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The construction of nanotubular Ni-Mg phyllosilicate solid solution catalyst for boosting CO2 catalytic conversion: Identifying the species variations and interactions.

Authors :
Wang, Dehui
Liu, Jia
Li, Hai
Liu, Qing
Cheng, Yu
Fan, Xing
Liang, Peng
Source :
Applied Catalysis B: Environmental. Jun2023, Vol. 327, pN.PAG-N.PAG. 1p.
Publication Year :
2023

Abstract

Addressing the problems of easy collapse, Ni sintering and low catalytic activity over the nanotubular nickel phyllosilicate catalyst, the Mg species was doped via a simple hydrothermal method to construct the nanotubular Ni-Mg bimetallic phyllosilicate solid solution. The high thermal stability, nonreducible property and strong basicity of magnesium species led to the enhancement of anti-collapse, Ni-sintering resistance and basicity. As a result, the fine Ni particles and enhanced H 2 and CO 2 chemisorption and activation properties resulted in boosting the catalytic activity of both CO 2 methanation and CH 4 -CO 2 reforming reactions. The Ni/Mg ratios and the reduction temperatures were detailed optimized, and the 600oC-reduced Ni 8 Mg 2 -NT catalyst with the Ni/Mg ratio of 8:2 was the optimal, which also exhibited high long-term stability. In short, the formed Ni-Mg-phyllosilicate solid solution structure and the special interactions of different species brought about high catalytic performance of the nanotubular Ni-Mg phyllosilicate catalyst. [Display omitted] • The nanotubular Ni-Mg bimetallic phyllosilicate solid solution was synthesized. • Nanotubular Ni-Mg phyllosilicate obtained high anti-collapse and Ni-sintering resistance properties. • The Ni/Mg ratio of 8:2 and the reduction temperature of 600 oC were the optimum. • This catalyst was versatile for both CO 2 methanation and CH 4 -CO 2 reforming reactions. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09263373
Volume :
327
Database :
Academic Search Index
Journal :
Applied Catalysis B: Environmental
Publication Type :
Academic Journal
Accession number :
162008526
Full Text :
https://doi.org/10.1016/j.apcatb.2023.122452