The effects of Co3O4 loading, precalcination temperature acid ZnO treatment on the catalytic properties of the Co3O4/Al2O3 system were investigated. The amounts of Co3O4 were varied between 5.57 wt% and 32.0 wt% and the resulting solids subjected to heat treatment at temperatures in the range 300-60DoC. The amounts of ZnO were varied between 0.36 wt% and 2.12 wt%. The results obtained indicated that ZnO treatment of Co3O4/Al2O3 solids followed by precalcination at 400 degreesC resulted in a progressive decrease in the particle size of the Co3O4 crystallites in the resulting samples. The catalytic activity of such solids towards H2O2 decomposition decreased progressively as the precalcination temperature employed was increased in the range 400-600 degreesC. The relationship between the catalytic activity expressed as a plot of the reaction rate constant, k, versus the amount of Co3O4 in the samples showed a progressive increase in the range 5.6-17.7 wt% followed by an abrupt increase when the extent of loading exceeded this limit. Treatment with ZnO effected a measurable increase (42%) in the specific surface area (S-BET) of the treated solids. However, such treatment also resulted in a considerable increase in the value of the reaction rate constant for the catalyzed reaction. Thus, the maximum increase in the value of k(20 degreesC) due to doping with 2.12 wt% ZnO attained a value of 543% while the corresponding increase in the value of the reaction rate constant per unit surface area, (k) over bar (20 degreesC) was 331%. Precalcination at 400-600 degreesC of Co3O4Al2O3 solids subjected to ZnO treatment did not modify the mechanism whereby the catalytically active constituents (surface cobalt species) were involved in the reaction although their concentration was altered without affecting their energetic nature.
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Department of Physical Chemistry, National Research Centre, Dokki, Cairo, EgyptDepartment of Physical Chemistry, National Research Centre, Dokki, Cairo, Egypt
El-Shobaky, Gamil A.
Radwan, Nagi R. E.
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Department of Chemistry, Faculty of Education, Suez Canal University, Suez, EgyptDepartment of Physical Chemistry, National Research Centre, Dokki, Cairo, Egypt
Radwan, Nagi R. E.
Radwan, Farouk M.
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Department of Chemistry, Faculty of Science, Suez Canal University, Ismailia, EgyptDepartment of Physical Chemistry, National Research Centre, Dokki, Cairo, Egypt