ABSTRACT
Brønsted acid zeolites catalyze alkene oligomerization reactions, an important route to produce fuels and chemicals from light hydrocarbon feedstocks. Propene dimerization rates (per H+, 503 K) decrease monotonically with increasing crystallite size in MFI zeolites because heavy oligomer products remain occluded within microporous voids and restrict intrazeolite diffusion of reactants and products. Here, we show that the preferential zoning of framework Al centers and their associated H+ sites toward exterior surfaces of MFI crystallites in an "egg-shell" architecture minimizes the extent of diffusion-enhanced secondary reactions within a given crystallite, which increases both propene dimerization rates (per H+) and selectivity to true oligomer products. These results show that tailoring Al distributions to be spatially zoned toward external surfaces of medium-pore zeolite crystallites is efficacious at minimizing diffusion path lengths to increase alkene oligomerization rates and selectivity to true oligomer products.
