TY - JOUR
T1 - Development of TiO2 Films by Sol–Gel/Sedimentation for the Inactivation of Multidrug-Resistant Escherichia coli and Salmonella Typhimurium in Greywater
AU - Rincón-Barón, Luz Adriana
AU - Forero-Carvajal, María Paula
AU - Ramírez-Alemán, Laura Gabriela
AU - Mejía-Gómez, Augusto Enrique
AU - Salcedo-Reyes, Juan Carlos
AU - Carrascal-Camacho, Ana Karina
AU - Velez, Camilo
AU - Pedroza-Rodríguez, Aura Marina
N1 - Publisher Copyright:
© 2025 by the authors.
PY - 2025/11/30
Y1 - 2025/11/30
N2 - Crystalline TiO2 films were synthesized on hydrophilic glass substrates by Peroxo sol–gel and sedimentation (S1–S4) and compared with conventional sol–gel protocols (S5–S10). The films were deposited on soda-lime glass and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and UV–Vis absorption. Photocatalytic activity was evaluated through the inactivation of multidrug-resistant Escherichia coli and Salmonella Typhimurium, and the removal of chemical oxygen demand (COD) from greywater under UV irradiation. The obtained films exhibited anatase crystallinity, crystallite sizes of ~60 nm, and grain sizes between 1.5 and 3.0 µm. S1 films showed a bandgap of 3.26 eV (380 nm). Under UV exposure, S1 reduced E. coli and S. Typhimurium by 4.78 and 3.00 Log10 units, respectively, at pH 5.0 after 30 min, while COD decreased to 380 mg L−1 compared to 433 mg L−1 with UV photolysis alone. Increasing TiO2 loading and extending irradiation to 120 min further enhanced bacterial inactivation (93 and 78% for E. coli and S. Typhimurium), COD (33%), NH4+ (90%), and H2S (89%) oxidation, outperforming UV-light controls. These results indicate that S1 films exhibited superior crystallinity, photocatalytic performance, and bacterial inactivation compared to other protocols, although complete mineralization was not achieved.
AB - Crystalline TiO2 films were synthesized on hydrophilic glass substrates by Peroxo sol–gel and sedimentation (S1–S4) and compared with conventional sol–gel protocols (S5–S10). The films were deposited on soda-lime glass and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and UV–Vis absorption. Photocatalytic activity was evaluated through the inactivation of multidrug-resistant Escherichia coli and Salmonella Typhimurium, and the removal of chemical oxygen demand (COD) from greywater under UV irradiation. The obtained films exhibited anatase crystallinity, crystallite sizes of ~60 nm, and grain sizes between 1.5 and 3.0 µm. S1 films showed a bandgap of 3.26 eV (380 nm). Under UV exposure, S1 reduced E. coli and S. Typhimurium by 4.78 and 3.00 Log10 units, respectively, at pH 5.0 after 30 min, while COD decreased to 380 mg L−1 compared to 433 mg L−1 with UV photolysis alone. Increasing TiO2 loading and extending irradiation to 120 min further enhanced bacterial inactivation (93 and 78% for E. coli and S. Typhimurium), COD (33%), NH4+ (90%), and H2S (89%) oxidation, outperforming UV-light controls. These results indicate that S1 films exhibited superior crystallinity, photocatalytic performance, and bacterial inactivation compared to other protocols, although complete mineralization was not achieved.
KW - Escherichia coli
KW - Salmonella Typhimurium
KW - TiO photocatalysis
KW - conventional sol–gel
KW - greywater
KW - peroxo-solz–gel
KW - sedimentation
KW - TiO2 photocatalysis
UR - https://www.scopus.com/pages/publications/105025786587
UR - https://www.mendeley.com/catalogue/9557ec4e-8d2c-3d4d-a65d-7df682688f68/
U2 - 10.3390/catal15121115
DO - 10.3390/catal15121115
M3 - Article
AN - SCOPUS:105025786587
SN - 2073-4344
VL - 15
JO - Catalysts
JF - Catalysts
IS - 12
M1 - 1115
ER -