Gold partitioning in melt-vapor-brine systems

被引:122
作者
Simon, AC
Frank, MR
Pettke, T
Candela, PA
Piccoli, PM
Heinrich, CA
机构
[1] Univ Maryland, Dept Geol, Lab Mineral Deposits Res, College Pk, MD 20742 USA
[2] No Illinois Univ, Dept Geol & Environm Geosci, De Kalb, IL 60115 USA
[3] ETH Zentrum NO, Fed Inst Technol, CH-8092 Zurich, Switzerland
基金
美国国家科学基金会;
关键词
D O I
10.1016/j.gca.2005.01.028
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
We used laser-ablation inductively coupled plasma mass spectrometry to measure the solubility of gold in synthetic sulfur-free vapor and brine fluid inclusions in a vapor + brine + haplogranite + magnetite + gold metal assemblage. Experiments were conducted at 800 degrees C, oxygen fugacity buffered at Ni-NiO (NNO), and pressures ranging from 110 to 145 MPa. The wt% NaCl eq. of vapor increases from 2.3 to 19 and that of brine decreases from 57 to 35 with increasing pressure. The composition of the vapors and brines are dominated by NaCl + KCl + FeCl2 + H2O. Gold concentrations in vapor and brine decrease from 36 to 5 and 50 to 28 mu g/g, respectively, and the calculated vapor:brine partition coefficients for gold decrease from 0.72 to 0.17 as pressure decreases from 145 to 110 MPa. These data are consistent with the thermodynamic boundary condition that the concentration of gold in the vapor and brine must approach a common value as the critical pressure is approached along the 800 degrees C isotherm in the NaCl-KCI-FeCl2-HCl-H2O system. We use the equilibrium constant for gold dissolution as AuOHO, extrapolated from lower temperature and overlapping pressure range, to calculate expected concentrations of AuOHO in our experimental vapors. These calculations suggest that a significant quantity of gold in our experimental vapors is present as a non-hydroxide species. Possible chloridogold(I) species are hypothesized based on the positively correlated gold and chloride concentrations in our experimental vapors. The absolute concentration of gold in our synthetic vapor, brine, and melt and calculated mass partition coefficients for gold between these physicochemically distinct magmatic phases suggests that gold solubility in aqueous fluids is a function of aqueous phase salinity, specifically total chloride concentration, at magmatic conditions. However, though we highlight here the effect of salinity, the combination of our data with data sets from lower temperatures evinces a significant decrease in gold solubility as temperature drops from 800 degrees C to 600 degrees C. This decrease in solubility has implications for gold deposition from ascending magmatic fluids. Copyright (C) 2005 Elsevier Ltd.
引用
收藏
页码:3321 / 3335
页数:15
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