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
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.