Laboratory to bench-scale evaluation of an integrated CO2 capture system using a thermostable carbonic anhydrase promoted K2CO3 solvent with low temperature vacuum stripping. (1st January 2018)

• Record Type: Journal Article
• Authors: Qi, Guojie; Liu, Kun; House, Alan; Salmon, Sonja; Ambedkar, Balraj; Frimpong, Reynolds A.; Remias, Joseph E.; Liu, Kunlei
• Is Part Of: Applied energy. Volume 209(2018)
• Page Start: 180
• Page End: 189
• Publication Date: 2018-01-01
• Subjects: Post-combustion CO2 capture -- Vacuum stripping -- K2CO3 -- Carbonic anhydrase; Power (Mechanics) -- Periodicals; Energy conservation -- Periodicals; Energy conversion -- Periodicals; 621.042
• DOI: 10.1016/j.apenergy.2017.10.083
• Languages: English
• ISSNs: 0306-2619

Abstract

Graphical abstract: Highlights: CA promoted K2 CO3 solvent based CO2 capture system with vacuum stripping was evaluated. Decreasing the total cycle time spent at high temperature can extend CA longevity. 2 g/L CA enhanced K2 CO3 solvent has a dramatic 5-fold increase in CO2 mass transfer coefficient. CO2 capture performance with various key operational parametric variables was accessed. An integrated bench-scale system operated successfully for an accumulated 500 h. Abstract: An advanced post-combustion CO2 capture process with combined attributes of a thermostable carbonic anhydrase (CA) enzyme catalyst, low-enthalpy K2 CO3 solvent, and vacuum stripping utilizing low exergy steam was evaluated from laboratory concept to application performance testing in an integrated 30 standard liters per minute gas flow bench-scale system operated for 500 h. Laboratory concept studies were performed using a wetted wall column to characterize solvent CO2 absorption kinetics and using a recirculating temperature loop to evaluate CA thermo-stability. Wetted wall column tests showed a dramatic 5-fold increase in CO2 mass transfer coefficient when combining 2 g/L CA with aqueous 23.5 wt% K2 CO3 solvent. Further increasing the CA concentration resulted in a gradual increase in mass transfer coefficient until a performance plateau was observed beyond a 4 g/L CA dose. Operating temperature had limited impact on CO2 capture over the range 30–50 °C. Surface tension measurements of 23.5 wt% K2 CO3 solvent exhibited a gradual decrease with increasing CA concentration. Thermo-stability tests in a temperature cycling loop designed to mimic the temperature swings between absorption and desorption showed that CA longevity could be extended by decreasing the total cycle time spent at high temperature. Parametric tests in the bench-scale unit resulted in a CO2 capture efficiency increase of 4.6-fold when increasing the CA concentration from zero to 2.5 g/L. Capture efficiency increased with higher reboiler duty (i.e. reboiler temperature) and lower absorber temperature. Tests with a 30 °C absorber temperature delivered >90% capture. Variation in solvent flow rate had little impact on capture efficiency because the reaction closely reached equilibrium at the top of the absorber. The integrated bench-scale system operated successfully for an accumulated 500 h under conditions of 40 °C absorber temperature and stripper at 35 kPa pressure with an approximate 77 °C stripper bottom temperature, delivering an average 84% CO2 capture with 23.5 wt% K2 CO3 -based solvent containing 2.5 g/L CA. Dissolved CA replenishment and conventional process controls were demonstrated as straightforward approaches to maintain system performance of this benign, low-temperature, CA-promoted process for CO2 capture.