The influence of calcination and reduction conditions, the metal-incor
poration technique, and metal loading on the hydroisomerization of n-b
utane over bifunctional Pt/HZSM-5 catalysts was studied. Temperature-p
rogrammed desorption of ammonia (TPDA), atomic absorption spectroscopy
(AA), BET surface area/pore size distributions, chemisorption measure
ments, temperature-programmed reduction (TPR), and transmission electr
on microscopy (TEM) techniques were used to characterize the catalysts
. The calcination conditions have a significative influence on ion-exc
hanged catalysts, as they control the final metal distribution. The re
duction conditions and the method used for platinum incorporation were
found to be important factors that affected both the activity and sel
ectivity of the catalysts. Thus, the highest selectivity to isobutane
was achieved over an ion-exchanged catalyst.