• journal_title：American Mineralogist
• Contributor：Yi-Gang Zhang ; John D. Frantz
• Publisher：Mineralogical Society of America
• Date：2000-
• Format：text/html
• Language：en
• journal_abbrev：American Mineralogist
• issn：0003-004X
• volume：85
• issue：7-8
• firstpage：918
• section：Articles

The compositions of aqueous fluids in equilibrium with enstatite + forsterite were investigated at temperatures from 900 to 1200 °C and pressures from 1.0 to 2.0 GPa. Experiments, performed in a piston-cylinder apparatus, involved the location of phase boundaries between the stability fields of enstatite and enstatite + forsterite, and enstatite + forsterite and forsterite. The intersection of these two phase-boundaries near the H₂O apex was used to define the fluid composition. The results indicated a systematic increase in the concentration of silica in the fluid phase with increasing temperature. The experiments indicated that the concentration of dissolved MgO was below 0.3 mol% and not resolvable using our techniques. This finding was corroborated by microprobe analyses of quench precipitates from the fluid phase, which gave on average 0.2 mol% MgO. Because of the low MgO concentrations, the mean values of the intercepts with SiO₂-H₂O binary of the fitted lines representing, respectively, the phase boundaries between the enstatite and enstatite + forsterite and between the enstatite + forsterite and forsterite stability fields were taken to represent the concentrations of dissolved silica at the various temperatures and pressures of the present study. The concentrations increased from 0.6 mol% at 900 °C to 3.9 mol% at 1200 °C at 1.0 GPa. The pressure effect from 1.0 to 2.0 GPa at 1000 °C appeared to be minor and not resolvable using our techniques. At 1.0 GPa, the base 10 logarithm of the molal concentration of dissolved silica in equilibrium with enstatite + forsterite was obtained combining data from the present study with those from Nakamura and Kushiro (1978) and Manning and Boettcher (1994):

Comparison with studies of the solubility of quartz (Manning 1994) indicated that thermodynamic properties of aqueous silica derived from silica-saturated systems may not be applicable to calculations in silica-deficient systems at high pressure.