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In relation to this article, we declare that there is no conflict of interest.
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Received July 10, 2016
Accepted March 7, 2017
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Phase separation characteristics in biphasic solvents based on mutually miscible amines for energy efficient CO2 capture

Department of Chemical and Biological Engineering, Korea National University of Transportation, Chungju, Chungbuk 27469, Korea 1Green Energy Process Laboratory, Korea Institute of Energy Research, 152 Gajeong-ro, Yuseong-gu, Daejeon 34129, Korea
Korean Journal of Chemical Engineering, June 2017, 34(6), 1840-1845(6), 10.1007/s11814-017-0067-4
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Abstract

One of the challenges with regard to the aqueous amine-based CO2 capture process is the considerable energy requirement for solvent regeneration. To overcome this challenge, a biphasic solvent was employed in this study. Here, the phase separation behavior of amine blends depending on the characteristic structures of the solvent component was investigated using a turbidity measurement apparatus. Amines were classified as (1) primary/secondary amines or tertiary/sterically hindered amines depending on the CO2 reaction species, such as carbamate and bicarbonate (2) alkyl and alkanolamines, depending on the presence of a hydroxyl group, (3) chain and cyclic amines, and (4) mono- and polyamines depending on the molecular structure. Easy phase separation occurred in solvent blends containing polyamines such as DETA (diethylenetriamine), TETA (triethylenetetramine), and DEEA (2-(diethylamino) ethanol). The types with the greatest potential were the DETA/DEEA blended solvents. A phase separation could be determined based on the difference in the reaction rate with CO2 and the low solubility between the carbamate species of DETA and DEEA.

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