甲烷氧化偶联
材料科学
掺杂剂
催化作用
甲烷
氧化磷酸化
联轴节(管道)
化学
兴奋剂
光电子学
冶金
有机化学
生物化学
作者
Sven Schardt,Simon Bastian,Ahmet Çelik,Jaspreet Chawla,Patrick Lott
出处
期刊:Catalysts
[Multidisciplinary Digital Publishing Institute]
日期:2024-11-05
卷期号:14 (11): 785-785
标识
DOI:10.3390/catal14110785
摘要
Autothermal oxidative coupling of methane (OCM) is a highly attractive approach for methane utilization. If platinum-based catalysts are operated in short-contact-time reactors with high space velocities, high methane conversion can be achieved. Using a 1 wt.% Pt/Al2O3 catalyst as a benchmark, the present study elucidates how different dopants, namely Ni, Sn, and V2O5, affect the OCM reaction. Kinetic catalyst tests reveal that acetylene (C2H2) is the predominant C2 product, irrespective of the catalyst formulation or operation conditions. Furthermore, the use of bimetallic catalysts allows either for the maintenance or even the improvement of the C2 selectivity during OCM, which is attributed to synergistic effects that occur when expensive Pt is partially replaced by cheaper dopants. In particular, the 1 wt.% Pt/Al2O3 reference catalyst yielded a maximum C2 selectivity of 8.2%, whereas the best-performing doped sample 0.25 wt.% Pt 0.75 wt.% V2O5/Al2O3 yielded a total C2 selectivity of 11.3%.
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