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      Impact of dissolved carbon dioxide concentration on the process parameters during its conversion to acetate through microbial electrosynthesis

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          Abstract

          The reduction of carbon dioxide (CO 2) released from industry can help to reduce the emissions of greenhouse gases (GHGs) to the atmosphere while at the same time producing value-added chemicals and contributing to carbon fixation.

          Abstract

          The reduction of carbon dioxide (CO 2) released from industry can help to reduce the emissions of greenhouse gases (GHGs) to the atmosphere while at the same time producing value-added chemicals and contributing to carbon fixation. Microbial electrosynthesis (MES) is a recently developed process which accomplishes this idea by using cathodic bacteria at the expense of only minimum energy. In this study, enriched mixed homoacetogenic bacteria as cathodic biocatalysts for the reduction of CO 2 with five different concentrations were evaluated to produce acetate at a constant potential. Increasing the carbon concentration showed an improved acetate production rate and carbon conversion efficiency. A maximum acetate production rate of 142.2 mg L per day and a maximum carbon conversion efficiency of 84% were achieved, respectively, at 4.0 and 2.5 g HCO 3 L −1. The changes in pH due to interactive reactions between the bicarbonate (substrate) and acetate (products) were able to create a buffering nature in the catholyte controlling the operating parameters of the MES process, such as pH and substrate specificity. A higher acetate production shifted the catholyte pH toward acidic conditions, which further triggered favorable conditions for the bioelectrochemical reduction of acetate to ethanol.

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          Electrobiocommodities: powering microbial production of fuels and commodity chemicals from carbon dioxide with electricity.

          Electricity can be an energy source for microbially catalyzed production of fuels and other organic commodities from carbon dioxide. These electrobiocommodities (E-BCs) can be produced directly via electrode-to-microbe electron transfer or indirectly with electrochemically generated electron donors such as H2 or formate. Producing E-BCs may be a more efficient and environmentally sustainable strategy for converting solar energy to biocommodities than approaches that rely on biological photosynthesis. A diversity of microbial physiologies could potentially be adapted for E-BC production, but to date acetogenic microorganisms are the only organisms shown to covert electrically generated low potential electrons and carbon dioxide into multi-carbon organic products with high recovery of electrons in product. Substantial research and development will be required for E-BC commercialization. Copyright © 2013 Elsevier Ltd. All rights reserved.
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            Efficient and selective molecular catalyst for the CO2-to-CO electrochemical conversion in water

            Substitution of the four paraphenyl hydrogens of iron tetraphenylporphyrin by trimethylammonio groups provides a water-soluble molecule able to catalyze the electrochemical conversion of carbon dioxide into carbon monoxide. The reaction, performed in pH-neutral water, forms quasi-exclusively carbon monoxide with very little production of hydrogen, despite partial equilibration of CO2 with carbonic acid-a low pKa acid. This selective molecular catalyst is endowed with a good stability and a high turnover frequency. On this basis, prescribed composition of CO-H2 mixtures can be obtained by adjusting the pH of the solution, optionally adding an electroinactive buffer. The development of these strategies will be greatly facilitated by the fact that one operates in water. The same applies for the association of the cathode compartment with a proton-producing anode by means of a suitable separator.
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              An overview on emerging bioelectrochemical systems (BESs): Technology for sustainable electricity, waste remediation, resource recovery, chemical production and beyond

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                Author and article information

                Journal
                RCEEBW
                Reaction Chemistry & Engineering
                React. Chem. Eng.
                Royal Society of Chemistry (RSC)
                2058-9883
                2018
                2018
                : 3
                : 3
                : 371-378
                Affiliations
                [1 ]Separation & Conversion Technology
                [2 ]Flemish Institute for Technological Research (VITO)
                [3 ]2400 Mol
                [4 ]Belgium
                [5 ]Department of Chemical Engineering
                Article
                10.1039/C7RE00220C
                dae4ef27-c49c-4cc7-9f99-866270b7acb0
                © 2018

                http://rsc.li/journals-terms-of-use

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