Document Type
Article
Publication Date
7-2018
Abstract
In the present study, pyrrhotite (Fe7S8) was investigated for the removal of Pb2+ and Cu2+ ions from aqueous solution. The Fe7S8 material was prepared through a solvothermal method and was characterized using XRD. The average particle size for the nanomaterial was determined to be 29.86 ± 0.87 nm using XRD analysis and Scherrer's equation. Batch studies were performed to investigate the effects of pH, time, temperature, interfering ions, and the binding capacity of Pb2+ and Cu2+ ions to the Fe7S8 nanomaterial. During the pH profile studies, the optimum pH for the binding of Pb2+ and Cu2+ was determined to be pH 5 for both cations. Isotherm studies were conducted from which the thermodynamics and binding capacities for both Cu2+ and Pb2+ were determined. The binding capacity for Pb2+ and Cu2+ binding to the Fe7S8 were determined to be 0.039 and 0.102 mmol/g, respectively at 25°C. The thermodynamic parameters indicated a ΔG for the sorption of Pb2+ ranged from 5.07 kJ/mol to -2.45 kJ/mol indicating a non-spontaneous process was occurring. Whereas, the ΔG for Cu2+ ion binding ranged from 9.78 kJ/mol to -11.23 kJ/mol indicating a spontaneous process at higher temperatures. The enthalpy indicated an endothermic reaction was occurring for the binding of Pb2+ and Cu2+ to the Fe7S8 nanomaterial with ΔH values of 55.8 kJ/mol and 153.5 kJ/mol, respectively. Furthermore, the ΔS values for the reactions were positive indicating an increase in the entropy of the system after metal ion binding. Activation energy studies indicated the binding for both Pb2+ and Cu2+ occurred through chemisorption.
Recommended Citation
Cantu, J., Gonzalez, D. F., Cantu, Y., Eubanks, T., & Parsons, J. G. (2018). Thermodynamic and Kinetic study of the removal of Cu2+ and Pb2+ ions from aqueous solution using Fe7S8 nanomaterial. Microchemical journal : devoted to the application of microtechniques in all branches of science, 140, 80–86. https://doi.org/10.1016/j.microc.2018.04.003
Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial-No Derivative Works 4.0 International License.
Publication Title
Microchemical Journal
DOI
10.1016/j.microc.2018.04.003