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Ultra-thin enzymatic liquid membrane for CO(2) separation and capture
The limited flux and selectivities of current carbon dioxide membranes and the high costs associated with conventional absorption-based CO(2) sequestration call for alternative CO(2) separation approaches. Here we describe an enzymatically active, ultra-thin, biomimetic membrane enabling CO(2) captu...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5841395/ https://www.ncbi.nlm.nih.gov/pubmed/29515116 http://dx.doi.org/10.1038/s41467-018-03285-x |
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author | Fu, Yaqin Jiang, Ying-Bing Dunphy, Darren Xiong, Haifeng Coker, Eric Chou, Stanley S. Zhang, Hongxia Vanegas, Juan M. Croissant, Jonas G. Cecchi, Joseph L. Rempe, Susan B. Brinker, C. Jeffrey |
author_facet | Fu, Yaqin Jiang, Ying-Bing Dunphy, Darren Xiong, Haifeng Coker, Eric Chou, Stanley S. Zhang, Hongxia Vanegas, Juan M. Croissant, Jonas G. Cecchi, Joseph L. Rempe, Susan B. Brinker, C. Jeffrey |
author_sort | Fu, Yaqin |
collection | PubMed |
description | The limited flux and selectivities of current carbon dioxide membranes and the high costs associated with conventional absorption-based CO(2) sequestration call for alternative CO(2) separation approaches. Here we describe an enzymatically active, ultra-thin, biomimetic membrane enabling CO(2) capture and separation under ambient pressure and temperature conditions. The membrane comprises a ~18-nm-thick close-packed array of 8 nm diameter hydrophilic pores that stabilize water by capillary condensation and precisely accommodate the metalloenzyme carbonic anhydrase (CA). CA catalyzes the rapid interconversion of CO(2) and water into carbonic acid. By minimizing diffusional constraints, stabilizing and concentrating CA within the nanopore array to a concentration 10× greater than achievable in solution, our enzymatic liquid membrane separates CO(2) at room temperature and atmospheric pressure at a rate of 2600 GPU with CO(2)/N(2) and CO(2)/H(2) selectivities as high as 788 and 1500, respectively, the highest combined flux and selectivity yet reported for ambient condition operation. |
format | Online Article Text |
id | pubmed-5841395 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58413952018-03-09 Ultra-thin enzymatic liquid membrane for CO(2) separation and capture Fu, Yaqin Jiang, Ying-Bing Dunphy, Darren Xiong, Haifeng Coker, Eric Chou, Stanley S. Zhang, Hongxia Vanegas, Juan M. Croissant, Jonas G. Cecchi, Joseph L. Rempe, Susan B. Brinker, C. Jeffrey Nat Commun Article The limited flux and selectivities of current carbon dioxide membranes and the high costs associated with conventional absorption-based CO(2) sequestration call for alternative CO(2) separation approaches. Here we describe an enzymatically active, ultra-thin, biomimetic membrane enabling CO(2) capture and separation under ambient pressure and temperature conditions. The membrane comprises a ~18-nm-thick close-packed array of 8 nm diameter hydrophilic pores that stabilize water by capillary condensation and precisely accommodate the metalloenzyme carbonic anhydrase (CA). CA catalyzes the rapid interconversion of CO(2) and water into carbonic acid. By minimizing diffusional constraints, stabilizing and concentrating CA within the nanopore array to a concentration 10× greater than achievable in solution, our enzymatic liquid membrane separates CO(2) at room temperature and atmospheric pressure at a rate of 2600 GPU with CO(2)/N(2) and CO(2)/H(2) selectivities as high as 788 and 1500, respectively, the highest combined flux and selectivity yet reported for ambient condition operation. Nature Publishing Group UK 2018-03-07 /pmc/articles/PMC5841395/ /pubmed/29515116 http://dx.doi.org/10.1038/s41467-018-03285-x Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Fu, Yaqin Jiang, Ying-Bing Dunphy, Darren Xiong, Haifeng Coker, Eric Chou, Stanley S. Zhang, Hongxia Vanegas, Juan M. Croissant, Jonas G. Cecchi, Joseph L. Rempe, Susan B. Brinker, C. Jeffrey Ultra-thin enzymatic liquid membrane for CO(2) separation and capture |
title | Ultra-thin enzymatic liquid membrane for CO(2) separation and capture |
title_full | Ultra-thin enzymatic liquid membrane for CO(2) separation and capture |
title_fullStr | Ultra-thin enzymatic liquid membrane for CO(2) separation and capture |
title_full_unstemmed | Ultra-thin enzymatic liquid membrane for CO(2) separation and capture |
title_short | Ultra-thin enzymatic liquid membrane for CO(2) separation and capture |
title_sort | ultra-thin enzymatic liquid membrane for co(2) separation and capture |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5841395/ https://www.ncbi.nlm.nih.gov/pubmed/29515116 http://dx.doi.org/10.1038/s41467-018-03285-x |
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