Influence of nitrogen surface functionalities on the catalytic activity of activated carbon in low temperature SCR of NO with NH3

2004 ◽  
Vol 90 (1-2) ◽  
pp. 51-59 ◽  
Author(s):  
Grzegorz S. Szymański ◽  
Teresa Grzybek ◽  
Helmut Papp
2014 ◽  
Vol 633 ◽  
pp. 121-124 ◽  
Author(s):  
Liang Jing Zhang ◽  
Su Ping Cui ◽  
Hong Xia Guo ◽  
Xiao Yu Ma ◽  
Xiao Gen Luo

Catalysts of Mn/TiO2 and Mn-Ce /TiO2 prepared by co-precipitation method for low temperature selective catalytic reduction (SCR) of NO with NH3 were investigated in this study. The experimental results showed that co-precipitation method after improvement, the NO conversion of Mn-Ce/TiO2 catalyst increased sharply. Meanwhile, the addition of cerium has significant effects on the catalytic activity. Characterizations of catalysts were carried out by XRD, BET and H2-TPR. The characterized results indicated that co-precipitation method after improvement, in temperature windows 150 to 300 °C, showed higher NOx conversion.


Energies ◽  
2018 ◽  
Vol 12 (1) ◽  
pp. 123 ◽  
Author(s):  
Guangli Liu ◽  
Dongtai Han ◽  
Jie Cheng ◽  
Yongshi Feng ◽  
Wenbin Quan ◽  
...  

Hydrocarbons as reductants show promising results for replacing NH3 in SCR technology. Therefore, considerable interest exists for developing low-temperature (<200 °C) and environmentally friendly HC-SCR catalysts. Hence, C2H4 was examined as a reductant using activated-carbon-supported MnOx-based catalyst in low-temperature SCR operation. Its sensitivity to Mn concentration and operating temperature was parametrically studied, the results of which showed that the catalyst activity followed the order of 130 °C > 150 °C > 180 °C with an optimized Mn concentration near 3.0 wt.%. However, rapid deactivation of catalytic activity also occurred when using C2H4 as the reductant. The mechanism of deactivation was explored and is discussed herein in which deactivation is attributed to two factors. The manganese oxide was reduced to Mn3O4 during reaction testing, which contained relatively low activity compared to Mn2O3. Also, increased crystallinity of the reduced manganese and the formation of carbon black occurred during SCR reaction testing, and these constituents on the catalyst’s surface blocked pores and active sites from participating in catalytic activity.


2011 ◽  
Vol 12 (6) ◽  
pp. 394-398 ◽  
Author(s):  
Lili Zhu ◽  
Bichun Huang ◽  
Wenhui Wang ◽  
Zhengle Wei ◽  
Daiqi Ye

2020 ◽  
Vol 379 ◽  
pp. 122398 ◽  
Author(s):  
Jie Yang ◽  
Shan Ren ◽  
Tianshi Zhang ◽  
Zenghui Su ◽  
Hongming Long ◽  
...  

2014 ◽  
Vol 2 (48) ◽  
pp. 20486-20493 ◽  
Author(s):  
Sihui Zhan ◽  
Mingying Qiu ◽  
Shanshan Yang ◽  
Dandan Zhu ◽  
Hongbing Yu ◽  
...  

MnO2 doped Fe2O3 hollow nanofibers were successfully synthesized by the electrospinning method, which exhibit superior catalytic activity for low temperature NH3-SCR.


Catalysts ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. 873 ◽  
Author(s):  
Zenghui Su ◽  
Shan Ren ◽  
Zhichao Chen ◽  
Jie Yang ◽  
Yuhan Zhou ◽  
...  

In this study, the poisoning effect of CaO on activated carbon (AC)-based Mn-Ce catalysts was discussed. Loading CaO inhibited the catalytic activity of the catalyst and the NO conversion of the catalyst decreased from 69.5% to 38.2% at 75 °C. The amount of MnO2 in AC surface decreased in the process of loading CaO, which was detrimental to the Selective Catalytic Reduction (SCR) performance of the catalyst. The change of manganese oxide form inhibited generation rate for the chemisorption oxygen and NO2, which was the most critical reason for the decrease of catalytic activity. Besides, loaded CaO entered into the pores of the catalyst, which led to the blockage of the pores and further resulted in the decrease of the Brunauer-Emmett-Teller (BET) surface area and total pore volume. It also destroyed the oxygen-containing functional groups and acid site on the surface of AC. All of these caused the deactivation of Mn-Ce/AC catalyst after loading CaO.


Fuel ◽  
2015 ◽  
Vol 156 ◽  
pp. 47-53 ◽  
Author(s):  
Boxiong Shen ◽  
Jianhong Chen ◽  
Shiji Yue ◽  
Guoliang Li

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