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Effect of oxygen dosing point and mixing on the microaerobic removal of hydrogen sulphide in sludge digesters
► Microaerobic removal of H2S achieved an efficiency higher than 98%. ► Headspace was found the optimal dosing point. ► Dissolved sulphide was removed with biogas recirculation. ► The main result of H2S oxidation was S0, partly accumulated in the headspace. ► Sulphide-oxidising bacteria developed in...
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Published in: | Bioresource technology 2011-02, Vol.102 (4), p.3768-3775 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | ► Microaerobic removal of H2S achieved an efficiency higher than 98%. ► Headspace was found the optimal dosing point. ► Dissolved sulphide was removed with biogas recirculation. ► The main result of H2S oxidation was S0, partly accumulated in the headspace. ► Sulphide-oxidising bacteria developed in the headspace.
Limited oxygen supply to anaerobic sludge digesters to remove hydrogen sulphide from biogas was studied. Micro-oxygenation showed competitive performance to reduce considerably the additional equipment necessary to perform biogas desulphurization. Two pilot-plant digesters with an HRT of ∼20d were micro-oxygenated at a rate of 0.25 NL per L of feed sludge with a removal efficiency higher than 98%. The way of mixing (sludge or biogas recirculation) and the point of oxygen supply (headspace or liquid phase) played an important role on hydrogen sulphide oxidation. While micro-oxygenation with sludge recirculation removed only hydrogen sulphide from the biogas, dissolved sulphide was removed if micro-oxygenation was performed with biogas recirculation. Dosage in the headspace resulted in a more stable operation. The result of the hydrogen sulphide oxidation was mostly elemental sulphur, partially accumulated in the headspace of the digester, where different sulphide-oxidising bacteria were found. |
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ISSN: | 0960-8524 1873-2976 |
DOI: | 10.1016/j.biortech.2010.12.016 |