FeOx magnetization enhancing E. coli inactivation by orders of magnitude on Ag-TiO 2 nanotubes under sunlight

Citation data:

Applied Catalysis B: Environmental, ISSN: 0926-3373, Vol: 202, Page: 438-445

Publication Year:
2017
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DOI:
10.1016/j.apcatb.2016.09.064
Author(s):
Marco Mangayayam; John Kiwi; Stefanos Giannakis; Cesar Pulgarin; Ivica Zivkovic; Arnaud Magrez; Sami Rtimi
Publisher(s):
Elsevier BV
Tags:
Chemical Engineering; Environmental Science
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article description
Drastic bacterial enhancement was observed when the Ag(3%)-TiO 2 nanotubes were modified with FeOx (3%) magnetic oxide. On bare TiO 2 - nanotubes a reduction of 0.2log 10 CFU was observed within one hour under simulated low intensity solar light. Under similar conditions, a bacterial reduction of 2.5log 10 CFU was observed on Ag(3%)TiO 2 increasing to 6.0log 10 CFU on Ag(3%)-TiO 2 -FeOx(3%) magnetic nanotubes. The bacterial inactivation kinetics is strongly influenced by the addition of FeOx. The fast inactivation induced by the composite catalyst seems to involve an increase in the interfacial charge transfer (IFCT) compared to a 2-oxide composite photocatalyst. Stable recycling of the photocatalyst was observed leading to bacterial oxidation. The unambiguous identification of the radical intermediates: OH-radicals, O-singlet and the valence holes vb(h + ) on the Ag-TiO 2 -FeOx interface showed that the valence band holes vb(h + ) were the main oxidative intermediates leading to bacterial inactivation. Nanotubes size, crystallinity and bulk composition of magnetite 1% (θ = 51.0°), anatase 5% (θ = 8.9°), goethite 37.3% (θ = 9.0°), silver 1% (θ = 2.7°) was obtained by the Rietveld refinement for the Ag(3%)-TiO 2 -FeOx(3%) nanotubes. The redox chemistry during bacterial inactivation was determined by X-ray photoelectron spectroscopy (XPS).