Affiliation:
1. Pacific Northwest National Laboratory Battelle Blvd 99352 Richland WA USA
2. Department of Chemical & Biological Engineering University of Alabama 35487-0203 Tuscaloosa AL USA
3. Present address: Oak Ridge National Laboratory 37830 Oak Ridge TN USA
4. Washington State University 99164-1067 Pullman WA USA
Abstract
AbstractEfficient direct air capture (DAC) of CO2 will require strategies to deal with the relatively low concentration in the atmosphere. One such strategy is to employ the combination of a CO2‐selective membrane coupled with a CO2 capture solvent acting as a draw solution. Here, the interactions between a leading water‐lean carbon‐capture solvent, a polyether ether ketone (PEEK)‐ionene membrane, CO2, and combinations were probed using advanced NMR techniques coupled with advanced simulations. We identify the speciation and dynamics of the solvent, membrane, and CO2, presenting spectroscopic evidence of CO2 diffusion through benzylic regions within the PEEK‐ionene membrane, not spaces in the ionic lattice as expected. Our results demonstrate that water‐lean capture solvents provide a thermodynamic and kinetic funnel to draw CO2 from the air through the membrane and into the bulk solvent, thus enhancing the performance of the membrane. The reaction between the carbon‐capture solvent and CO2 produces carbamic acid, disrupting interactions between the imidazolium (Im+) cations and the bistriflimide anions within the PEEK‐ionene membrane, thereby creating structural changes through which CO2 can diffuse more readily. Consequently, this restructuring results in CO2 diffusion at the interface that is faster than CO2 diffusion in the bulk carbon‐capture solvent.
Funder
U.S. Department of Energy
Office of Science
Basic Energy Sciences
Subject
General Energy,General Materials Science,General Chemical Engineering,Environmental Chemistry
Cited by
3 articles.
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