کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
41726 45897 2011 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
NO removal by activated carbon-supported copper catalysts prepared by impregnation, polyol, and microwave heated polyol processes
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
پیش نمایش صفحه اول مقاله
NO removal by activated carbon-supported copper catalysts prepared by impregnation, polyol, and microwave heated polyol processes
چکیده انگلیسی

The effect of HNO3 pretreatment of activated carbon (AC)-supported copper catalysts for NO removal with NH3 was studied. In addition, the effects of various preparation methods for Cu/AC catalysts, namely, impregnation (IM), polyol process (P), and microwave heated polyol process (MP), on the activity of NO removal with NH3 were compared. HNO3 pretreatment increased the number of carboxyl sites and promoted good dispersion of active sites. In addition, the chemical states of active phases were found to be affected when the catalysts were prepared by the microwave heated polyol process. More Cu2O particles were observed on the Cu/AC-N-MP catalyst than on the Cu/AC-N-P catalyst. The experimental results indicated that HNO3 pretreatment of the AC support led to increased catalytic activity for NO removal with NH3. The catalytic activity of the Cu/AC catalysts for NO removal at 200 °C decreased in the following order: Cu/AC-N-MP > Cu/AC-N-P > Cu/AC-N-IM. The microwave heated polyol process is a facile method for the rapid synthesis of carbon-supported Cu catalysts for NO removal at low temperature.

Figure optionsDownload high-quality image (145 K)Download as PowerPoint slideHighlights
► Pretreatment of AC support with HNO3 increased the number of carboxyl sites.
► The active phases of Cu/AC prepared by the MP were Cu, CuO, and Cu2O.
► The MP is an easy and effective preparation method for Cu/AC catalyst for NO removal.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Applied Catalysis A: General - Volume 397, Issues 1–2, 30 April 2011, Pages 234–240
نویسندگان
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