Selective inhibition of methanogenesis by acetylene in single chamber microbial electrolysis cells

•1–5% acetylene can effectively inhibit methanogens in single chamber MECs.•Acetylene didn’t reduce the exoelectrogenic activity in the MECs fed with acetate.•Acetylene didn’t reduce the current generation in the MECs fed with glucose.•Acetylene can be used as a selective inhibitor against methanoge...

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Veröffentlicht in:Bioresource technology 2019-02, Vol.274 (C), p.557-560
Hauptverfasser: Wang, Luguang, Trujillo, Stephanie, Liu, Hong
Format: Artikel
Sprache:eng
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Zusammenfassung:•1–5% acetylene can effectively inhibit methanogens in single chamber MECs.•Acetylene didn’t reduce the exoelectrogenic activity in the MECs fed with acetate.•Acetylene didn’t reduce the current generation in the MECs fed with glucose.•Acetylene can be used as a selective inhibitor against methanogens in MECs. Microbial electrolysis cells (MECs) for hydrogen production exhibit great advantages over many other biohydrogen production techniques in terms of versatility of substrate and hydrogen yield. However, hydrogen and acetate scavenging by methanogens puts forward a great challenge to the application of single chamber MECs when using mixed culture. In this study, we investigated the feasibility of using acetylene, a low-cost fuel and chemical building block, to selectively inhibit methanogenesis in single chamber MECs. Results demonstrate that the periodical injection of low concentration acetylene (1% and 5%) can successfully inhibit methanogenesis in MECs using both acetate and glucose as substrates. Current generation by exoelectrogens and the syntrophy between fermentative bacteria and exoelectrogens, however, were not negatively affected. Compared with the classic methanogen inhibitor, 2-Bromoethanesulfonate (BES), the low concentration acetylene demonstrates superior effectiveness in MECs. These results demonstrate the great potential of using acetylene as a cost-effective inhibitor against methanogenesis in MECs.
ISSN:0960-8524
1873-2976
DOI:10.1016/j.biortech.2018.12.039