合成气
催化作用
甲烷
合金
二氧化碳重整
化学工程
空间速度
材料科学
氧化物
贵金属
金属
冶金
化学
有机化学
选择性
工程类
作者
Defang Liang,Yishuang Wang,Yaolin Wang,Mingqiang Chen,Xuanlan Xie,Chang Li,Jun Wang,Yuan Liang
标识
DOI:10.1016/j.ijhydene.2023.07.135
摘要
High tendency to sinter and carbon deposition becomes the choke point of Ni-based catalyst for its performance optimization in syngas generation via dry reforming of methane (DRM). Uniting the encapsulation of support with the construction of alloy interfaces, is a bright strategy to protect metallic Ni sites and synthesize highly efficient and stable Ni-based catalyst. Herein, M-Ni@S-1 catalysts (M = Pt, Pd, Ru, Au) with the same noble metal content (0.5 wt%) rather than moles were fabricated, and evaluated in DRM process. Results reveal that the type of noble metals influences the cooperating effect of the formed M − Ni alloy interface and support encapsulation degree, which achieves the best in Pt–Ni@S-1 catalyst. Therefore, Pt–Ni@S-1 catalyst exhibited outstanding sinter resistance and carbon tolerance as well as high catalytic stability, and obtained the highest methane conversion of approximately 80% at 700 °C and 60,000 mL·min−1·gcat−1 of GHSV. This can attribute to the small particle size of 3 nm, suitable metal-support interaction, abundant surface alkaline sites and stably existed Pt–Ni binary alloy interfaces.
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