Surface modification of PtSn/Al2O3 catalyst by organic acid chelation and its effect on propane dehydrogenation performance

被引:17
作者
Cao, Lei [1 ,2 ]
Qian, Rong [2 ]
Zhang, Yuanyuan [3 ]
Luo, Shizhong [2 ]
Jiang, Chengfa [2 ]
Jing, Fangli [1 ,2 ]
机构
[1] Southwest Petr Univ, Coll Chem & Chem Engn, 8 Ave Xindu, Chengdu 610500, Peoples R China
[2] Sichuan Univ, Sch Chem Engn, 24 South Sect 1,Yihuan Rd, Chengdu 610065, Peoples R China
[3] Xihua Univ, Sch Sci, 999 Tuqiao Jinzhou Rd, Chengdu 610039, Peoples R China
关键词
Propane dehydrogenation; Pt dispersion; Lewis acid sites; Chelating agent; Heterogeneous catalysis; ISOBUTANE DEHYDROGENATION; LIGHT ALKANES; ONE-POT; FT-IR; STABILITY; METAL; CE; ETHANE; PT-SN/AL2O3; ADSORPTION;
D O I
10.1016/j.jpcs.2023.111331
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of Pt-based catalysts has been prepared by a chelating-agent-assisted impregnation method, and char-acterized by N2 adsorption/desorption, XRD, XPS, H2-TPR, NH3-TPD, pyridine-FTIR, CO-DRIFT-IR, Raman, and TG techniques to investigate the influence of organic acids on physicochemical properties. It was found that, except in the case of tartaric acid, organic acid-assisted preparation not only led to higher dispersion of Pt particles in comparison with organic acid-free catalyst PtSn/Al2O3, but also changed the concentration of Lewis acid sites and modified the interaction between the metallic Pt sites and the support. Experiments on the catalytic dehydrogenation of propane have revealed that the optimal dehydrogenation performance, with a propane conversion of 35% and a propylene selectivity of 93%, was obtained over the citric acid-assisted catalyst (PtSn/ Al2O3-CA). Lewis acid sites are mainly responsible for activating C-H bonds during the tandem activation- -cleavage process, whereas coke deposition and the aggregation of Pt sites are mainly responsible for deactivation of the catalyst.
引用
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页数:12
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