摘要
This study was aimed to investigate Pb(II) and Cu(II) ions removal ability from aqueous solution by cassava root husks (CRH) as a cheap, sustainable and eco<span>-</span><span><span>friendly bioadsorbent. The CRH was characterized by Fourier Transform Infrared (FTIR) spectroscopy which indicated the availability of various functional groups for metal coordination and the result was supported by elemental analysis studies. UV-Visible spectral studies indicated the presence of oxalate (</span><img src="Edit_88f5f86a-6e96-4764-8dc0-31bbb7ac83c6.png" width="34" height="18" alt="" /></span><span><span></span><span><span>) </span><span>and it could possibly interact with metal ions to give rise to a stable chelated coordination complex which affects metal ions removal efficiency. Bioadsorption process was carried out as a function of metal concentration, contact time, pH of the solution, particle size</span></span><span>,</span><span> and dosage of the adsorbent. Experimental results indicated the optimal adsorption condition of pH 4 for both Pb(II) and Cu(II) ions, dosage of 0.1</span><span style="font-family:;" "=""> </span><span>g/0.1L and 1</span><span style="font-family:;" "=""> </span><span>g/0.1L for Pb(II) and Cu(II) ions respectively, adsorption equilibrium time of 2 and 25 minutes for Pb(II) and Cu(II) respectively, and concentration of 0.5 mg/L for both metal ions. Kinetic data best</span><span style="font-family:;" "=""> </span><span>fitted pseudo-second-order model and not </span><span>the </span><span>pseudo-first-order model. Equilibrium data best fitted </span><span>the </span><span>Freundlich model than </span><span>the </span><span>Langmuir model. Specific surface area and pore volume studies indicated that CRH is non-porous and hence rapid adsorption kinetics is expected. Supporting the experimental results, molecular modeling studies performed using Schr<span style="white-space:nowrap;">ö</span>dinger software predicted several sites in the structure capable of docking with metal ions.</span></span>
This study was aimed to investigate Pb(II) and Cu(II) ions removal ability from aqueous solution by cassava root husks (CRH) as a cheap, sustainable and eco<span>-</span><span><span>friendly bioadsorbent. The CRH was characterized by Fourier Transform Infrared (FTIR) spectroscopy which indicated the availability of various functional groups for metal coordination and the result was supported by elemental analysis studies. UV-Visible spectral studies indicated the presence of oxalate (</span><img src="Edit_88f5f86a-6e96-4764-8dc0-31bbb7ac83c6.png" width="34" height="18" alt="" /></span><span><span></span><span><span>) </span><span>and it could possibly interact with metal ions to give rise to a stable chelated coordination complex which affects metal ions removal efficiency. Bioadsorption process was carried out as a function of metal concentration, contact time, pH of the solution, particle size</span></span><span>,</span><span> and dosage of the adsorbent. Experimental results indicated the optimal adsorption condition of pH 4 for both Pb(II) and Cu(II) ions, dosage of 0.1</span><span style="font-family:;" "=""> </span><span>g/0.1L and 1</span><span style="font-family:;" "=""> </span><span>g/0.1L for Pb(II) and Cu(II) ions respectively, adsorption equilibrium time of 2 and 25 minutes for Pb(II) and Cu(II) respectively, and concentration of 0.5 mg/L for both metal ions. Kinetic data best</span><span style="font-family:;" "=""> </span><span>fitted pseudo-second-order model and not </span><span>the </span><span>pseudo-first-order model. Equilibrium data best fitted </span><span>the </span><span>Freundlich model than </span><span>the </span><span>Langmuir model. Specific surface area and pore volume studies indicated that CRH is non-porous and hence rapid adsorption kinetics is expected. Supporting the experimental results, molecular modeling studies performed using Schr<span style="white-space:nowrap;">ö</span>dinger software predicted several sites in the structure capable of docking with metal ions.</span></span>
作者
Kaupa Philip
Rebecca Jacob
Janarthanan Gopalakrishnan
Kaupa Philip;Rebecca Jacob;Janarthanan Gopalakrishnan(Department of Applied Sciences, PNG University of Technology, Lae, Papua New Guinea;School of Chemistry, University of Sydney, Sydney, Australia)