Investigation mechanism of DEA as an activator on aqueous MEA solution for postcombustion CO2 capture

被引:43
|
作者
Liu, Helei [1 ]
Li, Moxia [2 ]
Luo, Xiao [2 ]
Liang, Zhiwu [2 ]
Idem, Raphael [1 ]
Tontiwachwuthikul, Paitoon [1 ]
机构
[1] Univ Regina, CETRI, Regina, SK S4S 0A2, Canada
[2] Hunan Univ, Joint Int Ctr Capture & Storage iCCS CO2, Prov Hunan Key Lab Cost Effect Utilizat Fossil Fu, Coll Chem & Chem Engn, Changsha 410082, Hunan, Peoples R China
基金
加拿大自然科学与工程研究理事会;
关键词
mechanism; CO2; absorption; blended solvent; NMR; STOPPED-FLOW TECHNIQUE; CARBON-DIOXIDE; ABSORPTION; BLENDS; MONOETHANOLAMINE; SOLVENT; SYSTEM; METHYLDIETHANOLAMINE; DIETHANOLAMINE; KINETICS;
D O I
10.1002/aic.16165
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
In this work, Diethanolamine (DEA) was considered as an activator to enhance the CO2 capture performance of Monoethanolamine (MEA). The addition of DEA into MEA system was expected to improve disadvantages of MEA on regeneration heat, degradation, and corrosivity. To understand the reaction mechanism of blended MEA-DEA solvent and CO2, C-13 nuclear magnetic resonance (NMR) technique was used to study the ions (MEACOO(-), DEACOO(-), MEA, DEA, MEAH(+), DEAH(+), HCO3-, CO32-) speciation in the blended MEA-DEA-CO2-H2O systems with CO2 loading range from 0 to 0.7 mol CO2/mol amine at the temperature of 301 K. The different ratios of MEA and DEA (MEA: DEA=2.0:0, 1.5:0.5, 1.0:1.0, and 0:2.0) were studied to comprehensively investigate the role of DEA in the system of MEA-DEA-CO2-H2O. The results revealed that DEA performs the coordinative role at the low CO2 loading and the competitive role at high CO2 loading. Additionally, the mechanism was also proposed to interpret the reaction process of the blended solvent with CO2. (c) 2018 American Institute of Chemical Engineers AIChE J, 64: 2515-2525, 2018
引用
收藏
页码:2515 / 2525
页数:11
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