加氢脱硫
加氢脱氧
二苯并噻吩
催化作用
化学
X射线光电子能谱
解吸
程序升温还原
核化学
无机化学
选择性
吸附
化学工程
有机化学
工程类
作者
Bolong Jiang,Tianhan Zhu,Hua Song,Feng Li
标识
DOI:10.1016/j.jallcom.2019.07.242
摘要
The Fe-doped Ni2P/Fe-SBA-15 was prepared by the temperature programmed reduction method at a relative low temperature of 673 K. The effect of Fe on the catalytic performance for benzofuran (BF) hydrodeoxygenation (HDO) and dibenzothiophene (DBT) hydrodesulfurization (HDS) were investigated. The catalysts were characterized by means of X-ray diffraction (XRD), N2 adsorption-desorption, inductively coupled plasma mass spectrometry (ICP-MS), X-ray photoelectron spectroscopy (XPS), temperature-programmed desorption of ammonia (NH3-TPD), and transmission electron microscope (TEM) and CO uptakes. The results indicate the incorporation of Fe into SBA-15 contributes to the exposure of smaller Ni2P particles (5.6 nm) with an uniform dispersion, along with enhancement of weak and medium acid strengths. Compared with Ni2P/SBA-15, the Fe-doped Ni2P/Fe-SBA-15 exhibited a much higher BF conversion of 91.7% with an improved total deoxygenated product yield of 83.3%. The excellent HDO performance of Ni2P/Fe-SBA-15 can be ascribed to the exposure of highly-dispersed smaller Ni2P particles. Meanwhile, the improved dehydration of 2-EtPh to EB and the high deoxygenated product selectivity can be attributed to the enhanced acidity. As compared to the Ni2P/SBA-15, the Fe-doped Ni2P/Fe-SBA-15 showed a higher DBT HDS activity of 96.3% with the BP formation at a great proportion of 90.3%, indicating that DBT was mainly transformed through the desulfurization pathway during HDS.
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