Evaluation of photoassisted treatments for norfloxacin removal in water using mesoporous Fe 2 O 3 -TiO 2 materials
We report the synthesis of mesoporous TiO and mesoporous Fe O -TiO catalysts by using a structure-directing-surfactant method, their characterization and their employment as photocatalysts for norfloxacin degradation in aqueous solution. The main findings show that in the presence of both O and H O...
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Veröffentlicht in: | Journal of environmental management 2019-03, Vol.238, p.243 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | We report the synthesis of mesoporous TiO
and mesoporous Fe
O
-TiO
catalysts by using a structure-directing-surfactant method, their characterization and their employment as photocatalysts for norfloxacin degradation in aqueous solution. The main findings show that in the presence of both O
and H
O
, Fe-containing mesoporous titania (Fe
O
-TiO
), with iron percentages between 1 and 3 wt%, exhibited norfloxacin degradation rates more than 60% greater than otherwise identical mesoporous titania without iron. Furthermore, the activity of the mesoporous composite catalysts also exceeds that of titania when illuminated with 405 nm light-emitting diodes. Iron loading improved the photocatalytic activity for norfloxacin degradation with values of apparent reaction rate constants of 0.037 min
and 0.076 min
with 1 and 3 surface wt.% of iron, respectively. An optimum of activity was found with the 3 wt% Fe
O
-TiO
catalyst. Under these conditions, 10 mg/L of norfloxacin is reacted essentially to completion and 90% of total organic carbon conversion was obtained within 120 min of reaction. This higher organic carbon conversion degree was reached due to the photo-oxidation of short-chain organic acids. The high activity of the as-synthesized mesoporous composites is attributed to the additional iron phase which led to the different reactions for H
O
decomposition, but also due to the improvement in light absorbance. Finally, the activity of the most active catalyst was found to be stable over multiple sequential runs, which was related to a negligible amount of iron leaching ( |
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ISSN: | 1095-8630 |