Photocatalytic degradation of reactive black 5 from synthetic and real wastewater under visible light with TiO2 coated PET photocatalysts
The photocatalytic removal of Reactive Black 5 (RB5) was investigated using a titanium dioxide-polyethylene terephthalate (TiO<sub>2</sub>-PET) catalyst under visible (VIS) light. The sol-gel method was employed for the fabrication of the TiO<sub>2</sub>-coated PET catalyst, which was then characterized using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and elemental mapping (MAP) analysis. This study examined the reaction kinetics using the one-factor-at-a-time (OFAT) approach and evaluates the effects of various parameters, including pH (3-11), catalyst dosage (0.1-1 g L<sup>- 1</sup>), contact time (15-120 min), RB5 concentration (10-50 mg L<sup>- 1</sup>), hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) content (2-100 mM), purging gases, organic compound types, and ionic strength, on the photocatalytic removal of RB5. Under optimal conditions (pH= 3, [RB5]<sub>°</sub>= 20 mg L<sup>- 1</sup>, nanocatalyst dosage= 0.5 g L<sup>- 1</sup>), 99.99% of the dye was removed after 120 min. Increasing the RB5 concentration (10-50 mg L<sup>- 1</sup>) resulted in a decrease in the observed reaction rate constant (k<sub>obs</sub>) from 0.052 to 0.0017 min<sup>- 1</sup>, while the calculated electrical energy per order (EEO) increased from 11.08 to 338.82 kWh m<sup>- 3</sup>. Furthermore, the total operating cost of the light emitting diode (LED)/TiO<sub>2</sub>-PET process (3 USD kg<sup>- 1</sup>) was lower than that of other photocatalytic processes, including LED/TiO<sub>2</sub> (4.73 USD kg<sup>- 1</sup>), LED/PET (40 USD kg<sup>- 1</sup>), and LED (63.16 USD kg<sup>- 1</sup>). The removal of RB5 was negatively affected by the presence of H<sub>2</sub>O<sub>2</sub>, O<sub>2</sub> and N<sub>2</sub> gases, organic compounds, and ionic species. Radical quenching experiments confirmed that hydroxyl radicals (<sup>·</sup>OH) were the dominant reactive species responsible for RB5 degradation. The RB5 removal efficiency using the LED/TiO<sub>2</sub>-PET method (99.99%) was significantly higher than that of the LED/TiO<sub>2</sub> method (63.42%). Desorption experiments demonstrated excellent catalyst stability, maintaining catalytic activity for up to five sequential cycles. GC-MS analysis identified several intermediate degradation products, including 1,2-benzenedicarboxylic acid, benzoic acid (2-amino-, methyl ester), benzene [(methylsulfonyl) methyl], phenol, 4-naphthalenedione, acetic acid, and propionic acid. Moreover, the removal efficiency in drinking water samples was approximately 63.31%, whereas for real textile wastewater samples, it reached 96.66%. Toxicity tests conducted on the final treated solutions confirmed no toxicity toward Daphnia magna, demonstrating the effectiveness of the LED/TiO<sub>2</sub>-PET method in degrading both RB5 dye and its toxic by-products.
Authors
- Mehdi Shirzad‐Siboni (ORCID: https://orcid.org/0000-0002-2085-2548)
- Seyed Hossein Mousavi (ORCID: https://orcid.org/0000-0003-3454-0243)
- Mohsen Mohammadi-Galangash
Institutions
- University of Guilan (IR)
Publication Details
- Journal
- Scientific Reports
- Published
- 2025-04-24
- DOI
- https://doi.org/10.1038/s41598-025-95091-x
- Citations
- 17
- Primary Topic
- TiO2 Photocatalysis and Solar Cells
- Type
- article
- Field-Weighted Citation Impact
- 6.18
Funders
- University of Guilan
- Guilan University of Medical Sciences