Developing silicalite-1 encapsulated Ni nanoparticles as sintering-/coking-resistant catalysts for dry reforming of methane

被引:33
|
作者
Xu, Shanshan [1 ]
Slater, Thomas J. A. [2 ]
Huang, Hong [3 ]
Zhou, Yangtao [4 ]
Jiao, Yilai [4 ]
Parlett, Christopher M. A. [1 ,2 ,5 ,6 ]
Guan, Shaoliang [7 ]
Chansai, Sarayute [1 ]
Xu, Shaojun [5 ,8 ]
Wang, Xinrui [1 ]
Hardacre, Christopher [1 ]
Fan, Xiaolei [1 ]
机构
[1] Univ Manchester, Sch Engn, Dept Chem Engn & Analyt Sci, Oxford Rd, Manchester M13 9PL, England
[2] Diamond Light Source Ltd, Electron Phys Sci Imaging Ctr, Didcot OX11 0DE, Oxon, England
[3] Forschungszentrum Julich, Electrochem Proc Engn IEK 14, D-52425 Julich, Germany
[4] Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, 72 Wenhua Rd, Shenyang 110016, Peoples R China
[5] Res Complex Harwell, Rutherford Appleton Lab, UK Catalysis Hub, Harwell OX11 0FA, Oxon, England
[6] Univ Manchester Harwell, Diamond Light Source, Harwell Sci & Innovat Campus, Didcot OX11 0DE, Oxon, England
[7] Res Complex Harwell, Harwell XPS The EPSRC Natl Facil Photoelectron Sp, Didcot OX11 0FA, Oxon, England
[8] Cardiff Univ, Cardiff Catalysis Inst, Sch Chem, Cardiff CF10 3AT, Wales
基金
英国工程与自然科学研究理事会;
关键词
Silicalite-1; Encapsulated Ni catalyst; Dry reforming of methane; Anti-sintering; Anti-coking; CARBON-DIOXIDE; PARTICLE-SIZE; ZEOLITE; CO2; SHELL; CONFINEMENT; PERFORMANCE; CH4; NANOCATALYSTS; PROMOTER;
D O I
10.1016/j.cej.2022.137439
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The stability of catalysts in dry reforming of methane (DRM) is a known issue. In this paper an encapsulation strategy has been employed to improve the stability compared with conventional impregnation methods. Herein, nickel nanoparticles encapsulated in silicalite-1 were prepared using a range of methods including post treat-ment, direct hydrothermal and seed-directed methods to investigate the effect of synthesis protocol on the properties of catalysts, such as degree of encapsulation and Ni dispersion, and anti-coking/-sintering perfor-mance in DRM. The Ni@SiO2-S1 catalysts obtained by the seed-directed synthesis presented the full encapsu-lation of Ni NPs by the zeolite framework with small particle sizes (similar to 2.9 nm) and strong metal-support interaction, which could sterically hinder the migration/aggregation of Ni NPs and carbon deposition. There-fore, Ni@SiO2-S1 showed stable CO2/CH4 conversions of 80% and 73%, respectively, with negligible metal sintering and coking deposition (-0.5 wt%) over 28 h, which outperformed the other catalysts prepared. In contrast, the catalysts developed by the post-treatment and ethylenediamine-protected hydrothermal methods showed the co-existence of Ni phase on the internal and external surfaces, i.e. incomplete encapsulation, with large Ni particles, contributing to Ni sintering and coking. The correlation of the synthesis-structure-performance in this study sheds light on the design of coking-/sintering-resistant encapsulated catalysts for DRM.
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页数:12
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