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Conventional methods are inefficient to treat water contaminated with persistent organic contaminants. To decontaminate bacteria and 2,4,5‐trichlorophenol (TCP) contaminated water, a heterogeneous photocatalysis‐based advanced oxidation process was applied in this study. A Li‐doped ternary Zn0.5Ni0.5Fe2O4 (ZNF) photocatalyst (Li/ZNF) was synthesized via a facile co‐precipitation technique and characterized. The Li/ZNF has a sufficient specific surface area (69.8 m2.g−1), and an appropriate bandgap of 2.89 eV. Under optimal conditions, 10 mg of Li/ZNF photocatalyst degraded 80 % of 50 mg L−1 TCP in 6 h at pH 3 in the presence of 4 mM H2O2. After use, the Li/ZNF photocatalyst was magnetically separated and reused numerous times, with an efficiency of 66 % after the fifth reuse cycle. In the antibacterial time‐kill assay, 15 and 25 mg of Li/ZNF inhibited 1×107 CFU.mL−1 of S. Aureus and E. coli bacteria after 60 min of UV exposure, respectively. [ABSTRACT FROM AUTHOR]

Conventional methods are inefficient to treat water contaminated with persistent organic contaminants. To decontaminate bacteria and 2,4,5‐trichlorophenol (TCP) contaminated water, a heterogeneous photocatalysis‐based advanced oxidation process was applied in this study. A Li‐doped ternary Zn0.5Ni0.5Fe2O4 (ZNF) photocatalyst (Li/ZNF) was synthesized via a facile co‐precipitation technique and characterized. The Li/ZNF has a sufficient specific surface area (69.8 m2.g−1), and an appropriate bandgap of 2.89 eV. Under optimal conditions, 10 mg of Li/ZNF photocatalyst degraded 80 % of 50 mg L−1 TCP in 6 h at pH 3 in the presence of 4 mM H2O2. After use, the Li/ZNF photocatalyst was magnetically separated and reused numerous times, with an efficiency of 66 % after the fifth reuse cycle. In the antibacterial time‐kill assay, 15 and 25 mg of Li/ZNF inhibited 1×107 CFU.mL−1 of S. Aureus and E. coli bacteria after 60 min of UV exposure, respectively. [ABSTRACT FROM AUTHOR]

With the growing concern of biofilm-associated infections and drug-resistant bacteria, an increasing interest in developing novel antibacterial agents is an urgent priority. Metal oxide-based polymeric materials are able to distinguish mammalian cells from bacterial cells and thus provide long-term antibacterial growth inhibition. Herein, we report the preparation of MgO, NiO and chitosan-coated metal oxide (CS–MO) nanocomposites via a simple in situ chemistry approach. Fourier transform infrared spectroscopy, X-ray diffraction patterns and X-ray photoelectron spectra results proved the formation of CS–MgO and CS–NiO nanocomposites. Also, the particle sizes were observed to be 18.3 and 25.5 nm for CS–NiO and CS–MgO, respectively. All the samples exhibited antibacterial activities against the Escherichia coli and Staphylococcus aureus strains; however, more effective against S. aureus compared to E. coli. Noticeably, 5 μg/mL CS–NiO comparatively exhibited highest bactericidal capability where E. coli and S. aureus viabilities were reduced to 25–47% after 12 h incubation. After treatment with 15 μg/mL of CS–NiO, ∼98% of S. aureus and 92.3% of E. coli cells were inhibited. [ABSTRACT FROM AUTHOR]

• Through green synthesis, a new bimetallic licu-ferrite nanospinel was developed. • LiCu-F has a mean particle size of 59.8 nm and a crystallite size of 45.9 nm. • LiCu-F exhibited sufficient antimicrobial activity and can be used in biological applications. • Within 60 min, LiCu-F exhibited bacteriostatic and bactericidal effects on S. aureus and E. coli. • LiCu-F had lower binding energy (−29.16 kcal/mol) for E. coli than for S. aureus (−38.89 kcal/mol). An aqueous carob leaf extract was employed in the current study as a biogenic agent (reducing and capping agents) for the synthesis of novel bimetallic lithium and copper-based nanospinel ferrites (LiCu-F) with antibacterial activity. LiCu-F has a considerable number of surface -OH groups, a BET-specific surface area of 72.5 m2/g, a mean particle size of 59.8 nm, and a crystallinity index of 78.9%, according to the results of the physicochemical characterisation of the ferrite. Within the first 60 min, LiCu-F showed bacteriostatic and bactericidal effects on S. aureus and E. coli based on the time-kill assay. 0.4 mg of LiCu-F demonstrated 67.9% bacteriostatic effects on E. coli while exhibiting 100% inactivation of S. aureus strains, demonstrating that the gram-positive bacteria are more susceptible to LiCu-F. The computational molecular docking analysis demonstrated that LiCu-F has a higher binding affinity for S. aureus (-38.89 kcal/mol) than E. coli (-29.16 kcal/mol), which is consistent with the experimental findings. With an LD 50 of 1000 mg per kg of body weight based on a computational prediction tool, LiCu-F is cytotoxic to bacteria and can cause DNA damage and cell death in bacterial strains. [Display omitted] [ABSTRACT FROM AUTHOR]