Abstract

This paper reports on an investigation using steady-state isotopic transient kinetic analysis (SSITKA) of Al 2O 3-promotion of sulfated zirconia (SZ) for n-butane isomerization. SZ promoted with Al 2O 3 showed an approximately 30% increase in n-butane isomerization activity at 250 °C. The average surface residence times of the reaction intermediates on unpromoted and Al 2O 3-promoted SZ measured by SSITKA suggest that the active sites on both catalysts were identical. There was, however, a significant increase in the concentration of surface intermediates upon Al 2O 3-promotion, leading to the increased activity. Al 2O 3-promotion also appeared to improve catalyst site stability resulting in a slower rate of deactivation.

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