Abstract
In this study, an efficient adsorbent was proposed for the removal of mercury from saline water contaminated with mercury ions. Fe3O4 nanoparticles were modified using tetraethylenepentamine and carbon disulfide to incorporate dithiocarbamate functional group on the surface of the adsorbent. CHNS analysis confirmed successful modification of magnetic nanoparticles. The XRD pattern of adsorbent indicated a proper match with the standard XRD pattern of cubic Fe3O4. The saturation magnetization of final adsorbent was 27 emu g−1. The morphology of bare and silica-coated Fe3O4 and final product were investigated using FE-SEM analysis. For optimizing the adsorption process, response surface methodology was applied, which was resulted in a significant quadratic model. The effect of adsorbent dosage and initial concentration of Hg (II) was much more significant than that of pH. Different concentrations of dissolved solids up to 2000 mg L−1 had no adverse effect on the adsorption process due to the strong interaction between dithiocarbamate functional group of adsorbent and Hg (II). The least values of RMSE (0.0950) and χ2 (0.0009) were observed for Radke-Prausnitz, Redlich-Peterson, and UT isotherms. Maximum adsorption capacities calculated using Langmuir and UT models were 109.5 and 95.07 mg g−1, respectively. The investigation of adsorption isotherm was conducted at the pH range of 2.0–6.5. The results showed an increase in the adsorption capacity by increasing pH. Thermodynamic studies demonstrated that the nature of the adsorption process was spontaneous and endothermic. Recovery of adsorbent was successfully carried out using HCl 0.5 mol L−1. The prepared adsorbent was successfully applied for mercury removal from a real groundwater.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
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.