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Background of the study: The genus Morinda of the Madder family, (Rubiaceae) has been widely documented in traditional medicine due to its therapeutic properties and also, contributed a great deal in chemical industry. Different parts of Morinda species have traditionally been used to treat malaria, diabetes, memory loss, cancer, inflammation, skin infections, and typhoid fever. Aim and Objectives: The review provide a critical and innovative information on the traditional uses, phytochemical constituents, and industrial applications of the genus Morinda. This will help researchers understand future research trends by bridging the gap between documented literature and contemporary uses. Methodology: All the systematic literature data or information on the genus Morinda was collected via selected electronic databases, including Scopus, PubMed, Web of Science, Springer, Medline, ChemSpider, Taylor and Francis, Google Scholar, SciFinder, ScienceDirect and Wiley. Relevant book chapters, Wikipedia and books were also explored. Results: The study reveals that different parts of Morinda plants have been extensively used for folkloric therapeutic purposes and are a plethora of mineral or nutritional benefits and secondary metabolites. Several classes of bioactive compounds have been elucidated from Morinda plants via spectroscopic and chromatographic phytochemical analyses. Compounds such as terpenoids, glycosides, anthraquinones, polyphenols, steroids, saponins and reducing sugars are among the bioactive substances reported in the genus. Plant extracts, fractions and isolates of Morinda plants have exhibited pronounced antidiabetic, antioxidant, antiplasmodial, antidepressant, wound healing, anticancer, and anti-inflammatory effects (in vitro and in vivo). These pharmacological activities exhibited could be linked to the presence of secondary metabolites reported. The applications of this genus is well documented in textile, metallurgical, agrochemicals and food industries. Conclusion: A number of reports on Morinda showed significant therapeutic effect against several diseases such as cancer, dermal infection, diabetes, inflammation, malaria, typhoid, cholera and memory loss, however, there were several drawback in previous reports including mechanism of action, drug dose, controls and toxicological data of extracts or isolates. In view of this, further studies should emphasis on targeting active secondary metabolites which responsible for the therapeutic activities, structural elucidation and toxicological assessment. Furthermore, industrial uses require authentication.

The large capacity of wastewater production due to rapid growth of industries has resulted in limited water resources. The need to protect and conserved water resources have enforced researchers worldwide to focus on the development of an effective, economical and environmentally friendly novel materials. In this study, green synthesis of zinc oxide nanoparticles (ZnONPs) using T. diversifolia leaf extract by hydrothermal method was loaded on the surface of flamboyant pods (Delonix regia) activated carbon (FPAC). The developed ZnONPs loaded on the surface flamboyant pods activated carbon (ZnONPs-FPAC) was used successfully to remove of methylene blue (MB) from aqueous solution. The developed FPAC, ZnONPs and ZnONPs-FPAC were characterized UV–Vis spectroscopy, Fourier-transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), Scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM/EDX), Transmission electron microscope (TEM) and Brunauer-Emmett-Teller (BET) techniques. The antibacterial activity of the synthesized FPAC, ZnONPs and ZnONPs-FPAC were screened and the results revealed that ZnONPs has an excellent antibacterial activity when compared. Batch adsorption studies were conducted to investigate the influence of process parameters such as initial concentration, contact time, pH, adsorbent dosage and temperature on MB uptake. The high BET surface area of 794.48 m2/g and mesoporous ZnONPS-FPAC developed gave good adsorption capacity of 186 mg/g. Equilibrium adsorption data of MB were modelled using Langmuir, Freundlich, Temkin and Dubinin–Radushkevich (D–R) isotherm model. The adsorption of MB onto ZnONPs-FPAC was best described by Freundlich model indicating surface heterogeneity, and pseudo-second-order kinetics according to %Δqe (normalized standard deviation), SSE (sum of square error), and R2 (coefficient of determination) values. The results of the thermodynamic suggest that the adsorption process of MB onto ZnONPs-FPAC is endotherm, favourable, spontaneous, and physical. In nature. The reusability of ZnONPs-FPAC was examined upto five cycles with no significant loss in removal efficiency. The mean free energy (E), and Enthalpy (ΔH) values calculated, suggested that the adsorption mechanism of MB on ZnONPs-FPAC is dominated by physical adsorption.

Single pot system in chemical reduction via bottom-up approach was used for the synthesis of core shell nanoscale zerovalent iron (CS-nZVI). CS-nZVI was characterized by a combination of physicochemical and spectroscopic techniques. Data obtained showed BET surface area 20.8643 m2/g, t-Plot micropore volume 0.001895 cm3/g, BJH volume pores 0.115083 cm3/g, average pore width 186.9268 Å, average pore diameter 240.753 Å, PZC 5.24, and pH 6.80. Surface plasmon Resonance from UV-Vis spectrophotometer was observed at 340 nm. Surface morphology from SEM and TEM revealed a spherical cluster and chain-like nanostructure of size range 15.425 nm −97.566 nm. Energy Dispersive XRF revealed an elemental abundance of 96.05% core shell indicating the dominance of nZVI. EDX showed an intense peak of nZVI at 6.2 keV. FTIR data revealed the surface functional groups of Fe–O with characteristics peaks at 686.68 cm−1, 569.02 cm−1 and 434 cm−1. In a batch technique, effective adsorption of endocrine disruptive Cu(II) ions was operational parameters dependent. Isotherm and kinetics studies were validated by statistical models. The study revealed unique characteristics of CS-nZVI and its efficacy in waste water treatment.

Chemically prepared activated carbon derived from Gmelina aborea leaves (GALAC) were used as adsorbent for the removal of Rhodamine B (Rh–B) dye from aqueous solutions. The adsorptive characteristics of activated carbon (AC) prepared from Gmelina aborea leaves (GAL) were studied using SEM, FTIR, pH point of zero charge (pHpzc) and Boehm Titration (BT) techniques respectively. The effects of pH, contact time, initial dye concentration and solution temperature were also examined. Experimental data were analyzed using four different isotherm models: Langmuir, Freundlich, Temkin and Dubinin-Radushkevich. Four adsorption kinetic models: Pseudo-first-order (PFO), Pseudo-second-order (PSO), Elovich and Intraparticle diffusion models to establish the kinetics of adsorption process. The RhB dye adsorption on GALAC was best described by Langmuir isotherm model with maximum monolayer coverage of 1000 mg g−1 and R2 value of 0. 9999. The EDX analysis revealed that GALAC contained 82.81% by weight and 91.2% by atom of carbon contents which are requisites for high adsorption capacity. Adsorption kinetic data best fitted the PSO kinetic model. Thermodynamic parameters obtained for GALAC are (ΔGo ranged from -22.71 to -18.19 kJmol-1; ΔHo: 1.51 kJmol-1; and ΔSo: 0.39 kJmol-1 K−1respectively) indicating that the RhB dye removal from aqueous solutions by GALAC was spontaneous and endothermic in nature. The cost analysis established that GALAC is approximately eleven times cheaper than CAC thereby providing a saving of 351.41USD/kg. Chemically treated GAL was found to be an effective absorbent for the removal of RhB dye from aqueous solution.

Single pot green synthesis of silver nanoparticles (AgNPs) was successfully carried out using medicinal plant extract of Acalypha wilkesiana via bottom-up approach. Five imperative operational parameters (pH, contact time, concentration, volume ratio and temperature) pivotal to the synthesis of silver nanoparticles were investigated. The study showed pH 9, 90 min contact time, 0.001 M Ag+ concentration, volume ratio 1:9 (extract: Ag+ solution), and temperature between 90 – 100 °C were important for the synthesis of Acalypha wilkesiana silver nanoparticles (AW-AgNPs). Phytochemical screening confirmed the presence of saponins, flavonoids, phenols and triterpenes for A. wilkesiana. These phytomolecules served as both capping and stabilizing agent in the green synthesis of silver nanoparticles. AW-AgNPs was characterized by UV-Vis Spectroscopy, Fourier Transform Infrared (FTIR) Spectroscopy and Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM) and Energy Dispersive X-ray (EDX). The surface Plasmon resonance (SPR) was observed at 450 nm which is a characteristic absorbance region of AW-AgNPs formation as a result of the collective oscillation of free electron of silver nanoparticles. FTIR Spectroscopy confirmed the presence of functional groups responsible for bioreduction of Ag+. SEM and TEM results confirmed a well dispersed AW-AgNPs of spherical shape. EDX shows the elemental distribution and confirmed AgNPs with a characteristic intense peak at 3.0 keV. AW-AgNPs showed significant inhibition against selected Gram negative and Gram positive prevailing bacteria. AW-AgNPs can therefore be recommended as potential antimicrobial and therapeutic agent against multidrug resistant pathogens.

Novel silver nanoparticles from Gleichenia Pectinata (Willd.) C. Presl. was synthesized. A combination of spectroscopic and microscopic techniques were utilized to characterize the newly synthesized Gleichenia Pectinata Silver Nanoparticles (GPAgNPs) vis-à-vis UV-Vis Spectroscopy, Fourier Transform Infra-Red (FTIR) Spectroscopy, Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), Energy Dispersive X-ray Spectroscopy (EDX) and X-Ray Diffraction (XRD) Analyses. Significant absorption was observed at 460 nm resulting from the surface Plasmon resonance (SPR). A rapid rate of synthesis was observed and the best surface plasmon resonance was obtained at 105 minutes contact time. SEM and TEM showed an spherical shape of GPAgNPs with an average size of 7.51 nm. The XRD result revealed a crystalline and polydispersed GPAgNPs. GPAgNPs were effective against four antibiotic resistant pathogens and they exhibited excellent antimicrobial activity against Pseudomonas aeruginosa, Escherichia coli, Klebsiella pneumoniae and Candida albicans. GPAgNPs favorably competed with standard antibiotics. This therefore enlisted GPAgNPs as potential antimicrobial and therapeutic agents against multidrug resistant micro-organisms (MDRM).