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Two forms of activated carbon (i.e., granular and powdered forms) used to test mercury removal in solution. These activated carbons were obtained from the shells of a palmae biomass and used in mercury ion removal in aquatic systems. The African palmae shell taken out from a broadly and simply full-fledged palm tree. This biomass serves as a precursor in the formulation of activated carbons not documented. The powdered and granular fractions of activated carbons described for chemical composition, isoelectric point, and surface area. The mechanism of reactions and the kinetics involved were studied using the results of protonation and rate limitations. The parameters used in the batch mode study included pH, contact time, initial concentration of the adsorbate and the dose of the activated carbons. A comparison of performances, contact time demonstrated the highest adsorption efficiency of 93% for the powdered activated carbon and 92% for the granular activated carbon. The dosage recorded the lowest adsorption efficiency of 84% using granular activated carbon. Comparatively, this study brought to the fore that activated carbon derived from the Plamae biomass remains a novel bio-sorbent

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The removal of Lead (Pb 2+) ions from waste water in the aquatic environment by copper oxide-kaolinite composite forms an important step involved in the reduction of Lead ions in the environment. The study investigated the synthesis, characterization, and application of copper oxide-kaolinite composite in the removal of Lead ions from aqueous systems. The synthesis of the composite involved a trimetric process to produce the copper oxide (CuO)-kaolinite composite. The characterization involved the determination of cation exchange capacity, specific surface area, and spectral analysis by sodium saturation method, nitrogen gas adsorption techniques, and scanning electron spectroscopy, respectively. The determination of parameters affecting the reaction mechanism and reaction kinetics involved the use of batch mode techniques. The findings indicated a reaction mechanism that was less than one proton coefficient, higher mass transfer rates when compared with uncoated kaolinite. Here, the intraparticle diffusion was higher than the value for the uncoated kaolinite. The reactions based on Pb 2+ initial concentration indicated that the coated kaolinite gradually became saturated as the concentration was increased. The reactions based on solid concentration (Cp) demonstrated a complex change in the capacity of adsorption over different Pb 2+ concentrations (10-40 mgL −1) and solid concentrations (2-10 gL −1). Here, the reduction in specific surface area, particle size increase, mineral aggregation, and concentration gradient effect controlled the complex changes in adsorption. In conclusion, the copper oxide-kaolinite composite significantly enhanced the adsorption of Pb 2+ ions.