期刊
ACS SUSTAINABLE CHEMISTRY & ENGINEERING
卷 10, 期 14, 页码 4451-4461出版社
AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.1c08186
关键词
natural amino acids; flue gas desulfurization; SO2; regeneration; density-functional theory
资金
- Shihezi University Young Innovative Talents Program [CXBJ201902]
- National Natural Science Foundation of China [31800828]
- Double First-Class General Science and Technology Project of Shihezi University [SHYL-YB201902]
This study systematically investigated the performance of natural amino acid solutions in absorbing SO2 from flue gas. It was found that monoamino amino acids exhibited good absorption performance, while polyamino amino acids performed poorly. The complex interaction mechanisms between amino acid solutions and SO2 were revealed through various characterization and analysis techniques.
In previous research, we have found and reported for thefirst time that beta-alanine aqueous solution could be employed to efficiently separate SO2fromflue gas. However, the performance of most natural amino acids (AAs) on SO2absorptionand their interaction mechanisms are not fully understood. In this work, the performance of 20 natural AA aqueous solutions on SO2absorption from flue gas was systematically studied. The experimental data showed that monoamino AAs (MAAs) exhibited good absorption performance, especially glycine, of which thesaturation uptake of SO2reached 0.461 g/g. All the MAAs showedexcellent regeneration performance, while the polyamino AAs oflysine, arginine, and histidine performed poorly. Based on thecharacterization and analysis using Fourier transform infraredspectroscopy, Raman spectroscopy,13C-nuclear magnetic resonance, and the density-functional theory simulation, it was found that the interaction mechanism between MAA aqueous solutions represented by glycine and SO2is complex, including the hydrolysis ofSO2and the protonation of MAAs, the formation of hydrogen bonds between cationic MAAs and HSO3-, and the interaction between zwitterionic MAAs and SO2. In addition, cationic glycine could form a carboxylic acid dimer, which further interacted withHSO3-through hydrogen bonds.
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