催化作用
化学
X射线光电子能谱
氨
解吸
空间速度
分解
过渡金属
离解(化学)
吸附
热脱附光谱法
钼
透射电子显微镜
无机化学
核化学
分析化学(期刊)
物理化学
化学工程
纳米技术
选择性
材料科学
有机化学
工程类
作者
Jun Xu,Han Yan,Jin Zhao,Chun‐Jiang Jia
标识
DOI:10.1002/cjoc.201900016
摘要
Summary of main observation and conclusion In the present work, high quality γ‐Mo 2 N catalysts for ammonia decomposition were successfully synthesized via temperature programmed nitridation of α‐MoO 3 nanobelts. The optimal conditions for the synthesis of MoO 3 precursors were obtained by using the orthogonal experimental method. The MoO 3 precursors and the corresponding fresh and used Mo 2 N catalysts were characterized by various characterization techniques, including transmission electron microscopy, X‐ray diffraction and N 2 adsorption‐desorption. Furthermore, temperature‐ programmed desorption by N 2 or NH 3 and X‐ray photoelectron spectroscopy analysis were performed to better understand the chemical properties of Mo 2 N catalysts. The results revealed that Mo 2 N catalyst has good NH 3 adsorption ability and facilitates the dissociation adsorption of N 2 . Moreover, the morphology and structure of Mo 2 N catalysts well maintained after the reaction. Therefore, among the three transition metal nitrides (Mo 2 N, W 2 N and VN) and some Mo‐based catalysts previously reported, Mo 2 N catalysts showed very high activity and stability. Nearly 94% conversion of NH 3 could be reached at 550°C with the gas hourly space velocity of 22000 cm 3 ∙g cat –1 ∙h –1 and no obvious deactivation was observed during a 72 h test.
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