Creating a sustainable and effective approach to handling organic contaminants from industrial waste is an ongoing problem. In the present study, ZnO nanoparticles (ZnO NPs) were synthesized under a controlled ultrasound cavitation technique using the extract of Passiflora foetida fruit peels, which act as a reducing (i.e., reduction of metal salt) and stabilizing agent. The formation of monodispersed and hexagonal morphology (average size approximately 58 nm with BET surface area 30.83m2/g). The synthesized ZnO NPs were characterized by a various technique such as UV–visible spectroscopy, X-ray diffraction (XRD), Fourier-transform infrared (FTIR), Scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), Transmission electron microscopy (TEM), Thermogravimetric analysis (TGA) and Dynamic light scattering (DLS). Further, the XRD pattern confirmed the hexagonal wurtzite structure of synthesized ZnONPs. The ZnO NPs exhibit excellent degradation efficiency towards organic pollutant dyes, i.e., Methylene blue (MB) (93.25% removal) and Rhodamine B (91.06% removal) in 70 min, under natural sunlight with apparent rate constant 0.0337 min−1 (R2 = 0.9749) and 0.0347 min−1 (R2 = 0.9026) respectively.Zeta potential study shows the presence of a negative charge on the surface of ZnO NPs. The use of green synthesized ZnO NPs is a good choice for wastewater treatment, given their high reusability and photocatalytic efficiency, along with adaptability to green synthesis.

The present study deals with the synthesis of ZnO and Ag‐ZnO nanoparticles using Excoecaria agallocha leaf extract under a controlled ultrasound cavitation technique. The characterization of the as‐synthesized ZnO and Ag‐ZnO nanoparticles (different molar concentration of Ag) were subjected to Fourier transform infrared spectroscopy (FTIR), X‐ray diffraction analysis (XRD), UV‐Visible Diffuse reflectance spectroscopy (UV‐Vis DRS), Thermogravimetric analysis (TGA), N2 adsorption‐desorption isotherm (BET), scanning electron microscopy(SEM) and transmission electron microscopy (TEM). The photocatalytic performance of ZnO and Ag‐ZnO nanoparticles as catalysts were studied for hazardous organic dyes such as methylene blue (MB) and rhodamine‐B (Rh−B) under solar light irradiation. The degradation study follows pseudo‐first‐order kinetics. The effective degradation of MB was found to be 56.44 % (ZnO nanoparticles) and 98.44 % Ag‐ZnO nanoparticles, respectively at 100 min at the molar ratio (0.25 : 1). Whereas, Rh−B shows 27.50 % (ZnO nanoparticles) and 98.83 % at the same molar ratio of Ag‐ZnO nanoparticles at 80 min. Among the as‐synthesized nanoparticles, Ag‐ZnO at molar ratio 0.25 : 1 shows effective photocatalytic activity. Besides these as‐synthesized nanoparticles exhibited good antimicrobial activity with an increase in Ag nanoparticles decorated into ZnO. A similar trend was observed in antioxidant and anti‐inflammatory activity.

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Objective:The present study is deals with the green synthesis of silver (AgNPs), iron oxide (α-Fe2O3NPs) and core-shell (Ag-α-Fe2O3CNPs) nanoparticles using the aqueous extract ofAlstonia scholariswithout any catalyst, template or surfactant or any intermediate under ultrasound cavitation technique. The purpose was to facilitate the high level of dispersion with increase in rate of reaction. Further AgNPs and α-Fe2O3NPs were used to synthesis Ag-Fe2O3CNPs in aqueous extract ofAlstonia scholarisunder controlled ultrasound cavitation technique.Methods:The size of AgNPs and Ag-Fe2O3CNPs can be tuned by optimizing various reaction parameters. UV-visible, X-ray diffraction spectroscopy (XRD), Transmission electron microscopy (TEM), Field emission scanning electron microscope (FE-SEM) and Fourier transform infra-red spectroscopy has been used for the characterization of silver and core shell Ag@Fe2O3nanoparticles. TEM images clearly show the formation of core shell nanoparticles with spherical morphology.Result:Fourier transform infra-red spectroscopy analysis revealed that carbohydrate, polyphenols, and protein molecules were involved in the synthesis and capping of silver, iron oxide and Ag@Fe2O3CNPs.

The focus of the present research is on the biodegradation of low density polyethylene (LDPE):polylactic acid (PLA) and LDPE:PLA:organo modified montmorillonite (OMMT) polymer nanocomposites. PLA was synthesized using the polycondensation method. The surface modification of nanomaterials is affected by various factors such as modifying agent, dispersion medium, and the dispersion of nanoparticles. Ultrasound cavitation technique improves the better dispersion of MMT in reaction mixture and enhances the interaction rate of a modifying agent with clay layered structure. A mixture of aminopropyltriethoxysilane and octadecyl amine was used for the surface modification of MMT. Polymer nanocomposite was prepared using the melt mixing method and used further for the biodegradation study. The mesophilic bacterium isolated from the dumping yard, identified by the 16rRNA technique, was capable of biodegradation of LDPE:PLA and LDPE:PLA:OMMT polymer nanocomposites. Isolated bacterial AP1 is 96.05% identical to the current MCCC1A02146 strain of Bacillus albus. After 50 days of incubation, the polymer nanocomposite sheet was characterized using Fourier transform infrared, X‐ray powder diffractometer, UV–Visible spectroscopy, Field Emission Scanning Electron Microscope (FESEM), etc. Further, LDPE:PLA30% (17.5%) and LDPE:PLA30%:OMMT4.5phr (19.20%), shows maximum percentage degradation. It has been observed that the addition of OMMT contributes to an enhancement in the polymer nanocomposite degradation because it has a large d‐spacing gap that is (21 Å) that enables the water to penetrate in the polymer matrix and increases the growth of bacteria within the polymer matrix. The highest change in biomass and change in extracellular protein content was found to be (39.11 mg/L and OD 0.38) LDPE:PLA30%:OMMT4.5phr composites. In addition, the mechanical properties decrease effectively after the incubation period, for LDPE:PLA 30% and LDPE:PLA30%:OMMT4.5phr.