Global warming, driven by the accumulation of anthropogenic greenhouse gases, particularly CO, in the atmosphere, has garnered significant attention due to its detrimental environmental impacts. To combat this critical issue, the deployment of CO capture and utilization (CCU) strategies has been considered as one of the technology-based solutions, leading to extensive scientific and engineering research. Electrochemical pH-swing (EPS) processes offer a promising approach to diverse CCU pathways, such as the delivery of pure CO gas, the delivery of bicarbonate (e.g., for microalgae cultivation), and the formation of carbonate minerals. In this study, we discuss several CCU pathways using EPS and provide an in-depth analysis of its mechanisms and potential applications, outlining its limitations from both thermodynamic and kinetic standpoints. The EPS process has demonstrated remarkable capabilities, achieving a CO capture efficiency of over 90% and unlocking valuable opportunities for CCU applications. We also develop an initial techno-economic assessment and provide the perspectives and challenges for future development and deployment of EPS. This study sheds light on the integration of EPS with CCU, closing the carbon cycle by effectively utilizing the products generated through the process, such as carbonate minerals and bicarbonate solution. For instance, the bicarbonate product can serve as a viable feedstock for bicarbonate-based microalgae production systems, with the added benefit of reducing costs by 40-80% compared to traditional gaseous CO delivery approaches. By integration of electrochemical technologies with CCU methods, this study underscores the immense potential for mitigating CO emissions and advancing sustainable practices to combat global warming. This study not only addresses the urgent need for effective solutions but also paves the way for a greener and more sustainable future.
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http://dx.doi.org/10.1021/acs.iecr.3c02183 | DOI Listing |
Environ Sci Technol
December 2024
Department of Mechanical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States.
In recent years, marine carbon removal technologies have gained attention as a means of reducing greenhouse gas concentrations. One family of these technologies is electrochemical systems, which employ Faradaic reactions to drive alkalinity-swings and enable dissolved inorganic carbon (DIC) removal as gaseous CO or as solid minerals. In this work, we develop a thermodynamic framework to estimate upper bounds on performance for Faradaic DIC removal systems.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
November 2024
Department of Materials Science and Engineering, Stanford University, Stanford, CA 94305.
Electrochemical pH-swing strategies offer a promising avenue for cost-effective and energy-efficient carbon dioxide (CO) capture, surpassing the traditional thermally activated processes and humidity-sensitive techniques. The concept of elevating seawater's alkalinity for scalable CO capture without introducing additional chemical as reactant is particularly intriguing due to its minimal environmental impact. However, current commercial plants like chlor-alkali process or water electrolysis demand high thermodynamic voltages of 2.
View Article and Find Full Text PDFACS Org Inorg Au
August 2024
Department of Chemistry, University of California, Irvine, 1102 Natural Sciences II, Irvine, California 92697-2025, United States.
Escalating levels of carbon dioxide (CO) in the atmosphere have motivated interest in CO capture and concentration from dilute streams. A guanidino-functionalized aromatic 1,4-bis(tetramethylguanidino)benzene (1,4-btmgb) was evaluated both as a redox-active sorbent and as a pH swing mediator for electrochemical CO capture and concentration. Spectroscopic and crystallographic studies demonstrate that 1,4-btmgb reacts with CO in water to form 1,4-btmgbH(HCO ).
View Article and Find Full Text PDFACS Sustain Chem Eng
May 2024
Wetsus, European Centre of Excellence for Sustainable Water Technology, P.O. Box 1113, 8900CC Leeuwarden, The Netherlands.
Carbon capture is widely acknowledged as a promising strategy for achieving negative emissions. Electrochemical carbon capture technologies are considered a viable alternative to conventional temperature swing processes. Among these, employing the hydrogen oxidation and hydrogen evolution reactions as a redox couple, along with an ion exchange membrane, offers an effective means of establishing a pH swing for desorbing CO and regenerating the alkaline solvent.
View Article and Find Full Text PDFAcc Chem Res
February 2024
Smith School of Chemical and Biomolecular Engineering, Cornell University, Ithaca, New York 14853, United States.
ConspectusAchieving carbon neutrality requires realizing scalable advances in energy- and material-efficient pathways to capture, convert, store, and remove anthropogenic CO emission in air and flue gas while cogenerating multiple high-value products. To this end, earth-abundant Ca- and Mg-bearing alkaline resources can be harnessed to cogenerate Ca- and Mg-hydroxide, silica, H, O, and a leachate bearing high-value metals in an electrochemical approach with the generation of a pH gradient, which is a significant departure from existing pH-swing-based approaches. To accelerate CO capture and mineralization, CO in dilute sources is captured using solvents to produce CO-loaded solvents.
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