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1 Department of Mineralogy, Geological Institute, University of Copenhagen, Øster Voldgade 10, DK-1350 Copenhagen K, Denmark
2 Institute for Geology and Geological Engineering, The Danish Technical University, Building 205, DK-2800 Lyngby, Denmark
* E-mail: emilm{at}geo.geol.ku.dk
Phase relations in the S-poor portions of the dry condensed Pt-Ir-Fe-S system were determined at 1000° and 1100°C with a particular emphasis on delineation of the solid solubility fields of the Pt-Ir-Fe alloys. At both temperatures, a broad field of
(Ir,Fe,Pt) alloy coexists with
-(Pt,Fe), Pt3Fe and PtFe which dissolve respectively at least 5.1, 29.3 and 24.0 at.% Ir at 1100°C (2.2, 23.6 and
17.2 at.% Ir at 1000°C). Gaps between the nearly Ir-free Pt-Fe alloys
(Pt,Fe), Pt3Fe s.s., PtFe s.s. and
(Fe,Pt) were estimated as 2023 at.%, 4042 at.% and 54.2~57 at.% Fe at 1100°C (1823, 39.542.5 and 5962 at.% Fe at 1000°C). The first gap agrees with data from natural phases by Cabri et al. (1996). The Fe-rich sulphide melt dissolves only traces of Pt and Ir; Fe1xS dissolves up to 5.8 at.% Ir at 1100°C and 3.4 at.% Ir at 1000°C. These solubilities and the compositions of coexisting alloys (before low-temperature exsolution) may serve as geothermometers. The S-rich melt dissolves up to 8.2 at.% Pt and 2.5 at.% Ir (measured on a solidified melt) at 1100°C. The Fe-Ir thiospinel dissolves up to 2.2 at.% Pt (for the composition Fe21.6Ir18.9Pt2.2S57.3 at 1100°C). The 2528 at.% Fe portions of Pt3Fe with <10 at.% Ir partake in all important sulphide (± melt)-alloy assemblages (with PtS, Ir2S3, pyrrhotite, S-rich melt and thiospinel). Therefore, their use in recognizing distinct natural assemblages of genetic importance is of limited value.
KEYWORDS: Pt-Ir-Fe-S phase system, Pt-Fe alloys, isoferroplatinum, tetraferroplatinum, platinum-group metal deposits
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