Publication | Open Access
Solution combustion synthesis of Ni/La<sub>2</sub>O<sub>3</sub> for dry reforming of methane: tuning the basicity <i>via</i> alkali and alkaline earth metal oxide promoters
33
Citations
62
References
2021
Year
The production of syngas <i>via</i> dry reforming of methane (DRM) has drawn tremendous research interest, ascribed to its remarkable economic and environmental impacts. Herein, we report the synthesis of K, Na, Cs, Li, and Mg-promoted Ni/La<sub>2</sub>O<sub>3</sub> using solution combustion synthesis (SCS). The properties of the catalysts were determined by N<sub>2</sub> physisorption experiments, scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectrometry (XPS), and H<sub>2</sub>-TPR (temperature programmed reduction). In addition, their catalytic performance towards DRM was evaluated at 700 °C. The results demonstrated that all catalysts exhibited porous structures with high specific surface area, in particular, Mg-promoted Ni/La<sub>2</sub>O<sub>3</sub> (Mg-Ni-La<sub>2</sub>O<sub>3</sub>) which depicted the highest surface area and highest pore volume (54.2 m<sup>2</sup> g<sup>-1</sup>, 0.36 cm<sup>3</sup> g<sup>-1</sup>). Furthermore, Mg-Ni-La<sub>2</sub>O<sub>3</sub> exhibited outstanding catalytic performance in terms of activity and chemical stability compared to its counterparts. For instance, at a gas hourly space velocity (GHSV) of 30 000 mL g<sup>-1</sup> h<sup>-1</sup>, it afforded 83.2% methane conversion and 90.8% CO<sub>2</sub> conversion at 700 °C with no detectable carbon deposition over an operating period of 100 h. The superb DRM catalytic performance of Mg-Ni-La<sub>2</sub>O<sub>3</sub> was attributed to the high specific surface area/porosity, strong metal-support interaction (MSI), and enhanced basicity, in particular the strong basic sites compared to other promoted catalysts. These factors remarkably enhance the catalytic performance and foster resistance to coke deposition.
| Year | Citations | |
|---|---|---|
Page 1
Page 1