Volume 47 Issue 6
Jun.  2019
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Article Contents
QIE Zhi-qiang, ZHANG Zi-yi, JING Jie-ying, YANG Zhi-fen, FENG Jie, LI Wen-ying. Effect of Ni2P loading on the structure and naphthalene hydrogenation performance of Ni2P/Ce-Al2O3 catalyst[J]. Journal of Fuel Chemistry and Technology, 2019, 47(6): 718-724.
Citation: QIE Zhi-qiang, ZHANG Zi-yi, JING Jie-ying, YANG Zhi-fen, FENG Jie, LI Wen-ying. Effect of Ni2P loading on the structure and naphthalene hydrogenation performance of Ni2P/Ce-Al2O3 catalyst[J]. Journal of Fuel Chemistry and Technology, 2019, 47(6): 718-724.

Effect of Ni2P loading on the structure and naphthalene hydrogenation performance of Ni2P/Ce-Al2O3 catalyst

Funds:

the National Natural Science Foundation of China U1610221

Natural Science Foundation of Shanxi Province 201701D221237

Program for the Top Young Academic Leaders of Higher Learning Institutions of Shanxi 164010121-S

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  • Corresponding author: JING Jie-ying, Tel/Fax: 86-351-6018453, E-mail: jingjieying@tyut.edu.cn
  • Received Date: 2019-01-30
  • Rev Recd Date: 2019-04-16
  • Available Online: 2021-01-23
  • Publish Date: 2019-06-10
  • A series of Ni2P/Ce-Al2O3 catalysts were prepared by temperature-programmed reduction method, and the influence of Ni2P loading on the catalyst structure and naphthalene hydrogenation saturation performance was investigated. The results show that the specific surface area, the Ni2P particle size and the active site number of the as-synthesized catalysts are greatly affected by Ni2P loading, which is derived from the variable interaction between active component Ni2P and the support Ce-Al2O3. When the Ni2P loading is 17% (mass ratio), the catalyst possesses a large specific surface area (40 m2/g), a small Ni2P particle size (26.3 nm), and the maximum number of active sites (26.7 μmol/g). Meanwhile, the conversion rate of naphthalene and the selectivity of decalin reach to 95% and 76%, respectively, and the activity stability of the catalyst is good, which is mainly attributed to the large specific surface area and high number of active sites of the catalyst providing more sites for the reaction.
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