolysis temperature) was synthesized through a one-step pyrolysis of hemin (Hem) and polyacrylate (PA). The reported method enables high dispersion and exposure of both Fe and N active sites on PA derived carbon. The PA@Hemx samples were then used for peroxymonosulfate (PMS) activated diclofenac (DCF) degradation. Results from the character ization studies verified the successful incorporation of hemin in the composite. Approximately 99.2 % DCF degradation at pH = 6.01 was achieved in 60 min using 0.1 g L− 1 PA@Hem700 and 1.0 mM PMS. The pseudo second-order kinetic model and Langmuir model were used to described the uptake and equilibrium process in DCF/PA@Hem700 system. Scavenging and electron-spin-resonance studies showed a non-radical singlet oxygen species ( 1 O2) dominates over • OH and SO4 •− radicals in the system. The role of electron transfer was also verified via chronoamperometry and electrochemical-impedance spectroscopy techniques. Furthermore, the PA@Hem700/PMS remained highly active towards DCF degradation even in the presence of common anions, humic acid, and various water matrices. The developed catalyst exhibited a TOC removal of 65.8 %. The study also established the potential of PA@Hem700/PMS to degrade other organic pollutants (e.g., tetracycline (TC),
dc.identifier.otherhttps://doi.org/10.1016/j.chemosphere.2025.144388
dc.identifier.urihttps://ugspace.ug.edu.gh/handle/123456789/43379
dc.language.isoen
dc.publisherChemosphere
dc.subjectDiclofenac
dc.subjectPeroxymonosulfate
dc.subjectPolymer
dc.titleNovel hemin-derived Fe/N–C magnetic catalyst for enhanced peroxymonosulfate activation and diclofenac degradation
dc.typeArticle

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