Evaluation of promoted Ni-based nanocatalysts in wall-coated microchannel reactor on the dry reforming of methane and effect of ultrasound waves on physiochemical properties of synthesized nanocatalysts

The deactivation of nickel catalysts in the dry reforming of methane (DRM) process has been one of the issues of interest to researchers. In this research, the effect of active phase and support promoter uses and synthesis method on synthesized Ni-Co/Al2O3-MgO nanocatalysts efficiency in wall coated microreactor on dry reforming of methane process studied. To determine the characteristics of the synthesized samples, XRD, BET, FESEM, and Ft-IR analyses have been performed. Analyses show that the use of ultrasound waves in the synthesis of catalysts improves the catalyst surface morphology so that about 82% of the particles of the synthesized sample are smaller than 100 nm and , increases the specific surface area to an average of 10%, and makes its structure smaller. Also, the total pore volume on the surface of the samples also shows a 10% increase. The use of promoters increases the catalyst activity and makes it more stable up to 18 h on stream. The use of a wall-coated microreactor improves heat transfer, easier access of reactants to active sites, no pressure drop, and higher activity than a conventional U-type fixed bed reactor. Nanocatalysts with Ni/Co = 5 and Al/Mg = 5 has shown the highest and most stable activity throughout the temperature range in the DRM process.

Automated summary

The deactivation of nickel catalysts in the dry reforming of methane process has been a concern for researchers. This study investigates the efficiency of synthesized Ni-Co/Al2O3-MgO nanocatalysts with different active phase and support promoter uses in a wall coated microreactor. The use of ultrasound waves in catalyst synthesis improves surface morphology and increases specific surface area and pore volume. Promoters enhance catalyst activity and stability, while the wall-coated microreactor improves heat transfer and access to active sites.