脱氢
丙烷
催化作用
价(化学)
氧化物
X射线光电子能谱
氧气
热处理
化学工程
热解
化学
无机化学
材料科学
有机化学
工程类
复合材料
作者
Zhiqian Lin,Hualiang Zuo,Rui Ma,Huaiqing An,P. W. Zhao,Kaijun Liang,Mingshan Wang,Fushen Lu,Guojun Zou
标识
DOI:10.1016/j.mcat.2023.113018
摘要
Propane dehydrogenation (PDH) has emerged as an efficient complementary process for producing propylene. The fundamental understanding of reaction mechanism of traditional CrOx-based catalysts is important for designing novel PDH catalysts. Here, the evolution of surface Cr species was investigated by means of steam pre-treatment to introduce a certain amount of hydroxyl groups on deeply reductive Cr2O3/Al2O3 catalysts without influencing the valence states and aggregated states. The surface structural features of CrOx/Al2O3 catalysts were investigated by FT-IR, TGA, XPS, NH3-TPD, and Py-IR characterization techniques. It demonstrated that more hydroxyls were produced on the surface of catalysts under steam treatment. Subsequently, hydroxyl groups were mostly removed during the H2 thermal treatment and abundant oxygen defect sites were generated. These defect sites showed an increasing number of acidic sites, thus exhibiting a relatively high PDH activity. This strategy of introducing hydroxyl groups to construct oxygen defect sites is also applicable to other oxide materials, which offers a novel perspective for rational catalyst design.
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