Structural investigation of platinum solubility in silicate glasses

Abstract : The coordination environment of 20-200 ppm Pt in yellowish glasses from the CaO-Al2O3-SiO2 (CAS) ternary was studied using X-ray absorption fine structure spectroscopy at the Pt-L-III edge. Analysis of the Pt-L-III edge region suggests that Pt in these glasses is mainly tetravalent and sixfold-coordinated by O (with a mean Pt-O distance of 2.08 +/- 0.02 Angstrom). No evidence for Pt2+ or Pt6+ was found in any of the glasses studied, suggesting that one can not derive valence information easily from solubility data. No second-neighbor contribution was observed around Pr4+O6 polyhedra. However, bond-valence modeling suggest that these polyhedra are likely to bond mostly to Ca-[VI](2+), which should promote high positional disorder of second-neighbor cations around Pt. This particular bonding arrangement may explain the relatively high solubility of Pt in these relatively depolymerized melts, as CaPtO3-type units.
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Article dans une revue
American Mineralogist, Mineralogical Society of America, 1999, 84 (10), pp.1562--1568
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F Farges, Dr Neuville, Ge Brown. Structural investigation of platinum solubility in silicate glasses. American Mineralogist, Mineralogical Society of America, 1999, 84 (10), pp.1562--1568. 〈hal-00693854〉

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