The Effect of Composition on the Properties and Application of CuO-NiO Nanocomposites Synthesized Using a Saponin-Green/Microwave-Assisted Hydrothermal Method.

In this study, we explored the formation of CuO nanoparticles, NiO nanoflakes, and CuO-NiO nanocomposites using saponin extract and a microwave-assisted hydrothermal method. Five green synthetic samples were prepared using aqueous saponin extract and a microwave-assisted hydrothermal procedure at 200 °C for 30 min. The samples were pristine copper oxide (100C), 75% copper oxide-25% nickel oxide (75C25N), 50% copper oxide-50% nickel oxide (50C50N), 25% copper oxide-75% nickel oxide (25C75N), and pristine nickel oxide (100N). The samples were characterized using FT-IR, XRD, XPS, SEM, and TEM. The XRD results showed that copper oxide and nickel oxide formed monoclinic and cubic phases, respectively. The morphology of the samples was useful and consisted of copper oxide nanoparticles and nickel oxide nanoflakes. XPS confirmed the +2 oxidation state of both the copper and nickel ions. Moreover, the optical bandgaps of copper oxide and nickel oxide were determined to be in the range of 1.29-1.6 eV and 3.36-3.63 eV, respectively, and the magnetic property studies showed that the synthesized samples exhibited ferromagnetic and superparamagnetic properties. In addition, the catalytic activity was tested against para-nitrophenol, demonstrating that the catalyst efficiency gradually improved in the presence of CuO. The highest rate constants were obtained for the 100C and 75C25N samples, with catalytic efficiencies of 98.7% and 78.2%, respectively, after 45 min.

Effect of Synthesis Conditions on CuO-NiO Nanocomposites Synthesized via Saponin-Green/Microwave Assisted-Hydrothermal Method.

This work presents the synthesis of CuO-NiO nanocomposites under different synthesis conditions. Nanocomposites were synthesized by merging a green synthesis process with a microwave-assisted hydrothermal method. The synthesis conditions were as follows: concentration of the metal precursors (0.05, 0.1, and 0.2 M), pH (9, 10, and 11), synthesis temperature (150 °C, 200 °C, and 250 °C), microwave treatment time (15, 30, and 45 min), and extract concentration (20 and 40 mL of 1 g saponin/10 mL water, and 30 mL of 2 g saponin/10 mL water). The phases and crystallite sizes of the calcined nanocomposites were characterized using XRD and band gap via UV-Vis spectroscopy, and their morphologies were investigated using SEM and TEM. The XRD results confirmed the formation of a face-centered cubic phase for nickel oxide, while copper oxide has a monoclinic phase. The calculated crystallite size was in the range of 29-39 nm. The direct band gaps of the samples prepared in this work were in the range of 2.39-3.17 eV.

Methylene Blue Dye Adsorption on Iron Oxide-Hydrochar Composite Synthesized via a Facile Microwave-Assisted Hydrothermal Carbonization of Pomegranate Peels' Waste.

The toxicity of dyes has a long-lasting negative impact on aquatic life. Adsorption is an inexpensive, simple, and straightforward technique for eliminating pollutants. One of the challenges facing adsorption is that it is hard to collect the adsorbents after the adsorption. Adding a magnetic property to the adsorbents makes it easier to collect the adsorbents. The current work reports the synthesis of an iron oxide-hydrochar composite (FHC) and an iron oxide-activated hydrochar composite (FAC) through the microwave-assisted hydrothermal carbonization (MHC) technique, which is known as a timesaving and energy-efficient method. The synthesized composites were characterized using various techniques, such as FT-IR, XRD, SEM, TEM, and N2 isotherm. The prepared composites were applied in the adsorption of cationic methylene blue dye (MB). The composites were formed of crystalline iron oxide and amorphous hydrochar, with a porous structure for the hydrochar and a rod-like structure for the iron oxide. The pH of the point of zero charge (pHpzc) of the iron oxide-hydrochar composite and the iron oxide-activated hydrochar composite were 5.3 and 5.6, respectively. Approximately 556 mg and 50 mg of MB dye was adsorbed on the surface of 1 g of the FHC and FAC, respectively, according to the maximum adsorption capacity calculated using the Langmuir model.

Acacia nilotica Pods' Extract Assisted-Hydrothermal Synthesis and Characterization of ZnO-CuO Nanocomposites.

This work represents a novel combination between Acacia nilotica pods' extract and the hydrothermal method to prepare nanoparticles of pure zinc oxide and pure copper oxide and nanocomposites of both oxides in different ratios. Five samples were prepared with different ratios of zinc oxide and copper oxide; 100% ZnO (ZC0), 75% ZnO: 25% CuO (ZC25), 50% ZnO: 50% CuO (ZC50), 25% ZnO: 75% CuO (ZC75), and 100% CuO (ZC100). Several techniques have been applied to characterize the prepared powders as FTIR, XRD, SEM, and TEM. The XRD results confirm the formation of the hexagonal wurtzite phase of zinc oxide and the monoclinic tenorite phase of copper oxide. The microscopy results show the formation of a heterostructure of nanocomposites with an average particle size of 13-27 nm.

Experimental Design Modeling of the Effect of Hexagonal Wurtzite-ZnO Synthesis Conditions on Its Characteristics and Performance as a Cationic and Anionic Adsorbent.

Surface composite design was used to study the effect of the ZnO synthesis conditions on its adsorption of methyl orange (MO) and methylene blue (MB). The ZnO was prepared via hydrothermal treatment under different conditions including temperature (T), precursor concentration (C), pH, and reaction time (t). Models were built using four Design expert-11 software-based responses: the point of zero charge (pHzc), MO and MB removal efficiencies (RMO, RMB), MO and MB adsorption capacities (qMO, qMB), and hydrodynamic diameter of ZnO particles (Dh). ZnO was characterized by X-ray diffraction (XRD), Fourier-transform infrared (FTIR) spectroscopy, UV/VIS spectroscopy, thermal gravimetric analysis (TGA), and dynamic light scattering (DLS). The formation of ZnO was confirmed by the XRD, UV, and FTIR spectra. Results showed a very high efficiency for most of the samples for adsorption of MB, and more than 90% removal efficiency was achieved by 8 samples among 33 samples. For MO, more than 90% removal efficiency was achieved by 2 samples among 33 samples. Overall, 26 of 31 samples showed higher MB adsorption capacity than that of MO. RMB was found to depend only on the synthesis temperature while RMO depends on temperature, pH, and reaction time. pHzc was found to be affected by the synthesis pH only while Dh depends on the synthesis pH and precursor concentration.

Nanocrystalline iron oxide synthesised within Hierarchical Porous Silica prepared by nanoemulsion templating.

PIC (Phase Inversion Composition) O-W nanoemulsions was used as a template for the synthesis of Hierarchical Porous Silica (HPS), and the oil phase of the nanoemulsion was used as a nanoreactor for the preparation of magnetic gamma-Fe(2)O(3) nanoparticles, confined within the silica matrix.

Stability and tunability of O/W nanoemulsions prepared by phase inversion composition.

We report on an analysis of the parameters that control both the stability and tunability of O/W nanoemulsions prepared by the phase inversion composition (PIC). These nanoemulsions are prepared with Tween 80 and Span 80, two nonionic surfactants, that can be mixed to adjust the hydrophilic lipophilic balance (HLB). We used a process mixture design method, which combines mixture and process design with phase diagrams, to describe the cross-link between parameters like composition, temperature of preparation, and HLB. Nanoemulsions, stable for several days, are obtained by this method, and they remain unchanged even at high concentration. We have identified the different critical distances of interactions that control the degree of freedom in the motion of the oil droplets. The diameter of these oil droplets could be adjusted between 50 and 300 nm. Different parameters, among them the temperature of preparation, the surfactant over oil ratio (S/O), and the HLB, allow control the final size of the nanoemulsions. As these parameters can exhibit opposite effects on the oil droplet size, the process mixture design method allowed us to illustrate these cross-interactions.