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Jennifer L. Wade

Publications and source records attributed to Jennifer L. Wade.

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Vacuum Moisture Swing Direct Air Capture: A Low-Thermal, Water-Managed Pathway for Scalable CO2 Removal

Direct Air Capture remains highly energy intensive, with most systems relying on high-temperature regeneration of amines or metal oxides. Here we present the first comprehensive evaluation of a low-temperature DAC process based on a moisture-swing mechanism that reversibly captures and releases CO2 using commercial ion exchange resins. The proposed vacuum moisture swing, VMS, process replaces thermal regeneration with a low-temperature water vapor stripping step driven by vacuum evaporation. A cyclic model, informed by experimentally measured water and CO2 sorption kinetics, was optimized across air relative humidity of 20 to 80 percent and kinetic regimes of 0.5 to 2.0x baseline. Optimized VMS operation at 20 percent relative humidity achieves CO2 productivities of 0.2 to 0.6 kg CO2 per kg sorbent per day, comparable to or exceeding high-temperature amine systems without external heat input. Electrical energy required for gas and vapor flow and CO2 compression to 0.1 MPa ranges from 1 to 15 MJ per kg CO2, driven primarily by vapor flow in the stripping step. At a representative productivity of 0.5 kg CO2 per kg sorbent per day, energy demand is about 2.5 MJ per kg CO2, surpassing typical productivity, energy tradeoffs, but with water losses of 1.4 to 3.5 kg water per kg CO2 due to evaporation, similar to liquid-based systems. Water loss scales with productivity and decreases under higher humidity and faster kinetics. The VMS process manages water through vacuum-driven evaporation and condensation, enabling the use of non-fresh or saline water sources. This work establishes a low-temperature DAC pathway that integrates realistic CO2 and water transport with built-in water management.

physics.chem-ph

SERS Raman detection of the CO$_2$ Moisture Swing

The development of scalable, energy-efficient carbon dioxide capture technologies is critical for achieving net-zero emissions. Moisture swing sorbents offer a promising alternative to traditional thermal regeneration methods by enabling reversible CO$_2$ binding through humidity-driven ion hydrolysis. In this study, we investigate the anion speciation dynamics in two classes of MS materials, an anion-exchange resin with bicarbonate anion and activated carbon impregnated with potassium bicarbonate salt using both sorption measurements and in situ surface-enhanced Raman spectroscopy. Ni coated Ag nanowires were employed as SERS substrates to enhance signal intensity and enable the real-time detection of carbonate , bicarbonate , and hydroxide species under controlled humidity conditions in both air and nitrogen atmospheres. The results reveal humidity-dependent interconversion between anionic species, with significant spectral shifts confirming the reversible hydrolysis reactions that drive the MS mechanism. Under humid conditions, we observed the depletion of bicarbonate signals and a concurrent increase in carbonate species, consistent with moisture-induced desorption of CO$_2$. These findings not only validate the mechanistic models of humidity-driven anion exchange in moisture swing sorbents but also demonstrate the practical potential of SERS as an operando diagnostic tool for monitoring CO$_2$ capture media. The ability to resolve and quantify the reversible transformation of carbonate, bicarbonate, and hydroxide ions under realistic environmental conditions provides valuable insight for the rational design, performance optimization, and quality control of next-generation sorbent materials for direct air capture applications.

cond-mat.mtrl-sci