Abstract
This study examined the electro dissolution mechanism of five impure sphalerite samples, which differ significantly in purity levels, along with their partially oxidized counterparts in a 0.5 M H2SO4. Partially oxidized samples were prepared through an incomplete leaching of sphalerite using H2SO4 with Fe2(SO4)3.H2O as an oxidizing agent. The original sphalerite samples and the partially oxidized samples were referred to as SP and POS samples, respectively. Analyses using XRD, SEM, Raman spectroscopy, and electrochemical techniques suggested presence of elemental sulfur and a metal-deficient layer on the surface of the POS samples. Cyclic voltammetry revealed that the sample with the highest iron content exhibited the highest electrochemical response, while the sphalerite with the highest lead concentration had the lowest activity. Electrochemical impedance spectroscopy (EIS) studies showed that impedance values were higher in the POS samples compared to the PS samples, indicating a correlation within the passivation phenomenon. In conclusion, these findings suggested that the sphalerite dissolution process is primarily controlled by charge transfer and kinetic polarization. This understanding can lead to the development of more selective and sustainable extraction methods and improving the overall economic viability of zinc hydrometallurgical operations.
Recommended Citation
G. Khodadadmahmoudi et al., "Electrochemical Insights into the Direct Dissolution of Impure Sphalerites and Their Partial Oxidation in an Acidic Environment," Scientific reports, vol. 15, no. 1, p. 3005, Nature Research, Jan 2025.
The definitive version is available at https://doi.org/10.1038/s41598-025-87270-7
Department(s)
Mining Engineering
Publication Status
Open Access
Keywords and Phrases
Cyclic voltammetry; Electrochemical impedance spectroscopy; Electrometallurgy; Partial leaching; Sphalerite
International Standard Serial Number (ISSN)
2045-2322
Document Type
Article - Journal
Document Version
Final Version
File Type
text
Language(s)
English
Rights
© 2025 The Authors, All rights reserved.
Creative Commons Licensing

This work is licensed under a Creative Commons Attribution 4.0 License.
Publication Date
23 Jan 2025
PubMed ID
39849067
