Dry reforming of methane catalysed by molten metal alloys

被引:183
|
作者
Palmer, Clarke [1 ]
Upham, D. Chester [2 ]
Smart, Simon [3 ]
Gordon, Michael J. [1 ]
Metiu, Horia [2 ]
McFarland, Eric W. [1 ]
机构
[1] Univ Calif Santa Barbara, Dept Chem Engn, Santa Barbara, CA 93106 USA
[2] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
[3] Univ Queensland, Sch Chem Engn, St Lucia, Qld, Australia
基金
美国国家科学基金会;
关键词
REDUCTION-OXIDATION CYCLE; HYDROGEN-PRODUCTION; SYNTHESIS GAS; CO2; WATER; CARBON; DECOMPOSITION; SYNGAS; TECHNOLOGY; CONVERSION;
D O I
10.1038/s41929-019-0416-2
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
Dry reforming of methane can so far afford syngas with equimolar CO and H-2, which is suboptimal for Fischer-Tropsch chemistry. Now a process is reported based on a Ni-In molten metal alloy catalyst that is capable of producing syngas with practically relevant H-2/CO ratios together with separable carbon. Dry reforming of methane usually affords low-quality syngas with equimolar amounts of CO and H-2. Here we report the high conversion of CH4 and CO2 to syngas and solid carbon through simultaneous pyrolysis and dry reforming of methane in a bubble column reactor using a molten metal alloy catalyst (65:35 mol% Ni:In). The H-2 to CO ratio can be increased above 1:1 using feed ratios of CH4:CO2 greater than 1:1 to produce stoichiometric solid carbon as a co-product that is separable from the molten metal. A coupled reduction-oxidation cycle is carried out in which CO2 is reduced by a liquid metal species (for example, In) and methane is partially oxidized to syngas by the metal oxide intermediate (for example, In2O3), regenerating the native metal. Moreover, the H-2:CO product ratio can be easily controlled by adjusting the CH4:CO2 feed ratio, temperature, and residence time in the reactor.
引用
收藏
页码:83 / 89
页数:7
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