Effect of titanium content on dibenzothiophene HDS performance over Ni2P/Ti-MCM-41 catalyst

被引:137
作者
Song, Hua [1 ,2 ]
Wang, Jian [1 ]
Wang, Zidong [1 ]
Song, Hualin [3 ]
Li, Feng [1 ,2 ]
Jin, Zaishun [3 ]
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, Key Lab Canc Prevent & Treatment Heilongjiang Pro, Mudanjiang 157011, Heilongjing, Peoples R China
基金
中国国家自然科学基金;
关键词
Nickel phosphide; Ti-MCM-41; Titanium content; Hydrodesulfurization; Dibenzothiophene; NICKEL PHOSPHIDE CATALYSTS; TRANSITION-METAL PHOSPHIDES; MESOPOROUS MOLECULAR-SIEVE; THIOPHENE HYDRODESULFURIZATION; HYDROGEN SPILLOVER; HYDROTREATING CATALYSTS; BENZENE HYDROGENATION; MICROWAVE PREPARATION; ACTIVE PHASE; BULK NI2P;
D O I
10.1016/j.jcat.2013.11.021
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
Ni2P/Ti-MCM-41 catalysts were successfully prepared under a lower reduction temperature of 400 degrees C, and the effects of Ti on the catalytic properties for hydrodesulfurization (HDS) were investigated. The prepared catalysts were characterized by X-ray diffraction, N-2-adsorption specific surface area measurements, Fourier transform infrared spectroscopy of adsorbed pyridine, X-ray photoelectron spectroscopy, transmission electron microscope (TEM) and CO uptake. The incorporation of Ti can enhance the Lewis acidity and the Bronsted acidity of MCM-41 supports and induce proper Lewis acidity of the Ni2P/Ti-MCM-41 catalyst. An appropriate amount of Ti can promote the formation of the Ni2P phase and induce a better Ni2P dispersion. The catalyst prepared with a Ti/Si molar ratio of 1.5% exhibited the highest HDS activity of 99.4%. The Ti electronic effect (through the direct desulfurization route) and the moderate surface Lewis acidity (through the hydrogenation route) may explain the improved HDS catalytic activity of the Ti-doped samples. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:257 / 265
页数:9
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