388930 Regenerable Sorbent System for Post Combustion CO2 Capture

Monday, November 17, 2014: 1:10 PM
M101 (Marriott Marquis Atlanta)
Ambalavanan Jayaraman1, Gökhan Alptekin2, Steve Dietz2, Robert Copeland2 and Ashok Rao3, (1)TDA Research, Inc., Wheat Ridge, CO, (2)TDA Research Inc., Wheat Ridge, CO, (3)Advanced Power & Energy Program, University of California, Irvine, CA

TDA Research, Inc (TDA) is developing a low cost, high capacity CO2 adsorbent and demonstrating its technical and economic viability for post-combustion CO2 capture for existing pulverized coal-fired power plants.  TDA uses an advanced physical adsorbent to selectively remove CO2 from the flue gas.  The sorbent exhibits a much higher affinity for CO2 than N2, H2O or O2.  The sorbent binds CO2 more strongly than common adsorbents, providing the chemical potential needed to remove the CO2. However, because CO2 does not form a true covalent bond with the surface sites, the regeneration can be carried out with only a very small energy input (4.9 kcal per mol of CO2) compared to amines (14.2 kcal/mol CO2). We demonstrated the sorbent’s efficacy through multiple cycles for removing CO2 from coal derived flue gas and the sorbent achieved a stable capacity.  The presence of acid gases such as SO2 and NOx (80 and 200 ppmv, respectively) and water vapor up to 15% vol. caused no adverse effect on the CO2 capacity.  The regeneration of the sorbent and the recovery of CO2 and its pressurization can be achieved by several approaches, including temperature and vacuum swing.  A detailed techno-economic analysis using Aspen PlusTM software is conducted in collaboration with University of California Irvine to estimate the impact of the TDA’s CO2 capture system on plant efficiency and cost of electricity. Our system analysis showed that TDA’s CO2 capture process will reduce plant efficiency only by 19.4% (compared to 31.2% reduction for amine scrubbers) while providing 90% capture and the increase in 1st year levelized cost of electricity (COE) is 18.4% point lower than that of amines. We will present the latest results from the DOE sponsored work at the AIChE meeting.

Extended Abstract: File Not Uploaded