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Design and development of 3D hierarchical ultra-microporous CO2-sieving carbon architectures for potential flow-through CO2 capture at typical practical flue gas temperatures

Liu, Xin; Liu, Jingjing; Sun, Chenggong; Liu, Hao; Wang, Wenlong; Smith, Emily; Jiang, Long; Chen, Xinyong; Snape, Colin

Design and development of 3D hierarchical ultra-microporous CO2-sieving carbon architectures for potential flow-through CO2 capture at typical practical flue gas temperatures Thumbnail


Authors

Xin Liu

Jingjing Liu

Chenggong Sun

HAO LIU LIU.HAO@NOTTINGHAM.AC.UK
Professor of Energy Engineering

Wenlong Wang

Emily Smith

LONG JIANG LONG.JIANG@NOTTINGHAM.AC.UK
Surface Analytical Officer

Xinyong Chen

COLIN SNAPE COLIN.SNAPE@NOTTINGHAM.AC.UK
Professor of Chemical Technology & Chemical Eng



Abstract

Developing effective carbon materials for post-combustion CO2 capture (PCC) has received great attentions over many recent years, owing to their desirable adsorption−desorption performance and exceptional thermo-oxidative stability compared to virtually any other capture materials typically the wide array of amine-based sorbent materials. However, due to the nature of physical adsorption, virtually none of the carbon materials reported so far can be practically used for PCC applications without deep flue gas cooling to ambient or even lower temperatures in order to achieve appreciable levels of CO2 uptake capacities at low CO2 partial pressures. Here, we present a category of 3D hierarchical molecular sieving carbon architectures that are able to operate at realistic flue gas temperatures with exceedingly high reversible CO2 capacities. The breakthrough CO2-sieving carbon materials are prepared from using a cost-effective and commercially widely available precursor of polymeric polyisocyanurates with a facile one-step compaction-activation methodology. Tested at sensible flue gas temperatures of 40−70 o C and a low CO2 partial pressure of 0.15 bar, the best performing materials are found to have exceedingly high reversible CO2 capacities of up to 2.30mmol/g at 40 o C and 1.90mmol/g at 70 o C. Advanced characterisations suggest that the unique geometry and chemistry of the easily available precursor material coupled with the characteristics of the compaction-activation protocol used are responsible for the CO2-sieving structures and capacities of the 3D carbon architectures. The findings essentially change the general perception that carbon-based materials can hardly find applications in post-combustion capture due to their low CO2 uptake capacity at low CO2 partial pressures and realistic flue gas temperatures.

Citation

Liu, X., Liu, J., Sun, C., Liu, H., Wang, W., Smith, E., …Snape, C. (2020). Design and development of 3D hierarchical ultra-microporous CO2-sieving carbon architectures for potential flow-through CO2 capture at typical practical flue gas temperatures. Journal of Materials Chemistry A, 8(33), 17025-17035. https://doi.org/10.1039/d0ta01417f

Journal Article Type Article
Acceptance Date Mar 8, 2020
Online Publication Date Aug 5, 2020
Publication Date Sep 7, 2020
Deposit Date May 1, 2020
Publicly Available Date Aug 6, 2021
Journal Journal of Materials Chemistry A
Print ISSN 2050-7488
Electronic ISSN 2050-7496
Peer Reviewed Peer Reviewed
Volume 8
Issue 33
Pages 17025-17035
DOI https://doi.org/10.1039/d0ta01417f
Keywords General Materials Science; Renewable Energy, Sustainability and the Environment; General Chemistry
Public URL https://nottingham-repository.worktribe.com/output/4369015
Publisher URL https://pubs.rsc.org/en/content/articlelanding/2020/ta/d0ta01417f
Additional Information : This document is Similarity Check deposited; : Supplementary Information; : Xin Liu (ORCID); : Chenggong Sun (ORCID); : Hao Liu (ORCID); : Long Jiang (ORCID); : Single-blind; : Received 6 February 2020; Accepted 8 March 2020; Advance Article published 5 August 2020

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