Hydrogen uptake in palladium and ruthenium exchanged zeolite X
Hydrogen uptake in palladium and ruthenium exchanged zeolite X
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DOI:
10.1016/j.jallcom.2007.11.058
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发表时间:
2008-10
影响因子:
6.2
通讯作者:
K. Prasanth;Renjith S Pillai;Sunil A Peter;H. Bajaj;R. Jasra;H. Chung;T. H. Kim;S. D. Song
中科院分区:
文献类型:
--
作者:
K. Prasanth;Renjith S Pillai;Sunil A Peter;H. Bajaj;R. Jasra;H. Chung;T. H. Kim;S. D. Song
The hydrogen adsorption properties and uptake capacities of NaX and its palladium and ruthenium exchanged forms were investigated at 77K in a static volumetric adsorption setup up to 1bar, and at 303K and 333K in a gravimetric adsorption system up to 5bar. All the hydrogen adsorption isotherms were of Type I with a maximum adsorption capacity shown in NaX at 77K temperature. Hydrogen adsorption capacities at 77K were found to be decreasing as palladium and ruthenium exchange levels increases. Chemisorption of hydrogen was observed at 303K and 333K and was due to the chemical interaction between the transition metal cations and the hydrogen molecules. The maximum hydrogen uptake at 303K and 5bar was observed for palladium exchanged zeolite X with a value of around 85cm3/g. Grand canonical Monte Carlo simulations were also performed to study the adsorption of H2in these zeolites at 77K as well as 303K and 333K. The simulation studies are suitable for establishing a correlation between the microscopic behavior of the zeolite and adsorbate system with the macroscopic properties which are measured experimentally, such as adsorption isotherms.