کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
54803 | 47027 | 2013 | 7 صفحه PDF | دانلود رایگان |

The direct reduction of NO over mesoporous manganese oxide (m-MnOx) and in the presence of CO was studied at reaction temperatures in the range from 150 to 460 °C. The conversion of NO without the reducing agent CO was limited to less than 10%, but when CO was added to the reactor feed up to 70% of the NO was reduced at a reaction temperature of 340 °C. However, the m-MnOx catalyst activity deteriorated at temperature above 340 °C due to a transformation of MnO2 to the less active Mn2O3 and Mn3O4 phases. The activity of the m-MnOx catalyst at high temperatures was enhanced by the addition of CuO. Two methods to load CuO on the m-MnOx were investigated: wet impregnation and co-precipitation. Both methods produced catalysts that achieved close to 97% NO conversion in CO at a reaction temperature of 430 °C.
This figure outlines the activity of mesoporous MnOx and CuO supported on mesoporous MnOx synthesized by two different methods for removal of NO using CO as reducing agent.Figure optionsDownload high-quality image (104 K)Download as PowerPoint slideHighlights
► Mesoporous MnOx studied for catalytic reduction of NO with CO.
► Above 340 °C, an irreversible phase change of MnO2 to Mn2O3 and Mn3O4 observed.
► The above phase change reduced the catalyst activity.
► Wet impregnation and co-precipitation methods used to synthesize CuO/meso-MnOx.
► CuO/meso-MnOx catalysts show superior activity at high temperatures.
Journal: Catalysis Today - Volume 212, 1 September 2013, Pages 38–44