Sub-nanometer ceria-promoted Ni 13X zeolite catalyst for CO2 methanation

被引:23
|
作者
Wei, Liangyuan [1 ]
Grenman, Henrik [2 ]
Haije, Wim [4 ]
Kumar, Narendra [2 ]
Aho, Atte [2 ]
Eranen, Kari [2 ]
Wei, Liangfu [3 ]
de Jong, Wiebren [1 ]
机构
[1] Delft Univ Technol, Fac 3mE, Dept Proc & Energy, Sect Large Scale Energy Storage, Delft, Netherlands
[2] Abo Akad Univ, Fac Sci & Engn, Johan Gadolin Proc Chem Ctr, Lab Ind Chem & React Engn, Turku, Finland
[3] Delft Univ Technol, Fac CiTG, Dept Sanit Engn, Delft, Netherlands
[4] Delft Univ Technol, Fac Sci Appl, Dept Chem Engn, Sect Mat Energy Convers & Storage, Delft, Netherlands
关键词
Sub-nanometer nickel-ceria on zeolite 13X; Citrate complexes; Nickel citrate; Cerium citrate; CO < sub > 2 <; sub > methanation; SINGLE-ATOM CATALYSTS; REDUCTION; OXIDE; ACID; HYDROGENATION; SPECTROSCOPY; CARBON; SITES; EFFICIENT; COPPER;
D O I
10.1016/j.apcata.2021.118012
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
Sub-nanometer zeolite 13X-supported Ni-ceria catalysts were synthesized for CO2 methanation. XRD and SEM results show the structure and morphology of 13X zeolite after impregnation and calcination. Ce loading affected the catalysts' metal dispersion, reducibility, basicity and acidity, and thence their activity and selectivity. STEMEDX elemental mappings showed that Ce and Ni are predominantly highly dispersed. Ce has a positive effect on the reduction of NiO and leads to a relatively high number of medium basic sites with a low Ce loading. Highly stable 5%Ni2.5%Ce13X had high activity and nearly 100% CH4 selectivity in CO2 methanation at 360 ?C, which is mainly due to the high dispersion of metals and relatively high amount of medium basic sites. It can be inferred that this catalyst synthesis strategy has great potential for good catalyst dispersion, since metal uptake by the zeolite is selective for the metal citrate complexes in solution.
引用
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页数:12
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