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Journal ArticleDOI

Partitioning of molybdenum between magnetite and melt; a preliminary experimental study of partitioning of ore metals between silicic magmas and crystalline phases

R. C. Tacker, +1 more
- 01 Nov 1987 - 
- Vol. 82, Iss: 7, pp 1827-1838
TLDR
In this article, the Nernst partition coefficients of molybdenum between magnetite and two rhyolitic melts have been determined at 800 degrees C, 1 kb of pressure, and at two oxygen fugacities.
Abstract
The partitioning of molybdenum between magnetite (mt) and two rhyolitic melts has been determined at 800 degrees C, 1 kb of pressure, and at two oxygen fugacities. At an oxygen fugacity one-half a log unit above nickel-nickel oxide, D (super mt/melt) Mo = 0.21 + or - 0.08. A decrease in the oxygen fugacity to the graphite-methane buffer is accompanied by an increase in D (super mt/melt) Mo to 0.52 + or - 0.13. The differences in melt composition have no discernible effect.These data are interpreted by writing balanced chemical potential relationships involving independently variable phase components. The Nernst partition coefficients given above are then formulated as a function of these equilibria. Given the observed variation in D (super mt/melt) Mo with oxygen fugacity, and assuming that Fe 2 MoO 4 is the molybdenum-bearing phase component in magnetite, our data suggest that Mo(III) may be present in naturally occurring silicic magmas. Further, we suggest the establishment of critical bulk partition coefficients for ore-forming systems, defined in terms of critical values of the efficiency of removal function defined by Candela and Holland (1986). These preliminary results indicate that the crystallization of ferromagnesian or titanium-bearing phases may be important in reducing the amount of molybdenum available for orthomagmatic-hydrothermal ore formation. Oxygen fugacity may play a large role in the melt-crystal-vapor equilibria ofmolybdenum under magmatic conditions.

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Journal ArticleDOI

The chemistry of hydrothermal magnetite: A review

TL;DR: The most important factors that govern compositional variations in hydrothermal magnetite are (A) temperature, (B) fluid composition, (C) oxygen and sulfur fugacity, (D) silicate and sulfide activity, (E) host rock buffering, (F) reequilibration processes, and (G) intrinsic crystallographic controls such as ionic radius and charge balance as mentioned in this paper.
Journal ArticleDOI

The role of magma sources, oxidation states and fractionation in determining the granite metallogeny of eastern Australia

TL;DR: In this article, the authors found that the ore-element associations of granite-related ore deposits in the eastern Australian Palaeozoic fold belts can be related to the inferred relative oxidation state, halogen content and degree of fractional crystallisation within the associated granite suites.
Book ChapterDOI

Controls on ore metal ratios in granite-related ore systems: an experimental and computational approach

TL;DR: The size and composition (bulk metal ratios) of magmatic hydrothermal mineral deposits are affected by a number of chemical and physical processes including the nature of the source region and mode of emplacement as mentioned in this paper.
Journal ArticleDOI

Exsolution of magmatic volatile phases from Cl-enriched mineralizing granitic magmas and implications for ore metal transport

TL;DR: In this article, the solubility behavior of H2O and Cl is very similar to that of CO2 and H 2O in felsic liquids, and experiments were conducted to determine the Solubility of NaCl, KCl, and H2Os in felic liquids at 0.5 and 2 kbar.
Journal ArticleDOI

Apatite trace element and halogen compositions as petrogenetic-metallogenic indicators: Examples from four granite plutons in the Sanjiang region, SW China

TL;DR: In this article, the abundances of trace elements including Sr, Ga and rare earth elements (REE) and halogens in apatite crystals from four intermediate-felsic plutons in the Zhongdian terrane in the Sanjiang region have been determined using electron microprobe and laser ablation inductively coupled plasma mass spectrometry to evaluate the potential of APatite as a petrogenic-metallogenic indicator.
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