Low-temperature steam reforming of methanol to produce hydrogen over various metal-doped molybdenum carbide catalysts

被引:130
作者
Ma, Yufei [1 ]
Guan, Guoqing [1 ,2 ]
Shi, Chuan [3 ]
Zhu, Aimin [3 ]
Hao, Xiaogang [4 ]
Wang, Zhongde [4 ]
Kusakabe, Katsuki [5 ]
Abudula, Abuliti [1 ,2 ]
机构
[1] Hirosaki Univ, Grad Sch Sci & Technol, Hirosaki, Aomori 0368561, Japan
[2] Hirosaki Univ, North Japan Res Inst Sustainable Energy, Aomori 0300813, Japan
[3] Dalian Univ Technol, Lab Plasma Phys Chem, Dalian City 116024, Liaoning, Peoples R China
[4] Taiyuan Univ Technol, Dept Chem Engn, Taiyuan 030024, Peoples R China
[5] Sojo Univ, Dept Nanosci, Nishi Ku, Kumamoto 8600082, Japan
基金
日本科学技术振兴机构;
关键词
Steam reforming of methanol; Molybdenum carbide; TPR method; Transition metal; Hydrogen production; SOLID-STATE TRANSFORMATION; GAS; MO2C; DECOMPOSITION; TRIOXIDE; ETHANOL; PD/ZNO; COBALT;
D O I
10.1016/j.ijhydene.2013.09.150
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
Various transition metals (M = Pt, Fe, Co, and Ni) were selected to support on molybdenum carbides by in-situ carburization metal-doped molybdenum oxide (M-MoOx) via temperature-programmed reaction (TPR) with a final temperature of 700 degrees C in a reaction gas mixture of 20% CH4/H-2. XRD analysis results indicated that beta-Mo2C phase was formed in the case of Fe, Co, or Ni doping while alpha-Mo2C phase was appeared with the beta-MoC1-x phase in the case of Pt doping. With the increase in Pt doping amount, more alpha-MoC1-x phase was produced. As-prepared metal doped molybdenum carbides were investigated as alternative catalysts for the steam reforming of methanol. Comparing with the undoped molybdenum carbide such as beta-Mo2C, metal-doped one showed higher methanol conversion and hydrogen yield. It is found that Pt doped molybdenum carbide had the highest catalytic activity and selectivity among the prepared catalysts and methanol conversion reached 100% even at a temperature as low as 200 degrees C, and remained a long-time stability with a stable methanol conversion. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:258 / 266
页数:9
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