Hydrogen production by methane decomposition: A comparative study of supported and bulk ex-hydrotalcite mixed oxide catalysts with Ni, Mg and Al

被引:40
|
作者
Garcia-Sancho, C. [1 ]
Guil-Lopez, R. [1 ]
Sebastian-Lopez, A. [1 ]
Navarro, R. M. [1 ]
Fierro, J. L. G. [1 ]
机构
[1] CSIC, Sustainable Energy & Chem Grp EQS, ICP, C Marie Curie 2, Madrid 28049, Spain
关键词
Hydrogen; Methane decomposition; Hydrotalite; Nickel catalysts; Supported catalysts; FEITKNECHT COMPOUND PRECURSOR; COX-FREE HYDROGEN; THERMOCATALYTIC DECOMPOSITION; NI/AL2O3; CATALYST; ACTIVATED CARBONS; PYROLYSIS; COPRODUCTION; DEACTIVATION; REGENERATION; NANOCARBON;
D O I
10.1016/j.ijhydene.2018.04.021
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
A catalytic comparative study of COx-free hydrogen production by methane decomposition was carried out. Catalytic performances of bulk Ni-mixed oxides derived from Ni/Mg/Alhydrotalcites (ex-HTs-Ni) were compared with those obtained with Ni supported on mixed oxides derived from Mg/Al-hydrotalcites (Ni/ex-HTs), or on commercial supports (gamma Al2O3, MgO and MgO-modified gamma-Al2O3). Catalyst characterization and their catalytic performance showed both ex-HTs-Ni and Ni/ex-HTs appear to be a similar regardless of their method of preparation. Ni/y-Al2O3 was the best supported catalyst, although the catalytic performances of the ex-HTs catalysts were better. Higher Ni-Mg interaction in ex-HTs provides higher resistance to deactivation. Characterization by TG, Raman spectroscopy and TEM of spent catalysts in the reaction suggest the degree of ordering of the graphitic layers of the carbon deposit onto the catalyst surface is the key factor in the catalyst deactivation. The higher degree of ordering or graphitization of the carbon produced with the higher concentration of sp2 carbons on the surface of the Ni/y-Al2O3 favours its faster deactivation by Ni-coverage than the bulk catalyst (ex-HT-Ni), in which the MWNT type carbon is mainly obtained. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:9607 / 9621
页数:15
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