Neodymium promoted ceria and alumina supported nickel catalysts for CO2 methanation reaction

被引:11
|
作者
Gac, Wojciech [1 ]
Zawadzki, Witold [1 ]
Kusmierz, Marcin [1 ]
Slowik, Grzegorz [1 ]
Grudzinski, Wojciech [2 ]
机构
[1] Marie Curie Sklodowska Univ, Fac Chem, 3 M Curie Sklodowska Sq, PL-20031 Lublin, Poland
[2] Marie Curie Sklodowska Univ, Inst Phys, Dept Biophys, 2 M Curie Sklodowska Sq, PL-20031 Lublin, Poland
关键词
CO2; methanation; Neodymium; Nickel catalyst; Ceria; Alumina; Basicity; CARBON-DIOXIDE; LOW-TEMPERATURE; DOPED CERIA; METAL; SURFACE; NI; OXIDE; HYDROGENATION; KINETICS; CE;
D O I
10.1016/j.apsusc.2023.157542
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
Two series of catalysts containing 20 wt.% nickel, promoted with different amounts of neodymium from 1 to 10 wt.% were prepared by the impregnation method, using nano-CeO2 and gamma-Al2O3 as supports. Ceria supported nickel catalysts showed high activity in CO2 methanation reaction and weak activity changes were observed with an increase in Nd content. X-ray diffraction, hydrogen chemisorption and transmission electron microscopy studies evidenced a decrease in the average size of nickel crystallites and an increase in the active surface area of catalysts. The temperature-programmed reduction, oxidation and CO2 desorption, XPS, Raman and in-situ FTIR spectroscopy indicated complex changes in the nature of their redox and base centres. Non-promoted alumina supported nickel catalyst despite higher surface area showed lower activity than similar catalyst with ceria as support. However, an introduction of Nd-promoter led to strong increase in their activity. Such effect was mainly ascribed to the increase in their basicity, facilitation of CO2 activation and subsequent transformation of the intermediate surface species to methane with participation of hydrogen atoms activated on metallic nickel crystallites.
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页数:22
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