MCM-41 supported nickel-based bimetallic catalysts with superior stability during carbon dioxide reforming of methane: Effect of strong metal–support interaction

Nickel-based bimetallic catalysts supported on MCM-41 mesoporous molecular sieves (Ni–Ti-, Ni–Mn-, and Ni–Zr–MCM-41) were prepared by direct hydrothermal synthesis. The catalytic properties were tested in methane reforming with CO2. All Zr-promoted catalysts exhibited comparable or enhanced initial catalytic activity as compared to Ni–MCM-41. Adding Zr4+ remarkably improved the long-term stability, whereas decreased lower initial activity and stability were observed for Ti- and Mn-modified catalysts. The addition of Zr4+ enhanced the structural stability and the dispersion of active Ni sites. The strong anchoring effect of Zr4+ and the partial activation of CO2 by Zr4+ contributed to the high catalytic activity and long-term stability. On the contrary, the decoration of Ni clusters with TiOx and MnOx species on Ni–Ti and Ni–Mn catalysts hindered the accessibility of Ni-active centers, thus decreasing their catalytic performance. The partial transformation of amorphous silica matrix into quartz and/or tridymite phases over Ni–Mn, Ni–Ti, and Ni–MCM-41 catalysts also played a negative role on their catalytic stability.

Graphical abstractNi–Zr–MCM-41 catalysts exhibited remarkably enhanced catalytic activity and long-term stability due to the anchoring effect of Zr4+ and partial activation of CO2 by Zr4+.Figure optionsDownload full-size imageDownload high-quality image (116 K)Download as PowerPoint slide