Abstract

A series of experiments were carried out in a batch system to assess the removal of cobalt ion (Co2+) by intact and modified Ficus carica leaves (FCLs) from the aqueous solutions in laboratory experiments. Adsorption kinetics and thermodynamic parameters, as well as equilibrium adsorption isotherms, were examined. The effects of pH, initial concentration of metal ions, biosorbent dose, and the treatment of biosorbent on the biosorption process were also studied. Results showed that the optimum uptake (20.2 mg/g with the removal efficiency of 31.02%) was reached at pH 4. It was also found that the FCLs treated with MgCl2 caused an increase in the uptake capacity, 33.9 mg/g (qexp) at pH 6, and removal efficiency was 57.15%. The biosorption data followed the Freundlich (R2 = 0.974), Langmuir (R2 = 0.978), Dubinin–Radushkevich (R2 = 0.982), and Temkin (R2 = 0.915) isotherms. Langmuir, Freundlich, and Dubinin–Radushkevich models exhibited a higher and better fit of the data. The Freundlich constants Kf and n were found to be 0.75 and 1.014, respectively, and the maximum sorption capacity (qmax) was 82.64 mg/g. Dubinin–Radushkevich parameters were KD–R = 0.00142, Xm = 0.0067 mol/g, and ED–R value was 18.782 kJ/mol. The overall biosorption process of Co2+ ion was best described by pseudo-second-order kinetic model. The negative ∆G° (−0.124) observed at 20°C revealed that biosorption of Co2+ ions onto FCLs was spontaneous at this temperature. Thermodynamic studies also demonstrated positive ∆S° (+0.705), showing increased disorder of the cobalt ion removal process. Ion-exchange mechanism and dominant sorption functional groups determination accomplished using Fourier transform infrared (FTIR) and X-ray fluorescence (XRF) techniques, and hence pseudo-second-order kinetic model. The results from this study showed the raw and modified FCLs are a new biomass for the removal of Co2+ from aqueous solutions.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.