In this study Ag nanoparticles (AgNPs), ZnO nanoparticles (ZnONPs), and Ag/ZnO nanocomposites were greenly synthesized and loaded on activated carbon via three different routes: simple impregnation, successive precipitation, and co-precipitation. Neem leaf extract was used as a reducing and stabilizing agent. The morphological and structural properties of the synthesized nanocomposites have been examined using different analytical techniques such as XRD, SEM, FTIR, and UV. The antibacterial and catalytic activity of the synthesized nanocomposites were examined and compared. The results showed that AgNPs loaded on activated carbon (Ag/AC) has the best catalytic activity compared to the other nanocomposites, which is attributed to the good dispersal of AgNPs on the surface of activated carbon. Furthermore, AgNPs showed the best antibacterial effect on eight out of 16 tested pathogens. Results also showed that the order of precipitation is an important factor, as both antibacterial activities and photodegradation activities were higher for ZnO/Ag/AC than Ag/ZnO/AC. Furthermore, the co-precipitation method was shown to be better than the successive precipitation method for 4-nitrophenol photodegradation and 14 out of the 16 antibacterial tests performed.

Iron nanoparticles (FeNP) were synthesized using Acacia nilotica seedless pods extract. The synthesized FeNP were characterized by Fourier transform infrared (FTIR), UV/Vis spectroscopy, dynamic light scattering (DLS), electron microscopy (TEM), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), and X-ray diffraction (XRD). The XRD pattern confirmed the synthesis of crystalline phase of α-Fe₂O₃. EDS spectroscopy showed the presence of elemental iron and oxygen, indicating that the nanoparticles are essentially present in oxide form. UV absorption in the range of 450–550 nm confirmed the formation of FeNP. DLS indicated an average FeNP particle size of 229 nm. The synthesized FeNP was tested for adsorption and oxidation degradation of methyl orange (MO) under different conditions and found to be effective in both degradation and adsorption processes. Furthermore, the synthesized FeNP has the potential to terminate the pathogenicity of several human opportunistic pathogens; belongs to gram-negative and gram-positive bacteria and one species of Candida as well.

Water pollution with dye effluents from different industries is a broadly established environmental and health problem that needs serious attention. In this study, making use of Acacia nilotica seed extract, greenly synthesized MnO₂ nanoparticles were loaded on the surface of biochar derived from palm waste (MnO₂/PF), with specific surface areas of 70.97 m²/g. Batch experiments were adopted, aiming to evaluate the performance of palm fronds, biochar, and the MnO₂/PF adsorbents in methyl orange (MO) removal from an aqueous solution. The feedstock and synthesized biochars were comprehensively characterized using XRD, SEM-EDX, FTIR, and BET surface area techniques. Moreover, the influences of the modification of palm fronds, initial dye concentrations, pH, and adsorbent dosage on MO uptake were examined. The results demonstrated that MnO₂/PF biochar nanocomposite led to an increase in the removal efficiency by 6 and 1.5 times more than those of palm fronds and biochar, respectively. In addition, it was found that the second-order kinetic model presented the kinetic adsorption very well. This paper demonstrates that the depositing of greenly synthesized MnO₂ nanoparticles on the date palm waste biochar forms a novel adsorbent (MnO₂/PF) for the removal of MO from aqueous solutions. Furthermore, this adsorbent was easy to synthesize under moderate conditions without the need for chemical capping agents, and would thus be cost-effective and eco-friendly.

P-nitrophenol (pNP) is a highly toxic organic compound and is considered carcinogenic and mutagenic. It is a very stable compound with high resistance to chemical or biological degradation. As a result, the elimination of this pollutant has been very challenging for many researchers. Catalytic reduction is one of the most promising techniques, if a suitable catalyst is developed. Thus, this work aims to prepare an eco-friendly catalyst via a simple and low-cost route and apply it for the conversion of the toxic p-nitrophenol (pNP) into a non-toxic p-aminophenol (pAP) that is widely used in industry. Manganese oxide was prepared in an environmentally friendly manner with the aid of Lawsonia inermis (henna) extract as a stabilizing and capping agent and loaded on the surface of 13X molecular sieve zeolite. The UV-Vis spectrum, EDS, and XRD patterns confirmed the formation of the pure MnO₂ loaded on the zeolite crystalline network. The TGA analysis showed that the samples prepared by loading MnO₂ on zeolite (Mn2Z, Mn3Z, and Mn4Z) lost more mass than pure MnO₂ (Mn) or zeolite (Z), which is mainly moisture adsorbed on the surface. This indicates a better dispersion of MnO₂ on the surface of zeolite compared to pure MnO₂, and thus a higher number of active adsorption sites. SEM images and EDS confirmed the dispersion of the MnO₂ on the surface of the zeolite. Results showed a very fast reduction rate, following the order Mn2Z > Mn3Z > Mn4Z > Mn > Z. With sample Mn2Z, 96% reduction of pNP was achieved in 9 min and 100% in 30 min. For Mn3Z, Mn4Z, and Mn, 98% reduction was achieved in 20 min and 100% in 30 min. Zeolite was the slowest, with only a 40% reduction in 30 min. Increasing the amount of zeolite in the synthesis mixture resulted in lower reduction efficiency. The kinetic study indicated that the reduction of p-nitrophenol on the surface of the prepared nanocomposite follows the pseudo-first-order model. The results show that the proposed nanocomposite is very effective and very promising to be commercially applied in water treatment, due to its low cost, simple synthesis procedure, and reusability.