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A rocking multianvil: elimination of chemical segregation in fluid-saturated high-pressure experiments
Authors:Max W Schmidt  Peter Ulmer
Institution:1 Institute for Mineralogy and Petrology, ETH Zentrum, CH 8092 Zurich, Switzerland
Abstract:Fluid saturated high-pressure experiments often result in strongly zoned experimental charges, this hinders experimentation in chemically homogeneous systems which in turn has serious consequences on equilibration, reaction progress, and (apparent) phase stabilities. In order to overcome these problems, a 600-ton press accommodating either a multianvil or end-loaded piston cylinder module has been mounted in such a way that it can be turned by 180°, thus inverting its position in the gravity field. During turning, hydraulic pressure, heating power, and cooling water remain connected allowing fully controlled pressures and temperatures during experiments.A series of experiments at 13 GPa, 950°C, on a serpentine bulk composition in the MgO-SiO2-H2O system demonstrates that continuous turning at a rate of 2 turns/min results in a nearly homogeneous charge composed of phase E + enstatite. The same experiment at static conditions resulted in four mineral zones: quench phase E, enstatite, enstatite + phase E, and phase E + phase A. Phase A disappears in experiments at a turning rate ≥1 turn/min. A static 15-min experiment shows that zonation already forms within this short time span. Placing two short capsules within a single static experiment reveals that the fluid migrates to the hot spot in each capsule and is not gravitationally driven toward the top. The zonation pattern follows isotherms within the capsule, and the degree of zonation increases with temperature gradient (measured as 10 °C within a capsule) and run time.Our preferred interpretation is that Soret diffusion causes a density-stratified fluid within the capsule that does not convect in a static experiment and results in temperature dependant chemical zonation. The aggravation of zonation and appearance of additional phases with run time can be explained with a dissolution-reprecipitation process where the cold spot of the capsule is relatively MgO enriched and the hot spot relatively SiO2 and H2O enriched (at 13 GPa and 950°C). Rocking and tilting of a stratified fluid induces Rayleigh-Taylor instabilities, causing chemical rehomogenization. If turning is faster than the time required to build significant chemical potential gradients in the fluid, chemical zonation in the distribution of the solids is suppressed.
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