In-situ DRIFTS study of two-step CO2 capture and catalytic methanation over Ru,"Na2O"/Al2O3 Dual Functional Material

被引:192
作者
Proano, Laura [1 ]
Tello, Edisson [1 ]
Arellano-Trevino, Martha A. [2 ]
Wang, Shuoxun [2 ]
Farrauto, Robert J. [2 ]
Cobo, Martha [1 ]
机构
[1] Univ La Sabana, Dept Chem Engn, Energy Mat & Environm Lab, Campus Univ Puente del Comun,Km 7 Autopista Norte, Bogota, Colombia
[2] Columbia Univ, Earth & Environm Engn, New York, NY USA
关键词
Alkaline adsorbents; CO2; capture; Catalytic CO2 conversion to CH4; Dual Function Materials; In-situ DRIFTS; SYNTHETIC NATURAL-GAS; POWER-TO-GAS; CARBON-DIOXIDE; LOW-TEMPERATURE; RENEWABLE ENERGY; FLUE-GAS; ADSORPTION; CONVERSION; HYDROGENATION; SURFACE;
D O I
10.1016/j.apsusc.2019.01.281
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Dual Function Materials (DFM) are composed of an alkali or alkaline earth CO2 adsorbent phase and a supported catalyst. It selectively captures CO2 which is then methanated using renewable H-2. Both the capture and methanation steps are conducted at about 320 degrees C so no temperature swings are required allowing for continuous operation using two parallel reactors operating in tandem. This process approaches carbon neutral power generation by recycling the CH4 produced for re-combustion. This two-step process was studied by in-situ DRIFTS at 320 degrees C over 5%Ru-6.1%"Na2O"/Al2O3 DFM and compared with the 5%Ru/Al2O3 traditional methanation catalyst. In the DFM the Na2CO3/Al2O3 pre-curser is reduced to "Na2O" catalyzed by Ru metal. For both Ru/ Al2O3 and DFM CO2 adsorbs on Ru active sites and Al2O3 OH groups during the capture step. For DFM large amounts of CO2 absorb on the Al-O--Na+ species forming bidentate carbonates. During the H-2 reduction step (Le., methanation step), adsorbed bicarbonates and bidentate carbonates spill over onto the Ru-support interface, where methanation takes place through sequential hydrogenation with formates as reaction intermediaries. Although CO2 was mainly adsorbed on the alkaline support methanation occurs over Ru, supporting the hypothesis that the reaction occurs at the Ru-support interface. Therefore, the multiple adsorption sites over the DFM explain the high CO2 adsorption capacity by the formation of bidentate carbonates that spill over onto the Ru-support interface, during the two-step methanation process.
引用
收藏
页码:25 / 30
页数:6
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