Water-assisted oxygen activation during selective oxidation reactions

被引:27
作者
Hung-Vu Tran [1 ]
Doan, Hieu A. [1 ]
Chandler, Bert D. [2 ]
Grabow, Lars C. [1 ]
机构
[1] Univ Houston, Dept Chem & Biomol Engn, Houston, TX 77204 USA
[2] Trinity Univ, Dept Chem, San Antonio, TX 78212 USA
基金
美国国家科学基金会;
关键词
TEMPERATURE CO OXIDATION; PROPENE EPOXIDATION; THEORETICAL INSIGHTS; CARBON-MONOXIDE; GOLD CATALYSIS; METHANE; AU; CONVERSION; REACTIVITY; HYDROGEN;
D O I
10.1016/j.coche.2016.08.010
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The selective functionalization of hydrocarbons with oxygen to produce valuable commodity chemicals is inherently challenging, because of the thermodynamic stability of the complete combustion products. Emerging green synthesis routes and sustainable energy production also rely on the success of selective oxidation reactions. As one of the unselective by-products, water is always present under reaction conditions and numerous studies indicate that the catalytic activity and selectivity of selective oxidation reactions may be tuned by judiciously controlling the water content during the reaction. Some experimentally verified examples include the preferential oxidation of carbon monoxide, direct hydrogen peroxide synthesis, propene epoxidation and alcohol oxidation. Finally, it has been predicted that the direct conversion of methane to methanol can benefit from the right amount of water near the active site during oxygen activation.
引用
收藏
页码:100 / 108
页数:9
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