Several studies have reported that the hydrothermal carbonization method (HTC) of agricultural waste is able to produce a solid residue with interesting properties for the adsorption of organic pollutants from contaminated water. This work represents a facile method to prepare hydrochar (HC) from pomegranate peels’ waste using the microwave-assisted hydrothermal carbonization method (MHTC) at 200 °C for 1 h with a mass ratio of peel to water = 1:10. Activated hydrochar (AHC) was prepared by in situ chemical activation using ZnCl₂ and MHTC. Several techniques have been applied to characterize the prepared samples as FTIR, XRD, TEM and SEM. The samples were investigated for their possible use as adsorbents of methylene blue (MB) dye. The results confirm the formation of amorphous hydrochar with a porous structure. The pH of zero point charge (pH_zpc) is 4.3 and 4.6 for HC and AHC samples, respectively. The maximum adsorption capacity of HC and AHC samples are 194.9 and 12.55 mg/g (i.e., mg of adsorbate/g of adsorbent), respectively.

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.

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.

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 (R_MO, R_MB), MO and MB adsorption capacities (q_MO, q_MB), and hydrodynamic diameter of ZnO particles (D_h). 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. R_MB was found to depend only on the synthesis temperature while R_MO depends on temperature, pH, and reaction time. pHzc was found to be affected by the synthesis pH only while D_h depends on the synthesis pH and precursor concentration.

A novel henna-green/microwave-assisted hydrothermal method was applied to synthesize cobalt-manganese spinel ferrite nanocomposites. This eco-friendly approach, utilizing henna extract as a capping agent, combined with a microwave-assisted hydrothermal technique, offers advantages such as environmental sustainability, time, and energy efficiency. Examined parameters included pH (10 ± 1), temperatures (175 ± 25 °C), durations (15, 30 ± 15 min), and forty milliliters of henna extract prepared with varying henna quantities (five, ten, or fifteen grams per hundred milliliters of water). Post-optimization, various substituents like nickel and chromium were explored. Samples were calcined at 500 °C, 700 °C, and 900 °C, and analyzed using Fourier Transform Infrared Spectroscopy (FTIR), X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and magnetic property assessments. XRD revealed a cubic face-centered spinel ferrite and hematite structure. SEM and TEM showed diverse morphologies (rod-like, flower-like, polygonal) influenced by synthesis conditions and substituents. XPS confirmed Co²⁺, Mn²⁺, Ni²⁺, Fe³⁺, and Cr³⁺ presence in the spinel lattice. The nanocomposites exhibited ferromagnetic behavior with saturation magnetization (M_s) values from 23.53 to 55.15 emu/g. Chromium substitution showed the best antimicrobial activity against Escherichia coli, Staphylococcus aureus, and Candida albicans. This study highlights the potential of the henna-green/microwave-assisted hydrothermal method for controlled synthesis of substituted cobalt spinel ferrite nanocomposites with tunable properties for various applications.

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.