Oxygen solubility and speciation in sulphide-rich mattes

• Published in: Geochimica et cosmochimica acta 2008-06, Vol.72 (11), p.2619-2635
• Main Authors: Fonseca, Raúl O.C., Campbell, Ian H., O’Neill, Hugh St.C., Fitzgerald, John D.
• Format: Article
• Language: English
• ISSN: 0016-7037; 1872-9533
• DOI: 10.1016/j.gca.2008.03.009

Sulphide-rich liquids are common in magmatic environments forming over a wide range of temperature, pressure, fO 2 and fS 2. They are economically important because they sequester valuable metals such as Cu, Ni, Au and Pt from silicate melts. The presence of accessory amounts of primary oxides associated with sulphide mineralisations is often ignored or unexplained. Experimental work has shown that large amounts of oxygen can dissolve into mattes at fO 2 typical of terrestrial environments. At the quartz–fayalite–magnetite fO 2 buffer, the molar fraction of O in the matte exceeds that of S, placing the composition of the matte to the magnetite side of the mss (monosulphide solid solution)–magnetite join in the Fe–S–O system. However, sulphides crystallise before magnetite in most sulphide mineralisations and are much more abundant. Moreover, the speciation of O in a matte is not well known. Here we report the results of an experimental study of the solubility of O in mattes as a function of fS 2, fO 2, temperature, and composition. We confirm previous observations that Ni and Cu have a negative effect on the solubility of O in mattes. We show evidence for the existence of FeSO as a structural constituent of mattes in the Fe–S–O system. We present a simple parameterisation of the amount of O dissolved in mattes under relevant geological conditions, and use this parameterisation to discuss mechanisms for the crystallisation of primary spinels associated with sulphides in the Kambalda massive sulphide deposit (Western Australia) and the Sudbury Igneous Complex (Ontario, Canada).