CO from carbonate-based capture solutions requires a substantial energy input. Replacing this step with (bi)carbonate electrolysis has been commonly proposed as an efficient alternative that coproduces CO/syngas. Here, we assess the feasibility of directly integrating air contactors with (bi)carbonate electrolyzers by leveraging process, multiphysics, microkinetic, and technoeconomic models. We show that the copresence of CO with HCO in the contactor effluent greatly diminishes the electrolyzer performance and eventually results in a reduced CO capture fraction to ≤1%. Additionally, we estimate suitable effluents for (bi)carbonate electrolysis to require 5-14 times larger contactors than conventionally needed contactors, leading to unfavorable process economics. Notably, we show that the regeneration of the capture solvent inside (bi)carbonate electrolyzers is insufficient for CO recapture. Thus, we suggest process modifications that would allow this route to be operationally feasible. Overall, this work sheds light on the practical operation of integrated direct air capture with (bi)carbonate electrolysis.
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http://dx.doi.org/10.1021/acsenergylett.4c00807 | DOI Listing |
Molecules
December 2024
Department of Mechatronics, Faculty of Technical Sciences, University of Warmia and Mazury in Olsztyn, 10-719 Olsztyn, Poland.
This study investigates the influence of prolonged electrolysis on the electrochemical performance and surface characteristics of NiFe-modified compressed graphite electrodes used in alkaline water electrolysis. The electrochemical experiment was conducted over a two-week period at a constant temperature of 60 °C. The electrodes were evaluated for changes in surface morphology and composition using scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and X-ray diffraction (XRD).
View Article and Find Full Text PDFSmall
December 2024
Department of Chemical Engineering, Queen's University, Kingston, ON, K7L 3N6, Canada.
Electrochemical carbon dioxide (CO) reduction from aqueous solutions offers a promising strategy to overcome flooding and salt precipitation in gas diffusion electrodes used in gas-phase CO electrolysis. However, liquid-phase CO electrolysis often exhibits low CO reduction rates because of limited CO availability. Here, a macroporous Ag mesh is employed and activated to achieve selective CO conversion to CO with high rates from an aqueous bicarbonate solution.
View Article and Find Full Text PDFACS Sustain Chem Eng
October 2024
Laboratory for the Chemistry of Construction Materials (LC2), Department of Civil and Environmental Engineering, University of California, Los Angeles, California 90095, United States.
Limestone (calcite, CaCO) is an abundant and cost-effective source of calcium oxide (CaO) for cement and lime production. However, the thermochemical decomposition of limestone (∼800 °C, 1 bar) to produce lime (CaO) results in substantial carbon dioxide (CO) emissions and energy use, i.e.
View Article and Find Full Text PDFChemSusChem
September 2024
Process and Energy Department, Faculty of Mechanical Engineering, Delft University of Technology, 2628 CB, Delft, Zuid-Holland, The Netherlands.
Electrolytic bicarbonate conversion holds the promise to integrate carbon capture directly with electrochemical conversion. Most research has focused on improving the faradaic efficiencies of the system, however, the stability of the system has not been thoroughly addressed. Here, we find that the bulk electrolyte pH has a large effect on the selectivity, where a higher pH results in a lower selectivity.
View Article and Find Full Text PDFACS Appl Energy Mater
September 2024
School of Physics, Trinity College Dublin, Dublin D02 PN40, Ireland.
In pursuit of commercial viability for carbon dioxide (CO) electrolysis, this study investigates the operational challenges associated with membrane electrode assembly (MEA)-type CO electrolyzers, with a focus on CO loss into the solution phase through bicarbonate (HCO ) and carbonate (CO ) ion formation. Utilizing a silver electrode known for selectively facilitating CO to CO conversion, the molar production of CO, CO, and H is measured across a range of current densities from 0 to 600 mA/cm, while maintaining a constant CO inlet flow rate of 58 mL/min. The dynamics of CO loss are monitored through measurements of pH changes in the electrolyte and carbon elemental balance analysis.
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