Kinetic performance of CO2 absorption into a potassium carbonate solution promoted with the enzyme carbonic anhydrase: Comparison with a monoethanolamine solution

被引:69
|
作者
Zhang, Shihan [1 ]
Lu, Yongqi [1 ]
机构
[1] Univ Illinois, Illinois State Geol Survey, Prairie Res Inst, Champaign, IL 61820 USA
关键词
CO2; capture; Carbonic anhydrase; Potassium carbonate; Kinetics; Mass transfer; DIOXIDE ABSORPTION; AQUEOUS-SOLUTIONS; DIFFUSIVITY; BIOCATALYST; SOLUBILITY; STABILITY; GASES;
D O I
10.1016/j.cej.2015.05.034
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Development of enzyme-mediated solvents are regarded as a potential option to overcome the energy use disadvantages associated with the benchmark monoethanolamine (MEA) solvent for post-combustion CO2 capture. In this work, the kinetics of CO2 absorption into a 20 wt% potassium carbonate (PC) solution promoted with the enzyme carbonic anhydrase (CA) was investigated using a stirred tank reactor. Experimental results showed no noticeable change in the intrinsic activity of the CA enzyme with increasing CO2 loading in PC solution. A rate-based mass transfer analysis was conducted using the enzymatic kinetics measured, and results revealed that in a packed-bed column, the CO2 absorption rates into a lean and rich PC solution with 3 g L-1 CA were 50% lower and 2.2 times higher, respectively, than those into their 5 M MEA counterparts. The liquid-phase mass transfer resistance was dominant for both PC- and MEA-based systems. Modeling results revealed the effective packing volume of the absorber with PC in the presence of 10 g L-1 CA was only slightly larger than that with MEA for post-combustion CO2 capture. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:335 / 343
页数:9
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