Supported Cobalt Nanoparticles with a Single Active Phase for Fischer-Tropsch Synthesis

被引:25
|
作者
Lyu, Shuai [1 ,2 ]
Peng, Bo [3 ]
Kuang, Ting [1 ,2 ]
Rappe, Kenneth G. [3 ]
Zhang, Yuhua [1 ,2 ]
Li, Jinlin [1 ,2 ]
Wang, Li [1 ,2 ]
机构
[1] South Cent Univ Nationalities, State Ethn Affairs Commiss, Key Lab Catalysis & Mat Sci, Wuhan 430074, Hubei, Peoples R China
[2] South Cent Univ Nationalities, Minist Educ, Coll Chem & Mat Sci, Wuhan 430074, Hubei, Peoples R China
[3] Pacific Northwest Natl Lab, Inst Integrated Catalysis, 902 Battelle Blvd,POB 999, Richland, WA 99352 USA
来源
ACS APPLIED NANO MATERIALS | 2019年 / 2卷 / 04期
关键词
Fischer-Tropsch synthesis; carbon nanofibers; hcp-Co; single phase; syngas chemistry; reduction-caburization-reduction; phase evolution; IN-SITU XRD; CO ACTIVATION; CATALYSTS; DEACTIVATION; DESIGN; SIZE; HCP;
D O I
10.1021/acsanm.9b00187
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Cobalt (Co) with a hexagonal-close-packed structure (hcp-Co) has been documented as a preferred active phase for Co versus face-centered-cubic structure (fcc-Co) in a Fischer-Tropsch synthesis (FTS) reaction. Thus, hcp-Co with high dispersion and durability is highly attractive, and in this work, its controlled formation was targeted. This is challenging, however, because of the complexity of the phase transition during the materials synthesis and processing. With the use of carbon nanofiber (CNF) as the catalyst support, a two-step approach through the controlled formation of an oxide precursor CoO, followed by its reduction, has been demonstrated to synthesize single-phase Co. The obtained Co/CNF catalysts were thoroughly characterized by using in situ and ex situ techniques, and it is revealed that the formation of pure-phase CoO nanocrystals was responsible for the final pure-phase Co that was formed. Compared to the conventional reduction-carburization-reduction (RCR) process, this method allows for a higher dispersion of Co particles with higher activity by avoiding agglomeration of the nanoparticles before or after reduction. Equally important, under FTS conditions, no catalyst deactivation and phase transformation were observed for 400 h.
引用
收藏
页码:2266 / 2272
页数:13
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