氨氧化法合成乙腈:钼/沸石催化剂筛选

F. Ayari, Emna Mannei, E. Asedegbega-Nieto, M. Mhamdi, G. Delahay
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引用次数: 3

摘要

研究了Mo/沸石催化剂在乙烷和乙烯氨氧化制乙腈中的催化作用。通过改变不同的工艺参数,分别在固-固界面和液-固界面制备催化剂。交换时Mo的稳定性取决于沸石的亲疏水性和Mo前驱体的类型。事实上,低Si/Al摩尔比的沸石应避免使用,因为它们的脱水焓值较高(Δdehyd.H)。另一方面,使用MoOCl4、Mo(CO)6和MoCl3前驱体以及高Si/Al比的沸石,导致低效的[Mo7O24]6 -和无定形的MoO3催化燃烧反应。然而,MoCl5、MoO3和MoO2(C5H7O2)2的使用导致了有希望的活性。在催化作用中,需要[MoO4]2 -类催化C2H6生成C2H4,而[MoxO3x+1]2 - (x = 1,2)类催化C2H4的氨化和乙胺脱氢生成CH3CN。有趣的是,通过湿浸渍和同时氧化处理可以获得活性催化剂。这样的处理改善了结晶MoO3的分散状态,从而激活了乙烷分子。在氨氧化之前进行C2H6氧化脱氢是明智的,因为可以注意到不同研究参数之间的干扰。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acetonitrile Synthesis via Ammoxidation: Mo/zeolites Catalysts Screening
Mo/zeolites catalysts were investigated in ethane and ethylene ammoxidation into acetonitrile. The catalysts were prepared either in solid‒solid or liquid‒solid interface after varying different parameters. The stabilization of Mo species upon the exchange is dependent on the hydrophilic/hydrophobic character of the zeolite and the type of Mo precursor. In fact, zeolites with low Si/Al molar ratios should be avoided due to their higher dehydration enthalpy values (Δdehyd.H). On the other hand, the use of MoOCl4, Mo(CO)6 and MoCl3 precursors and zeolites with high Si/Al ratios led to inefficient [Mo7O24]6‒ species and amorphous MoO3 which catalyzes the combustion reaction. Nevertheless, the use of MoCl5, MoO3 and MoO2(C5H7O2)2 led to promising activities. In catalysis, [MoO4]2‒ species are required to activate C2H6 into C2H4, while [MoxO3x+1]2‒ (x =1, 2) species catalyze the ammoniation of C2H4 and the ethylamine dehydrogenation into CH3CN. Interestingly, active catalysts could be obtained by humid impregnation and a simultaneous oxidative treatment. Such a treatment improves the dispersion state of crystalline MoO3, which activate ethane molecules. It is judicious to perform C2H6 oxidative dehydrogenation before ammoxidation since the interference between the different investigated parameters could be noted.
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