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  • 关珺 ( 副教授 )

    的个人主页 http://faculty.dlut.edu.cn/2002011088/zh_CN/index.htm

  •   副教授   硕士生导师
论文成果 当前位置: 中文主页 >> 科学研究 >> 论文成果
Naphthalene Hydrogenation over Silica Supported Nickel Phosphide in the Absence and Presence of N-Containing Compounds

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论文类型:期刊论文
发表时间:2010-07-01
发表刊物:ENERGY & FUELS
收录刊物:SCIE、EI、Scopus
卷号:24
期号:7
页面范围:3796-3803
ISSN号:0887-0624
摘要:Silica supported nickel phosphide catalysts with initial Ni/P molar ratios from 0.5 to 2.0 and the sum of NiO and P(2)O(5) loadings from 10 to 40 wt % in their precursors have been prepared by the temperature-programmed reduction method and characterized by means of X-ray diffraction, N(2) physisorption, CO chemisorption, and pyridine adsorption with in situ Fourier transform-infrared (FT-IR) spectroscopy. Naphthalene hydrogenation was carried out at 340 degrees C and 4.0 MPa over the as-prepared Ni(2)P/SiO(2) catalysts. Mutual influences of naphthalene hydrogenation and guillotine hydrodenitrogenation were investigated under similar conditions. The catalyst with Ni/P = 1.25 and 30 wt % loading showed the complete naphthalene conversion as well as 92.1% of selectivity to decalin. It was observed that cis-decalin converted partly into trans-decalin under the studied conditions. Addition of quinoline into naphthalene hydrogenation obviously decreased naphthalene conversion and selectivity to decalin over the Ni(2)P/SiO(2) catalysts due to the strong adsorption of guillotine on active sites. The similar effects of the guillotine hydrogenated compounds on naphthalene hydrogenation were also observed over the Ni(2)P/SiO(2) catalysts. The addition of naphthalene had no effect on guillotine hydrogenation to tetrahydroquinoline but inhibited tetrahydroquinoline hydrogenation to decahydroguinoline. Naphthalene conversion over the Ni(2)P/SiO(2) catalyst in the presence of quinoline and dibenzothiophene decreased with the increase of their contents. It is noteworthy that naphthalene conversion could be recovered after the removal of guillotine while the hydrogenation activity could not in the case of dibenzothiophene.

 

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