脱氢
丙烷
催化作用
介孔材料
选择性
物理吸附
焦炭
化学工程
化学
X射线光电子能谱
化学吸附
无机化学
材料科学
有机化学
工程类
作者
Qiao Chen,Lidan Deng,Zewei Wu,Fang Wang,Xingmao Jiang
标识
DOI:10.1021/acs.iecr.2c00646
摘要
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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