CO2 Absorption and Desorption in an Aqueous Solution of Heavily Hindered Alkanolamine: Structural Elucidation of CO2-Containing Species
- Authors
- Choi, Young-Seop; Im, Jinkyu; Jeong, Jun Kyo; Hong, Sung Yun; Jang, Ho Gyeom; Cheong, Minserk; Lee, Je Seung; Kim, Hoon Sik
- Issue Date
- 1-4월-2014
- Publisher
- AMER CHEMICAL SOC
- Citation
- ENVIRONMENTAL SCIENCE & TECHNOLOGY, v.48, no.7, pp.4163 - 4170
- Indexed
- SCIE
SCOPUS
- Journal Title
- ENVIRONMENTAL SCIENCE & TECHNOLOGY
- Volume
- 48
- Number
- 7
- Start Page
- 4163
- End Page
- 4170
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/98786
- DOI
- 10.1021/es405036m
- ISSN
- 0013-936X
- Abstract
- The pathways for the CO2 absorption and desorption in an aqueous solution of a heavily hindered alkanolamine, 2-(t-butylamino)ethanol (TBAE) were elucidated by X-ray crystallographic and C-13 NMR spectroscopic analysis. In the early stage of the CO2 absorption, the formation of carbonate species ([TBAEH](2)CO3) was predominant, along with the generation of small amounts of zwitterionic species. With the progress of the absorption, the carbonate species was rapidly transformed into bicarbonate species ([TBAEH]HCO3), and the amounts of the zwitterionic species increased gradually. During desorption at elevated temperature in the absence of CO2, [TBAEH]HCO3 was found to transform into [TBAEH](2)CO3, where CO32- strongly interacts with two [TBAEH](+) via hydrogen bondings.
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