Carbon dioxide (CO) electrolysis is a promising route to utilise captured CO as a building block to produce valuable feedstocks and fuels such as carbon monoxide and ethylene. Very recently, CO electrolysis has been proposed as an alternative process to replace the amine recovery unit of the commercially available amine-based CO capture process. This process would replace the most energy-intensive unit operation in amine scrubbing while providing a route for CO conversion. The key enabler for such process integration is to develop an efficient integrated electrolyser that can convert CO and recover the amine simultaneously. Herein, this review provides an overview of the fundamentals and recent progress in advancing integrated CO conversion in amine-based capture media. This review first discusses the mechanisms for both CO absorption in the capture medium and electrochemical conversion of the absorbed CO. We then summarise recent advances in improving the efficiency of integrated electrolysis innovating electrodes, tailoring the local reaction environment, optimising operation conditions (, temperatures and pressures), and modifying cell configurations. This review is concluded with future research directions for understanding and developing integrated CO electrolysers.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1039/d2nr03310k | DOI Listing |
Environ Sci Technol
January 2025
Zhejiang Key Laboratory of Clean Energy Conversion and Utilization, Science and Education Integration College of Energy and Carbon Neutralization, Zhejiang University of Technology, Hangzhou 310014, China.
ACS Omega
December 2024
Faculty of Materials Science and Engineering, Kyoto Institute of Technology, Matsugasaki, Sakyo-ku, Kyoto 606-8585, Japan.
ACS Omega
December 2024
Department of Chemistry, Graduate School of Science, Tokyo Metropolitan University, Hachioji, Tokyo 192-0397, Japan.
CO chemisorption using amine-based sorbents is one of the most effective techniques for carbon capture and storage. Solid CO sorbents with amines immobilized on their surface have been attracting attention due to the easy collection of sorbents and reusability. In this study, we developed a solid CO adsorbent by co-condensation of a silanizing reagent having a chloroalkyl group and tetraethyl ethoxysilane, followed by alkylation of the chloroalkyl group with diamine.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Chemical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37830, United States.
Direct air capture (DAC) technologies are limited by the poor understanding of the dynamic role of interfaces in modulating the chemisorption of CO from air into solutions. While the reactivity of aqueous amine-based solvents in the bulk environment is strongly inhibited by nonequilibrium solvent effects, promoting DAC at interfaces posits a possibility to reduce the coupling with the solvent and significantly accelerate DAC. Building on an experimentally proven concept to bring an anionic glycine absorbent to the interface through ion-pairing interactions with a positively charged surfactant, we establish the fundamental time scales for key elementary steps involved in DAC with rate theory and enhanced-sampling molecular dynamics simulations.
View Article and Find Full Text PDFChemphyschem
November 2024
Department of Chemistry, University of Tennessee, 37996, Knoxville, Tennessee, United States.
Carbon capture, sequestration and utilization offers a viable solution for reducing the total amount of atmospheric CO concentrations. On an industrial scale, amine-based solvents are extensively employed for CO capture through chemisorption. Nevertheless, this method is marked by the high cost associated with solvent regeneration, high vapor pressure, and the corrosive and toxic attributes of by-products, such as nitrosamines.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!