Preparation of Ni2P/TiO2-Al2O3 and the Catalytic Performance for Hydrodesulfurization of 3-Methylthiophene

被引:39
|
作者
Wang, Kaile [1 ]
Yang, Bolun [1 ]
Liu, Yu [1 ]
Yi, Chunhai [1 ]
机构
[1] Xi An Jiao Tong Univ, Dept Chem Engn, State Key Lab Multiphase Flow Power Engn, Xian 710049, Shaanxi, Peoples R China
基金
高等学校博士学科点专项科研基金;
关键词
HYDROTREATING ACTIVITY; NICKEL; DIBENZOTHIOPHENE; NI2P;
D O I
10.1021/ef9002523
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Composite TlO2-Al2O3 supports were prepared by the sol-gel technique using tetra-n-butyl-titanate and gamma-Al2O3 as raw materials, and the Ni2P/TiO2-Al2O3 catalysts were obtained by incipient wetness impregnation of aqueous metal phosphate precursors, followed by temperature-programmed reduction of inflowing H-2. The supports and catalysts were characterized by X-ray diffraction, infrared spectroscopy, transmission electron microscopy, and N-2 adsorption. The hydrodesulfurization (HDS) activity was examined in a fixed-bed reactor. Experimental results indicate that the composite support can effectively prevent the formation of aluminum phosphates based on the strong interaction between P and gamma-Al2O3, overcome the disadvantage of low surface titania, and improve metal support interaction, which significantly increase catalyst activity and selectivity. The Ni2P/TiO2-Al2O3 Catalyst exhibits good activity for the HDS of 3-methylthiopliene (3-MT), used as a model compound. The activity and stability of the Ni2P/TiO2-Al2O3 catalyst are affected by the phosphorus content, both achieving a maximum with an initial Ni/P molar ratio of 1:2. The reaction temperature and the weight hourly space velocity (WHSV) show significant influence, but the reaction pressure and the volume ratio of hydrogen/oil have little effect oil the HDS performance of the Ni2P/TiO2-Al2O3 catalyst. The conversion of 3-MT is close to 100% when the reaction temperature reaches 603 K, reaction pressure reaches 2.0 MPa, WHSV reaches 1,275 h(-1), and volume ratio of hydrogen/oil reaches 400.
引用
收藏
页码:4209 / 4214
页数:6
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