Mechanism of silicate elution by hydrogen sulfide from bottom sediment in a brackish lake

Abstract

Highly concentrated dissolved silicate was detected in pore water from anoxic-reducing sediment in Lake Nakaumi, a brackish lake. Silicate concentration also simultaneously increased with total hydrogen sulfide concentration during the summer. Generally, dissolved silicate is readily adsorbed onto ferric hydroxide and precipitates in an oxidative environment. In this study, we focused on the behavior of ferric hydroxide adsorbing silicate in sediment and determined that hydrogen sulfide was the main cause of dissolved silicate elution from ferric hydroxide adsorbing silicate because the hydrogen sulfide produced via microbiological processes in the anoxic-reducing environment was reducible for other metal oxides. According to laboratory experiments, silicate was released from ferric hydroxide by reacting with sodium sulfide, causing increasing elution of dissolved silicate from anoxic-reducing sediments with increasing concentration of sodium sulfide in the solutions. This result shows that hydrogen sulfide is very crucial for silicate release under a reducing environment. Therefore, in Lake Nakaumi, silicate would be released from the bottom after ferric hydroxide adsorbing silicate reacted with hydrogen sulfide in a summer reductive environment.

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“…So, accurate measurement of silicate is of great significance. [29] At present, the main methods for the determination of silicates in water are spectrophotometry, [30][31][32] voltammetry, [33] etc., but these methods are complex, timeconsuming and costly, which severely limits the real-time monitoring of silicate in water environment.…”