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Journal Article

An amperometric microsensor for the determination of H2S in aquatic environments

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Kühl,  Michael
Permanent Research Group Microsensor, Max Planck Institute for Marine Microbiology, Max Planck Society;

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Citation

Jeroschewski, P., Steuckart, C., & Kühl, M. (1996). An amperometric microsensor for the determination of H2S in aquatic environments. Analytical Chemistry, 68(24), 4351-4357. doi:10.1021/ac960091b.


Cite as: https://hdl.handle.net/21.11116/0000-0005-0A0D-3
Abstract
A new amperometric microsensor for detection of dissolved H2S in aquatic environments was developed. The design of the microsensor is based on the same principle as the Clark-type oxygen microsensor. The sensor is equipped with a glass-coated platinum working electrode and a platinum guard electrode positioned in an outer glass casing (tip diameter 20-100 mu m). Both working electrode and guard electrode were polarized at a fixed value in the range from +85 to +150 mV with respect to a counter electrode. The outer casing is sealed with a thin silicone membrane and filled with a buffered electrolyte solution containing ferricyanide (K-3[Fe(CN)(6)]) as redox mediator. Hydrogen sulfide penetrates the silicone membrane and is oxidized by K-3[Fe(CN)(6)], resulting in the formation of elemental sulfur and ferrocyanide (K-4-[Fe(CN)(6)]). The latter is electrochemically reoxidized at the exposed end of the platinum working electrode, thereby creating a current that is directly proportional to the dissolved H2S concentration at the sensor tip. The sensor was characterized and calibrated in a flow-through cell combined with a coulometric sulfide generator. Difficult studies including the determination of H2S with high spatial and temporal resolution seem to be possible.