Hierarchically porous carbon foams coated with carbon nitride : insights into adsorbents for pre-combustion and post-combustion CO2 separation
Vorokhta, Maryna and Kusdhany, Muhammad Irfan Maulana and Švábová, Martina and Nishihara, Masamichi and Sasaki, Kazunari and Lyth, Stephen Matthew (2025) Hierarchically porous carbon foams coated with carbon nitride : insights into adsorbents for pre-combustion and post-combustion CO2 separation. Separation and Purification Technology, 354 (5). 129054. ISSN 1383-5866 (https://doi.org/10.1016/j.seppur.2024.129054)
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Abstract
Adsorption is fundamental to many industrial processes, including separation of carbon dioxide from other gases in pre- or post-combustion gas mixtures. Adsorbents should have high capacity and selectivity, which are both intimately linked with surface area, pore size distribution, and surface energy. Porous carbons are cheap and scalable adsorbents, but greater understanding of how their textural properties and surface chemistry affects their performance is needed. Here, we investigate the effect of nitrogen doping on CO2 adsorption. Microporous carbon foams with large surface area (>2500 m2 g−1) and pore volume (1.6 cm3 g−1) are synthesized, then coated with varying amounts of carbon nitride (up to 17 at% nitrogen) to achieve high CO2 uptake (25.5 mmol g−1) and selectivity (CO2:N2 = 21), whilst also giving insights into the relationship between structure and function. At low pressure (relevant to post-combustion capture), moderate carbon nitride loading leads to enhanced uptake and selectivity by combining large ultramicropore volume with the introduction of Lewis base sites, leading to high isosteric heat of adsorption. Higher carbon nitride loading further increases selectivity but lowers uptake by blocking micropores. Conversely, at high pressure (relevant to pre-combustion capture) the uncoated carbon foam displays superior uptake, because mesoporosity is the dominant factor in this regime, rather than the presence of ultramicropores. Finally, the samples displayed excellent regeneration under repeated adsorption–desorption cycles, and breakthrough curves were measured. These results underscore the delicate balance required for optimal material design when applying porous carbon adsorbents to CO2 separation processes. Moving forward, improved adsorbents will contribute to the proliferation of carbon capture and storage (CCS) and carbon capture and utilisation (CCU) technologies, ultimately contributing reduced anthropogenic CO2 emissions.
ORCID iDs
Vorokhta, Maryna, Kusdhany, Muhammad Irfan Maulana, Švábová, Martina, Nishihara, Masamichi, Sasaki, Kazunari and Lyth, Stephen Matthew ORCID: https://orcid.org/0000-0001-9563-867X;-
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Item type: Article ID code: 90305 Dates: DateEvent19 February 2025Published8 August 2024Published Online30 July 2024Accepted4 June 2024SubmittedSubjects: Science > Chemistry
Technology > Chemical engineeringDepartment: Faculty of Engineering > Chemical and Process Engineering Depositing user: Pure Administrator Date deposited: 20 Aug 2024 11:25 Last modified: 22 Nov 2024 01:22 URI: https://strathprints.strath.ac.uk/id/eprint/90305