Fate of H(2) in an Upflow Single-Chamber Microbial Electrolysis Cell Using a Metal-Catalyst-Free Cathode. Environmental science & technology [Environ Sci Technol] Journal article

With the goal of maximizing the H(2)-harvesting efficiency, we designed an upflow single-chamber microbial electrolysis cell (MEC) by placing the cathode on the top of the MEC and carried out a program to track the fate of H(2) and electron equivalents in batch experiments. When the initial acetate concentration was 10 mM in batch-evaluation experiments lasting 32 h, the cathodic conversion efficiency (CCE) from coulombs (i.e., electron equivalents in current from the anode to the cathode) to H(2) was 98 +/- 2%, the Coulombic efficiency (CE) was 60 +/- 1%, the H(2) yield was 59 +/- 2%, and methane production was negligible. However, longer batch reaction time ( approximately 7 days) associated with higher initial acetate concentrations (30 or 80 mM) led to significant H(2) loss due to CH(4) accumulation: up to 14 +/- 1% and 16 +/- 2% of the biogas at 30 and 80 mM of acetate, respectively. Quantitative PCR proved that no acetoclastic methanogens were present, but that hydrogenotrophic methanogens (i.e., Methanobacteriales) were present on both electrodes. The hydrogenotrophic methanogens decreased the CCE by diverting H(2) generated at the cathode to CH(4) in the upflow single-chamber MEC. In some experiments, the CE was greater than 100%. The cause was anode-respiring bacteria oxidizing H(2) and producing current, which recycled H(2) between the cathode and the anodes, increasing CE to over 100%, but with a concomitant decline in CCE, despite negligible CH(4) formation.

Environmental science & technology [Environ Sci Technol]