4.7 Article

Mass transfer enhanced CaO pellets for CO2 sorption: Utilization of CO2 emitted from CaCO3 pellets during calcination

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 421, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2021.129584

Keywords

Carbon dioxide capture and storage; CO2 sorption; CaO; Pellet; Mass transfer

Funding

  1. Energy Technology Development Business of the Korea Institute of Energy Technology Evaluation and Planning (KETEP) - Korean government Ministry of Trade, Industry Energy [20182020201260]
  2. National Research Foundation of Korea (NRF) through the Super Ultra Low Energy - Korean government Ministry of Science and ICT [NRF-2016R1A5A1009592]

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In this study, mass transfer enhanced CaO pellets were prepared by utilizing CO2 evacuation to form channels, which significantly improved the initial stage of CO2 sorption and accelerated the sorption kinetics. The enhanced mass transfer not only increased the CO2 sorption uptake at different temperatures, but also had a positive effect on CO2 release after capture. The fast CO2 sorption and regeneration kinetics of the new pellets significantly enhanced the energy efficiency of continuous CO2 capture processes.
In the preparation of CaO-based CO2 sorbents, particle densification during pelletization significantly limits the mass transfer of CO2, thereby decreasing the CO2 sorption performance. In this study, mass transfer enhanced CaO pellets (CaO-PC) were prepared through the formation of channels using CO2 evacuation from the inside of the pellets. Calcination of CaCO3 pellets induced CO2 evacuation and the remaining evacuation pathways provided excellent mass transfer channels for CaO-PC. Conventional CaO pellets (CaO-CP) were also prepared for comparison. Unlike the severely agglomerated (or blocked) morphology of CaO-CP, well-developed channels were observed in CaO-PC. It was experimentally confirmed that these channels directly contributed to the initial stage of CO2 sorption in CaO-PC, which significantly accelerated the CO2 sorption kinetics. CaO-PC had increased CO2 sorption uptakes of 58.9, 65.1, and 67.0 wt% at 500, 600, and 700 degrees C, respectively, whereas those for CaO-CP were 47.6, 55.4, and 56.8 wt%. In addition to CO2 sorption, enhanced mass transfer had a positive effect on CO2 release after capture. Under CO2 flow, the regeneration of CaO-PC was faster than that of CaO-CP, even at lower temperatures. Both the fast CO2 sorption and regeneration kinetics of CaO-PC significantly enhance the energy efficiency of continuous CO2 capture processes. These improvements were accomplished easily without the need of any additional energy-consuming treatments other than the conventional preparation methods.

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