Journal
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 47, Issue 75, Pages 32071-32080Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2022.07.104
Keywords
Dry reforming of methane; Glycine; Carbon dioxide utilization; Ni catalyst; High dispersion; Metal-support interaction
Categories
Funding
- Open Research Subject of Zhejiang Key Laboratory of Petrochemical Environmental Pollution Control [2021Z01]
- Science and Technol- ogy Foundation of Zhoushan [2018C21013]
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Ni-based catalysts with glycine-assisted impregnation method were prepared and studied for the dry reforming of methane. The addition of glycine increased Ni dispersion and metal-support interaction, resulting in improved catalytic performance. Among the catalysts, Ni/SiO2-0.7G showed the best catalytic performance in the dry reforming of methane test.
Ni-based catalysts have been widely studied in reforming methane with carbon dioxide. However, Ni-based catalysts tends to form carbon deposition at low temperatures (<= 600 ?), compared with high temperatures. In this paper, a series of Ni/SiO2-XG catalysts were prepared by the glycine-assisted incipient wetness impregnation method, in which X means the molar ratio of glycine to nitrate. XRD, H-2-TPR, TEM and XPS results confirmed that the addition of glycine can increase Ni dispersion and enhance the metal-support interaction. When X >= 0.3, these catalysts have strong metal-support interaction and small Ni particle size. The Ni/SiO2-0.7G catalyst has the best catalytic performance in dry reforming of methane (DRM) test at 600 ?, and its CH4 conversion is 3.7 times that of Ni/SiO2-0G catalyst. After 20 h reaction under high GHSV (6 x 10(5) ml/g(cat)/h), the carbon deposition of Ni/SiO2-0.7G catalyst is obviously lower than that of Ni/SiO2-0G catalyst. Glycine-assisted impregnation method can enhance the metal-support interaction and decrease the metal particle size, which is a method to prepare highly dispersed and stable Ni-based catalyst. (c) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
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