Study on the promotional effect of lanthana addition on the performance of hydroxyapatite-supported Ni catalysts for the CO2 methanation reaction

被引:48
|
作者
Boukha, Zouhair [1 ]
Bermejo-Lopez, Alejandro [1 ]
Pereda-Ayo, Benat [1 ]
Gonzalez-Marcos, Jose A. [1 ]
Gonzalez-Velasco, Juan R. [1 ]
机构
[1] Univ Basque Country UPV EHU, Fac Sci & Technol, Dept Chem Engn, Chem Technol Environm Sustainabil Grp, POB 644, E-48080 Bilbao, Spain
关键词
Methanation; Nickel catalyst; lanthana; Hydroxyapatite; CO; 2; adsorption; methanation cycles; KINETICS; CAPTURE; GAS; LA; HYDROGENATION; TEMPERATURE; REDUCTION; BETA; CH4;
D O I
10.1016/j.apcatb.2022.121500
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
The performance of nickel supported on lanthana-modified hydroxyapatite (HAP) catalysts is investigated in the CO2 methanation. The addition of La (1-6.6 wt%) leads to a surface enrichment following a sequential multilayer deposition model. Moreover, La addition systematically improves the dispersion of Ni particles and their reducibility, which in turn increases spectacularly the amounts of basic sites and their thermal stability. Such physicochemical changes impact positively on the activity of the catalysts in CO2 methanation. The estimated turnover frequency (TOF) suggest that the small Ni particles are the most efficient. The latter seem to provide a large density of very active defects on Ni-La2O3 interface. The optimized catalyst proves to be highly resistant to deactivation during 100 h time-on-stream (TOS). The samples were also assayed as dual function materials (DFMs) for CO2 adsorption and methanation. A scheme is proposed to describe the different steps involved in a CO2 adsorption/hydrogenation cycle.
引用
收藏
页数:14
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