Abstract

Abstract 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 μm 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.

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