journal article·2021-08

Promotional Effect of Ni−Sn Interaction over Ni Supported on Sn‐incorporated MCM‐41 Catalysts for CO2 Reforming of CH4

Yutong Zhao, Zichun Wang, Wenjie Yang, Shengshen Gu, Xiaoxia Yang, Amanj Kheradmand, Xingmo Zhang, Yongming Luo, Jun Huang, Yijiao Jiang

ChemNanoMat· Volume 7· Issue 8
Publisher page

Abstract

Abstract Sintering of active Ni sites and deposition of coke remain challenging issues for catalytic dry reforming of methane. Herein, Ni supported on the Sn‐incorporated MCM‐41 catalysts were synthesized and tested for DRM process. The structural and physicochemical properties of fresh and spent samples were studied by N2 adsorption‐desorption, XRD, H2‐TPR, XPS, TEM, STEM‐EDS, Raman, and TGA techniques. It was revealed that Sn addition improved the dispersion and decreased the size of active Ni nanoparticles by tuning the charger transfer between Ni and Sn. The formation of Ni−SnOx interface provides more possibilities to activate CO2. The best results were obtained by 2Ni/Sn−MCM‐41 sample with the Ni/Sn mole ratio of 2 : 1, contributing CH4 conversion of 95% and CO2 conversion of 94% at 800 °C. Moreover, the presence of Sn increased the resistance to sintering of Ni‐based catalysts during the severe conditions, thereby the Ni nanoparticle size only appeared a slight growth after 32 h TOS. Combined with the characterization of the spent 2Ni/Sn−MCM‐41 sample, it was revealed that the coke deposition of the deactivated catalyst was dominated by amorphous carbon, which could be responsible for the desirable regeneration ability of the catalyst.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Catalysts for Methane Reforming · Catalytic Processes in Materials Science · CO2 Reduction Techniques and Catalysts

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

School of Engineering Macquarie University Sydney New South Wales 2109 Australia

Faculty of Environmental Science and Engineering Kunming University of Science and Technology Kunming 650500 P. R. China

School of Chemical and Biomolecular Engineering The University of Sydney Sydney New South Wales 2006 Australia

Funding

Australian Research Council

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