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

[Display omitted] •Ti-incorporated Ni2P/Ti-MCM-41 was prepared under a lower reduction temperature of 400°C.•The Ti addition can modify the Ni2P electronic atmosphere and improve the DDS activity.•The improved HYD activity of the Ti-doped samples can be attributed to moderate surface acidity sites.•...

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Veröffentlicht in:Journal of catalysis 2014-03, Vol.311, p.257-265
Hauptverfasser: Song, Hua, Wang, Jian, Wang, Zidong, Song, Hualin, Li, Feng, Jin, Zaishun
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Sprache:eng
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Zusammenfassung:[Display omitted] •Ti-incorporated Ni2P/Ti-MCM-41 was prepared under a lower reduction temperature of 400°C.•The Ti addition can modify the Ni2P electronic atmosphere and improve the DDS activity.•The improved HYD activity of the Ti-doped samples can be attributed to moderate surface acidity sites.•DBT HDS conversion of Ni2P/Ti-MCM-41 reached 99.4%, which improved by 17.5% compared to Ni2P/MCM-41. Ni2P/Ti-MCM-41 catalysts were successfully prepared under a lower reduction temperature of 400°C, and the effects of Ti on the catalytic properties for hydrodesulfurization (HDS) were investigated. The prepared catalysts were characterized by X-ray diffraction, N2-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 Brönsted 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.
ISSN:0021-9517
1090-2694
DOI:10.1016/j.jcat.2013.11.021