Electron-rich/poor reaction sites enable ultrafast confining Fenton-like processes in facet-engineered BiOI membranes for water purification
Heterogeneous Fenton-reaction accomplishes the destruction of pollutants via the oxidation of hydroxyl radicals during water purification. Herein, two facet-engineered (control of different exposed crystal planes) BiOI nanocatalysts (BI-001 and BI-110) as the dual-reaction-center catalysts were load...
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Veröffentlicht in: | Applied catalysis. B, Environmental Environmental, 2022-05, Vol.304, p.120970, Article 120970 |
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Sprache: | eng |
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Zusammenfassung: | Heterogeneous Fenton-reaction accomplishes the destruction of pollutants via the oxidation of hydroxyl radicals during water purification. Herein, two facet-engineered (control of different exposed crystal planes) BiOI nanocatalysts (BI-001 and BI-110) as the dual-reaction-center catalysts were loaded on the polyvinylidene fluoride membrane, remarkably accelerating the occurrence of Fenton-reaction and leading to the enhanced degradation of the pollutants in complex water matrices. The degradation efficiency of paracetamol by BI-110 membrane (~96.0%) was significantly higher than that of BI-001 membrane (~26.1%) in catalytic activity. The electron paramagnetic resonance tests and theoretical calculations proved that BI-110 possesses more oxygen vacancies, which acts as the electron-rich sites to trigger the Fenton-reaction. Correspondingly, the pollutants were adsorbed on the electron-poor Bi3+ sites and donate electrons during the degradation process. This study provides a candidate strategy to break the limitations of Fenton reaction advanced oxidation processes for water purification using the tunable facet-engineered BiOI membrane.
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•Facet-engineered BiOI membranes are first proposed for water purification.•Enhanced AOP kinetics is due to the spatial nanoconfinement effect.•Fenton-like processes are realized on the electron-rich/poor reaction sites.•BI-110 membrane/H2O2 showed excellent performance in complex water matrix. |
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ISSN: | 0926-3373 1873-3883 |
DOI: | 10.1016/j.apcatb.2021.120970 |