volume 37 issue 23 pages 18001-18020

Mesoporous nanocrystalline ceria–zirconia solid solutions supported nickel based catalysts for CO2 reforming of CH4

Publication typeJournal Article
Publication date2012-12-01
scimago Q1
wos Q1
SJR1.685
CiteScore13.3
Impact factor8.3
ISSN03603199, 18793487
Condensed Matter Physics
Energy Engineering and Power Technology
Fuel Technology
Renewable Energy, Sustainability and the Environment
Abstract
A series of mesoporous nanocrystalline ceria–zirconia solid solutions with different Ce/Zr ratios were facilely synthesized via improved evaporation induced self-assembly strategy. The obtained materials with advantageous structural properties and excellent thermal stabilities were characterized by various techniques and investigated as the supports of the Ni based catalysts for CO 2 reforming of CH 4 . The effects of Ce/Zr ratio and mesopore structure on promoting catalytic performances had been investigated. It was found that the catalyst supported on carrier with 50/50 Ce/Zr ratio behaved the highest catalytic activity. The reason for this might be that the mesoporous ceria–zirconia solid solution carrier contributed to the activation of CO 2 by its own redox property. Compared with the catalyst without obvious mesostructure, the current mesoporous catalyst performed higher catalytic activity and better catalytic stability, demonstrating the advantages of the mesostructure. On the one hand, the predominant textural properties such as large surface area, big pore volume, and uniform channel helped to the high dispersion of the Ni particles among the mesoporous framework, finally leading to higher catalytic activity. On the other hand, the mesoporous matrix could stabilize the Ni nanoparticles under severe reduction and reaction conditions by the “confinement effect”, committed to better catalytic stability. Besides, the properties of the coke over the mesoporous catalyst were also carefully studied. Generally, these mesoporous nanocrystalline ceria–zirconia solid solutions were a series of promising catalytic carriers for CO 2 reforming of CH 4 . ► Mesoporous Ce–Zr solid solutions with various Ce/Zr ratios prepared by EISA method. ► These materials were utilized as supports for Ni based catalysts for dry reforming. ► The effect of Ce/Zr ratio on the catalytic activity was investigated. ► The role of mesopore in promoting catalytic activity and stability was examined. ► Properties of the coke over the mesoporous catalyst were studied.
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GOST Copy
Xu L., Song H., Chou L. Mesoporous nanocrystalline ceria–zirconia solid solutions supported nickel based catalysts for CO2 reforming of CH4 // International Journal of Hydrogen Energy. 2012. Vol. 37. No. 23. pp. 18001-18020.
GOST all authors (up to 50) Copy
Xu L., Song H., Chou L. Mesoporous nanocrystalline ceria–zirconia solid solutions supported nickel based catalysts for CO2 reforming of CH4 // International Journal of Hydrogen Energy. 2012. Vol. 37. No. 23. pp. 18001-18020.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/j.ijhydene.2012.09.128
UR - https://doi.org/10.1016/j.ijhydene.2012.09.128
TI - Mesoporous nanocrystalline ceria–zirconia solid solutions supported nickel based catalysts for CO2 reforming of CH4
T2 - International Journal of Hydrogen Energy
AU - Xu, Leilei
AU - Song, Huanling
AU - Chou, Lingjun
PY - 2012
DA - 2012/12/01
PB - Elsevier
SP - 18001-18020
IS - 23
VL - 37
SN - 0360-3199
SN - 1879-3487
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2012_Xu,
author = {Leilei Xu and Huanling Song and Lingjun Chou},
title = {Mesoporous nanocrystalline ceria–zirconia solid solutions supported nickel based catalysts for CO2 reforming of CH4},
journal = {International Journal of Hydrogen Energy},
year = {2012},
volume = {37},
publisher = {Elsevier},
month = {dec},
url = {https://doi.org/10.1016/j.ijhydene.2012.09.128},
number = {23},
pages = {18001--18020},
doi = {10.1016/j.ijhydene.2012.09.128}
}
MLA
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MLA Copy
Xu, Leilei, et al. “Mesoporous nanocrystalline ceria–zirconia solid solutions supported nickel based catalysts for CO2 reforming of CH4.” International Journal of Hydrogen Energy, vol. 37, no. 23, Dec. 2012, pp. 18001-18020. https://doi.org/10.1016/j.ijhydene.2012.09.128.