2003 Seattle Annual Meeting (November 2–5, 2003)

Paper No. 4
Presentation Time: 9:00 AM

PLATINUM AND GOLD SOLUBILITY AND PARTITIONING BEHAVIOR IN SYNTHETIC MAGMATIC MELT – BRINE MIXTURES


HANLEY, Jacob, Department of Geology, Univ of Toronto, Earth Sciences Centre, 22 Russell Street, Toronto, ON M5S 3B1, Canada, PETTKE, Thomas, Isotope Geochemistry and Mineral Resources, Federal Institute of Technology, ETH Zentrum NO, CH-8092, Zurich, Switzerland, MUNGALL, James E., Geology, Univ of Toronto, 22 Russell St, Toronto, ON M5S 3B1, Canada and HEINRICH, Christoph A., Department of Earth Sciences, Institute for Isotope Geochemistry and Mineral Resources, ETH Zurich, ETH Zentrum NO, Sonneggstr. 5, Zurich, 8092, hanley@geology.utoronto.ca

The behavior of Pt and Au in brines associated with silicate melt (relevant to Pt-bearing layered intrusions, and Au-bearing porphyry systems) was investigated by reacting the metals with high-T (500-850ºC), S-free brine (20-70 wt% NaCl) ± peraluminous melt, trapping the brine in synthetic fluid inclusions (quartz-hosted) and vesicles (melt-hosted), and quantifying the metal content of the trapped brine and glass by LA-ICPMS. HCl activity was buffered using albite-andalusite-qtz; fO2 using Ni-NiO and MnO-Mn3O4. The following observations were made: (i) transient ablation signals for the inclusions demonstrate coincidence between metal and Na signals, suggesting that the metals are dissolved in solution and not present as accidentally trapped particles; (ii) CPtbrine and CAubrine are very high, with ranges in conc. over all experimental conditions of 10-103 ppm Pt, and 102-105 ppm Au (wt% Au contents indicated by visible Au daughter crystals); (iii) trapped brines exhibit a wide range of Cmetal (due to premature fracture healing and slow metal-brine-melt equilibration) allowing for only minimum estimates of metal solubility; (iv) CPtmelt and CAumelt are ~500 ppb and 2 ppm, respectively, and are invariant over the range of experimental conditions, but exhibit some heterogeneity within a single run (formation of micronuggets during quench?); (v) apparent brine-melt partition coefficients vary only as a function of Cmetalbrine, independent of Cmetalmelt; D*Ptbrine/meltbrine/melt range from 3x102-5.2x104, D*Au brine/melt range from 1.4x104-4.9x105; (vi) at fixed T and NaCltot, maximum and mean Cmetalbrine increases with increasing fO2 in accordance with oxidation states Pt2+ and Au1+; (vii) the maximum and mean Cmetalbrine decreases with increasing NaCltot at fixed T, but increases with increasing T at fixed NaCltot. The observed behavior is consistent with hydroxide complexing; the following mass action expressions are proposed: (i) NaAlSi3O8 + Au(s) + ¼O2 + HClaq=AuOH + ½Al2SiO5 + 2.5SiO2 + NaClaq, (ii) 2NaAlSi3O8 + Pt(s) + ½O2 + 2HClaq=Pt(OH)2 + Al2SiO5 + 5SiO2 + 2NaClaq. The results demonstrate that S-free, aqueous brines which exsolve from/interact with residual magmatic liquids have the ability to carry large amounts of both Pt and Au across the magmatic-hydrothermal interface, even at moderately oxidizing conditions (Ni-NiO).