Tailoring the activity and selectivity of Rh/SiO2 for the selective hydrogenation of phenol by CoOx promotion

被引:7
|
作者
Zhang, Fei [1 ,2 ]
Wu, Chunzheng [3 ]
Wang, Shuibo [1 ]
Wang, Shiwei [1 ]
Li, Tong [1 ]
Zou, Laixi [2 ]
Yu, Hongbo [1 ]
Yin, Hongfeng [1 ]
机构
[1] Chinese Acad Sci, Ningbo Inst Mat Technol & Engn, 1219 Zhongguan West Rd, Ningbo 315201, Zhejiang, Peoples R China
[2] Jiangxi Univ Sci & Technol, Sch Met & Chem Engn, Ganzhou, Jiangxi 341000, Peoples R China
[3] Zhejiang A&F Univ, Chem & Mat Engn, Hangzhou 311300, Zhejiang, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
RHODIUM NANOPARTICLES; LOW-TEMPERATURE; CYCLOHEXANONE; PD; CATALYSTS; SILICA; TPR; RH; RU; HYDRODEOXYGENATION;
D O I
10.1039/d1cy02324a
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
Although supported Rh nanoparticles (NPs) are one of the best catalysts for the selective hydrogenation of phenol to cyclohexanol, they still suffer from poor selectivity problems. In this study, we promoted the selectivity of Rh NPs with CoOx through an in situ transformation of the bimetallic RhCo NPs on SiO2. Among the obtained Rh-CoOx/SiO2 catalysts, the one with a Co/Rh molar ratio of 1/3 exhibited the highest phenol conversion (i.e., 98.1%) and the highest selectivity to cyclohexanol (i.e., 99.4%). Our study showed that CoOx promoters modified the electronic states of Rh and created new active sites at their interface, which are beneficial to the activation of phenol and the desorption of cyclohexanol. Excessive coverage of Rh by CoOx, however, would cause deactivation due to the less exposure of the Rh-CoOx interface.
引用
收藏
页码:2257 / 2264
页数:8
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