Phosphate assisted integrated carbon dioxide capture and conversion to methane

被引:7
|
作者
Koch, Christopher J.
Alagaratnam, Anushan
Goeppert, Alain
Prakash, G. K. Surya [1 ]
机构
[1] Univ Southern Calif, Loker Hydrocarbon Res Inst, Univ Pk, Los Angeles, CA 90089 USA
基金
美国国家科学基金会;
关键词
CATALYTIC TRANSFER HYDROGENATION; CO2; CAPTURE; HOMOGENEOUS HYDROGENATION; RUTHENIUM; DEGRADATION; SOLUBILITY; ALUMINA; AIR;
D O I
10.1039/d3se00390f
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
Phosphate salts have been previously studied as carbon dioxide capture reagents. However, the direct conversion of the captured carbon dioxide species to hydrogenated products is not well studied with phosphate-assisted systems. Herein, we report the conversion of captured carbon dioxide to methane in such a system. When a nickel-based catalyst was used, the reactivity was strongly inhibited due to unwanted interaction of nickel with the phosphate species present in the system. However, with 5% Ru/Al2O3 as the catalyst, 100% conversion of captured CO2 to methane was achieved after 6 hours under 50 bar H-2 at 200 degrees C. 5% Ru/Al2O3 was also able to maintain its reactivity over several capture/hydrogenation cycles.
引用
收藏
页码:2824 / 2829
页数:6
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