暴露CeO2不同晶面的VOx-MnOx/CeO2催化剂低温NH3-SCR脱硝的原位红外研究

in-situ DRIFTs study on different exposed facets of VOx-MnOx/CeO2 catalysts for low-temperature NH3-SCR

  • 摘要: 为实现低温(200-250℃)NH3-SCR烟气脱硝,开发出了一种高分散暴露CeO2不同晶面的VOx-MnOx/CeO2低温脱硝催化剂。脱硝性能评价实验结果表明,暴露110晶面的VOx-MnOx/CeO2-R催化剂在很宽的温度范围内(220-330℃)都保持了>95%的脱硝效率。原位漫反射红外分析结果可知,暴露110晶面的VOx-MnOx/CeO2-R催化剂表面更易发生NH3和NO吸附,进而提高NO的转化效率。气态NH3在VOx-MnOx/CeO2-R催化剂上吸附生成NH3(L)和NH4+(B),该中间体与NO吸附的中间体桥联硝酸盐和双齿硝酸盐反应生成N2和H2O,并遵循Langmuir-Hinshelwood机理。

     

    Abstract: In order to achieve the low-temperature (200-250℃) NH3-SCR, highly dispersed VOx-MnOx/CeO2 catalysts with different exposed facets were produced. The NH3-SCR performance results indicate that the NO conversion over VOx-MnOx/CeO2-R with preferentially exposed 110 facets can achieve NO conversion >95% over a wide temperature span of 220-330℃. From the in-situ DRIFTs, gaseous NH3 and NO are favorable to be absorbed on the surface of the VOx-MnOx/CeO2-R catalyst with preferentially exposed 110 facets, which improves the efficiency of NO conversion. The mechanism study via in situ DRIFTs demonstrates that the well dispersed vanadium species on CeO2 110 absorb NH3 to generate NH3(L) and NH4+(B) species, which in turn become highly reactive toward bridging nitrate and bidentate nitrate species to form N2 and H2O according to the Langmuir-Hinshelwood mechanism.

     

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