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The Effect of Different Promoters (La(2)O(3), CeO(2), and ZrO(2)) on the Catalytic Activity of the Modified Vermiculite-Based Bimetallic NiCu/EXVTM-SiO(2) Catalyst in Methane Dry Reforming

[Image: see text] An X-NiCu/EXVTM-SiO(2) (X = La, Ce, and Zr) catalyst was successfully prepared by using modified vermiculite as a support by the impregnation method. This experiment investigated the effects of La(2)O(3), CeO(2), and ZrO(2) promoters on the activity of the NiCu/EXVTM-SiO(2) catalys...

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Detalles Bibliográficos
Autores principales: Meng, Zhaojun, Wang, Zijun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8587639/
https://www.ncbi.nlm.nih.gov/pubmed/34778636
http://dx.doi.org/10.1021/acsomega.1c03959
Descripción
Sumario:[Image: see text] An X-NiCu/EXVTM-SiO(2) (X = La, Ce, and Zr) catalyst was successfully prepared by using modified vermiculite as a support by the impregnation method. This experiment investigated the effects of La(2)O(3), CeO(2), and ZrO(2) promoters on the activity of the NiCu/EXVTM-SiO(2) catalyst. The study found that the addition of three different metal oxides did not improve the activity of the NiCu/EXVTM-SiO(2) catalyst. On the contrary, some Ni active sites were covered by the promoter, which reduced the number of active sites, resulting in its catalytic activity lower than NiCu/EXVTM-SiO(2). In addition, the promoted catalysts that were repeatedly calcined two times can significantly reduce the textural property as well as active sites of the catalyst, resulting in the lower activity. However, in X-NiCu/EXVTM-SiO(2), Ce-NiCu/EXVTM-SiO(2) showed relatively high initial catalytic activity, with the initial conversion rate of CH(4) reaching 60.1% and the initial conversion rate of CO(2) reaching 89.1%. This is mainly because the catalyst has a stronger basic site on the surface to facilitate the adsorption of CO(2) molecules, and the smaller metal particle size is also conducive to the cleavage of C–H bonds.