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MnOx-TiO2,CeO2-MnOx-TiO2 and V2O5-MnOx-TiO2 catalysts for low-temperature NH3-SCR were prepared by sol-gel method.The results showed that both cerium and vanadium prevented the transformation of anatase TiO2 to the rutile phase.The addition of vanadium oxide induced the segregation of crystalline Mn2O3,which contributed little to low-temperature SCR and ammonia oxidation,from the MnOx-TiO2 solid solutions.However,the selectivity of the V-containing catalyst was almost 100% due to the decreased ammonia consump-tion and enhanced adsorption capacity of ammonia on Br(?)nsted acid sites at relatively high temperatures.The electron-donating effect of ce-rium reduced the Mn4+/Mn3+ ratio to some extent,resulting in a decreased activity for ammonia oxidation.This,in combination with the en-hanced ammonia adsorption capacity by Cen+ as additional Lewis acid sites,endowed the Ce-doped catalyst a higher N2 selectivity than MnOx-TiO2 despite the slightly elevated light-off temperature for NO conversion.
MnOx-TiO2, CeO2-MnOx-TiO2 and V2O5-MnOx-TiO2 catalysts for low-temperature NH3-SCR were prepared by sol-gel method. The results showed that both cerium and vanadium prevented the transformation of anatase TiO2 to the rutile phase. The addition of vanadium oxide induced the segregation of crystalline Mn2O3, which contributed little to low-temperature SCR and ammonia oxidation, from the MnOx-TiO2 solid solutions. Still, the selectivity of the V-containing catalyst was almost 100% due to the decreased ammonia consump-tion and enhanced adsorption capacity of ammonia on Br (?) nsted acid sites at relatively high temperatures. The electron-donating effect of ce-rium reduced the Mn4 + / Mn3 + ratio to some extent, resulting in a decreased activity for ammonia oxidation .This, in combination with the en-hanced ammonia adsorption capacity by Cen + as additional Lewis acid sites, endowed the Ce-doped catalyst a higher N2 selectivity than MnOx-TiO2 with the slightly elevated light-off temperature for NO convergent sion.