Thermophilic sulphate and sulphite reduction in lab-scale gas-lift reactors using H(2) and CO(2) as energy and carbon source

Feasibility of thermophilic (55 degrees C) sulphate and sulphite reduction with H(2) and CO(2) gas-mixtures was studied in gas-lift reactors, which contained pumice particles as carrier material. Particular attention was paid to biomass retention and the competition between hydrogenotrophic sulphate...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Biotechnology and bioengineering 1997-09, Vol.55 (5), p.807-814
Hauptverfasser: van Houten, R T, Yun, S Y, Lettinga, G
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Feasibility of thermophilic (55 degrees C) sulphate and sulphite reduction with H(2) and CO(2) gas-mixtures was studied in gas-lift reactors, which contained pumice particles as carrier material. Particular attention was paid to biomass retention and the competition between hydrogenotrophic sulphate-reducers and other hydrogenotrophic thermophiles. A model medium with defined mineral nutrients was used.The results of the experiments clearly demonstrate that sulphate conversion rates up to 7.5 g SO(4) (2-)/L per day can be achieved. With sulphite, a reduction rate of 3.7 g S/L per day was obtained, which equals a sulphate conversion rate of 11.1 g SO(4) (2-)/L per day. Under the applied conditions, a strong competition for hydrogen between hydrogenotrophic sulphate-reducers, tentatively designated as Desulfotomaculum sp., and hydrogenotrophic methanogens was observed. The outcome of the competition could not be predicted. Growth of the mixed culture was totally inhibited at an H(2)S concentration of 250 mg/L. Poor attachment of sulphate-reducing bacteria was observed in all experiments. The biomass concentration did not exceed 1.2 g/L, despite the presence of 50 g/L of pumice. The reason for this phenomenon remains to be understood. (c) 1997 John Wiley & Sons, Inc. Biotechnol Bioeng 55: 807-814, 1997.
ISSN:0006-3592
DOI:10.1002/(SICI)1097-0290(19970905)55:5<807::AID-BIT11>3.0.CO;2-8