Coke Formation on Pt-Sn/Al2O3 Catalyst for Propane Dehydrogenation

被引:125
|
作者
Wang, Hai-Zhi [1 ]
Sun, Li-Li [1 ]
Sui, Zhi-Jun [1 ]
Zhu, Yi-An [1 ]
Ye, Guang-Hua [1 ]
Chen, De [2 ]
Zhou, Xing-Gui [1 ]
Yuan, Wei-Kang [1 ]
机构
[1] East China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
[2] Norwegian Univ Sci & Technol, Dept Chem Engn, N-7491 Trondheim, Norway
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
PT-SN; CARBONACEOUS MATERIALS; PTSN/ZSM-5; CATALYST; RAMAN-SPECTROSCOPY; HYDROGENATION; DEACTIVATION; TIME; HYDROCARBONS; PERFORMANCE; ADSORPTION;
D O I
10.1021/acs.iecr.8b01313
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Catalyst deactivation by coking is one major problem for propane dehydrogenation (PDH). To develop catalysts with high resistance to coke, the analysis of coke becomes essential. In this work, an analysis procedure is proposed and validated to acquire the detailed locations and compositions of the coke formed on an assynthesized Pt-Sn/Al2O3 catalyst. This procedure combines highresolution transmission electron microscopy (HRTEM), FT-IR, Raman, thermogravimetric analysis (TG), and pyrolysis GC-MS; with this procedure, the systematic and quantitative analysis of coke can be achieved. The results show that the coke is located on the metal, in the vicinity of the metal, and on the support. Besides, aliphatics, aromatics, and pregraphite cokes are identified, and they account for 69.0, 4.4, and 26.6 wt %, respectively. Finally, an in situ DRIFT study is performed, and the results show that the aliphatic coke can be transformed into the aromatic coke and this transformation is related to the deep dehydrogenation reactions.
引用
收藏
页码:8647 / 8654
页数:8
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