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Exact(8)
Ceria-zirconia mixed oxide was chosen as a support because of its properties to activate CO2.
The presence of molybdenum specie in the intermediate (Bi,Mo 2O3 mixed oxide was ascertained by EDS during complementary ex situ experiments.
The Zr0.1Ti0.9On mixed oxide was of bicrystalline TiO2 anatase-brookite structure (67 33 wt.%) showing small crystallite-sizes, which allowed the optimal surface phase junction.
A SiO2/Nb2O5 mixed oxide was prepared by a sol gel processing method based on TEOS and NbCl5 as precursors and HCl as catalysts.
The ternary mixed oxides containing Mn were more active than the binary Cu Mn, Co Mn, and Ni Mn ones as well as the ternary Al-containing catalysts; the Cu Ni Mn mixed oxide was the most active.
The Ce75Zr25O2 mixed oxide was prepared by co-precipitation of hydroxides and was characterized by X-ray diffraction (XRD) before and after pre-treatments, thermogravimetric analysis (TG) and temperature programmed desorption of NO (TPD).
Similar(52)
Monometallic noble metal catalysts supported on ceria zirconia mixed oxide were prepared by impregnation and tested in the oxidation of chlorobenzene (100 ppm in air).
MgAlLaO mixed oxide is also a strong solid base in spite of much lower La content.
The redox properties of model Mn-containing mixed oxide are studied.
Films of Ce Zr mixed oxide were produced by sol gel and r.f.
For comparison, other anode materials such as platinum and mixed oxide were also tested.
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