Effects of rehydration of alumina on its structural properties, surface acidity, and HDN activity of quinoline

被引:37
|
作者
Li, Guangci [1 ]
Liu, Yunqi [1 ]
Tang, Zhe [1 ]
Liu, Chenguang [1 ]
机构
[1] China Univ Petr, CNPC, Key Lab Catalysis, State Key Lab Heavy Oil Proc, Qingdao 266555, Peoples R China
关键词
Alumina; Mesoporous materials; Nanostructures; Lewis acidity; HDN; GAMMA-ALUMINA; HYDROGEN SPILLOVER; CRYSTALLITE SIZE; BOND LENGTHS; CATALYSTS; BOEHMITE; HYDRODENITROGENATION; OXIDE; HYDRODESULFURIZATION; ALOOH;
D O I
10.1016/j.apcata.2012.06.017
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A series of aluminas were obtained through rehydration-dehydration of the initial alumina under different hydrothermal conditions. To investigate the influences of rehydration temperature on the physicochemical properties of the as-obtained aluminas, several techniques were applied, such as X-ray powder diffraction, nitrogen adsorption, scanning/transmission electron microscopy, Fourier transform infrared, thermogravimetric analysis, and (27)AI MAS NMR. The results show that crystal size and morphology of alumina particles changed as the treatment temperature was increased, and alumina crystallites grew mainly along two surface orientations. Consequently, the changes in textural properties of the aluminas took place. In addition, the rehydration process increased not only the weak acid sites but also the strong acid sites, which is closely related to the growth of the (1 1 1) and (1 1 0) surfaces of gamma-Al2O3. The two type acid sites were originated from coordinately unsaturated four-fold aluminum atoms. TPR for a series of Ni(Mo) catalysts were carried out and the results show that rehydration process increased the surface acidity and basicity of alumina simultaneously, which enhanced the interacting force of Ni and Mo species with aluminas respectively. This interaction is closely related to the hydrodenitrogenation (HDN) activity of quinoline over the corresponding NiMo/gamma-Al2O3 catalysts. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:79 / 89
页数:11
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