Rapid start-up of a bioelectrochemical system under alkaline and saline conditions for efficient oxalate removal

•A bioelectrochemical system (BES) was successfully started up for oxalate removal.•Aerobic oxalotrophic biofilm pre-grown on graphite granules was used as inoculum.•The biofilm could rapidly switch from using oxygen to graphite as electron acceptor.•Highest coulombic efficiency (>70%) for anodic...

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Veröffentlicht in:Bioresource technology 2018-02, Vol.250, p.317-327
Hauptverfasser: Weerasinghe Mohottige, Tharanga N., Ginige, Maneesha P., Kaksonen, Anna H., Sarukkalige, Ranjan, Cheng, Ka Yu
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Sprache:eng
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Zusammenfassung:•A bioelectrochemical system (BES) was successfully started up for oxalate removal.•Aerobic oxalotrophic biofilm pre-grown on graphite granules was used as inoculum.•The biofilm could rapidly switch from using oxygen to graphite as electron acceptor.•Highest coulombic efficiency (>70%) for anodic oxalate oxidation in the literature.•Oxalobacteraceae strains became abundant signifying their role in the BES process. This study examined a new approach for starting up a bioelectrochemical system (BES) for oxalate removal from an alkaline (pH > 12) and saline (NaCl 25 g/L) liquor. An oxalotrophic biofilm pre-grown aerobically onto granular graphite carriers was used directly as both the microbial inoculum and the BES anode. At anode potential of +200 mV (Ag/AgCl) the biofilm readily switched from using oxygen to graphite as sole electron acceptor for oxalate oxidation. BES performance was characterised at various hydraulic retention times (HRTs, 3–24 h), anode potentials (−600 to +200 mV vs. Ag/AgCl) and influent oxalate (25 mM) to acetate (0–30 mM) ratios. Maximum current density recorded was 363 A/m3 at 3 h HRT with a high coulombic efficiency (CE) of 70%. The biofilm could concurrently degrade acetate and oxalate (CE 80%) without apparent preference towards acetate. Pyro-sequencing analysis revealed that known oxalate degraders Oxalobacteraceae became abundant signifying their role in this novel bioprocess.
ISSN:0960-8524
1873-2976
DOI:10.1016/j.biortech.2017.11.009