Structure - Catalytic Activity Correlation in Aluminium Hydroxide Supported Vanadia Catalysts

Shanty Mathew, J. B. Nagy, Nagaraju N.
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Abstract

            Aluminium hydroxide samples containing vanadium in the range 5 - 25 wt % have been prepared by incipient wetness impregnation method. The catalysts have been characterized through % composition of vanadium, BET surface area, FTIR, PXRD, SEM and solid state V-NMR. Liquid phase conversion of benzyl alcohol over the above materials into various products has been used as a chemical probe to investigate the activity of these catalysts. Benzyl alcohol has been converted into benzaldehyde, toluene and 1, 2-diphenyl ethane (dibenzyl). Formation of various products at different loadings of vanadium is found to be related to structural features of vanadium oxo-species. Oxidation- reduction products and 1, 2-diphenyl ethane have been formed selectively, at lower loadings of vanadium, which was in the tetrahedral environment of oxygen and at higher loading when vanadium was in square pyramidal environment catalytic activity increased but with low selectivity. When aluminum hydroxide was used as a support monolayer coverage was completed only at higher loading indicating better dispersion of metal - oxo species over this support.
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氢氧化铝负载钒催化剂的结构-催化活性相关性研究
采用初湿浸渍法制备了钒含量在5 ~ 25wt %的氢氧化铝样品。通过钒含量、BET比表面积、FTIR、PXRD、SEM和固态V-NMR对催化剂进行了表征。用苄醇在上述材料上液相转化成各种产物作为化学探针来考察这些催化剂的活性。苯甲醇已转化为苯甲醛、甲苯和1,2 -二苯乙烷(二苯基)。发现不同钒负载下不同产物的形成与钒氧态的结构特征有关。氧化还原产物和1,2 -二苯乙烷在低负荷的氧四面体环境下有选择性地形成,在高负荷的氧四面体环境下有选择性地形成,而在高负荷的氧四面体环境下有选择性地形成。当使用氢氧化铝作为支撑层时,只有在较高的负载下才完成覆盖,这表明金属氧在该支撑层上的分散更好。
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