陆安慧

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教授

博士生导师

硕士生导师

主要任职:校长助理

其他任职:精细化工国家重点实验室副主任,辽宁省低碳资源高值化利用重点实验室主任

性别:男

毕业院校:中科院山西煤化所

学位:博士

所在单位:化工学院

学科:工业催化. 化学工艺. 能源化工

办公地点:大连市凌工路2号大连理工大学西部校区化工楼,邮编:116024

联系方式:0411-84986112

电子邮箱:anhuilu@dlut.edu.cn

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Spatially and Size Selective Synthesis of Fe-Based Nanoparticles on Ordered Mesoporous Supports as Highly Active and Stable Catalysts for Ammonia Decomposition

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论文类型:期刊论文

发表时间:2021-01-12

发表刊物:JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

卷号:132

期号:40

页面范围:14152-14162

ISSN号:0002-7863

摘要:Uniform and highly dispersed gamma-Fe(2)O(3) nanoparticles with a diameter of similar to 6 nm supported on CMK-5 carbons and C/SBA-15 composites were prepared via simple impregnation and thermal treatment. The nanostructures of these materials were characterized by XRD, Mossbauer spectroscopy, XPS, SEM, TEM, and nitrogen sorption. Due to the confinement effect of the mesoporous ordered matrices, gamma-Fe(2)O(3) nanoparticles were fully immobilized within the channels of the supports. Even at high Fe-loadings (up to about 12 wt %) on CMK-5 carbon no iron species were detected on the external surface of the carbon support by XPS analysis and electron microscopy. Fe(2)O(3)/CMK-5 showed the highest ammonia decomposition activity of all previously described Fe-based catalysts in this reaction. Complete ammonia decomposition was achieved at 700 degrees C and space velocities as high as 60 000 cm(3) g(cat)(-1) h(-1). At a space velocity of 7500 cm(3) g(cat)(-1) h(-1), complete ammonia conversion was maintained at 600 degrees C for 20 h. After the reaction, the immobilized gamma-Fe(2)O(3) nanoparticles were found to be converted to much smaller nanoparticles (gamma-Fe(2)O(3) and a small fraction of nitride), which were still embedded within the carbon matrix. The Fe(2)O(3)/CMK-5 catalyst is much more active than the benchmark NiO/Al(2)O(3) catalyst at high space velocity, due to its highly developed mesoporosity. gamma-Fe(2)O(3) nanoparticles supported on carbon-silica composites are structurally much more stable over extended periods of time but less active than those supported on carbon. TEM observation reveals that iron-based nanoparticles penetrate through the carbon layer and then are anchored on the silica walls, thus preventing them from moving and sintering. In this way, the stability of the carbon-silica catalyst is improved. Comparison with the silica supported iron oxide catalyst reveals that the presence of a thin layer of carbon is essential for increased catalytic activity.