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Electrochemical carbon dioxide capture to close the carbon cycle

Journal Article · · Energy & Environmental Science
DOI:https://doi.org/10.1039/d0ee03382k· OSTI ID:1853750
 [1];  [2];  [3];  [3];  [4]
  1. Delft Univ. of Technology (Netherlands); Wetsus, European Centre of Excellence for Sustainable Water Technology, Leeuwarden (Netherlands); OSTI
  2. Wetsus, European Centre of Excellence for Sustainable Water Technology, Leeuwarden (Netherlands)
  3. California Institute of Technology (CalTech), Pasadena, CA (United States)
  4. Delft Univ. of Technology (Netherlands)

Electrochemical CO2 capture technologies are gaining attention due to their flexibility, their ability to address decentralized emissions (e.g., ocean and atmosphere) and their fit in an electrified industry. In the present work, recent progress made in electrochemical CO2 capture is reviewed. The majority of these methods rely on the concept of “pH-swing” and the effect it has on the CO2 hydration/dehydration equilibrium. Through a pH-swing, CO2 can be captured and recovered by shifting the pH of a working fluid between acidic and basic pH. Such swing can be applied electrochemically through electrolysis, bipolar membrane electrodialysis, reversible redox reactions and capacitive deionization. In this review, we summarize main parameters governing these electrochemical pH-swing processes and put the concept in the framework of available worldwide capture technologies. We analyse the energy efficiency and consumption of such systems, and provide recommendations for further improvements. Although electrochemical CO2 capture technologies are rather costly compared to the amine based capture, they can be particularly interesting if more affordable renewable electricity and materials (e.g., electrode and membranes) become widely available. Furthermore, electrochemical methods have the ability to (directly) convert the captured CO2 to value added chemicals and fuels, and hence prepare for a fully electrified circular carbon economy.

Research Organization:
California Institute of Technology (CalTech), Pasadena, CA (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES)
Grant/Contract Number:
SC0021266
OSTI ID:
1853750
Journal Information:
Energy & Environmental Science, Journal Name: Energy & Environmental Science Journal Issue: 2 Vol. 14; ISSN 1754-5692
Publisher:
Royal Society of ChemistryCopyright Statement
Country of Publication:
United States
Language:
English

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  • Mitchell, Mark J.; Jensen, Oliver E.; Cliffe, K. Andrew
  • Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences, Vol. 466, Issue 2117 https://doi.org/10.1098/rspa.2009.0349
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