Surface-Specific Catalytic Activity of Carbon Nanotube Encapsulated with Metal-Oxide Clusters

2014 ◽  
Vol 490-491 ◽  
pp. 113-117
Author(s):  
Lei Wang ◽  
Chang Qing Dong

It is first attempted to demonstrate the catalytic efficiency and structure-sensitivity reactions on the surface of carbon nanotube (CNT) encapsulated with metal oxide particle. The results shows that the encapsulated nanoparticle CuO activate the outer orbits of CNT, and hence the surface of CuO@CNT is chemically active for hydroxyl radical generation. The results obtained from DFT calculation and experiments verified the highly active of CuO@CNT catalysts for the generation of hydroxyl radicals, and the structure-sensitivity for the oxidation of dichlorophenol. This suggests a novel strategy to design well-defined interfaces, controlling the structure-sensitivity reaction, can hence markedly improve the performance of catalysts.

2004 ◽  
Vol 10 (7) ◽  
pp. 1747-1751 ◽  
Author(s):  
François Ribot ◽  
Virginie Escax ◽  
José C. Martins ◽  
Monique Biesemans ◽  
Laurent Ghys ◽  
...  

1999 ◽  
Vol 48 (9) ◽  
pp. 1670-1672
Author(s):  
M. M. Levitsky ◽  
A. R. Arutyunyan ◽  
B. G. Zavin ◽  
V. V. Erokhin ◽  
A. L. Buchachenko

2012 ◽  
Vol 84 (3) ◽  
pp. 495-508 ◽  
Author(s):  
Ekaterina S. Lokteva ◽  
Anton A. Peristyy ◽  
Natalia E. Kavalerskaya ◽  
Elena V. Golubina ◽  
Lada V. Yashina ◽  
...  

Laser electrodispersion (LED) of metals is a promising technique for the preparation of heterogeneous catalysts as an alternative to wet impregnation of supports with the corresponding salt solutions. The LED technique can be used to deposit highly active chloride- and nitrate-free metal nanoparticles onto carbon or oxide supports. We report preparation and properties of new Ni-, Pd-, and Au-containing alumina-supported catalysts with low metal loadings (10–3–10–4 % mass) and their comparison with the previously studied carbon (Sibunit) supported systems. The catalysts demonstrate high stability and extremely high specific catalytic activity (by 2–3 orders of magnitude higher than for traditional catalysts) in the gas-phase hydrodechlorination (HDC) of chlorobenzene (CB).


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