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Evaluation of Pt/MCM-41//MgAPO-n composite catalysts for isomerization and hydrocracking of n-decane

机译:Pt / MCM-41 // MgAPO-n复合催化剂对正癸烷异构化和加氢裂化的评价

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摘要

The hydroconversion of n-decane has been investigated over bifunctional Pt/MCM-41//MgAPO-n (n=5,11) composite catalysts consisting of Pt/MCM-41 as the metal function and different Mg-containing aluminophosphates MgAPO-n as the acidic function. Hydrocracking is dominant over the catalysts containing MgAPO-5, while the isomerization selectivity is high over composite catalysts containing MgAPO-11. The higher isomerization selectivity of the latter catalysts is explained in terms of shape selectivity. The acid site density was varied by adding different quantities of MgAPO-n to the composite catalyst without changing the overall metal content. The highest selectivity for n-decane isomerization is found for a 50/50 physical mixture of 1.0Pt/MCM-41 with MgAPO-11. The distance between the two catalytic functions was varied by mixing of different sized pellets. It was found that the particles with diameters ranging from 1 to ca. 250 mum can be mixed without significant decrease in catalytic activity. The results of this study confirm that the classical bifunctional mechanism for isomerization and hydrocracking of n-alkanes is operative under our experimental conditions.
机译:已在由Pt / MCM-41作为金属官能团和不同的含Mg的铝磷酸盐MgAPO-n组成的双功能Pt / MCM-41 // MgAPO-n(n = 5,11)复合催化剂上研究了正癸烷的加氢转化作为酸性功能。加氢裂化作用优于含MgAPO-5的催化剂,而异构化选择性高于含MgAPO-11的复合催化剂。根据形状选择性解释了后者催化剂的较高的异构化选择性。通过向复合催化剂中添加不同量的MgAPO-n来改变酸位密度,而无需改变总金属含量。对于1.0Pt / MCM-41与MgAPO-11的50/50物理混合物,发现正癸烷异构化的最高选择性。两种催化功能之间的距离通过混合不同大小的颗粒而变化。发现直径范围为1至约1μm的颗粒。可以混合250 mum,而不会明显降低催化活性。这项研究的结果证实,在我们的实验条件下,正构烷烃异构化和加氢裂化的经典双功能机理是可行的。

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