A vibrational spectroscopic<sup>18</sup>O tracer study of pyrite oxidation

Publication Type:
Journal Article
Citation:
Geochimica et Cosmochimica Acta, 1991, 55 (6), pp. 1609 - 1614
Issue Date:
1991-01-01
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Pyrite was oxidised under18O2gas in H216O solutions, with and without added ferric ion, and the sulfate produced was analysed by vibrational spectroscopy to determine the relative amounts of sulfate isotopomers (S16On18O4-n2-) formed. At 70°C and pH 1, with no added Fe3+, the majority of the sulfate formed was that which derived all four oxygen atoms from water (i.e., S16O42-), but significant amounts of two other isotopomers, S16O318O2-and S16O218O22-, which derive one or two oxygen atoms from molecular oxygen were observed. When Fe3+was added at the start under identical conditions, no S16O218O22-was observed. The major isotopomer formed was still S16O42-, with S16O318O2-present as a minor product. Experiments which were performed at initial pH 7 yielded similar results, as did others performed at 20°C, although the amounts of the minor isotopomers formed vary with temperature. All of the results were confirmed by performing identical experiments with the source of the oxygen isotopes reversed, that is, by oxidising pyrite under air in H218O solutions and obtaining the same products in isotopic reverse. © 1991.
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