Degradation of doxycycline antibiotics using lanthanum copper oxide microspheres under simulated sunlight

In this study, lanthanum copper oxide was synthesized under hydrothermal techniques and characterized for doxycycline degradation. The catalyst exhibited enhanced photocatalytic doxycycline degradation under visible light owing to its compatible bandgap energy (1.7 eV). The XRD data revealed high crystallinity of the material with no noticeable impurities. Three-dimensional microspheres of varying sizes (average diameter of 2.52 μm) were observed from SEM. EDX confirms the successful synthesis of La2CuO4. The effect of DC concentration, catalyst dosage, and initial pH on the degradation rate of DC was studied methodically. Interestingly, about 85% of doxycycline (10 mg/L) was degraded within 120 min of light-emitting diode irradiation at pH 10. Oxygen vacancies and surface defects were determined through photoluminescence spectra. The recyclability experiments suggested that the catalyst is capable of degrading DC for three consecutive runs. Radical trapping trials suggested that holes (h+), superoxide radicals (●O2−), and hydroxyl radicals (●OH) are involved in the photodegradation of DC. Herein, the novel approach of La2CuO4 synthesis and the efficient visible-light harvesting capability of as-prepared catalyst reveal the potentiality for DC degradation thereby opening a new horizon of research employing La2CuO4 used for various environmental applications.</p

Visible light responsive AgBiS₂ nanomaterials for photocatalytic applications in removal of antimicrobial compounds and bacterial pathogens: Possible electrochemical pathways

Potential synthesis of ternary chalcogenide nanocomposite to showcase a practical electronic pathway to improve photocatalytic efficiency was carried out. In the present study, AgBiS2 nanorod-shaped with remarkably visible-light absorption was prepared using solvothermal techniques. This material was employed in photocatalytic degradation of amoxicillin (AMX) under visible light irradiation. The results indicated more than 90% degradation of AMX under 60 min having a corresponding bandgap of ∼2.19 eV. In the verge of understanding the photogenerated separation of electron-hole pair, VB and CB potentials were calculated to be 2.06 eV and − 0.76 eV, proposing a possible pathway for the degradation study. The photogenerated intermediates were identified using LC-MS analysis and the mineralization was followed using TOC analysis. A scavenging experiment showed a potential reactive oxygen species involved in the oxidation of organics that proved effective in three consecutive trials.In addition, antibacterial and antibiofilm activity showcased fair efficiency of the material, especially the presence of Ag+ in AgBiS2 improves antimicrobial activity. In case of antibiofim activity, 4 × 107 CFU/mL were seen to be most effective for the biomass formation of the biofilms.</p