首页> 外文会议>International Zeolite Conference pt.C; 20040425-30; Cape Town(ZA) >HYDROISOMERIZATION OF n-HEXADECANE ON ZEOLITE CATALYSTS
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HYDROISOMERIZATION OF n-HEXADECANE ON ZEOLITE CATALYSTS

机译:分子筛催化剂上正十六烷的加氢异构化

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摘要

Bifunctional platinum catalysts containing MCM-22, ZSM-5, SAPO-11 and H-Beta were tested for their hydroisomerization of n-hexadecane(n-C_(16)), and their catalytic activities and selectivity were compared. Pt/MCM-22 and Pt/ZSM-5 catalysts showed lower isomerization selectivity due to their strong acidity, while Pt/SAPO-11 and Pt/H-Beta catalysts showed higher selectivity. Through the analysis of the product distribution, the hydroisomerization mechanism on Pt/SAPO-11 was discussed. It was showed that the isomerization of long chain n-paraffins on medium pore zeolite took place at the external surface and pore mouth of the zeolite. The hydroisomerization selectivity was greatly influenced by the catalyst acidity. Weak and mild acids were favorable to isomerization.
机译:测试了含有MCM-22,ZSM-5,SAPO-11和H-Beta的双功能铂催化剂的正十六烷(n-C_(16))加氢异构化反应,并比较了它们的催化活性和选择性。 Pt / MCM-22和Pt / ZSM-5催化剂由于其强酸性而显示出较低的异构化选择性,而Pt / SAPO-11和Pt / H-Beta催化剂则显示出较高的选择性。通过分析产物分布,探讨了Pt / SAPO-11加氢异构化机理。结果表明,长孔正构烷烃在中孔沸石上的异构化发生在沸石的外表面和孔口。加氢异构化的选择性受催化剂酸度的影响很大。弱酸和弱酸有利于异构化。

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