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Received May 27, 2005
Accepted December 11, 2005
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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The effect of water on the activation and the CO2 capture capacities of alkali metal-based sorbents

Department of Chemical Engineering, Kyungpook National University, Daegu 702-701, Korea 1Korea Electric Power Research Institute, Daejeon 305-380, Korea 2Korea Institute of Energy Research, Daejeon 305-343, Korea 3Department of Chemical Engineering, Yeungnam University, Kyongsan 712-749, Korea
kjchang@mail.knu.ac.kr
Korean Journal of Chemical Engineering, May 2006, 23(3), 374-379(6), 10.1007/BF02706737
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Abstract

Alkali metal-based sorbents were prepared by the impregnation either of potassium carbonate (K2CO3) or of sodium carbonate (Na2CO3) on the supports (activated carbon (AC) and Al2O3). The CO2 absorption and regeneration properties were measured in a fixed bed reactor at the low temperature conditions (CO2 absorption at 60 °C and regeneration at 150 °C). The potassium carbonate which was supported on the activated carbon (K2CO3/AC) was clarified as a leading sorbent, of which the total CO2 capture capacity was higher than those of other sorbents. This sorbent was completely regenerated and transformed to its original phase by heating the used sorbent. The activation process before CO2 absorption needed moisture nitrogen containing 1.3-52 vol% H2O for 2 hours either at 60 °C or at 90 °C. The activation process played an important role in CO2 absorption, in order to form new active species defined as K2CO3· 1.5 H2O, by X-ray diffraction. It was suggested that the new active species (K2CO3·1.5H2O) could be formed by drying the K4H2(CO3)3·1.5H2O phase formed after pre-treatment with excess water.

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