郭新闻

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教授

博士生导师

硕士生导师

主要任职:盘锦校区管委会副主任兼教学与科研工作部部长

性别:男

毕业院校:大连理工大学

学位:博士

所在单位:化工学院

学科:工业催化. 物理化学

办公地点:化工实验楼B427

联系方式:18641143913

电子邮箱:guoxw@dlut.edu.cn

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Cobalt-modified molybdenum carbide as an efficient catalyst for chemoselective reduction of aromatic nitro compounds

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论文类型:期刊论文

发表时间:2014-01-01

发表刊物:GREEN CHEMISTRY

收录刊物:SCIE、Scopus

卷号:16

期号:3

页面范围:1274-1281

ISSN号:1463-9262

摘要:This work presents a facile and clean transformation for synthesizing diverse functionalized arylamines through chemoselective reduction reaction of their corresponding substituted nitroarenes catalyzed by the supported cobalt-promoted molybdenum carbide catalyst on modified activated carbon (Co-Mo2C/AC, AC is denoted as the modified activated carbon by H2O2 oxidation treatment). Various characterization techniques including X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), inductively coupled plasma (ICP) and H-2 temperature-programmed reduction (H-2-TPR) were employed to reveal the relationship between catalyst nature and catalytic performance, and the plausible reaction mechanism is also proposed. The characterization results suggest that the addition of a small amount of transition metals, especially cobalt could significantly promote the formation of a perfect molybdenum carbide crystal phase, resulting in the improvement in catalytic properties of the supported molybdenum carbide catalyst. Reaction results demonstrate that the optimized Co-Mo2C/AC catalyst shows comparable catalytic performance towards precious metals for chemoselective reduction of various aromatic nitro compounds, affording 100% yield for all substrates involved in this work (99.3% of isolated yield for model substrate). Moreover, it can be found that the catalyst could be easily recovered by filtration and recycled without obvious loss in its catalytic properties. Therefore, the developed Co-Mo2C/AC catalyst in this work can be considered as an industrially viable and cheap candidate for clean and highly-efficient production of diverse functionalized arylamines.