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Generation of NH3 Selective Catalytic Reduction Active Catalysts from Decomposition of Supported FeVO4
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The effect of catalyst loading, composition, and calcination temperature on NH3 selective catalytic reduction (SCR) activity was investigated for metal vanadates of the type FexAl1鈥搙VO4 (0 鈮?x 鈮?1, MeVO4) supported on TiO2鈥揥O3鈥揝iO2 (TWS). The optimized catalyst (4.5 wt % FeVO4/TWS calcined at 650 掳C) showed an enhanced NOx reduction activity compared to the reference material 2.3 wt % V2O5/TWS. An activation effect was observed above a calcination at 600 掳C and was investigated by means of X-ray diffraction, Brunauer鈥揈mmett鈥揟eller, diffuse reflectance infrared Fourier transform, and X-ray absorption near edge structure analyses. It was shown that the activation is due to the decomposition of FeVO4. VOx species disperse and migrate to the support material, while the iron species sinter to Fe2O3 particles. We provide strong evidence that the active species responsible for NH3鈥揝CR in a FeVO4/TWS catalyst is not FeVO4 but VOx species that possess a similar coordination environment to the VOx species on conventional V-based catalysts. Due to the remarkable effect of the activation upon calcination, a very active and thermally stable SCR catalyst up to 700 掳C was obtained.

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