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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).