A combined cycle of capture and conversion of CO
2 performed under isothermal conditions may be an advantageous process intensification approach compared to traditional CO
2 capture and sequestration in that the combined cycle can remove energy intensive temperature or pressure swing steps and minimize process units.
1 Furthermore, the produced fuel source from conversion of CO
2 can be directly used again as an energy source for power generation. A first generation of catalytic sorbents, such as Ru+CaO/Al
2O
3, for such an application has previously been reported.
1,2 In this work, sodium promoted MgO and loaded with ruthenium metal was used for capture and methanation of CO
2 in a combined cycle. The MgO support with various NaNO
3 and NaNO
2 promoter loadings was tested for CO
2 capture at 250 °C. MgO_NaNO
3 (1:0.1 molar ratio) showed adsorption capacity of 7.6 mmol CO
2/g in 12 h. MgO_NaNO
3_NaNO
2 (1:0.1:0.1 molar ratio) showed adsorption capacity of 8.6 mmol CO
2/g in 12 h. To evaluate performance of these materials in a capture and methanation cycle, the methanation capacity, which is equivalent to number of moles of methane produced per mass of catalytic sorbents in a cycle of capture and methanation, was measured for the prepared catalytic sorbents. It was found that a physical mixture of MgO_NaNO
3 and Ru supported MgO showed the highest methanation capacity at 250 °C with 1.1 mmol CH
4/g. This methanation capacity is comparable to the highest methanation capacity reported up to date, making sodium promoted MgO sorbent promising materials for such applications.
Reference:
(1) Duyar, M. S.; Treviño, M. A. A.; Farrauto, R. J. Dual Function Materials for CO2 Capture and Conversion Using Renewable H2. Appl. Catal. B Environ. 2015, 168â169, 370â376.
(2) Duyar, M. S.; Wang, S.; Arellano-Treviño, M. A.; Farrauto, R. J. CO2 Utilization with a Novel Dual Function Material (DFM) for Capture and Catalytic Conversion to Synthetic Natural Gas: An Update. J. CO2 Util. 2016, 15, 65â71.