Cerium oxide (CeO2) was recently reported
to function
as a highly active heterogeneous catalyst in the flow synthesis of
2-imidazolidinone (EU) without gas-phase CO2 from ethylenediamine
carbamate (EDA-CA), the latter of which can be synthesized easily
from ethylenediamine (EDA) and ambient CO2, in an EDA solvent.
However, catalyst deactivation due to the surface deposition of polyurea-like
compounds has remained a grand challenge. In this study, in an attempt
to develop new catalysts with better stability than conventional CeO2 by tuning surface properties, the addition of a second metal
to CeO2 was examined in the kinetic region. Mn-doped CeO2 (Mn content = 1 wt %) prepared via a coprecipitation method
was found to be a more stable catalyst in the EU production with a
lower deactivation rate constant of 0.018 h–1 than
the pure CeO2 (0.058 h–1). Mn species
incorporated in the CeO2 lattice exhibited good resistance
against their leaching during the reactions operated in the EDA solvent,
leading to a higher stability of Mn-doped CeO2 catalysts
than the pure CeO2 and also Mn-loaded CeO2 that
readily underwent the leaching of Mn species during the reaction.
The origin of the better stability of Mn-doped CeO2 than
pure CeO2 was suggested from various characterization data
to be the decreased density of the acid sites. The high density of
acid sites of the pure CeO2 possibly leads to the multipoint
adsorption of polyurea-like compounds, resulting in the catalyst deactivation.
In contrast, the low density of acid sites has been suggested to retard
such undesirable interactions with catalyst poisons and thus improved
the catalyst stability in the EU production from EDA-CA in the EDA
solvent.