In the present study, titanium (IV) sulfide (TiS2) was synthesized and investigated for the removal of Cu2+ and Pb2+ ions from aqueous solutions. TiS2 nanoparticles synthesized through a solvothermal synthesis were characterized using x-ray diffraction (XRD) and scanning electron microscopy (SEM). The average particle size for the TiS2 material was determined to be 8.03 ± 0.98 nm from the diffraction pattern. Studies were performed to examine the effects of pH, temperature, time, and interfering ions on the binding of Cu2+ and Pb2+ to the TiS2. As well isotherm studies were performed to determine the binding capacity of TiS2 for both Cu2+ and Pb2+ ions. The pH profile studies showed optimal binding occurred at pH 2 for the sorption of both Cu2+ and Pb2+ to the TiS2. The isotherm studies showed the adsorption capacities at temperatures of 4, 22, and 45 °C for Cu2+ were 243, 222, and 153 mg/g, respectively. An opposite trend in the adsorption was observed for Pb2+ binding to the TiS2. The observed binding capacities for Pb2+ were 32, 166, and 357 mg/g, at temperatures of 4, 22, and 45 °C, respectively. The thermodynamic parameters for binding showed a non-spontaneous process for the sorption of Cu2+ whereas a spontaneous binding process was observed for the sorption of Pb2+. Additionally, the binding of Cu2+ on TiS2 in the presence of interfering ions (Na+, K+, Mg2+, and/or Ca2+) was observed to decrease at high concentrations; however, the binding of Pb2+ was unaffected by the presence of the same cations.
Cantu, J., Valle, J., Flores, K., Gonzalez, D., Valdes, C., Lopez, J., Padilla, V., Alcoutlabi, M., & Parsons, J. (2019). Investigation into the thermodynamics and kinetics of the binding of Cu2+ and Pb2+ to TiS2 nanoparticles synthesized using a solvothermal process. Journal of Environmental Chemical Engineering, 7(6), 103463. https://doi.org/10.1016/j.jece.2019.103463
Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial-No Derivative Works 4.0 International License.
Journal of Environmental Chemical Engineering