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However, the origin of the promoting effect of, for instance, vanadium in mixed oxides is largely unknown.
The effect of adsorbed hydrogen and of mixed oxides is discussed.
The redox behaviour under flowing 5%CO/He and 5%H2/Ar of two Ce0.62Zr0.38O2 mixed oxides is investigated.
Based on a careful investigation on the structural characterizations, the growth mechanism of the 3D nanostructured α MnO2/RuO2 mixed oxides is discussed in detail.
Eoc-data and CV-spectra support surface electrochemistry of mixed oxides is governed by the Ru III)/Ru(IV) redox couple.
For the first time, single-cell operation to separate U from Ln in mixed oxides is shown to be feasible by using AlCl3 as chlorination agent followed by electrodeposition.
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Slight acetaldehyde formation during ethanol deep oxidation over the supported mixed oxides was observed.
The CO oxidation activity of the mixed oxides was found to be dependent on Ce/Zr ratio, which relates to the degree of reducibility.
In particular, supported CeO2 and CeO2-based mixed oxides are effective catalysts for the oxidation of different hydrocarbons and for the removal of organics from polluted water from different sources [6].
Also, the CeO2-based mixed oxides are effective catalysts for the oxidation of different hydrocarbons and for the removal of total organic carbon from polluted waters from different sources [26, 27].
All the mixed oxides were considerably more active for methane oxidation than pure CeO2 prepared by the same citrate route.
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