Acidic Treatment of CaO-Based Materials for Medium-High Temperature CO2 Capture

Article Preview

Abstract:

In this work, a series of CaO-based materials for medium-high temperature (500-800 °C) CO2 capture were synthesized from limestone by acidic treatment. In order to enhance its thermal stability, CaO-based materials were modified with Al(NO3)3. With various stirring time of 24, 48 and 72 hours, three types of CO2 capture sorbent were synthesized, named LA24, LA48 and LA72, respectively. TGA results showed the CaO-based materials were activated in the CO2 capture reaction of temperature range of 500-800 °C. LA24 exhibited the best CO2 capture capacity of 53.8 wt % as well as stability of 93.2 % after 10 cycles test. Furthermore, all of the modified CaO-based materials showed good thermal resistance upon 900 °C. It was consistent with expectation by the contributions of alumina coexistence with calcium oxide. XRD results indicated that CaO dominated in the diffraction spectrum before capturing CO2, and a side diffraction peak of Al2O3 was also observed. The characterization of CaO-based materials was also investigated by BET and SEM, respectively.

You might also be interested in these eBooks

Info:

Periodical:

Key Engineering Materials (Volumes 656-657)

Pages:

18-22

Citation:

Online since:

July 2015

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2015 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

* - Corresponding Author

[1] S. Sjostrom, H. Krutka, Fuel 89 (2010) 1298–1306.

Google Scholar

[2] A. Samanta, A. Zhao, G. K. H. Shimizu, P. Sarkar, R. Gupta, Ind. Eng. Chem. Res. 51 (2012) 1438–1463.

Google Scholar

[3] Q. Wang, J. Luo, Z. Zhong, A. Borgna, Energy Environ. Sci. 4 (2011) 42–55.

Google Scholar

[4] R. Filitz, A. M. Kierzkowska, M. Broda, C. R. Müller, Environ. Sci. Technol. 46 (2012) 559–565.

Google Scholar

[5] Y. J. Wu, F. Díaz Alvarado, J. C. Santos, F. Gracia, A. F. Cunha, A. E. Rodrigues, Chem. Eng. Technol. 35 (2012) 847–858.

DOI: 10.1002/ceat.201100534

Google Scholar

[6] W.Q. Liu, H. An, C.L. Qin, J.J. Yin, G.X. Wang, B. Feng, M.H. Xu, Energy & Fuels 26 (2012) 2751–2767.

Google Scholar

[7] B. Feng, H. An, E. Tan, Energy Fuels 21 (2007) 426–434.

Google Scholar

[8] S. N. Li, F. Y. Wang, X. Y. Jing, J. Wang, J. Saba, Q. Liu, L. Ge, D. L. Song, M. L. Zhang, Mater. Chem. Phys. 132 (2012) 39–43.

Google Scholar

[9] E. R. Bobicki, Q. X. Liu, Z. H. Xu, H. B. Zeng, Prog. Energy Combust. Sci. 38 (2012) 302–320.

Google Scholar

[10] N. Rodríguez, R. Murillo, J. C. Abanades, Environ. Sci. Technol. 46 (2012) 2460–2466.

Google Scholar

[11] N. Phalak, N. Deshpande, L. S. Fan, Energy Fuels 26 (2012) 3903–3909.

Google Scholar

[12] S. F. Wu, Y. Q. Zhu, Ind. Eng. Chem. Res. 49 (2010) 2701–2706.

Google Scholar

[13] J. M. Valverde, A. Perejon, L. A. Perez-Maqueda, Environ. Sci. Technol. 46 (2012) 6401–6408.

Google Scholar