选择性
石脑油
化学
氧合物
沸石
催化作用
己烷
烷烃
烷基
偶联反应
有机化学
组合化学
作者
Changcheng Wei,Qijun Yu,Jinzhe Li,Zhongmin Liu
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2020-03-10
卷期号:10 (7): 4171-4180
被引量:27
标识
DOI:10.1021/acscatal.9b05619
摘要
The coupling conversion of n-hexane (a model compound of naphtha) and CO was conducted over an HZSM-5 zeolite catalyst. A significant increase in the aromatic selectivity and dramatic decrease in the alkane selectivity were simultaneously achieved by adjusting the H/C ratio of the reactants. Under suitable conditions, the aromatic selectivity was 80%, which far exceeds the theoretical value for the conversion of only n-hexane over HZSM-5. Detailed studies revealed that the high aromatic selectivity originated from the direct incorporation of CO into the products. Different characterization methods were used to elucidate the coupling reaction mechanism. Important reaction intermediates, such as acyl groups and oxygenates (substituted cyclopentenones), were detected. Isotope labeling studies revealed that oxygenates were formed by 13CO incorporation into alkyl species, and they could transform into aromatic products. Based on these findings, a plausible reaction mechanism of the coupling transformation was proposed. The coupling effect between n-hexane and CO over HZSM-5 demonstrated in this work contradicts the traditional view that metal catalysts are indispensable for the highly selective conversion of naphtha to aromatics. This type of coupling reaction might have great potential for industrial applications, considering the large existing supply capacities of CO and alkanes.
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