Abstract
Propane dehydrogenation is one of the most admired technologies for propylene production. However, the development of an active and stable catalyst presents a significant challenge. In this study, Pt–Ga/SBA-15 catalysts were prepared via coimpregnation, followed by H2 reduction, and applied in propane dehydrogenation. The Pt–Ga/SBA-15 catalyst with a Ga/Pt molar ratio of 1 exhibited a high propane conversion of up to 60% and high selectivity toward propylene of 98.2% at 550 °C for 10 min, with a propane conversion of 51.6% and propylene selectivity of 99.5% after reaction for 25 h. The physicochemical properties characterized using N2 physisorption, XRD, TEM, XPS, CO chemisorption, and in situ CO–DRIFT spectroscopy reveal that the Pt–Ga alloy nanoparticles were formed on the SBA-15 support after direct reduction with H2. The study of coke formation via temperature-programmed oxidation showed that a large amount of coke was deposited over the support of spent Pt–Ga/SBA-15 catalyst, indicating coke mobility from the active sites to the supports and its contribution to catalyst stability. The activities of spent catalysts could be almost completely recovered via reduction regeneration, during which Pt–Ga alloy retains the original geometrical and electronic structure well. The dilution of Pt ensembles due to the addition of Ga, e.g., Pt–Ga alloy formation, plays an important role in enhancing the catalytic performance for propane dehydrogenation.
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