No abstract

A series of unmodified bulk Al2O3 materials show an intrinsic activity for selectively catalyzing propane dehydrogenation.

Summary Sulfated zirconia (SZ) and its modified versions attract great interest in recent years, because of their promising potential in n‐alkane isomerization. The oxidative and protonation routes are active and interactional in n‐alkane activation over SZ catalysts. The bimolecular reaction becomes dominant with increasing the density of active sites on SZ surface and decreasing the carbon chain of feed. Pentane and hexane are mainly isomerized by protonated cyclopropane mechanism, while which is thermodynamically unflavored for n‐butane isomerization. The deactivation of SZ catalysts is primarily caused by the loss of superacidity and oxidizing ability, resulted from the structure changes of sulfate species. Several strategies for improving the activity of SZ are reviewed. The intrinsic structure‐reactivity relationship of SZ catalysts in alkane isomerization is updated to illuminate the prerequisite for the highly active catalysts and the mechanism of active sites formation. The applications of Pt/SZ in fixed‐bed and unmodified SZ in circulating fluidizing bed in light alkanes isomerization are compared with the conventional technologies based on the chlorinated alumina catalysts. Finally, the future study of SZ catalysts is outlooked from the academic investigations to the industrial applications.

No abstract

No abstract