Comparison study on strategies to prepare nanocrystalline Li2ZrO3-based absorbents for CO2 capture at high temperatures

Qiang XIAO, Xiaodan TANG, Yefeng LIU, Yijun ZHONG, Weidong ZHU

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PDF(233 KB)
Front. Chem. Sci. Eng. ›› 2013, Vol. 7 ›› Issue (3) : 297-302. DOI: 10.1007/s11705-013-1346-1
RESEARCH ARTICLE
RESEARCH ARTICLE

Comparison study on strategies to prepare nanocrystalline Li2ZrO3-based absorbents for CO2 capture at high temperatures

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Abstract

A comparison study has been conducted on the strategies for synthesizing nanocrystalline Li2ZrO3 and K-doped Li2ZrO3 absorbents for CO2 capture at high temperatures, including solid-state and liquid-phase methods, citrate route, and starch-assisted sol-gel method combined with freeze-drying technique. The absorption properties, including uptake rate and absorption capacity, of synthesized absorbents were investigated by thermogravimetric analysis (TGA) at different CO2 partial pressures. The nanosized Li2ZrO3 crystals synthesized by the citrate route exhibit a faster uptake and a higher, nearly stoichiometric absorption capacity than those synthesized by the solid-state and liquid-phase methods. The doping of K into Li2ZrO3 can significantly improve the uptake rate of CO2, especially at low CO2 partial pressures. For the synthesis of K-doped Li2ZrO3, the citrate route has poor reproducibility and scalability, whereas the starch-assisted sol-gel method combined with freeze-drying technique is reproducible and easily scaled up, and the thus synthesized absorbents possess excellent CO2 capture properties.

Keywords

CO2 capture / Li2ZrO3 / K-doped Li2ZrO3 / citrate / starch / freeze-drying technique

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Qiang XIAO, Xiaodan TANG, Yefeng LIU, Yijun ZHONG, Weidong ZHU. Comparison study on strategies to prepare nanocrystalline Li2ZrO3-based absorbents for CO2 capture at high temperatures. Front Chem Sci Eng, 2013, 7(3): 297‒302 https://doi.org/10.1007/s11705-013-1346-1

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Acknowledgements

The financial supports from the National Basic Research Program of China (2009CB626607), the National Natural Science Foundation of China (21036006), the Program for Changjiang Scholars and Innovative Research Team in Chinese Universities (IRT0980), and the Program for Zhejiang Leading Team of Science and Technology Innovation (2011R09020-05) are gratefully acknowledged.

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2014 Higher Education Press and Springer-Verlag Berlin Heidelberg
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