In this work, the CuCo2O4 nanowires (CuCo2O4 NWs) were grown on carbon cloth electrode (CCE) and then coated with polypyrrole (pPy) layer (CuCo2O4 NWs-pPy@CCE). The morphology and structure characterization of as-prepared CuCo2O4 NWs-pPy@CCE were carried out using Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDX), field-emission scanning electron microscope (FESEM), thermogravimetric analysis (TGA), and transmission electron microscope (TEM). The CuCo2O4 NWs-pPy@CCE was applied directly as an electrocatalyst toward nonenzymatic glucose oxidation. Due to the advantages of this 3D structure, it offer high availability to the analyte/electrolyte, abundant electrochemical-active sites, and high stability and conductivity. As a glucose sensor, the CuCo2O4 NWs-pPy@CCE shows wide linear range (0.01 to 21.3 mM), excellent sensitivity (4.41 μA μM−1 cm−2), good selectivity, low detection limit (0.2 μM), and rapid response time (<1 s) toward glucose detection. Furthermore, the designed sensor shows a great ability in detection of glucose in biological real samples.

In this study, zinc acetate (as a precursor) and activated carbon carboxylic acid derivative were used to create the nanostructure of zinc oxide (ZnO) as a matrix. The carboxylic acid derivative was produced by modifying the oxidized activated carbon with nitric acid (AC-COOH). The modified activated carbon's surface was then impregnated with zinc to load it. By using BET, XRD, and SEM to characterize the ZnO nanostructure, it was discovered that it was composed of nanoparticles with a surface area capacity of 17.78 m2 g-1 and a size range of 21–31 nm. The photocatalytic hydrolysis of the dye methyl orange in an aqueous medium served as a test case for the catalyst's performance. The primary variables were considered, including pH, catalyst dose, stirring effect, and starting dye concentration. Measurements of activity below UV light revealed satisfactory outcomes for photocatalytic hydrolysis of the methyl orange (MO). In addition, the efficiency of the methyl orange (MO) photolysis catalyst prepared with unmodified activated carbon was also evaluated. The outcomes proved that zinc oxide (ZnO), made using a derivative carboxylic acid of activated carbon molecules by a matrix, had more good photocatalytic action than zinc oxide (ZnO) made by the real activated carbon matrix.

Humic acid (HA) has a complex chemical composition and the ability to chelate, adsorb, and exchange ions with organic and inorganic contaminants in bodies of water, which worsens water quality and poses a threat to human health and the environment. In this research, an Ultraviolet-activated sodium perborate (UV/SPB) symbiotic method (UV/SPB) was developed to eliminate humic acid in water. The major synergistic and degradative processes of the humic acid were investigated, as well as the impact of the starting humic acid concentration, sodium perborate dose, and primary pH value on the humic acid elimination. Results indicate that just 0.5 % and 1.5 % of humic acid were eliminated mostly by sole UV and sole sodium perborate (SPB) methods, respectively. More effectively than other methods, UV/SPB removed humic acid with an efficiency of 88.83%. An experiment using free radicals to mask them revealed that the primary catalyst for humic acid removal is the hydroxyl radical generated by sodium perborate activation. The excitation-emission matrix spectroscopy, Ultraviolet-visible absorption (UV-Vis) spectrum, absorbance ratio values, specific Ultraviolet-visible absorbance values (SUVA), and UV/SPB method performance findings demonstrated the UV/SPB method's capability to degrade and mineralize humic acid.

This study focused on the adsorption behavior of the cationic CrystalViolet (CV) dye from aqueous solutions using a Co+2‒hectoritecomposite as an adsorbent surface. The initial and equilibrium CV dyeconcentrations were determined using a UV-Vis spectrophotometer. Theresults were discussed and presented for the impacts of pH, primary CVdye concentration, composite dosage, and temperature. The optimumconditions were found for eliminating Crys tal Violet dye from theaqueous solution at a pH 4, ideal temperature 293 K, and 0.5 g L-1of composite dose. The pseudo-second-order kinetic, intraparticlediffusion analyzed the tes ts’ data and film diffusion models. Eachmodel’s defining features have been identified, and these models werein good agreement and in charge of regulating the adsorption reaction.The adsorption operation was also thermodynamically examined todetermine thermodynamic variables such as Gibbs free energy (ΔGo),entropy (ΔSo), activation energy (Ea), and enthalpy (ΔHo). The negativevalue of Gibbs free energy (ΔGo) and enthalpy (ΔHo) indicated thatthe adsorption process was a spontaneous and exothermic reaction.While the activation energy (Ea) data which fell within the normalrange for physisorption, was showed at  22.434 kJ mol-1. The physical adsorption occurs between  CV dye and adsorbent .

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