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An anodic syntrophic consortium (exoelectrogenic plus fermentative bacteria) able to use methanol as sole carbon source was developed for the first time in a bioelectrochemical system. In this frame, promising results were obtained in single chamber MFC, comparable to those obtained with readily biodegradable substrates. Regarding MEC operation, the presence of homoacetogenic bacteria led to electron recycling, avoiding net hydrogen production in single chamber MEC. In a double chamber MEC, satisfying results (in terms of coulombic efficiency and cathodic gas recovery) were obtained even though energy recovery still restrained the feasibility of the process. The approach used in this work with methanol opens a new range of possibilities for other complex substrates as electron donors for bioelectrosynthesis.

BACKGROUND The microbial fuel cell (MFC) technology transforms the chemical energy present in substrates into electricity. Starting-up these systems, i.e. enriching the anodic community in exoelectrogenic bacteria, is a lengthy process or requires expensive equipment. RESULTS An easy and low-cost procedure based on a sediment MFC was developed to select microbial communities with exoelectrogenic activity from the anaerobic sludge of a waste water treatment plant (WWTP). The configuration was based on a simple vessel working as a single chamber MFC with a cathode of stainless steel wool in the liquid surface and a submerged graphite fibre brush as anode. In 30 days of operation, a biofilm with remarkable exoelectrogenic activity was grown on the anode of the MFC. This graphite fibre brush anode was able to supply 0.9 W m-2 when working in an air-cathode MFC (AC-MFC) for 45 days. CONCLUSION The procedure presented was demonstrated to be a successful, low-cost and low-maintenance procedure to obtain exoelectrogenic activity and had performances comparable with other more costly and complex inoculation procedures. The Sed-MFC does not require a potentiostat, external aeration, stirring, membranes or an enriched inoculum in the exoelectrogenic biomass. © 2013 Society of Chemical Industry

Nickel foam (NF), stainless steel wool (SSW), platinum coated stainless steel mesh (Pt), and molybdenum disulfide coated stainless steel mesh (MoS2) electrodes have been proposed as catalysts for hydrogen gas production, but previous tests have primarily examined their performance in well buffered solutions. These materials were compared using two-chamber microbial electrolysis cells (MECs), and linear sweep voltammetry (LSV) in unbuffered saline solutions at two different initial pHs (7 and 12). There was generally no appreciable effect of initial pH on production rates or total gas production. NF produced hydrogen gas at a rate of 1.1 m3 H2/m3·d, which was only slightly less than that using Pt (1.4 m3 H2/m3·d), but larger than that obtained with SSW (0.52 m3 H2/m3·d) or MoS2 (0.67 m3 H2/m3·d). Overall hydrogen gas recoveries with SSW (29.7 ± 0.5 mL), MoS2 (28.6 ± 1.3 mL) and NF (32.4 ± 2 mL) were only slightly less than that of Pt (37.9 ± 0.5 mL). Total energy recoveries, based on the gas produced versus electrical energy input, ranged from 0.75 ± 0.02 for Pt, to 0.55 ± 0.02 for SSW. An LSV analysis showed no effect of pH for NF and Pt, but overpotentials were reduced for MoS2 and SSW by using an initial lower pH. At cathode potentials more negative than −0.85 V (vs Ag/AgCl), NF had lower overpotentials than the MoS2. These results provide the first assessment of these materials under practical conditions of high pH in unbuffered saline catholytes, and position NF as the most promising inexpensive alternative to Pt.