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Study of Pt/MCM-22 based catalystsin the transformation of n-hexane: effect of rare earthelements and mode of platinum introduction

机译:Pt / MCM-22基催化剂在正己烷转化中的研究:稀土元素的影响和铂的引入方式

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The bifunctional transformation of n-hexane was carried out over Pt/MCM-22 based catalysts. MCM-22 was synthesized and submitted to ion exchange with rare earth nitrate solutions of La, Nd and Yb, followed by Pt introduction. Three different methods were used to introduce about 1 wt% of Pt in the zeolite: ion exchange, incipient wetness impregnation and mechanical mixture with Pt/Al2O3. The bifunctional catalysts were characterized by transmission electron microscopy and by the model reaction of toluene hydrogenation. These experiments showed that, in the ion exchanged sample, Pt is located both within the inner micropores and on the outer surface, whereas in the impregnated one, the metal is essentially located on the outer surface under the form of large particles. The presence of RE elements increases the hydrogenating activity of Pt/MCM-22 since the location of these species at the vicinity of metal particles causes modification on its electronic properties. Whatever the mode of Pt introduction, a fast initial decrease in conversion is observed for n-hexane transformation, followed by a plateau related to the occurrence of the catalytic transformations at the hemicages located at the outer surface of the crystals. The effect of rare earth elements on the hydrogenating function leads to a lower selectivity in dibranched isomers and increased amounts of light products.
机译:正己烷的双功能转化是在基于Pt / MCM-22的催化剂上进行的。合成了MCM-22,并与La,Nd和Yb的稀土硝酸盐溶液进行离子交换,然后引入Pt。三种不同的方法用于将约1 wt%的Pt引入沸石中:离子交换,初湿浸渍和与Pt / Al2O3的机械混合。通过透射电子显微镜和甲苯氢化的模型反应来表征双功能催化剂。这些实验表明,在离子交换样品中,Pt既位于内部微孔内,又位于外表面,而在浸渍的Pt中,金属基本上以大颗粒的形式位于外表面。 RE元素的存在增加了Pt / MCM-22的氢化活性,因为这些物质在金属颗粒附近的位置导致其电子性质的改变。无论引入Pt的方式如何,对于正己烷转化而言,都会观察到转化率的快速初始下降,然后是与位于晶体外表面的半个位上催化转化发生有关的平稳期。稀土元素对氢化功能的影响导致二支链异构体的选择性降低和轻质产物的增加。

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