Abstract
The electrochemical behavior of mineral and coal pyrites in basic borate/sulfate solutions was investigated using cyclic voltammetry with both stationary and rotating disk electrodes. Emphasis was centered on transpassive oxidation. In the transpassive region, 0.4 to 0.8 V (SCE), aggressive oxidation of pyrite occurred. The reaction products in this region are Fe(III) oxides, sulfate ion, and partially oxidized sulfur intermediates. The formation of sulfur and polysulfides was identified by in situ Raman spectroscopy. Exposure of pyrite to anodic potentials higher than the transpassive region resulted in rapid oxidation of sulfur intermediates to sulfate ion. The effect of electrode rotation speed, electrode precondition time, and upper potential of the scan in the transpassive region was observed to be critical to the formation of sulfur intermediates. Sulfur intermediates, formed in the transpassive region, dramatically affected subsequent oxidation reactions occurring in the lower potential region. The magnitude of two dominant oxidation peaks, a ferrous hydroxide peak and an iron sulfide peak, observed in this region correlated directly with the quantity of sulfur intermediates formed in the transpassive region. This effect was less pronounced for coal pyrites compared to mineral pyrite.
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