Title of article :
Physicochemical properties of solid–solid interactions in nanosized NiO-substituted Fe2O3/TiO2 system at 1200 °C
Author/Authors :
Khedr، نويسنده , , M.H. and Sobhy، نويسنده , , M.S. and Tawfik، نويسنده , , A.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2007
Pages :
8
From page :
213
To page :
220
Abstract :
The solid–solid interactions between nanosized pure and NiO-substituted ferric and titanium(IV) oxides have been investigated using XRD technique and microstructure studies, also magnetic properties were studied using vibrating samples magnetometer (VSM). The amounts of substituting Ni2+ were x = 0, 0.2, 0.4, 0.6, 0.8 and 1 mole. A mixture equimolar proportions of finely powdered Fe2O3 and TiO2 were mixed with NiO, ball milled, compressed at 250 kg/cm2 and fired at 1200 °C for 4 h. tained results showed that with substituting Ni2+ concentration x = 0 only Fe2TiO5 phase is present (∼80 nm) which showed a very small saturation magnetic flux density (Bs), remnant magnetic flux density (Br) and the maximum energy product (BH)max. By the addition of x = 0.2 NiO, new phases were observed NiTiO3 and NiFe2O4 of crystallite sizes 160 and 110 nm, respectively. By the increase of substituting Ni2+ concentration the NiTiO3 and NiFe2O4 phases increased on the expense of Fe2TiO5 up to x = 0.4, then the increase in substituting Ni2+ concentration led to a decrease in Fe2TiO5 and NiTiO3 while NiFe2O4 increases which results in a great improvement of magnetic properties. mples exhibit a catalytic activity towards H2O2 decomposition and the values of rate constant increase with increasing amount of Ni2+ substituting. The most acidic active sites are shown by specimens substituted with x = 0 this concludes that H2O2 decomposition is not favored on acidic active sites.
Keywords :
A. Nanostructure , B. Chemical synthesis , D. Catalytic properties , D. Crystal structure , D. Magnetic properties
Journal title :
Materials Research Bulletin
Serial Year :
2007
Journal title :
Materials Research Bulletin
Record number :
2098091
Link To Document :
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