首页 | 本学科首页   官方微博 | 高级检索  
     


Effect of preparation methods on the hydrocracking performance of NiMo/Al2O3 catalysts
Authors:Jiake Yang  Tongjiu Zuo  Jiangyin Lu
Affiliation:Key Laboratory of Oil&Gas Fine Chemicals, Ministry of Education, College of Chemistry and Chemical Engineering, Xinjiang University, Urumqi 830046, China
Abstract:In this work, NiMo catalysts with various contents of MoO3 were prepared through incipient wetness impregnation by a two-step method (NM-xA) and one-pot method (NM-xB). The catalysts were then characterized by XRD, XPS, NH3-TPD, H2-TPR, HR-TEM, and N2 adsorption–desorption technologies. The performance of the NiMo/Al2O3 catalysts was investigated by hydrocracking low-temperature coal tar. When the MoO3 content was 15 wt%, the interaction between Ni species and Al2O3 on the NM-15B catalyst was stronger than that on the NM-15A catalyst, resulting in the poor performance of the former. When the MoO3 content was 20 wt%, MoO3 agglomerated on the surface of the NM-20A catalyst, leading to decreased number of active sites and specific surface area and reduced catalytic performance. The increase in the number of MoS2 stack layers strengthened the interaction between Ni and Mo species of the NM-20B catalyst and consequently improved its catalytic performance. When the MoO3 content reached 25 wt%, the active metals agglomerated on the surface of the NiMo catalysts, thereby directly decreasing the number of active sites. In conclusion, the two-step method is suitable for preparing cat-alysts with large pore diameter and low MoO3 content loading, and the one-pot method is more appro-priate for preparing catalysts with large specific surface area and high MoO3 content. Moreover, the NM-xA catalysts had larger average pore diameter than the NM-xB catalysts and exhibited improved desul-furization performance.
Keywords:Preparation methods  Hydrocracking performance  The NiMo catalysts  MoO3 content
本文献已被 CNKI 万方数据 等数据库收录!
点击此处可从《中国化学工程学报》浏览原始摘要信息
点击此处可从《中国化学工程学报》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