Remarkable enhancement of the catalytic performance of molybdenum sulfide catalysts via an in situ decomposition method for higher alcohol synthesis from syngas

被引:3
|
作者
Wang, Na [1 ,2 ,3 ]
Li, Jianli [2 ]
Liu, Xuemin [2 ]
Hu, Ruijue [2 ]
Zhang, Yulong [2 ]
Su, Haiquan [1 ,2 ]
Gu, Xiaojun [2 ]
机构
[1] Inner Mongolia Univ Technol, Chem Engn Coll, Hohhot 010051, Inner Mongolia, Peoples R China
[2] Inner Mongolia Univ, Sch Chem & Chem Engn, Inner Mongolia Key Lab Coal Chem, Hohhot 010021, Inner Mongolia, Peoples R China
[3] Baotou Teachers Coll, Baotou 014030, Inner Mongolia, Peoples R China
来源
RSC Advances | 2016年 / 6卷 / 113期
关键词
TEMPERATURE-PROGRAMMED REDUCTION; SYNTHESIS GAS; CO HYDROGENATION; MOS2; CATALYSTS; MIXED ALCOHOLS; HYDRODESULFURIZATION CATALYSTS; K2CO3/MOS2; CATALYST; SELECTIVITY; HDS; POTASSIUM;
D O I
10.1039/c6ra24406h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nickel-containing and nickel-free molybdenum sulfide catalysts were prepared by an in situ thermal decomposition method. Their catalytic performance was investigated for higher alcohol synthesis from syngas. It is surprising that the Ni-promoted and the nickel-free catalysts prepared by in situ decomposition showed significantly higher activity featuring space-time-yield (STY, mg g(-1) h(-1)) values of 520 and 510 respectively, while the ex situ method resulted in K-Ni-MoS2-E and K-MoS2-E catalysts with low activities featuring STY values of 370 and 170 mg g(-1) h(-1), respectively. The remarkable difference in catalytic activities was due to the fact that the in situ decomposition method can result in disordered MoS2 domains and exposure to more coordinated unsaturated sites by the formation of smaller particles. In addition, the excellent catalytic performance was also associated with the combined impact of the in situ preparation method and Ni promotion.
引用
收藏
页码:112356 / 112362
页数:7
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