环己酮
环己烷
催化作用
路易斯酸
选择性
化学
原子层沉积
微型多孔材料
无机化学
沉积(地质)
化学工程
沸石
ZSM-5型
有机化学
图层(电子)
生物
工程类
古生物学
沉积物
作者
Liming Zhai,Bin Zhang,Haojie Liang,Huibin Wu,Xinchun Yang,Gen Luo,Shichao Zhao,Yong Qin
标识
DOI:10.1007/s11426-020-9968-x
摘要
The design of efficient iron-based catalysts remains a great challenge for selective cyclohexane oxidation to cyclohexanone under mild conditions. Because of the complex distribution of iron location on the support, the selectivity is always low. Here, we report a general strategy to selectively deposit highly-dispersed FeOx into the micropore of ZSM-5 by atomic layer deposition (ALD). The framework of ZSM-5 and the Bronsted acid sites are intact during ALD, and the Fe species are selectively deposited onto the defect and Lewis acid sites of ZSM-5. Besides, more Fe-O-Si bonds are formed over FeOx/ZSM-5 with a low loading of Fe, while FeOx nanoparticles are generated at high Fe loading. They cannot be realized by the traditional solution method. The obtained FeOx/ZSM-5 catalysts perform high selectivity of cyclohexanone (92%–97%), and ALD cycle numbers of FeOx control the activity. Compared with the Fe nanoparticles, the Fe-O-Si species performs higher turnover frequency and stability in the oxidation reaction.
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