TY - JOUR
T1 - Mass transfer enhanced CaO pellets for CO2 sorption
T2 - Utilization of CO2 emitted from CaCO3 pellets during calcination
AU - Yoon, Hyung Jin
AU - Lee, Chan Hyun
AU - Lee, Ki Bong
N1 - Funding Information:
This work was supported by the Energy Technology Development Business of the Korea Institute of Energy Technology Evaluation and Planning (KETEP) grant funded by the Korean government Ministry of Trade, Industry & Energy ( 20182020201260 ) and the National Research Foundation of Korea (NRF) through the Super Ultra Low Energy and Emission Vehicle Engineering Research Center funded by the Korean government Ministry of Science and ICT ( NRF-2016R1A5A1009592 ).
Publisher Copyright:
© 2021 Elsevier B.V.
PY - 2021/10/1
Y1 - 2021/10/1
N2 - 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 °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.
AB - 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 °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.
KW - CO sorption
KW - CaO
KW - Carbon dioxide capture and storage
KW - Mass transfer
KW - Pellet
UR - http://www.scopus.com/inward/record.url?scp=85104671306&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2021.129584
DO - 10.1016/j.cej.2021.129584
M3 - Article
AN - SCOPUS:85104671306
SN - 1385-8947
VL - 421
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 129584
ER -