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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Reactivity of olefins and thiophenes in hydrodesulfurization of FCC gasoline

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论文类型:期刊论文

发表时间:2013-12-10

发表刊物:Advanced Materials Research

收录刊物:EI、CPCI-S、Scopus

卷号:881-883

页面范围:271-278

ISSN号:9783037859940

关键字:FCC gasoline; CoMoS/Al2O3; Hydrogenation; Hydrodesulfurization; Graded catalyst bed

摘要:The reactivity of olefins and S-compounds and their distributions in different catalyst-bed lengths were experimentally evaluated with a FCC gasoline in a high-pressure fixed-bed continuous flow pilot unit over the CoMoS/gamma-Al2O3 catalyst. The evaluation results demonstrated that the increased steric hindrances around the double bond (C=C) and that to the thiophene molecules could suppress the hydrogenation of olefins and hydrodesulfurization (TADS) of S-compounds, respectively. Meanwhile, the reaction temperatures could influence the acidic property of the CoMoS active phase confirmed by FT-IR. analysis, and thus induced the different reactions. It was found that the isomerization of terminal olefins to internal olefins was promoted by the Bronsted acid sites (-SH) at low temperatures, as well as the skeletal isomerization by the strong Lewis acid sites occurred to a minor extent at high temperatures. Besides, the distributions of olefins and S-compounds in different catalyst-bed lengths showed that the removal of S-compounds reached 80% of its maximum conversion at the first 40% of the reactor length, however, the saturation of olefins increased linearly as the reactor length increased. Therefore, a new catalyst-loading method was developed, i.e., the upper 40% of the reactor length filling with catalyst of high HDS activity and the bottom 60% with catalyst of low olefin saturation activity, respectively. The evaluation results showed that the graded catalyst loading process showed higher selectivity in BIDS of FCC gasoline.