PARTITIONING OF NICKEL, COPPER, IRIDIUM, RHENIUM, PLATINUM, AND PALLADIUM BETWEEN MONOSULFIDE SOLID-SOLUTION AND SULFIDE LIQUID - EFFECTS OF COMPOSITION AND TEMPERATURE
C. Li et al., PARTITIONING OF NICKEL, COPPER, IRIDIUM, RHENIUM, PLATINUM, AND PALLADIUM BETWEEN MONOSULFIDE SOLID-SOLUTION AND SULFIDE LIQUID - EFFECTS OF COMPOSITION AND TEMPERATURE, Geochimica et cosmochimica acta, 60(7), 1996, pp. 1231-1238
Partitioning of Ni, Cu, and Pt-group elements (Ir, Rh, Pt, Pd) between
monosulfide solid solution (Mss) and sulfide liquid has been investig
ated in the Fe-Ni-Cu-S system at 1000 and 1100 degrees C and one atmos
phere pressure. The Nernst partition coefficients (D = wt% in Mss/wt%
in sulfide liquid) for Ni vary significantly from 0.19 to 1.17, while
the values of D-Cu show a limited range of 0.17-0.27. The partition co
efficients for Ir range from 1.06 to 13. Rhodium has a partition coeff
icient slightly lower than that of Ir under the same conditions, rangi
ng from 0.37 to 8.23. The partition coefficients for Pt and Pd vary fr
om 0.05 to 0.16, and from 0.08 to 0.27, respectively. The partition co
efficients depend strongly on the bulk S contents of the system. They
increase with increasing S contents in both Mss and liquid. Platinum,
Pd, and Cu behave incompatibly during Mss crystallization, strongly pa
rtitioning into sulfide liquid. Nickel is incompatible in S-undersatur
ated systems and S-saturated systems. It becomes compatible when the s
ystem is S-oversaturated, Rhodium is compatible in S-saturated and S-o
versaturated systems, but incompatible in S-undersaturated systems. Ir
idium changes from highly compatible through moderately compatible to
slightly compatible when the system changes from S-oversaturated throu
gh S-saturated to S-undersaturated. The effect of temperature on metal
partitioning is observed only in S-oversaturated systems, in which th
e partition coefficients for Ni and Rh increase with decrease of tempe
rature. The compatible behavior of Ir and Ph, and incompatible behavio
r of Pt and Pd and Cu under S-saturated conditions appears to support
the hypothesis that the observed metal zonation in many sulfide ore de
posits such as Sudbury, Ontario and Noril'sk, Siberia resulted from su
lfide liquid fractionation.