王安杰

个人信息Personal Information

教授

博士生导师

硕士生导师

性别:男

毕业院校:大连理工大学

学位:博士

所在单位:化工学院

学科:工业催化

办公地点:西部校区化工实验楼B321

联系方式:大连市高新区凌工路2号大连理工大学西部校区B321

电子邮箱:ajwang@dlut.edu.cn

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Hydrodesulfurization of dibenzothiophene and its hydrogenated intermediates over bulk MoP

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论文类型:期刊论文

发表时间:2012-03-01

发表刊物:JOURNAL OF CATALYSIS

收录刊物:EI、SCIE

卷号:287

页面范围:161-169

ISSN号:0021-9517

关键字:Hydrodesulfurization; Dibenzothiophene; Hydrogenated intermediates; Molybdenum phosphide; Piperidine

摘要:The hydrodesulfurization (HDS) of dibenzothiophene (DBT) and its hydrogenated intermediates 1,2,3,4-tetrahydro-dibenzothiophene (TH-DBT) and 1,2,3,4,4a,9b-hexahydro-dibenzothiophene (HH-DBT) over a bulk MoP catalyst was studied at 340 degrees C and 4 MPa both in the presence and absence of piperidine. The results indicated that sulfur was incorporated on the surface of MoP during HDS reactions, probably leading to the formation of new active sites, which possessed higher direct desulfurization (DDS) activity than the fresh MoP. The hydrogenation pathway and DDS pathway played an equally important role in the HDS of DBT. The desulfurization of TH-DBT was much faster than that of DBT, whereas HH-DBT mainly desulfurized by dehydrogenation to TH-DBT and subsequent desulfurization of TH-DBT. Piperidine decreased the rates of all reactions, but that of hydrogenation more than of desulfurization. It not only competed with the sulfur-containing molecules for adsorption on the active sites but also slowed down the sulfidation of MoP surface. (C) 2011 Elsevier Inc. All rights reserved.