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A novel synthesis of Ni2P/MCM-41 catalysts by reducing a precursor of ammonium hypophosphite and nickel chloride at low temperature
被引:55
|作者:
Song, Hua
[1
,2
]
Dai, Min
[1
,4
]
Song, Hualin
[3
]
Wan, Xia
[1
,4
]
Xu, Xiaowei
[1
]
机构:
[1] Northeast Petr Univ, Coll Chem & Chem Engn, Daqing 163318, Heilongjing, Peoples R China
[2] Northeast Petr Univ, Coll Chem & Chem Engn, Prov Key Lab Oil & Gas Chem Technol, Daqing 163318, Heilongjing, Peoples R China
[3] Mudanjiang Med Univ, Dept Image Coll, Mudanjiang 157011, Heilongjing, Peoples R China
[4] CPE Survey & Design Inst Xinjiang Oil, Karamay 834000, Xinjiang, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Nickel phosphide;
Ammonium hypophosphite;
Nickel chloride;
MCM-41;
Hydrodesulfurization;
Dibenzothiophene;
TRANSITION-METAL PHOSPHIDES;
HYDRODESULFURIZATION ACTIVITY;
THERMAL-DECOMPOSITION;
DEEP DESULFURIZATION;
SURFACE SITES;
ACTIVE PHASE;
LIQUID-PHASE;
IN-SITU;
GAS OIL;
NI2P;
D O I:
10.1016/j.apcata.2013.05.015
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 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 H-2, to form Ni2P catalysts. The catalysts were characterized by H-2 temperature-programmed reduction (H-2-TPR), X-ray diffraction (XRD), N-2-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 613K, a pressure of 3.0 MPa, a H-2/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. (C) 2013 Elsevier B.V. All rights reserved.
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页码:247 / 255
页数:9
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