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Synthesis and thermal evolution of structure in alkoxide-derived niobium pentoxide gels
Author(s) -
Narottam P. Bansal
Publication year - 1994
Publication title -
journal of materials science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.813
H-Index - 177
eISSN - 1573-4803
pISSN - 0022-2461
DOI - 10.1007/bf00376270
Subject(s) - niobium pentoxide , materials science , differential scanning calorimetry , crystallization , amorphous solid , thermogravimetric analysis , alkoxide , differential thermal analysis , niobium , thermal analysis , powder diffraction , activation energy , inorganic chemistry , chemical engineering , chemistry , crystallography , organic chemistry , thermodynamics , catalysis , diffraction , thermal , physics , engineering , metallurgy , optics
Niobium pentoxide gels in the form of transparent monoliths and powder have been synthesized from the controlled hydrolysis and polycondensation of niobium pentaethoxide under different experimental conditions using various mole ratios of Nb(OC2H5)5:H2O:C2H5OH:HCl. Alcohol acted as the mutual solvent and HCl as the deflocculating agent. In the absence of HCl, precipitation of colloidal particles was encountered on the addition of any water to the alkoxide. The gels were subjected to various thermal treatments and characterized by differential thermal analysis, thermogravimetric analysis, X-ray diffraction and infra-red spectroscopy. After drying at 400°C, the gels were amorphous to X-rays. The amorphous powder crystallized into the low temperature orthorhombic form of Nb2O5 at ~ 500°C, which transformed irreversibly into the high temperature monoclinic a-Nb2O5 between 900 to 1000°C. The kinetics of crystallization of the amorphous niobium pentoxide have been investigated by non-isothermal differential scanning calorimetry. The crystallization activation energy was determined to be 399 kJ mol-1.

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