选择性
催化作用
乙醛
纳米复合材料
纳米结构
化学工程
空间速度
材料科学
氧化物
乙醇
化学
无机化学
纳米技术
有机化学
冶金
工程类
作者
Guofeng Zhao,Songyua Fan,Xiaxia Pan,Pengjing Chen,Ye Liu,Yong Lu
出处
期刊:Chemsuschem
[Wiley]
日期:2017-01-23
卷期号:10 (7): 1380-1384
被引量:14
标识
DOI:10.1002/cssc.201601848
摘要
A high-performance SiC-foam-structured nanocomposite catalyst of CoO@Cu2 O (i.e., 50-100 nm CoO partially covered with ca. 10 nm Cu2 O) was engineered from nano- to macro-scales in one step for the high-throughput gas-phase aerobic oxidation of bioethanol to acetaldehyde. This special CoO@Cu2 O nanostructure shows much higher activity/selectivity than other binary metal-oxide assemblies such as CuOx &CoO nano-mixtures or inverse Cu2 O@CoO nanostructures. The catalyst was facilely but exclusively obtainable by in situ reaction-induced transformation of the respective metal nitrates supported on SiC-foam into the CoO@Cu2 O nanostructure in the reaction stream. It achieved 95 % conversion with 98 % selectivity under mild conditions and was stable for at least 150 h for a feed of 20 vol % ethanol (much higher than in the literature: 1-6 vol %) at a high EtOH weight hourly space velocity of 8.5 h-1 . Abundant Cu2 O-CoO interfaces and high stability of the CoO@Cu2 O nanostructure were responsible for the high activity/selectivity and promising stability in this reaction.
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