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Structure and catalysis of mesoporous titania-supported vanadium oxide

机译:介孔二氧化钛负载钒氧化物的结构与催化

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We successfully prepare vanadium catalysts supported on mesoporous titania with the mesostructural order and extremely high surface area. Vanadium was incorporated into mesoporous titania by co-condensation (direct incorporation, V-meso TiO_2) and by post synthesis impregnation (impregnation, V/meso TiO_2). The peak in X-ray diffraction remained until the loading reached 5 wt percent as V metal for V-meso TiO_2, while no diffraction was observed in 6 wt percent V/meso TiO_2. The position and intensity of pre-edge absorption in V K edge spectra revealed that the valence of V is 4 +in V-meso TiO_2 under atmospheric conditions. Both V-meso TiO_2 and V/meso TiO_2 were highly active in a propene oxidation reaction producing carbon monoxide and dioxide. The oxidation rates per unit V were enhanced by a factor of 3.9 and 18 for V-meso TiO_2 and V/meso TiO_2, respectively, from the activity of V/JRC-TIO-4.
机译:我们成功地制备了介孔二氧化钛上具有介孔结构级和极高表面积的钒催化剂。钒通过共缩合(直接引入,V-介孔TiO_2)和后合成浸渍(浸渍,V /介孔TiO_2)掺入介孔二氧化钛。 X射线衍射的峰值一直保持到V-介观TiO_2的负载量达到V金属的5%(重量),而在6%(重量)的V /介观TiO_2中没有观察到衍射。在V K边缘光谱中,前边缘吸收的位置和强度表明,在大气条件下,V-介观TiO_2中V的化合价为4 +。 V-间位TiO_2和V /间位TiO_2在产生一氧化碳和二氧化碳的丙烯氧化反应中均具有高活性。从V / JRC-TIO-4的活性来看,V-间位TiO_2和V /间位TiO_2的单位V的氧化速率分别提高了3.9和18倍。

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