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High-Selective Catalyst Based on Intermetallic Rh1In1 Particles for Nitrobenzene Hydrogenation
Kinetics and Catalysis ( IF 1.1 ) Pub Date : 2021-09-25 , DOI: 10.1134/s0023158421050062
A. V. Rassolov 1 , G. A. Ivanov 1 , G. O. Bragina 1 , G. N. Baeva 1 , N. S. Smirnova 1 , A. V. Kazakov 1 , N. Ya. Usachev 1 , A. Yu. Stakheev 1
Affiliation  

Abstract

The catalytic performance of a bimetallic RhIn/SiO2 catalyst was studied in the liquid-phase hydrogenation of nitrobenzene. The formation of intermetallic Rh1In1 nanoparticles was revealed by X-ray diffraction (XRD) analysis and confirmed by transmission electron microscopy (TEM) and IR spectroscopy of adsorbed CO. It was shown that, in comparison with monometallic Rh/SiO2, the hydrogenation of nitrobenzene on the RhIn/SiO2 catalyst proceeded at a higher rate and with higher selectivity. In contrast to the monometallic catalyst, the formation of by-products and the hydrogenation of the benzene ring did not proceed on the intermetallic sample. It was assumed that the higher selectivity of RhIn/SiO2 can be associated both with a change in the electronic state of Rh atoms and with the geometry of the active sites.



中文翻译:

基于金属间化合物 Rh1In1 颗粒的高选择性硝基苯加氢催化剂

摘要

研究了双金属RhIn/SiO 2催化剂在硝基苯液相加氢中的催化性能。X 射线衍射 (XRD) 分析揭示了金属间化合物 Rh 1 In 1纳米粒子的形成,并通过透射电子显微镜 (TEM) 和吸附 CO 的红外光谱证实。结果表明,与单金属 Rh/SiO 2 相比, RhIn/SiO 2催化剂上硝基苯的加氢反应速率较高,选择性较高。与单金属催化剂相反,副产物的形成和苯环的加氢在金属间化合物样品上没有进行。据推测,RhIn/SiO 的更高选择性2可能与 Rh 原子的电子态变化和活性位点的几何形状有关。

更新日期:2021-09-27
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