Facile fabrication of Ag decorated MnFeO3 catalyst: Comparative analysis of visible light driven antibiotic reduction and antibacterial performance.

Photocatalysis is an effective method with the potential to eliminate pharmaceutical compounds from water sources. Manganese ferrite (MnFeO3), a type of multiferroic perovskite catalyst, has attracted significant attention due to its small band gap, however its application was limited due to its high recombination rate and low quantum efficiency. It was therefore aimed to improve the properties of MnFeO3 by doping silver (Ag)-particles. In this study, Ag-MnFeO3 photocatalysts with different Ag content (1-3 mmol%) were synthesized by performing a facile hydrothermal method. The as-prepared samples were characterized using x-ray diffraction (XRD), scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM/EDS), transmission electron microscopy (TEM), x-ray photoelectron spectroscopy (XPS), ultraviolet-visible spectroscopy (DRS), photoluminescence spectroscopy (PL), electrochemical impedance spectroscopy (EIS) and Brunauer-Emmett-Teller (BET) method, showing successful addition of Ag-particles with the MnFeO3 structure. Then, the as-synthesized materials were investigated as: (i) photocatalysts for degradation tetracycline (TC) antibiotic and (ii) antibacterial agents for bacteria. The Ag-MnFeO3 catalyst demonstrated superior catalytic performance (95.7%), which was 1.6 times higher than that of pristine MnFeO3 (59.7%). The positive effect was ascribed to oxygen vacancies, enhanced light absorption ability, and lower recombination rate. The Ag-MnFeO3 catalyst also showed satisfactory removal performances in real water matrices. Furthermore, radical trapping tests depicted that the superoxide radicals played a dominant role in the photodegradation system. In addition, Box-Behnken design (BBD) was performed to determine the optimum conditions, which were determined as catalyst dosage of 0.45 g/L, initial TC concentration of 5.10 mg/L, and initial solution pH value of 3.69. In terms of antibacterial tests, the incorporation of Ag into the MnFeO3 structure greatly increased the antimicrobial resistance against bacteria. Our findings disclose that the incorporation of Ag into the MnFeO3 structure can be regarded as a feasible and promising approach to improve both photocatalytic degradation and antibacterial performances.

Deposition of CaFe2O4 and LaFeO3 perovskites on polyurethane filter: A new photocatalytic support for flowthrough degradation of tetracycline antibiotic.

The immobilization of powder catalysts on substrates has been the subject of increasing interest in the field of photocatalysis. For the first time, highly efficient LaFeO3 and CaFe2O4 perovskites were hydrothermally deposited on polyurethane filters (LFO/PU, CFO/PU). Furthermore, the photo-Fenton catalytic decomposition of tetracycline antibiotic by the new catalyst filters was explored under visible light irradiation. The structural, optical, and morphological characteristics of the photo-active filters were investigated using Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM-EDS), X-ray diffraction (XRD), UV-visible diffusion spectra (UV-vis DRS), X-Ray fluorescence (XRF), and thermogravimetric/dynamic thermal analyses (TG-DTG). The decomposition studies were conducted in both batch and micro-flow reactor systems. The effects of solution pH, reactive species, and water type on the reaction mechanism were examined. It was found that the photo-Fenton degradation of tetracycline improved when the perovskite proportions on the filter were increased; the removal rates reached 94% and 80% forLFO/PU and CFO/PU, respectively. The high degradation performance obtained in lake (∼71%) and seawater (∼76%) demonstrated the great potential of photo-active catalyst filters, and their excellent stability was confirmed by reusability tests. In the continuous flow system, the photocatalytic filters kept the degradation rate stable at 83% and 44% after 7 h of examination forLFO/PU and CFO/PU, respectively. These results suggest that the as-prepared catalytic filters may be suitable for industrial photocatalytic applications.

Determination of total antioxidant capacity of humic acids using CUPRAC, Folin-Ciocalteu, noble metal nanoparticle- and solid-liquid extraction-based methods.

Total antioxidant capacity (TAC) of humic acid (HA) samples was determined using CUPRAC (CUPric Reducing Antioxidant Capacity), FC (Folin-Ciocalteu), QUENCHER-CUPRAC, QUENCHER-FC, Ag-NP (Silver nanoparticle)‒ and Au-NP (Gold nanoparticle)‒based methods. Conventional FC and modified FC (MFC) methods were applied to solid samples. Because of decreased solubility of Folin-Ciocalteu's phenol reagent in organic solvents, solvent effect on TAC measurement was investigated using QUENCHER-CUPRAC assay by using ethanol:distilled water and dimethyl sulfoxide:distilled water with varying ratios. To see the combined effect of solubilization (leaching) and TAC measurement of humic acids simultaneously, QUENCHER experiments were performed at 25°C and 50°C; QUENCHER-CUPRAC and QUENCHER-FC methods agreed well and had similar precision in F-statistics. Although the Gibbs free energy change (ΔG°) of the oxidation of HA dihydroxy phenols with the test reagents were negative, the ΔG° was positive only for the reaction of CUPRAC reagent with isolated monohydric phenols, showing CUPRAC selectivity toward polyphenolic antioxidants. This is the first work on the antioxidant capacity measurement of HA having a sparingly soluble matrix where enhanced solubilization of bound phenolics is achieved with coupled oxidation by TAC reagents.