摘要
The upgrading of underutilized methane in shale gas with anthropogenic CO 2 can produce the value-added syngas via dry reforming. Nickel-based catalysts, due to their efficiency and cost-effectiveness, have received widespread attention. However, Ni-catalyzed dry reforming of methane is usually subjected to sintering or coking-induced instability. To address these issues, a series of Al 2 O 3 -supported nickel nanoparticle catalysts with uniform sizes are synthesized by varying the calcination temperatures and applied in methane dry reforming (DRM). Ni/Al 2 O 3 -700 °C catalyst behaves better catalytic performance compared to the other catalysts, which can be attributed to its higher metal dispersion and stronger metal-support interaction. In addition, the abundant moderate-strength basic sites and optimal Al IV /Al VI ratio can promote the adsorption and activation of CO 2 and suppress the deep cracking of CH 4 for Ni/Al 2 O 3 -700 °C catalyst, respectively, causing the enhancement of anti-coking performance. Furthermore, combining CH 4 -temperature programmed surface reaction and in situ Fourier transform infrared spectroscopy demonstrates that the presence of CO 2 can promote the activation of CH 4 for Ni/Al 2 O 3 -700 °C catalyst, which is rate-determining step for DRM system. These findings provide valuable theoretical guidance for the rational design of Ni-based catalysts with enhanced catalytic performance.
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