New evidences of redox mechanism in n-butane oxidative dehydrogenation over undoped and Cs-doped nickel molybdates
2002
Abstract Redox-type mechanisms of the n -butane oxidative dehydrogenation (ODH), over unpromoted and 3% cesium-promoted nickel molybdate, are clearly put in evidence by a study of the catalyst’s electrical conductivity. The in situ data, recorded submitting the catalysts to a sequence of gaseous atmospheres (oxygen–butane–oxygen–reaction mixture), also evidences the n-type semiconductor behavior of the nickel molybdate. The above-mentioned mechanism is also confirmed by temperature-programmed reduction (TPR) and catalytic data. The experiments show that cesium inhibits strongly NiMoO 4 reduction under the reaction conditions, keeping the catalyst in a higher oxidation state, which can be useful for practical applications.
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