4.7 Article

Direct formation of hierarchically porous MgO-based sorbent bead for enhanced CO2 capture at intermediate temperatures

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 371, Issue -, Pages 64-77

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2019.04.020

Keywords

Pelletization; Magnesium oxide; Cerium oxide; CO2 capture; Sorbent

Funding

  1. Korea Institute of Energy Technology Evaluation and Planning (KETEP)
  2. Ministry of Trade, Industry & Energy of the Republic of Korea [20158510011280, 20172010202070]
  3. Korea Evaluation Institute of Industrial Technology (KEIT) [20172010202070] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Solid CO2 sorbents operating at elevated temperatures have been extensively studied for pre-combustion CO2 capture and sorption-enhanced H-2 production. The sorbent must be prepared as a structured one for integration in a process, retaining high and stable working capacity, though this remains the most overlooked challenge. Herein, a novel combustion-assisted method was used to develop MgO-CeO2 beads with dimensions of several hundred micrometers, featuring homogeneous metal oxide composites and hierarchical pore structure. With the coordination complex of cerium, the controlled release of water and volatile gases by the temperature allows the ground gel to grow into a sphere-like structure for minimizing the interfacial surface. The sorption capacity of the beads impregnated with alkali metal salts was 45 wt% at 325 degrees C and 240 min., and 43 wt% at the 30th cycle during repeated sorption (under 100% CO2 for 60 min at 325 degrees C) and regeneration (with 100% N-2 for 15 min at 425 degrees C). In addition, compared to the corresponding power and pressed-pellet sorbents, the beads impregnated with alkali metal salts showed significantly enhanced stability with high working capacity for CO2 capture. The results indicate that the MgO-CeO2 beads developed via environmentally benign and industrially feasible route provide a promising platform not only for CO2 capture, but also for sorption-enhanced H-2 production.

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