Semiclathrate-based CO2 capture from flue gas mixtures: An experimental approach with thermodynamic and Raman spectroscopic analyses

被引:69
|
作者
Kim, Soyoung [1 ]
Seo, Yongwon [1 ]
机构
[1] Ulm Natl Inst Sci & Technol, Sch Urban & Environm Engn, Ulsan 689798, South Korea
基金
新加坡国家研究基金会;
关键词
Carbon dioxide; Semiclathrate; Gas hydrate; Quaternary ammonium salts; Flue gas; HYDRATE PHASE-EQUILIBRIA; BUTYL AMMONIUM BROMIDE; CARBON-DIOXIDE; HYDROGEN STORAGE; TETRABUTYLAMMONIUM BROMIDE; NATURAL-GAS; LATENT-HEAT; PLUS WATER; SEPARATION; CHLORIDE;
D O I
10.1016/j.apenergy.2015.05.107
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Semiclathrate-based CO2 capture from flue gas in the presence of various quaternary ammonium salts (QASs) such as tetra-n-butyl ammonium bromide (TBAB), tetra-n-butyl ammonium chloride (TBAC), and tetra-n-butyl ammonium fluoride (TBAF) was investigated with a primary focus on the thermodynamic, kinetic, and spectroscopic aspects. The thermodynamic stability of the CO2 (20%) + N-2 (80%) + QAS semiclathrates was examined with an isochoric method using a high pressure reactor as well as with dissociation enthalpy measurement using a high pressure micro-differential scanning calorimeter (HP mu-DSC). The TBAF semiclathrate with CO2 (20%) + N-2 (80%) showed the most significant equilibrium pressure reduction at a specified temperature. However, the TBAC semiclathrate had the highest gas uptake and steepest CO2 concentration change in the vapor phase, which indicates the largest gas storage capacity for CO2 capture. CO2 was observed to be preferentially captured and enriched to approximately 60% in the semiclathrate phase. The CO2 selectivity was independent of the type of QASs used. The Raman spectroscopic results revealed that both CO2 and N-2 are enclathrated in the small cages of the QAS semiclathrates and that the enclathration of guest gas molecules does not change the structure of the semiclathrates. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:987 / 994
页数:8
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