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Journal of Environmental Science and Health, Part A
Toxic/Hazardous Substances and Environmental Engineering
Volume 54, 2019 - Issue 14
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Articles

Simultaneous removal of hydrogen sulfide and ammonia using a combined system with absorption and electrochemical oxidation

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Pages 1430-1440 | Received 30 Apr 2019, Accepted 29 Jul 2019, Published online: 18 Aug 2019
 

Abstract

Hydrogen sulfide (H2S) and ammonia (NH3), common impurities in biogas, need to be removed before utilizing it. In this study, a combined system, which consisted of an absorption column and an electrochemical oxidation reactor, was tested to simultaneously remove these impurities. The effects of the current density and the chemical loading rate on the system performance were investigated. Firstly, the mass transfer coefficients for the absorption column were determined at various gas flow rates. More mass of NH3 was transferred, compared with that of H2S, because of its higher solubility. In the electro-oxidation reactor, reactive chlorine species (RCSs) were generated and oxidized both H2S and NH3; however, NH3 started to degrade only after H2S was completely eliminated. At a current density of 400 A/m2, the current efficiencies of H2S and NH3 were 23.1% and 5.9%, respectively. In the combined system, the removal efficiency of H2S was closely related to the mass ratio of the H2S transferred and the RCSs generated. The removal efficiency of H2S was greater than 99% when the ratio was less than 1. The mass transfer potential and the oxidation kinetics should be balanced to improve the system performance for the simultaneous removal of H2S and NH3.

Additional information

Funding

This work was supported by Korea Environment Industry & Technology Institute (KEITI) through Public Technology Program based on Environmental Policy Program, funded by Korea Ministry of Environment (MOE) (2017000700002). It was also supported by the Technology Development Program to Solve Climate Changes of the Korean National Research Foundation (NRF) funded by Korean Ministry of Science, ICT (2017M1A2A2086642).

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