کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
55315 47047 2012 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Higher activity of Diesel soot oxidation over polycrystalline ceria and ceria–zirconia solid solutions from more reactive surface planes
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
پیش نمایش صفحه اول مقاله
Higher activity of Diesel soot oxidation over polycrystalline ceria and ceria–zirconia solid solutions from more reactive surface planes
چکیده انگلیسی

High temperature treatment under air of samples of polycrystalline ceria and ceria–zirconia is shown to induce a rearrangement of crystals, with a surface structural evolution of the oxides toward the formation of more reactive exposed planes belonging to the {1 0 0} and {1 1 0} families, associated with a decrease of the exposure of the less reactive {1 1 1} facets. This is dependent on the amount of ceria, being more evident with pure CeO2, and less important with increasing ZrO2 content. A correlation between the exposure of more reactive planes and the specific rate of carbon soot oxidation is found, in agreement with previous results obtained in monodimensional nanoshaped and polycrystalline ceria samples for CO oxidation. This suggests that Diesel soot oxidation catalysts might be designed by keeping into consideration also these effects.

Figure optionsDownload high-quality image (215 K)Download as PowerPoint slideHighlights
► After high temperature calcination ceria and ceria–zirconia undergo structural evolution with exposure of more reactive surfaces.
► The exposure of reactive {1 0 0} and {1 1 0} type surfaces in ceria–zirconia is dependent on the amount of CeO2.
► {1 0 0} and {1 1 0} family type surfaces of ceria and ceria–zirconia are more reactive toward carbon soot oxidation.
► Any processing condition which favor the formation of (1 0 0) and (1 1 0) surfaces in ceria will result in enhanced activity toward soot oxidation.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Catalysis Today - Volume 197, Issue 1, 15 December 2012, Pages 119–126
نویسندگان
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