Abstract

Base metal exchange reactions between magnetite and a supercritical aqueous chloride solution have been experimentally calibrated at T = 600 to 800°C, P = 2 kb, and total chloride = 2.06 M. The results are expressed as the distribution coefficients Kd MFe= (X MX Fe ) fl (X MX Fe ) s , where fl and s represent the fluid and the solid solution, respectively, and X M= m M (m M + m Fe total (m M + m Fe total ) are the mole fractions of the metal of interest and of total Fe, respectively. The experimentally determined distribution coefficients are Kd MnFe = 64, 33, and 18, and Kd ZnFe=161, 87, and 53, at T=600, 700, and 800°C, respectively. Linear regression yields the best fit equations: ln Kd ZnFe = 5198/ T(K) − 0.872 ( r 2 = 0.9999) and ln Kd MnFe = 5941/ T(K) − 2.63 ( r 2 = 0.9995). Kd values were independent of composition over the range of concentrations investigated. Clearly, both Mn and Zn are strongly fractionated into the fluid with respect to Fe. A combination of Kd MnFe and Kd ZnFe yields Kd ZnMn = 2.54, 2.67, and 2.94 at 600, 700, and 800°C, where Kd = (X Zn X Mn ) fl / (X Zn X Fe ) s . The partitioning and temperature dependence described by Kd ZnMn are significantly weaker than those shown by Kd MnFe and Kd ZnFe. Results for the CdFe and CuFe exchange reactions indicate that both Cd and Cu are extremely partitioned into the fluid with respect to Fe and very strongly partitioned into the fluid with respect to Zn and Mn. The experimental results suggest that even minor to trace concentrations of these base metals in natural magnetites indicate strong enrichment of Zn, Mn, Cu, and Cd relative to Fe in chloride-rich hydrothermal fluids. In particular, Kd MnFe was applied to magnetites from skarn deposits. Calculations at 360 to 420°C suggest that skarn fluids in equilibrium with magnetites containing only minor concentrations of Mn can have Mn/Fe ratios greater than 1.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.