甲烷氧化偶联
甲烷
环氧乙烷
氧化物
乙烯
联轴节(管道)
材料科学
化学工程
膜
氧化磷酸化
化学
有机化学
工程类
冶金
催化作用
聚合物
生物化学
共聚物
作者
Luke H Denoyer,Kannan Pasupathikovil Ramaiyan,Fernando H. Garzón
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2025-07-15
卷期号:39 (29): 13905-13930
被引量:6
标识
DOI:10.1021/acs.energyfuels.5c02114
摘要
Methane is a highly abundant, low-cost hydrocarbon; hence, effective conversion of methane toward value-added products such as olefins has been a highly researched field for over 40 years. Oxidative coupling of methane (OCM) is one of the most studied methods for direct methane conversion due to favorable thermodynamics; however, at industrially relevant methane conversion rates, the overoxidation to CO 2 inhibits the selectivity toward desired C 2 products. Electrochemical OCM (E-OCM) using high-temperature solid oxide electrolyzer cells (SOECs) has recently gained attention, as it can alter product selectivity by catalyst selection and externally applied potential. However, the material requirements for E-OCM applications are seldom addressed. For example, the anode of an E-OCM cell must possess high electronic and ionic conductivity while showing tolerance toward coke or carbonate formation under methane-rich conditions under applied potentials for successfully activating methane toward C 2 products. This paper reviews the E-OCM literature to provide a perspective on materials’ properties governing catalytic activity, electrical conductivity, and chemical stability under E-OCM conditions. Methane coupling in SOECs utilizing oxide ion conductors, proton conductors, and catalytic membrane reactors is reviewed in detail. An outlook for future directions for material development and catalytic requirements is provided.
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