Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6477343 | Journal of Environmental Chemical Engineering | 2017 | 9 Pages |
â¢Cu-decorated TiO2 supported on Raschig rings were used for MB degradation.â¢Effect of the Cu-amount decorating RR@TiO2 on the photocatalytic performance.â¢Leaching of TiO2 and/or Cu showed to be way below sanitary regulations.â¢RR@TiO2-Cu led to MB-degradation with acceptable kinetics up to 5 reuse cycles.
The methylene blue (MB) discoloration on innovative photocatalysts made up of Raschig-rings coated by pre-formed TiO2 nanoparticles decorated with CuOx (RR@TiO2-Cu) is presented. The MB-discoloration was drastically accelerated by the subsequent addition of 0.004% Cu. This Cu-content being â¼3000 times below the TiO2 present in the RR@TiO2 samples led to MB-discoloration in shorter times. The Cu-ions released from the RR@TiO2-Cu 0.004% were determined â¤1ppb by inductively coupled plasma mass-spectrometry (ICP-MS). Cu-percentages >0.018% decreased the MB-discoloration kinetics due to the Cu acting as recombination sites for the photogenerated charges. The total organic carbon (TOC) reduction concomitant with the MB-discoloration is reported as well as the effect of the initial MB-concentration and pH on the discoloration kinetics. The Cu-addition shifted significantly the TiO2 absorption into the visible region even when added in sub-microgram quantities (0.004%) to RR@TiO2 as detected by diffuse reflectance spectroscopy (DRS). The Cu level added to RR@TiO2 was too low to be detected by X-ray diffraction (XRD). The roughness of the RR@TiO2-Cu (0.018%-0.081% Cu) presented Rg-values between 11.8 nm and 23.9 nm. The RR@TiO2Cu presented agglomerate sizes of â¼200 nm for TiO2 and for the Cu aggregates sizes of â¼20 nm. The MB discoloration kinetics and reuse of the RR@TiO2-Cu suggest the potential as a supported catalyst in environmental cleaning process. A reaction mechanism is suggested taking into consideration the role of the Cu1+/2+ intra-gap states involving redox catalysis as detected by X-ray photoelectron-spectroscopy (XPS).
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