Use of nonedible seed pods ofMoringa oleifera(Moringa) tree and nutshells ofSclerocarya birrea(Morula) tree for removal of selected metal ions (lead, cadmium, copper, manganese, iron, zinc, and magnesium) from wastewater and borehole water samples was investigated. Removal parameters such as contact time, pH, temperature, particle size, sorbent dose, and initial metal concentration were optimized. Determination of residual metal ions after employing sorbent was done using flame atomic absorption spectroscopy (FAAS). Using 200 ng synthetic metal ion mixture in 50 mL of water sample, the optimized parameters for Moringa seed pods were 60 min contact time, 1.0 g of sorbent dose, pH 8, 100 μm sorbent particle size, and extraction temp 35°C. While using Morula nutshells, the optimized conditions were 120 min contact time, 2.0 g sorbent dose, pH 8, 100 μm sorbent particle size, and extraction temp of 35°C. The removal efficiency of acid treated sorbents was compared to that of untreated sorbents and it was found to be higher for acid treated sorbents. These nonedible plant parts for Morula and Moringa plants are proposed as a cheap, simple, and an effective alternative for purification of water contaminated with heavy metals.

The growing worldwide environmental and water pollution challenges require the use of renewable biomass-based materials to purify water systems. The remarkable qualities of nanocellulose (NC) and its eco-friendliness make it a desirable material for this purpose. Hence, many investigations have been conducted on the optimization of NC-based materials for water purification. This review presents the first examination of the progress made in creating emerging NC composites using molecularly imprinted polymers (MIPs), metal organic frameworks (MOFs), and aluminosilicates. MIPs, MOFs, and aluminosilicates endow NC composites with stability, multifunctionality, and extended reusability. The applications of these composites to wastewater treatment, such as the removal of toxic heavy metals, dyes, pharmaceuticals, and microorganisms are discussed. Finally, the economic viability, challenges, and future perspectives of these emerging NC composites and their applications are discussed. The research gaps demonstrated in this review will enable the exploration of new areas of study on functionalised NC composites, leading to enhanced industrial applications. Moreover, the utilisation of NC composites with suitably modified components results in multifunctional adsorbents that have great potential for effectively eliminating many contaminants simultaneously.

The ever-increasing population growth and economic developments have heightened demand for energy. This has resulted in depletion and ever-rising prices of petroleum diesel, thus increasing environmental degradation. These complications have motivated this study for the search of an alternative eco-friendly and renewable source of energy such as biodiesel. Biodiesel has been found to be a potential alternative fuel for diesel. Biodiesel was produced by transesterification reaction of Schinziophyton rautanenii (mongongo) nut oil in the presence of a base heterogeneous catalyst: CaO derived from eggshell ash and synthesised CaO-nanoparticles (CaO-NPs). The catalysts were calcined at a temperature of 800°C for 3 h and characterized by scanning electron microscope-energy dispersive X-ray (SEM-EDX) where both catalysts showed agglomerated particles and high elemental composition of Ca and O. Powder X-ray diffraction (XRD) showed that CaO was present in both catalysts, and the average crystalline size obtained was 42 and 50 nm for CaO-NPs and eggshell ash, respectively. Fourier transmission infrared (FTIR) spectrometer showed absorption bands of CaO in both catalysts which were at 875 and 713.46 cm⁻¹ for CaO-NPs and eggshell ash, respectively. The analysis of mongongo nut oil (MNO) and mongongo methyl esters (MMEs) was done according to the European biodiesel specification (EN 1421) and American Society for Testing and Materials (ASTM D675). Statistically, there was no significant difference between CaO-NPs and eggshell in terms of optimum yield ( ) using a sample t-test. However, in terms of catalyst loading, the eggshell was a better catalyst as it required a low catalyst load to obtain an optimum yield of 83% at 6 wt.% compared to CaO-NPs with an optimum yield of 85% at 12 wt.%. The reactions were all performed at constant reaction conditions of 9 : 1 methanol to oil ratio, 3 h reaction time, and 65°C reaction temperature.

A new hexadentate 2-picolyl-polypyridyl-based ligand (4, 4'-(butane-1, 4-diylbis(oxy))bis(N, N-bis(pyridin-2-ylmethyl)aniline)) (2BUT) (1) and its corresponding Ru(II/III) complexes were synthesized and characterized, followed by assessment of their possible bioactive properties towards drug-resistant and non-drug-resistant bacteria. Spectroscopic characterization of the ligand was done using proton NMR, FTIR, and ESI-MS, which showed that the ligand was successfully synthesized. The Ru(II/III) complexes were characterized by FTIR, UV/Vis, elemental analysis, proton NMR, ESI-MS, and magnetic susceptibility studies. The analysis of ESI-MS data of the complexes showed that they were successfully synthesized. Empirical formulae derived from elemental analysis of the complexes also indicated successful synthesis and relative purity of the complexes. The important functional groups of the ligands could be observed after complexation using FTIR. Magnetic susceptibility data and electronic spectra indicated that both complexes adopt a low spin configuration. The disc diffusion assay was used to test the compounds for antibiotic activity on two bacteria species and their drug-resistant counterparts. The compounds displayed antibiotic activity towards the two non-drug-resistant bacteria. As for the drug-resistant organisms, only [Ru₂(2BUT)(DMF)₂(DPA)₂](BH₄)₄3 and 2, 2-dipyridylamine inhibited the growth of MRSA. Gel electrophoresis DNA cleavage studies showed that the ligands had no DNA cleaving properties while all the complexes denatured the bacterial DNA. Therefore, the complexes may have DNA nuclease activity towards the bacterial genomic material.

The management of HIV in the human body has been a major research area in the quest to either find the cure or the preventative scientific measure. The quest to manage the virus has been successful using some organic molecules which target one or more of the stages of the replication cycle of HIV rendering it inhibited to continue infecting other host cells. However, the approach is now moving to use of transition metal complexes to manage the HIV infection in the host cells and this review highlights the relevant contributions of such as HIV/AIDS inhibitors. There have been increasing number of reports on the trends for transition metal complexes with anticancer and antimicrobial activity hence this probed the need of such a review. Complexes of vanadium, manganese, iron, copper, cobalt, nickel, zinc, ruthenium, platinum and gold have been reported to be active against HIV-1 virus. The complexes discussed in this review showed anti-viral activity compared to the vehicle control.

A new polypyridyl ligand 4‐(4‐nitrophenoxy)‐N,N‐bis (pyridin‐2‐ylmethyl)aniline (L1) and its three ruthenium (II/III) complexes, [Ru (Cl)₃L1] (C1), [Ru(L1)₂]Cl (C2), and [RuCl (dpa)L1] (C3) where dpa = 2,2‐dipyridylamine, have been successfully synthesized and characterized using Fourier‐transform infrared spectroscopy (FTIR), elemental analysis, proton nuclear magnetic resonance (¹H NMR), high‐resolution electrospray ionization mass spectrometry (HR‐ESI‐MS), thermal analysis (thermogravimetric analysis [TGA] and differential scanning calorimetry [DSC]), UV/Vis absorption, and magnetic susceptibility. The structures of the ligand and the complexes were optimized, and the structural characteristics were determined by density functional theory (DFT) using the B3LYP‐GD3/6‐311G++(d,p) method. Optimized FTIR vibrational frequencies and ¹H NMR chemical shifts agreed well with the corresponding experimental FTIR and ¹H NMR data. In vitro cytotoxicity of the ligand and the complexes were evaluated against the MCF‐7 breast cancer cell line. Ligand L1 was the most potent with an IC₅₀ of 38.45 μM, followed by C2 with an IC₅₀ of 45.23 μM. However, the ligand and the complexes showed low antiproliferative activity compared to cisplatin, which had an IC₅₀ of 9.67 μM. To predict the reactivity trend of L1 and the complexes, frontier molecular orbital (FMO) analysis was performed. The FMO energy gap (Eg = E_LUMO − E_HOMO) for C2 was found to be 1.675 eV, which was the lowest among all the complexes or L1. In addition, molecular docking studies were carried out so as to predict the binding capacity of L1 and the complexes to estrogen receptor alpha (ER‐α). The results showed that C2 has the most negative binding energy score (−9.63 kcal/mol), which indicates more stable adducts with the key amino acid residues at the active sites of ER‐α. Furthermore, C2 displayed the lowest inhibition constant (K_i) of 0.09 μM compared to all the complexes or L1. These results are very promising and show that the novel complex C2 may help in the development of anticancer drugs.