Mesoporous zeolite-supported metal sulfide catalysts with high activities in the deep hydrogenation of phenanthrene

被引:71
作者
Fu, Wenqian [1 ]
Zhang, Lei [2 ]
Wu, Dongfang [1 ]
Xiang, Mei [2 ]
Zhuo, Qian [1 ]
Huang, Kai [1 ]
Tao, Zhongdong [1 ]
Tang, Tiandi [2 ]
机构
[1] Southeast Univ, Sch Chem & Chem Engn, Nanjing 211189, Jiangsu, Peoples R China
[2] Wenzhou Univ, Coll Chem & Mat Engn, Wenzhou 325035, Peoples R China
基金
美国国家科学基金会;
关键词
Mesoporous zeolite ZSM-5; NiMo catalyst; Phenanthrene; Deep hydrogenation; DIESEL FUELS; HYDRODESULFURIZATION CATALYST; HYDROTREATING CATALYSTS; NIMO/SBA-15; CATALYSTS; SULFUR TOLERANCE; CHELATING-AGENTS; MO CATALYSTS; ACTIVE PHASE; CITRIC-ACID; 4,6-DIMETHYLDIBENZOTHIOPHENE;
D O I
10.1016/j.jcat.2015.07.026
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Developing highly active hydrogenation catalysts for deep aromatics saturation is of great importance in the production of ultraclean diesel fuel at a low cost. Toward this goal, we synthesized a mesoporous zeolite ZSM-5 (MZSM-5) that was cost-effective and available on a large scale, and used it as a support for the preparation of highly efficient metal sulfide catalysts (NiMoS/MZSM-5 and CoMoS/MZSM-5) for the deep hydrogenation of phenanthrene. The intrinsic activity of the NiM0S/MZSM-5 catalyst (7.4 x 10(-4) mol kg(-1) s(-1)) was much higher than that of the alumina-supported NiMo catalyst (NiMOS/gamma-Al2O3, 4.8 x 10(-4) mol kg(-1) s(-1)), and the selectivity of the deep hydrogenation products over NiM0S/MZSM-5 (20.9%) was higher than for NiMOS/gamma-Al2O3 (15.2%). Compared with gamma-Al2O3, the relatively weak metal-support interaction could facilitate the formation of polymolybdates on MZSM-5. After sulfidation, the more multistacked MoS2 active phases were formed on the MZSM-5, enhancing the hydrogenation activity of the NiMOS/MZSM-5 catalyst. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:423 / 433
页数:11
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