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Potassium-promoted magnesium ferrite on 3D porous graphene as highly efficient catalyst for CO hydrogenation to lower olefins.

Authors :
Cheng, Yi
Tian, Jing
Lin, Jun
Wang, Shunwu
Xie, Songhai
Pei, Yan
Yan, Shirun
Qiao, Minghua
Xu, Hualong
Zong, Baoning
Source :
Journal of Catalysis. Jun2019, Vol. 374, p24-35. 12p.
Publication Year :
2019

Abstract

• Honeycomb-structured graphene (HSG) was used to support the K-MgFe catalysts. • Unprecedentedly high activity and productivity of lower olefins were obtained in FTO. • The synergetic effect of Mg and K enhanced the adsorption and dissociation of CO. • The catalyst also showed better durability than typical FTO catalysts. • HSG enabled fast heat dissipation and confined the sintering of the active phase. Three-dimensional (3D) honeycomb-like structured graphene (HSG)-supported ternary K-promoted magnesium ferrite catalysts (K-MgFe/HSG) are prepared and evaluated in Fischer–Tropsch synthesis to the lower olefins (FTO). The catalysts bear interconnected mesoporous-macroporous framework of graphene nanosheets decorated with homogeneously sized magnesium ferrite nanoparticles (NPs). Under typical FTO reaction conditions, the composition-optimized 1K-MgFe/HSG catalyst affords a reduced CO 2 selectivity of 40.4%, an excellent weight specific activity to hydrocarbons of 1825 μmol CO g Fe −1 s−1, and an appreciable selectivity to the lower olefins (C 2 C 4 olefins) of 57.8%, thus giving rise to a record high productivity of the lower olefins of 1055 μmol CO g Fe −1 s−1. The excellent catalytic efficiency is tentatively attributed to the synergetic effect of Mg and K on adsorption and dissociation of CO. The catalyst also exhibits better durability than previously reported iron-based FTO catalysts, without significant changes in the catalytic performance and the size of the iron carbide NPs after 120 h on stream, highlighting the crucial role of the 3D porous HSG support in restricting the agglomeration of the active phase during the challenging high-temperature and exothermic FTO reaction. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00219517
Volume :
374
Database :
Academic Search Index
Journal :
Journal of Catalysis
Publication Type :
Academic Journal
Accession number :
137432629
Full Text :
https://doi.org/10.1016/j.jcat.2019.04.024