Selective Hydrogenation of Crotonaldehyde over Ir-FeOx/SiO2 Catalysts: Enhancement of Reactivity and Stability by Ir-FeOx Interaction

被引:31
|
作者
Yu, Qin [1 ]
Bando, Kyoko K. [2 ]
Yuan, Ju-Fang [1 ]
Luo, Ce-Qi [1 ]
Jia, Ai-Ping [1 ]
Hu, Geng-Shen [1 ]
Lu, Ji-Qing [1 ]
Luo, Meng-Fei [1 ]
机构
[1] Zhejiang Normal Univ, Inst Phys Chem, Minist Educ Adv Catalysis Mat, Key Lab, Jinhua 321004, Peoples R China
[2] Natl Inst Adv Ind Sci & Technol, Res Inst Chem Proc Technol, Tsukuba 3058565, Japan
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2016年 / 120卷 / 16期
基金
中国国家自然科学基金;
关键词
GAS-PHASE HYDROGENATION; CHEMOSELECTIVE HYDROGENATION; STRUCTURE SENSITIVITY; PT/ZRO2; CATALYSTS; CROTYL ALCOHOL; CO OXIDATION; WATER; TEMPERATURE; PT/TIO2; NANOPARTICLES;
D O I
10.1021/acs.jpcc.6b00456
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
A series of FeOx-promoted Ir/SiO2 catalysts were prepared and tested for gas phase selective hydrogenation of crotonaldehyde. It was found that a catalyst containing Ir nanoparticles contacting with highly dispersed FeOx clusters (3Ir/0.1Fe/SiO2) showed excellent activity and stability, with a 5-fold enhanced steady state crotyl alcohol yield (59.6%) compared to that of the bare Ir/SiO2 (12.4%), while a catalyst promoted with high content of Fe (3Ir/3.5Fe/SiO2) had high initial activity but deactivated rapidly. A catalyst with similar highly dispersed FeOx clusters but prepared by an, inverse 0 impregnation sequence (0.1Fe/3Ir/SiO2) also suffered severe deactivation. Various characterizations revealed that the observed behaviors were closely related to the Ir-FeOx interactions induced by different morphologies of the catalysts. The active sites generated at Ir-FeOx interface were responsible for the better performance. The catalyst deactivation was attributed to the deposit of heavy compound and strong adsorption of CO on the surface, which was induced by the strong Ir-FeOx interaction due to heavy decoration of FeOx on the Ir surface.
引用
收藏
页码:8663 / 8673
页数:11
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