Attainment of solution and gas equilibrium in Japanese geothermal systems

The geothermal fluids in seven Japanese geothermal systems are tested for attainment of aqueous and gaseous equilibrium. The pH of fluids in the geothermal reservoir is approximately buffered by the assemblage K-feldspar—K-mica—quartz. (Na ^f)/(K⁺) and (Na⁺)/ V(Ca³⁺) activity ratios are ther-modynamically approximated by reactions between albite and K-feldspar, and between albite and anor-thite (or Ca-zeolites), respectively. The (Mg²⁺)/(K⁺)²activity ratio of high temperature geothermal fluids of Japan can be represented, by the reaction involving Mg-chlorite and K-bearing silicate minerals, though at lower temperatures other reactions may be responsible. The geothermal fluids are also com-monly saturated with respect to anhydrite and calcite. A small amount of steam loss in the reservoir does not significantly affect the aqueous composition of the fluids. The partial pressure of C0₂is controlled by the reaction involving calcite, K-bearing silicate minerals, and albite or Ca-zeolite in geothermal systems which are not affected by steam loss and dilution. Equilibrium between CH₄, C0₂and H₂ is at-tained at high temperatures but not maintained to lower temperatures in most Japanese geothermal systems. The H₂/H₂S ratio is probably equilibrated with Fe-bearing minerals. Gaseous compositions are very good indicators to identify processes in the geothermal reservoir, such as boiling and dilution. Last-ly, the major aqueous composition and pH of Japanese neutral Na-Cl type geothermal fluid are predic-table if two variables (e.g., temperature and one of the cation activities) are provided.