Improving the Stability of CeO2Catalyst by Rare Earth Metal Promotion and Molecular Insights in the Dimethyl Carbonate Synthesis from CO2and Methanol with 2-Cyanopyridine

Identifier:  imarina:4090799

Handle: https://hdl.handle.net/20.500.11797/imarina4090799

Authors:  Stoian, D; Urakawa, A; Medina, F

Abstract:
© 2018 American Chemical Society. The unmatched efficiency of the direct dimethyl carbonate (DMC) synthesis from CO2and methanol over CeO2catalysts in the presence of an organic dehydrating agent (2-cyanopyridine, 2-CP) was recently reported with high DMC yield (>90%) in both batch and continuous operations. However, the CeO2catalyst gradually deactivates in the time scale of days due to suggested surface poisoning by 2-picolinamide (2-PA) produced by hydration of 2-CP. This work seeks active and stable CeO2-based catalysts and aims to understand the material factors influencing the catalytic performance. Surface modification of CeO2by the addition of rare earth metal (REM) was found to be effective for improving the catalyst stability. Surface basicity and reducibility of the Ce4+species play important roles in preventing catalyst deactivation by stabilizing the reactive methoxy species in comparison to the poisoning species (2-PA or species alike). This has been evidenced by in situ attenuated total reflection infrared spectroscopy. CeO2materials promoted with 1 wt % rare earth metals (La, Gd, and Pr) greatly enhanced the catalyst stability while retaining the high catalytic activity of CeO2. Among them, 1 wt % Pr promotion to CeO2was the most effective, affording 35% higher DMC yield in comparison to that of bare CeO2after 150 h on stream under the optimized reaction conditions of 30 bar and 120 °C.