Journal
JOURNAL OF MATERIALS CHEMISTRY A
Volume 2, Issue 15, Pages 5481-5489Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4ta00438h
Keywords
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Funding
- UK EPSRC [EP/G063176/1, EP/G061785/1, EP/I010955/1]
- National Nature Science Foundation of China [51172251, 51061130536]
- Shanxi Province Science and Technology Innovation Program [2012102007]
- Shanxi Province International Collaboration Program [2013081016]
- Institute of Coal Chemistry, Chinese Academy of Sciences
- Department of Chemistry, University College London
- Department of Chemical and Environmental Engineering, University of Nottingham
- EPSRC [EP/G063176/1, EP/G061785/1, EP/I010955/1] Funding Source: UKRI
- Engineering and Physical Sciences Research Council [EP/I010955/1, EP/G061785/1, EP/G063176/1] Funding Source: researchfish
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A facile and efficient spheridization method is developed to produce nitrogen-enriched hierarchically porous carbon spheres of millimeters in diameter, with intricate micro-, meso-and macro-structural features. Such spheres not only show exceptional working capacity for CO2 sorption, but also satisfy practical requirements for dynamic flow in post-combustion CO2 capture. Those were achieved using co-polymerized acrylonitrile and acrylamide as the N-enriched carbon precursor, a solvent-exchange process to create hierarchically porous macro-sphere preforms, oxidization to induce cyclization of the polymer chains, and carbonization with concurrent chemical activation by KOH. The resulting carbon spheres show a relatively high CO2 uptake of 16.7 wt% under 1 bar of CO2 and, particularly, an exceptional uptake of 9.3 wt% under a CO2 partial pressure of 0.15 bar at 25 degrees C. Subsequent structural and chemical analyses suggest that the outstanding properties are due to highly developed microporous structures and the relatively high pyridinic nitrogen content inherited from the co-polymer precursor, incorporated within the hierarchical porous structures.
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