梁长海

个人信息Personal Information

教授

博士生导师

硕士生导师

任职 : 大连理工大学成都研究院院长

性别:男

毕业院校:中科院大连化学物理研究所

学位:博士

所在单位:化工学院

学科:化学工艺. 物理化学. 功能材料化学与化工

办公地点:大连理工大学西部校区化工综合楼A401室

联系方式:辽宁省大连市高新区凌工路2号,邮编116024

电子邮箱:changhai@dlut.edu.cn

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Structure Investigation and Dibenzothiophene Hydrodesulfurization Properties of Fe-Substituted Ni-Si Intermetallics

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论文类型:期刊论文

发表时间:2015-12-31

发表刊物:JOURNAL OF PHYSICAL CHEMISTRY C

收录刊物:SCIE、EI、Scopus

卷号:119

期号:52

页面范围:29052-29061

ISSN号:1932-7447

摘要:Development of highly active and sulfur-tolerant catalysts for deep hydrodesulfurization (HDS) is of great importance in petroleum refining. Here, the discovery of Fe-substituted Ni Si intermetallic catalysts (Ni1-x,FexSi2) that efficiently removes dibenzothiophene (DBT) by HDS is reported. The structure of the catalyst was identified through X-ray diffraction, Mossbauer spectroscopy, transmission electron microscopy, and X-ray photoelectron spectroscopy. The results showed that Fe atoms substituted Ni atoms in Nii_xFe Si, catalysts, which preferentially bond with Ni to form alloy and combine with Si to form silicide. The DBT activity for the Ni1-xFexSi2 has the following order: Ni0.75Fe0.25Si2 > NiSi2 > N10.50Fe0.50Si2 Ni0.25Fe0.75Si2 i Fe Si. The positive synergistic effect on HDS activity can be correlated to that the formation of Ni Fe and Fe Si bonds makes the metal site to have high d-electron density, which promotes the hydrogenation activity. Comparison with the fresh and spent catalysts revealed the stability and sulfur resistance of these catalysts. The present findings suggest that Fe-substituted Ni Si intermetallics catalysts provide a good starting point for a new catalyst development in the HDS field.