Environmental pollutants such as organic dyes are major focal areas of the current era. For this reason, excellent photocatalytic substances are needed time to degrade such water bodies and get pollution‐free water. In this study, Sulphur doped zinc oxide nanoparticles were fabricated utilizing a solution‐free technique, while graphene oxide was synthesized using a modified hummer‘s method. Sulphur‐doped zinc oxide nanoparticles were mixed with graphene oxide in five distinct weight percentages to achieve the S‐ZnO/GO (SZO) composites. The 8 % SZO NC demonstrated superior photocatalytic efficiency, degrading 100 % of MB in 110 minutes under sunlight irradiation. The synthesized composites were characterized by the techniques viz. TEM, SEM, EDXS, FTIR, XPS, and UV spectrophotometry to determine their chemical nature and morphological features. Methylene blue was used as a reference pollutant to evaluate the photocatalytic activity of the composites. According to the radical scavenger‘s test observations, •OH and •O2– were the primary species responsible for MB decomposition. Furthermore, the nanocomposites were found highly stable, with a continuously high degree of dye degradation throughout six catalytic cycles. As a result, the SZO nanocomposites have the prospective to be an extremely effective and versatile photocatalyst for the photodegradation of organic wastes.

The poly(o-anisidine)/BaSO4 nanocomposites were prepared by oxidative polymerization of o-anisidine monomer with BaSO4 filler for the potential antibacterial properties of the composite materials. To achieve the optimal and tunable properties of the nanocomposites, the ratio of BaSO4 filler was changed at the rates of 1%, 3%, 5%, 7%, and 10% with respect to matrix. Different analytical techniques, i.e., FTIR and UV-visible spectroscopy, were employed for functional identification and optical absorption of the poly(o-anisidine)/BaSO4 nanocomposites. The FTIR data revealed the significant interaction between POA and BaSO4, as well as the good absorption behavior of the UV-visible spectra. The conducting properties were controllable by varying the load percentage of the BaSO4 filler. Furthermore, different bacterial strains, i.e., Pseudomonas aeruginosa (Gram-negative) and Staphylococcus aureus (Gram-positive), were used to evaluate the antibacterial activity of the POA/BaSO4 nanocomposites. The largest zones of inhibition 0.8 and 0.9 mm were reached using 7% and 10% for Staphylococcus aureus and Pseudomonas aeruginosa, respectively.

The clinical significance of benzimidazole-containing drugs has increased in the current study, making them more effective scaffolds. These moieties have attracted strong research interest due to their diverse biological features. To examine their various biological significances, several research synthetic methodologies have recently been established for the synthesis of benzimidazole analogs. The present study aimed to efficiently and quickly synthesize a new series of benzimidazole analogs. Numerous spectroscopic techniques, including 1H-NMR, 13C-NMR, and HREI-MS, were used to confirm the synthesized compounds. To explore the inhibitory activity of the analogs against α-amylase and α-glucosidase, all derivatives (1–17) were assessed for their biological potential. Compared to the reference drug acarbose (IC50 = 8.24 ± 0.08 µM), almost all the derivatives showed promising activity. Among the tested series, analog 2 (IC50 = 1.10 ± 0.10 & 2.10 ± 0.10 µM, respectively) displayed better inhibitory activity. Following a thorough examination of the various substitution effects on the inhibitory capacity of α-amylase and α-glucosidase, the structure-activity relationship (SAR) was determined. We looked at the potential mechanism of how active substances interact with the catalytic cavity of the targeted enzymes in response to the experimental results of the anti-glucosidase and anti-amylase. Molecular docking provided us with information on the interactions that the active substances had with the various amino acid residues of the targeted enzymes for this purpose.

We constructed a catechol detection biosensor that is enzyme-free and extremely selective using a glassy carbon electrode (GCE) modified with a copper-polypyrrole (Cu-PPy) composite.

In the modern era, problems like eutrophication caused by increased nutrients such as ammonia and phosphorous in freshwater bodies have become the cause of freshwater ecosystem deterioration. To save freshwater by reducing eutrophication, new cost-effective strategies and methods are urgently needed. In this study, titanium oxide nanoparticles dispersed on zeolite were chemically synthesized for the simultaneous removal of phosphate and ammonium ions from aqueous solutions. SEM and XRD analysis were used to characterize the synthesized TiO2/zeolite nanocomposites, which revealed that the synthesized material was more stable and dispersed than zeolite. The nanocomposites removed 38.8% NH4+ and 98.1% PO43− from an initial concentration of both ions of 20 mg 100 ml−1. The removal of both ions was investigated under various conditions including different concentrations of nanocomposites, initial concentration of the solution, temperature, time, and pH. The maximum adsorption of nanocomposites for PO43- was 38.63 mg g−1 at optimal conditions, and 3.75 mg g−1 for NH4+. Kinematics studies showed that both the ions were adsorbed by a pseudo-second-order model. Ion chemisorption occurred as a result of ligand exchange or electrostatic adsorption between ions and nanocomposites. Overall, it was determined that this strategy is a viable and efficient method for simultaneously removing both ions (anionic phosphate and cationic ammonium) from eutrophic waters.