Effect of Strontium on the Catalytic Activity and Physicochemical Properties of Ru/Mn Catalysts for CO2 Methanation Reaction

Article Preview

Abstract:

The recycling technology by the catalytic conversion offers a very promising technique for reducing greenhouse CO2 gas from flue gases of coal burning power plant by converting the carbon dioxide gas to methane. The methane produced from the reaction can be used as other fuel to run turbine for electricity generation. Therefore, the strontia based catalysts was prepared by impregnated with RuMn/Al2O3 catalyst and then calcined at 1000°C for 5 hour. Strontia catalyst is an effective material because of its highly basic properties which could enhance carbon dioxide adsorption and chemisorption on the catalyst surface but not been widely explored. The result obtained revealed that the addition of Sr to RuMn/Al2O3 as based catalyst had increased the catalytic activity and found to be more active for promoting the CO2 methanation reaction. Under reducing pretreatment at 300°C, the activity of CO2 conversion increased about 30.98% which is from 50.45% over RuMn-65/Al2O3 catalyst to 73.10% over RuMnSr-65/Al2O3 catalyst with 40% of methane yielded at reaction temperature of 210°C. The Sr addition did not modify the crystalline structure of the catalyst but gave higher surface area, smaller particle size and high metal dispersion as well as increased the degree of reduction and CO chemisorption.

You might also be interested in these eBooks

Info:

Periodical:

Pages:

371-376

Citation:

Online since:

June 2015

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2015 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

* - Corresponding Author

[1] T.E. Hoost, J.G. Goodwin Jr, Potassium Effects on the Deactivation by Carbon of Ruthenium Catalysts. Stud Surf Sci Catal. 68 (1991) 691-698.

DOI: 10.1016/s0167-2991(08)62701-9

Google Scholar

[2] L.J. Lakshmi, E.C. Alyea, S.T. Srinivas, P. Kanta Rao, Influence of metal oxide modification of alumina on the dispersion and activity of vanadia catalysts. J. Phys. Chem. B. 101 (1997) 3324-3328.

DOI: 10.1021/jp963450f

Google Scholar

[3] J. Shen, R.D. Cortright, Y. Chen, J.A. Dumesic, Microcalorimetric and infrared spectroscopic studies of γ-Al2O3 modified by basic metal oxides. J. Phys. Chem. 98 (1994) 8067-8073.

DOI: 10.1021/j100084a025

Google Scholar

[4] P. A. U. Aldana, F. Ocampo, K. Kobl, B. Louisb, F. Thibault-Starzyka, M. Daturia, P. Bazina, S. Thomasa, A.C. Rogerb, Catalytic CO2 valorization into CH4 on Ni-based ceria-zirconia. Reaction mechanism by operando IR spectroscopy, Cat Today. 215 (2013).

DOI: 10.1016/j.cattod.2013.02.019

Google Scholar

[5] Y-H. Huang, J-J. Wang, Z-M. Liu, G-D. Lin, H-B. Zhang, Highly efficient Ni-ZrO2 catalyst doped with Yb2O3 for co-methanation of CO and CO2, Appl Cat A General. 466 (2013) 300-306.

DOI: 10.1016/j.apcata.2013.06.021

Google Scholar

[6] N. Perkas, G. Amirian, Z. Zhong, J. Teo, Y. Gofer, A. Gedanken, Methanation of carbon dioxide on Ni catalysts on mesoporous ZrO2 doped with rare earth oxides. Catal Lett. 130 (2009) 455-462.

DOI: 10.1007/s10562-009-9952-8

Google Scholar