Magnetite solubility and iron transport in magmatic-hydrothermal environments

Details Magnetite solubility and iron transport in magmatic-hydrothermal environments Magnetite solubility and iron transport in magmatic-hydrothermal environments

Dec 2004

adsabs.harvard.edu/cgi-bin/nph-data_query?bibcode=2004gecoa..68.4905s&link_type=abstract

Geochimica et Cosmochimica Acta, Volume 68, Issue 23, p. 4905-4914.

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We have examined the effect of pressure on the apparent equilibrium constant, K′, for magnetite solubility (Fe3O4mt + 6HClfluid + H2fluid = 3FeCl2fluid + 4H2Ofluid) and the relative iron-carrying capacities of magmatic vapor and brine by conducting experiments in a rhyolite melt-vapor-brine-magnetite system at 800°C, fO2 = NNO and pressures ranging from 100 to 145 MPa. Iron concentrations in synthetic vapor and brine fluid inclusions were quantified by using laser-ablation inductively-coupled-plasma-mass-spectrometry (LA-ICPMS). Hydrogen chloride (HCl) concentrations in magmatic vapor were inferred by potentiometric measurements of H+ in quenched run product fluids. These data yield calculated values for log K′, assuming aH2O = XH2O, of 1.7, 4.9, 6.2, 6.8 and 9.1 at 100, 110, 130, 140 and 145 MPa, respectively. The concentration of iron in magmatic vapor increases by an order of magnitude, whereas the concentration of iron in magmatic brine remains constant (within 1σ) with increasing pressure as the 800°C critical pressure is approached along the vapor-brine solvus. The concentrations of iron in vapor and brine fluid inclusions yield calculated partition coefficients (DFev/b) of 0.05, 0.14, 0.27 and 0.56 at 110, 130, 140 and 145 MPa, respectively. Our data reveal that pressure fluctuations may significantly affect the value of log K′. More importantly, the data demonstrate conclusively that a significant amount of iron can be transported by a low-density aqueous vapor in the magmatic-hydrothermal environment.

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