Ca-Ag compounds in ethylene epoxidation reaction

被引:8
作者
Antonyshyn, Iryna [1 ]
Sichevych, Olga [1 ]
Ormeci, Alim [1 ]
Burkhardt, Ulrich [1 ]
Rasim, Karsten [1 ]
Titlbach, Sven [2 ]
Armbruester, Marc [3 ]
Schunk, Stephan A. [2 ]
Grin, Yuri [1 ]
机构
[1] Max Planck Inst Chem Phys Fester Stoffe, Chem Met Sci Dept, Dresden, Germany
[2] Hte GmbH, Heidelberg, Germany
[3] Tech Univ Chemnitz, Fac Nat Sci, Inst Chem, Mat Innovat Energy Concepts, Chemnitz, Germany
关键词
Intermetallic compound; crystal structure; chemical bonding; reactivity; heterogeneous catalysis; ethylene epoxidation; ethylene oxide; CATALYZED SELECTIVE OXIDATION; SILVER BIMETALLIC CATALYSTS; CRYSTAL-STRUCTURES; HETEROGENEOUS CATALYSIS; INTERMETALLIC COMPOUNDS; ALLOY CATALYSTS; CALCIUM; COPPER; PROMOTERS; CHEMISTRY;
D O I
10.1080/14686996.2019.1655664
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The ethylene epoxidation is a challenging catalytic process, and development of active and selective catalyst requires profound understanding of its chemical behaviour under reaction conditions. The systematic study on intermetallic compounds in the Ca-Ag system under ethylene epoxidation conditions clearly shows that the character of the oxidation processes on the surface originates from the atomic interactions in the pristine compound. The Ag-rich compounds Ca2Ag7 and CaAg2 undergo oxidation towards fcc Ag and a complex Ca-based support, whereas equiatomic CaAg and the Ca-rich compounds Ca5Ag3 and Ca3Ag in bulk remain stable under harsh ethylene epoxidation conditions. For the latter presence of water vapour in the gas stream leads to noticeable corrosion. Combining the experimental results with the chemical bonding analysis and first-principles calculations, the relationships among the chemical nature of the compounds, their reactivity and catalytic performance towards epoxidation of ethylene are investigated. [GRAPHICS] .
引用
收藏
页码:902 / 916
页数:15
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