氨氧化
丙烷
催化作用
氮化物
材料科学
化学
丙烯腈
有机化学
纳米技术
图层(电子)
共聚物
聚合物
作者
Xiaoqiang Fan,Huimin Zhang,Jianmei Li,Zhen Zhao,Chunming Xu,Jian Liu,Aijun Duan,Guiyuan Jiang,Yuechang Wei
出处
期刊:Chinese Journal of Catalysis
[China Science Publishing & Media Ltd.]
日期:2014-03-01
卷期号:35 (3): 286-293
被引量:7
标识
DOI:10.1016/s1872-2067(14)60015-2
摘要
Five different methods were used to prepare the Ni-Mo oxide precursors including sol-gel, rotary evaporation-microwave drying, co-precipitation, impregnation, and mechanical mixing. Ni-Mo nitride catalysts have been synthesized by temperature-programmed nitration of the oxide precursors in a flow of H2 and N2. The structure and physico-chemical properties of the Ni-Mo oxide precursors and their corresponding nitride catalysts were determined by X-ray diffraction, total nitrogen content analysis, X-ray photoelectron spectroscopy and H2 temperature-programmed reduction, and their catalytic performance for propane ammoxidation was also tested. The catalytic activity and selectivity towards the formation of acrylonitrile over the Ni-Mo nitride catalysts are strongly dependent on the preparation methods for the oxide precursors. The N species in the Ni-Mo nitrides and their mobility and reactivity affect the selectivity for acrylonitrile. The Ni-Mo nitride prepared by co-precipitation, with the largest amount and more reactive N species, exhibited the highest catalytic activity and selectivity for acrylonitrile.
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