首页 | 本学科首页   官方微博 | 高级检索  
     

以SBA-15为载体担载Ni-Mo制备深度加氢脱硫催化剂
引用本文:任靖,曹光伟,王安杰,胡永康.以SBA-15为载体担载Ni-Mo制备深度加氢脱硫催化剂[J].石油学报(石油加工),2008,24(5):503-503.
作者姓名:任靖  曹光伟  王安杰  胡永康
作者单位:1. 中国石化催化剂抚顺分公司,辽宁,抚顺,113001
2. 中国石化催化剂抚顺分公司,辽宁,抚顺,113001;大连理工大学精细化工国家重点实验室,辽宁,大连,116012
3. 大连理工大学精细化工国家重点实验室,辽宁,大连,116012
4. 大连理工大学精细化工国家重点实验室,辽宁,大连,116012;中国石化抚顺石油化工研究院,辽宁,抚顺,113001
摘    要: 以TEOS为硅源、聚环氧乙烷-聚环氧丙烷-聚环氧乙烷三嵌段共聚物表面活性剂(P123)为模板剂,在水热条件下合成了SBA-15,用XRD、N2 吸附、HRTEM等方法对其进行了表征。以SBA-15作载体,担载Ni-Mo制备了深度加氢脱硫(HDS)催化剂,在高压固定床反应器上以二苯并噻吩(DBT)和4,6-二甲基-二苯并噻吩(4,6-DMDBT)为模型化合物,考察了以SBA-15作载体的催化剂对DBT和4,6-DMDBT的HDS活性。结果表明,合成的SBA-15具有较高的比表面积、均匀的孔径。SBA-15担载Ni-Mo制备的催化剂表现出较高的加氢脱硫活性,其中Ni/Mo原子比为0.25时,催化剂的加氢脱硫活性最高。

关 键 词:SBA-15  Ni-Mo  深度加氢脱硫
收稿时间:2007-10-25
修稿时间:2007-12-6

PREPARATION OF DEEP HYDRODESULFURIZATION CATALYSTS BY DEPOSITING Ni-Mo SPECIES ON SILICEOUS SBA-15
REN Jing,CAO Guang-wei,WANG An-jie,HU Yong-kang.PREPARATION OF DEEP HYDRODESULFURIZATION CATALYSTS BY DEPOSITING Ni-Mo SPECIES ON SILICEOUS SBA-15[J].Acta Petrolei Sinica (Petroleum Processing Section),2008,24(5):503-503.
Authors:REN Jing  CAO Guang-wei  WANG An-jie  HU Yong-kang
Abstract:Siliceous SBA-15 was synthesized by a conventional hydrothermal method with TEOS as Si resource and PEO-PPO-PEO copolymer (P123) as template. The structure and properties of the synthesized SBA-15 were studied by means of XRD, N2 adsorption, TEM. A deep hydrodesulfurization (HDS) catalyst, which was considerably active to desulfurize dibenzothiophene (DBT) and 4,6-dimethyl dibenzothiophene (4,6-DMDBT), was prepared by depositing Ni-Mo species over SBA-15. It was indicated that the SBA-15 possessed extremely high surface area and even pore diameter, favoring the dispersion of the active species, resulting in very high HDS activity. The optimal Ni/Mo atomic ratio for this series of catalysts is 0.25, with which the Ni-Mo(0.25)/SBA-15 exhibited excellent performance in HDS of DBT and 4,6-DMDBT.
Keywords:SBA-15  Ni-Mo
本文献已被 维普 万方数据 等数据库收录!
点击此处可从《石油学报(石油加工)》浏览原始摘要信息
点击此处可从《石油学报(石油加工)》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号