This study investigates the performance of acetate feed membrane less single chamber microbial fuel cell and physical characterization of the bio film present on the anode surface using Scanning Electron Microscope (SEM) and 16S rRNA analyzer. The performance has been investigated using Teflon treated carbon paper with 0.3 mg/cm2 Pt/C loaded as a cathode and carbon paper as an anode. The maximum open circuit potential is noticed as 791 mV, the system successfully revealed a maximum power density of 86.1 mW m−2 at stable current density of 354 mA m−2 with high coulombic efficiency of 65% at maximum degradation rate of 96%. SEM showed the dense adherence of microorganisms on the anode. 16S rRNA sequencing results indicates phylogenetic mixture in the communities of anodic biofilm and there is no single dominant bacterial species. The dominant phyla are Firmicutes, Gamma Proteobacteria, Alpha Proteobacteria, Actinobacteria, with ten dominant microbial strains: Bacillus firmus, Shewanella profunda, Bacillus isronensis, Brevundimonas bullata, Pseudomonas putida, Planococcus citreus, Micrococcus endophyticus, Acinetobacter tandoii, Bacillus safensis and Shewanella xiamenensis.

Mixed transition metal (Co, Mn, and Cu) oxide electrocatalysts anchored on different carbon supports for oxygen reduction reaction.

In the microbial electrochemical system (MES), the microbial-electrode interactions are often regulated by the metabolic pathway and respiratory activities. To improve the efficiency of MES, there is a need to introduce a microbial community that provides a continuous oxidation of organic substrates with a sustainable current output. Thus, activated sludge was suggested and the rapid evaluation of its biodegradation activity, using cyclic voltammetry, was performed. Stimulation of the metabolic pathway led to the appearance of an oxidation peak current (22 μA/cm(2), at about 750 mV), whereas the electrochemical signals were originated only from the metabolically active microbes. Cell viability, cultivation time, type, and concentration of the degradable organic substrates have been identified as major regulators for the electrocatalytic performance. From two different microbial communities, the generated electrochemical signal of the aerobic activated sludge was more than twofold higher in converting the degradable organic substrates (glucose, acetate, and succinate at 10 g/L) into oxidation current. On the other hand, the secretion of electroactive metabolite(s) in the extracellular matrix was determined as a source of electrochemical signal. Moreover, the mechanism(s) of the microbe-electrode interactions were demonstrated. Therefore, the current bioelectrochemical system could be used as a platform for monitoring the rate of substrate degradation as well as measuring the metabolic pathway activity.

Due to the potential interest, bioelectrochemical responses of activated sludge using the three-electrode system are tested. From the cyclic voltammograms, the oxidation current output is increasing due to incubation time increase, whereas 5, 25 and 39.33 μA are obtained after 3, 72 and 96 h, respectively. Changing the working electrode from glassy carbon to carbon paste led to the increase in the electrochemical signal from 0.3 to be 3.72 μA. On the other hand, the use of the lipophilic redox mediator (2,6-dichlorophenolindophenol (DCIP)) amplified the oxidation current to reach 19.9 μA instead of 2.1 μA. Based on these findings, the mixed microbial community of the activated sludge is exploited as a catalyst for the bio-oxidation of the degradable organic substrates, while DCIP is used as a mobile electron carrier from the intracellular matrix of the metabolically active cells to the carbon paste electrode which served as the final electron acceptor. Therefore, the extracellular electron transfer from the formed active biofilm at the electrode surface is assisted by the existence of DCIP.

Construction of efficient performance of microbial fuel cells (MFCs) requires certain practical considerations. In the single chamber microbial fuel cell, there is no border between the anode and the cathode, thus the diffusion of the dissolved oxygen has a contrary effect on the anodic respiration and this leads to the inhibition of the direct electron transfer from the biofilm to the anodic surface. Here, a fed-batch single chambered microbial fuel cells are constructed with different distances 3 and 6 cm (anode- cathode spacing), while keeping the working volume is constant. The performance of each MFC is individually evaluated under the effects of vitamins & minerals with acetate as a fed load. The maximum open circuit potential during testing the 3 and 6 cm microbial fuel cells is about 946 and 791 mV respectively. By decreasing the distance between the anode and the cathode from 6 to 3 cm, the power density is decreased from 108.3 mW m −2 to 24.5 mW m −2 . Thus, the short distance in membrane-less MFC weakened the cathode and inhibited the anodic respiration which affects the overall performance of the MFC efficiency. The system is displayed a maximum potential of 564 and 791 mV in absence & presence of vitamins respectively. Eventually, the overall functions of the acetate single chamber microbial fuel cell can be improved by the addition of vitamins & minerals and increasing the distance between the cathode and the anode.