TY - JOUR
T1 - Designing, building and operating an up-scaled methane producing bioelectrochemical system for power-to-methane
AU - Brandão Lavender, Micaela
AU - Steller, Jos
AU - Liu, Dandan
AU - de Rink, Rieks
AU - Tofik, Shiba
AU - ter Heijne, Annemiek
PY - 2025/2/15
Y1 - 2025/2/15
N2 - A 17 L scale up methane producing bioelectrochemical system (BES) for power-to-gas application was built taking into account: (1) use of granular activated carbon as cathode material to provide a large surface area for the reaction to take place; (2) a commercially available tubular membrane separating the anaerobic cathodic reaction from the anodic oxygen production; (3) an hexagonal prism design that can be further up-scaled in modules, specially avoiding the hurdle of producing electrodes in non-commercially available sizes. The BES was operated for 470 days with step wise increase in applied current density between −6 and −125 A m−3BES, with resulting methane production rates between 10 NL m−3BES d−1 and 280 NL m−3BES d−1 and faradaic efficiency ranging between 80% and 100%. A stable performance was observed after a start-up period of around 70 days. Furthermore, changes in the electrolyte composition and anode dimensions were made in order to decrease losses associated to the electrolyte and anode reaction, respectively. The distribution of the voltage losses is assessed in this paper and for the majority of the experimental time the energy efficiency ranged around 40%, specifically when operating with an electrolyte with [Figure presented] / [Figure presented] carbonate/bicarbonate concentrations of 0.2 M, 0.4 M and 0.6 M and with an anode surface area equal to or larger than 0.02 m2. Besides the BES itself, the reactor line-up included a bubble column, an oxygen stripping unit and an interchange vessel, all of which essential for its operation.
AB - A 17 L scale up methane producing bioelectrochemical system (BES) for power-to-gas application was built taking into account: (1) use of granular activated carbon as cathode material to provide a large surface area for the reaction to take place; (2) a commercially available tubular membrane separating the anaerobic cathodic reaction from the anodic oxygen production; (3) an hexagonal prism design that can be further up-scaled in modules, specially avoiding the hurdle of producing electrodes in non-commercially available sizes. The BES was operated for 470 days with step wise increase in applied current density between −6 and −125 A m−3BES, with resulting methane production rates between 10 NL m−3BES d−1 and 280 NL m−3BES d−1 and faradaic efficiency ranging between 80% and 100%. A stable performance was observed after a start-up period of around 70 days. Furthermore, changes in the electrolyte composition and anode dimensions were made in order to decrease losses associated to the electrolyte and anode reaction, respectively. The distribution of the voltage losses is assessed in this paper and for the majority of the experimental time the energy efficiency ranged around 40%, specifically when operating with an electrolyte with [Figure presented] / [Figure presented] carbonate/bicarbonate concentrations of 0.2 M, 0.4 M and 0.6 M and with an anode surface area equal to or larger than 0.02 m2. Besides the BES itself, the reactor line-up included a bubble column, an oxygen stripping unit and an interchange vessel, all of which essential for its operation.
KW - Bioelectrochemical system
KW - Granular activated carbon
KW - Hexagonal prism shape
KW - Power-to-methane
KW - Scaling up
U2 - 10.1016/j.jpowsour.2024.236010
DO - 10.1016/j.jpowsour.2024.236010
M3 - Article
AN - SCOPUS:85211445812
SN - 0378-7753
VL - 629
JO - Journal of Power Sources
JF - Journal of Power Sources
M1 - 236010
ER -