Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
4715069 | Journal of Volcanology and Geothermal Research | 2011 | 10 Pages |
The geochemistry and mineralization of H2S in the geothermal system hosted by basaltic rock formation at Hellisheidi, SW Iceland, was studied. Injection of mixtures of H2S with geothermal waste water and condensed steam into the > 230 °C geothermal aquifer is planned, where H2S will hopefully be removed in the form of sulphides. The natural H2S concentrations in the aquifer average 130 ppm. They are considered to be controlled by close approach to equilibrium with pyrite, pyrrhotite, prehnite and epidote. Injection of H2S will increase significantly the reservoir H2S equilibrium concentrations, resulting in mineralization of pyrite and possibly other sulphides as well as affecting the formation of prehnite and epidote. Based on reaction path modelling, the main factors affecting the H2S mineralization capacity are related to the mobility and oxidation state of iron. At temperatures above 250 °C the pyrite mineralization is greatly reduced upon epidote formation leading to the much greater basalt dissolution needed to sequestrate the H2S. Based on these findings, the optimum conditions for H2S injection are aquifers with temperatures below ~ 250 °C where epidote formation is insignificant. Moreover, the results suggest that sequestration of H2S into the geothermal system is feasible. The total flux of H2S from the Hellisheidi power plant is 12,950 tonnes yr− 1. Injection into 250 °C aquifers would result in dissolution of ~ 1000 tonnes yr− 1 of basalt for mineralization of H2S as pyrite, corresponding to ~ 320 m3 yr− 1.
Research highlights► The sequestration of H2S in geothermal systems was investigated. ► The sequestration of H2S is favorable at < 250 °C where iron is considered to quantitatively remove H2S into pyrites. ► The addition of H2S to geothermal fluids at 200–300 °C does not change the overall reaction path but affects the mass quantity of various secondary minerals.