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Microbial Reverse-Electrodialysis Electrolysis and Chemical-Production Cell for H(2) Production and CO(2) Sequestration
[Image: see text] Natural mineral carbonation can be accelerated using acid and alkali solutions to enhance atmospheric CO(2) sequestration, but the production of these solutions needs to be carbon-neutral. A microbial reverse-electrodialysis electrolysis and chemical-production cell (MRECC) was dev...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3982931/ https://www.ncbi.nlm.nih.gov/pubmed/24741666 http://dx.doi.org/10.1021/ez500073q |
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author | Zhu, Xiuping Hatzell, Marta C. Logan, Bruce E. |
author_facet | Zhu, Xiuping Hatzell, Marta C. Logan, Bruce E. |
author_sort | Zhu, Xiuping |
collection | PubMed |
description | [Image: see text] Natural mineral carbonation can be accelerated using acid and alkali solutions to enhance atmospheric CO(2) sequestration, but the production of these solutions needs to be carbon-neutral. A microbial reverse-electrodialysis electrolysis and chemical-production cell (MRECC) was developed to produce these solutions and H(2) gas using only renewable energy sources (organic matter and salinity gradient). Using acetate (0.82 g/L) as a fuel for microorganisms to generate electricity in the anode chamber (liquid volume of 28 mL), 0.45 mmol of acid and 1.09 mmol of alkali were produced at production efficiencies of 35% and 86%, respectively, along with 10 mL of H(2) gas. Serpentine dissolution was enhanced 17–87-fold using the acid solution, with approximately 9 mL of CO(2) absorbed and 4 mg of CO(2) fixed as magnesium or calcium carbonates. The operational costs, based on mineral digging and grinding, and water pumping, were estimated to be only $25/metric ton of CO(2) fixed as insoluble carbonates. Considering the additional economic benefits of H(2) generation and possible wastewater treatment, this method may be a cost-effective and environmentally friendly method for CO(2) sequestration. |
format | Online Article Text |
id | pubmed-3982931 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-39829312014-04-14 Microbial Reverse-Electrodialysis Electrolysis and Chemical-Production Cell for H(2) Production and CO(2) Sequestration Zhu, Xiuping Hatzell, Marta C. Logan, Bruce E. Environ Sci Technol Lett [Image: see text] Natural mineral carbonation can be accelerated using acid and alkali solutions to enhance atmospheric CO(2) sequestration, but the production of these solutions needs to be carbon-neutral. A microbial reverse-electrodialysis electrolysis and chemical-production cell (MRECC) was developed to produce these solutions and H(2) gas using only renewable energy sources (organic matter and salinity gradient). Using acetate (0.82 g/L) as a fuel for microorganisms to generate electricity in the anode chamber (liquid volume of 28 mL), 0.45 mmol of acid and 1.09 mmol of alkali were produced at production efficiencies of 35% and 86%, respectively, along with 10 mL of H(2) gas. Serpentine dissolution was enhanced 17–87-fold using the acid solution, with approximately 9 mL of CO(2) absorbed and 4 mg of CO(2) fixed as magnesium or calcium carbonates. The operational costs, based on mineral digging and grinding, and water pumping, were estimated to be only $25/metric ton of CO(2) fixed as insoluble carbonates. Considering the additional economic benefits of H(2) generation and possible wastewater treatment, this method may be a cost-effective and environmentally friendly method for CO(2) sequestration. American Chemical Society 2014-03-24 2014-04-08 /pmc/articles/PMC3982931/ /pubmed/24741666 http://dx.doi.org/10.1021/ez500073q Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) |
spellingShingle | Zhu, Xiuping Hatzell, Marta C. Logan, Bruce E. Microbial Reverse-Electrodialysis Electrolysis and Chemical-Production Cell for H(2) Production and CO(2) Sequestration |
title | Microbial Reverse-Electrodialysis Electrolysis and
Chemical-Production Cell for H(2) Production and CO(2) Sequestration |
title_full | Microbial Reverse-Electrodialysis Electrolysis and
Chemical-Production Cell for H(2) Production and CO(2) Sequestration |
title_fullStr | Microbial Reverse-Electrodialysis Electrolysis and
Chemical-Production Cell for H(2) Production and CO(2) Sequestration |
title_full_unstemmed | Microbial Reverse-Electrodialysis Electrolysis and
Chemical-Production Cell for H(2) Production and CO(2) Sequestration |
title_short | Microbial Reverse-Electrodialysis Electrolysis and
Chemical-Production Cell for H(2) Production and CO(2) Sequestration |
title_sort | microbial reverse-electrodialysis electrolysis and
chemical-production cell for h(2) production and co(2) sequestration |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3982931/ https://www.ncbi.nlm.nih.gov/pubmed/24741666 http://dx.doi.org/10.1021/ez500073q |
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