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Structure and catalysis of mesoporous titania-supported vanadium oxide

机译:中孔二氧化钛支撑钒氧化物的结构和催化

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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:我们成功地制备钒催化剂,其具有介孔的二氧化钛和极高的表面积。 通过共聚(直接掺入,V-Meso TiO_2)并通过合成浸渍(浸渍,v / meso tiO_2),钒掺入中孔二氧化钛中。 X射线衍射中的峰仍然保持在载荷达到5重量%的V-Meso TiO_2,而在6wt%V / Meso TiO_2中没有观察到衍射。 V k边缘光谱中预先偏压吸收的位置和强度显示V在大气条件下V-Meso TiO_2中的4 +。 V-Meso TiO_2和V / MESO TiO_2均在生产一氧化碳和二氧化碳的丙烯氧化反应中具有高活性。 从V / JRC-TiO-4的活性,分别从V / JRC-TiO-4的活性增加每单位v的氧化速率3.9和18。

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