个人信息Personal Information
教授
博士生导师
硕士生导师
性别:女
毕业院校:大连理工大学
学位:博士
所在单位:化工学院
学科:化学工艺. 能源化工. 工业催化
办公地点:大连市凌工路2号大连理工大学西部校区化工实验楼C331室
联系方式:0411-84986355
电子邮箱:wencuili@dlut.edu.cn
Supported Boron Oxide Catalysts for Selective and Low-Temperature Oxidative Dehydrogenation of Propane
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论文类型:期刊论文
发表时间:2019-09-01
发表刊物:ACS CATALYSIS
收录刊物:SCIE、EI
卷号:9
期号:9
页面范围:8263-8270
ISSN号:2155-5435
关键字:boron oxide; supported catalysts; low temperature; selectivity; oxidative dehydrogenation; propane
摘要:Oxidative dehydrogenation (ODH) of light alkanes catalyzed by metal oxides is considered to be a thermodynamically favorable process for olefin production. The strong interaction between the unoccupied d-orbital of metal atom and the pi-electrons of olefins, however, leads to deep oxidation of olefin to CO2, especially at elevated temperatures. The challenge lies in the development of selective and low-temperature active catalysts to avoid such unwanted deep oxidation. Here, we report unambiguous evidence on properly prepared mesoporous silica-supported boron oxide catalysts showing high selectivity for ODH of propane. The catalysts are active at a temperature as low as 405 degrees C, showing a propane conversion of 2.8% and a propene selectivity of 84.1% (C-2-(3)=: 94.6%). Upon raising the temperature to 450 degrees C, a propane conversion of 14.8% can be achieved, with a selectivity of 73.3% toward propene or 87.4% for both propene and ethene (C-2-(3)=). Both experimental and theoretical studies indicate tricoordinated boroxol and hydroxylated linear boron species are the active sites for the ODH of propane. In addition, the oxophilicity of boron sites is responsible for suppressing deep oxidation by eliminating the alkoxyl species, leading to high selectivity toward olefin products.