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Titel Preferential partitioning of copper into the vapor phase: fact or a natural artifact?
VerfasserIn Linda Lerchbaumer, Andreas Audétat
Konferenz EGU General Assembly 2011
Medientyp Artikel
Sprache Englisch
Digitales Dokument PDF
Erschienen In: GRA - Volume 13 (2011)
Datensatznummer 250056193
 
Zusammenfassung
Studies on natural assemblages of coexisting vapor and brine inclusions revealed that copper (±Â Au, As, B, Mo) commonly occurs in higher concentrations in the vapor phase than in the brine. It is believed that this is due to the formation of stable hydrosulfide-bearing complexes in the vapor phase, a theory that is supported by experiments proving the existence of copper-hydrosulfide complexes, experiments noting an increase in the vapor/brine partition coefficients of Cu (DCuvap-ˆ•brine) with increasing sulfur content of the fluid, and observations showing that in natural boiling assemblages DCuvap-ˆ•brine correlates positively with DSvap-ˆ•brine. On the other hand, none of the experimental studies conducted so far has succeeded in reproducing conditions under which copper clearly fractionates into the vapor phase (i.e., DCuvap-ˆ•brine >1). An exception seemed to be the study of Nagaseki and Hayashi (2008) who claimed to have obtained DCuvap-ˆ•brine values up to 30. However, mass balance constraints and results of experiments performed at identical conditions in our laboratory suggest that these values are wrong and in fact are below unity. In view of recent experimental studies demonstrating that quartz-hosted fluid inclusions can diffusively loose or gain copper after their formation we wanted to check whether such a process could also lead to artificially high vapor/brine partition coefficients. For this purpose we synthesized vapor and brine inclusions from a Cu2S-saturated H2O-NaCl-S fluid at 800 ˚ C / 1.3 kbar and re-equilibrated them in a second experiment with similar fluid at 800 ˚ C / 700 bar. After each step some of the inclusions were analyzed by LA-ICP-MS. Although the Au capsule featured a leak after the second experiment, the result is quite spectacular: while vapor and brine inclusions analyzed after the first step contained only 250 ppm Cu (n=1) and 530 ±Â 150 ppm Cu (n=8), respectively, vapor and brine inclusions analyzed after re-equilibration contained 5.1 ±Â 3.2 wt% Cu (n=7) and 0.4 ±Â 0.2 wt% Cu (n=7), respectively. Results of subsequent experiments suggest that copper in these inclusions was gained in response to a change in pH, which changed from