Promoting n-Butane Dehydrogenation over PtMn/SiO2 through Structural Evolution Induced by a Reverse Water-Gas Shift Reaction

被引:15
作者
Liu, Yi [1 ]
Zhang, Guanghui [1 ]
Liu, Shida [2 ]
Zhu, Jie [1 ]
Liu, Jiaxu [1 ]
Wang, Jianyang [3 ]
Li, Rongtan [3 ]
Wang, Mingrui [1 ]
Fu, Qiang [3 ]
Hou, Shuandi [1 ,2 ]
Song, Chunshan [1 ,4 ]
Guo, Xinwen [1 ]
机构
[1] Dalian Univ Technol, Frontier Sci Ctr Smart Mat, PSU DUT Joint Ctr Energy Res, Sch Chem Engn,State Key Lab Fine Chem, Dalian 116024, Peoples R China
[2] Sinopec Dalian Fushun Res Inst Petr & Petrochem, Dalian 116045, Peoples R China
[3] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
[4] Chinese Univ Hong Kong, Fac Sci, Dept Chem, Hong Kong 999077, Peoples R China
基金
中国国家自然科学基金;
关键词
alkane dehydrogenation; PtMn alloy; structural evolution; reverse water-gas shift reaction; PROPANE DEHYDROGENATION; CO2; HYDROGENATION; CATALYSTS; DISPERSION; PLATINUM; PHASE; CU;
D O I
10.1021/acscatal.2c04471
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Structural evolution of heterogeneous catalysts often occurs during catalytic reactions. In this contribution, the structural evolution of a PtMn/SiO2 catalyst during the reverse water-gas shift (RWGS) reaction was investigated using detailed spectroscopic characterizations. The results show that Mn atoms on the PtMn nanoparticle surface were partially removed during the RWGS reaction, which increases the ratio of Pt sites with a lower coordination number on the surface, leading to a 10-fold increase of the rate in n-C4H10 dehydrogenation from 1.85 to 21.93 mol g(Pt)(-1) h(-1) and a decrease of the apparent activation energy from 50 to 33 kJ mol(-1). This work provides a dimension of improving the catalytic performance of alkane dehydrogenation over Pt-based bimetallic catalysts through structural evolution during CO2 hydrogenation.
引用
收藏
页码:13506 / 13512
页数:7
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