催化作用
柠檬酸
氨
钼
无机化学
氨生产
加氢脱硫
氢
化学
分解
氮化物
X射线光电子能谱
核化学
材料科学
化学工程
有机化学
图层(电子)
工程类
作者
Seetharamulu Podila,Sharif F. Zaman,Hafedh Driss,Abdulrahim A. Al‐Zahrani,Muhammad A. Daous,L. Petrov
标识
DOI:10.1016/j.ijhydene.2017.01.044
摘要
Hydrogen production from ammonia decomposition was studied using a series of unsupported high surface area molybdenum nitride (Mo2N) and cobalt promoted molybdenum nitride (3%Co-Mo2N) catalysts prepared with citric acid (CA) as a chelating agent. To elucidate the influence of citric acid amount in preparation conditions on the structure and catalytic activity, we prepared catalysts with different citric acid to Mo molar ratios i.e. CA/Mo = 1, 2, 3 and 4. The catalytic activity was evaluated in the temperature range of 300–600 °C at atmospheric pressure. The catalytic activity of the tested samples has changed in the following order of CA/Mo atomic ratio of 1 < 2 < 3 > 4. Therefore, the catalyst prepared by using CA/Mo ratio = 3 showed the highest catalytic activity. BET, XRD, XPS, SEM and TEM-EDS techniques were been used to characterize the catalysts. The increased activity of Mo2N-3:1 and 3%Co-Mo2N-3:1 catalysts was due to increased surface area, decreased particle size and increased relative proportions of Mo2N and Co3Mo3N phases. The ammonia conversion for 3%Co-Mo2N catalyst was increased from 75 to 97% at 550 °C with the increase of CA/Mo ratio from 1 to 3. This enrichment of activity in 3%Co-Mo2N-3:1 catalyst is due to increased dispersion of Co3Mo3N microstructure on γ-Mo2N platelets confirmed by SEM and TEM results. No deactivation was observed for any catalysts investigated in this study for ammonia decomposition.
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