Title of article :
A novel synthesis of Ni2P/MCM-41 catalysts by reducing a precursor of ammonium hypophosphite and nickel chloride at low temperature Original Research Article
Author/Authors :
Hua Song، نويسنده , , Min Dai، نويسنده , , Hualin Song، نويسنده , , Xia Wan، نويسنده , , Xiaowei Xu، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2013
Pages :
9
From page :
247
To page :
255
Abstract :
A novel method to prepare Ni2P/MCM-41 catalysts at low reduction temperature based on ammonium hypophosphite and nickel chloride by temperature programmed reduction is described. The catalysts were prepared using incipient wetness impregnation of the siliceous MCM-41 support with aqueous solutions of ammonium hypophosphite and nickel chloride, followed by reducing the obtained precursor at 483–663 K for 2 h in flowing H2, to form Ni2P catalysts. The catalysts were characterized by H2 temperature-programmed reduction (H2-TPR), X-ray diffraction (XRD), N2-adsorption specific surface area measurements (BET), CO uptake, transmission electron microscope (TEM), and X-ray photoelectron spectroscopy (XPS). With sample of initial P/Ni molar ratio >0.5, the Ni2P was successfully obtained at lower reduction temperature, and a high initial P/Ni molar ratio favors the formation of Ni2P at lower temperature. Using less oxidic phosphorus precursor of hypophosphite enabled the Ni2P to be formed at low reduction temperature. Evaluation of the activity for DBT HDS of the catalysts shows that the catalyst prepared with initial P/Ni ratios of 2 exhibited the highest activity. At a reaction temperature of 613 K, a pressure of 3.0 MPa, a H2/oil ratio of 500 (V/V), and a weight hourly space velocity (WHSV) of 2.0 h−1, the HDS conversion reached 99%, and no catalyst deactivation was observed within 120 h.
Keywords :
Nickel chloride , Hydrodesulfurization , Ammonium hypophosphite , Nickel phosphide , MCM-41 , Dibenzothiophene
Journal title :
Applied Catalysis A:General
Serial Year :
2013
Journal title :
Applied Catalysis A:General
Record number :
1157477
Link To Document :
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