THE HYDROGEN STORAGE BEHAVIOUR OF PT AND PD LOADED TRANSITION METAL OXIDES

被引:0
|
作者
Molendowska, A. [1 ,2 ]
Hall, P. J. [1 ]
Donet, S. [2 ]
机构
[1] Univ Strathclyde, Dept Chem & Proc Engn, James Weir Bldg,75 Montrose St, Glasgow G1 1XJ, Lanark, Scotland
[2] French Atom Commission, Lab Innovat New Energy Technol & Nanomat LITEN, F-38000 Grenoble, France
关键词
WALLED CARBON NANOTUBES; SUPPORT IONICITY; PARTICLE-SIZE; ADSORPTION; TEMPERATURE; CATALYSTS; PT/TIO2; NANOSTRUCTURES; FTIR;
D O I
暂无
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
The catalytic properties of Pt and Pd deposited on commercial porous MnO2 and TiO2 powders for hydrogen adsorption were examined to determine whether hydrogen molecules and diffuse onto the support. Fluidised-Bed Metal-Organic Catalyst deposition was achieved using metal-organic Chemical Vapour Deposition. Scanning Electron Microscopy showed that the average diameter of metal particles was < 1 mu m. The amount of catalyst loading was determined from the deposition conditions and was < 1%wt. Hydrogen uptakes at 77K were determined volumetrically. Experiments were carried in 77K and measurements were performed for samples before and after deposition. Physically adsorbed hydrogen was determined form the uptake of metal oxides without catalyst loading and it was found that the hydrogen uptakes exceeded both the amount of physically adsorbed hydrogen and the theoretical capacity for Pt and Pd. From this it was inferred that some hydrogen had been transferred from the support although the mechanism for this process is still not clear.
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页码:51 / +
页数:3
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