Development and catalytic mechanism of a highly efficient Pt/K? catalyst for n-Heptane aromatization

Development of a high-performance naphtha aromatization catalyst has been paid many attentions as this re-action is generally employed to elevate the octane number of FCC gasoline and Fischer-Tropsch-synthesized oil. Here, a hierarchical porous Pt/K beta catalyst is developed. It shows much higher activity, selectivity and stability than conventional Pt/KL. The catalytic performance of Pt/K beta depends on Br phi nsted acidity and mesoporosity of zeolite beta and nanoparticles (NPs) size and electronic state of Pt. The catalytic mechanism was investigated by combining TPSR, GC-MS, reaction kinetic studies and DFT calculations. Pt NPs catalyze dehydrogenations of alkanes/cycloalkenes to alkenes and dienes, while Br phi nsted acid sites facilitate alkene cyclization and ring-expansion of cycloalkenes despite that they can also dehydrogenate alkanes/alkenes through hydrogen trans-fer reactions. The n-heptane is mainly aromatized by dehydrogenating to 1-heptene and 2-heptene, 1,6-and 1,5-cyclizing into methylcyclohexane and ethyl-cyclopentane, and successively ring-expanding and/or dehydro-genating to toluene that may be further dealkylated to benzene.