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This work aimed to synthesize an effective material having greater potential to reduce water pollution caused by industrial waste and exhibit efficient antibacterial potential. The transition metals (Manganese-Mn, Zinc-Zn) and post transition metal (Tin-Sn) reacted with TeO2 in a stoichiometric ratio by adopting a solid-state reaction. The crystallite size of the synthesized compounds MnTeO3 (D1), ZnTeO3 (D2), and SnTe3O8 (D3) was measured by the Debye-Scherrer formula by extracting data from the FWHM. D1 and D2 exhibit the orthorhombic structure whereas D3 has a simple cubic structure and crystalline size was measured by FWHM i.e., 221 nm, 458 nm, and 153 nm. Catalytic degradation efficiency for the removal of MB dye was found to be in the range of 66%-73%. Additionally, these substances have strong antimicrobial action alongside both bacteria and fungi, such as Escherichia coli, Staphylococcus aureus with maximal zone inhibitions of 35.0 mm and 12.5 mm for each kind of bacterium. The highest antifungal activity of Mn integrated was estimated to be 37.2 mm versus Aspergillus niger and 15.1 mm alongside Coccidioides. According to the findings, the manufactured material has effective photocatalytic and antimicrobial activities.

Metal-organic frameworks have been used as antibacterial agents because of their effective antibacterial properties. In this research, nanocomposites of copper (II)- benzene-1,4-dicarboxylic acid metal–organic framework with iron oxide [Cu-MOF@Fe3O4] were prepared via a simple hydrothermal route. X-ray analysis reveals the crystallinity of the structure while FTIR analysis confirms the existence of Cu-based MOFs functional group. Cu-MOF@Fe3O4 scans using Scanning Electron Microscopy (SEM) reveal irregular clusters of cubic particles fused with Fe3O4 nanoparticles. Energy Dispersive X-ray (EDX) spectrum of Cu-MOF@Fe3O4 provides the evidence of elemental composition by showing the peaks of iron, oxygen, copper and carbon. Using the minimum inhibitory concentration (MIC) and zone of inhibition assays, the antimicrobial activity of the Cu-MOF and Cu-MOF@Fe3O4 against E. coli and B. subtilis were evaluated. The antibacterial results have shown that the Cu-MOF@Fe3O4 has higher antibacterial performance against E. coli as compared with B. subtilis as compared to Cu-MOF, Fe3O4 and ligands only. On the other hand, the Cu-MOF@Fe3O4 composites exhibit excellent antifungal potential when compared to the ligand, commercial nanoparticles, Cu(NO3)2·3H2O, iron oxide, Cu-MOF. The exploration of antibacterial mechanism revealed that the Cu-MOF@Fe3O4 composite favors slow release of metal ions and prolonged biocidal effect.

This research work includes the fabrication of iron oxide nanoparticles (Fe2O3 NPs) by green construction approach using Wisteria sinensis leaves extract. Due to its eco-friendly approach, the synthesis of iron oxide NPs (Fe2O3 NPs) using various plant sources, such as plant parts, and microbial cells have gained a lot of attention in recent years. Cost-effectiveness and ease of availability make Wisteria sinensis leaves extract a potential candidate for the construction of iron oxide NPs. The various key features like biocompatibility, non-toxicity capping, and stabilizing agents present in biological sources are advantageous for usage in a variety of applications. The phytoconstituents present in the leaf extract of Wisteria sinensis serve as reducing and stabilizing agents. The biologically fabricated (Fe2O3 NPs) were analyzed using FT-IR, XRD, UV–vis spectroscopy, and SEM. In the present work, the antioxidant and photocatalytic dye degradation efficiency of Fe2O3 NPs has been studied. The dye degradation efficiency of methylene blue dye was found to be 87% at 180 min upon exposure to sunlight. The capacity of Fe2O3 NPs to scavenge 2,2-diphenyl-1-picrylhydrazyl hydrate free radicals (DPPH) was examined using a UV–Vis spectrophotometer. The study compared the radical scavenging activity (RSA) of Fe2O3 nanoparticles (NPs) with that of the standard antioxidant ascorbic acid. The results demonstrated that Fe2O3 NPs have a greater ability to scavenge radicals than ascorbic acid. The half-maximal inhibitory concentration (IC50) of Fe2O3 NPs was observed to range from 0.12 to 0.17. Furthermore, Fe2O3 NPs displayed the highest antifungal activity, with an inhibition zone of 26.8 mm against F. oxysporum. These findings suggest that the biologically synthesized Fe2O3 NPs possess potent antimicrobial and dye degradation properties.

Besides natural sunlight and expensive artificial lights, economical indoor white light can play a significant role in activating a catalyst for photocatalytic removal of organic toxins from contaminated water. In the current effort, CeO2 has been modified with Ni, Cu, and Fe through doping methodology to study the removal of 2-chlorophenol (2-CP) in the illumination of 70 W indoor LED white light. The absence of additional diffractions due to the dopants and few changes such as reduction in peaks’ height, minor peak shift at 2θ (28.525°) and peaks’ broadening in XRD patterns of modified CeO2 verifies the successful doping of CeO2. The solid-state absorption spectra revealed higher absorbance of Cu-doped CeO2 whereas a lower absorption response was observed for Ni-doped CeO2. An interesting observation regarding the lowering of indirect bandgap energy of Fe-doped CeO2 (∼2.7 eV) and an increase in Ni-doped CeO2 (∼3.0 eV) in comparison to pristine CeO2 (∼2.9 eV) was noticed. The process of e-– h+ recombination in the synthesized photocatalysts was also investigated through photoluminescence spectroscopy. The photocatalytic studies revealed the greater photocatalytic activity of Fe-doped CeO2 with a higher rate (∼3.9 × 10−3 min-1) among all other materials. Moreover, kinetic studies also revealed the validation of the Langmuir-Hinshelwood kinetic model (R2 = 0.9839) while removing 2-CP in the exposure of indoor light with a Fe-doped CeO2 photocatalyst. The XPS analysis revealed the existence of Fe3+, Cu2+ and Ni2+ core levels in doped CeO2. Using the agar well-diffusion method, the antifungal activity was assessed against the fungus M. fructicola and F. oxysporum. Compared to CeO2, Ni-doped CeO2, and Cu-doped CeO2 nanoparticles, the Fe-doped CeO2 nanoparticles have outstanding antifungal properties.

Bacteria develop resistance against antimicrobial drugs, and new remediations are constantly being introduced in the market. Silver and its compounds have strong resistance against different bacteria. The vegetable waste extract-synthesized silver nanoparticles (VWE-AgNPs) have distinct properties and potential applications because of their unique size and morphology. The fundamental purpose of this study was to develop an environment-friendly method for the synthesis of VWE-AgNPs to avoid the use of hazardous chemicals that cause danger to the environment as well as recycling vegetable waste material. The VWE-AgNPs were synthesized by mixing 1 mM AgNO3 solution and VWE at room temperature. The VWE-AgNPs were characterized by UV-visible spectroscopy, FTIR, SEM, and EDX. The synthesized particles showed good antibacterial properties against poultry bacteria Salmonella gallinarum and Salmonella enteritidis (growth reduction of 31 mm and 18 mm at 80 mg/mL AgNPs, respectively). The results demonstrated that VWE-AgNPs inhibited the growth of tested bacterial strains. The fabricated VWE-AgNPs also had the potential to act as a green photocatalyst for degradation of 87.7% of methylene blue (MB) and 90.76% of methyl orange (MO) nearly at 3.25 h and 1 h sunlight exposure time, respectively. The highest antifungal activity, which was determined to be 36.5 mm and 31.8 mm against Alternata sp. and C. albican, was discovered to be in VWE-AgNPs.