کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
40332 45850 2013 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Effect of heat treatment conditions on the structure and catalytic properties of MnOx/Al2O3 in the reaction of CO oxidation
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
پیش نمایش صفحه اول مقاله
Effect of heat treatment conditions on the structure and catalytic properties of MnOx/Al2O3 in the reaction of CO oxidation
چکیده انگلیسی


• Catalytic properties of MnOx/Al2O3 catalysts were studied in the CO oxidation.
• Activity of the Ar-calcined catalysts was related to the Mn3−xAlxO4 formation.
• Active component in the air-catalysts contains Mn3O4 and amorphous Mn–Al–O phase.

Catalytic properties of MnOx/Al2O3 catalysts were studied in the CO oxidation reaction. The catalysts were prepared by co-precipitation and then the product was calcined in Ar or air at temperatures of 700–1200 °C. It was found that increase in the calcination temperature to 950–1000 °C lead to the growth of catalytic activity for both series, especially for catalysts calcined in air.An increase in the catalytic activity of the catalysts calcined in Ar was related to the formation of Mn3−xAlxO4 cubic spinel which was stable during specimen cooling in inert atmosphere. It was found that active component in the air-calcined catalysts was formed via decomposition of the high-temperature precursor (cubic spinel Mn3−xAlxO4) followed by the appearance of aggregates consisting of imperfect Mn3O4+δ oxide and amorphous Mn–Al–O phase. The decomposition was accompanied by the formation of weakly bound oxygen which appears to be active in oxidation reactions. The structure of the active component was directly related to the composition of the high-temperature precursor – the higher the concentration of manganese cations are in the Mn3−xAlxO4 cubic spinel, the more Mn3O4 and weakly bound oxygen appear in the decomposition product.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Applied Catalysis A: General - Volume 459, 24 May 2013, Pages 73–80
نویسندگان
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