کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
41885 45903 2010 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Copper–manganese oxide catalysts supported on alumina: Physicochemical features and catalytic performances in the aerobic oxidation of benzyl alcohol
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
پیش نمایش صفحه اول مقاله
Copper–manganese oxide catalysts supported on alumina: Physicochemical features and catalytic performances in the aerobic oxidation of benzyl alcohol
چکیده انگلیسی

We report the facile synthesis of alumina supported copper–manganese mixed oxide catalysts by a homogeneous deposition–precipitation method and the catalytic applications of these catalysts in the oxidation of benzyl alcohol using molecular oxygen. Benzyl alcohol conversion of ca. 90.9% was achieved with benzaldehyde as the main product. The catalyst can be recycled consecutively up to seven runs without appreciable loss of its activity and selectivity. Characterizations with X-ray diffraction, transmission electron microscopy, Raman, X-ray absorption spectroscopy, and hydrogen temperature-programmed reduction suggested the formation of a mixed oxide (Mn1.5Cu1.5O4) microcrystalline phase after adding copper to the manganese supported on alumina. Such formation would account for the high catalytic performance. Calcination under high temperature decomposed this mixed oxide phase, resulting in a poor catalytic activity.

Figure optionsDownload high-quality image (90 K)Download as PowerPoint slideResearch highlights▶ Copper–manganese bimetallic catalysts were synthesized by a facile method. ▶ Adding copper remarkably improves the catalytic activity of Mn/Al2O3. ▶ Mn1.5Cu1.5O4 microcrystalline phase is responsible for enhanced activity. ▶ High temperature calcination results in the decomposition of this mixed oxide. ▶ The Mn3O4 formed shows poor catalytic activity in benzyl alcohol oxidation.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Applied Catalysis A: General - Volume 389, Issues 1–2, 1 December 2010, Pages 101–107
نویسندگان
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