EXPERIMENTAL SIMULATION OF ALKALINE SEAFLOOR HYDROTHERMAL SYSTEMS
Brine-rock reaction decreases pH from 7.4 to ~5, consumes ~50 mMol of aqueous magnesium and nearly all of the aqueous sodium and potassium. Approximately 2 to 4 mol percent CO2 was injected into these experiments after achieving steady-state. Calcium concentrations decrease (~1 to 2 mMol) following CO2 injection, whereas magnesium concentrations rebound (~1 mMol), as do the silica concentrations (3 to 7 mMol), both likely a result of increased brine acidity. Significant dissolution of olivine and pyroxenes occurred, as shown by surface pits and etching. The powdered solid reactants have been extensively serpentinized, and mineral fragments developed serpentine overgrowths. Needle-like laths of calcium sulfate and rhombs of magnesium carbonate were extensively precipitated on the reactants and the inner surfaces of the reaction cell. The experiments experienced a gradual pressure decrease following CO2 injection (27 bars); this pressure decrease is a result of dissolution and mineralization of CO2.
These reactions provide initial constraints as to the extent and rate of reactions occurring in alkaline hydrothermal systems. Additionally, the extensive formation of magnesium carbonate minerals indicates that direct injection of CO2 into magnesium silicate rich terranes, as such peridotite hosted hydrothermal systems, may be a viable means of sequestering anthropogenic CO2.