The Influence of Water Vapor and Sulfur Dioxide on the Catalytic Decomposition of Nitrous Oxide

Author(s):  
C. Yalamas ◽  
R. Heinisch ◽  
M. Cournil ◽  
M. Barz
Author(s):  
K. Yanagida ◽  
W. Kurniawan ◽  
C. Salim ◽  
H. Hinode

Decomposition of nitrous oxide (N2O) over titania (TiO2) supported copper (Cu) catalyst was investigated with the existence of oxygen and water vapor. The catalytic activity of TiO2 was promoted by copper loading. It was found that there are optimum levels of copper loading on TiO2, and these values are correlated to the specific surface area of TiO2 support being used. The relationship between the catalytic activity for decomposition of N2O and the crystal structure of TiO2 was also investigated. The result revealed that Cu/TiO2 catalysts with the rutile structure has a higher activity toward N2O decomposition than those with the anatase structure. In this research, Cu(5wt%)/TiO2 prepared from TiO2 JRC-TIO-4 (reference catalyst provided by Catalysis Society of Japan) which was mainly constituted of rutile showed the highest activity for N2O decomposition and it could decompose N2O completely at 650℃. The catalytic activity was inhibited by the existence of oxygen. However, there was no influence of water vapor to the catalytic activity of Cu/TiO2 for N2O decomposition. 


2008 ◽  
Vol 9 (14) ◽  
pp. 2303-2307 ◽  
Author(s):  
P. Siva Sankar Reddy ◽  
N. Seshu Babu ◽  
Nayeem Pasha ◽  
N. Lingaiah ◽  
P.S. Sai Prasad

The bimolecular reaction 2N 2 O = 2N 2 + 2N 2 was recently shown to belong to the rather rare class of homogeneous reactions. Decomposition of two molecules of nitrous oxide takes place when a collision of a certain critical degree of violence occurs in the gas. At the moment of collision the two molecules must possess a combined energy of at least 58,000 calories (per 2 gram molecules), and it is probable that most of the collision in which this condition is fulfilled are fruitful. A comparison between the kinetics of this homogeneous decomposition and the corresponding reaction proceeding catalytically at the surface of a solid might be expected to throw light on the mechanism of heterogeneous catalysis. Previous efforts ( loc. cit .) to accelerate the reaction catalytically by the introduction of metals into the bulb in which the homogeneous reaction was going on were fruitless, since the reaction, if any, which took place at the surface of the metal was slow in camparison with the gaseous reaction. This difficulty was overcome by using as a catalyst a fine metal wire heated electrically. This could be raised to a sufficiently high temperature to cause the surface reaction to proceed with measurable velocity while the bulk of the gas was kept cold, thus eliminating the homogeneous reaction. Experiments made with platinum wires in this way were successful. The kinetics of the decomposition of nitrous oxide on the surface of platinum are summarized in the equation – d [N 2 O]/ dt = k [N 2 O]/1 + b [O 2 ]. The reaction is unimolecular, but is complicated by the strong retarding action of the oxygen formed.


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