Electrochemical study of hydrothermal and sedimentary pyrite dissolution |
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| Authors: | Ran Liu Amy L Wolfe David A Dzombak Colin P Horwitz Brian W Stewart Rosemary C Capo |
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| Institution: | 1. Department of Civil and Environmental Engineering, Carnegie Mellon University, Pittsburgh, PA 15213, USA;2. Department of Geology and Planetary Science, University of Pittsburgh, Pittsburgh, PA 15260, USA;3. Department of Chemistry, Carnegie Mellon University, Pittsburgh, PA 15213, USA |
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| Abstract: | The dissolution of pyrite is of interest in the formation of acid mine drainage and is a complex electrochemical process. Being able to measure the rate of dissolution of particular pyrite samples under particular conditions is important for describing and predicting rates of AMD generation. Electrochemical techniques offer the promise of performing such measurements rapidly and with small samples. The oxidation of pyrite and the reduction of Fe3+ ions and/or O2 half reactions involved in the pyrite dissolution process were investigated by cyclic voltammetry and steady-state voltammetry using three pyrite materials formed in both sedimentary and hydrothermal environments. For each sample, two kinds of pyrite working electrodes (conventional constructed compact solid electrode, and carbon paste electrode constructed from fine-grained pyrite particles) were employed. Results indicated that for both the hydrothermal and sedimentary pyrite samples the oxidation and reduction half reactions involved in dissolution were governed by charge transfer processes, suggesting that hydrothermal and sedimentary pyrites obey the same dissolution mechanism despite their different formation mechanisms. In addition, the results showed that it is feasible to use a C paste electrode constructed from fine-grained or powdered pyrite to study the pyrite dissolution process electrochemically and to derive approximate rate expressions from the electrochemical data. |
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