کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
41662 45895 2011 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Reactivity studies of Au–Pd supported nanoparticles for catalytic applications
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
پیش نمایش صفحه اول مقاله
Reactivity studies of Au–Pd supported nanoparticles for catalytic applications
چکیده انگلیسی

The utilisation of gold–palladium nanoparticles either in the form of colloids or supported nanoparticles has received enormous attention in recent years. These materials are very effective for the transformation of organic compounds to highly useful chemical products. The catalytic materials are usually prepared using deposition–precipitation and impregnation techniques, but recently significant attention has been focused on the use of colloidal methods. Here we compare and contrast the preparation and catalytic reactivity of Au–Pd supported nanoparticles synthesised by deposition–precipitation and colloidal methods. The catalyst materials have been evaluated for three different reactions, namely, the oxidation of benzyl alcohol, the direct synthesis of hydrogen peroxide and the oxidation of carbon monoxide. In addition, we have focused our attention on the pre-treatment temperature and the improvement of the deposition–precipitation method by using urea and sodium borohydride for the preparation of highly active Au–Pd supported nanoparticles.

The catalytic reactivity of Au–Pd supported nanoparticles synthesised by deposition–precipitation and colloidal methods have been compared. We have focused our attention on the calcination temperature and the improvement of the deposition–precipitation method by using urea and sodium borohydride for the preparation of Au–Pd supported nanoparticles that are very active for both the direct synthesis of H2O2 and CO oxidation.Figure optionsDownload high-quality image (67 K)Download as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Applied Catalysis A: General - Volume 391, Issues 1–2, 4 January 2011, Pages 400–406
نویسندگان
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