负载型金属催化剂上正石蜡加氢异构反应的研究进展

M. Safaat, I. B. Adilina, S. Tursiloadi
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引用次数: 1

摘要

正石蜡催化加氢异构化的目的是制备支链石蜡异构体,抑制低浊点生物柴油生产中的裂化反应。金属和催化剂载体的种类、金属负载量和反应条件的发展是提高催化剂活性的重要因素。一种高性能的加氢异构化催化剂具有高水平的加氢活性位点和低酸度的双功能特征,与竞争性裂化反应相比,可以最大限度地提高加氢异构化的进展。此外,孔径较小的催化剂载体可以阻止大分子结构的异石蜡在孔内的酸位发生反应,从而为正石蜡的转化提供了良好的选择性。负载贵金属(Pt或Pd)的催化剂对长链石蜡加氢异构化的选择性明显高于Ni、Co、Mo和w等非贵金属过渡金属。反应温度和接触时间也是长链石蜡加氢异构化的重要参数,因为长接触时间和高温容易产生不良的裂解副产物。本文报道了几种负载型金属催化剂在优化反应条件下用于长链烷烃正构烷烃的加氢异构化反应,以最低的副产物量获得了最佳的异构化选择性。各种金属及其载体的作用将主要解释为双功能催化剂。
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A Review on the Hydroisomerisasion of n-Parafins over Supported Metal Catalysts
Catalytic hydroisomerization of n-paraffin aims to produce branched paraffin isomers and suppress cracking reactions in the production of the low cloud point of biodiesel. The development of the type of metal and catalyst support, amount of metal loading, and reaction conditions are important to increase the catalyst activity. A high performace catalyst for hydroisomerization bears bifunctional characteristics with a high level of hydrogenation active sites and low acidity, maximizing the progress of hydroisomerization compared to the competitive cracking reaction. In addition, a catalyst support with smaller pore size can hinder large molecular structure isoparaffins to react on the acid site in the pore thus providing good selectivity for converting n-paraffin. Catalysts loaded with noble metals (Pt or Pd) showed significantly higher selectivity for hydroisomerization than non-noble transition metals such as Ni, Co, Mo and W. The reaction temperature and contact time are also important parameters in hydroisomerization of long chain paraffin, because long contact times and high temperatures tend to produce undesired byproducts of cracking. This review reports several examples of supported metal catalyst used in the hydroisomerization of long chain hydrocarbon n-paraffins under optimized reaction conditions, providing the best isomerization selectivity results with the lowest amount of byproducts. The role of various metals and their supports will be explained mainly for bifunctional catalysts.
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