The dehydrocyclisation of
n-octane to
iso-octane, ethylbenzene and
o-,
m- and
p-xylene was investigated on monofunctional (non-acidic) and bifunctional (acidic) Pt/Al
2O
3 catalyst in a microcatalytic reactor with hydrogen as carrier at 1.8 atm and 563–673 K. On bifunctional Pt/Al
2O
3, the total conversion of
n-octane started from a high value and decreased with increasing temperature for all pulse sizes investigated. The primary product of
n-octane conversion on acidic Pt/Al
2O
3 was
iso-octane. The product yield-temperature profiles showed a large initial production of
iso-octane which decreased to a minimum as the catalyst temperature increased due to its conversion to ethylbenzene and
o-xylene. On non-acidic Pt/Al
2O
3, the total conversion of
n-octane increased initially and then went through a maximum as the catalyst temperature increased. The primary products of the reaction were found to be ethylbenzene and
o-xylene, indicative of the activity of the metal to effect these ring closure reactions.
相似文献