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A procedure to prepare Pt-promoted sulfated zirconia (SZ) catalysts which results in highly active and stable catalyst for n-pentane isomerization
at atmospheric conditions, is described. High temperature calcination of SZ prior to Pt addition leads to elimination of loosely-bound
sulfur species from the zirconia surface. Reducing the catalyst after Pt addition results in further increase in apparent activity. Upon repeated
regenerations, an increase of up to 60% in conversion with iso-pentane selectivity of over 80% is observed. It is proposed that regenerative
oxidation/reduction cycles lead to a restructuring of the acid and metal sites which facilitates hydrogen migration and helps to arrest
deactivation.

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