氨基甲酸
化学
溶剂
深共晶溶剂
胺气处理
粘度
二氧化碳
稀释剂
水溶液
二甲基亚砜
相(物质)
有机化学
热力学
共晶体系
物理
合金
作者
Xiaobin Zhou,Chao Liu,Yinming Fan,Lihao Zhang,Shen Tang,Shengpeng Mo,Yinian Zhu,Zongqiang Zhu
出处
期刊:Energy
[Elsevier]
日期:2022-06-17
卷期号:255: 124570-124570
被引量:41
标识
DOI:10.1016/j.energy.2022.124570
摘要
Biphasic solvents have been widely studied for CO2 capture due to their remarkable energy-saving potentiality. However, most existing biphasic solvents suffer from the high viscosity of their CO2-rich phase. This study proposed a novel low-viscous secondary amine-based nonaqueous biphasic solvent for CO2 capture. With dimethyl sulfoxide (DMSO) as the organic diluent and pentamethyldiethylenetriamine (PMDETA) as the phase splitting agent, the secondary amine of 2-methyl-ethynolamine (MAE) was proved to be the optimal candidate for preparing the biphasic solvent. The MAE/DMSO/PMDETA (M/D/P) biphasic solvent could realize a high CO2 loading of 0.84 mol mol−1 and the viscosity of its CO2-rich phase was only 8.87 mPa s, which was significantly lower than that of most reported biphasic solvents. The reaction mechanism analysis revealed that M/D/P absorbed CO2 to form products of protonated amines, carbamate, and carbamic acid species. Since the products were polar and showed a stronger affinity to polar DMSO, while less polar PMDETA was isolated, thereby resulting in a phase change. Thermodynamics analysis showed that the M/D/P biphasic solvent could sharply cut down the sensible heat and latent heat during CO2 desorption. Eventually, the total regeneration energy penalty of M/D/P was significantly reduced by 46.3% compared with the benchmark aqueous MEA solution.
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