Ultra-thin enzymatic liquid membrane for CO2 separation and capture

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作者
Yaqin Fu
Ying-Bing Jiang
Darren Dunphy
Haifeng Xiong
Eric Coker
Stanley S. Chou
Hongxia Zhang
Juan M. Vanegas
Jonas G. Croissant
Joseph L. Cecchi
Susan B. Rempe
C. Jeffrey Brinker
机构
[1] University of New Mexico,Department of Chemical and Biological Engineering
[2] University of New Mexico,Center for Micro
[3] University of New Mexico,Engineered Materials
[4] Sandia National Laboratories,Department of Earth and Planetary Sciences
[5] Angstrom Thin Film Technologies LLC,Department of Physics
[6] University of Vermont,undefined
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The limited flux and selectivities of current carbon dioxide membranes and the high costs associated with conventional absorption-based CO2 sequestration call for alternative CO2 separation approaches. Here we describe an enzymatically active, ultra-thin, biomimetic membrane enabling CO2 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 CO2 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 CO2 at room temperature and atmospheric pressure at a rate of 2600 GPU with CO2/N2 and CO2/H2 selectivities as high as 788 and 1500, respectively, the highest combined flux and selectivity yet reported for ambient condition operation.
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