Dramatic liquid-phase dehydrogenation rate enhancements using gas-phase hydrogen acceptors

被引:19
作者
Hindle, K. T.
Burch, R.
Crawford, P.
Hardacre, C. [1 ]
Hu, P.
Kalirai, B.
Rooney, D. W.
机构
[1] Queens Univ Belfast, CenTACat, Sch Chem & Chem Engn, Belfast BT9 5AG, Antrim, North Ireland
[2] Robinson Bros Ltd, W Bromwich B70 0AH, Ireland
基金
英国工程与自然科学研究理事会;
关键词
dehydrogenation; palladium; carbazole; tetrahydrocarbazole; hydrogen acceptor; tetrahydronaphthalene; naphthalene; DFF;
D O I
10.1016/j.jcat.2007.07.032
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The dehydrogenation of 1,2,3,4-tetrahydrocarbazole (THCZ) to form carbazole (CZ) over supported palladium catalysts was examined in the presence of hydrogen acceptors. As expected, liquid hydrogen acceptors increased the rate of reaction but, importantly, gaseous hydrogen acceptors also have been used. Ethene, propene, and but-1-ene showed up to a fivefold increase in the rate of dehydrogenation. Moreover, compared with the analogous liquid systems, the gaseous alternatives are a potentially more economic method of enhancing the activity and provide a simpler workup. The mechanism for the increase in rate was examined by density functional theory calculations, which showed that the propene hydrogenation competes effectively with the back-hydrogenation of the intermediates formed during the THCZ dehydrogenation, resulting in a shift in the equilibrium toward to the formation of CZ. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:338 / 344
页数:7
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