Enhancements in mass transfer for carbon capture solvents part I: Homogeneous catalyst
- Univ. of Kentucky, Lexington, KY (United States)
The novel small molecule carbonic anhydrase (CA) mimic [CoIII(Salphen-COO-)Cl]HNEt3 (1), was synthesized as an additive for increasing CO2 absorption rates in amine-based post-combustion carbon capture processes (CCS), and its efficacy was verified. 1 was designed for use in a kinetically slow but thermally stable blended solvent, containing the primary amines 1-amino-2-propanol (A2P) and 2-amino-2-methyl-1-propanol (AMP). Together, the A2P/AMP solvent and 1 reduce the overall energy penalty associated with CO2 capture from coal-derived flue gas, relative to the baseline solvent MEA. 1 is also effective at increasing absorption kinetics of kinetically fast solvents, such as MEA, which can reduce capital costs by requiring a smaller absorber tower. The transition from catalyst testing under idealized laboratory conditions, to process relevant lab- and bench-scale testing adds many additional variables that are not well understood and rarely discussed. As a result, the stepwise testing of both 1 and the novel A2P/AMP solvent blend is described through a transition process that identifies many of these process and evaluation challenges not often addressed when designing a chemical or catalytic additive for industrial CCS systems, where consideration of solvent chemistry is typically the primary goal.
- Research Organization:
- Univ. of Kentucky, Lexington, KY (United States). Center for Applied Energy Research
- Sponsoring Organization:
- USDOE Office of Fossil Energy (FE)
- Grant/Contract Number:
- FE0012926; 3048110942
- OSTI ID:
- 1362045
- Alternate ID(s):
- OSTI ID: 1550337
- Journal Information:
- International Journal of Greenhouse Gas Control, Vol. 63, Issue C; ISSN 1750-5836
- Publisher:
- ElsevierCopyright Statement
- Country of Publication:
- United States
- Language:
- English
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