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GeoRef Categories
Era and Period
Book Series
Date
Availability
Crystal chemistry of tetrahedrite Available to Purchase
Sphalerite compositional variations in sulfide ores of the Norwegian Caledonides Available to Purchase
Reconnaissance of the Cu-Fe-Zn-S system; sphalerite phase relationships Available to Purchase
Ore mineralogy of the Great Gossan Lead, Virginia Available to Purchase
Phase relations in the Cu-Co-S system and mineral associations of the carrollite (CuCo 2 S 4 )-linnaeite (Co 3 S 4 ) series Available to Purchase
Sulfidation of synthetic biotites Available to Purchase
Cobalt-bearing sulfide assemblages from the Shinkolobwe Deposit, Katanga, Zaire Available to Purchase
Fletcherite, Cu(Ni,Co) 2 S 4 , a new thiospinel from the Viburnum Trend (New Lead Belt), Missouri Available to Purchase
Stability of Fe-Mg amphiboles with respect to oxygen fugacity Available to Purchase
Stability of Fe-Mg amphiboles with respect to sulfur fugacity Available to Purchase
Synthesis and X-ray properties of Fe-Mg orthoamphiboles Available to Purchase
Orientation of exsolved pentlandite in natural and synthetic nickeliferous pyrrhotite Available to Purchase
Pyrrhotite; the nA (or 2A, 3C) superstructure reviewed Available to Purchase
Sulfide mineralogy of metamorphosed ultramafic rocks, western Sierra Nevada foothills, California Available to Purchase
Phase Relations in the Cu-Fe-Ni-S System and Their Application to Magmatic Ore Deposits Available to Purchase
Abstract The phase relations in the Cu-Fe-Ni-S system are discussed in the light of experimental results from liquidus temperatures to below 550° C. Although liquidus temperatures vary greatly throughout the system, beginning of melting of a typical ore composition (1.5% Cu, 4.5% Ni, 38.5% S, 55.5% Fe) was found to occur at 1,105° C. Magnetite lowers the beginning-of-melting temperature to 1,019° C. In contrast, water influences the beginning-of-melting temperature by less than 20° C. Under conditions encountered in typical massive Ni-Cu sulfides fractionation leading to formation of a Cu-enriched liquid is possible only above 850° C. Ni enrichment in a liquid phase is not encountered below 1,000° C except under sulfur pressure conditions much lower than those encountered in typical Ni-Cu ores. The bulk compositions of Ni-Cu sulfide ores commonly lie within the confines of a quaternary monosulfide solid solution at temperatures above 500° C. This suggests that such ores formed a homogenous phase at the time of their emplacement. Cooling below 600° C may result in exsolution of chalcopyrite and/or pyrite or chalcopyrite and/or pentlandite depending on sulfur pressure. The commonly observed pentlandite +pyrite assemblage is stable only well below 300° C and cannot crystallize directly from a Cu-Fe-Ni sulfide melt. The absence of natural analogues even of a ternary (Fe,Ni) 1–x S monosulfide solid solution and the frequent occurrence of monoclinic pyrrhotite and the pyrite + pentlandite assemblage indicate low-temperature reequilibration of mineral assemblages and mineral compositions subsequent to original emplacement which may have occurred at or near liquidus temperatures. Such reequilibration negates usage of the pyrrhotite-pyrite geothermometer in magmatic Ni-Cu ores. The present study offers a new view of the paragenesis of Ni-Cu ores and demonstrates that the observed mineral assemblages may be explained in terms of phase changes occurring in a system of isochemical bulk composition in response to decreasing temperature.