Abstract
Arsenopyrite is an important component of many ore deposits and dissolves in the O2-rich, acidic surface waters that are commonly found in the vicinity of active mines, releasing As, Fe and S to the environment. However, despite the potentially serious effect of this pollution on the human and animal population, the rate at which such oxidation occurs is poorly known. Kinetic experiments were therefore conducted in a mixed flow reactor to investigate the oxidation of arsenopyrite in Fe2(SO4)3 solutions (pH=l.8) having a concentration of l×l0−2 to 1 ×l0−5 mol kg−1 at temperatures of 45, 35, 25 and 15 °C. The results of these experiments show that the rate of oxidation of arsenopyrite increases with increasing concentration of dissolved Fe2(SO4)3 and temperature. They also show that As released during the oxidation of arsenopyrite has the form As(III), and that the rate of conversion of As(III) to As(V) is relatively low, although it tends to increase with increasing concentration of dissolved Fe2(SO4)3 and temperature. In the presence of Cl−, oxidation of arsenopyrite is accelerated, as is the conversion of As(III) to As(V). These findings indicate that exploitation of arsenopyrite-bearing ores will cause contamination of groundwaters by As at levels sufficient to have a major negative effect on the health of humans and animals.
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