Application of gas diffusion biocathode in microbial electrosynthesis from carbon dioxide

Microbial catalysis of carbon dioxide (CO 2 ) reduction to multi-carbon compounds at the cathode is a highly attractive application of microbial electrosynthesis (MES). The microbes reduce CO 2 by either taking the electrons or reducing the equivalents produced at the cathode. While using gaseous CO...

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Published inEnvironmental science and pollution research international Vol. 23; no. 22; pp. 22292 - 22308
Main Authors Bajracharya, Suman, Vanbroekhoven, Karolien, Buisman, Cees J.N., Pant, Deepak, Strik, David P. B. T. B.
Format Journal Article
LanguageEnglish
Published Berlin/Heidelberg Springer Berlin Heidelberg 01.11.2016
Springer Nature B.V
Subjects
acetates
Acetates - chemistry
Activated carbon
Alternative energy sources
Anaerobiosis
Aquatic Pollution
Atmospheric Protection/Air Quality Control/Air Pollution
Autotrophic bioproduction
bacteria
Bacteria - classification
Bacteria - metabolism
Biocatalysts
Biocathode
biocathodes
Bioelectric Energy Sources - microbiology
Biomass
Bioreactors
butyrates
Carbon
Carbon dioxide
Carbon Dioxide - chemistry
Carbon sources
Catalysis
catalytic activity
Chemicals
Climate change
CO reduction
Conservation of Natural Resources
Earth and Environmental Science
Ecotoxicology
Electric rates
Electrodes
Electrolytes
electrons
Environment
Environmental Chemistry
Environmental Health
Environmental Pollutants
Environmental science
Ethanol
Flue gas
Gas diffusion electrode
Gases
Hydrogen
Hydrogen - chemistry
hydrophobicity
inoculum
Mass transfer
Microbial electrosynthesis
polytetrafluoroethylene
Renewable resources
Sewage - microbiology
silver
silver chloride
Sludge
Studies
Technoeconomic Perspectives on Sustainable CO2 Capture and Utilization
Waste Water Technology
Water Management
Water Pollution Control
Gas diffusion electrode
Microbial electrosynthesis
Biocathode
CO
reduction
Autotrophic bioproduction
CO2 reduction
Online AccessGet full text

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Abstract Microbial catalysis of carbon dioxide (CO 2 ) reduction to multi-carbon compounds at the cathode is a highly attractive application of microbial electrosynthesis (MES). The microbes reduce CO 2 by either taking the electrons or reducing the equivalents produced at the cathode. While using gaseous CO 2 as the carbon source, the biological reduction process depends on the dissolution and mass transfer of CO 2 in the electrolyte. In order to deal with this issue, a gas diffusion electrode (GDE) was investigated by feeding CO 2 through the GDE into the MES reactor for its reduction at the biocathode. A combination of the catalyst layer (porous activated carbon and Teflon binder) and the hydrophobic gas diffusion layer (GDL) creates a three-phase interface at the electrode. So, CO 2 and reducing equivalents will be available to the biocatalyst on the cathode surface. An enriched inoculum consisting of acetogenic bacteria, prepared from an anaerobic sludge, was used as a biocatalyst. The cathode potential was maintained at −1.1 V vs Ag/AgCl to facilitate direct and/or hydrogen-mediated CO 2 reduction. Bioelectrochemical CO 2 reduction mainly produced acetate but also extended the products to ethanol and butyrate. Average acetate production rates of 32 and 61 mg/L/day, respectively, with 20 and 80 % CO 2 gas mixture feed were achieved with 10 cm 2 of GDE. The maximum acetate production rate remained 238 mg/L/day for 20 % CO 2 gas mixture. In conclusion, a gas diffusion biocathode supported bioelectrochemical CO 2 reduction with enhanced mass transfer rate at continuous supply of gaseous CO 2 . Graphical abstract ᅟ
AbstractList Microbial catalysis of carbon dioxide (CO2) reduction to multi-carbon compounds at the cathode is a highly attractive application of microbial electrosynthesis (MES). The microbes reduce CO2 by either taking the electrons or reducing the equivalents produced at the cathode. While using gaseous CO2 as the carbon source, the biological reduction process depends on the dissolution and mass transfer of CO2 in the electrolyte. In order to deal with this issue, a gas diffusion electrode (GDE) was investigated by feeding CO2 through the GDE into the MES reactor for its reduction at the biocathode. A combination of the catalyst layer (porous activated carbon and Teflon binder) and the hydrophobic gas diffusion layer (GDL) creates a three-phase interface at the electrode. So, CO2 and reducing equivalents will be available to the biocatalyst on the cathode surface. An enriched inoculum consisting of acetogenic bacteria, prepared from an anaerobic sludge, was used as a biocatalyst. The cathode potential was maintained at −1.1 V vs Ag/AgCl to facilitate direct and/or hydrogen-mediated CO2 reduction. Bioelectrochemical CO2 reduction mainly produced acetate but also extended the products to ethanol and butyrate. Average acetate production rates of 32 and 61 mg/L/day, respectively, with 20 and 80 % CO2 gas mixture feed were achieved with 10 cm2 of GDE. The maximum acetate production rate remained 238 mg/L/day for 20 % CO2 gas mixture. In conclusion, a gas diffusion biocathode supported bioelectrochemical CO2 reduction with enhanced mass transfer rate at continuous supply of gaseous CO2. [Figure not available: see fulltext.]
Microbial catalysis of carbon dioxide (CO2) reduction to multi-carbon compounds at the cathode is a highly attractive application of microbial electrosynthesis (MES). The microbes reduce CO2 by either taking the electrons or reducing the equivalents produced at the cathode. While using gaseous CO2 as the carbon source, the biological reduction process depends on the dissolution and mass transfer of CO2 in the electrolyte. In order to deal with this issue, a gas diffusion electrode (GDE) was investigated by feeding CO2 through the GDE into the MES reactor for its reduction at the biocathode. A combination of the catalyst layer (porous activated carbon and Teflon binder) and the hydrophobic gas diffusion layer (GDL) creates a three-phase interface at the electrode. So, CO2 and reducing equivalents will be available to the biocatalyst on the cathode surface. An enriched inoculum consisting of acetogenic bacteria, prepared from an anaerobic sludge, was used as a biocatalyst. The cathode potential was maintained at -1.1 V vs Ag/AgCl to facilitate direct and/or hydrogen-mediated CO2 reduction. Bioelectrochemical CO2 reduction mainly produced acetate but also extended the products to ethanol and butyrate. Average acetate production rates of 32 and 61 mg/L/day, respectively, with 20 and 80 % CO2 gas mixture feed were achieved with 10 cm2 of GDE. The maximum acetate production rate remained 238 mg/L/day for 20 % CO2 gas mixture. In conclusion, a gas diffusion biocathode supported bioelectrochemical CO2 reduction with enhanced mass transfer rate at continuous supply of gaseous CO2. [Figure not available: see fulltext.]
Microbial catalysis of carbon dioxide (CO 2 ) reduction to multi-carbon compounds at the cathode is a highly attractive application of microbial electrosynthesis (MES). The microbes reduce CO 2 by either taking the electrons or reducing the equivalents produced at the cathode. While using gaseous CO 2 as the carbon source, the biological reduction process depends on the dissolution and mass transfer of CO 2 in the electrolyte. In order to deal with this issue, a gas diffusion electrode (GDE) was investigated by feeding CO 2 through the GDE into the MES reactor for its reduction at the biocathode. A combination of the catalyst layer (porous activated carbon and Teflon binder) and the hydrophobic gas diffusion layer (GDL) creates a three-phase interface at the electrode. So, CO 2 and reducing equivalents will be available to the biocatalyst on the cathode surface. An enriched inoculum consisting of acetogenic bacteria, prepared from an anaerobic sludge, was used as a biocatalyst. The cathode potential was maintained at −1.1 V vs Ag/AgCl to facilitate direct and/or hydrogen-mediated CO 2 reduction. Bioelectrochemical CO 2 reduction mainly produced acetate but also extended the products to ethanol and butyrate. Average acetate production rates of 32 and 61 mg/L/day, respectively, with 20 and 80 % CO 2 gas mixture feed were achieved with 10 cm 2 of GDE. The maximum acetate production rate remained 238 mg/L/day for 20 % CO 2 gas mixture. In conclusion, a gas diffusion biocathode supported bioelectrochemical CO 2 reduction with enhanced mass transfer rate at continuous supply of gaseous CO 2 . Graphical abstract ᅟ
Microbial catalysis of carbon dioxide (CO₂) reduction to multi-carbon compounds at the cathode is a highly attractive application of microbial electrosynthesis (MES). The microbes reduce CO₂ by either taking the electrons or reducing the equivalents produced at the cathode. While using gaseous CO₂ as the carbon source, the biological reduction process depends on the dissolution and mass transfer of CO₂ in the electrolyte. In order to deal with this issue, a gas diffusion electrode (GDE) was investigated by feeding CO₂ through the GDE into the MES reactor for its reduction at the biocathode. A combination of the catalyst layer (porous activated carbon and Teflon binder) and the hydrophobic gas diffusion layer (GDL) creates a three-phase interface at the electrode. So, CO₂ and reducing equivalents will be available to the biocatalyst on the cathode surface. An enriched inoculum consisting of acetogenic bacteria, prepared from an anaerobic sludge, was used as a biocatalyst. The cathode potential was maintained at −1.1 V vs Ag/AgCl to facilitate direct and/or hydrogen-mediated CO₂ reduction. Bioelectrochemical CO₂ reduction mainly produced acetate but also extended the products to ethanol and butyrate. Average acetate production rates of 32 and 61 mg/L/day, respectively, with 20 and 80 % CO₂ gas mixture feed were achieved with 10 cm² of GDE. The maximum acetate production rate remained 238 mg/L/day for 20 % CO₂ gas mixture. In conclusion, a gas diffusion biocathode supported bioelectrochemical CO₂ reduction with enhanced mass transfer rate at continuous supply of gaseous CO₂. Graphical abstract ᅟ
Microbial catalysis of carbon dioxide (CO2) reduction to multi-carbon compounds at the cathode is a highly attractive application of microbial electrosynthesis (MES). The microbes reduce CO2 by either taking the electrons or reducing the equivalents produced at the cathode. While using gaseous CO2 as the carbon source, the biological reduction process depends on the dissolution and mass transfer of CO2 in the electrolyte. In order to deal with this issue, a gas diffusion electrode (GDE) was investigated by feeding CO2 through the GDE into the MES reactor for its reduction at the biocathode. A combination of the catalyst layer (porous activated carbon and Teflon binder) and the hydrophobic gas diffusion layer (GDL) creates a three-phase interface at the electrode. So, CO2 and reducing equivalents will be available to the biocatalyst on the cathode surface. An enriched inoculum consisting of acetogenic bacteria, prepared from an anaerobic sludge, was used as a biocatalyst. The cathode potential was maintained at -1.1 V vs Ag/AgCl to facilitate direct and/or hydrogen-mediated CO2 reduction. Bioelectrochemical CO2 reduction mainly produced acetate but also extended the products to ethanol and butyrate. Average acetate production rates of 32 and 61 mg/L/day, respectively, with 20 and 80 % CO2 gas mixture feed were achieved with 10 cm2 of GDE. The maximum acetate production rate remained 238 mg/L/day for 20 % CO2 gas mixture. In conclusion, a gas diffusion biocathode supported bioelectrochemical CO2 reduction with enhanced mass transfer rate at continuous supply of gaseous CO2. Graphical abstract ᅟ.Microbial catalysis of carbon dioxide (CO2) reduction to multi-carbon compounds at the cathode is a highly attractive application of microbial electrosynthesis (MES). The microbes reduce CO2 by either taking the electrons or reducing the equivalents produced at the cathode. While using gaseous CO2 as the carbon source, the biological reduction process depends on the dissolution and mass transfer of CO2 in the electrolyte. In order to deal with this issue, a gas diffusion electrode (GDE) was investigated by feeding CO2 through the GDE into the MES reactor for its reduction at the biocathode. A combination of the catalyst layer (porous activated carbon and Teflon binder) and the hydrophobic gas diffusion layer (GDL) creates a three-phase interface at the electrode. So, CO2 and reducing equivalents will be available to the biocatalyst on the cathode surface. An enriched inoculum consisting of acetogenic bacteria, prepared from an anaerobic sludge, was used as a biocatalyst. The cathode potential was maintained at -1.1 V vs Ag/AgCl to facilitate direct and/or hydrogen-mediated CO2 reduction. Bioelectrochemical CO2 reduction mainly produced acetate but also extended the products to ethanol and butyrate. Average acetate production rates of 32 and 61 mg/L/day, respectively, with 20 and 80 % CO2 gas mixture feed were achieved with 10 cm2 of GDE. The maximum acetate production rate remained 238 mg/L/day for 20 % CO2 gas mixture. In conclusion, a gas diffusion biocathode supported bioelectrochemical CO2 reduction with enhanced mass transfer rate at continuous supply of gaseous CO2. Graphical abstract ᅟ.
Microbial catalysis of carbon dioxide (CO sub(2)) reduction to multi-carbon compounds at the cathode is a highly attractive application of microbial electrosynthesis (MES). The microbes reduce CO sub(2) by either taking the electrons or reducing the equivalents produced at the cathode. While using gaseous CO sub(2) as the carbon source, the biological reduction process depends on the dissolution and mass transfer of CO sub(2) in the electrolyte. In order to deal with this issue, a gas diffusion electrode (GDE) was investigated by feeding CO sub(2) through the GDE into the MES reactor for its reduction at the biocathode. A combination of the catalyst layer (porous activated carbon and Teflon binder) and the hydrophobic gas diffusion layer (GDL) creates a three-phase interface at the electrode. So, CO sub(2) and reducing equivalents will be available to the biocatalyst on the cathode surface. An enriched inoculum consisting of acetogenic bacteria, prepared from an anaerobic sludge, was used as a biocatalyst. The cathode potential was maintained at -1.1 V vs Ag/AgCl to facilitate direct and/or hydrogen-mediated CO sub(2) reduction. Bioelectrochemical CO sub(2) reduction mainly produced acetate but also extended the products to ethanol and butyrate. Average acetate production rates of 32 and 61 mg/L/day, respectively, with 20 and 80 % CO sub(2) gas mixture feed were achieved with 10 cm super(2) of GDE. The maximum acetate production rate remained 238 mg/L/day for 20 % CO sub(2) gas mixture. In conclusion, a gas diffusion biocathode supported bioelectrochemical CO sub(2) reduction with enhanced mass transfer rate at continuous supply of gaseous CO sub(2). [Figure not available: see fulltext.]
Microbial catalysis of carbon dioxide (CO ) reduction to multi-carbon compounds at the cathode is a highly attractive application of microbial electrosynthesis (MES). The microbes reduce CO by either taking the electrons or reducing the equivalents produced at the cathode. While using gaseous CO as the carbon source, the biological reduction process depends on the dissolution and mass transfer of CO in the electrolyte. In order to deal with this issue, a gas diffusion electrode (GDE) was investigated by feeding CO through the GDE into the MES reactor for its reduction at the biocathode. A combination of the catalyst layer (porous activated carbon and Teflon binder) and the hydrophobic gas diffusion layer (GDL) creates a three-phase interface at the electrode. So, CO and reducing equivalents will be available to the biocatalyst on the cathode surface. An enriched inoculum consisting of acetogenic bacteria, prepared from an anaerobic sludge, was used as a biocatalyst. The cathode potential was maintained at -1.1 V vs Ag/AgCl to facilitate direct and/or hydrogen-mediated CO reduction. Bioelectrochemical CO reduction mainly produced acetate but also extended the products to ethanol and butyrate. Average acetate production rates of 32 and 61 mg/L/day, respectively, with 20 and 80 % CO gas mixture feed were achieved with 10 cm of GDE. The maximum acetate production rate remained 238 mg/L/day for 20 % CO gas mixture. In conclusion, a gas diffusion biocathode supported bioelectrochemical CO reduction with enhanced mass transfer rate at continuous supply of gaseous CO . Graphical abstract ᅟ.
Author Strik, David P. B. T. B.
Buisman, Cees J.N.
Bajracharya, Suman
Vanbroekhoven, Karolien
Pant, Deepak
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  givenname: Suman
  surname: Bajracharya
  fullname: Bajracharya, Suman
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– sequence: 2
  givenname: Karolien
  surname: Vanbroekhoven
  fullname: Vanbroekhoven, Karolien
  organization: Separation and Conversion Technologies, Flemish Institute for Technological Research (VITO)
– sequence: 3
  givenname: Cees J.N.
  surname: Buisman
  fullname: Buisman, Cees J.N.
  organization: Sub-department of Environmental Technology, Wageningen University
– sequence: 4
  givenname: Deepak
  orcidid: 0000-0002-1425-9588
  surname: Pant
  fullname: Pant, Deepak
  email: deepak.pant@vito.be, pantonline@gmail.com
  organization: Separation and Conversion Technologies, Flemish Institute for Technological Research (VITO)
– sequence: 5
  givenname: David P. B. T. B.
  surname: Strik
  fullname: Strik, David P. B. T. B.
  organization: Sub-department of Environmental Technology, Wageningen University
BackLink https://www.ncbi.nlm.nih.gov/pubmed/27436381$$D View this record in MEDLINE/PubMed
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Keywords Gas diffusion electrode
Microbial electrosynthesis
Biocathode
CO
reduction
Autotrophic bioproduction
CO2 reduction
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Snippet Microbial catalysis of carbon dioxide (CO 2 ) reduction to multi-carbon compounds at the cathode is a highly attractive application of microbial...
Microbial catalysis of carbon dioxide (CO ) reduction to multi-carbon compounds at the cathode is a highly attractive application of microbial electrosynthesis...
Microbial catalysis of carbon dioxide (CO2) reduction to multi-carbon compounds at the cathode is a highly attractive application of microbial electrosynthesis...
Microbial catalysis of carbon dioxide (CO sub(2)) reduction to multi-carbon compounds at the cathode is a highly attractive application of microbial...
Microbial catalysis of carbon dioxide (CO₂) reduction to multi-carbon compounds at the cathode is a highly attractive application of microbial electrosynthesis...
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StartPage 22292
SubjectTerms acetates
Acetates - chemistry
Activated carbon
Alternative energy sources
Anaerobiosis
Aquatic Pollution
Atmospheric Protection/Air Quality Control/Air Pollution
Autotrophic bioproduction
bacteria
Bacteria - classification
Bacteria - metabolism
Biocatalysts
Biocathode
biocathodes
Bioelectric Energy Sources - microbiology
Biomass
Bioreactors
butyrates
Carbon
Carbon dioxide
Carbon Dioxide - chemistry
Carbon sources
Catalysis
catalytic activity
Chemicals
Climate change
CO reduction
Conservation of Natural Resources
Earth and Environmental Science
Ecotoxicology
Electric rates
Electrodes
Electrolytes
electrons
Environment
Environmental Chemistry
Environmental Health
Environmental Pollutants
Environmental science
Ethanol
Flue gas
Gas diffusion electrode
Gases
Hydrogen
Hydrogen - chemistry
hydrophobicity
inoculum
Mass transfer
Microbial electrosynthesis
polytetrafluoroethylene
Renewable resources
Sewage - microbiology
silver
silver chloride
Sludge
Studies
Technoeconomic Perspectives on Sustainable CO2 Capture and Utilization
Waste Water Technology
Water Management
Water Pollution Control
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Title Application of gas diffusion biocathode in microbial electrosynthesis from carbon dioxide
URI https://link.springer.com/article/10.1007/s11356-016-7196-x
https://www.ncbi.nlm.nih.gov/pubmed/27436381
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https://www.proquest.com/docview/2000439228
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Volume 23
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