Characterization and catalytic behavior of hydrotalcite-derived Ni-Al catalysts for methane decomposition

被引:33
作者
Shi, Zemin [1 ]
Wan, Chunsheng [1 ]
Huang, Min [1 ]
Pan, Jinhua [1 ]
Luo, Ruizhi [1 ]
Li, Dalin [1 ]
Jiang, Lilong [1 ]
机构
[1] Fuzhou Univ, Coll Chem Engn, Natl Engn Res Ctr Chem Fertilizer Catalyst, Xueyuan Rd 1, Quanzhou, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
Catalytic methane decomposition; Hydrogen; Carbon nanomaterials; Nickel catalyst; Hydrotalcite-like compounds; COX-FREE HYDROGEN; THERMAL-DECOMPOSITION; NI/AL2O3; CATALYST; NI-AL2O3; CARBON NANOFIBERS; NI/SIO2; MG; PERFORMANCE; GENERATION; ALLOY;
D O I
10.1016/j.ijhydene.2020.04.141
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 series of Ni catalysts were prepared from Ni-Al hydrotalcite-like compounds (HTlcs) by varying the Ni/Al molar ratio (1-4) and calcination temperature (773-1173 K) of HTlcs. The catalysts were reduced with H-2 at 1073 K and tested for CH4 decomposition at 773-923 K on a thermal gravimeter. Various techniques including N-2 physical adsorption, XRD, H-2-TPR, XPS, HAADF-STEM, TEM, and Raman were applied to characterize the catalysts and the as-produced carbon. The characterizations show that calcination of Ni-Al HTlcs leads to Ni(Al)O solid solution and minor NiO and/or NiAl2O4 spinel may be formed depending on the Ni/Al ratio and calcination temperature; upon reduction at 1073 K, most nickel species are reduced to metallic Ni. In CH4 decomposition, carbon yield shows a volcano-type dependence on the Ni content with the optimum Ni/Al ratio equal to 3. On the otherhand, carbon yield is affected by the calcination temperature of the Ni3Al HTlcs to a small extent. Carbon yield is also significantly affected by the reaction temperature, which decreases remarkably with a rise of temperature to 923 K. TEM and Raman indicate that fish-bone carbon nanofibers are formed at 773-823 K, whereas multi-walled carbon nanotubes are formed at 873-923 K. (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:17299 / 17310
页数:12
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