甲烷
材料科学
催化作用
电极
纤维
电化学
电催化剂
化学工程
无机化学
化学
复合材料
有机化学
工程类
物理化学
作者
Zhi-Kai Guo,Wei Chen,Yanfang Song,Xiao Dong,G. Li,Wei Wei,Yuhan Sun
出处
期刊:Chinese Journal of Catalysis
[China Science Publishing & Media Ltd.]
日期:2020-07-01
卷期号:41 (7): 1067-1072
被引量:18
标识
DOI:10.1016/s1872-2067(20)63548-3
摘要
Natural gas and shale gas, with methane as the main component, are important and clean fossil energy resources. Direct catalytic conversion of methane to valuable chemicals is considered a crown jewel topic in catalysis. Substantial studies on processes including methane reforming, oxidative coupling of methane, non-oxidative coupling of methane, etc. have been conducted for many years. However, owing to the intrinsic chemical inertness of CH 4 , harsh reaction conditions involving either extremely high temperatures or highly oxidative reactants are required to activate the C–H bonds of CH 4 in such thermocatalytic processes, which may cause the target products, such as ethylene or methanol, to be further converted into coke or CO and CO 2 . It is desirable to adopt a new strategy for direct CH 4 conversion under mild conditions. Herein, we report that efficient electrocatalytic oxidation of methane to alcohols at ambient temperature and pressure can be achieved using a NiO/Ni hollow fiber electrode. This work opens a new avenue for direct catalytic conversion of CH 4 . Electrocatalytic methane conversion was carried out using a porous hollow fiber NiO/Ni anode, in which CH 4 is converted into methanol and ethanol in a 0.1 mol/L aqueous NaOH solution at ambient temperature and pressure.
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