Abstract
In the oligomerization of ethene, the chain-length distributions obtained over heterogeneous nickel catalysts at a low reaction temperature (ca. 110 °C) depend on the acidity of the silica–alumina support, the nickel loading and the olefin feed. Most significantly, ion-exchanged catalysts based on a silica–alumina of high acidity (ca. 0.7 mass% Ni), and those based on a highly-exchanged medium-acidity support (ca. 1.6% Ni), show a distinct superimposed activity for the dimerization of the intermediate butenes. This causes a desirable shift to higher hydrocarbon products, and it is possible to obtain 41 mass% C10+ oligomers, while the corresponding value predicted from Schulz–Flory statistics is only 24 mass%. No such deviation from Schulz–Flory statistics is observed in propene oligomerization.
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