共 55 条
Phosphate assisted integrated carbon dioxide capture and conversion to methane
被引:7
作者:

Koch, Christopher J.
论文数: 0 引用数: 0
h-index: 0
机构: Univ Southern Calif, Loker Hydrocarbon Res Inst, Univ Pk, Los Angeles, CA 90089 USA

Alagaratnam, Anushan
论文数: 0 引用数: 0
h-index: 0
机构: Univ Southern Calif, Loker Hydrocarbon Res Inst, Univ Pk, Los Angeles, CA 90089 USA

论文数: 引用数:
h-index:
机构:

Prakash, G. K. Surya
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Southern Calif, Loker Hydrocarbon Res Inst, Univ Pk, Los Angeles, CA 90089 USA Univ Southern Calif, Loker Hydrocarbon Res Inst, Univ Pk, Los Angeles, CA 90089 USA
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.
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页码:2824 / 2829
页数:6
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