Title of article :
Kinetics and mechanism of hydrothermally prepared copper oxide nanorod catalyzed decomposition of ammonium nitrate Original Research Article
Author/Authors :
Anuj A. Vargeese، نويسنده , , Krishnamurthi Muralidharan، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2012
Pages :
7
From page :
171
To page :
177
Abstract :
One of the key aspects in the development of materials science is the synthesis of particles with specific size and morphology for catalytic applications. Nowadays, nanostructured materials with specific morphology are gaining great importance in the field of catalysis. Thin, one-dimensional, monodispersed CuO nanorods with a significantly higher aspect ratio of 5, were successfully prepared by the hydrothermal method with subsequent ultrasonication. The formation of pure monoclinic CuO nanorods was confirmed by powder XRD and SAED. The CuO nanorod growth mechanism is investigated by using TEM and further characterized by FTIR, UV–visible spectroscopy and thermogravimetry. The catalytic decomposition of ammonium nitrate, an environmental friendly rocket propellant oxidizer, over the synthesized CuO nanorods was investigated. The thermal kinetic constants for the catalytic and noncatalytic decomposition of ammonium nitrate samples were computed by using model free (differential and non-linear integral) and model fitting approaches. The catalytic influence was evident even with 1% catalyst concentration. The model fitting method suggested contracting cylinder mechanism as the effective mechanism for all the investigated samples. Apparently, the CuO nanorods provide Lewis acid and/or active metal sites, facilitating the removal of ammonium nitrate decomposition inhibition species such as NH3 and thereby enhance the rate of decomposition.
Keywords :
CuO nanorods , Ammonium nitrate , Surface reactions , Reaction kinetics , Catalyzed decomposition
Journal title :
Applied Catalysis A:General
Serial Year :
2012
Journal title :
Applied Catalysis A:General
Record number :
1157140
Link To Document :
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