Bismuth-based nanostructured photocatalysts for the remediation of antibiotics and organic dyes.

A serious threat to human health and the environment worldwide, in addition to the global energy crisis, is the increasing water pollution caused by micropollutants such as antibiotics and persistent organic dyes. Nanostructured semiconductors in advanced oxidation processes using photocatalysis have recently attracted a lot of interest as a promising green and sustainable wastewater treatment method for a cleaner environment. Due to their narrow bandgaps, distinctive layered structures, plasmonic, piezoelectric and ferroelectric properties, and desirable physicochemical features, bismuth-based nanostructure photocatalysts have emerged as one of the most prominent study topics compared to the commonly used semiconductors (TiO2 and ZnO). In this review, the most recent developments in the use of photocatalysts based on bismuth (e.g., BiFeO3, Bi2MoO6, BiVO4, Bi2WO6, Bi2S3) to remove dyes and antibiotics from wastewater are thoroughly covered. The creation of Z-schemes, Schottky junctions, and heterojunctions, as well as morphological modifications, doping, and other processes are highlighted regarding the fabrication of bismuth-based photocatalysts with improved photocatalytic capabilities. A discussion of general photocatalytic mechanisms is included, along with potential antibiotic and dye degradation pathways in wastewater. Finally, areas that require additional study and attention regarding the usage of photocatalysts based on bismuth for removing pharmaceuticals and textile dyes from wastewater, particularly for real-world applications, are addressed.

Dual function Mg-doped binary metal ferrite: Photocatalytic degradation of trichlorophenol, bactericidal activity and molecular docking analysis.

A new Mg-doped Zn0.5Ni0.5Fe2O4 (Mg-FZN) photocatalyst was synthesised using a simple co-precipitation-doping technique to develop a dual-function material with the ability to degrade hazardous and refractory pollutants and inactivate bacterial strains. The characterization results revealed that Mg-FZN is an n-type semiconductor with a conduction band of -0.413 eV, an average pore width of 2.32 nm, and a crystal size of 31.45 nm. The photocatalytic activity of Mg-FZN was assessed based on the degradation of 2,4,5-trichlorophenol and achieved 83.8% degradation efficiency under optimised conditions. The radical quenching results revealed that h+ significantly contributed to the photodegradation process while •OH, and •O2- played key roles. Additionally, within 60 min, 25 mg of Mg-FZN had bactericidal effects on the bacteria E. coli and S. aureus in both the presence and absence of UV light. Mg-FZN showed H-bonding, electrostatic, and metal-contact interactions with the amino acid residues of the bacterial protein with high binding scores (-4.711 kcal/mol and -5.872 kcal/mol), according to molecular docking.

Efficient removal of antibiotic in single and binary mixture of nickel by electrocoagulation process: Hydrogen generation and cost analysis.

In discharged water, antibiotics and heavy metals frequently coexist, forming stable and recalcitrant complexes. Environmental concerns about how to efficiently treat this type of pollution are growing. Using Fe and Al electrodes, electrocoagulation (EC) was applied to remove tetracycline (TC) as a single pollutant as well as TC-nickel ions in a binary mixture from water. The effects of critical variables and the TC-Ni molar ratio (1:1, 1:2, and 2:1) were studied. The Fe electrode achieved 99.3% TC removal after 60 min in a single pollutant system containing 15 mgL-1 of TC, while the Al electrode achieved 99.8% removal in 20 min at optimal conditions. The EC process demonstrated excellent electrodegradation efficiency towards TC-Ni complexes. When the TC to Ni2+ ratio was 1:1 and 1:2, respectively, TC elimination was 100% in 10 min and 99.6% in 20 min. We noted that a sufficient amount of Ni2+ could increase TC decomposition by electrocatalysis. The amount of hydrogen gas produced after treatment of a 0.2 L TC solution alone is 22.2-13.99 mol m-3, whereas it was 27.2-40.8 mol m-3 in the TC-Ni binary mixture, which can generate more than 35% of the electrical energy needed to power the EC system. To evaluate the generated sludge, FTIR analysis was performed.

Fabrication of a novel nontoxic trichlorophenol-epichlorohydrin-based compound with high antimicrobial activity and thermal stability.

The aim of this study was to modify a discontinued, toxic antiseptic agent 2,4,5-trichlorophenol (TCP) by reacting it with epichlorohydrin (ECH) to obtain a nontoxic novel compound with similar antimicrobial effectiveness. A novel compound named {[1,3-bis(2,4,5-trichlorophenoxy) propan-2-yl] oxy}-3-(2,4,5-trichlorophenoxy) hexan-2-ol (TPTH) was synthesized from this reaction. Chemical and physical structures of the product were characterized by FTIR, MS, Uv-vis, NMR, SEM and TEM. The thermal stability of TPTH was evaluated by conducting thermogravimetric analysis. Biological interactions of the compound were investigated by performing antimicrobial activity and cytotoxicity assays. The compound displayed a good antimicrobial activity where minimum inhibitor concentrations were found to be 0.02, 0.08, and 0.15 µg mL-1 against Staphylococcus aureus (S. aureus), Methicillin-resistant Staphylococcus aureus (MRSA) and Escherichia coli (E. coli) respectively. Additionally, well diffusion assay demonstrated that, the zone of inhibitions for S. aureus, MRSA and E. coli were 24 mm, 22 mm and 18 mm, respectively. Cytotoxicity assay results revealed that TPTH is nontoxic against cells at effective anti-microbial concentrations. TPTH shows thermal stability up to 220 °C. Results here demonstrate the successful conversion of toxic TCP to a nontoxic form; TPTH with a good anti-microbial activity and thermal stability.