Bimetallic catalysts for hydrogenation in liquid phase

被引:13
|
作者
Especel, Catherine [1 ]
Duprez, Daniel [1 ]
Epron, Florence [1 ]
机构
[1] Univ Poitiers, UMR CNRS 7285, Inst Chim Milieux & Mat Poitiers, IC2MP, F-86073 Poitiers 9, France
关键词
Bimetallic catalysts; Surface redox reactions; Citral hydrogenation; Nitrate reduction; Liquid phase; SURFACE REDOX REACTIONS; PT-GE CATALYSTS; CITRAL HYDROGENATION; RH-GE; SELECTIVE HYDROGENATION; INFRARED-SPECTROSCOPY; PD-SN/SIO2; CATALYSTS; SUPPORTED PALLADIUM; NITRATE REDUCTION; CO ADSORPTION;
D O I
10.1016/j.crci.2013.12.009
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Activity and selectivity of bimetallic catalysts for two model reactions, citral hydrogenation in isopropanol and nitrate reduction in water, are reviewed on the basis of results obtained over bimetallic systems prepared in our laboratory, notably by redox techniques. The parent metal is generally a noble metal (Rh, Pd, Pt), while the additive is most often a non-noble metal (Ge, Sn, Cu...) whose oxidation state plays an important role in hydrogenation. Dramatic improvements of the selectivity to unsaturated alcohols are observed in citral hydrogenation with adequate deposition of the additive and pretreatment of the final catalyst. In nitrate reduction, the second metal essentially affects the first step of the process (conversion of nitrate to nitrite) but the global selectivity (limitation of NH3 formation) may be significantly improved by tuning the couple parent metal additive. Other aspects such as the choice of the support and the optimization of reaction conditions (temperature, pressure, pH effects in water) are also discussed. (C) 2013 Academie des sciences. Published by Elsevier Masson SAS. All rights reserved.
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页码:790 / 800
页数:11
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