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Ni/LaBO3 (B = Al, Cr, Fe) Catalysts for Steam Reforming of Methane (SRM): On the Interaction Between Ni and LaBO3 Perovskites with Differed Fine Structures.

Authors :
Yang, Menghe
Wang, Yingao
Zhang, Rui
Liu, Teng
Xia, Lianghui
Chen, Zijian
Fang, Xiuzhong
Xu, Xianglan
Xu, Junwei
Wang, Xiang
Source :
Catalysis Surveys from Asia. Dec2021, Vol. 25 Issue 4, p424-436. 13p.
Publication Year :
2021

Abstract

With the target to fabricate more feasible catalysts for SRM to produce hydrogen, the interaction between Ni and LaBO3 (B = Al, Cr and Fe) perovskite supports with different B-sites has been explored. To avoid the formation of big Ni grains, the Ni loading is intentionally set as low as 2 wt%. XRD and Raman results revealed that the three LaBO3 supports are composed of pure perovskite phase, but have differed fine crystal structures. While LaFeO3 and LaCrO3 can be indexed to the orthorhombic perovskite phase, LaAlO3 can be indexed to the hexagonal phase. H2-TPR and XPS results have validated that NiO has varied interfacial interactions with the LaBO3 supports through partial electron transfer from the supports to Ni. As a consequence, the active metallic Ni surface areas are in the order of 2%Ni/LaAlO3 > 2%Ni/LaCrO3 > 2%Ni/LaFeO3, well consistent with the reaction performance. Furthermore, by varying the B-site element, the abundance of the active surface oxygen species (mainly O22−) is varied, obeying the sequence of 2%Ni/LaCrO3 > 2%Ni/LaAlO3 > 2%Ni/LaFeO3, well consistent with the anti-coking ability of the catalysts. It is discovered that the change of the fine crystal structure of LaBO3 supports can influence the SRM performance of the 2%Ni/LaBO3 catalysts evidently. The reaction performance of the catalysts is mainly determined by the active Ni surface area, but the anti-coking ability is majorly decided by the amount of active oxygen species. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15711013
Volume :
25
Issue :
4
Database :
Academic Search Index
Journal :
Catalysis Surveys from Asia
Publication Type :
Academic Journal
Accession number :
153097658
Full Text :
https://doi.org/10.1007/s10563-021-09343-7