This review is designed to foster the discussion regarding the viability of postcombustion CO capture by water-lean solvents, by separating fact from fiction for both skeptics and advocates. We highlight the unique physical and thermodynamic properties of notable water-lean solvents, with a discussion of how such properties could translate to efficiency gains compared to aqueous amines. The scope of this review ranges from the purely fundamental molecular-level processes that govern solvent behavior to bench-scale testing, through process engineering and projections of process performance and cost. Key discussions of higher than expected CO mass transfer, water tolerance, and compatibility with current infrastructure are presented along with current limitations and suggested areas where further solvent development is needed. We conclude with an outlook of the status of the field and assess the viability of water-lean solvents for postcombustion CO capture.
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http://dx.doi.org/10.1021/acs.chemrev.6b00768 | DOI Listing |
ACS Omega
November 2024
Pacific Northest National Laboratory, 902 Battelle Blvd, Richland, Washington 99352, United States.
Here, we demonstrate an integrated semibatch simultaneous CO capture and conversion to methanol process using a water-lean solvent, -(2-ethoxyethyl)-3-morpholinopropan-1-amine (2-EEMPA), that serves as both the capture solvent and subsequent condensed-phase medium for the catalytic hydrogenation of CO. CO is captured from simulated coal-derived flue gas at a target >90 mol % capture efficiency, with a continuous slipstream of CO-rich solvent delivered to a fixed bed catalytic reactor for catalytic hydrogenation. A single-pass conversion rate >60 C-mol % and selectivity >80 C-mol % are observed for methanol at relatively low temperatures (<200 °C) in the condensed phase of the carbon capture solvent.
View Article and Find Full Text PDFNat Chem
July 2024
Pacific Northwest National Laboratory, Richland, WA, USA.
Carbon capture, utilization and storage is a key yet cost-intensive technology for the fight against climate change. Single-component water-lean solvents have emerged as promising materials for post-combustion CO capture, but little is known regarding their mechanism of action. Here we present a combined experimental and modelling study of single-component water-lean solvents, and we find that CO capture is accompanied by the self-assembly of reverse-micelle-like tetrameric clusters in solution.
View Article and Find Full Text PDFAnal Chem
October 2023
Pacific Northwest National Laboratory, Richland, Washington 99352, United States.
Carbon capture represents a key pathway to meeting climate change mitigation goals. Powerful next-generation solvent-based capture processes are under development by many researchers, but optimization and testing would be significantly aided by integrating in situ monitoring capability. Further, real-time water analysis in water-lean solvents offers the potential to maintain their water balance in operation.
View Article and Find Full Text PDFChemSusChem
July 2023
Pacific Northwest National Laboratory, Battelle Blvd, 99352, Richland, WA, USA.
Efficient direct air capture (DAC) of CO will require strategies to deal with the relatively low concentration in the atmosphere. One such strategy is to employ the combination of a CO -selective membrane coupled with a CO 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, CO , and combinations were probed using advanced NMR techniques coupled with advanced simulations.
View Article and Find Full Text PDFInd Eng Chem Res
November 2022
Department of Chemical Engineering, NTNU, NO-7491Trondheim, Norway.
Water-lean solvents have been proposed as a possible alternative to aqueous amine systems in postcombustion carbon capture. There is however little data available on how amine degradation is affected by different solvents. This study presents new insights on the effect of solvent on thermal degradation of alkanolamines from laboratory-scale degradation experiments.
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