4.8 Article

Facile and environmentally friendly synthesis of ultramicroporous carbon spheres: A significant improvement in CVD method

Journal

CARBON
Volume 171, Issue -, Pages 426-436

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.carbon.2020.08.056

Keywords

Carbon spheres; Ultramicropores; CVD; Green; CO2 capture

Funding

  1. European Union [663830]
  2. Engineering and Physical Sciences Research Council-Impact Acceleration Account (EPSRC-IAA) [RIF67]
  3. Reduced Industrial Carbon Emissions (RICE) research operation - EU's European Regional Development Fund through the Welsh Government
  4. Flexible Integrated Energy Systems (FLEXIS) research operation - EU's European Regional Development Fund through the Welsh Government
  5. EPSRC [EP/M028267/1]
  6. European Regional Development Fund through the Welsh Government [80708]
  7. Ser Solar project via theWelsh Government
  8. EPSRC [EP/K006061/1, EP/D049245/1, EP/E005918/1, EP/M028267/1, EP/E004563/1, EP/D037794/1, EP/K006061/2] Funding Source: UKRI

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A new environmentally friendly method for synthesizing ultramicroporous carbon spheres was developed using a simple one-step non-catalytic CVD process at 800 degrees C. The carbon spheres exhibited high CO2 capture capacity and good regeneration performance.
A new and environmentally friendly non-caustic route to synthesize ultramicroporous carbon spheres (CS) via a simple one-step non-catalytic and activation-free chemical vapor deposition (CVD) method is described. The CVD method was applied at different temperatures, 600-900 degrees C; 800 degrees C was identified as the optimum for CS formation using a safe solid feedstock. The ultramicropores allow the effective interaction of the sorbent with CO2, resulting in high carbon capture capacity at both atmospheric and lower pressures. Specific surface area and total pore volume were influenced by the deposition temperature, leading to an appreciable change in overall carbon dioxide capture capacity. At atmospheric pressure, the highest CO2 adsorption capacities were ca. 4.0 mmol.g(-1) and 2.9 mmol.g(-1) at 0 degrees C and 25 degrees C, respectively, for the best CS. At lower pressure, 0.15 bar, the CO2 adsorption capacities were 2.0 mmol.g(-1) and 1.1 mmol.g(-1), again at 0 degrees C and 25 degrees C. The CS showed good sorption/desorption cyclability, ease of regeneration, favorable selectivity over N-2 of 30:1 at 25 degrees C, and rapid kinetics. The proposed method is suitable for large-scale adoption since high pyrolysis temperatures are already used in multi-million-ton industries such as that of carbon black production. (C) 2020 Elsevier Ltd. All rights reserved.

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