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Updated: Jul 11, 2026

Preparation of Authigenic Pyrite from Methane-bearing Sediments for In Situ Sulfur Isotope Analysis Using SIMS
Published on: August 31, 2017
Aqueous geochemical and surface science investigation of the effect of phosphate on pyrite oxidation
A R Elsetinow1, M A Schoonen, D R Strongin
1Department of Chemistry, Temple University, Philadelphia, Pennsylvania 19122, and Department of Geosciences, SUNY-Stony Brook, Stony Brook, New York 11794-2100, USA.
Abstract:
Aqueous geochemical and surface science techniques were used to investigate the effect of phosphate on the oxidation of crushed and (100) pyrite. Studies showed that the presence of phosphate in solution significantly impeded the oxidation rate of crushed pyrite at pH values equal to or greater than 4. At pH 3, the presence of phosphate had almost no experimentally discernible effect on pyrite oxidation. X-ray photoelectron spectroscopy (XPS) studies showed that phosphate, at pH values greater than 4, became irreversibly bound to an Fe(3+)-bearing product on the pyrite surface during the oxidation process. Once bound to this region on the pyrite surface, the adsorbed phosphate inhibited further oxidation of the pyrite (based on XPS determinations of sulfur and iron oxide product concentrations) under our experimental conditions. These results suggested that the rate of pyrite oxidation in the absence of phosphate was facilitated at or near Fe(3+)-bearing oxidation phases on the surface. Phosphate bound on iron(III) oxide product either prevents O2 adsorption on this phase or electronically modifies these surface regions, but in either case it inhibits electron transfer from pyrite-Fe2+ sites to molecular O2.
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