Syed Muhammad Salman, Muhammad Zahoor, Afsheen, Latif-ur-Rahman, Farman Ali, Hizbullah Khan, Muhammad Wahab, Qaisar Khan, Rozina, Riaz Ullah, Essam A. Ali, Muhammad Naveed Umar, Abdul Waheed Kamran
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引用次数: 0
Abstract
Herein, an efficient adsorbent was prepared at high temperature using sawdust of Melia azedarach plant. The prepared adsorbent was characterized by instrumental techniques like EDX, XRD, SEM, FTIR, TGA, and surface area analyzer. The fabricated activated carbon (AC) was used as an adsorbent for the removal of Pb2+ Ni2+, and Cu2+ from aqueous solution utilizing batch adsorption approaches. At pH 6, the highest elimination of Pb2+ and Cu2+ was achieved, whereas for Ni2+ the optimum pH was 5. The recorded time interval for reaching equilibrium was 60 min in the case of Pb2+ and Ni2+ metal, whereas 80 min in the case of Cu2+ ion. The adsorbent was found to be more effective at high doses, with an optimum dose of 0.05 g. The isotherm models, including Langmuir, Freundlich, Temkin, Jovanovich, and Harkins-Jura models, were utilized to decide the best fit model for explaining the isotherm adsorption data. Out of the tested models, the Langmuir model was more effective with high R2 values of 0.997, 0.991, and 0.984, respectively, for Pb2+, Ni2+, and Cu2+ ions. The pseudo-second order model best fitted the kinetics data with high R2 values of 0.980, 0.991, and 0.987 correspondingly, for the mentioned ions. The estimated ∆H° values were −22.699, −31.147, and −33.199 J·mol−1 respectively for Pb2+, Ni2+ and Cu2+, indicated the process to be an exothermic one. The favorable nature of the studied adsorption was obvious from the recorded negative values of Gibbs free energy. The fabricated AC could thus be considered as an efficient and cheap alternative to commercially available activated carbon; however, further confirmation and validation of the present findings by other researchers is mandatory.
期刊介绍:
As the leading archival journal devoted exclusively to chemical kinetics, the International Journal of Chemical Kinetics publishes original research in gas phase, condensed phase, and polymer reaction kinetics, as well as biochemical and surface kinetics. The Journal seeks to be the primary archive for careful experimental measurements of reaction kinetics, in both simple and complex systems. The Journal also presents new developments in applied theoretical kinetics and publishes large kinetic models, and the algorithms and estimates used in these models. These include methods for handling the large reaction networks important in biochemistry, catalysis, and free radical chemistry. In addition, the Journal explores such topics as the quantitative relationships between molecular structure and chemical reactivity, organic/inorganic chemistry and reaction mechanisms, and the reactive chemistry at interfaces.