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Low-temperature catalytic reduction of nitrogen oxides with ammonia over supported manganese oxide catalysts

机译:负载型氧化锰催化剂上的氨低温催化还原氮氧化物

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摘要

MnOx supported on γ-Al_2O_3, TiO_2, Y-ZrO_2 and SiO_2 was prepared by an impregnation and a deposition-precipitation method, and their catalytic activities for the low-temperature selective catalytic reduction (SCR) of NOx with NH_3 in the presence of excess O_2 were examined. The catalytic activity of the catalysts prepared by a deposition-precipitation method was higher than that of catalysts prepared by an impregnation method. The activity follows in the order: MnOx/TiO_2≈MnOx/γ-Al_2O_3 > MnOx/SiO_2 > MnOx/Y-ZrO_2. Supported MnOx catalysts prepared by a deposition-precipitation method appeared to have an amorphous manganese oxide phase and those prepared by an impregnation method exhibited a crystalline MnO_2 phase, respectively. The addition of SO_2 with H_2O in the feeding gas slightly deactivates the SCR activity of MnOx/TiO_2 catalysts.
机译:通过浸渍和沉积-沉淀法制备了负载在γ-Al_2O_3,TiO_2,Y-ZrO_2和SiO_2上的MnOx,并在过量存在下用NH_3对NOx进行低温选择性催化还原(SCR)。检查了O_2。通过沉积沉淀法制备的催化剂的催化活性高于通过浸渍法制备的催化剂的催化活性。活性依次为:MnOx /TiO_2≈MnOx/γ-Al_2O_3> MnOx / SiO_2> MnOx / Y-ZrO_2。通过沉积-沉淀法制备的负载型MnOx催化剂似乎具有非晶态的氧化锰相,而通过浸渍法制备的负载型MnOx催化剂则分别呈现结晶态的MnO_2相。在进料气中添加SO_2和H_2O会稍微降低MnOx / TiO_2催化剂的SCR活性。

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