Title of article :
Effects of Fe substitutions by Ni in La–Ni–O perovskite-type oxides in reforming of methane with CO2 and O2
Author/Authors :
Jahangiri، نويسنده , , Alireza and Aghabozorg، نويسنده , , Hamidreza and Pahlavanzadeh، نويسنده , , Hassan، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2013
Pages :
10
From page :
10407
To page :
10416
Abstract :
LaNiO3 and LaNi1−xFexO3 (x = 0.2, 0.4, 0.6, 0.8 and 1) perovskites were prepared by the citrate sol–gel method. The prepared compounds were characterized by using thermogravimetric analysis (TGA) and X-ray diffraction (XRD), temperature programmed reduction (TPR), and inductively coupled plasma (ICP) techniques. Specific surface area of the samples was measured by BET method. Morphology study of the prepared catalysts was performed using scanning and transmission electron microscopy (SEM and TEM, respectively). The XRD patterns of fresh catalysts indicated the formation of well-crystallized perovskite structure as the main phase present in the prepared samples. The results showed that the highly homogeneous and pure solids with particle sizes in the range of nanometers were obtained through this synthesis method. TPR analysis revealed that by increasing the degree of substitution (x) the reduction of the prepared samples became difficult. The effects of the partial substitution of Ni by Fe and reaction temperatures at atmospheric pressure were investigated in the combined reforming of methane with CO2 and O2 (CRM), after reduction of the samples under hydrogen. LaNiO3 exhibited high activity and selectivity without coke formation between all of the studied perovskites. Among Fe-substituted catalysts, the following order of activity was observed: LaNiO3>LaNi0.4Fe0.6O3>LaNi0.6Fe0.4O3 > LaNi0.8Fe0.2O3 > LaNi0.2Fe0.8O3 > LaFeO3.
Keywords :
Sol–gel , CRM process , Ni-substitution by Fe , catalytic activity , Perovskite
Journal title :
International Journal of Hydrogen Energy
Serial Year :
2013
Journal title :
International Journal of Hydrogen Energy
Record number :
1864083
Link To Document :
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