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Theoretical study of CO2 capture mechanisms of SrO and Sr(OH)2.nH2O (n=0,1,8)

Conference ·
DOI:https://doi.org/10.2172/2560286· OSTI ID:2560286
<span style="font-family: Roboto; font-size: 11pt;">In this presentation, the adsorption reactions of CO</span><sub style="font-family: Roboto; font-size: 11pt;">2</sub><span style="font-family: Roboto; font-size: 11pt;"> on SrO surfaces and its hydrated counterparts are examined. The predicted energies of CO</span><sub style="font-family: Roboto; font-size: 11pt;">2</sub><span style="font-family: Roboto; font-size: 11pt;"> adsorption on follows the order of increasing H</span><sub style="font-family: Roboto; font-size: 11pt;">2</sub><span style="font-family: Roboto; font-size: 11pt;">O content. The carbonation on the monohydrate surface is barrierless, whereas the CO</span><sub style="font-family: Roboto; font-size: 11pt;">2</sub><span style="font-family: Roboto; font-size: 11pt;"> reaction on the Sr(OH)</span><sub style="font-family: Roboto; font-size: 11pt;">2</sub><span style="font-family: Roboto; font-size: 11pt;"> and the octahydrate surfaces follows pathways with finite activation barriers. The thermodynamics of bulk reaction is also addressed.</span>
Research Organization:
National Energy Technology Laboratory (NETL), Pittsburgh, PA, Morgantown, WV, and Albany, OR (United States)
Sponsoring Organization:
USDOE Office of Fossil Energy and Carbon Management (FECM)
OSTI ID:
2560286
Country of Publication:
United States
Language:
English