Confined Pt and CoFe2O4 Nanoparticles in a Mesoporous Core/Shell Silica Microsphere and Their Catalytic Activity

被引:6
|
作者
Kang, Donghyeon [1 ]
Eum, Min-Sik [1 ]
Lee, Byeongno [1 ]
Bae, Tae-Sung [2 ]
Lee, Kyu Reon [1 ]
Lim, Heung Bin [3 ]
Hur, Nam Hwi [1 ]
机构
[1] Sogang Univ, Dept Chem, Seoul 121742, South Korea
[2] Korea Basic Sci Inst, Jeonju 561765, South Korea
[3] Dankook Univ, Dept Chem, Gyeonggi Do 448701, South Korea
来源
基金
新加坡国家研究基金会;
关键词
Magnetic nanoparticles; Core/Shell silica; Catalyst; Proximity effect; METAL-SUPPORT INTERACTION; GAS SHIFT REACTION; PHASE SELECTIVE HYDROGENATION; GOLD CATALYSTS; CO OXIDATION; CHEMOSELECTIVE HYDROGENATION; OXYGEN REDUCTION; OXIDE CATALYSTS; MILD CONDITIONS; TIO2;
D O I
10.5012/bkcs.2011.32.10.3712
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Confined Pt and CoFe2O4 nanoparticles (NPs) in a mesoporous core/shell silica microsphere, Pt-CoFe2O4@meso-SiO2, were prepared using a bi-functional linker molecule. A large number of Pt NPs in Pt-CoFe2O4@meso-SiO2, ranging from 5 to 8 nm, are embedded into the shell and some of them are in close contact with CoFe2O4 NPs. The hydrogenation of cyclohexene over the Pt-CoFe2O4@meso-SiO2 microsphere at 25 degrees C and 1 atm of H, yields cyclohexane as a major product. In addition, it gives oxygenated products. Control experiments with O-18-labelled water and acetone suggest that surface-bound oxygen atoms in CoFe2O4 are associated with the formation of the oxygenated products. This oxidation reaction is operative only if CoFe2O4 and Pt NPs are in close contact. The Pt-CoFe2O4@meso-SiO2 catalyst is separated simply by a magnet, which can be re-used without affecting the catalytic efficiency.
引用
收藏
页码:3712 / 3719
页数:8
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