4.7 Article

Promotional effects of nitrogen doping on catalytic performance over manganese-containing semi-coke catalysts for the NH3-SCR at low temperatures

期刊

JOURNAL OF HAZARDOUS MATERIALS
卷 387, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.jhazmat.2019.121704

关键词

Nitrogen doping; MnOx/semi-coke catalyst; Low-temperature SCR; Surface chemistry; Promotional mechanism

资金

  1. National Natural Science Foundation of China [51874058, 51604048]
  2. Fund of Chongqing Science and Technology [cstc2017shms-zdyfx0055, cstc2016zdcy-ztzx20001]
  3. Chongqing Key Technology Innovation of Industries [cstc2016zdcy-ztzx20006]
  4. Cheng Tou Road and Bridge Administration Co. Ltd.

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A series of nitrogen-doped MnOx/semi-coke catalysts were studied for low-temperature (LT) de-NOx performance in the NH3-SCR reaction. Changes in morphology, structure, and surface chemistry of the semi-coke catalysts were systematically investigated to analyze the promotional effects of nitrogen doping on catalytic performance. The catalytic activity of ASC-10U10 Mn was found to be enhanced significantly in a broad temperature range of 100-300 degrees C, improving 44.2 % at 150 degrees C-the largest jump in this temperature range-and reaching 94.5 % at 275 degrees C. Nitrogen doping results in aromatic pyridinic-N, pyrrolic-N, and quatemary-N; the unpaired electrons on these groups play a critical role in enhancing the adsorption and oxidation of NO center dot NH3 adsorption is enhanced due to numerous diverse Lewis acid sites on ASG10U10 Mn. The electron distribution of MnOx/semi-coke catalysts and the electron mobility between manganese and oxygen species are improved by nitrogen doping. The resulting nitrate intermediates, especially bridging nitrates, can be reduced by NH3 species at low temperatures. The increase in the number of oxygen vacancies improves oxidation of coordinated NH3. In addition, DRIFTS results suggest that coordinated NH3 and intermediate -NH2 are much more active and make a considerable positive contribution to the LT SCR reaction.

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