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Experimental determination of the phase relations of Pt and Pd antimonides and bismuthinides in the Fe-Ni-Cu sulfide systems between 1100 and 700 °C

  • Hassan M. Helmy and Roman Botcharnikov
Published/Copyright: March 1, 2020
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Abstract

The stability relations of Pt and Pd antimonides and bismuthinides in the Sb- and Bi-bearing Fe-Ni-Cu sulfide systems have been experimentally determined at temperatures between 1100 and 700 °C in evacuated silica tubes. Both PtSb and PdSb are stable as immiscible liquids at temperatures above 1100 and 1000 °C, respectively. The Fe-Ni-Cu-sulfide melt that coexists with the immiscible antimonide melt can dissolve up to 3.8 wt% Sb at 1100 °C, whereas monosulfide solid solution (mss) dissolves very low amounts of Sb over the entire 1100–700 °C temperature range. The liquidus of Pt-antimonides and Pd-antimonides are above 980 and 750 °C, respectively. Bismuth does not form immiscible melt at 1100 °C but may partially partition into a vapor phase at 1050 °C. The Pt- and Pd-bismuthinides crystallize directly from immiscible bismuthinide melt only after crystallization of the sulfide melt into intermediate solid solution (iss). Insizwaite (PtBi2) and froodite (PdBi2) are stable at 780 and 700 °C, respectively. At the last stage of evolution of Sb-bearing magmatic Fe-Ni-Cu sulfide melts, Sb will form immiscible antimonide melt that will extract Pt and Pd from the sulfide melt. During cooling, Pt and Pd-antimonides will crystallize directly from the immiscible antimonide melt, and Pt-phases will form at higher temperatures relative to Pd-phases. Bismuth will partition into vapor phase and concentrate into a low-temperature melt in hydrothermal and porphyry systems that scavenge precious metals. The Sb and Bi (like Te) will be highly incompatible at moderate degrees of mantle partial melting.

Acknowledgments and Funding

H.M. Helmy’s research was funded by the Alexander von Humboldt Society through a Georg Forster Research Award. We thank Iain McDonald and another anonymous reviewer for critical comments on the manuscript and Kate Kiseeva for editorial handling.

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Received: 2019-06-12
Accepted: 2019-11-15
Published Online: 2020-03-01
Published in Print: 2020-03-26

© 2020 Walter de Gruyter GmbH, Berlin/Boston

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