Microbial Electrosynthesis Cells Research Articles

Microbial electrosynthesis system with dual biocathode arrangement for simultaneous acetogenesis, solventogenesis and carbon chain elongation.

A microbial electrosynthesis cell comprising two biological cathode chambers sharing the same anode compartment is used to promote the production of C2-C4 carboxylic acids and alcohols from carbon dioxide. Each cathode chamber provides ideal pH conditions to favor acetogenesis/carbon chain elongation (pH = 6.9), and solventogenesis (pH = 4.9), respectively, without the requirement of external acid/base dosing.

Porous Hollow Fiber Nickel Electrodes for Effective Supply and Reduction of Carbon Dioxide to Methane through Microbial Electrosynthesis

AbstractMicrobial electrochemical reduction of CO2 gas to value‐added chemical products requires the development of an electrode architecture with a three‐phase interface for efficient mass transport. A hybrid bioinorganic system for CO2 reduction to CH4 is developed by coupling a new electrode architecture with enriched methanogenic community. The novel electrode design consists of porous nickel hollow fibers, which act as an inorganic electrocatalyst for hydrogen generation from proton reduction and as a gas‐transfer membrane for direct CO2 delivery to CO2‐fixing hydrogenotrophic methanogens (biological catalyst) on the cathode through the pores of the hollow fibers. These unique features of the electrode create a suitable environment for the enrichment of methanogens, which utilize the hydrogen as a source of reducing equivalents for the conversion of CO2 to CH4. The performance of the nickel electrode is tested in microbial electrosynthesis cells operated at cathode potential of −1 V versus Ag/AgCl, achieving high faradaic efficiency of 77% for CH4. The superior performance of the hybrid bioinorganic system is attributed to the electrode architecture, which provides a three‐phase boundary for gas–liquid reactions, with the reactions supported by the inorganic and biological catalysts.

Stainless Steel-Based Bioanodes for Applications in Bioelectrochemical Systems

The majority of studies focusing on bioelectrochemical systems (BES) report the utilization of carbon-based electrodes. However, in order to overcome the limitations related to the scale-up of Microbial Fuel Cells (MFC) and Microbial Electro Synthesis (MES) cells technologies, the utilization of metal-based electrodes need to be considered due to their conductivity, cost and robustness. Stainless steel fiber felts (SSFF) as bioanode material for BES applications was investigated in this study. The unmodified SSFF was tested alongside with electrodes modified with reduced graphene oxide (rGO), magnetite nanoparticles (Fe3O4), manganese oxide (MnO2) and flame-oxidation (FO). The performance of the metal-based electrodes as bioanodes were investigated in half-cells in terms of stability and current densities. In addition, the impact of the capacitance of the abiotic electrode materials on the performance of the bioanodes and MFCs was evaluated (Fig. a), especially to assess how these materials can increase the energy harvested compared to non-capacitive bioanodes. The results showed that the stainless steel- based electrodes studied are competitive alternatives to the carbon-based electrodes. Current densities recorded in half-cells were 1.96, 1.95 and 2.26 mA/cm2 for FO-MnO2-SS, rGO-SS and carbon cloth, respectively. In addition, charge/discharge experiments carried out with the bioanodes developed (Fig. c) showed that the modified SSFF electrodes allow the storage of electrical charge from the biofilm to the capacitive layers of the electrodes when cells are left at open circuit potential (OCP). These results demonstrate the potential of these materials for energy generation and storage applications from waste in BES. Figure 1

Increasing methane content in biogas and simultaneous value added product recovery using microbial electrosynthesis.

Electrosynthesis of multi-carbon compounds from the carbon dioxide present in biogas is a nascent approach towards purification of biogas. Microbial electrosynthesis (MES) cells, fabricated using different electrode materials, were operated using different electrolytes and mixed anaerobic culture as biocatalysts in the cathodic chamber under an applied cathode potential of -0.7 V vs standard hydrogen electrode (SHE). The rate of production of acetate, isobutyrate, propionate and 2-piperidinone from reduction of CO2 in the cathodic chamber of the MES was 0.81 mM/day, 0.63 mM/day, 0.44 mM/day and 0.53 mM/day, respectively. As methane was also present in the biogas, methyl derivatives of these acids were also found in traces in catholyte. It was observed that the use of nickel foam as an anode, 1 M NiSO4 solution as anolyte, graphite felt as a cathode, phosphate buffer solution as catholyte at a pH of 5.2 proved to be the best possible combination for MES for this study to get enhanced product yield at higher energy efficiency.

Efficiently "pumping out" value-added resources from wastewater by bioelectrochemical systems: A review from energy perspectives.

Bioelectrochemical systems (BES) can accomplish simultaneous wastewater treatment and resource recovery via interactions between microbes and electrodes. Often deemed as "energy efficient" technologies, BES have not been well evaluated for their energy performance, such as energy production and consumption. In this work, we have conducted a review and analysis of energy balance in BES with parameters like normalized energy recovery, specific energy consumption, and net energy production. Several BES representatives based on their functions were selected for analysis, including direct electricity generation in microbial fuel cells, hydrogen production in microbial electrolysis cells, nitrogen recovery in BES, chemical production in microbial electrosynthesis cells, and desalination in microbial desalination cells. Energy performance was normalized to water volume (kWh m-3), organic removal (kWh kg COD-1), nitrogen recovery (kWh kg N-1), chemical production (kWh kg-1), or removed salt during desalination (kWh kg-1). The key operating factors such as pumping system (recirculation/feeding pumps) and external power supply were discussed for their effects on energy performance. This is an in-depth analysis of energy performance of various BES and expected to encourage more thinking, analysis, and presentation of energy data towards appropriate research and development of BES technology for resource recovery from wastewater.

Microbial fuel cells: From fundamentals to applications. A review

In the past 10–15 years, the microbial fuel cell (MFC) technology has captured the attention of the scientific community for the possibility of transforming organic waste directly into electricity through microbially catalyzed anodic, and microbial/enzymatic/abiotic cathodic electrochemical reactions. In this review, several aspects of the technology are considered. Firstly, a brief history of abiotic to biological fuel cells and subsequently, microbial fuel cells is presented. Secondly, the development of the concept of microbial fuel cell into a wider range of derivative technologies, called bioelectrochemical systems, is described introducing briefly microbial electrolysis cells, microbial desalination cells and microbial electrosynthesis cells. The focus is then shifted to electroactive biofilms and electron transfer mechanisms involved with solid electrodes. Carbonaceous and metallic anode materials are then introduced, followed by an explanation of the electro catalysis of the oxygen reduction reaction and its behavior in neutral media, from recent studies. Cathode catalysts based on carbonaceous, platinum-group metal and platinum-group-metal-free materials are presented, along with membrane materials with a view to future directions. Finally, microbial fuel cell practical implementation, through the utilization of energy output for practical applications, is described.

The Effect of Membrane Type on the Performance of Microbial Electrosynthesis Cells for Methane Production

This study evaluated the influence of the membrane type on the performance of bioelectromethanogenesis reactors. The functional activities and taxonomic composition of bioelectrochemical systems (BES) with Nafion 117 or Ultrex CMI-7000 membranes were assessed. Functional activity was measured as methane production and current consumption rates throughout operation. Microbial biomass and phylogenetic diversity were characterized at strategic intervals related to the membrane type used. The Nafion-BES reactor showed the best performance in terms of current consumption and methane production in the early operational period and a strong selection for fermentative bacteria. However, the Nafion-BES was not able to sustain this activity over the course of 7 subpassages since methanogenic species were ultimately selected against and did not appear in the community composition for the last two subpassages. In contrast, the Ultrex-BES had a lower pH concentration gradient and lower overall current consumption activity; however, the methane production activity from the Ultrex-BES was equivalent or better than the Nafion-BES reactor and was sustained throughout the seven subpassages. The membrane type appeared to be responsible not only for differences in the electrochemical operation of the BESs but it also influenced microbial taxonomic composition and dynamics.

Modelling the simultaneous production and separation of acetic acid from CO2 using an anion exchange membrane microbial electrosynthesis system

AbstractBACKGROUNDMicrobial electrosynthesis is a carbon capture technology capable of transforming CO2 into valuable organic compounds. The aim of this article is to model the simultaneous production and separation of acetate in an anion‐exchange membrane microbial electrosynthesis cell which employs CO2 as feedstock.RESULTSThe maximum amount of acetate product produced was 0.72 mmol after 19 operational days. Simultaneous production and separation of acetate began after 4 days when 0.95 mol m−3 and 0.04 mol m−3 of acetate were detected in the cathode and anode MES cell chambers, respectively. A model that fits the simultaneous production and separation of acetate in the microbial electrosynthesis cell was successfully developed and validated.CONCLUSIONThe microbial electrosynthesis model developed in this work can be used to predict the product concentrations of a carbon capture technology which simultaneously produces and separates acetate product. © 2016 Society of Chemical Industry

Long-term operation of microbial electrosynthesis cell reducing CO2 to multi-carbon chemicals with a mixed culture avoiding methanogenesis

In microbial electrosynthesis (MES), CO2 can be reduced preferably to multi-carbon chemicals by a biocathode-based process which uses electrochemically active bacteria as catalysts. A mixed anaerobic consortium from biological origin typically produces methane from CO2 reduction which circumvents production of multi-carbon compounds. This study aimed to develop a stable and robust CO2 reducing biocathode from a mixed culture inoculum avoiding the methane generation. An effective approach was demonstrated based on (i) an enrichment procedure involving inoculum pre-treatment and several culture transfers in H2:CO2 media, (ii) a transfer from heterotrophic to autotrophic growth and (iii) a sequential batch operation. Biomass growth and gradual acclimation to CO2 electro-reduction accomplished a maximum acetate production rate of 400mgLcatholyte−1d−1 at −1V (vs. Ag/AgCl). Methane was never detected in more than 300days of operation. Accumulation of acetate up to 7–10gL−1 was repeatedly attained by supplying (80:20) CO2:N2 mixture at −0.9 to −1V (vs. Ag/AgCl). In addition, ethanol and butyrate were also produced from CO2 reduction. Thus, a robust CO2 reducing biocathode can be developed from a mixed culture avoiding methane generation by adopting the specific culture enrichment and operation procedures without the direct addition of chemical inhibitor.

An enriched electroactive homoacetogenic biocathode for the microbial electrosynthesis of acetate through carbon dioxide reduction.

In the direction of generating value added chemicals from carbon dioxide (CO2) reduction through microbial electrosynthesis (MES), considering the crucial impact of the electrode material for the biofilm development and electron delivery, an attempt was made in this study to evaluate the efficiency of two different materials as biocathodes and their respective output in terms of electrosynthesis. The electrode material is a key component in the MES process. Several electrodes such as platinum, graphite foil, dimentionally stable anode (DSA) and graphite rod, and VITO-CoRE™ derived electrodes were tested for their suitability for ideal electrode combination in a three electrode cell setup. Bicarbonates (the dissolved form of CO2) was reduced to acetate by a selectively developed biocathode under a mild applied cathodic potential of -400 mV (vs. SHE) in 500 mL of single chamber MES cells operating for more than four months. Among the two electrode combinations evaluated, VITO-CoRE™-PL (VC-IS, plastic inert support) as the cathode and VITO-CoRE™-SS (VC-SS, stainless steel metal support) as the counter electrode showed higher production (4127 mg L(-1)) with a volumetric production rate of 0.569 kg per m(3) per d than the graphite rod (1523 mg L(-1)) with a volumetric production rate of 0.206 kg per m(3) per d. Contrary to the production efficiencies, the coulombic efficiency was higher with the second electrode combination (40.43%) than the first electrode combination (29.91%). Carbon conversion efficiency to acetate was higher for VC-IS (90.6%) than the graphite rod (82.0%).

Improved cathode for high efficient microbial-catalyzed reduction in microbial electrosynthesis cells

Microbial electrosynthesis cells (MECs) are devices wherein microorganisms can electrochemically interact with electrodes, directly donating or accepting electrons from electrode surfaces. Here, we developed a novel cathode by using nickel nanowires anchored to graphite for the improvement of microbial-catalyzed reduction in MEC cathode chamber. This porous nickel-nanowire-network-coated graphite electrode increased the interfacial area and interfacial interactions between the cathode surface and the microbial biofilm. A 2.3 fold increase in bio-reduction rate over the untreated graphite was observed. Around 282 mM day(-1) m(-2) of acetate resulting from the bio-reduction of carbon dioxide by Sporomusa was produced with 82 ± 14% of the electrons consumed being recovered in acetate.