A controllable synthesis of nitrogen-doped mesoporous carbon supported MoS2 catalysts for hydrodesulfurization of thiophene

被引:14
|
作者
Hu, Jianheng [1 ]
Zhang, Zhenwei [2 ]
Wang, Fei [1 ]
Zheng, Shifu [1 ]
Cai, Jinpeng [1 ]
Qin, Jilong [1 ]
Liu, Wenwen [1 ]
Liang, Shuai [1 ]
Jiang, Xingmao [1 ,3 ]
机构
[1] Changzhou Univ, Sch Petrochem & Engn, Adv Catalysis & Green Mfg Collaborat Innovat Ctr, Changzhou 213164, Peoples R China
[2] Changzhou Inst Technol, Dept Chem & Engn, Changzhou 213022, Peoples R China
[3] Wuhan Inst Technol, Sch Chem Engn & Pharm, Wuhan 430205, Peoples R China
基金
美国国家科学基金会;
关键词
PERFORMANCE; CARBONIZATION; POLYMERS;
D O I
10.1039/c6ra22554c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A highly active and stable catalyst for hydrodesulfurization (HDS) was developed based on the in situ formation of MoS2 on nitrogen-doped mesoporous carbon (MoS2/NMC). N-Doped mesoporous carbon (NMC) was prepared using urea and glucose as precursors and silica nanospheres as templates for achieving mesoporous structures via an in situ self-assembly process. Taking advantage of its high specific surface area and its uniform and adjustable pore size, MMC provides a favourable microenvironment for deposit of highly dispersed MoS2. It was demonstrated that the resulting MoS2/NMC catalysts exhibited an excellent catalytic activity and recycling stability in HDS of thiophene. Pore size and N content of NMC support can be adjusted by the size of the silica template and the amount of urea. The as-prepared 30MoS(2)/NMC-10 catalyst achieved a compete conversion of thiophene, indicating that an appropriate amount of N content in carbon support can enhance HDS activity. This simple and versatile method also can be extended to cover many kinds of other supported catalysts for broad applications in many other catalytic reactions in the future.
引用
收藏
页码:101544 / 101551
页数:8
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