Cermets Ni/(Ce0.9Ln0.1O1.95)(Ln = Gd, La, Nd and Sm) prepared by solution combustion method as catalysts for hydrogen production by partial oxidation of methane

被引:13
作者
Alvarez-Galvan, Consuelo [1 ]
Falcon, Horacio [2 ]
Cascos, Vanessa [3 ]
Troncoso, Loreto [3 ]
Perez-Ferreras, Susana [1 ]
Capel-Sanchez, Maricarmen [1 ]
Campos-Martin, Jose M. [1 ]
Antonio Alonso, Jose [3 ]
Fierro, Jose L. G. [1 ]
机构
[1] CSIC, Inst Catalisis & Petroleoquim, E-28049 Madrid, Spain
[2] Univ Tecnol Nacl, Fac Reg Cordoba, Ctr Invest & Tecnol Quim CITeQ, X5016ZAA, Cordoba, Argentina
[3] CSIC, Inst Ciencia Mat Madrid, E-28049 Madrid, Spain
关键词
Cermets; SCS; Methane; Partial oxidation; Hydrogen; STRUCTURAL-CHARACTERIZATION; NI/CEO2; CATALYSTS; SYNTHESIS GAS; CERIA; PT/CEO2; FUEL;
D O I
10.1016/j.ijhydene.2018.04.025
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
Catalysts based on Ni/(Ce(0.9)Ln(0.1)O(1.95)) (Ln = Gd, La, Nd and Sm) have been developed and tested for hydrogen production by partial oxidation of methane. The synthesis method (SCS, solution combustion synthesis) produces macroporous composite materials composed of ceramic (cer, Ce(0.9)Ln(0.1)O(1.95)) and metallic (met, Ni) phases, without the need of an activation stage prior to the catalytic reaction. The catalysts have been characterized by different techniques: X-ray diffraction, N-2 adsorption-desorption, Hg porosimetry, Scanning Electron Microscopy, Temperature Programmed Reduction, H-2 and O-2 pulse chemisorption, X-ray photoelectron spectroscopy and Raman spectroscopy. With the exception of the lanthanum-loaded catalyst, the catalysts are highly active, selective and stable; being the one doped with gadolinium the most efficient. Correlations structure activity point out that the excellent catalytic performance is related to the high catalytic surface area per unit mass of catalyst and to an appropriate balance of nickel dispersion to oxygen vacancies of the support. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:16834 / 16845
页数:12
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