Author/Authors :
Palizdar, M Training Department - CPG Industrial - Mining and Technical Services, Germany , Aslam, Z Institute for Materials Research - Leeds University, U.K , Aghababazadeh, R Graduate , Mirhabibi, A Iran University of Science and Technology , Sangpour, P Graduate , Palizdar, Y Graduate , Brydson, R Institute for Materials Research - Leeds University, U.K , Abadi, Z Graduate
Abstract :
In this paper, the chemical interaction between catalyst and support was studied to understand the observed
different growth rate of CNTs in our previous paper. Both pure MgO and Mg(NO3)2 . 6H2O as sources of the MgO
catalyst support and Fe2(SO4)3 · xH2O as the source of the Fe catalyst, were employed. A Fe catalyst supported on
MgO was synthesized using the wet impregnation method followed by calcination. To compare the catalyst grain size
and its distribution, the sample were characterized by scanning electron microscopy (SEM), transmission electron
microscopy (TEM), X-ray powder diffraction (XRD), BET specic surface area (SSA) measurement, and X-ray
photoelectron spectroscopy (XPS). XPS technique was utilized complementary to demonstrate the existence of
chemical interaction between MgO support and Fe catalyst. Results revealed that the type of precursor used to prepare
the support had a signicant inuence on the morphology of the support and the associated distribution of the Fe
catalysts. The highest yield of MgFe2O4 phase was obtained using a pure MgO precursor which after calcination
resulted in a homogenous distribution of nano-sized Fe particles over the support surface.