ملخص: The hydroconversion of n-heptane on 1 wt.% palladium supported on sulfated zirconium pillared montmorillonite (PdZMS) under isothermal and isobar conditions (PHC=7.99 kPa and PTot=101.3 kPa) is studied. The catalyst activity of PdZMS is compared to those obtained on 1 wt.% palladium supported on [gamma]-alumine (PdAl) and on sulfated zirconia (PdZS).The PdZMS catalyst develops an intermediary catalytic behavior between that of PdAl and that of PdZS and shows a very important isomerization selectivity at 300-330 [deg]C. The monobranched isomers are the major reaction products formed on this catalyst and suggest a classical bifunctional mechanism.On the PdAl catalyst, it is rather a metallic mechanism charaterized by hydrogenolysis on Pd particles (demethylation reaction) and by a bond shift isomerization occurring through a cyclic intermediate.On the PdZS catalyst, a high selectivity in cracking products (propane and butane) suggests a mechanism involving a cyclopropanic protonated intermediate, followed by a [beta]-scission attributed to the strong acidity of the sulfated zirconia.

لغة: إنجليزية