Influence of the chemical nature of deposited metal ions on their catalytic properties in oxidation of methane by nitrous oxide

1989 ◽  
Vol 24 (4) ◽  
pp. 440-445
Author(s):  
N. I. Il'chenko ◽  
A. I. Bostan ◽  
G. I. Golodets
1984 ◽  
Vol 106 (15) ◽  
pp. 4117-4121 ◽  
Author(s):  
H. F. Liu ◽  
R. S. Liu ◽  
K. Y. Liew ◽  
R. E. Johnson ◽  
J. H. Lunsford

2001 ◽  
Vol 166 (2) ◽  
pp. 323-330 ◽  
Author(s):  
Shigeru Sugiyama ◽  
Yoshiharu Fujii ◽  
Keiichi Abe ◽  
Hiromu Hayashi ◽  
John B Moffat

The chemical nature of the cool flame of hexane at 300°C, maintained stationary in a flow system at atmospheric pressure, has been investigated. The relative intensities of cool flames obtained from mixtures of differing composition have been measured, using a photomultiplier cell, and correlated with analyses made of the complex mixture of reaction products. The stationary two-stage flames which may be obtained at either higher oxygen concentrations or higher pressures than the cool flame are also described, and investigated similarly. The results are examined in the light of a theory of combustion of the higher hydrocarbons via aldehydes and hydroxyl radicals, which is an extension of a mechanism derived for the oxidation of methane. This receives considerable support, particularly from the identification of the complete homologous series of saturated aldehydes which can result from the hexane molecule. Associated with these reactions are others due to the greater stability of peroxide radicals at 300°C than at the higher temperatures of methane oxidation. Thus the building up of a partial pressure of hydroperoxide sufficient to ignite in the presence of oxygen may initiate the cool flame, and considerable amounts of cyclic ethers have been found which probably had a peroxidic precursor.


RSC Advances ◽  
2015 ◽  
Vol 5 (115) ◽  
pp. 94949-94979 ◽  
Author(s):  
Parthasarathi Bera ◽  
M. S. Hegde

CeO2 and TiO2 based noble metal ionic catalysts show very high catalytic activities toward several reactions such as auto exhaust, water gas shift, H2 + O2 recombination compared to supported nanometal catalysts due to their electronic interactions.


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