Highly coke resistant Mg-Ni/Al2O3 catalyst prepared via a novel magnesiothermic reduction for methane reforming catalysis with CO2: the unique role of Al-Ni intermetallicsElectronic supplementary information (ESI) available. See DOI: 10.1039/c8nr08447e

Addition of alkaline promoters is considered to be an effective way to improve the coking resistance of the metal/support composite catalysts for dry reforming of methane (DRM). The traditional metal/promoter/support composites for DRM catalysis are generally obtained from alkaline species impregnat...

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Bibliographic Details
Main Authors Feng, Xiaoqian, Liu, Jing, Zhang, Peng, Zhang, Qing, Xu, Luyang, Zhao, Liping, Song, Xuefeng, Gao, Lian
Format Journal Article
LanguageEnglish
Published 17.01.2019
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Summary:Addition of alkaline promoters is considered to be an effective way to improve the coking resistance of the metal/support composite catalysts for dry reforming of methane (DRM). The traditional metal/promoter/support composites for DRM catalysis are generally obtained from alkaline species impregnation and then high temperature H 2 reduction. This two-step process leads to a random distribution of metal-promoter interaction. We herein report a novel magnesiothermic method to reduce Ni from spinel precursor and introduce alkaline Mg( ii ) into the composite at the same time, which also gratifies the interaction between the promoter and metal nanoparticles (NPs). The reaction paths to Mg reduction are proposed. The as prepared catalysts show good activity and outstanding coking resistance in DRM. The Ni-Al intermetallics in the catalyst were found for the first time to play an important role in coking resistance as they can be in situ transformed into Ni nanoparticles and MgAl 2 O 4 with strong metal-support interaction during the DRM. Magnesiothermic method was used to synthesize Mg-Ni/Al 2 O 3 catalysts and Al-Ni intermetallics were found effective in coking resistance in DRM for the first time.
Bibliography:10.1039/c8nr08447e
Electronic supplementary information (ESI) available. See DOI
ISSN:2040-3364
2040-3372
DOI:10.1039/c8nr08447e