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首页> 外文期刊>Journal of Catalysis >High selectivity of MCM-22 for cyclopentanol formation in liquid-phase cyclopentene hydration
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High selectivity of MCM-22 for cyclopentanol formation in liquid-phase cyclopentene hydration

机译:MCM-22对液相环戊烯水合中环戊醇形成的高选择性

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Highly effective formation of cyclopentanol through the liquid-phase hydration of cyclopentene has been attempted on various zeolites catalysts. MCM-22 zeolite was the most selective catalyst, which actively converted cyclopentene to cyclopentanol with a selectivity up to 99%. The effect on the hydration of catalyst preparation method, reaction atmosphere and temperature have been investigated for the MCM-22 catalysts. On the basis of the effect of reaction atmosphere, the mechanism of liquid-phase cyclopentene hydration was proposed. The thermodynamic equilibrium between cyclopentene and cyclopentanol was suggested to control greatly the cyclopentene conversion. The cyclopentene conversion was increased to 10% by increasing the water/cyclopentene ratio. Poisoning using organic amines with different molecular sizes revealed that the hydration occurred mainly in the 10-membered ring channels of MWW structure, which had an elliptic aperture smaller than that of MFI structure, exhibiting a significant shape selectivity by suppressing the etherification cyclopentanol.
机译:已经尝试在各种沸石催化剂上通过环戊烯的液相水合高效形成环戊醇。 MCM-22沸石是最具选择性的催化剂,它能以高达99%的选择性将环戊烯主动转化为环戊醇。研究了MCM-22催化剂对水合催化剂制备方法,反应气氛和温度的影响。根据反应气氛的影响,提出了液相环戊烯水合机理。提出了环戊烯和环戊醇之间的热力学平衡极大地控制了环戊烯的转化。通过增加水/环戊烯的比例,将环戊烯的转化率提高到10%。使用具有不同分子大小的有机胺中毒显示,水合作用主要发生在MWW结构的10元环通道中,该通道的椭圆孔径小于MFI结构,通过抑制醚化环戊醇表现出显着的形状选择性。

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