Location and activity of VOx species on TiO2 particles for NH3-SCR catalysis

被引:65
作者
Ganjkhanlou, Yadolah [1 ]
Janssens, Ton V. W. [2 ]
Vennestrom, Peter N. R. [2 ]
Mino, Lorenzo [1 ]
Paganini, Maria Cristina [1 ]
Signorile, Matteo [1 ]
Bordiga, Silvia [1 ]
Berlier, Gloria [1 ]
机构
[1] Univ Torino, NIS & INSTM Ctr, Dept Chem, Via P Giuria 7, I-10125 Turin, Italy
[2] Umicore Denmark ApS, Nojsomhedsvej 20, DK-2800 Lyngby, Denmark
关键词
VOx-TiO2; catalyst; NH3-SCR; Infrared spectroscopy; Electron paramagnetic resonance; CO adsorption; VANADIA-TITANIA CATALYSTS; IN-SITU RAMAN; TEMPERATURE CO ADSORPTION; OXIDE CATALYSTS; NITRIC-OXIDE; MOLECULAR-STRUCTURES; SURFACE-PROPERTIES; SUPPORTED VANADIA; IR SPECTROSCOPY; FT-IR;
D O I
10.1016/j.apcatb.2020.119337
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The role of anatase TiO2 on the performance of VOx-TiO2 is studied by in situ spectroscopies on a series of catalysts with 1.9-9.7 V at/nm(2). At low coverages, VOx is preferentially located at defect sites, spreading on the main TiO2 {101} and {100} facets at intermediate coverages. Bronsted sites concentration is maximum around 6 V atoms/nm(2), and EPR shows a significant amount of V4+ at intermediate VOx densities, indicating the influence of TiO2 on their reducibility. The activity is proportional to the square of the VOx density up to 5.8 V atoms/nm(2). All catalysts show the same activation energy for NH3-SCR of 56.9 +/- 1.0 kJ/mol in the temperature range 160-280 degrees C, indicating that the reaction path does not change in the studied V coverage range. The activity does not follow the observed trends for Bronsted acid sites or reducibility, and it seems that the ability to form V-pairs is the only requirement for catalytic activity.
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页数:10
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